应对恶性血液肿瘤在新型冠状病毒肺炎疫情中的挑战

Weathering the storm: COVID-19 infection in patients with hematological malignancies 应对恶性血液肿瘤在新型冠状病毒肺炎疫情中的挑战 1 2 3 4 first-author 1 2 3 4 1 2 3 4 1 2 3 4 corresp ‡Corresponding Authors ‡Corresponding Authors †E-mail:huyongxian2000@aliyun.comArnon.Nagler@sheba.health.gov.ilhuanghe@zju.edu.cn †E-mail:huyongxian2000@aliyun.comArnon.Nagler@sheba.health.gov.ilhuanghe@zju.edu.cn huyongxian2000@aliyun.com 5 corresp ‡Corresponding Authors ‡Corresponding Authors †E-mail:huyongxian2000@aliyun.comArnon.Nagler@sheba.health.gov.ilhuanghe@zju.edu.cn †E-mail:huyongxian2000@aliyun.comArnon.Nagler@sheba.health.gov.ilhuanghe@zju.edu.cn huyongxian2000@aliyun.com 1 2 3 4 corresp ‡Corresponding Authors ‡Corresponding Authors †E-mail:huyongxian2000@aliyun.comArnon.Nagler@sheba.health.gov.ilhuanghe@zju.edu.cn †E-mail:huyongxian2000@aliyun.comArnon.Nagler@sheba.health.gov.ilhuanghe@zju.edu.cn huyongxian2000@aliyun.com Bone Marrow Transplantation Center, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China Bone Marrow Transplantation Center, the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310003, China Zhejiang Province Engineering Laboratory for Stem Cell and Immunity Therapy, Hangzhou 310058, China Zhejiang Province Engineering Laboratory for Stem Cell and Immunity Therapy, Hangzhou 310058, China Institute of Hematology, Zhejiang University, Hangzhou 310058, China Institute of Hematology, Zhejiang University, Hangzhou 310058, China Zhejiang Laboratory for Systems & Precision Medicine, Zhejiang University Medical Center, Hangzhou 310058, China Zhejiang Laboratory for Systems & Precision Medicine, Zhejiang University Medical Center, Hangzhou 310058, China Hematology and Bone Marrow Transplantation Division, Chaim Sheba Medical Center, Tel-Hashomer 52621, Israel Hematology and Bone Marrow Transplantation Division, Chaim Sheba Medical Center, Tel-Hashomer 52621, Israel The coronavirus disease 2019 (COVID-19) is an emerging infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Within a matter of months, this highly contagious novel virus has led to a global outbreak and is still spreading rapidly across continents. In patients with COVID-19, underlying chronic diseases and comorbidities are associated with dismal treatment outcomes. Owing to their immunosuppressive status, patients with hematological malignancies (HMs) are at an increased risk of infection and have a worse prognosis than patients without HMs. Accordingly, intensive attention should be paid to this cohort. In this review, we summarize and analyze specific clinical manifestations for patients with coexisting COVID-19 and HMs. Furthermore, we briefly describe customized management strategies and interventions for this susceptible cohort. This review is intended to guide clinical practice. 新型冠状病毒肺炎(COVID-19)是一种由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的新型传染病.SARS-CoV-2具有极强的传染性,因此在引发流行病后又使其迅速升级为全球大流行,至今仍在部分国家迅速传播.在COVID-19的感染者中,存在肿瘤等慢性病或伴有相关合并症的患者预后往往较差.同时,由于恶性血液肿瘤患者长期处于免疫抑制状态,往往感染风险更高且预后更差,所以十分值得我们关注.这篇综述归纳并分析了恶性血液肿瘤患者合并COVID-19后的临床表现.此外,归纳了疫情期间恶性肿瘤的管理策略和感染后的综合干预措施,旨在为临床提供指导. Coronavirus disease 2019 (COVID-19) Hematological malignancies Immunosuppressive status Management strategies Treatment regimen 新型冠状病毒肺炎(COVID-19) 恶性血液肿瘤 免疫抑制 管理策略 治疗方案 Introduction 1 The coronavirus disease 2019 (COVID-19) has spread worldwide in the past ten months. By Oct. 9, 2020, according to the World Health Organization ( 2020 2020 ), a total of 36 361 054 cumulative confirmed cases and 1 056 186 deaths had been documented globally in 216 countries and territories across six continents. Recent epidemiological study has revealed that the highly infectious causal pathogen, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is commonly transmitted through respiratory droplets and close contact (Gu et al., 2020 2020 ). It has also been detected in the sputum, blood, stool (Gu et al., 2020 2020 ), urine (Jones et al., 2020 2020 ), and even tears (Xia et al., 2020 2020 ). At the molecular level, SARS-CoV-2 can enter host cells via interacting with angiotensin-converting enzyme 2 (ACE2) receptors located in various organs (Hamming et al., 2004 2004 ; Zhou P et al., 2020 2020 ), and therefore, could induce multiple-organ manifestations of infection (Gavriatopoulou et al., 2020 2020 ). The severity and clinical outcomes of COVID-19 vary among individuals. Up to now, an advanced age, high sequential organ failure assessment score, high D -dimer level on admission, and preexisting chronic diseases have been recognized as risk factors for dismal outcomes (Wang XH et al., 2020 2020 ; Zhou F et al., 2020 2020 ). In particular, patients with cancer have a remarkably elevated risk of COVID-19 and poorer outcomes than those in non-cancer cohorts, which can be explained by the systemic immunosuppressive state caused by the malignancies and anti-cancer therapies (Liang et al., 2020 2020 ). Hematological malignancies (HMs) are a group of heterogeneous blood diseases, including leukemias, lymphomas, and multiple myelomas (MMs) (Li et al., 2018 2018 ). According to the most recent statistics, both leukemia and non-Hodgkin lymphoma are among the top ten cancers in terms of incidence and death rates (Siegel et al., 2019 2019 ). As cancer progresses, malignant cells proliferate extensively and inhibit normal hematopoiesis. The suppression of leukopoiesis confers increased susceptibility to several infections, such as bacterial, fungal, and viral infections (Busca, 2012 2012 ). Though HMs remain challenging, the survival period and quality of life of patients with HMs have improved remarkably as a result of the introduction of chemotherapy, targeted therapy, monoclonal antibodies, and lately cell-based immunotherapy. However, these anti-cancer therapies might also expose patients to a higher risk of infection (Byrne et al., 2017 2017 ). Amid the COVID-19 outbreak, clinicians need to optimize the clinical management of HM patients in terms of treatment regimens, preventive measures for infection, clinical trials of novel therapies, and long-term follow-up. Recently, detailed case reports and cohort studies of COVID-19 in patients with preexisting HMs have become increasingly available in databases like PubMed, Web of Science, and medRxiv. Given the unfavorable outcomes of this susceptible group, strict vigilance is necessary to recognize and differentiate clinical manifestations, radiologic patterns, and laboratory findings. Moreover, the timely detection of COVID-19 and positive interventions are not only necessary to improve the survival rate of patients with HMs, but also to limit transmission among patients and caregivers. In this review, we outline recent reports of patients with coexisting COVID-19 and HMs. Also, we summarize the specific clinical manifestations. Based on recent guidelines and clinical experience, we have compiled a set of management strategies for HM patients and interventional strategies for patients with HMs and COVID-19. Regional reports of SARS-CoV-2 infections in patients with HMs 1 Owing to the characteristics of COVID-19 in HM cohorts, increasing numbers of case reports, large-cohort studies, and scattered clinical experiences have recently been presented. In this section, we summarize details of recent cases (Table 1 1 ) and provide an overview of several large-cohort studies. ALC, absolute lymphocyte count; ALL, acute lymphoblastic leukemia; ALT, alanine aminotransferase; AML, acute myeloid leukemia; ANC, absolute neutrophil count; APL, acute promyelocytic leukemia; Ara-C, cytarabine; AST, aspartate aminotransferase; ATO, arsenic trioxide; ATRA, all-trans retinoic acid; BNP, B-type natriuretic peptide; CLL, chronic lymphocytic leukemia; CML, chronic myeloid leukemia; COVID-19, coronavirus disease 2019; CPAP, continuous positive airway pressure; Cr, creatine; CRP, C-reactive protein; CRS, cytokine release syndrome; CTX, cyclophosphamide; DS, differentiation syndrome; FDG, fluorodeoxyglucose; GGO, ground-glass opacity; Hb, hemoglobin; HCQ, hydroxychloroquine; HGB, hemoglobin; HL, Hodgkin lymphoma; HMs, hematological malignancies; ICU, intensive care unit; IFN, interferon; IL, interleukin; IVIG, intravenous immunoglobulin; LDH, lactate dehydrogenase; MM, multiple myeloma; NA, not available; NHL, non-Hodgkin lymphoma; PET/CT, positron emission tomography/computed tomography; PLT, platelet; PT, prothrombin time; PCT, procalcitonin; PD1, programmed cell death protein 1; RT-PCR, real-time polymerase chain reaction; SaOЂ2ɽ, oxygen saturation; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; TKI, tyrosine kinase inhibitor; WBC, white blood cell Type of HM Patient demographics (gender, age, place) Symptom and incubation period Laboratory finding 2 Radiologic finding Treatment regimen (for COVID-19 and HM) Clinical outcome Comment Reference 3 T-cell ALL 3 Male, 8 years, China 3 Intractable fever, paroxysmal dry cough 3 WBC↓, ANC↓, ALC↓, HGB↓, PLT↓, IL-6↑, IL-10↑; Nucleic acid detection of SARS-CoV-2 ever turned to negative and soon back to positive 2 3 Lung inflammation and consolidation (initially); Floc-density shadow with GGOs (after antibiotic therapies) 3 CTX, Ara-C, up-leveled antibiotics, oxygen therapy, Arbidol, ribavirin, IFN, IVIG, etc. 3 Unstable and low SaOЂ2ɽ; Referral to ICU 1. Patients with agranulocytosis tend to develop multiple infections or secondary viral infections and have dismal outcomes; 3 Chen et al., 2020 2020 2. SARS-CoV-2 might exist for an extended period in HM patients; 3. Repetitive SARS-CoV-2 nucleic acid tests are needed to reduce false-negative rates and to detect the recurrence of infections. 2 B-cell ALL 2 Male, 3 years and 10 months, China 2 Cough (for nearly 33 d), fever 2 WBC↓, ALC↓, AST↑, ALT↑, CRP↑; Initial negative results of RT-PCR 2 2 Dense texture in both sides of the lungs 2 Discontinued chemotherapy, IFN, sulfamethoxazole, others 2 Recovery 1. Pediatric patients might bear longer durations of diagnosis than adults; 2 Zhao et al., 2020 2020 2. Prolonged duration of cough might be caused by a low viral load. 2 ALL 2 Female, 62 years, China 2 Initial stage: productive cough, fatigue; Progressive stage: fever, shortness of breath 2 Initial stage: normal; Progressive stage: hemocytopenia, PCT↑, BNP↑ 2 2 Mild infiltration in the right lung 2 Lopinavir/ritonavir, antibiotics 2 Recovery 1. Early symptoms of HM patients were uncharacteristic of the typical presentations of COVID-19; 2 Wu et al., 2020 2020 2. Mild COVID-19 might exacerbate the underlying hematologic diseases. 2 AML 2 Female, 13 years, Italy 2 Persistent fever 2 WBC↓, Hb↓, PLT↓, CRP↑ 2 2 Bilateral increased reticular marking 2 Anti-microbial and antifungal therapy, HCQ, lopinavir/ritonavir 2 Recovery 2 Highly immunocompromised children on anticancer therapy might have a favorable outcome under proper interventions. 2 Sieni et al., 2020 2020 2 APL 2 Male, 36 years, UK 2 Fever, cough, sweats 2 WBC↓, ANC↓, ALC↓, PLT↓, PT↑, d-dimer↑, ferritin↑, LDH↑, CRP↑ 2 2 Extensive, predominantly peripheral, consolidative changes 2 ATRA+ATO, enoxaparin, supportive management for COVID-19 2 NA 1. Both APL and COVID-19 are associated with coagulopathy, which raised diagnostic and therapeutic challenges; 2 Farmer et al., 2020 2020 2. Prophylactic corticosteroids to prevent DS should be reappraised in the context of COVID-19. 2 CLL (progressed) and NHL 2 Male, 39 years, China 2 Moderate fever, productive cough, dyspnea; 25 d 2 WBC↑, lymphocyte percentage↑ 2 2 GGOs and pleural fluid 2 Oral chlorambucil (reduced dose), IFN, IVIG, methylprednisolone 2 Remarkably improved 1. Laboratory findings are not reliable in HM patients; 2 Jin et al., 2020 2020 2. HM patients, as well as the glucocorticoids-therapy receivers, might have a longer incubation period. 2 CLL (4 cases) 2 Male, >70 years, Spain 2 Fever (4/4), dry cough (2/4), diarrhea (1/4) 2 Ferritin↑ (3/4), lymphocytopenia (2/4), d-dimer↑ (1/4) 2 2 Bilateral or single-lung infiltration 2 Lopinavir/ritonavir, hydroxychloroquine, azithromycin, others 2 Recovery (4/4) 1. The prevalence of CLL was defined as 0.95% (4/420); 2 Baumann, et al., 2020 2. Despite coexisting with various comorbidity, the course of COVID-19 was mild and controllable. 2 CML (accelerated phase) 2 Male, 47 years, China 2 Cough, fever, dyspnea, pharyngalgia 2 Lymphocytopenia 2 2 No sign of pneumonia 2 NA 2 Cured 2 Radiological findings of COVID-19 could be negative in CML. 2 Wang DY et al., 2020 2020 2 CML (chronic phase) 2 Female, 89 years, China 2 Cough, dyspnea (oxygen therapy ineffective) 2 Lymphocytopenia, ALT and AST↑, Cr↑, troponin- positive 2 2 Typical pneumonia patterns 2 NA 2 Succumbed after a 3-d hospitalization 1. Elderly patients with comorbidities have a poor prognosis and high mortality; 2 Wang DY et al., 2020 2020 2. The degree of lymphopenia is related to the severity of the disease. 2 CML (chronic phase) 2 Pregnant female, 26 years, Italy 2 Fever 2 Testing positive on the swab 2 2 NA 2 Paracetamol, antibiotics 2 Recovery 2 Chronic phase CML patients on TKI are not at higher risk of developing COVID-19. 2 Abruzzese et al., 2020 2020 2 MM 2 Male, 60 years, China 2 Aggravating chest tightness without fever or cough 2 ALC↓, CRP↑, IL-6↑ 2 2 Bilateral, multiple GGOs and pneumatocele located in both subpleural spaces 2 Thalidomide, moxifloxacin IV, methylprednisolone, tocilizumab, Arbidol tablets 2 Recovery 1. Symptoms of COVID-19 might be atypical with coexisting comorbidities; 2 Zhang et al., 2020 2020 2. IL-6 receptor inhibitor might be effective in alleviating cytokine storm in COVID-19. 2 HL 2 Female, 22 years, Ireland 2 Cough, fever, sore throat, chills, rigors 2 Lymphocytopenia, CRP↑, LDH↑, PLT↓ (transiently) 2 2 Infiltrates in the lower zones bilaterally 2 Pembrolizumab, lopinavir/ritonavir, antibiotics, HCQ and azithromycin, corticosteroids 2 Better 1. PD1-inhibitor-induced pneumonitis should be carefully differentiated in the context of COVID-19; 2 O'Kelly et al., 2020 2020 2. Amid COVID-19, dual pathology for lung injury, CRS should be noted when using a PD1 inhibitor. 2 NHL 2 Male, 78 years, Italy 2 Persistent fever, cough, dyspnea 2 RT-PCR on pharyngeal swab was twice tested negative for COVID-19 and turned to positive later 2 2 PET-CT: multiple FDG-avid lymphadenopathies and non-FDG-avid peripheral rounded GGO in the right upper lobe 2 Tocilizumab, CPAP ventilation 2 Worsen 1. False or delayed results of RT-PCR should be taken into consideration; 2 Zanoni et al., 2020 2020 2. Co-infection with other pathogens might influence the accuracy of RT-PCR. 2 Mantle cell lymphoma 2 Female, 52 years, France 2 Asthenia, abdominal pain, dry cough 2 Leukocytosis, LDH↑ 2 Early CT: no sign of pulmonary infection but multiple adenomegalies 2 NA 2 NA 2 The PET/CT features of COVID-19 were in accordance with recent publications. 2 Playe et al., 2020 2020 2 PET/CT: FDG-avid bilateral ground glass and subpleural curvilinear opacities In Wuhan, China, 128 hospitalized patients with HMs and 226 caregivers from two centers were included in a cohort study (He et al., 2020 2020 ). The calculated incidences of SARS-CoV-2 infection in HM and caregiver cohorts were 10% and 7%, respectively. Though no significant difference was found in terms of prevalence, subjects with HMs tended to develop severe COVID-19. Based on the data of 530 individuals with chronic myeloid leukemia (CML), another local study group in Hubei Province reported a SARS-CoV-2 infection prevalence of 0.9% in patients and 0.1% in healthy individuals (Baumann et al., 2020 2020 ). Note that advanced phase CML could enhance the risk of COVID-19, even if patients attained a complete cytogenetic response or significant molecular response. Meanwhile, in the UK, Cook et al. ( 2020 2020 ) conducted a real-world assessment, focusing on the clinical impact of COVID-19 in individuals with MMs. The risk of death was found to be significantly associated with male gender, advancing age, and other comorbidities. The authors also noted that patients with relapsed or refractory MM might be at the highest risk of dismal outcomes once infected. Moreover, multicenter retrospective research in China that focused on the same topic reported that HM patients have a poorer prognosis than solid tumor patients (Yang et al., 2020 2020 ). The European Myeloma Network (Terpos et al., 2020b 2020b ) and Malard and Mohty ( 2020 2020 ) published detailed management strategies for MM during the COVID-19 pandemic. In France, Malard et al. ( 2020 2020 ) studied consecutive adult patients with hematologic disorders at the Hematology Department of the Saint-Antoine Hospital, beginning on Mar. 9, 2020. After nearly one month, 25 patients with hemopathies had confirmed COVID-19. In this cohort, fever (22/25), cough (19/25), and shortness of breath (19/25) were the most common complaints at diagnosis. Complementary examinations were also typical, for example, lymphopenia (23/25) and bilateral ground-glass opacities (25/25). The HM cohort was at a higher risk of developing severe COVID-19 with acute respiratory distress syndrome. Within this cohort, patients with MM accounted for a high proportion, emphasizing the impact of steroid-involved chemotherapy. Foà et al. ( 2020 2020 ) collected data on adult patients with acute lymphoblastic leukemia (ALL) from 40 hematological centers in Italy during the COVID-19 outbreak. Notably, in the Philadelphia chromosome-positive (ph+) cohort, only one individual had verified COVID-19, and one was symptomatic but tested negative. The low infection rate supported the effectiveness of the tyrosine kinase inhibitor (TKI)-based “soft” approach for the treatment of ph+ ALL. Moreover, the effectiveness of this regimen has been identified in GIMEMA (Gruppo Italiano Malattie Ematologiche dell'Adulto) nationwide trials. More importantly, amid the COVID-19 pandemic, this regimen has reduced the hospitalization days and enabled home-based treatment. Subsequently, in Barcelona, Spain, 804 chronic lymphocytic leukemia (CLL) patients were registered, 420 of whom maintained follow-up. Of this CLL cohort, only four patients (0.95%) were diagnosed with symptomatic COVID-19. The details of the four infected individuals with CLL are summarized in Table 1 1 . These published case reports and cohort studies were performed at different research centers, with differences in various factors, such as medical level and treatment planning. Thus, an overview of their experiences could provide insight into optimal choices for patient care. Specific clinical manifestations, radiologic patterns, and laboratory findings in patients with COVID-19 and HMs 1 Clinical manifestations 2 In 2002 and 2003, most patients with SARS had a fever (99%–100%). In contrast, fever (43.8% on admission, 88.7% during hospitalization) and non-productive cough (67.8%) are not specific symptoms for COVID-19 (Guan et al., 2020 2020 ; Han et al., 2020 2020 ). Those asymptomatic SARS-CoV-2 carriers might contribute to the acceleration of COVID-19 transmission. Based on recent literature, patients with HMs are more likely to be asymptomatic carriers presenting with atypical and delayed COVID-19 symptoms. As shown in Table 1 1 , some COVID-19 patients with HMs might experience extended incubation periods (Jin et al., 2020 2020 ). Patients with HMs, along with COVID-19, might be non-febrile on admission or during the entire period of illness (Zhang et al., 2020 2020 ). Moreover, mild initial symptoms (e.g., a slight cough, dyspnea, or chest tightness) might be followed by rapid deterioration. Worse still, overlapping clinical manifestations of the infection and tumor would hinder diagnosis, as discussed in detail later. Radiologic findings 2 In most patients with COVID-19, the initial radiologic findings show multiple patchy shadows and interstitial changes in the lungs before the appearance of ground-glass opacities (Guan et al., 2020 2020 ). In HM cohorts, radiologic imaging findings might not be significantly typical or recognizable. Because of their low immunity, lung imaging of patients might initially show mixed lesions of bacterial, viral, or fungal infections. Signs of viral infection would take time to emerge after the administration of antimicrobial and antifungal medications. In immunocompromised patients, the critical viral infection could lead to “extensive white lung,” which is caused mainly by the respiratory syncytial virus, cytomegalovirus, or SARS-CoV-2, individually or collectively. In clinical practice, we also discovered that patients with COVID-19 would have radiographic images and patterns of disease progression based on chest imaging (X-ray and computed tomography (CT) scan) similar to those of patients with cytomegalovirus-related pneumonia with diffuse large B-cell lymphoma (Fig. 1 1 ). Therefore, besides radiologic imaging, a definite diagnosis would be required with nasopharyngeal swabs or bronchoalveolar lavage samples, testing for COVID-19 and other pathogens. These two types of pneumonia (COVID-19 vs. CMV) showed a somewhat similar progression in the initial stage, progressive stage, and consolidation stage/diffuse infiltration stage of infection. Initially, both presented with typical GGOs. (a) Chest imaging of COVID-19 pneumonia. A 51-year-old male was confirmed with COVID-19 and received CT scans on 4, 8, and 15 February, 2020. (b) Chest imaging of CMV pneumonia. A 26-year-old male with diffuse large B cell lymphoma (non-GCB, IVB stage) was diagnosed with CMV pneumonia during chemotherapy. He received CT scans on 4, 7, 22 March, 2020. COVID-19, coronavirus disease 2019; CMV, cytomegalovirus; CT, computed tomography; GCB, germinal center B-cell-like lymphoma; GGOs, ground-glass opacities Laboratory tests 2 The characteristic laboratory features of COVID-19 include lymphocytopenia, leukopenia, and thrombocytopenia (Guan et al., 2020 2020 ). However, in patients with HMs, laboratory results are not as reliable as those for COVID-19 patients without such malignancies. Hematological neoplasms and treatment regimens might influence the blood system to variable degrees. For example, leukemia cells could boost leukocyte counts to abnormally high levels, whereas other malignant cells could impair the function of hematopoiesis and leukopoiesis. Moreover, the unexplained phenomenon of “COVID-induced lymphocytosis (CIL),” with remarkably elevated levels of leukocytes and lymphocytes, was observed in patients with CLL (Paneesha et al., 2020 2020 ). Additionally, high-dose chemotherapeutic agents and lymphocyte-targeted immunotherapy would influence normal hematopoiesis and deplete lymphocytes non-selectively. For example, rituximab, an anti-CD20 monoclonal antibody, and chimeric antigen receptor (CAR) T-cell therapy were designed to effectively recognize and lyse malignant and non-malignant B-cells (Freeman and Sehn, 2018 2018 ; June and Sadelain, 2018 2018 ). Furthermore, severe COVID-19 could be characterized by a hyper-inflammatory status with a significant elevation of serum cytokines and chemokines (Mehta et al., 2020 2020 ). High serum procalcitonin, ferritin, C-reactive protein, lactate dehydrogenase, interleukin-6 (IL-6), and D -dimer levels are associated with a dismal prognosis for COVID-19, prompting timely intervention to improve clinical outcomes (Lagunas-Rangel, 2020 2020 ; Terpos et al., 2020a 2020a ). Undeniably, microbial pathogen detection and serological tests are the most accurate methods to diagnose COVID-19, even in patients with HMs. Using real-time polymerase chain reaction (RT-PCR) and next-generation sequencing, it is possible to identify SARS-CoV-2 nucleic acids from various specimen types like nasopharyngeal swabs, sputum samples, and blood samples. With respect to serological tests, immunoglobulin M (IgM) specific to SARS-CoV-2 can be detected nearly 3 d after infection, and IgG levels increase four-fold during the recovery phase. However, for subjects with negative RT-PCR results, typical CT patterns could be found in more than 70% of suspected individuals (Ai et al., 2020 2020 ). Therefore, it is better to increase the frequency of examination or combine nucleic acid tests with serological tests (or imaging results) to improve the COVID-19 detection rate in patients with HMs. Clinical diagnostic criteria and differential diagnoses of patients with COVID-19 and HMs 1 During the COVID-19 pandemic, clinical diagnostic criteria are essential to differentiate between infected and non-infected cohorts efficiently. In line with the certainty of diagnosis, these criteria divide patients into three categories, specifically “surveillance cases,” “clinically COVID-19 suspected cases,” and “confirmed COVID-19 cases” (Table 2 2 ). In clinical practice, the efficient identification of “suspected cases” is an urgent and challenging issue, especially in HM cohorts, due to diverse manifestations with various confounding factors. Besides SARS-CoV-2, pneumonia in patients with HM could be induced by other viruses, fungal pathogens, or even medications. Table 3 3 clearly describes the similarities and unique features of various types of pneumonia in patients with HMs. According to the Chinese guidelines for COVID-19, suspected cases can be ruled out if an individual tests negative twice in the SARS-CoV-2 nucleic acid test and achieves negative serological results 7 d after disease onset. As a side note, samples for nucleic acid detection should be collected using a throat swab or nasal swab (at longer than a 1-d interval). # Involvement of lung was graded by “+/++/+++/++++”: +, 10%– < 25%; ++, 25%– < 50%; +++, 50%– < 75%; ++++, no less than 75%. Allo-HCT, allogeneic hematopoietic cell transplantation; ARDS, acute respiratory distress syndrome; BAL, bronchoalveolar lavage; CMV, cytomegalovirus; GGO, ground-glass opacity; HMs, hematological malignancies; HPIV, human parainfluenza virus; MTX, methotrexate; RSV, respiratory syncytial virus; RTX, rituximab; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2 2 Characteristics 6 Viral pneumonia 2 Fungal pneumonia 2 Drug-induced pneumonia 1 COVID-19 1 Adenovirus pneumonia 1 CMV pneumonia 1 RSV pneumonia 1 Influenza virus pneumonia 1 HPIV pneumonia Causative factor SARS-CoV-2 Adenovirus CMV RSV Influenza virus HPIV Pneumocystis jirovecii Medicine (e.g., MTX, RTX) Epidemiology Travel history to an area with high prevalence or contact history with infected patients Year-round Mostly after allo-HCT Seasonal variation of incidence Seasonal variation of incidence Year-round Common in immunodeficiency patients 2 Symptoms and signs 6 Common symptoms: onset with symptoms of upper respiratory infection, such as fever, headache, sore throat, and nasal congestion. When it progresses to pneumonia, most develop a non-productive cough with persistent high fever, dyspnea, etc. Their manifestations vary from asymptomatic patterns to end-organ damage, such as ARDS. 2 Fever, non-productive cough, dyspnea, etc. 2 Dyspnea, fever, cough 6 Common signs: diminished breath sounds with wheezing rales or crackles. 2 Laboratory findings 6 Most viral infection induces a reduction of leukocytes and lymphocytes, whereas a routine blood test is not always reliable and typical. 2 Special staining of the sample from BAL 2 6 Combination of viral nucleic acid detection and antibody detection could differentiate various infections. CT imaging 6 Diffuse bilateral ground-glass infiltrates small multifocal nodules, bronchial vascular thickening, and/or airspace consolidation. Bilateral, patchy GGOs, and cystic lesions Diffuse interstitial infiltrates Distribution of lesions Peripheral Multifocal Diffuse Airway, multifocal Airway, multifocal Airway, multifocal GGO + # +++ ++++ + + + Common (not as common as in patients without HMs) Common Consolidation Uncommon +++ ++ + + + Uncommon Nodule Rare Centrilobular+ ++ Centrilobular+++ ++ Centrilobular++ Uncommon Pleural effusion Uncommon Common Rare Common Uncommon Uncommon Rare 9 References 6 Koo et al., 2018 2018 ; Fontana and Strasfeld, 2019 2019 Cordonnier et al., 2017 2017 Atzeni et al., 2013 2013 Another significant issue is the partial overlap between the common complaints of patients with HMs and patients with COVID-19. Fever, as a systemic warning symptom of COVID-19, is commonly observed in the hematology department. The causative factors, including infection, cancer, and treatment, should be dissected with meticulous attention (Table 4 4 ). Organ-specific manifestations of COVID-19 also partly resemble the symptoms of HMs. In a large retrospective study, the neurological complication of COVID-19 was observed in over 36.4% of infected patients, and 24.8% of infected patients presented symptoms from the central nervous system (CNS) (Gavriatopoulou et al., 2020 2020 ; Mao et al., 2020 2020 ). The most common CNS symptoms were dizziness and headache, which overlapped with the CNS involvement of leukemia or myeloma in patients with HMs. Kidney involvement, a typical complication of MM, is also common in SARS-CoV-2-infected individuals. For instance, a large prospective study, which involved both moderate and severe COVID-19 cases, demonstrated that 43.9% presented with proteinuria and 26.7% with hematuria on admission (Boulware et al., 2020 2020 ; Gavriatopoulou et al., 2020 2020 ). Moreover, in acute promyelocytic leukemia (APL), petechia on the skin, gingival hemorrhaging, and other familiar manifestations of coagulation dysfunction might disguise COVID-19-induced coagulation abnormalities (Wang YD et al., 2020 2020 ). aGVHD, acute graft versus host reaction; Ara-C, cytarabine; CAR-T, chimeric antigen receptor T cell; CMV, cytomegalovirus; CRS, cytokine release syndrome; HL, Hodgkin lymphoma; HSCT, hematopoietic stem cell transplantation; L -ASP, L -asparaginase; MTX, methotrexate; NHL, non-Hodgkin lymphoma; RSV, respiratory syncytial virus; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2 Causative factor Example Infectious fever Viral infections, including SARS-CoV-2, CMV, and RSV Fungal infections Bacterial infections Others, such as mycoplasma Treatment-associated fever Chemotherapeutics, such as high-dose MTX, L -ASP, and Ara-C aGVHD after HSCT CRS induced by CAR-T therapy Others Oncological fever NHL: body temperature >38 °C accompanied by weight loss or (and) night sweats HL: patients could present with unknown persistent fever; 1/6 patients could develop Pel Ebstein fever Others Governments’ restrictive measures, public anxiety, and a shift in the primary focus of medical staff to SARS-CoV-2 infection amid the pandemic might lead to underdiagnosis of symptoms in HM patients, deferral of hematological laboratory and radiological tests, and postponement of other hematological exams. Most acute leukemias deteriorate rapidly with severe complications, making prompt diagnosis and treatment crucial. Therefore, telephone calls, telemedicine, or digital platforms should be used to screen for suspicious hematological symptoms (Molica et al., 2020 2020 ). After a referral to a hospital, a comprehensive evaluation of SARS-CoV-2 and hematological disease should be performed simultaneously. General management strategies for patients with HMs during the COVID-19 pandemic 1 The outbreak of COVID-19 has not only had a massive impact on patients with HMs, but also posed tremendous challenges for medical institutions and medical staff. Routine medical procedures and standards for the diagnosis, treatment, follow-up, and prevention of nosocomial infections need to be adjusted to account for COVID-19. Considerations for hospital admission procedures 2 Patients with HMs are advised to follow different hospital admission procedures in view of the prevalence of COVID-19 in different areas of a hospital (Fig. 2 2 ). On admission, patients with HMs should be classified according to the risk stratification system for COVID-19 (Table 2 2 ). Those patients with a history of COVID-19 exposure or suspicious symptoms should be further investigated. Detailed contact history with exact locations, time, and individuals should be tracked and recorded. Also, blood tests, biochemical analysis, viral nucleic acid detection, viral antibody detection, and chest CT imaging are strongly recommended, to aid in decision-making regarding subsequent diagnostic processes and cancer regimens. (a) Admission procedures in areas with a high prevalence of COVID-19; (b) Admission procedures in areas with a low prevalence of COVID-19. CAR-T, chimeric antigen receptor T cell; COVID-19, coronavirus disease 2019; CT, computed tomography; HM, hematological malignancy; HSCT, hematopoietic stem cell transplantation; MDT, multidisciplinary team; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2 Cases that are consistent with one of the diagnostic items should be kept under clinical observation. Suspected cases refer to any individuals with a confirmed history of exposure, accompanied by two of the clinical manifestations. Cases that are compatible with each of the diagnostic items can be diagnosed as a confirmed case of COVID-19. COVID-19, coronavirus disease 2019; HMs, hematological malignancies; Ig, immunoglobulin; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; RT-PCR, real-time polymerase chain reaction. Stratified diagnosis criteria refer to Liang et al. ( 2020 2020 ), China National Health Commission ( 2020 2020 ), and Subspecialty Group of Hematology and Oncology, Society of Pediatrics of Hubei ( 2020 2020 ) Case category Criteria for diagnosis Surveillance a a 1. The patient presents with systemic or respiratory signs and symptoms, such as fever, fatigue, nausea, vomiting, and diarrhea. 2. The patient had a close contact with clinically suspected or confirmed COVID-19 cases. Suspected b b 1. History of exposure: The patient had a living history or travel history in and around areas with high COVID-19 prevalence or stayed in the community with suspected COVID-19 cases. The patient had close contact with individuals who had been to areas with high COVID-19 prevalence or the community with suspected COVID-19 symptoms. The patient was from one of the COVID-19 clusters. The patient had a contact history with confirmed COVID-19 patients. 2. Clinical manifestations: The patient presents with fever or respiratory symptoms like non-productive cough, dyspnea, and chest tightness. The imaging test of the patient shows pneumonia features with multiple spot shadows and interstitial changes. It could progress into multiple infiltration shadows on bilateral lung and pulmonary consolidation in severe cases; however, pleural effusion is rare. The total leukocyte count, granulocyte count, and (or) lymphocyte count could be reduced. When there are no definite or convincing etiologies to explain the clinical manifestations thoroughly. Confirmed c c 1. Positive nucleic acid detection of the SARS-CoV-2 from the samples (respiratory tract secretion, blood, etc.) by RT-PCR; 2. Sequencing of the SARS-CoV-2 viral genomes from samples of the respiratory tract or blood; 3. Both IgM and IgG serological results of SARS-CoV-2 test positive. Furthermore, each medical team should carefully weigh the advantages and disadvantages of each inclusion for clinical trials. Clinical trials allow access to off-label drugs or combinations that can be highly beneficial but are otherwise unavailable (Malard and Mohty, 2020 2020 ). Additionally, routine SARS-CoV-2 testing is also applicable in clinical trials before inclusion. For highly suspected or confirmed COVID-19 cases, HM patients should be transferred to assigned hospitals for further treatment and isolation. Moreover, a multidisciplinary team (MDT) involving hematologists, infectious disease experts, and other related specialists is necessary to discuss and tailor individualized treatment plans. Throughout the entire medical process, medical staff should be well-protected with full personal protective equipment. Considerations for hematological therapeutic regimens 2 Current options for the treatment of HMs include chemotherapy, immunotherapy, targeted therapy, hematopoietic stem cell transplantation (HSCT), radiotherapy, and cell-based therapy. All of these options would cause detrimental effects on hemopoietic functions, to some extent. Therefore, treatment needs to be adjusted during the COVID-19 outbreak. 5.2.1 Chemotherapy High-dose chemotherapy would severely impair the immune system via non-selective anti-cancer activity. Then, overcoming the sequelae of chemotherapy typically requires extensive medical equipment, medicine, or blood products. However, most medical equipment has been mobilized to emergency departments or COVID-19 wards during this critical period. Therefore, it is necessary to adjust conventional chemotherapy regimens for patients with HMs. The core ideas for converted regimens are as follows: (1) safe and effective oral chemotherapeutic drugs are preferable to reduce the duration of hospitalization; (2) therapeutic regimens should be simplified, with less frequent visits and shorter duration; (3) for patients maintaining remission, the dose of chemotherapy or the frequency of follow-up visits could be reduced; and (4) non-urgent chemotherapy or medical procedures should be deferred. For newly diagnosed patients with a high tumor burden or multiple high-risk genetic aberrations, the risks and benefits should be carefully weighed because underdosing might not kill the malignant cells efficiently and may induce tolerance to therapy. In Tables 5 5 – 7 7 , we briefly summarize the considerations for treatment regimens of common hematological cancers during the COVID-19 pandemic based on recommendations from the American Society of Hematology (ASH), the European Hematology Association (EHA), and other published guidelines. Before the administration of myelosuppressive treatment, it is vital to rule out COVID-19 infection. ALL, acute lymphoblastic leukemia; Allo-HSCT, allogeneic hematopoietic stem cell transplantation; AML, acute myeloid leukemia; APL, acute promyelocytic leukemia; ATRA, all-trans retinoic acid; ATO, arsenic trioxide; B-ALL, B cell-ALL; CAR-T, chimeric antigen receptor T cell; CLL, chronic lymphoblastic leukemia; CML, chronic myeloid leukemia; COVID-19, coronavirus disease 2019; CR, complete remission; DS, differentiation syndrome; G-CSF, granulocyte-colony stimulating factor; IVIG, intravenous immunoglobulin; 6-MP, 6-mercapto-purine; MTX, methotrexate; Ph, Philadelphia chromosome; R/R, relapsed or refractory; T-ALL, T-cell ALL; TKI, tyrosine kinase inhibitors Leukemia Induction treatment Consolidation and maintenance therapy R/R patient Reference 5 Acute leukemia  ALL Ph-positive: 1. TKI+minimal corticosteroid exposure 2. TKI+low-dose chemotherapy Ph-positive: 1. Consolidation therapy is not suggested for CR patients 2. TKI+corticosteroids (for maintenance therapy) B-ALL: 1. Inotuzumab 2. Blinatumomab or CD22 CAR-T (with enough medical resources) Gruber et al., 2009 2009 ; Gavillet et al., 2020 2020 ; Stock et al., 2020 2020  ALL Ph-negative: 1. Standard chemotherapy 2. Reduced dose for patients with high risk of complications 3. Minimized corticosteroids to relieve symptoms 4. G-CSF to facilitate the recovery of leukocyte count Ph-negative: 1. Consolidation therapy is not suggested for CR patients 2. Allo-HSCT 3. Vincristine+prednisone+6-MP+MTX (for maintenance therapy) T-ALL: 1. Standard nelarabine-based regimens 2. Salvage chemotherapy and targeted therapies when necessary Gavillet et al., 2020 2020 ; NCCN, 2020; Stock et al., 2020 2020  AML APL: 1. Targeted oral drugs (e.g., ATO+ATRA), for low-risk patients; for high-risk patients, regimens should include a cytotoxic agent 2. Dexamethasone (to prevent DS) APL: ATO to achieve a low relapse rate 2 1. Salvage intensive re-induction 2. HSCT, aggressive chemotherapy or targeted therapies Raza et al., 2020 2020 ; Tallman et al., 2020 2020  AML Non-APL: 1. “7+3” regimen 2. Preventive antimicrobial drugs+G-CSF 3. Targeted drugs with reduced doses 4. Adjusted blood supply standards Non-APL: 1. High-dose cytarabine+reduced-dose cytarabine (decreased to three cycles) 2. Oral BCL-2 inhibitor alone or combined with 5-azacitidine Gavillet et al., 2020 2020 ; NCCN, 2020; Tallman et al., 2020 2020 5 Chronic leukemia  CLL 3 1. First-line treatment like ibrutinib could be continued with less frequent follow-ups 2. Monoclonal anti-CD20 antibodies and IVIG 3. Avoid the combination of targeted therapy 4. Venetoclax should be cautiously prescribed if necessary, owing to the need for frequent hemogram monitoring Shadman et al., 2020 2020  CML 3 1. Newly diagnosed: first-line treatment of TKI with the close monitoring of hemograms 2. Accelerated phase: continuing TKI if clinical response is positive 3. For others, dose interruptions or reductions could be considered Mauro et al., 2020 2020 AAVD, brentuximab vedotin, doxorubicin, vinblastine, and dacarbazine; ABVD, doxorubicin, bleomycin, vinblastine, and dacarbazine; ASCT, autologous stem cell transplantation; CAR-T, chimeric antigen receptor T cell; CHOP-21, three-weekly cyclophosphamide, doxorubicin, vincristine, and prednisolone; COVID-19, coronavirus disease 2019; DLBCL, diffuse large B-cell lymphoma; G-CSF, granulocyte-colony stimulating factor; HL, Hodgkin lymphoma; 6-MP, 6-mercapto-purine; MTX, methotrexate; NHL, non-Hodgkin lymphoma; PD1, programmed cell death protein 1; PET/CT, positron emission tomography/computed tomography; R/R, relapsed or refractory; RTX, rituximab Lymphoma Induction treatment Consolidation and maintenance therapy R/R patient Reference HL Early stage: Four cycles of ABVD with an interim of PET-CT (favorable disease) Advanced stage: 1. ABVD+PET/CT 2. AAVD+G-CSF Conventional HL regimens+prophylactic antibiotics 1. Second-line regimens (e.g., gemcitabine-based regimens) 2. Brentuximab vedotin or PD1 antibodies Advani et al., 2020b 2020b ; ESMO, 2020b NHL (mainly focused on DLBCL) High-risk: 1. CHOP-21 regimens 2. G-CSF to minimize neutropenia Medium-risk: 1. Non-curative treatment could be delayed 2. Avoid T-cell suppressive agents (e.g., bendamustine) High-risk: Lenalidomide+RTX (R2) or lenalidomide+corticosteroids Others: 6-MP+MTX 1. High-dose chemotherapy+ASCT 2. Second-line chemotherapy 3. Lenalidomide-based therapy 4. Polatuzamab+bendamustine 5. CAR-T cell therapy Advani et al., 2020a 2020a ; ESMO, 2020a ASCT, autologous stem cell transplantation; COVID-19, coronavirus disease 2019; CRd, cyclophosphamide, lenalidomide, and dexamethasone; CyBorD, cyclophosphamide, bortezomib, and dexamethasone; DRd, daratumumab, lenalidomide, and dexamethasone; IRd, ixazomib, lenalidomide, and dexamethasone; KRd, carfilzomib, lenalidomide, and dexamethasone; PCL, plasma cell leukemia; Rd, lenalidomide and dexamethasone; R/R, relapsed or refractory; RVd, lenalidomide, bortezomib, and dexamethasone Multiple myeloma Induction treatment Consolidation and maintenance therapy R/R patient Reference Standard-risk 1. Lenalidomide, bortezomib, and dexamethasone (RVd regimen) 2. Oral ixazomib, lenalidomide, and dexamethasone (IRd regimen; 28-d cycle) 3. CRd regimen; 28-d cycle 4. DRd regimen for elderly patients 5. CyBorD regiment: the only approved initial therapy 6. Clinic visits at an interval of 4 weeks 7. Consider administering additional cycles of induction, and delaying transplant until the first relapse 1. Reduced dose of dexamethasone with follow-up for those with good responses after 3–4 cycles 2. Bortezomib on a weekly basis after 6–8 cycles 3. If remission after 10–12 cycles, lenalidomide 2 1. Salvage ASCT (for aggressive relapse or secondary PCL) 2. Daratumumab-based treatment Al Saleh et al., 2020 2020 ; Malard and Mohty, 2020 2020 ; Rajkumar et al., 2020 2020 High-risk 1. Twenty-eight-day cycle of carfilzomib, lenalidomide, and dexamethasone (KRd regimen) 2. High-dose melphalan and ASCT as first-line treatments 3. Weekly outpatient clinic visits 1. RVd or Rd regimens 2. Acquiring ASCT post-pandemic Al Saleh et al., 2020 2020 ; Rajkumar et al., 2020 2020 5.2.2 Immunotherapy Unlike chemotherapy, novel therapies, like monoclonal antibodies, bispecific T-cell receptor-engaging antibodies, and chimeric antigen receptor T cell (CAR-T) therapies, aim to precisely eradicate malignant cells by recognizing surface antigens on tumor cells in relapsed or refractory HMs. However, for CAR-T therapy, long-term B-cell aplasia would increase susceptibility to infections. Also, cytokine release syndrome, the most common toxicity associated with CAR-T therapy, would promote cytokine storms with COVID-19. Fortunately, Bachanova et al. ( 2020 2020 ) proposed appropriate strategies and useful guidelines for CAR-T therapy during the COVID-19 pandemic. 5.2.3 Hematopoietic stem cell transplantation HSCT is an established and indispensable therapy for helping advanced-stage patients to achieve long-term survival (Gruber et al., 2009 2009 ). Before its administration, patients should be treated with high-dose chemotherapy, inducing a relatively long period of pancytopenia and increasing susceptibility to various infections. However, its implementation is challenging during the COVID-19 pandemic. Therefore, strict measures, such as the use of rooms with laminar flow hoods or positive pressure isolation wards, should be adopted for this cohort. Furthermore, non-urgent transplantation procedures for patients with stable diseases could be deferred. Moreover, COVID-19 screening should be conducted for both donors and recipients (Ljungman et al., 2020 2020 ). To reduce the false-negative rate, the combination of SARS-CoV-2 nucleic acid and antibody tests should be performed at least twice at an interval of at least 24 h prior to HSCT. To minimize the influence of unpredictable factors, the cryopreservation of stem cells before the conditioning regimen and the preparation of a back-up donor is recommended by the European Society for Blood and Marrow Transplantation (Ljungman et al., 2020 2020 ). If a transplant candidate is diagnosed with COVID-19, HSCT should be delayed for at least three months. For individuals who were in close contact with patients with COVID-19, HSCT should not be performed for at least 14 to 21 d (Ljungman et al., 2020 2020 ). 5.2.4 Recommendations for regimen adjustments 5.2.4.1 Acute leukemia In acute myeloid leukemia (AML), the regimens differ remarkably between APL and non-APL. For non-APL, following a negative COVID-19 test, intensive induction chemotherapy is recommended with a curative intent (Raza et al., 2020 2020 ). Lower-intensity therapies such as a hypomethylating agent with venetoclax can be administered to people as outpatients to reduce exposure (DiNardo et al., 2019 2019 ). Moreover, the consolidation with high-dose cytarabine should be offered to individuals with negative COVID-19 testing. The dose could be lowered (from 3.0 to 1.5 mg/m 2 ) to shorten the duration of myelosuppression, and the cycles could be reduced (Mayer et al., 1994 1994 ; Burnett et al., 2013 2013 ; Brissot et al., 2020 2020 ). For APL, the regimen of “oral all-trans retinoic acid (ATRA) and arsenic trioxide” is more desirable for low-risk individuals, owing to the reduced duration of myelosuppression (Zhu and Huang, 2014 2014 ). High-risk patients must still receive a regimen that includes a cytotoxic agent. In ALL, glucocorticoids should be prescribed in a recommended dose, given the paucity of information on their potential adverse role in SARS-CoV-2 infections. Meanwhile, bacterial and fungal infections and the inherent risk of thrombotic complications should be prevented in advance (Brissot et al., 2020 2020 ). 5.2.4.2 Chronic leukemia Among patients with CLL, a “watch and wait” policy has been widely adopted during this epidemic. Notably, given the dismal outcome of infection, self-isolating should be strictly performed to limit a patient’s exposure to viral infection (Paneesha et al., 2020 2020 ). Because of the potential of Bruton tyrosine kinase (BTK) inhibitors to disturb pulmonary inflammation and immune response in COVID-19, they could be reserved for the treatment of CLL and other indications, such as mantle cell lymphoma and Waldenstrom macroglobulinemia (Scarfò et al., 2020 2020 ; Treon et al., 2020 2020 ). As for CML, the absolute risk of contracting a severe SARS-CoV-2 infection was lower than 1% (Ector et al., 2020 2020 ; Li et al., 2020 2020 ). Leukemia-associated factors, including no complete hematologic response and subjects in advanced phase CML, were found to be the risk factors of infection, whereas the use of TKI was not (Li et al., 2020 2020 ). Therefore, it was safe to continue their TKI. 5.2.4.3 Lymphoma Diffuse large B-cell lymphoma is the most common aggressive non-Hodgkin lymphoma. For newly diagnosed patients, R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone), as the standard regimen, is recommended to be performed immediately. Moreover, the cycle of R-CHOP could be reduced to four cycles if the positron emission tomography (PET) is negative at the end of treatment (di Ciaccio et al., 2020 2020 ). 5.2.4.4 Multiple myeloma As for MM, high-dose melphalan and autologous HSCT (ASCT) remain the standard care. At the same time, hemopoietic recovery takes a long time after this therapy. Therefore, it was recommended to perform induction regimens of up to six cycles to postpone the ASCT. In the standard-risk group, transplant could be delayed until the first relapse because no significant effect on overall survival rate has been observed in this adjusted regimen. In the high-risk group, ASCT should still be regarded as first-line therapy, and SARS-CoV-2 screening should be highlighted throughout the therapy (Malard and Mohty, 2020 2020 ). Referring to the current guidelines, Table 7 7 summarizes induction, consolidation, and maintenance therapies, and regimens for relapsed or refractory MM. Considerations for follow-up plans 2 Unfortunately, routine follow-up has been strongly influenced by traffic restrictions and travel bans during the COVID-19 pandemic. In this context, patients should seek medical care at the nearest hospital to ensure treatment in the shortest time and minimize opportunities for exposure to COVID-19. Furthermore, telemedicine could be introduced to enable communication between patients and doctors. Video conferencing platforms, such as Zoom, WeChat, and Skype, could be used for collaborations among different medical institutions. If infection or disease progression is suspected, patients could search for timely medical assistance. Once the travel bans are lifted, pre-planned treatment and follow-up strategies could be resumed. However, the screening and testing of suspected COVID-19 cases should be continued. The precautions of proper handwashing methods, masking, social distancing, and good personal hygiene should be disseminated and strictly practiced among vulnerable cohorts. Above all, the most effective method to prevent COVID-19 transmission is still likely to be vaccination, once it becomes available. Comprehensive intervention strategies for patients with COVID-19 and preexisting HMs 1 The coexistence of HMs and COVID-19 infection is rather complicated and challenging for medical experts. During comprehensive care, in severely infected cases, COVID-19 should be prioritized over HMs. Generally, patients with COVID-19 and HMs should be isolated, and comprehensive treatment strategies should be designed according to the severity of the disease. The core interventions include the clearance of viremia, relieving cytokine storms, and improving organ function. Aiming to target the direct action of the virus on multiple organs, antivirals (e.g., lopinavir/ritonavir, remdesivir) and antibodies (e.g., convalescent plasma) are under evaluation for their safety and feasibility for managing COVID-19 (Wiersinga et al., 2020 2020 ). Emerging evidence shows the favorable effect of convalescent plasma infusion on improving symptoms and biomedical indices, and proves that early administration with convalescent plasma is preferable before seroconversion for SARS-CoV-2. Convalescent plasma also shows an acceptable safety profile (Psaltopoulou et al., 2020 2020 ). Most other medications did not show significant benefits for patients (Wiersinga et al., 2020 2020 ). A cytokine storm initiated by SARS-CoV-2 would induce a series of adverse effects, such as a hypercoagulable inflammatory state, increasing the risk of secondary infections, and impairing humoral immunity (Chauhan et al., 2020 2020 ; Jamilloux et al., 2020 2020 ). Therefore, targeted immunomodulatory agents (e.g., tocilizumab, ruxolitinib) and anti-inflammatory agents (e.g., dexamethasone) have been used to curb cytokine storms. Thromboprophylaxis is necessary among COVID-19 patients. Low-molecular weight heparins are the first-line choice, and other antithrombotic treatments such as antithrombin could be integrated (Terpos et al., 2020a 2020a ). The monitoring of blood oxygen saturation and oxygen therapy should be appropriately and promptly adopted as hypoxemia, or cytokine release syndrome would contribute to the development of shock, tissue perfusion disorders, and even multiple organ failure. Oxygen saturation should be maintained at 93%–96% for patients without chronic pulmonary disease and at 88%–92% for patients with chronic type II respiratory failure. Artificial liver support systems and blood purification efficiently reduce the incidence of shock, hypoxemia, and respiratory distress syndrome (Liang et al., 2020 2020 ). For patients with HMs and COVID-19, the prophylactic use of antibiotics is necessary (quinolones, second-or third-generation cephalosporins, and β-lactamase inhibitor compounds). Alternatives, such as carbapenems, β-lactamase inhibitor compounds, linezolid, and vancomycin, can be used in critically ill patients. Supportive treatment and nutritional support are crucial to maintaining the balance of the intracellular environment. A perturbation of the intestinal microecological balance in patients with COVID-19 can result in gastrointestinal symptoms, such as diarrhea, abdominal pain, and even secondary infection. Therefore, patients with severe COVID-19 infection would benefit from regular oral feeding and enteral nutrition. With the improvement of fever, respiratory symptoms, and radiologic and laboratory results, patients with HMs could be discharged after approval of the MDT. Importantly, two consecutive nucleic acid tests from throat swab specimens should test negative, with a sampling interval of at least 24 h (Liang et al., 2020 2020 ). After discharge, patients with COVID-19 and HMs must continue two weeks of home quarantine and isolation. Personal hygiene measures, such as handwashing and mask-wearing, should be emphasized. Re-examinations should include liver and kidney functions, blood tests, nucleic acid tests of sputum and stool samples, and a pulmonary function test or lung CT scan, according to the patient’s condition. Remote management and telemedicine should be introduced for follow-ups (Balduzzi et al., 2020 2020 ). Conclusions 1 We have summarized atypical symptoms and features of patients with COVID-19 and HMs based on our broad experience and data, as well as the recently published literature. The prolonged incubation period, complicated laboratory patterns, and confounding radiologic findings might eventually lead to the misdiagnosis of COVID-19 in patients with HMs. Furthermore, we have described additional considerations related to the diagnosis, differential diagnosis, and management of patients with HMs based on our clinical experiences. Amid the COVID-19 pandemic, patients with HM should be managed individually based on the severity and type of disease. Hematological cancer treatments during this critical period should be adjusted on a case-by-case basis. For patients with HMs and confirmed COVID-19, timely supportive treatment, antiviral regimens, oxygen therapy, and prophylactic antibiotics should be administered. An overview of management strategies for patients with HMs during the COVID-19 pandemic is illustrated in Fig. 3 3 . ALSS, artificial liver support system; HM, hematological malignancy; COVID-19, coronavirus disease 2019; CT, computed tomography; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2 We have also acknowledged the importance of home-based oral chemotherapy to reduce clinic visits. Moreover, a simplified chemotherapy regimen with higher therapeutic efficacy and lower toxicity for patients with HMs is indispensable. Lastly, hematology wards should be alert and prepared for emergencies and disease outbreaks. 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This article does not contain any studies with human or animal subjects performed by any of the authors. 10.1631/jzus.B2000423 Project supported by the National Natural Science Foundation of China (Nos. 81770201 and 81730008) 2020-08-02 2020-09-16 2022-01-05 Copyright © Zhejiang University and Springer-Verlag GmbH Germany, part of Springer Nature 2020 2020 Journal of Zhejiang University-SCIENCE B (Biomedicine and Biotechnology) 12 21