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December 05, 2020
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Registry sheds light on vulnerability of patients with hematologic malignancies, COVID-19

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Certain patients with hematologic malignancies and COVID-19 appeared at higher risk for severe infection and death, according to an analysis of data from an international registry presented at the virtual ASH Annual Meeting and Exposition.

The risk for death appeared highest among those who were older, had more severe infection, opted to forgo more intensive treatment and/or had a poorer cancer prognosis before COVID-19 infection, according to William A. Wood, MD, MPH, associate professor in the division of hematology/oncology at The University of North Carolina at Chapel Hill School of Medicine.

COVID-19 severity was strongly correlated with malignancy status at the time of diagnosis.
COVID-19 severity was strongly correlated with malignancy status at the time of diagnosis.

“In the early days of the COVID-19 pandemic, many hematologists were concerned that our patients could be at increased risk for adverse outcomes from COVID-19 infection for a variety of reasons — many of our patients are older, have underlying or treatment-induced comorbidities, have immune dysregulation or treatment-related immunosuppression and may already be susceptible to COVID-19 infection-related complications, such as thrombosis,” Wood, who also serves as a HemOnc Today Editorial Board Member, told Healio. “With this in mind, the ASH Research Collaborative facilitated the development of a COVID-19 registry.”

William Wood
William A. Wood

Launched in April, the ASH Research Collaborative COVID-19 Registry for Hematology includes voluntary contributions of clinical data from more than 100 international study sites. Researchers can aggregate de-identified data and make the results available to clinicians in near-real time, Wood added.

For the study, investigators pooled data from the registry on 656 patients (77% age 40 years; 60% men; 43% white) with various hematologic malignancies and laboratory-confirmed or presumptive diagnosis of COVID-19 infection. Among them, 57% had comorbidities reported, the most common of which included hypertension (50%) and diabetes (30%). More than half (57%) had leukemia, 25% had lymphoma and 18% had plasma cell neoplasms. Most (80%) had an expected survival of more than 12 months prior to COVID-19 infection.

The most common COVID-19-associated symptoms included fever (65%), cough (56%), dyspnea (39%) and fatigue (31%), whereas 11% reported no symptoms. Most patients received COVID-19-directed therapies, including azithromycin (n = 143), hydroxychloroquine (n = 137), convalescent plasma (n = 45) and remdesivir (Veklury, Gilead Sciences; n = 44).

Overall, 20% of patients died during the study period between April and November, including 33% of those who required hospital-level or ICU-level care. The mortality rate among those with ICU-level care was 65%.

Similar percentages (61% to 65%) of patients with leukemia, lymphoma or plasma cell disorders had moderate or severe COVID-19, Wood added.

COVID-19 severity was strongly correlated with malignancy status at the time of diagnosis, with 69% of those receiving initial treatment for a hematologic malignancy having moderate or severe disease compared with 50% in remission and 79% with relapsed or refractory disease.

Overall, 62% of patients with known severity status had moderate or severe COVID-19 infection. Among those aged younger than 19 years, 47% had moderate or severe disease, compared with 43% of those aged 19 to 39 years, 62% of those aged 40 to 69 years and 70% of those aged 70 years or older. The choice to forgo ICU care was strongly associated with age, with a 73% mortality rate among those who declined ICU-level care compared with 13% among those who did not.

Mortality rates differed significantly by prognosis. More than half (51%) of patients with pre-COVID-19 expected survival of less than 12 months died compared with 13% of patients with expected survival of more than 12 months. Mortality rates also differed significantly by malignancy status, with 21% mortality among those receiving initial treatment, 13% among those in remission and 36% among those with relapsed or refractory disease.

“Our findings suggest that patients with hematologic malignancies are a medically vulnerable group when it comes to COVID-19 infection,” Wood said. “It is therefore important for these patients and for the health care system to continue to take appropriate precautions to limit the risk [for] acquiring COVID-19.”

At the same time, most patients in study who acquired COVID-19 infection — and several who had severe disease and required ICU-level care — survived, Wood added.

“Thus, providing maximal care to patients with hematologic malignancies and COVID-19 infection appears appropriate if it is consistent with patient and family preferences. As the data mature, the registry may be able to better inform specific risks from specific treatments and specific underlying diseases, which could have an impact upon treatment decision-making,” he said.

The registry’s reliance on voluntary reporting, resulting in estimates that may not be the same as from a true population-based registry, served as a limitation of the study, according to Wood.

“This highlights the need for enhanced data-collection systems involving patients with underlying hematologic diseases,” he added. “The ASH Research Collaborative Data Hub is building programs that will help to address this gap, starting with sickle cell disease and multiple myeloma, and expanding to other diseases in the future. In the meantime, we encourage continued data collection to the ASH Research Collaborative COVID-19 Registry from hematologists around the world, so that the data resource we are building can be used to address further questions about COVID-19 and cancer that are relevant to hematologists. We encourage anyone who is interested to visit www.ashrc.org to learn more about the COVID-19 registry, view data summaries and, importantly, to contribute data.”