TY - JOUR
T1 - Association of Reduced-Intensity Conditioning Regimens with Overall Survival among Patients with Non-Hodgkin Lymphoma Undergoing Allogeneic Transplant
AU - Ghosh, Nilanjan
AU - Ahmed, Sairah
AU - Ahn, Kwang Woo
AU - Khanal, Manoj
AU - Litovich, Carlos
AU - Aljurf, Mahmoud
AU - Bacher, Vera Ulrike
AU - Bredeson, Christopher
AU - Epperla, Narendranath
AU - Farhadfar, Nosha
AU - Freytes, César O.
AU - Ganguly, Siddhartha
AU - Haverkos, Bradley
AU - Inwards, David
AU - Kamble, Rammurti T.
AU - Lazarus, Hillard M.
AU - Lekakis, Lazaros
AU - Murthy, Hemant S.
AU - Nishihori, Taiga
AU - Ramakrishnan, Praveen
AU - Rizzieri, David A.
AU - Yared, Jean A.
AU - Kharfan-Dabaja, Mohamed A.
AU - Sureda, Anna
AU - Hamadani, Mehdi
N1 - Funding Information:
Mayo Clinic and Foundation Rochester; Medac GmbH; Mediware; Memorial Sloan Kettering Cancer Center; Merck and Company Inc; Mesoblast; MesoScale Diagnostics Inc; Millennium, the Takeda Oncology Company; Miltenyi Biotec Inc; Mundipharma EDO; National Marrow Donor Program; Novartis Oncology; Novartis Pharmaceuticals Corporation; Omeros Corporation; Oncoimmune Inc; OptumHealth; Orca Biosystems Inc; the Patient-Centered Outcomes Research Institute; Pfizer Inc; Phamacyclics LLC; PIRCHE AG; Regeneron Pharmaceuticals Inc; REGiMMUNE Corporation; Sanofi Genzyme; Seattle Genetics; Shire; Sobi Inc; Spectrum Pharmaceuticals Inc; St Baldrick's Foundation; Swedish Orphan Biovitrum Inc; Takeda Oncology Company; The Medical College of Wisconsin; University of Minnesota; University of Pittsburgh; University of Texas–M. D. Anderson; University of Wisconsin–Madison; Viracor Eurofins; and Xenikos BV. Role of the Funder/Sponsor: The funding organizations had no role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. Disclaimer: The views expressed in this article do not reflect the official policy or position of the NIH, the Department of the Navy, the Department of Defense, the HRSA, or any other agency of the US Government. Additional Contributions: Jennifer Motl, BS (Medical College of Wisconsin), provided editorial support, which was funded by the Medical College of Wisconsin in accordance with Good Publication Practice guidelines.
Funding Information:
reported receiving grants and personal fees from Celgene Corporation, Janssen/Pharmacyclics, Seattle Genetics, and TG Therapeutics; receiving grants from Genentech and Forty Seven Inc; receiving personal fees from AbbVie, AstraZeneca, BMS, and Gilead/Kite outside the submitted work; participating in speakers bureaus for AbbVie, AstraZeneca, BMS, Celgene Corporation, Gilead, Janssen/Pharmacyclics, and Seattle Genetics; and consulting for Celgene Corporation, Gilead, Janssen/Pharmacyclics, Seattle Genetics, and TG Therapeutics. Dr Epperla reported receiving other compensation from AstraZeneca, Pharmacyclics, and Verastem Oncology outside the submitted work. Dr Ganguly reported receiving personal fees from Seattle Genetics outside the submitted work. Dr Lazarus reported receiving other compensation from Pharmacyclics, AstraZeneca, Seattle Genetics, and Genentech. Dr Nishihori reported receiving other compensation from Novartis AG and receiving other compensation from Karyopharm outside the submitted work. Dr Rizzieri reported receiving other compensation from the Center for International Blood & Marrow Transplant Research (CIBMTR) during the conduct of the study. Dr Kharfan-Dabaja reported receiving other compensation from Pharmacyclics and receiving other compensation from Daiichi Sankyo outside the submitted work. Dr Sureda reported receiving personal fees and nonfinancial support from Takeda; receiving personal fees from BMS, Celgene Corporation, Janssen, and Novartis AG; receiving grants and personal fees from Gilead Kite; receiving personal fees and nonfinancial support from Sanofi outside the submitted work; and receiving compensation from BMS, Celgene Corporation, Gilead, Incyte, Janssen, MSD, Novartis AG, Roche, Sanofi, Takeda, and the Lymphoma Working Party of the European Society for Blood and Marrow Transplantation. Dr Hamadani reported receiving grants from Astellas, Spectrum, and Takeda outside the submitted work; receiving research funding to their institution from Celgene Corporation, Janssen R&D, MedImmune, Merck, Millennium Pharmaceuticals, and Seattle Genetics; receiving consultancy fees from AbGenomics, ADC Therapeutics, AstraZeneca, Celgene Corporation, Cellerant Therapeutics, Incyte Corporation, Janssen R&D, Magenta Therapeutics, MedImmune LLC, Omeros, and Pharmacyclics; participating on the speakers bureaus for Sanofi Genzyme, TeneoBio, and Verastem; and receiving research support and funding from Astellas Pharma and Spectrum Pharmaceuticals. No other disclosures were reported.
Funding Information:
primarily by grant/cooperative agreement U24CA076518 from the Public Health Service and the National Cancer Institute (NCI), the National Heart, Lung, and Blood Institute (NHLBI), and the National Institute of Allergy and Infectious Diseases; grant/cooperative agreement U24HL138660 from the NHLBI and the NCI; grant U24CA233032 from the NCI; grants OT3HL147741, R21HL140314, and U01HL128568 from the NHLBI; contract HHSH250201700006C from the Health Resources and Services Administration (HRSA); grants N00014-18-1-2888 and N00014-17-1-2850 from the Office of Naval Research; subaward from prime contract award SC1MC31881-01-00 from the HRSA; subawards from prime grant awards R01HL131731 and R01HL126589 from the NHLBI; subawards from prime grant awards 5P01CA111412, 5R01HL129472, R01CA152108, 1R01HL131731, 1U01AI126612, and 1R01CA231141 from the NIH; and commercial funds from Actinium Pharmaceuticals Inc; Adaptive Biotechnologies; Allovir Inc; Amgen Inc; anonymous donation to the Medical College of Wisconsin; Anthem Inc; Astellas Pharma US; Atara Biotherapeutics Inc; Biomedical Advanced Research and Development Authority; Be the Match Foundation; bluebird bio Inc; Boston Children’s Hospital; Bristol-Myers Squibb Company; Celgene Corporation; Children’s Hospital of Los Angeles; Chimerix Inc; City of Hope Medical Center; CSL Behring; CytoSen Therapeutics Inc; Daiichi Sankyo Company Ltd; Dana Farber Cancer Institute; Enterprise Science and Computing Inc; Fred Hutchinson Cancer Research Center; Gamida-Cell Ltd; Genzyme; Gilead Sciences Inc; GlaxoSmithKline; HistoGenetics Inc; Immucor; Incyte Corporation; Janssen Biotech Inc; Janssen Pharmaceuticals Inc; Janssen Research and Development LLC; Janssen Scientific Affairs LLC; Japan Hematopoietic Cell Transplantation Data Center; Jazz Pharmaceuticals Inc; Karius Inc; Karyopharm Therapeutics Inc; Kite, a Gilead Company; Kyowa Kirin; Magenta Therapeutics;
Publisher Copyright:
© 2020 American Medical Association. All rights reserved.
PY - 2020/7
Y1 - 2020/7
N2 - Importance: Reduced-intensity conditioning and nonmyeloablative conditioning (RIC-NMAC) regimens are frequently used in allogeneic hematopoietic cell transplant (HCT) for non-Hodgkin lymphoma. However, the optimal RIC-NMAC regimen in allogeneic HCT for non-Hodgkin lymphoma is not known. Objective: To investigate whether RIC-NMAC regimens at a higher end of the intensity spectrum are associated with increased nonrelapse mortality and lower overall survival compared with RIC-NMAC regimens at the lower end of the intensity spectrum in patients with non-Hodgkin lymphoma undergoing allogeneic HCT. Design, Setting, and Participants: This cohort study used data from 1823 adult patients with non-Hodgkin lymphoma in the Center for International Blood and Marrow Transplant Research registry. Included patients underwent allogeneic HCT using matched related or unrelated donors between January 2008 and December 2016. Statistical analysis was performed from June 1, 2019, to February 10, 2020. Interventions: Patients received 1 of 4 RIC-NMAC regimens: fludarabine-intravenous busulfan (Flu-Bu), approximately 6.4 mg/kg (n = 458); fludarabine-melphalan (Flu-Mel140), 140 mg/m2(n = 885); fludarabine-cyclophosphamide (Flu-Cy) (n = 391); or Flu-Cy with 2 Gy total body irradiation (Flu-Cy-2GyTBI) (n = 89). Main Outcomes and Measures: The primary outcome was overall survival. Secondary outcomes were nonrelapse mortality, incidence of relapse, progression-free survival, and the incidence of acute and chronic graft-vs-host disease (GVHD). Results: Of 1823 patients, 1186 (65%) were male, with a mean (SD) age of 54.8 (9.9) years. The 4-year adjusted OS was 58% in the Flu-Bu cohort, 67% in the Flu-Cy-2GyTBI cohort, 49% in the Flu-Mel140 cohort, and 63% in the Flu-Cy cohort (P <.001). After adjustment for age, Karnofsky performance score, HCT comorbidity index, NHL subtype, remission status at HCT, and the use of antithymocyte globulin or alemtuzumab, the regression analysis showed a significantly higher mortality risk associated with Flu-Mel140 compared with Flu-Bu (hazard ratio [HR], 1.34; 95% CI, 1.13-1.59; P <.001). Compared with the Flu-Cy cohort, the Flu-Mel140 cohort had a higher risk of chronic GVHD (HR, 1.38; 95% CI, 1.15-1.65; P <.001). The Flu-Mel140 regimen was associated with a higher nonrelapse mortality risk (HR, 1.78; 95% CI, 1.37-2.31; P <.001) compared with the Flu-Bu regimen. Conclusions and Relevance: The findings suggest that use of the more intense RIC-NMAC regimen, Flu-Mel140, may have a negative association with overall survival and may be associated with higher nonrelapse mortality. The Flu-Bu and Flu-Cy regimens with or without 2GyTBI regimens appeared to provide comparable overall survival..
AB - Importance: Reduced-intensity conditioning and nonmyeloablative conditioning (RIC-NMAC) regimens are frequently used in allogeneic hematopoietic cell transplant (HCT) for non-Hodgkin lymphoma. However, the optimal RIC-NMAC regimen in allogeneic HCT for non-Hodgkin lymphoma is not known. Objective: To investigate whether RIC-NMAC regimens at a higher end of the intensity spectrum are associated with increased nonrelapse mortality and lower overall survival compared with RIC-NMAC regimens at the lower end of the intensity spectrum in patients with non-Hodgkin lymphoma undergoing allogeneic HCT. Design, Setting, and Participants: This cohort study used data from 1823 adult patients with non-Hodgkin lymphoma in the Center for International Blood and Marrow Transplant Research registry. Included patients underwent allogeneic HCT using matched related or unrelated donors between January 2008 and December 2016. Statistical analysis was performed from June 1, 2019, to February 10, 2020. Interventions: Patients received 1 of 4 RIC-NMAC regimens: fludarabine-intravenous busulfan (Flu-Bu), approximately 6.4 mg/kg (n = 458); fludarabine-melphalan (Flu-Mel140), 140 mg/m2(n = 885); fludarabine-cyclophosphamide (Flu-Cy) (n = 391); or Flu-Cy with 2 Gy total body irradiation (Flu-Cy-2GyTBI) (n = 89). Main Outcomes and Measures: The primary outcome was overall survival. Secondary outcomes were nonrelapse mortality, incidence of relapse, progression-free survival, and the incidence of acute and chronic graft-vs-host disease (GVHD). Results: Of 1823 patients, 1186 (65%) were male, with a mean (SD) age of 54.8 (9.9) years. The 4-year adjusted OS was 58% in the Flu-Bu cohort, 67% in the Flu-Cy-2GyTBI cohort, 49% in the Flu-Mel140 cohort, and 63% in the Flu-Cy cohort (P <.001). After adjustment for age, Karnofsky performance score, HCT comorbidity index, NHL subtype, remission status at HCT, and the use of antithymocyte globulin or alemtuzumab, the regression analysis showed a significantly higher mortality risk associated with Flu-Mel140 compared with Flu-Bu (hazard ratio [HR], 1.34; 95% CI, 1.13-1.59; P <.001). Compared with the Flu-Cy cohort, the Flu-Mel140 cohort had a higher risk of chronic GVHD (HR, 1.38; 95% CI, 1.15-1.65; P <.001). The Flu-Mel140 regimen was associated with a higher nonrelapse mortality risk (HR, 1.78; 95% CI, 1.37-2.31; P <.001) compared with the Flu-Bu regimen. Conclusions and Relevance: The findings suggest that use of the more intense RIC-NMAC regimen, Flu-Mel140, may have a negative association with overall survival and may be associated with higher nonrelapse mortality. The Flu-Bu and Flu-Cy regimens with or without 2GyTBI regimens appeared to provide comparable overall survival..
UR - http://www.scopus.com/inward/record.url?scp=85086233103&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85086233103&partnerID=8YFLogxK
U2 - 10.1001/jamaoncol.2020.1278
DO - 10.1001/jamaoncol.2020.1278
M3 - Article
C2 - 32496525
AN - SCOPUS:85086233103
SN - 2374-2437
VL - 6
SP - 1011
EP - 1018
JO - JAMA Oncology
JF - JAMA Oncology
IS - 7
ER -