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A phase II study of the orally administered negative enantiomer of gossypol (AT-101), a BH3 mimetic, in patients with advanced adrenal cortical carcinoma.
Xie, Hao; Yin, Jun; Shah, Manisha H; Menefee, Michael E; Bible, Keith C; Reidy-Lagunes, Diane; Kane, Madeleine A; Quinn, David I; Gandara, David R; Erlichman, Charles; Adjei, Alex A.
Afiliação
  • Xie H; Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.
  • Yin J; Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.
  • Shah MH; Division of Medical Oncology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
  • Menefee ME; FDA, Silver Spring, MD, 20993, USA.
  • Bible KC; Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.
  • Reidy-Lagunes D; Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Kane MA; Department of Medicine and Division of Medical Oncology, University of Colorado, Anschutz Medical Campus, Aurora, CO, USA.
  • Quinn DI; University of Southern California Norris Comprehensive Cancer Center, Hospital and Clinics, Los Angeles, CA, 90033, USA.
  • Gandara DR; UC Davis Comprehensive Cancer Center, Sacramento, CA, USA.
  • Erlichman C; Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.
  • Adjei AA; Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA. adjei.alex@mayo.edu.
Invest New Drugs ; 37(4): 755-762, 2019 08.
Article em En | MEDLINE | ID: mdl-31172443
ABSTRACT
Background Adrenal cortical carcinoma (ACC) is a rare cancer with treatment options of limited efficacy, and poor prognosis if metastatic. AT-101 is a more potent inhibitor of B cell lymphoma 2 family apoptosis-related proteins than its racemic form, gossypol, which showed preliminary clinical activity in ACC. We thus evaluated the efficacy of AT-101 in patients with advanced ACC. Methods Patients with histologically confirmed metastatic, recurrent, or primarily unresectable ACC were treated with AT-101 (20 mg/day orally, 21 days out of 28-day cycles) until disease progression and/or prohibitive toxicity. The primary endpoint was objective response rate, wherein a Response Evaluation Criteria In Solid Tumors (RECIST) partial response rate of 25% would be considered promising and 10% not, with a Type I error of 10% and 90% power. In a 2-stage design, 2 responses were required of the first 21 assessable subjects to warrant complete accrual of 44 patients. Secondary endpoints included safety, progression-free survival and overall survival. Results This study accrued 29 patients between 2009 and 2011; median number of cycles was 2. Seven percent experienced grade 4 toxicity including cardiac troponin elevations and hypokalemia. None of the first 21 patients attained RECIST partial response; accordingly, study therapy was deemed ineffective and the trial was permanently closed. Conclusions AT-101 had no meaningful clinical activity in this study in patients with advanced ACC, but demonstrated feasibility of prospective therapeutic clinical trials in this rare cancer.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gossipol / Neoplasias do Córtex Suprarrenal / Carcinoma Adrenocortical / Antineoplásicos Fitogênicos Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Gossipol / Neoplasias do Córtex Suprarrenal / Carcinoma Adrenocortical / Antineoplásicos Fitogênicos Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2019 Tipo de documento: Article