TY - JOUR
T1 - Allogeneic hematopoietic cell transplantation provides effective salvage despite refractory disease or failed prior autologous transplant in angioimmunoblastic T-cell lymphoma
T2 - A CIBMTR analysis
AU - Epperla, Narendranath
AU - Ahn, Kwang W.
AU - Litovich, Carlos
AU - Ahmed, Sairah
AU - Battiwalla, Minoo
AU - Cohen, Jonathon B.
AU - Dahi, Parastoo
AU - Farhadfar, Nosha
AU - Farooq, Umar
AU - Freytes, Cesar O.
AU - Ghosh, Nilanjan
AU - Haverkos, Bradley
AU - Herrera, Alex
AU - Hertzberg, Mark
AU - Hildebrandt, Gerhard
AU - Inwards, David
AU - Kharfan-Dabaja, Mohamed A.
AU - Khimani, Farhad
AU - Lazarus, Hillard
AU - Lazaryan, Aleksandr
AU - Lekakis, Lazaros
AU - Murthy, Hemant
AU - Nathan, Sunita
AU - Nishihori, Taiga
AU - Pawarode, Attaphol
AU - Prestidge, Tim
AU - Ramakrishnan, Praveen
AU - Rezvani, Andrew R.
AU - Romee, Rizwan
AU - Shah, Nirav N.
AU - Sureda, Ana
AU - Fenske, Timothy S.
AU - Hamadani, Mehdi
N1 - Publisher Copyright:
© 2019 The Author(s).
PY - 2019/1/10
Y1 - 2019/1/10
N2 - Background: There is a paucity of data on the role of allogeneic hematopoietic cell transplantation (allo-HCT) in patients with angioimmunoblastic T-cell lymphoma (AITL). Using the CIBMTR registry, we report here the outcomes of AITL patients undergoing an allo-HCT. Methods: We evaluated 249 adult AITL patients who received their first allo-HCT during 2000-2016. Results: The median patient age was 56 years (range = 21-77). Majority of the patients were Caucasians (86%), with a male predominance (60%). Graft-versus-host disease (GVHD) prophylaxis was predominantly calcineurin inhibitor-based approaches while the most common graft source was peripheral blood (97%). Median follow-up of survivors was 49 months (range = 4-170 months). The cumulative incidence of grade 2-4 and grade 3-4 acute GVHD at day 180 were 36% (95% CI = 30-42) and 12 (95% CI = 8-17), respectively. The cumulative incidence of chronic GVHD at 1 year was 49% (95%CI 43-56). The 1-year non-relapse mortality (NRM) was 19% (95% CI = 14-24), while the 4-year relapse/progression, progression-free survival (PFS), and overall survival (OS) were 21% (95% CI = 16-27), 49% (95% CI = 42-56), and 56% (95% CI = 49-63), respectively. On multivariate analysis, chemoresistant status at the time of allo-HCT was associated with a significantly higher risk for therapy failure (inverse of PFS) (RR = 1.73 95% CI = 1.08-2.77), while KPS < 90% was associated with a significantly higher risk of mortality (inverse of OS) (RR = 3.46 95% CI = 1.75-6.87). Conclusion: Our analysis shows that allo-HCT provides durable disease control even in AITL patients who failed a prior auto-HCT and in those subjects with refractory disease at the time of allografting.
AB - Background: There is a paucity of data on the role of allogeneic hematopoietic cell transplantation (allo-HCT) in patients with angioimmunoblastic T-cell lymphoma (AITL). Using the CIBMTR registry, we report here the outcomes of AITL patients undergoing an allo-HCT. Methods: We evaluated 249 adult AITL patients who received their first allo-HCT during 2000-2016. Results: The median patient age was 56 years (range = 21-77). Majority of the patients were Caucasians (86%), with a male predominance (60%). Graft-versus-host disease (GVHD) prophylaxis was predominantly calcineurin inhibitor-based approaches while the most common graft source was peripheral blood (97%). Median follow-up of survivors was 49 months (range = 4-170 months). The cumulative incidence of grade 2-4 and grade 3-4 acute GVHD at day 180 were 36% (95% CI = 30-42) and 12 (95% CI = 8-17), respectively. The cumulative incidence of chronic GVHD at 1 year was 49% (95%CI 43-56). The 1-year non-relapse mortality (NRM) was 19% (95% CI = 14-24), while the 4-year relapse/progression, progression-free survival (PFS), and overall survival (OS) were 21% (95% CI = 16-27), 49% (95% CI = 42-56), and 56% (95% CI = 49-63), respectively. On multivariate analysis, chemoresistant status at the time of allo-HCT was associated with a significantly higher risk for therapy failure (inverse of PFS) (RR = 1.73 95% CI = 1.08-2.77), while KPS < 90% was associated with a significantly higher risk of mortality (inverse of OS) (RR = 3.46 95% CI = 1.75-6.87). Conclusion: Our analysis shows that allo-HCT provides durable disease control even in AITL patients who failed a prior auto-HCT and in those subjects with refractory disease at the time of allografting.
KW - Allogeneic transplantation
KW - Angioimmunoblastic T-cell lymphoma
KW - GVL effects
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U2 - 10.1186/s13045-018-0696-z
DO - 10.1186/s13045-018-0696-z
M3 - Article
C2 - 30630534
AN - SCOPUS:85059829766
SN - 1756-8722
VL - 12
JO - Journal of Hematology and Oncology
JF - Journal of Hematology and Oncology
IS - 1
M1 - 6
ER -