Journal of Hematology & Oncology (Jan 2019)

Allogeneic hematopoietic cell transplantation provides effective salvage despite refractory disease or failed prior autologous transplant in angioimmunoblastic T-cell lymphoma: a CIBMTR analysis

  • Narendranath Epperla,
  • Kwang W. Ahn,
  • Carlos Litovich,
  • Sairah Ahmed,
  • Minoo Battiwalla,
  • Jonathon B. Cohen,
  • Parastoo Dahi,
  • Nosha Farhadfar,
  • Umar Farooq,
  • Cesar O. Freytes,
  • Nilanjan Ghosh,
  • Bradley Haverkos,
  • Alex Herrera,
  • Mark Hertzberg,
  • Gerhard Hildebrandt,
  • David Inwards,
  • Mohamed A. Kharfan-Dabaja,
  • Farhad Khimani,
  • Hillard Lazarus,
  • Aleksandr Lazaryan,
  • Lazaros Lekakis,
  • Hemant Murthy,
  • Sunita Nathan,
  • Taiga Nishihori,
  • Attaphol Pawarode,
  • Tim Prestidge,
  • Praveen Ramakrishnan,
  • Andrew R. Rezvani,
  • Rizwan Romee,
  • Nirav N. Shah,
  • Ana Sureda,
  • Timothy S. Fenske,
  • Mehdi Hamadani

DOI
https://doi.org/10.1186/s13045-018-0696-z
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 11

Abstract

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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.

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