1. Phase II clinical trial of docetaxel and trastuzumab for HER2-positive advanced extramammary Paget's disease (EMPD-HER2DOC).
- Author
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Hirai, Ikuko, Tanese, Keiji, Nakamura, Yoshio, Fukuda, Keitaro, Ouchi, Takeshi, Hayashida, Tetsu, Kameyama, Kaori, Abe, Takayuki, Amagai, Masayuki, and Funakoshi, Takeru
- Subjects
THERAPEUTIC use of antineoplastic agents ,DOCETAXEL ,ADENOCARCINOMA ,COMMUNICABLE diseases ,TRASTUZUMAB ,PATIENT safety ,RESEARCH funding ,SKIN diseases ,CLINICAL trials ,ANTINEOPLASTIC agents ,DESCRIPTIVE statistics ,GENE expression ,METASTASIS ,INTRAVENOUS therapy ,LONGITUDINAL method ,CANCER chemotherapy ,ONCOGENES ,DRUG efficacy ,CONFIDENCE intervals ,EPIDERMAL growth factor receptors ,NEUTROPENIA ,SERUM albumin ,EVALUATION - Abstract
Background No consensus has been reached regarding the optimal chemotherapy for metastatic extramammary Paget's disease (EMPD), a rare cutaneous adenocarcinoma, because of the lack of solid evidence from prospective trials. However, the immunohistochemical profile of EMPD reportedly resembles that of breast cancer, particularly in terms of human epidermal growth factor receptor 2 (HER2) expression, suggesting that HER2 is a promising therapeutic target for advanced HER2-positive EMPD. Methods In this phase II single-arm trial, 13 Japanese patients received intravenous trastuzumab (loading dose of 8 mg/kg and maintenance dose of 6 mg/kg) and docetaxel (75 mg/m
2 ) every 3 weeks for up to 2 years. The docetaxel dose was reduced or discontinued according to its toxicity. The primary trial endpoints were objective response rate (ORR) after 3 cycles of treatment and safety throughout the study period. Results All 13 patients completed 3 cycles of combination therapy. The median follow-up was 27.9 months. The ORR was 76.9% (n = 10/13; 90% CI, 50.5-93.4). Frequently observed adverse events were neutropenia (100%), hypoalbuminemia (84.6%), and mucocutaneous infection (84.6%), all of which were well tolerated. Conclusion The combination of docetaxel and trastuzumab demonstrated a favorable clinical effect and acceptable tolerability, which makes it a good treatment option for HER2-positive metastatic EMPD (ClinicalTrials.gov Identifier: UMIN000021311, jRCTs031180073). [ABSTRACT FROM AUTHOR]- Published
- 2024
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