TY - JOUR
T1 - Older Patients with Myeloma Derive Similar Benefit from Autologous Transplantation
AU - Sharma, Manish
AU - Zhang, Mei Jie
AU - Zhong, Xiaobo
AU - Abidi, Muneer H.
AU - Akpek, Görgün
AU - Bacher, Ulrike
AU - Callander, Natalie S.
AU - Dispenzieri, Angela
AU - Freytes, César O.
AU - Fung, Henry C.
AU - Gale, Robert Peter
AU - Gasparetto, Cristina
AU - Gibson, John
AU - Holmberg, Leona A.
AU - Kindwall-Keller, Tamila L.
AU - Klumpp, Thomas R.
AU - Krishnan, Amrita Y.
AU - Landau, Heather J.
AU - Lazarus, Hillard M.
AU - Lonial, Sagar
AU - Maiolino, Angelo
AU - Marks, David I.
AU - Mehta, Paulette
AU - Mikhael Med, Joseph R.
AU - Nishihori, Taiga
AU - Olsson, Richard
AU - Ramanathan, Muthalagu
AU - Roy, Vivek
AU - Savani, Bipin N.
AU - Schouten, Harry C.
AU - Scott, Emma
AU - Tay, Jason
AU - To, Luen Bik
AU - Vesole, David H.
AU - Vogl, Dan T.
AU - Hari, Parameswaran
N1 - Funding Information:
The CIBMTR is supported by Public Health Service Grant/Cooperative Agreement U24-CA076518 from the National Cancer Institute , the National Heart, Lung and Blood Institute (NHLBI) and the National Institute of Allergy and Infectious Diseases ; a Grant/Cooperative Agreement 5U10HL069294 from NHLBI and NCI ; a contract HHSH250201200016C with Health Resources and Services Administration ; two Grants N00014-12-1-0142 and N00014-13-1-0039 from the Office of Naval Research ; and grants from * Actinium Pharmaceuticals ; Allos Therapeutics, Inc.; * Amgen, Inc. ; Anonymous donation to the Medical College of Wisconsin ; Ariad; Be the Match Foundation ; * Blue Cross and Blue Shield Association ; * Celgene Corporation; Chimerix, Inc. ; Fred Hutchinson Cancer Research Center; Fresenius-Biotech North America, Inc. ; * Gamida Cell Teva Joint Venture Ltd. ; Genentech, Inc. ; * Gentium SpA ; Genzyme Corporation ; GlaxoSmithKline ; Health Research, Inc. ROSWELL PARK CANCER INSTITUTE ; HistoGenetics, Inc. ; Incyte Corporation ; Jeff Gordon Children's Foundation ; Kiadis Pharma ; The Leukemia & Lymphoma Society ; Medac GmbH ; The Medical College of Wisconsin ; Merck & Co., Inc. ; Millennium: The Takeda Oncology Co. ; * Milliman USA, Inc. ; * Miltenyi Biotec, Inc. ; National Marrow Donor Program ; Onyx Pharmaceuticals ; Optum Healthcare Solutions, Inc. ; Osiris Therapeutics, Inc. ; Otsuka America Pharmaceutical, Inc. ; Perkin Elmer, Inc. ; * Remedy Informatics ; * Sanofi US ; Seattle Genetics ; Sigma-Tau Pharmaceuticals ; Soligenix, Inc. ; St. Baldrick's Foundation ; StemCyte, A Global Cord Blood Therapeutics Co. ; Stemsoft Software, Inc. ; Swedish Orphan Biovitrum ; * Tarix Pharmaceuticals ; * Terumo BCT ; * Teva Neuroscience, Inc. ; * Texas Instruments Inc. ; University of Minnesota ; University of Utah ; and * WellPoint , Inc. The views expressed in this article do not reflect the official policy or position of the National Institute of Health, the Department of the Navy, the Department of Defense, Health Resources and Services Administration or any other agency of the US Government.
Publisher Copyright:
© 2014 American Society for Blood and Marrow Transplantation.
PY - 2014/11/1
Y1 - 2014/11/1
N2 - Autologous hematopoietic cell transplantation (AHCT) for plasma cell myeloma is performed less often in people >70 years old than in people ≤70 years old. We analyzed 11,430 AHCT recipients for plasma cell myeloma prospectively reported to the Center for International Blood and Marrow Transplant Research between 2008 and 2011, representing the majority of US AHCT activity during this period. Survival (OS) was compared in 3 cohorts: ages 18 to 59 years (n= 5818), 60 to 69 years (n= 4666), and >70 years (n= 946). Median OS was not reached for any cohort. In multivariate analysis, increasing age was associated with mortality (P= .0006). Myeloma-specific mortality was similar among cohorts at 12%, indicating an age-related effect on nonmyeloma mortality. Analyses were performed in a representative subgroup comparing relapse rate, progression-free survival (PFS), and nonrelapse mortality (NRM). One-year NRM was 0% for age >70 years and 2% for other ages (P= not significant). The three-year relapse rate was 56% in age 18 to 59 years, 61% in age 60 to 69 years, and 63% age >70 (P= not significant). Three-year PFS was similar at 42% in age 18 to 59 years, 38% in age 60 to 69 years, and 33% in age >70 years (P= not significant). Postrelapse survival was significantly worse for the older cohort (P= .03). Older subjects selected for AHCT derived similar antimyeloma benefit without worse NRM, relapse rate, or PFS.
AB - Autologous hematopoietic cell transplantation (AHCT) for plasma cell myeloma is performed less often in people >70 years old than in people ≤70 years old. We analyzed 11,430 AHCT recipients for plasma cell myeloma prospectively reported to the Center for International Blood and Marrow Transplant Research between 2008 and 2011, representing the majority of US AHCT activity during this period. Survival (OS) was compared in 3 cohorts: ages 18 to 59 years (n= 5818), 60 to 69 years (n= 4666), and >70 years (n= 946). Median OS was not reached for any cohort. In multivariate analysis, increasing age was associated with mortality (P= .0006). Myeloma-specific mortality was similar among cohorts at 12%, indicating an age-related effect on nonmyeloma mortality. Analyses were performed in a representative subgroup comparing relapse rate, progression-free survival (PFS), and nonrelapse mortality (NRM). One-year NRM was 0% for age >70 years and 2% for other ages (P= not significant). The three-year relapse rate was 56% in age 18 to 59 years, 61% in age 60 to 69 years, and 63% age >70 (P= not significant). Three-year PFS was similar at 42% in age 18 to 59 years, 38% in age 60 to 69 years, and 33% in age >70 years (P= not significant). Postrelapse survival was significantly worse for the older cohort (P= .03). Older subjects selected for AHCT derived similar antimyeloma benefit without worse NRM, relapse rate, or PFS.
KW - Autologous transplantation
KW - Myeloma
KW - Older patients
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UR - http://www.scopus.com/inward/citedby.url?scp=84908070200&partnerID=8YFLogxK
U2 - 10.1016/j.bbmt.2014.07.013
DO - 10.1016/j.bbmt.2014.07.013
M3 - Article
C2 - 25046833
AN - SCOPUS:84908070200
SN - 1083-8791
VL - 20
SP - 1796
EP - 1803
JO - Biology of Blood and Marrow Transplantation
JF - Biology of Blood and Marrow Transplantation
IS - 11
ER -