Blood Advances (Jan 2020)

PD-1 blockade for diffuse large B-cell lymphoma after autologous stem cell transplantation

  • Matthew J. Frigault,
  • Philippe Armand,
  • Robert A. Redd,
  • Erin Jeter,
  • Reid W. Merryman,
  • Kimberly C. Coleman,
  • Alex F. Herrera,
  • Parastoo Dahi,
  • Yago Nieto,
  • Ann S. LaCasce,
  • David C. Fisher,
  • Samuel Y. Ng,
  • Oreife O. Odejide,
  • Arnold S. Freedman,
  • Austin I. Kim,
  • Jennifer L. Crombie,
  • Caron A. Jacobson,
  • Eric D. Jacobsen,
  • Jeffrey L. Wong,
  • Jad Bsat,
  • Sanjay S. Patel,
  • Jerome Ritz,
  • Scott J. Rodig,
  • Margaret A. Shipp,
  • Yi-Bin Chen,
  • Robin M. Joyce

Journal volume & issue
Vol. 4, no. 1
pp. 122 – 126

Abstract

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Abstract: Disease relapse remains the leading cause of failure after autologous stem cell transplantation (ASCT) for patients with relapsed/refractory diffuse large B-cell lymphoma (R/R DLBCL). We conducted a phase 2, multicenter, single-arm study of the anti–PD-1 monoclonal antibody pembrolizumab given after ASCT in patients with chemosensitive DLBCL, hypothesizing that it would improve the progression-free survival (PFS) at 18 months after ASCT (primary endpoint) from 60% to 80%. Pembrolizumab was administered at 200 mg IV every 3 weeks for up to 8 cycles, starting within 21 days of post-ASCT discharge. Twenty-nine patients were treated on this study; 62% completed all 8 cycles. Seventy-nine percent of patients experienced at least one grade 3 or higher adverse event, and 34% experienced at least one grade 2 or higher immune-related adverse event. Overall, 59% of patients were alive and progression free at 18 months, which did not meet the primary endpoint. The 18-month overall survival was 93%. In conclusion, pembrolizumab was successfully administered as post-ASCT consolidation in patients with R/R DLBCL, but the PFS did not meet the protocol-specific primary objective and therefore does not support a larger confirmatory study. This trial was registered at www.clinicaltrials.gov as #NCT02362997.