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Phase II study of everolimus (RAD001) monotherapy as first-line treatment in advanced biliary tract cancer with biomarker exploration: the RADiChol Study.
Lau, David K; Tay, Rebecca Y; Yeung, Yvonne H; Chionh, Fiona; Mooi, Jennifer; Murone, Carmel; Skrinos, Effie; Price, Timothy J; Mariadason, John M; Tebbutt, Niall C.
Afiliación
  • Lau DK; Olivia Newton-John Cancer Research Institute, Melbourne, VIC, Australia.
  • Tay RY; School of Cancer Medicine, La Trobe University, Bundoora, VIC, Australia.
  • Yeung YH; Dept of Medical Oncology, Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Melbourne, VIC, Australia.
  • Chionh F; Dept of Medical Oncology, Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Melbourne, VIC, Australia.
  • Mooi J; Olivia Newton-John Cancer Research Institute, Melbourne, VIC, Australia.
  • Murone C; Dept of Medical Oncology, Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Melbourne, VIC, Australia.
  • Skrinos E; Olivia Newton-John Cancer Research Institute, Melbourne, VIC, Australia.
  • Price TJ; Olivia Newton-John Cancer Research Institute, Melbourne, VIC, Australia.
  • Mariadason JM; Olivia Newton-John Cancer Research Institute, Melbourne, VIC, Australia.
  • Tebbutt NC; Dept of Medical Oncology, Olivia Newton-John Cancer Wellness and Research Centre, Austin Health, Melbourne, VIC, Australia.
Br J Cancer ; 118(7): 966-971, 2018 04.
Article en En | MEDLINE | ID: mdl-29527009
ABSTRACT

BACKGROUND:

Advanced biliary tract cancers (BTCs) have a poor prognosis and limited treatment options. This exploratory phase II study aimed to evaluate the activity of the mTOR inhibitor everolimus in advanced BTC and explore prognostic biomarkers.

METHODS:

Patients with advanced BTCs, who had not received chemotherapy for advanced disease, were enroled to receive everolimus (10 mg daily). The primary endpoint was disease control rate (DCR) at 12 weeks. Secondary endpoints included overall response rate, progression-free survival (PFS), overall survival (OS) and adverse events. Activation status of the RAS and phosphatidylinositol 3-kinase (PI3K)/AKT/mTOR pathways was assessed by DNA sequencing and immunohistochemistry on archival tumour tissue.

RESULTS:

The study enroled 27 patients and the DCR at 12 weeks was 48%. Median PFS was 5.5 months (95% confidence interval (CI) 2.1-10.0 months) and median OS was 9.5 months (95% CI 5.5-16.6 months). DCR at 12 weeks was significantly worse for gall bladder carcinoma compared to other anatomical sites, and there was a trend towards a worsened PFS and OS. Treatment was well tolerated. KRAS (12%) and PIK3CA mutations (12%) were uncommon. Immunohistochemical staining for PI3K/AKT/mTOR pathways did not significantly correlate with outcome.

CONCLUSION:

In unselected patients, everolimus demonstrated clinical activity as first-line monotherapy in advanced BTC.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Sistema Biliar / Adenocarcinoma / Biomarcadores de Tumor / Everolimus Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Año: 2018 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias del Sistema Biliar / Adenocarcinoma / Biomarcadores de Tumor / Everolimus Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Br J Cancer Año: 2018 Tipo del documento: Article País de afiliación: Australia