Efficacy and safety of nivolumab with ipilimumab for recurrent malignant pleural mesothelioma after primary surgical intervention

Int J Clin Oncol. 2023 Mar;28(3):409-415. doi: 10.1007/s10147-023-02292-3. Epub 2023 Jan 7.

Abstract

Background: Treatment of recurrent malignant pleural mesothelioma (MPM) remains challenging. Our study examined the efficacy, tolerability, and safety of nivolumab with ipilimumab treatment for recurrent MPM after primary curative-intent surgery.

Methods: Treatment comprised 360 mg nivolumab every 3 weeks and 1 mg/kg of ipilimumab every 6 weeks, both administered intravenously. Both were discontinued for progressive disease or serious adverse events (AEs). Additional post-treatment data were evaluated, including objective response rate (ORR), disease control rate (DCR), post-treatment survival, progression-free survival (PFS), and AEs. Tumor response was assessed using the modified Response Evaluation Criteria in Solid Tumors (RECIST 1.1). Survival analysis was estimated using a Kaplan-Meier plot. Feasibility analysis was performed using the National Cancer Institute Common Terminology Criteria for AEs version 5.0.

Results: Forty-one patients received nivolumab with ipilimumab for recurrent MPM after primary curative-intent surgery (median follow-up, 10.4 months; median treatment, 5.1 months). Overall, 18 patients exhibited partial response, 13 exhibited stable disease, and 10 had documented progressive disease. ORR and DCR were 43.9 and 75.6%, respectively. The 12-month post-treatment survival rate and PFS rate were 74.2 and 40.0%, respectively (median survival, not calculated; median PFS, 7.3 months). Further, 47 AEs were reported in 29 patients (70.7%), including grade 3-4 AEs in 14 patients (34.1%). Grade 4 hepatobiliary disorders were observed in 2 patients and grade 4 neutropenia was observed in 1.

Conclusion: Nivolumab with ipilimumab treatment in patients with recurrent MPM after primary surgical treatment may be clinically efficacious, although serious AEs may be frequently observed.

Keywords: Adverse events; Anticytotoxic T lymphocyte antigen-4; Malignant pleural mesothelioma; Nivolumab plus ipilimumab; Postoperative recurrence; Programmed death-1 inhibition.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols
  • Humans
  • Ipilimumab / adverse effects
  • Ipilimumab / therapeutic use
  • Mesothelioma, Malignant* / chemically induced
  • Mesothelioma, Malignant* / drug therapy
  • Nivolumab / adverse effects
  • Progression-Free Survival
  • Survival Analysis

Substances

  • Nivolumab
  • Ipilimumab