Combination of Low-Dose Gemcitabine and PD-1 Inhibitors for Treatment in Patients With Advanced Malignancies

Front Immunol. 2022 Jul 13:13:882172. doi: 10.3389/fimmu.2022.882172. eCollection 2022.

Abstract

Purpose: This study determined the efficacy of low-dose gemcitabine combined with programmed death-1 (PD-1) inhibitors for treating multiple malignancies, providing a cost-effective and safe treatment option.

Study design: This study included 61 patients with advanced solid tumors treated with low-dose gemcitabine combined with PD-1 inhibitors at the Henan Cancer Hospital between January 2018 and February 2022. We retrospectively reviewed medical records to evaluate several clinical factors, including progression-free survival (PFS), overall survival (OS), adverse effects (AEs), and objective response to treatment.

Results: Sixty-one patients received treatment with low-dose gemcitabine combined with PD-1 inhibitors. The objective response rate (ORR) was 29.5% and the disease control rate (DCR) was 62.3%. The median PFS was 4.3 months (95% confidence interval, 2.3 to 6.3 months) and the median OS was 15.0 months (95% confidence interval, 8.8 to 21.2 months). Hematological toxicity, mainly leukopenia or thrombocytopenia, was the most common AE, with any-grade and grade 3/4 hematological toxicity reported in 60.7 and 13.1% of patients, respectively.

Conclusions: Low-dose gemcitabine combined with PD-1 inhibitors may offer a novel treatment option for patients with advanced malignancies.

Keywords: PD-1 inhibitors; combination immunotherapy; gemcitabine; low-dose chemotherapy; malignancy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Deoxycytidine / adverse effects
  • Deoxycytidine / analogs & derivatives
  • Gemcitabine
  • Humans
  • Immune Checkpoint Inhibitors*
  • Neoplasms* / chemically induced
  • Neoplasms* / drug therapy
  • Retrospective Studies

Substances

  • Immune Checkpoint Inhibitors
  • Deoxycytidine
  • Gemcitabine