Allogeneic hematopoietic cell transplantation provides effective salvage despite refractory disease or failed prior autologous transplant in angioimmunoblastic T-cell lymphoma: a CIBMTR analysis.
Adult
Aged
Aged, 80 and over
Autografts
Drug Resistance, Neoplasm
Female
Follow-Up Studies
Graft vs Host Disease
/ prevention & control
Hematopoietic Stem Cell Transplantation
/ methods
Humans
Lymphoma, T-Cell
/ therapy
Male
Middle Aged
Progression-Free Survival
Registries
Salvage Therapy
/ methods
Transplantation Conditioning
Transplantation, Autologous
/ adverse effects
Transplantation, Homologous
/ methods
Young Adult
Allogeneic transplantation
Angioimmunoblastic T-cell lymphoma
GVL effects
Journal
Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937
Informations de publication
Date de publication:
10 01 2019
10 01 2019
Historique:
received:
02
11
2018
accepted:
27
12
2018
entrez:
12
1
2019
pubmed:
12
1
2019
medline:
11
3
2020
Statut:
epublish
Résumé
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. We evaluated 249 adult AITL patients who received their first allo-HCT during 2000-2016. 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). 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.
Sections du résumé
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.
Identifiants
pubmed: 30630534
doi: 10.1186/s13045-018-0696-z
pii: 10.1186/s13045-018-0696-z
pmc: PMC6329157
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Research Support, U.S. Gov't, Non-P.H.S.
Research Support, U.S. Gov't, P.H.S.
Langues
eng
Sous-ensembles de citation
IM
Pagination
6Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA086862
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA076518
Pays : United States
Organisme : NHLBI NIH HHS
ID : U10 HL069294
Pays : United States
Références
Blood. 2010 Nov 4;116(18):3418-25
pubmed: 20660290
J Clin Oncol. 2013 Jan 10;31(2):240-6
pubmed: 22869878
J Clin Oncol. 2008 May 10;26(14):2264-71
pubmed: 18390969
Haematologica. 2003 Nov;88(11):1272-8
pubmed: 14607756
Bone Marrow Transplant. 1995 Jun;15(6):825-8
pubmed: 7581076
Leuk Lymphoma. 1999 Feb;32(5-6):545-52
pubmed: 10048427
Blood. 1998 Jul 1;92(1):76-82
pubmed: 9639502
J Clin Oncol. 2007 Feb 10;25(5):579-86
pubmed: 17242396
Biol Blood Marrow Transplant. 2008 Apr;14(4):480-3
pubmed: 18342792
Biol Blood Marrow Transplant. 2009 Dec;15(12):1628-33
pubmed: 19896087
Leukemia. 2012 Mar;26(3):520-6
pubmed: 21904377
Lifetime Data Anal. 1995;1(2):145-56; discussion 157-9
pubmed: 9385097
Biol Blood Marrow Transplant. 2015 Oct;21(10):1746-53
pubmed: 25981509
N Engl J Med. 2017 Dec 28;377(26):2531-2544
pubmed: 29226797
J Clin Oncol. 2009 Aug 20;27(24):3951-8
pubmed: 19620487
Am J Med. 1980 Aug;69(2):204-17
pubmed: 6996481
Biol Blood Marrow Transplant. 2017 Nov;23(11):1826-1838
pubmed: 28797780
J Clin Oncol. 2008 Sep 1;26(25):4124-30
pubmed: 18626005
Blood. 2008 May 1;111(9):4463-70
pubmed: 18292286
Ann Intern Med. 1992 Sep 1;117(5):364-70
pubmed: 1380221
Eur J Haematol. 2007 Apr;78(4):290-6
pubmed: 17378891
Biol Blood Marrow Transplant. 2007 Dec;13(12):1469-76
pubmed: 18022577
J Clin Oncol. 2012 Sep 1;30(25):3093-9
pubmed: 22851556
J Clin Oncol. 2013 Sep 1;31(25):3100-9
pubmed: 23897963
Biol Blood Marrow Transplant. 2017 May;23(5):853-856
pubmed: 28161608
J Clin Oncol. 2008 Jan 10;26(2):218-24
pubmed: 18182664
Br J Haematol. 2018 Sep;182(6):916-920
pubmed: 28771676