Journal article
Allogeneic hematopoietic cell transplantation provides effective salvage despite refractory disease or failed prior autologous transplant in angioimmunoblastic T-cell lymphoma: a CIBMTR analysis
Journal of hematology and oncology, Vol.12(1), pp.6-6
01/10/2019
DOI: 10.1186/s13045-018-0696-z
PMCID: PMC6329157
PMID: 30630534
Abstract
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.
Details
- Title: Subtitle
- Allogeneic hematopoietic cell transplantation provides effective salvage despite refractory disease or failed prior autologous transplant in angioimmunoblastic T-cell lymphoma: a CIBMTR analysis
- Creators
- Narendranath Epperla - The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research InstituteKwang W. Ahn - Center for International Blood and Marrow Transplant ResearchCarlos Litovich - Center for International Blood and Marrow Transplant ResearchSairah Ahmed - 1515 Holcombe Boulevard, Houston, TX 77030 USAMinoo Battiwalla - Sarah CannonJonathon B. Cohen - Emory UniversityParastoo Dahi - Memorial Sloan Kettering Cancer CenterNosha Farhadfar - University of Florida HealthUmar Farooq - University of Iowa Hospitals and ClinicsCesar O. Freytes - CHRISTUS Transplant InstituteNilanjan Ghosh - Levine Cancer InstituteBradley Haverkos - University of Colorado HospitalAlex Herrera - City Of Hope National Medical CenterMark Hertzberg - Prince of Wales HospitalGerhard Hildebrandt - Albert B. Chandler HospitalDavid Inwards - Mayo Clinic in FloridaMohamed A. Kharfan-Dabaja - Mayo Clinic in FloridaFarhad Khimani - Moffitt Cancer CenterHillard Lazarus - Case Western Reserve UniversityAleksandr Lazaryan - Moffitt Cancer CenterLazaros Lekakis - Case Western Reserve UniversityHemant Murthy - Florida CollegeSunita Nathan - Rush University Medical CenterTaiga Nishihori - Moffitt Cancer CenterAttaphol Pawarode - University of MichiganTim Prestidge - Starship Children's HealthPraveen Ramakrishnan - Southwestern Medical CenterAndrew R. Rezvani - Stanford Health CareRizwan Romee - Dana-Farber Cancer InstituteNirav N. Shah - Medical College of WisconsinAna Sureda - Duran i Reynals HospitalTimothy S. Fenske - Medical College of WisconsinMehdi Hamadani - Medical College of Wisconsin
- Resource Type
- Journal article
- Publication Details
- Journal of hematology and oncology, Vol.12(1), pp.6-6
- DOI
- 10.1186/s13045-018-0696-z
- PMID
- 30630534
- PMCID
- PMC6329157
- NLM abbreviation
- J Hematol Oncol
- ISSN
- 1756-8722
- eISSN
- 1756-8722
- Publisher
- BioMed Central
- Language
- English
- Date published
- 01/10/2019
- Academic Unit
- Hematology, Oncology, and Blood & Marrow Transplantation; Internal Medicine
- Record Identifier
- 9984359807102771
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