論文

査読有り 責任著者
2019年12月

A clinical trial to assess the feasibility and efficacy of nab-paclitaxel plus gemcitabine for elderly patients with unresectable advanced pancreatic cancer

International Journal of Clinical Oncology
  • Rikiya Hasegawa
  • Kosuke Okuwaki
  • Mitsuhiro Kida
  • Hiroshi Yamauchi
  • Yusuke Kawaguchi
  • Takaaki Matsumoto
  • Toru Kaneko
  • Eiji Miyata
  • Kazuho Uehara
  • Tomohisa Iwai
  • Masafumi Watanabe
  • Takahiro Kurosu
  • Hiroshi Imaizumi
  • Takashi Ohno
  • Wasaburo Koizumi
  • 全て表示

24
12
開始ページ
1574
終了ページ
1581
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1007/s10147-019-01511-0
出版者・発行元
Springer Science and Business Media LLC

BACKGROUND: The efficacy and safety of nanoparticle albumin-bound paclitaxel (nab-PTX) plus gemcitabine (GEM) in elderly Japanese patients with pancreatic cancer remain unclear. Therefore, we prospectively investigated the tolerability and efficacy of nab-PTX + GEM in Japanese patients aged ≥ 75 years with non-curatively resectable pancreatic cancer. METHODS: We treated eligible patients (n = 27) with nab-PTX + GEM until disease progression, appearance of adverse events, or withdrawal of consent. The primary endpoints included adverse events as well as dosing- and survival-related parameters. RESULTS: The rates of 2-cycle completion were 48.1% for nab-PTX and 55.6% for GEM; the relative dose intensities for the 7th (median) treatment cycle were 65.1% and 74.1%, respectively, whereas the dose-reduction rates were 81.5% and 48.1%, respectively. Grade 3 or higher hemotoxicity was observed in 14 of 27 subjects (51.9%); moreover, 22% experienced grade ≥ 3 peripheral nerve disorder and 1 patient (3.7%) died owing to chemotherapy-related interstitial pneumonia. The disease control rate was 92.6% (25/27), while the median progression-free and overall survival times were 7 and 10.3 months, respectively. CONCLUSION: The nab-PTX + GEM regimen is as efficacious in elderly patients who meet certain criteria as it is in previously reported non-elderly patients. The regimen is feasible with appropriate dose adjustments and attention to adverse events. TRIAL REGISTRATION: Clinical trial registration number: UMIN000018907.

リンク情報
DOI
https://doi.org/10.1007/s10147-019-01511-0
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31309381
URL
http://link.springer.com/content/pdf/10.1007/s10147-019-01511-0.pdf
URL
http://link.springer.com/article/10.1007/s10147-019-01511-0/fulltext.html
ID情報
  • DOI : 10.1007/s10147-019-01511-0
  • ISSN : 1341-9625
  • eISSN : 1437-7772
  • ORCIDのPut Code : 59491564
  • PubMed ID : 31309381

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