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BioPATH: A Biomarker Study in Asian Patients with HER2+ Advanced Breast Cancer Treated with Lapatinib and Other Anti-HER2 Therapy.
Kim, Sung-Bae; Do, In-Gu; Tsang, Janice; Kim, Tae-You; Yap, Yoon-Sim; Cornelio, Gerardo; Gong, Gyungyub; Paik, Soonmyung; Lee, Suee; Ng, Ting-Ying; Park, Sarah; Oh, Ho-Suk; Chiu, Joanne; Sohn, Joohyuk; Lee, Moonhee; Choi, Young-Jin; Lee, Eun Mi; Park, Kyong-Hwa; Nathaniel, Christos; Ro, Jungsil.
Afiliación
  • Kim SB; Department of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Do IG; Department of Pathology, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul, Korea.
  • Tsang J; Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
  • Kim TY; Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea.
  • Yap YS; Division of Medical Oncology, National Cancer Centre Singapore, Singapore.
  • Cornelio G; Department of Medicine, San Juan De Dios Hospital, Manila, Philippines.
  • Gong G; Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • Paik S; Department of Medical Oncology and Severance Biomedical Research Institute, Yonsei University College of Medicine, Seoul, Korea.
  • Lee S; Department of Internal Medicine, Dong-A University Hospital, Busan, Korea.
  • Ng TY; Department of Clinical Oncology, Tuen Mun Hospital, Hong Kong, China.
  • Park S; The Center for Anti-Cancer Companion Diagnostics, Bio-MAX/ N-Bio, Seoul National University, Seoul, Korea.
  • Oh HS; Department of Hematology- Oncology, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Korea.
  • Chiu J; Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
  • Sohn J; Division of Medical Oncology, Yonsei Cancer Center, Seoul, Korea.
  • Lee M; Division of Hematology-Oncology, Inha University Hospital, Incheon, Korea.
  • Choi YJ; Department of Hematology- Oncology, Pusan National University Hospital, Busan, Korea.
  • Lee EM; Department of Internal Medicine, Kosin University Gospel Hospital, Busan, Korea.
  • Park KH; Department of Internal Medicine, Korea University Anam Hospital, Seoul, Korea.
  • Nathaniel C; Novartis Pharmaceuticals Corporation, APSA, Midrand, South Africa.
  • Ro J; Graduate School of Cancer Science and Policy, National Cancer Center, Goyang, Korea.
Cancer Res Treat ; 51(4): 1527-1539, 2019 Oct.
Article en En | MEDLINE | ID: mdl-31163957
ABSTRACT

PURPOSE:

BioPATH is a non-interventional study evaluating the relationship of molecular biomarkers (PTEN deletion/downregulation, PIK3CA mutation, truncated HER2 receptor [p95HER2], and tumor HER2 mRNA levels) to treatment responses in Asian patients with HER2+ advanced breast cancer treated with lapatinib and other HER2-targeted agents. MATERIALS AND

METHODS:

Female Asian HER2+ breast cancer patients (n=154) who were candidates for lapatinib-based treatment following metastasis and having an available primary tumor biopsy specimen were included. The primary endpoint was progression-free survival (PFS). Secondary endpoints were response rate, overall survival on lapatinib, correlation between biomarker status and PFS for any previous trastuzumab-based treatment, and conversion/conservation rates of the biomarker status between tissue samples collected at primary diagnosis and at recurrence/metastasis. Potential relationships between tumor mRNA levels of HER2 and response to lapatinib-based therapy were also explored.

RESULTS:

p95HER2, PTEN deletion/downregulation, and PIK3CA mutation did not demonstrate any significant co-occurrence pattern and were not predictive of clinical outcomes on either lapatinib-based treatment or any previous trastuzumab-based therapy in the metastatic setting. Proportions of tumors positive for p95HER2 expression, PIK3CA mutation, and PTEN deletion/down-regulation at primary diagnosis were 32%, 31.2%, and 56.2%, respectively. Despite limited availability of paired samples, biomarker status patterns were conserved in most samples. HER2 mRNA levels were not predictive of PFS on lapatinib.

CONCLUSION:

The prevalence of p95HER2 expression, PIK3CA mutation, and PTEN deletion/downregulation at primary diagnosis were similar to previous reports. Importantly, no difference was observed in clinical outcome based on the status of these biomarkers, consistent with reports from other studies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / Inhibidores de Proteínas Quinasas / Lapatinib Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged País/Región como asunto: Asia Idioma: En Revista: Cancer Res Treat Año: 2019 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Biomarcadores de Tumor / Inhibidores de Proteínas Quinasas / Lapatinib Tipo de estudio: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Female / Humans / Middle aged País/Región como asunto: Asia Idioma: En Revista: Cancer Res Treat Año: 2019 Tipo del documento: Article
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