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A Phase III Study of Pafolacianine Injection (OTL38) for Intraoperative Imaging of Folate Receptor-Positive Ovarian Cancer (Study 006).
Tanyi, Janos L; Randall, Leslie M; Chambers, Setsuko K; Butler, Kristina A; Winer, Ira S; Langstraat, Carrie L; Han, Ernest S; Vahrmeijer, Alexander L; Chon, Hye Sook; Morgan, Mark A; Powell, Matthew A; Tseng, Jill H; Lopez, Alexis S; Wenham, Robert M.
  • Tanyi JL; Hospital of the University of Pennsylvania, Abramson Cancer Center, West Pavilion, Philadelphia, PA.
  • Randall LM; Virginia Commonwealth University Health, Massey Cancer Center, Richmond, VA.
  • Chambers SK; University of Arizona Cancer Center, Tucson, AZ.
  • Butler KA; Mayo Clinic Hospital-Phoenix, Phoenix, AZ.
  • Winer IS; Karmanos Cancer Institute, Detroit, MI.
  • Langstraat CL; Mayo Clinic-Rochester, Rochester, MI.
  • Han ES; City of Hope Comprehensive Cancer Center, Duarte, CA.
  • Vahrmeijer AL; Leiden University, Leiden, the Netherlands.
  • Chon HS; Moffitt Cancer Center, Tampa, FL.
  • Morgan MA; Hospital of the University of Pennsylvania, Abramson Cancer Center, Philadelphia, PA.
  • Powell MA; Washington University-St Louis, St Louis, MO.
  • Tseng JH; University of California-Irvine, Orange, CA.
  • Lopez AS; Moffitt Cancer Center, Tampa, FL.
  • Wenham RM; Moffitt Cancer Center, Tampa, FL.
J Clin Oncol ; 41(2): 276-284, 2023 01 10.
Article en En | MEDLINE | ID: mdl-36070540
ABSTRACT

PURPOSE:

The adjunctive use of intraoperative molecular imaging (IMI) is gaining acceptance as a potential means to improve outcomes for surgical resection of targetable tumors. This confirmatory study examined the use of pafolacianine for real-time detection of folate receptor-positive ovarian cancer.

METHODS:

This phase III, open-label, 11-center study included subjects with known or suspected ovarian cancer, scheduled to undergo cytoreductive surgery. The objectives were to confirm safety and efficacy of pafolacianine (0.025 mg/kg IV), given ≥ 1 hour before intraoperative near-infrared imaging to detect macroscopic lesions not detected by palpation and normal white light.

RESULTS:

From March 2018 through April 2020, 150 patients received a single infusion of pafolacianine (safety analysis set); 109 patients with folate receptor-positive ovarian cancer comprised the full analysis set for efficacy. In 33.0% of patients (95% CI, 24.3 to 42.7; P < .001), pafolacianine with near-infrared imaging identified additional cancer on tissue not planned for resection and not detected by white light assessment and palpation, exceeding the prespecified threshold of 10%. Among patients who underwent interval debulking surgery, the rate was 39.7% (95% CI, 27.0 to 53.4; P < .001). The sensitivity to detect ovarian cancer was 83%, and the patient false-positive rate was 24.8%. Investigators reported achieving complete R0 resection in 62.4% (68 of 109) of patients. Drug-related adverse events were reported by 30% of patients (45 of 150) and most commonly included nausea, vomiting, and abdominal pain. No drug-related serious adverse events or deaths were reported.

CONCLUSION:

This phase III study of pafolacianine met its primary efficacy end point, identifying additional cancers not otherwise identified or planned for resection. Pafolacianine may offer an important real-time adjunct to current surgical approaches for ovarian cancer.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Receptor 1 de Folato Límite: Female / Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Ováricas / Receptor 1 de Folato Límite: Female / Humans Idioma: En Año: 2023 Tipo del documento: Article