eJHaem (Nov 2020)

Phase II study of dose‐adjusted gemcitabine, dexamethasone, cisplatin, and rituximab in elderly relapsed diffuse large B‐cell lymphoma patients

  • Satoshi Yamasaki,
  • Akiko Kada,
  • Ilseung Choi,
  • Hiroatsu Iida,
  • Naohiro Sekiguchi,
  • Naoko Harada,
  • Morio Sawamura,
  • Takeshi Shimomura,
  • Takuya Komeno,
  • Takahiro Yano,
  • Isao Yoshida,
  • Shinichiro Yoshida,
  • Kazutaka Sunami,
  • Terutoshi Hishita,
  • Hiroshi Takatsuki,
  • Koichi Ohshima,
  • Morishige Takeshita,
  • Akiko M. Saito,
  • Hiromi Iwasaki,
  • Hirokazu Nagai

DOI
https://doi.org/10.1002/jha2.111
Journal volume & issue
Vol. 1, no. 2
pp. 507 – 516

Abstract

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Abstract High‐dose chemotherapy and autologous stem cell transplantation (ASCT) are too toxic for elderly patients with relapsed or refractory diffuse large B‐cell lymphoma (DLBCL). Therefore, effective and tolerable regimens for elderly patients are urgently needed. The present phase II study assessed the efficacy and safety of dose‐adjusted therapy with gemcitabine, dexamethasone, cisplatin, and rituximab (GDP‐R) in this population. ASCT‐ineligible elderly patients with relapsed or refractory DLBCL received dose‐adjusted GDP‐R in each 28‐day cycle for up to six cycles. The primary endpoint was overall response rate (ORR), and secondary endpoints were complete response (CR) rate, progression‐free survival (PFS), and safety. Thirty‐three patients were enrolled and received dose‐adjusted GDP‐R. The median age was 75 years (range: 68‐87 years). The ORR was 82.8% (90% confidence interval [CI], 67.1‐93.0%), with a CR rate of 58.6% (90% CI, 41.7‐74.1%). At a median follow‐up of 20.9 months, the 2‐year PFS rate was 46.8% (90% CI, 30.7‐61.5%) and the 2‐year overall survival rate was 63.2% (90% CI, 45.8‐76.3%). The most frequently observed grade 4 adverse events were neutropenia (63.6%), thrombocytopenia (57.6%), and lymphocytopenia (39.4%). Dose‐adjusted GDP‐R is a promising salvage regimen for ASCT‐ineligible elderly patients with relapsed DLBCL after rituximab‐containing chemotherapy and warrants further investigation.

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