Your browser doesn't support javascript.
loading
Tipifarnib in recurrent, metastatic HRAS-mutant salivary gland cancer.
Hanna, Glenn J; Guenette, Jeffrey P; Chau, Nicole G; Sayehli, Cyrus M; Wilhelm, Christian; Metcalf, Robert; Wong, Deborah J; Brose, Marcia; Razaq, Mohammad; Pérez-Ruiz, Elisabeth; Cohen, Ezra E W; Aggarwal, Rahul; Scholz, Catherine; Gualberto, Antonio; Ho, Alan L.
Afiliação
  • Hanna GJ; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Guenette JP; Division of Neuroradiology, Brigham & Women's Hospital, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Chau NG; Department of Medical Oncology, BC Cancer Vancouver Centre, Vancouver, British Columbia, Canada.
  • Sayehli CM; Department of Internal Medicine II, Early Clinical Trial Unit, University Hospital Wurzburg, Wurzburg, Germany.
  • Wilhelm C; Department of Otorhinolaryngology, Plastic, Aesthetic and Reconstructive Head and Neck Surgery, Julius Maximilian University of Wuerzburg, Wuerzburg, Germany.
  • Metcalf R; Medical Oncology, The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Wong DJ; Division of Hematology and Oncology, Department of Medicine, Ronald Reagan University of California at Los Angeles Medical Center, Los Angeles, California.
  • Brose M; Department of Otorhinolaryngology, Head and Neck Surgery, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.
  • Razaq M; Department of Hematology/Oncology, Stephenson Cancer Center, The University of Oklahoma, Oklahoma City, Oklahoma.
  • Pérez-Ruiz E; Department of Medical Oncology, Institute of Biomedical Research of Malaga, Costa del Sol Health Agency, Marbella, Spain.
  • Cohen EEW; Division of Hematology-Oncology, Moores Cancer Center, University of California at San Diego Health, San Diego, California.
  • Aggarwal R; Division of Hematology/Oncology, University of California at San Francisco Helen Diller Family Comprehensive Cancer Center, San Francisco, California.
  • Scholz C; Kura Oncology, San Diego, California.
  • Gualberto A; Kura Oncology, San Diego, California.
  • Ho AL; Department of Hematology/Oncology, Memorial Sloan Kettering Cancer Center, New York City, New York.
Cancer ; 126(17): 3972-3981, 2020 09 01.
Article em En | MEDLINE | ID: mdl-32557577
ABSTRACT

BACKGROUND:

To the authors' knowledge, there are no approved therapies for recurrent, metastatic (R/M) salivary gland carcinoma (SGC), but molecularly targeted therapies warrant ongoing investigation. In the current study, the authors have reported on the efficacy of tipifarnib in patients with aggressive HRAS-mutant, R/M SGC.

METHODS:

The current prospective, nonrandomized, multicenter, international cohort study involved 8 centers and was conducted from May 2015 to June 2019. The median follow-up was 22 months (range, 6-55 months). Subjects with HRAS-mutant R/M SGC (any histology) and disease progression within the last 6 months were enrolled. Tipifarnib was dosed orally twice daily. The authors determined the objective response rate using Response Evaluation Criteria in Solid Tumors (version 1.1), duration of response, and molecular predictors of response.

RESULTS:

A total of 13 patients with R/M SGC were enrolled; all had received prior systemic therapy (1-3 regimens). One objective response was observed; an additional 7 of 12 evaluable patients (58%) had stable disease as their best response with a median duration of 9 months (range, 3-14 months). Five of 7 patients had >10% tumor regression and 6 of 7 had stable disease lasting >6 months. Q61R was the most frequent activating HRAS mutation noted (7 of 13 patients; 54%), but gene variant and allele frequency did not correlate with outcomes. The median progression-free survival was 7 months (95% confidence interval, 5.9-10.1 months), and the median overall survival was 18 months (95% confidence interval, 9.6-22.4 months) with approximately 58.6% of patients alive at 1 year. Survival was similar regardless of HRAS mutant variant or co-occurring PIK3CA alterations. No participant discontinued treatment because of toxicity.

CONCLUSIONS:

Tipifarnib resulted in modest clinical activity with a promising disease control rate among patients with HRAS-mutant, R/M SGC who developed disease progression within the last 6 months.
Assuntos
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Salivares / Proteínas Proto-Oncogênicas p21(ras) / Quinolonas / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias das Glândulas Salivares / Proteínas Proto-Oncogênicas p21(ras) / Quinolonas / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cancer Ano de publicação: 2020 Tipo de documento: Article