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4443 Impact of Patient and Donor Factors on Successful Hematopoietic Stem Cell Transplantation for Acute T-Cell Leukemia/Lymphoma Patients in an Underserved Minority Population

Program: Oral and Poster Abstracts
Session: 625. T Cell, NK Cell, or NK/T Cell Lymphomas: Clinical and Epidemiological: Poster III
Hematology Disease Topics & Pathways:
Lymphoid Leukemias, ALL, Lymphomas, T Cell lymphoma, Diseases, Treatment Considerations, Biological therapies, Lymphoid Malignancies, Human, Transplantation (Allogeneic and Autologous)
Monday, December 9, 2024, 6:00 PM-8:00 PM

John Yan, MD1*, Parth Patel, MD2*, Simran Arjani, MD3*, Eliot A Rapoport, MD4, Brittany Moavero5*, Jhannine Verceles6*, Angela Czavar5*, Emma Cordover7*, Julie Nguyen8, Kira Gritsman, MD, PhD9, Noah Kornblum, MD9, Aditi Shastri, MD10, Ioannis Mantzaris, MD9, Nishi Shah, MBBS, MPH6, Ridhi Gupta, MD6, Marina Konopleva11, Amit Verma, MBBS8*, Eric J. Feldman, MD9*, Dennis L Cooper, MD6, Mendel Goldfinger6*, R. Alejandro Sica, MD9 and Lauren Shapiro, MD9

1Department of Medicine, Montefiore Medical Center, East Brunswick, NJ
2Dept of Medicine, Montefiore Medical Center, Bronx, NY
3Department of Internal Medicine, Montefiore Medical Center, Bronx, NY
4Department of Medicine, Montefiore Medical Center, Bronx, NY
5Montefiore Medical Center, Bronx, NY
6Montefiore Einstein Comprehensive Cancer Center, Blood Cancer Institute, Department of Oncology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY
7Montefiore Einstein Cancer Center, Montefiore Medical Center/Albert Einstein College of Medicine, New York, NY
8Albert Einstein College of Medicine, Bronx, NY
9Department of Oncology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY
10Hematology/Oncology, Montefiore Medical Center/ Albert Einstein College of Medicine, Bronx, NY
11Montefiore Einstein Comprehensive Cancer Center, Albert Einstein College of Medicine, Bronx, NY

Introduction

Adult T-cell leukemia/lymphoma (ATLL) is a rare but aggressive hematologic malignancy that disproportionately affects minorities. As minorities are currently underrepresented in the National Marrow Donor Program (NMDP), there remain significant challenges in achieving successful long-term outcomes through allogeneic hematopoietic stem cell transplantation (HSCT). There is currently limited data describing barriers that can delay timely access to this potentially curative treatment modality in this patient population. In this single-center retrospective study, we aimed to analyze various patient and donor factors impacting time and ability to reach successful HSCT for ATLL patients in an underserved minority population.

Methods

We retrospectively analyzed ATLL patients who were HLA typed at Montefiore Medical Center, Bronx, NY between 2013 and 2023. Demographic, clinical, and donor data were collected for each patient, including information from the NMDP registry search. Time-to-event data was collected relative to diagnosis date and included time to treatment initiation, patient HLA typing, donor HLA typing, and transplantation. We used chi-square and Mann-Whitney U Test for hypothesis testing to compare variable differences between the transplanted and non-transplanted cohorts. Univariate regression of time to transplant was then performed, with non-transplanted patients censored at last follow-up.

Results

Forty-four ATLL patients were HLA typed, and 20 (45%) underwent HSCT. The mean age at diagnosis was 54 years (range 25-76), with 23 (52%) being male. Ethnically, 33 (75%) were non-Hispanic black, 10 (23%) Hispanic, and one (2%) Asian. Subtypes included 21 (48%) with acute type and 23 (52%) with lymphomatous type ATLL. ECOG performance status was 0 or 1 in 41 patients (95%). Insurance coverage included Medicaid (50%), private and Medicare (18% each), and emergency Medicaid (9%). Excluding those in active transplant evaluation, there were no significant demographic or disease feature differences between transplant and non-transplant groups.

The median time to chemotherapy was 14 days, recipient HLA typing was 49 days, donor HLA typing was 100 days, and time to transplant was 274 days. Regarding treatment response, 45% had no response, 36% achieved complete remission (CR), 18% partial remission, and 5% relapsed. In the transplant cohort, 65% achieved CR and 5% were refractory, compared to 10% CR and 75% refractory in non-transplanted patients (p<0.001). On univariate analysis, relapsed/refractory disease before transplant significantly reduced transplant likelihood (p<0.01; HR 0.06). In addition, patients with three or more treatment lines (p=0.01, HR 0.23), recipient HLA typing beyond the median time of 49 days (p<0.01, HR 0.27), and donor HLA typing beyond the median of 100 days (p<0.01, HR 0.08) were also associated with lower transplant likelihood.

When analyzing NMDP match quality, only 30% of patients (n=13) had at least one potential 8/8 match, and 11% (n=5) had more than one. The transplant cohort had fewer full match donors (20%) compared to the non-transplant cohort (40%), and NMDP match presence was not significantly associated with transplant likelihood (p=0.82, HR 0.88). Among transplanted patients, 70% (n=14) used related donors (8 haploidentical, 6 full matches), 25% used unrelated donors (80% mismatched), and one patient (5%) underwent autologous HSCT. Among those excluded from transplant, 50% did not have any donor, 45% had related donors, and 5% had an unrelated donor. Reasons for transplant ineligibility included disease progression (60%), performance status decline (25%), patient choice (10%), and lastly social issues (5%).

Conclusions

Our retrospective study found that treatment refractoriness and prolonged time to HLA typing substantially reduced the likelihood of successfully reaching transplantation, underscoring an urgent need to improve frontline treatments and to prioritize expeditious patient/donor HLA typing. Surprisingly, NMDP match quality did not significantly affect transplant likelihood. This finding may be attributed to advancements in transplant techniques such as the use of post-transplant cyclophosphamide and abatacept, allowing greater access to HSCT in this minority population historically unable to find suitable quality matched donors, and mitigating other demographic and social barriers.

Disclosures: Gritsman: iOnctura: Research Funding. Shastri: Jassen: Consultancy; NACE & PeerView: Honoraria; Ryvu therapeutics: Research Funding; Geron: Speakers Bureau; Gilead, Rigel, Kymera: Consultancy; Kymera: Research Funding. Konopleva: MEI Pharma: Consultancy, Membership on an entity's Board of Directors or advisory committees; Servier: Speakers Bureau; Legend Biotech: Membership on an entity's Board of Directors or advisory committees; AbbVie: Consultancy, Membership on an entity's Board of Directors or advisory committees, Other: clinical trials, Research Funding; Intellisphere: Speakers Bureau; Adaptive: Consultancy; Dark Blue Therapeutics: Membership on an entity's Board of Directors or advisory committees; Syndax: Membership on an entity's Board of Directors or advisory committees; Klondike Biopharma: Research Funding; Sanofi Aventis: Consultancy; Vincerx: Consultancy; Novartis: Membership on an entity's Board of Directors or advisory committees; Curis: Consultancy; Auxenion GmbH: Membership on an entity's Board of Directors or advisory committees; Janssen: Consultancy, Other: clinical trials; Menarini Group: Consultancy, Membership on an entity's Board of Directors or advisory committees. Verma: Bakx: Current equity holder in publicly-traded company; Janssen: Honoraria; Stelexis: Honoraria; Eli Lilly: Research Funding; Curis: Research Funding; Medpacto: Research Funding; Incyte: Research Funding; BMS: Research Funding; prelude: Research Funding; Throws Exception: Current equity holder in publicly-traded company. Feldman: Stelexis: Consultancy.

*signifies non-member of ASH