Cancers (May 2022)

Allogeneic Stem Cell Transplantation in Mantle Cell Lymphoma; Insights into Its Potential Role in the Era of New Immunotherapeutic and Targeted Therapies: The GETH/GELTAMO Experience

  • Antonio Gutierrez,
  • Leyre Bento,
  • Silvana Novelli,
  • Alejandro Martin,
  • Gonzalo Gutierrez,
  • Maria Queralt Salas,
  • Mariana Bastos-Oreiro,
  • Ariadna Perez,
  • Rafael Hernani,
  • Maria Cruz Viguria,
  • Oriana Lopez-Godino,
  • Juan Montoro,
  • Jose Luis Piñana,
  • Christelle Ferra,
  • Rocio Parody,
  • Carmen Martin,
  • Ignacio Español,
  • Lucrecia Yañez,
  • Guillermo Rodriguez,
  • Joud Zanabili,
  • Pilar Herrera,
  • Maria Rosario Varela,
  • Antonia Sampol,
  • Carlos Solano,
  • Dolores Caballero,
  • on behalf of the Grupo Español de Trasplante de Progenitores Hematopoyéticos (GETH) and Grupo Español de Linfoma y Trasplante Autólogo (GELTAMO)

DOI
https://doi.org/10.3390/cancers14112673
Journal volume & issue
Vol. 14, no. 11
p. 2673

Abstract

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Allo-SCT is a curative option for selected patients with relapsed/refractory (R/R) MCL, but with significant NRM. We present the long-term results of patients receiving allo-SCT in Spain from March 1995 to February 2020. The primary endpoints were EFS, OS, and cumulative incidence (CI) of NRM, relapse, and GVHD. We included 135 patients, most (85%) receiving RIC. After a median follow-up of 68 months, 5-year EFS and OS were 47 and 50%, respectively. Overall and CR rates were 86 and 80%. The CI of relapse at 1 and 3 years were 7 and 12%. NRM at day 100 and 1 year were 17 and 32%. Previous ASCT and Grade 3–4 aGVHD were associated with a higher NRM. Grade 3–4 aGVHD, donor type (mismatch non-related), and the time-period 2006–2020 were independently related to worse EFS. Patients from 1995–2005 were younger, most from HLA-identical sibling donors, and were pretreated less. Our data confirmed that allo-SCT may be a curative option in R/R MCL with low a CI of relapse, although NRM is still high, being mainly secondary to aGVHD. The arrival of new, highly effective and low toxic immunotherapeutic or targeted therapies inevitably will relegate allo-SCT to those fit patients who fail these therapies, far away from the optimal timing of treatment.

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