A phase II study of the orally administered negative enantiomer of gossypol (AT-101), a BH3 mimetic, in patients with advanced adrenal cortical carcinoma.


Journal

Investigational new drugs
ISSN: 1573-0646
Titre abrégé: Invest New Drugs
Pays: United States
ID NLM: 8309330

Informations de publication

Date de publication:
08 2019
Historique:
received: 07 03 2019
accepted: 22 05 2019
pubmed: 7 6 2019
medline: 7 2 2020
entrez: 8 6 2019
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 31172443
doi: 10.1007/s10637-019-00797-1
pii: 10.1007/s10637-019-00797-1
pmc: PMC7515770
mid: NIHMS1628296
doi:

Substances chimiques

Antineoplastic Agents, Phytogenic 0
Proto-Oncogene Proteins c-bcl-2 0
Gossypol KAV15B369O
gossypol acetic acid S7RL72610R

Types de publication

Clinical Trial, Phase II Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

755-762

Subventions

Organisme : NCI NIH HHS
ID : UM1 CA186712
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA014089
Pays : United States
Organisme : NCI NIH HHS
ID : UM1 CA186717
Pays : United States

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Auteurs

Hao Xie (H)

Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.

Jun Yin (J)

Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.

Manisha H Shah (MH)

Division of Medical Oncology, Department of Internal Medicine, The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.

Michael E Menefee (ME)

FDA, Silver Spring, MD, 20993, USA.

Keith C Bible (KC)

Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.

Diane Reidy-Lagunes (D)

Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY, USA.

Madeleine A Kane (MA)

Department of Medicine and Division of Medical Oncology, University of Colorado, Anschutz Medical Campus, Aurora, CO, USA.

David I Quinn (DI)

University of Southern California Norris Comprehensive Cancer Center, Hospital and Clinics, Los Angeles, CA, 90033, USA.

David R Gandara (DR)

UC Davis Comprehensive Cancer Center, Sacramento, CA, USA.

Charles Erlichman (C)

Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA.

Alex A Adjei (AA)

Mayo Clinic Cancer Center, 200 First St. SW, Rochester, MN, 55905, USA. adjei.alex@mayo.edu.

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Classifications MeSH