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Pre- and Postoperative Neratinib for HER2-Positive Breast Cancer Brain Metastases: Translational Breast Cancer Research Consortium 022.
Freedman, Rachel A; Gelman, Rebecca S; Agar, Nathalie Y R; Santagata, Sandro; Randall, Elizabeth C; Gimenez-Cassina Lopez, Begoña; Connolly, Roisin M; Dunn, Ian F; Van Poznak, Catherine H; Anders, Carey K; Melisko, Michelle E; Silvestri, Kelly; Cotter, Christine M; Componeschi, Kathryn P; Marte, Juan M; Moy, Beverly; Blackwell, Kimberly L; Puhalla, Shannon L; Ibrahim, Nuhad; Moynihan, Timothy J; Nangia, Julie; Tung, Nadine; Burns, Robyn; Rimawi, Mothaffar F; Krop, Ian E; Wolff, Antonio C; Winer, Eric P; Lin, Nancy U.
Afiliación
  • Freedman RA; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA. Electronic address: rafreedman@partners.org.
  • Gelman RS; Department of Biostatistics and Computational Biology, Dana-Farber Cancer Institute, Boston, MA.
  • Agar NYR; Department of Neurosurgery, Brigham and Women's Hospital, Boston, MA.
  • Santagata S; Department of Pathology, Brigham and Women's Hospital, Boston, MA.
  • Randall EC; Department of Neurosurgery, Brigham and Women's Hospital, Boston, MA.
  • Gimenez-Cassina Lopez B; Department of Neurosurgery, Brigham and Women's Hospital, Boston, MA.
  • Connolly RM; Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD.
  • Dunn IF; Department of Neurosurgery, University of Oklahoma, Oklahoma City, OK.
  • Van Poznak CH; University of Michigan, Ann Arbor, MI.
  • Anders CK; Division of Medical Oncology, Department of Medicine, University of North Carolina, Chapel Hill, NC.
  • Melisko ME; Department of Medical Oncology, University of California at San Francisco, San Francisco, CA.
  • Silvestri K; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Cotter CM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Componeschi KP; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Marte JM; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Moy B; Massachusetts General Hospital, Boston, MA.
  • Blackwell KL; Department of Medicine, Duke University Medical Center, Durham, NC.
  • Puhalla SL; University of Pittsburgh Cancer Institute, Magee-Women's Hospital, Pittsburgh, PA.
  • Ibrahim N; The University of Texas MD Anderson Cancer Center, Houston, TX.
  • Moynihan TJ; Department of Medical Oncology, Mayo Clinic, Rochester, MN.
  • Nangia J; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX.
  • Tung N; Beth Israel Deaconess Medical Center, Boston, MA.
  • Burns R; The Emmes Corporation, Rockville, MD.
  • Rimawi MF; Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX.
  • Krop IE; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Wolff AC; Sidney Kimmel Comprehensive Cancer Center, Johns Hopkins School of Medicine, Baltimore, MD.
  • Winer EP; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
  • Lin NU; Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA.
Clin Breast Cancer ; 20(2): 145-151.e2, 2020 04.
Article en En | MEDLINE | ID: mdl-31558424
PURPOSE: This pilot study was performed to test our ability to administer neratinib monotherapy before clinically recommended craniotomy in patients with HER2-positive metastatic breast cancer to the central nervous system, to examine neratinib's central nervous system penetration at craniotomy, and to examine postoperative neratinib maintenance. PATIENTS AND METHODS: Patients with HER2-positive brain metastases undergoing clinically indicated cranial resection of a parenchymal tumor received neratinib 240 mg orally once a day for 7 to 21 days preoperatively, and resumed therapy postoperatively in 28-day cycles. Exploratory evaluations of time to disease progression, survival, and correlative tissue, cerebrospinal fluid (CSF), and blood-based analyses examining neratinib concentrations were planned. The study was registered at ClinicalTrials.gov under number NCT01494662. RESULTS: We enrolled 5 patients between May 22, 2013, and October 18, 2016. As of March 1, 2019, patients had remained on the study protocol for 1 to 75+ postoperative cycles pf therapy. Two patients had grade 3 diarrhea. Evaluation of the CSF showed low concentrations of neratinib; nonetheless, 2 patients continued to receive therapy without disease progression for at least 13 cycles, with one on-study treatment lasting for nearly 6 years. Neratinib distribution in surgical tissue was variable for 1 patient, while specimens from 2 others did not produce conclusive results as a result of limited available samples. CONCLUSION: Neratinib resulted in expected rates of diarrhea in this small cohort, with 2 of 5 patients receiving the study treatment for durable periods. Although logistically challenging, we were able to test a limited number of CSF- and parenchymal-based neratinib concentrations. Our findings from resected tumor tissue in one patient revealed heterogeneity in drug distribution and tumor histopathology.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Quinolinas / Neoplasias Encefálicas / Neoplasias de la Mama / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudio: Guideline Límite: Adult / Female / Humans / Middle aged Idioma: En Revista: Clin Breast Cancer Asunto de la revista: NEOPLASIAS Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Quinolinas / Neoplasias Encefálicas / Neoplasias de la Mama / Protocolos de Quimioterapia Combinada Antineoplásica Tipo de estudio: Guideline Límite: Adult / Female / Humans / Middle aged Idioma: En Revista: Clin Breast Cancer Asunto de la revista: NEOPLASIAS Año: 2020 Tipo del documento: Article