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This article is based on two webinars organized by European hematology institutions. The first was arranged by the International Academy of Clinical Hematology (IACH) and was entitled ‘COVID-19 in hematological malignancies: a few practical issues’. This webinar, held in a question and answer format, was chaired by Mohamad Mohty, who was joined by Christian Chabannon — both of whom are from France.1 The second was organized by the European Hematology Association (EHA) and European Society for Blood and Marrow Transplantation (EBMT) and was entitled ‘COVID-19 and hematology patient care’.2 The key messages from both webinars have been summarized in this article; we hope you will find the recommendations useful to your clinical practice.
The COVID-19 pandemic is an evolving situation, and the Multiple Myeloma Hub would like to remind readers to check current guidelines in their own country, as recommendations provided in this article may have been superseded by other guidelines as more data are released.
The risk is significant because patients with hematological malignancies may have a higher likelihood of contracting SARS-CoV-2 and of developing more severe disease. This is because
The United Kingdom has classified patients with hematological malignancies as ‘vulnerable’; this population are being told to stay inside for a period of 12 weeks.
Table 1. Recommendations of the EHA and EBMT for hematologic diseases2
ABVD, doxorubicin + bleomycin + vinblastine + dacarbazine; allo-SCT, allogeneic stem cell transplant; AML, acute myeloid leukemia; auto-SCT, autologous stem cell transplant; CLL, chronic lymphocytic leukemia; COVID-19, Coronavirus Disease 2019; CRAB, symptoms experienced by most patients with multiple myeloma: calcium (elevated), renal failure, anemia, bone lesions; FL, follicular lymphoma; MCL, mantle cell lymphoma; MM, multiple myeloma; PCR, polymerase chain reaction; R-CHOP, rituximab + cyclophosphamide + hydroxydaunorubicin + Oncovin + prednisone; R-COP, rituximab + cyclophosphamide + vincristine + prednisone; SCT, stem cell transplant |
|
Hematologic disease |
Recommendation |
---|---|
Aggressive lymphomas |
Initial therapy: no change, outpatient visits as much as possible Visits: replaced with telemedicine Rescue therapy: delivered in the outpatient setting if possible Auto-SCT: defer |
Indolent lymphomas |
Asymptomatic: watch-and-wait approach (instead of rituximab, for example) Chemotherapy: defer as much as possible; use R-COP/R-CHOP regimens in place of bendamustine Maintenance: defer onset of rituximab, e.g. in patients with FL, and increase the intervals between rituximab cycles. Use ibrutinib for MCL and CLL |
Hodgkin lymphoma |
Localized stages: avoid radiotherapy (multiple sessions) Advanced stages: Use ABVD regimens or similar, telemedicine, and outpatient regimens with bendamustine for relapse. Defer auto-SCT and allo-SCT |
AML |
Before therapy: conduct a PCR test (mandatory) Induction: use standard regimens and extreme prophylactic measures Consolidation: aim to use home protocols Allo-SCT: do not excessively delay Relapsed patients: enroll in clinical trials if possible |
Multiple myeloma |
MM without CRAB symptoms: delay onset of treatment Initial and maintenance therapy: do not change for patients both eligible and ineligible for transplant COVID-19 infection: interrupt maintenance until infection resolved Clinic visits: decrease as much as possible using remote labs, telemedicine, and prescription delivery via mail SCT: delay until the pandemic abates |
Prophylactic measures to protect patients from respiratory infections2
Patients with multiple myeloma (MM) may be particularly affected by disruption to SCTs, since auto-SCT is a key treatment for these patients. Additionally, numerous combination therapies used in the frontline and relapsed setting contain dexamethasone, which is associated with pneumonia — a severe complication of treatment in this population of patients.1
Auto-SCT requires multiple visits to the hospital, each of which increase the risk of infection. Hospitals are restricting access in order to reduce the spread of the virus, and so it is important to consider when and where to plan the auto-SCT1
For allo-SCT, it is difficult in the current situation to obtain grafts from unrelated donors, especially when the donor is located in a different country. Therefore, it is recommended that each patient is carefully evaluated, as patients undergoing SCT are at risk of needing access to intensive care unit (ICU) beds. Physicians should aim to reduce the burden on ICU beds and their ICU colleagues during the pandemic, so the timing of transplant must be carefully considered.1
In many cases, as with myeloproliferative neoplasms, second transplant, or patients with refractory disease, there is unlikely to be an impact on patient outcome if allo-SCT is delayed. Therefore, it is recommended to convert to non-transplant modalities. Additionally, it is important to consider whether the SCT is consolidative or curative.1
With regards to chimeric antigen receptor (CAR) T-cell therapy, where relapsed NHL and CD19-positive lymphomas are prime indications, the speakers noted the following1:
All decisions should account for the probability of needing to send the patient to ICU and the ICU bed availability.1
Read more about the EBMT recommendations for transplant centers and advice for donors and recipients of SCT here.
The speakers thanked all HCPs worldwide for their ongoing efforts and dedication in maintaining the excellent quality of care being given to patients. They encouraged everyone to stay safe and take good care of themself and their family.
Mohty M & Chabannon C International Academy of Clinical Hematology (IACH) webinar: COVID-19 in hematological malignancies: a few practical issues. Mar 26, 2020.
Rambaldi A, Ribera JM, von Lilienfeld-Toal M, Mikulska M. EHA and EBMT webinar: COVID-19 and hematology patient care. Apr 1, 2020.
Zhang X, Song K, Tong F, et al. First case of COVID-19 in a patient with multiple myeloma successfully treated with tocilizumab. Blood Adv. 2020;4(7):1307-1310. DOI: 1182/bloodadvances.2020001907
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