Outcomes with COVID-19 in hematopoietic stem cell transplant and cellular therapy patients.

Authors

Muhammad Umair Mushtaq

Muhammad Umair Mushtaq

Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS

Muhammad Umair Mushtaq , Mary Luder , Moazzam Shahzad , Nausheen Ahmed , Haitham Abdelhakim , Rajat Bansal , Ramesh Balusu , Sibgha Gull Chaudhary , Shaun DeJarnette , Clint Divine , Robert Kribs , Leyla Shune , Anurag K Singh , Sunil H. Abhyankar , Siddhartha Ganguly , Joseph McGuirk

Organizations

Division of Hematologic Malignancies and Cellular Therapeutics, University of Kansas Medical Center, Kansas City, KS

Research Funding

No funding received
None

Background: The Coronavirus Disease 2019 (COVID-19) has caused over 25 million infections in the US with over 0.4 million deaths. Hematogenic stem cell transplant (HCT) or cellular therapy (CT) recipients have a high risk of mortality with COVID-19 due to profound immune dysregulation. We aimed to assess the outcomes with COVID-19 in HCT/CT recipients. Methods: A single-center prospective study was conducted, including all (n=40) adult HCT/CT patients who were diagnosed with COVID-19 at the University of Kansas from Apr 2020 to Jan 2021. Baseline and disease-related characteristics were ascertained from medical records. Data were analyzed using SPSS version 21 (SPSS Inc, Chicago, IL). Bivariate analyses, using chi-square and t-test, and logistic regression analyses were conducted. Results: The study included 40 COVID-19 patients (72.5% Oct 2020-Jan 2021), including allogeneic HCT (n=25), autologous HCT (n=13) and CAR-T CT (n=2) with median time since HCT/CT of 12.4 (1-201.9), 37.2 (0.4-118.7), and 3.8 (2.8-4.8) months. Seventy percent were Caucasians and 17.5 were Hispanics. Primary hematologic malignancy was myeloid (37.5%), lymphoid (35%) or plasma cell disorder (27.5%). Myeloablative conditioning was performed in 65% of patients. Donors were autologous (37.5%), matched sibling (17.5%), matched unrelated (22.5%) and haploidentical (22.5%). COVID-19 was mild (42.5%), moderate (42.5%) or severe (15%). Clinical findings included pneumonia (62.5%), hypoxia (25%) and ICU admission (17.5%) while therapies included remdesivir (47.5%), convalescent plasma (40%), dexamethasone (25%) and monoclonal antibodies (17.5%). Concurrent cancer treatment, other infections and active GVHD were reported in 25% (all myeloma), 20% and 32.5% of patients. After a median follow-up of 74 days (7-269), the mortality rate was 12.5% in all patients and 20% in allo-HCT patients. Significant predictors of COVID-19 severity included allogeneic HCT, concurrent immune suppression and elevated inflammatory markers. (Table). Conclusions: Hematopoietic stem cell transplant recipients have an increased risk of mortality with COVID-19. Our findings confirm the need for vaccination prioritization, close monitoring, and aggressive treatment in HCT/CT patients.

Total (n=40)Mild COVID (n=17)Moderate-severe COVID (n=23)P valueDeaths (n=5)
Age yrs, median (range)58 (24-77)55.5 (24-72)60 (25-77)0.27362 (25-72)
Males, n (%)27 (67.5)11 (65)16 (70)0.7464 (80)
Months since HCT/CT, mean (SD)35 (41)44 (32)28 (32)0.27942 (47)
Allogeneic HCT, n (%)25 (62.5)7 (41)18 (78)0.0175 (100)
Autologous HCT/CAR-T, n (%)15 (37.5)10 (59)5 (22)0.0170
Concurrent immune suppression, n (%)19 (47.5)4 (23.5)15 (65)0.0095 (100)
CRP, mean (SD)0.10. 1 (0.2)5.7 (5.2)<0.0017 (5.3)
Ferritin, mean (SD)1535 (2109)129 (377)2275 (2274)0.0012451 (1739)
Neutrophil-lymphocyte ratio, mean (SD)15 (24)5.5 (6.3)19.7 (28)0.04142.5 (45.6)

Disclaimer

This material on this page is ©2024 American Society of Clinical Oncology, all rights reserved. Licensing available upon request. For more information, please contact licensing@asco.org

Abstract Details

Meeting

2021 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Hematologic Malignancies—Leukemia, Myelodysplastic Syndromes, and Allotransplant

Track

Hematologic Malignancies

Sub Track

Allogenic Stem Cell Transplantation

Citation

J Clin Oncol 39, 2021 (suppl 15; abstr 7033)

DOI

10.1200/JCO.2021.39.15_suppl.7033

Abstract #

7033

Poster Bd #

Online Only

Abstract Disclosures

Similar Abstracts

First Author: Sibgha Gull Chaudhary

First Author: Phyo Thazin Myint