論文

査読有り 筆頭著者 国際誌
2016年9月

Amrubicin in patients with platinum-refractory metastatic neuroendocrine carcinoma and mixed adenoneuroendocrine carcinoma of the gastrointestinal tract.

Anti-cancer drugs
  • Tomonori Araki
  • Atsuo Takashima
  • Tetsuya Hamaguchi
  • Yoshitaka Honma
  • Satoru Iwasa
  • Natsuko Okita
  • Ken Kato
  • Yasuhide Yamada
  • Hironobu Hashimoto
  • Hirokazu Taniguchi
  • Ryoji Kushima
  • Kazuhiko Nakao
  • Narikazu Boku
  • Yasuhiro Shimada
  • 全て表示

27
8
開始ページ
794
終了ページ
9
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1097/CAD.0000000000000393

Although the same treatment strategy as used for small cell lung cancer, including second-line chemotherapy, is generally applied to metastatic neuroendocrine carcinoma (NEC) and mixed adenoneuroendocrine carcinoma (MANEC) of the gastrointestinal tract (GIT; GIT-NEC/MANEC), the efficacy of amrubicin (AMR) for GIT-NEC/MANEC is not well known. We retrospectively analyzed platinum-refractory GIT-NEC/MANEC patients who received AMR between February 2004 and July 2012 at the National Cancer Center Hospital. The AMR dose administered was 30-45 mg/m on days 1-3 every 3-4 weeks. The overall response rate according to Response Evaluation Criteria in Solid Tumors guidelines, version 1.0, progression-free survival, overall survival, and adverse events by National Cancer Institute-Common Terminology Criteria for Adverse Events guidelines, version 4.0 were evaluated. Nineteen patients received AMR. The response rate for 16 assessable patients was 18.8% (95% confidence interval, 4.1-45.7), the median progression-free survival was 3.8 months (2.3-5.3), and the median overall survival was 7.7 months (7.1-8.2). Grade 3/4 neutropenia occurred in 52.6% of patients and febrile neutropenia occurred in 10.5%. Other nonhematological toxicities were mild and treatment-related deaths were not observed. AMR may have a modest effect, with tolerable toxicities, on patients with platinum-refractory GIT-NEC/MANEC. Further prospective evaluations are warranted.

リンク情報
DOI
https://doi.org/10.1097/CAD.0000000000000393
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/27341105
ID情報
  • DOI : 10.1097/CAD.0000000000000393
  • PubMed ID : 27341105

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