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Autologous transplantation versus allogeneic transplantation in patients with follicular lymphoma experiencing early treatment failure

  • Sonali M. Smith
  • , James Godfrey
  • , Kwang Woo Ahn
  • , Alyssa DiGilio
  • , Sairah Ahmed
  • , Vaibhav Agrawal
  • , Veronika Bachanova
  • , Ulrike Bacher
  • , Asad Bashey
  • , Javier Bolaños-Meade
  • , Mitchell Cairo
  • , Andy Chen
  • , Saurabh Chhabra
  • , Edward Copelan
  • , Parastoo B. Dahi
  • , Mahmoud Aljurf
  • , Umar Farooq
  • , Siddhartha Ganguly
  • , Mark Hertzberg
  • , Leona Holmberg
  • David Inwards, Abraham S. Kanate, Reem Karmali, Vaishalee P. Kenkre, Mohamed A. Kharfan-Dabaja, Andreas Klein, Hillard M. Lazarus, Matthew Mei, Alberto Mussetti, Taiga Nishihori, Praveen Ramakrishnan Geethakumari, Ayman Saad, Bipin N. Savani, Harry C. Schouten, Nirav Shah, Alvaro Urbano-Ispizua, Ravi Vij, Julie Vose, Anna Sureda, Mehdi Hamadani

Research output: Contribution to journalArticlepeer-review

Abstract

BACKGROUND: Early treatment failure (ETF) in follicular lymphoma (FL), defined as relapse or progression within 2 years of frontline chemoimmunotherapy, is a newly recognized marker of poor survival and identifies a high-risk group of patients with an expected 5-year overall survival (OS) rate of approximately 50%. Transplantation is an established option for relapsed FL, but its efficacy in this specific ETF FL population has not been previously evaluated. METHODS: This study compared autologous hematopoietic stem cell transplantation (auto-HCT) with either matched sibling donor (MSD) or matched unrelated donor (MUD) allogeneic hematopoietic cell transplantation (allo-HCT) as the first transplantation approach for patients with ETF FL (age ≥ 18 years) undergoing auto-HCT or allo-HCT between 2002 and 2014. The primary endpoint was OS. The secondary endpoints were progression-free survival, relapse, and nonrelapse mortality (NRM). RESULTS: Four hundred forty FL patients had ETF (auto-HCT, 240; MSD hematopoietic stem cell transplantation [HCT], 105; and MUD HCT, 95). With a median follow-up of 69 to 73 months, the adjusted probability of 5-year OS was significantly higher after auto-HCT (70%) or MSD HCT (73%) versus MUD HCT (49%; P =.0008). The 5-year adjusted probability of NRM was significantly lower for auto-HCT (5%) versus MSD (17%) or MUD HCT (33%; P <.0001). The 5-year adjusted probability of disease relapse was lower with MSD (31%) or MUD HCT (23%) versus auto-HCT (58%; P <.0001). CONCLUSIONS: Patients with high-risk FL, as defined by ETF, undergoing auto-HCT for FL have low NRM and a promising 5-year OS rate (70%). MSD HCT has lower relapse rates than auto-HCT but similar OS. Cancer 2018;124:2541-51.

Original languageEnglish (US)
Pages (from-to)2541-2551
Number of pages11
JournalCancer
Volume124
Issue number12
DOIs
StatePublished - Jun 15 2018

Bibliographical note

Publisher Copyright:
© 2018 American Cancer Society

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • allogeneic transplantation
  • autologous transplantation
  • chemoimmunotherapy
  • early treatment failure
  • follicular lymphoma
  • rituximab

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