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Patterns of survival in patients with recurrent mantle cell lymphoma in the modern era: progressive shortening in response duration and survival after each relapse. | LitMetric

AI Article Synopsis

  • The study examined 404 patients with mantle cell lymphoma (MCL) treated at Memorial Sloan Kettering Cancer Center from 2000 to 2014 to analyze outcomes after multiple treatment regimens.* -
  • Findings showed that median overall survival (OS) and progression-free survival (PFS) decreased with each subsequent therapy, with first-line treatment yielding 9.7 years OS and 4.0 years PFS.* -
  • Additionally, younger patients (<65 years) receiving stem cell transplant-based treatments had significantly better survival outcomes compared to those on other regimens, and early failure in treatment was linked to poorer long-term survival.*

Article Abstract

As the survival of patients with mantle cell lymphoma (MCL) continues to improve, patients are increasingly being treated with multiple regimens. However, outcome after each line remains poorly characterized in the modern era. To address this knowledge gap, we retrospectively studied 404 consecutive MCL patients who were managed between 2000 and 2014 at Memorial Sloan Kettering Cancer Center. Histologic diagnosis was centrally confirmed, and patients were followed longitudinally from diagnosis throughout their disease course. Progression-free survival (PFS) and overall survival (OS) were determined by Kaplan-Meier method. The median OS and PFS after first-line treatment were 9.7 and 4.0 years, respectively. After second-line therapy, the median OS and PFS were 41.1 and 14.0 months, third line were 25.2 and 6.5 months, and fourth line were 14.4 and 5.0 months. In patients less than 65 years, stem cell transplant (SCT)-based frontline regimens were associated with improved PFS compared with non-SCT regimens (median PFS: 86.2 versus 40.0 months; P < 0.01), with a trend toward longer OS (median OS: 165.0 versus 120.0 months; P = 0.06). Early treatment failure after first-line regimens was associated with worse OS (5.9 versus 2.5 years; P < 0.01). Our study should facilitate establishing proper endpoints for future clinical trials using novel treatment approaches.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527702PMC
http://dx.doi.org/10.1038/s41408-019-0209-5DOI Listing

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