TY - JOUR
T1 - Outcomes of Medicare-age eligible NHL patients receiving RIC allogeneic transplantation
T2 - A CIBMTR analysis
AU - Shah, Nirav N.
AU - Ahn, Kwang Woo
AU - Litovich, Carlos
AU - Fenske, Timothy S.
AU - Ahmed, Sairah
AU - Battiwalla, Minoo
AU - Bejanyan, Nelli
AU - Dahi, Parastoo B.
AU - Bolaños-Meade, Javier
AU - Chen, Andy I.
AU - Ciurea, Stefan O.
AU - Bachanova, Veronika
AU - DeFilipp, Zachariah
AU - Epperla, Narendranath
AU - Farhadfar, Nosha
AU - Herrera, Alex F.
AU - Haverkos, Bradley M.
AU - Holmberg, Leona
AU - Hossain, Nasheed M.
AU - Kharfan-Dabaja, Mohamed A.
AU - Kenkre, Vaishalee P.
AU - Lazarus, Hillard M.
AU - Murthy, Hemant S.
AU - Nishihori, Taiga
AU - Rezvani, Andrew R.
AU - D'Souza, Anita
AU - Savani, Bipin N.
AU - Ulrickson, Matthew L.
AU - Waller, Edmund K.
AU - Sureda, Anna
AU - Smith, Sonali M.
AU - Hamadani, Mehdi
N1 - Publisher Copyright:
© 2018 American Society of Hematology. All rights reserved.
PY - 2018/4/24
Y1 - 2018/4/24
N2 - The application of allogeneic hematopoietic cell transplantation (allo-HCT) in non-Hodgkin lymphoma (NHL) patients ≥65 years in the United States is limited by lack of Medicare coverage for this indication. Using the Center for International Blood and Marrow Transplant Research (CIBMTR) database, we report allo-HCT outcomes of NHL patients aged ≥65 years (older cohort; n = 446) compared with a cohort of younger NHL patients aged 55-64 years (n = 1183). We identified 1629 NHL patients undergoing a first reduced-intensity conditioning (RIC) or nonmyeloablative conditioning allo-HCT from 2008 to 2015 in the United States. Cord blood or haploidentical transplants were excluded. The median age was 68 years (range 65-77) for the older cohort vs 60 years (range 55-64) in the younger cohort. The 4-year adjusted probabilities of nonrelapse mortality (NRM), relapse/progression (R/P), progression-free survival (PFS), and overall survival (OS) of the younger and older groups were 24% vs 30% (P = .03), 41% vs 42% (P = .82), 37% vs 31% (P = .03), and 51% vs 46% (P = .07), respectively. Using multivariate analysis, compared with the younger group, the older cohort was associated with increased NRM, but there was no difference between the 2 cohorts in terms of R/P, PFS, or OS. The most common cause of death was disease relapse in both groups. In NHL patients eligible for allo-HCT, there was no difference in OS between the 2 cohorts. Age alone should not determine allo-HCT eligibility in NHL, and Medicare should expand allo-HCT coverage to older adults.
AB - The application of allogeneic hematopoietic cell transplantation (allo-HCT) in non-Hodgkin lymphoma (NHL) patients ≥65 years in the United States is limited by lack of Medicare coverage for this indication. Using the Center for International Blood and Marrow Transplant Research (CIBMTR) database, we report allo-HCT outcomes of NHL patients aged ≥65 years (older cohort; n = 446) compared with a cohort of younger NHL patients aged 55-64 years (n = 1183). We identified 1629 NHL patients undergoing a first reduced-intensity conditioning (RIC) or nonmyeloablative conditioning allo-HCT from 2008 to 2015 in the United States. Cord blood or haploidentical transplants were excluded. The median age was 68 years (range 65-77) for the older cohort vs 60 years (range 55-64) in the younger cohort. The 4-year adjusted probabilities of nonrelapse mortality (NRM), relapse/progression (R/P), progression-free survival (PFS), and overall survival (OS) of the younger and older groups were 24% vs 30% (P = .03), 41% vs 42% (P = .82), 37% vs 31% (P = .03), and 51% vs 46% (P = .07), respectively. Using multivariate analysis, compared with the younger group, the older cohort was associated with increased NRM, but there was no difference between the 2 cohorts in terms of R/P, PFS, or OS. The most common cause of death was disease relapse in both groups. In NHL patients eligible for allo-HCT, there was no difference in OS between the 2 cohorts. Age alone should not determine allo-HCT eligibility in NHL, and Medicare should expand allo-HCT coverage to older adults.
UR - http://www.scopus.com/inward/record.url?scp=85055419410&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85055419410&partnerID=8YFLogxK
U2 - 10.1182/bloodadvances.2018018531
DO - 10.1182/bloodadvances.2018018531
M3 - Article
C2 - 29685953
AN - SCOPUS:85055419410
SN - 2473-9529
VL - 2
SP - 933
EP - 940
JO - Blood Advances
JF - Blood Advances
IS - 8
ER -