PIVOT-10: Phase II study of bempegaldesleukin plus nivolumab in cisplatin-ineligible advanced urothelial cancer

Future Oncol. 2021 Jan;17(2):137-149. doi: 10.2217/fon-2020-0795. Epub 2020 Sep 17.

Abstract

The choice of first-line therapy for patients with metastatic urothelial cancer (mUC) is based on cisplatin-eligibility and programmed death-ligand 1 (PD-L1) status. For patients with mUC who are ineligible for cisplatin and with low PD-L1 expression, chemotherapy-based regimens are the only approved first-line option. In a Phase I/II trial of the chemotherapy-free regimen, bempegaldesleukin (BEMPEG; NKTR-214) plus nivolumab, patients with locally advanced or mUC experienced tumor responses regardless of baseline PD-L1 expression (objective response rates: 50 and 45% in patients with PD-L1-positive and -negative tumors, respectively). The Phase II PIVOT-10 study (NCT03785925), evaluates efficacy and safety of first-line BEMPEG plus nivolumab in cisplatin-ineligible patients with locally advanced or mUC. Most patients will have low PD-L1 expression. Primary end point: objective response rates (including complete response).

Keywords: IL-2 pathway; NKTR-214; PD-L1; PD-L1 negative; bempegaldesleukin; cisplatin-ineligible; immune checkpoint inhibitor combinations; immunotherapy; metastatic urothelial cancer; nivolumab.

Publication types

  • Clinical Trial, Phase II

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Biomarkers, Tumor
  • Cisplatin / administration & dosage
  • Humans
  • Interleukin-2 / administration & dosage
  • Interleukin-2 / analogs & derivatives
  • Molecular Targeted Therapy
  • Neoplasm Grading
  • Neoplasm Metastasis
  • Neoplasm Staging
  • Nivolumab / administration & dosage
  • Polyethylene Glycols / administration & dosage
  • Prognosis
  • Research Design*
  • Urologic Neoplasms / diagnosis
  • Urologic Neoplasms / drug therapy*
  • Urologic Neoplasms / etiology
  • Urologic Neoplasms / mortality

Substances

  • Biomarkers, Tumor
  • Interleukin-2
  • Nivolumab
  • Polyethylene Glycols
  • bempegaldesleukin
  • Cisplatin

Grants and funding