The negative impact of opioids on cancer patients treated with immune checkpoint inhibitors: a systematic review and meta-analysis

J Cancer Res Clin Oncol. 2023 Jun;149(6):2699-2708. doi: 10.1007/s00432-022-04513-0. Epub 2022 Dec 20.

Abstract

Purpose: As one of the most effective analgesics, opioids are essential for patients with cancer-related pain, even in the context of the opioid abuse crisis. The current meta-analysis aimed to identify whether concomitant exposure to opioids can affect the efficacy of ICIs and lead to a worse prognosis.

Methods: PubMed, Embase, and the Cochrane Library were searched based on the PRISMA checklist, through April 2022, for the following terms: ("opioids" OR "concomitant medication") AND ("Neoplasm" OR "Carcinoma" OR "Cancer" OR "Tumor") AND ("Immunotherapy" OR "Immune Checkpoint Inhibitor" OR "PD-L1 Inhibitor" OR "PD-1 Inhibitor" OR "CTLA-4 Inhibitor"). The outcomes considered were overall survival (OS) and progression-free survival (PFS) calculated using the random-effects or fixed-effects model.

Results: After screening 531 studies, a total of 7 articles involving 2690 patients were eligible for quantitative analysis. The use of opioids was negatively correlated with OS (HR 1.75, 95%CI 1.32-2.31, P < 0.001; I2 = 81%, P < 0.001) and significantly reduced the PFS (HR 1.61, 95%CI 1.41-1.83, P < 0.001; I2 = 0%, P = 0.63) of patients treated with ICIs. Similar results were obtained in each subgroup analysis. While NSAIDs could lead to poor OS (HR 1.25, 95% CI 1.03-1.51, P = 0.02; I2 = 0%, P = 0.60) but not PFS (HR 1.11, 95% CI = 0.89-1.39, P = 0.36) for ICIs patients. And sensitivity analyses confirmed the reliability of the results.

Conclusion: Opioids significantly reduced OS and PFS in patients receiving ICI therapy. Thus, the use of different types of opioids should be considered with caution, and it is necessary to actively develop alternative treatments.

Keywords: Immune checkpoint inhibitors; Meta-analysis; Opioids; Overall survival; Progression-free survival.

Publication types

  • Meta-Analysis
  • Systematic Review
  • Review

MeSH terms

  • Analgesics, Opioid* / adverse effects
  • Anti-Inflammatory Agents, Non-Steroidal
  • Carcinoma*
  • Humans
  • Immune Checkpoint Inhibitors / adverse effects
  • Reproducibility of Results

Substances

  • Analgesics, Opioid
  • Immune Checkpoint Inhibitors
  • Anti-Inflammatory Agents, Non-Steroidal