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Improved outcomes of high-risk relapsed Hodgkin lymphoma patients after high-dose chemotherapy: a 15-year analysis.
Nieto, Yago; Gruschkus, Stephen; Valdez, Benigno C; Jones, Roy B; Anderlini, Paolo; Hosing, Chitra; Popat, Uday; Qazilbash, Muzaffar; Kebriaei, Partow; Alousi, Amin; Saini, Neeraj; Srour, Samer; Rezvani, Katayoun; Ramdial, Jeremy; Barnett, Melissa; Gulbis, Alison; Shigle, Terri Lynn; Ahmed, Sairah; Iyer, Swaminathan; Lee, Hun; Nair, Ranjit; Parmar, Simrit; Steiner, Raphael; Dabaja, Bouthaina; Pinnix, Chelsea; Gunther, Jillian; Cuglievan, Branko; Mahadeo, Kris; Khazal, Sajad; Chuang, Hubert; Champlin, Richard; Shpall, Elizabeth J; Andersson, Borje S.
Afiliación
  • Nieto Y; From the Departments of Stem Cell Transplantation and Cellular Therapy. ynieto@mdanderson.org.
  • Gruschkus S; Biostatistics.
  • Valdez BC; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Jones RB; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Anderlini P; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Hosing C; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Popat U; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Qazilbash M; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Kebriaei P; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Alousi A; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Saini N; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Srour S; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Rezvani K; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Ramdial J; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Barnett M; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Gulbis A; Pharmacy.
  • Shigle TL; Pharmacy.
  • Ahmed S; Lymphoma and Myeloma.
  • Iyer S; Lymphoma and Myeloma.
  • Lee H; Lymphoma and Myeloma.
  • Nair R; Lymphoma and Myeloma.
  • Parmar S; Lymphoma and Myeloma.
  • Steiner R; Lymphoma and Myeloma.
  • Dabaja B; Radiation Oncology.
  • Pinnix C; Radiation Oncology.
  • Gunther J; Radiation Oncology.
  • Cuglievan B; Pediatrics.
  • Mahadeo K; Pediatrics.
  • Khazal S; Pediatrics.
  • Chuang H; Nuclear Medicine at the University of Texas MD Anderson Cancer Center.
  • Champlin R; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Shpall EJ; From the Departments of Stem Cell Transplantation and Cellular Therapy.
  • Andersson BS; From the Departments of Stem Cell Transplantation and Cellular Therapy.
Haematologica ; 107(4): 899-908, 2022 04 01.
Article en En | MEDLINE | ID: mdl-33951890
High-dose chemotherapy and autologous stem-cell transplant (HDC/ASCT) is standard treatment for chemosensitive relapsed classical Hodgkin lymphoma, although outcomes of high-risk relapse (HRR) patients remain suboptimal. We retrospectively analyzed all HRR classical Hodgkin lymphoma patients treated with HDC/ASCT at our institution between 01/01/2005 and 12/31/2019. HRR criteria included primary refractory disease/relapse within 1 year, extranodal extension, B symptoms, requiring more than one salvage line, or positron emission tomography (PET)-positive disease at ASCT. All patients met the same ASCT eligibility criteria. We treated 501 patients with BEAM (n=146), busulphan/melphalan (BuMel) (n=38), gemcitabine( Gem)/BuMel (n=189) and vorinostat/Gem/BuMel (n=128). The Gem/BuMel and vorinostat/Gem/BuMel cohorts had more HRR criteria and more patients with PET-positive disease at ASCT. Treatment with brentuximab vedotin (BV) or anti-PD1 prior to ASCT, PET-negative disease at ASCT, and maintenance BV increased over time. BEAM and BuMel predominated in earlier years (2005-2007), GemBuMel and BEAM in middle years (2008-2015), and vorinostat/GemBuMel and BEAM in later years (2016-2019). The median follow-up is 50 months (range, 6-186). Outcomes improved over time, with 2-year progressionfree survival (PFS)/overall survival (OS) rates of 58%/82% (2005-2007), 59%/83% (2008-2011), 71%/94% (2012-2015) and 86%/99% (2016- 2019) (P<0.0001). Five-year PFS/OS rates were 72%/87% after vorinostat/ GemBuMel, 55%/75% after GemBuMel, 45%/61% after BEAM, and 39%/57% after BuMel (PFS: P=0.0003; OS: P<0.0001). These differences persisted within the PET-negative and PET-positive subgroups. Prior BV and vorinostat/GemBuMel were independent predictors of more favorable outcome, whereas primary refractory disease, ≥2 salvage lines, bulky relapse, B symptoms and PET-positivity at ASCT correlated independently with unfavorable outcomes. In conclusion, post-HDC/ASCT outcomes of patients with HRR classic Hodgkin lymphoma have improved over the last 15 years. Pre-ASCT BV treatment and optimized synergistic HDC (vorinostat/GemBuMel) were associated with this improvement.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Haematologica Año: 2022 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Enfermedad de Hodgkin Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Haematologica Año: 2022 Tipo del documento: Article