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A phase II study of efficacy, toxicity, and the potential impact of genomic alterations on response to eribulin mesylate in combination with trastuzumab and pertuzumab in women with human epidermal growth factor receptor 2 (HER2)+ metastatic breast cancer.
Balch, Sara M; Vaz-Luis, Ines; Li, Tianyu; Tayob, Nabihah; Jain, Esha; Helvie, Karla; Buendia-Buendia, Jorge E; Shannon, Erin; Isakoff, Steven J; Tung, Nadine M; Krop, Ian E; Lin, Nancy U; Wagle, Nikhil; Freedman, Rachel A.
Afiliação
  • Balch SM; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Vaz-Luis I; Department of Medical Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Yawkey 1259, Boston, MA, 02215, USA.
  • Li T; Department of Medical Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Yawkey 1259, Boston, MA, 02215, USA.
  • Tayob N; Institut Gustave Roussy, Unit INSERM 981, Villejuif, France.
  • Jain E; Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Helvie K; Department of Data Sciences, Dana-Farber Cancer Institute, Boston, MA, USA.
  • Buendia-Buendia JE; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Shannon E; Department of Medical Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Yawkey 1259, Boston, MA, 02215, USA.
  • Isakoff SJ; Department of Medical Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Yawkey 1259, Boston, MA, 02215, USA.
  • Tung NM; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Krop IE; Cellarity, Inc., Cambridge, MA, USA.
  • Lin NU; The Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Wagle N; Massachusetts General Hospital, Boston, MA, USA.
  • Freedman RA; Harvard Medical School, Boston, MA, USA.
Breast Cancer Res Treat ; 189(2): 411-423, 2021 Sep.
Article em En | MEDLINE | ID: mdl-34302589
ABSTRACT

PURPOSE:

There are limited data on trastuzumab-pertuzumab (HP)-based treatments beyond the first-line, HER2+ metastatic breast cancer (MBC) setting. We conducted a phase II study of eribulin mesylate, which extends survival in MBC, with HP in patients with previously treated HER2+ MBC to evaluate efficacy, toxicity, and genomic alterations driving therapeutic response.

METHODS:

After a run-in phase for eribulin dosing, two cohorts were enrolled (Cohort A-no prior pertuzumab; Cohort B-prior pertuzumab). All patients received eribulin 1.4 mg/m2 on days 1, 8 with standard-dose HP on day 1 (21-day cycles). The primary endpoint was objective response rate (ORR). Genomic characterization via whole exome sequencing (WES) was completed on tumor DNA and matched germline DNA from 19 patients.

RESULTS:

The six-patient run-in established a dose of eribulin 1.4 mg/m2 with HP. Cohorts A and B enrolled 17 and 7 patients, respectively. Accrual stopped early due to an evolving treatment landscape and slow enrollment. The ORR was 26.3% (95% Confidence Interval [CI] 9.2-51.2%) in Cohort A and 0% in Cohort B (95% CI 0-41.0%). WES revealed more frequent alterations in TP53 (p < 0.05, q > 0.05) in patients without clinical benefit (disease control for < 24 weeks) which was not significant after multiple hypothesis correction.

CONCLUSION:

Eribulin-HP had manageable toxicity and modest clinical activity in patients without prior pertuzumab exposure. This study provides a preliminary landscape of somatic alterations in this patient cohort. Our data add to the literature on how genomic alterations may predict for therapy response/resistance, as we work to individualize choices in a quickly evolving HER2+ MBC treatment landscape. TRIAL REGISTRATION www.clinicaltrials.gov , NCT01912963. Registered 24 July 2013.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Breast Cancer Res Treat Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias da Mama Tipo de estudo: Prognostic_studies Limite: Female / Humans Idioma: En Revista: Breast Cancer Res Treat Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos