“Waitlist mortality” is high for myeloma patients with limited access to BCMA therapy

BackgroundThe first-in-class approved BCMA CAR-T therapy was idecabtagene vicleucel (ide-cel), approved in March 2021, for RRMM patients who progressed after 4 or more lines of therapy. Despite the promising outcomes, there were limited apheresis/production slots for ide-cel. We report outcomes of p...

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Main Authors: Nausheen Ahmed, William Wesson, Muhammad Umair Mushtaq, Rajat Bansal, Haitham AbdelHakim, Sarah Bromert, Allison Appenfeller, Batool Abu Ghazal, Anurag Singh, Sunil Abhyankar, Siddhartha Ganguly, Joseph McGuirk, Al-Ola Abdallah, Leyla Shune
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-08-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fonc.2023.1206715/full
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author Nausheen Ahmed
William Wesson
Muhammad Umair Mushtaq
Rajat Bansal
Haitham AbdelHakim
Sarah Bromert
Allison Appenfeller
Batool Abu Ghazal
Anurag Singh
Sunil Abhyankar
Siddhartha Ganguly
Siddhartha Ganguly
Joseph McGuirk
Al-Ola Abdallah
Leyla Shune
author_facet Nausheen Ahmed
William Wesson
Muhammad Umair Mushtaq
Rajat Bansal
Haitham AbdelHakim
Sarah Bromert
Allison Appenfeller
Batool Abu Ghazal
Anurag Singh
Sunil Abhyankar
Siddhartha Ganguly
Siddhartha Ganguly
Joseph McGuirk
Al-Ola Abdallah
Leyla Shune
author_sort Nausheen Ahmed
collection DOAJ
description BackgroundThe first-in-class approved BCMA CAR-T therapy was idecabtagene vicleucel (ide-cel), approved in March 2021, for RRMM patients who progressed after 4 or more lines of therapy. Despite the promising outcomes, there were limited apheresis/production slots for ide-cel. We report outcomes of patients at our institution who were on the “waitlist” to receive ide-cel in 2021 and who could not secure a slot.MethodsWe conducted a retrospective review of RRMM patients evaluated at the University of Kansas Cancer Center for ide-cel from 3/2021-7/2021. A retrospective chart review was performed to determine patient and disease characteristics. Descriptive statistics were reported using medians for continuous variables. Survival analysis from initial consult was performed using Kaplan-Meier Survival estimator.ResultsForty patients were eligible and were on the “waitlist” for CAR-T. The median follow-up was 14 months (2-25mo). Twenty-four patients (60%) secured a production slot and 16 (40%) did not. The median time from consult to collection was 38 days (8-703). The median time from collection to infusion was 42 days (34-132 days). The median overall survival was higher in the CAR-T group (NR vs 9 mo, p<0.001).Conclusion(s)Many patients who were eligible for ide-cel were not able to secure a timely slot in 2021. Mortality was higher in this group, due to a lack of comparable alternatives. Increasing alternate options as well as improvement in manufacturing and access is an area of high importance to improve RRMM outcomes.
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spelling doaj.art-2b8971cfcaa84a3c9175b572237e88142023-08-04T01:35:50ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2023-08-011310.3389/fonc.2023.12067151206715“Waitlist mortality” is high for myeloma patients with limited access to BCMA therapyNausheen Ahmed0William Wesson1Muhammad Umair Mushtaq2Rajat Bansal3Haitham AbdelHakim4Sarah Bromert5Allison Appenfeller6Batool Abu Ghazal7Anurag Singh8Sunil Abhyankar9Siddhartha Ganguly10Siddhartha Ganguly11Joseph McGuirk12Al-Ola Abdallah13Leyla Shune14Division of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesSchool of Medicine, University of Kansas, Kansas, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesMary and Ron Neal Cancer Center, Houston Methodist Hospital, Houston, TX, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesDivision of Hematologic Malignancies & Cellular Therapeutics, University of Kansas Cancer Center, Westwood, KS, United StatesBackgroundThe first-in-class approved BCMA CAR-T therapy was idecabtagene vicleucel (ide-cel), approved in March 2021, for RRMM patients who progressed after 4 or more lines of therapy. Despite the promising outcomes, there were limited apheresis/production slots for ide-cel. We report outcomes of patients at our institution who were on the “waitlist” to receive ide-cel in 2021 and who could not secure a slot.MethodsWe conducted a retrospective review of RRMM patients evaluated at the University of Kansas Cancer Center for ide-cel from 3/2021-7/2021. A retrospective chart review was performed to determine patient and disease characteristics. Descriptive statistics were reported using medians for continuous variables. Survival analysis from initial consult was performed using Kaplan-Meier Survival estimator.ResultsForty patients were eligible and were on the “waitlist” for CAR-T. The median follow-up was 14 months (2-25mo). Twenty-four patients (60%) secured a production slot and 16 (40%) did not. The median time from consult to collection was 38 days (8-703). The median time from collection to infusion was 42 days (34-132 days). The median overall survival was higher in the CAR-T group (NR vs 9 mo, p<0.001).Conclusion(s)Many patients who were eligible for ide-cel were not able to secure a timely slot in 2021. Mortality was higher in this group, due to a lack of comparable alternatives. Increasing alternate options as well as improvement in manufacturing and access is an area of high importance to improve RRMM outcomes.https://www.frontiersin.org/articles/10.3389/fonc.2023.1206715/fullBCMAide-celaccessproduction slotwaitlistmyeloma
spellingShingle Nausheen Ahmed
William Wesson
Muhammad Umair Mushtaq
Rajat Bansal
Haitham AbdelHakim
Sarah Bromert
Allison Appenfeller
Batool Abu Ghazal
Anurag Singh
Sunil Abhyankar
Siddhartha Ganguly
Siddhartha Ganguly
Joseph McGuirk
Al-Ola Abdallah
Leyla Shune
“Waitlist mortality” is high for myeloma patients with limited access to BCMA therapy
Frontiers in Oncology
BCMA
ide-cel
access
production slot
waitlist
myeloma
title “Waitlist mortality” is high for myeloma patients with limited access to BCMA therapy
title_full “Waitlist mortality” is high for myeloma patients with limited access to BCMA therapy
title_fullStr “Waitlist mortality” is high for myeloma patients with limited access to BCMA therapy
title_full_unstemmed “Waitlist mortality” is high for myeloma patients with limited access to BCMA therapy
title_short “Waitlist mortality” is high for myeloma patients with limited access to BCMA therapy
title_sort waitlist mortality is high for myeloma patients with limited access to bcma therapy
topic BCMA
ide-cel
access
production slot
waitlist
myeloma
url https://www.frontiersin.org/articles/10.3389/fonc.2023.1206715/full
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