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Clinical Efficacy and Molecular Response Correlates of the WEE1 Inhibitor Adavosertib Combined with Cisplatin in Patients with Metastatic Triple-Negative Breast Cancer.
Keenan, Tanya E; Li, Tianyu; Vallius, Tuulia; Guerriero, Jennifer L; Tayob, Nabihah; Kochupurakkal, Bose; Davis, Janae; Pastorello, Ricardo; Tahara, Rie K; Anderson, Leilani; Conway, Jake; He, Meng X; Shannon, Erin; Godin, Robert E; Sorger, Peter K; D'Andrea, Alan; Overmoyer, Beth; Winer, Eric P; Mittendorf, Elizabeth A; Van Allen, Eliezer M; Shapiro, Geoffrey I; Tolaney, Sara M.
Afiliación
  • Keenan TE; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Li T; Broad Institute of Massachusetts Institute of Technology and Harvard, Cambridge, Massachusetts.
  • Vallius T; Breast Oncology Program, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts.
  • Guerriero JL; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Tayob N; Breast Oncology Program, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts.
  • Kochupurakkal B; Breast Tumor Immunology Laboratory, Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Davis J; Laboratory of Systems Pharmacology, Department of Systems Biology, Harvard Medical School, Boston Massachusetts.
  • Pastorello R; Ludwig Center for Cancer Research at Harvard, Harvard Medical School, Boston, Massachusetts.
  • Tahara RK; Breast Tumor Immunology Laboratory, Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Anderson L; Laboratory of Systems Pharmacology, Department of Systems Biology, Harvard Medical School, Boston Massachusetts.
  • Conway J; Ludwig Center for Cancer Research at Harvard, Harvard Medical School, Boston, Massachusetts.
  • He MX; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Shannon E; Breast Oncology Program, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts.
  • Godin RE; Center for DNA Damage and Repair, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Sorger PK; Breast Tumor Immunology Laboratory, Department of Cancer Biology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • D'Andrea A; Laboratory of Systems Pharmacology, Department of Systems Biology, Harvard Medical School, Boston Massachusetts.
  • Overmoyer B; Ludwig Center for Cancer Research at Harvard, Harvard Medical School, Boston, Massachusetts.
  • Winer EP; Breast Oncology Program, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts.
  • Mittendorf EA; Division of Breast Surgery, Department of Surgery, Brigham and Women's Hospital, Boston, Massachusetts.
  • Van Allen EM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
  • Shapiro GI; Breast Oncology Program, Dana-Farber/Brigham and Women's Cancer Center, Boston, Massachusetts.
  • Tolaney SM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Clin Cancer Res ; 27(4): 983-991, 2021 02 15.
Article en En | MEDLINE | ID: mdl-33257427
ABSTRACT

PURPOSE:

We report results from a phase II study assessing the efficacy of the WEE1 inhibitor adavosertib with cisplatin in metastatic triple-negative breast cancer (mTNBC). PATIENTS AND

METHODS:

Patients with mTNBC treated with 0-1 prior lines of chemotherapy received cisplatin 75 mg/m2 i.v. followed 21 days later by cisplatin plus adavosertib 200 mg oral twice daily for five doses every 21 days. The study had 90% power to detect the difference between null (20%) and alternative (40%) objective response rates (ORR) with a one-sided type I error of 0.1 an ORR >30% was predefined as making the regimen worthy of further study. RNA sequencing and multiplex cyclic immunofluorescence on pre- and post-adavosertib tumor biopsies, as well as targeted next-generation sequencing on archival tissue, were correlated with clinical benefit, defined as stable disease ≥6 months or complete or partial response.

RESULTS:

A total of 34 patients initiated protocol therapy; median age was 56 years, 2 patients (6%) had BRCA2 mutations, and 14 (41%) had one prior chemotherapy. ORR was 26% [95% confidence interval (CI), 13-44], and median progression-free survival was 4.9 months (95% CI, 2.3-5.7). Treatment-related grade 3-5 adverse events occurred in 53% of patients, most commonly diarrhea in 21%. One death occurred because of sepsis, possibly related to study therapy. Tumors from patients with clinical benefit demonstrated enriched immune gene expression and T-cell infiltration.

CONCLUSIONS:

Among patients with mTNBC treated with 0-1 prior lines, adavosertib combined with cisplatin missed the prespecified ORR cutoff of >30%. The finding of immune-infiltrated tumors in patients with clinical benefit warrants validation.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pirazoles / Pirimidinonas / Protocolos de Quimioterapia Combinada Antineoplásica / Cisplatino / Neoplasias de la Mama Triple Negativas Tipo de estudio: Guideline Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Clin Cancer Res Asunto de la revista: NEOPLASIAS Año: 2021 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Pirazoles / Pirimidinonas / Protocolos de Quimioterapia Combinada Antineoplásica / Cisplatino / Neoplasias de la Mama Triple Negativas Tipo de estudio: Guideline Límite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Clin Cancer Res Asunto de la revista: NEOPLASIAS Año: 2021 Tipo del documento: Article