AI Article Synopsis

  • This report analyzed 65 patients with peripheral T cell lymphoma (PTCL) who underwent high-dose therapy and autologous hematopoietic stem cell transplantation (autoHCT) after induction or salvage chemotherapy.
  • Nineteen patients were in complete or partial remission post-induction, while 46 patients received second-line chemotherapy before proceeding to autoHCT.
  • The 5-year overall survival was 61.5%, with factors like bone marrow involvement and less than partial remission after induction identified as significant predictors for survival outcomes.

Article Abstract

This report is a retrospective analysis of 65 patients with peripheral T cell lymphoma (PTCL), who underwent high-dose therapy and autologous hematopoietic stem cell transplantation (autoHCT) as a consolidation of first response achieved with either induction or salvage chemotherapy. We intended to determine the prognostic factors that influenced outcome after autoHCT and to define the predictive value of the scoring systems most often applied for transplant outcomes. Nineteen patients in either complete or partial remission underwent autoHCT after induction chemotherapy. Forty-six patients received second-line chemotherapy as a consolidation of partial response after induction chemotherapy (n = 34) or as a salvage therapy after primary induction failure (n = 12), and thereafter proceeded to autoHCT. Finally, the 36 patients were in complete remission, and 29 in partial remission at autoHCT. The median follow-up of survivors was 53 months (range 7-157 months). The 5-year overall survival and progression-free survival for all patients were 61.5% (95% CI 47.0-74.2%) and 59.4% (95% CI 46.1-71.5%), respectively. In multivariate analysis, bone marrow involvement at diagnosis and less than partial remission after induction chemotherapy were factors independently predictive for overall survival and progression-free survival. The prognostic index for PTCL could reliably stratify the prognosis of PTCL in this analysis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674342PMC
http://dx.doi.org/10.1007/s00277-013-1716-2DOI Listing

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