Your browser doesn't support javascript.
loading
Phase 2 study of irinotecan plus cetuximab rechallenge as third-line treatment in KRAS wild-type metastatic colorectal cancer: JACCRO CC-08.
Masuishi, Toshiki; Tsuji, Akihito; Kotaka, Masahito; Nakamura, Masato; Kochi, Mitsugu; Takagane, Akinori; Shimada, Ken; Denda, Tadamichi; Segawa, Yoshihiko; Tanioka, Hiroaki; Hara, Hiroki; Sagawa, Tamotsu; Watanabe, Takanori; Takahashi, Takao; Negoro, Yuji; Manaka, Dai; Fujita, Hideto; Suto, Takeshi; Takeuchi, Masahiro; Ichikawa, Wataru; Fujii, Masashi.
Afiliação
  • Masuishi T; Department of Clinical Oncology, Aichi Cancer Center Hospital, 1-1 Kanokoden, Chikusa-ku, Nagoya, Aichi, 464-8681, Japan. tmasuishi@aichi-cc.jp.
  • Tsuji A; Department of Gastroenterology, Tsuchiura Kyodo General Hospital, 1-1, Ootsuno, Tsuchiura, Ibaraki, 300-0028, Japan. tmasuishi@aichi-cc.jp.
  • Kotaka M; Department of Medical Oncology, Kagawa University Hospital, 1750-1 Ikenobe, Miki-cho, Kita-gun, Kagawa, 761-0793, Japan.
  • Nakamura M; Gastrointestinal Cancer Center, Sano Hospital, 2-5-1 Shimizugaoka, Tarumi-ku, Kobe, Hyogo, 655-0031, Japan.
  • Kochi M; Aizawa Comprehensive Cancer Center, Aizawa Hospital, 2-5-1 Honjyou, Matsumoto, Nagano, 390-8510, Japan.
  • Takagane A; Department of Digestive Surgery, Nihon University School of Medicine, 30-1 Oyaguchikamimachi, Itabashi-ku, Tokyo, 173-8610, Japan.
  • Shimada K; Department of Surgery, Hakodate Goryoukaku Hospital, 38-3 Goryoukaku-cho, Hakodate, Hokkaido, 040-8611, Japan.
  • Denda T; Department of Internal Medicine, Showa University Koto Toyosu Hospital, 5-1-38 Toyosu, Koto-ku, Tokyo, 135-8577, Japan.
  • Segawa Y; Department of Gastroenterology, Chiba Cancer Center, 666-2 Nitona-cho, Chuo-ku, Chiba, 350-1298, Japan.
  • Tanioka H; Department of Medical Oncology, Saitama Medical University International Medical Center, 1397-1 Yamane, Hidaka, Saitama, 350-1298, Japan.
  • Hara H; Clinical Oncology, Kawasaki Medical School Hospital, 577 Matsushima, Kurashiki, Okayama, 701-0192, Japan.
  • Sagawa T; Department of Gastroenterology, Saitama Cancer Center, 780 Komuro, ina, Kita-adachi-gun, Saitama, 362-0806, Japan.
  • Watanabe T; Department of Gastroenterology, Hokkaido Cancer Center, 2-3-54 Kikusuishijyo, Shiroishi-ku, Sapporo, Hokkaido, 003-0804, Japan.
  • Takahashi T; Department of Surgery, Japanese Red Cross Society Himeji Hospital, 1-12-1 Shimoteno, Himeji, Hyogo, 670-8540, Japan.
  • Negoro Y; Department of Surgical Oncology, Gifu University, Graduate School of Medicine, 1-1 Yanagido, Gifu, 501-1194, Japan.
  • Manaka D; Department of Gastroenterology, Kochi Health Sciences Center, 2125-1 Ike, Kochi, 781-8555, Japan.
  • Fujita H; Department of Surgery, Kyoto Katsura Hospital, 17 Yamadahirao-cho, Nishikyo-ku, Kyoto, 615-8256, Japan.
  • Suto T; Department of Digestive Surgery, Kanazawa Medical University Hospital, 1-1 Daigaku, Uchinadamachi, Kahoku-gun, Ishikawa, 920-0293, Japan.
  • Takeuchi M; Department of Gastroenterological Surgery, Yamagata Prefectural Central Hospital, 1800 Ooazaaoyagi, Yamagata, 990-2292, Japan.
  • Ichikawa W; Department of Clinical Medicine (Biostatistics), Kitasato University School of Pharmacy, 5-9-1 Shirokane, Minato-ku, Tokyo, 108-8641, Japan.
  • Fujii M; Division of Medical Oncology, Showa University Fujigaoka Hospital, 1-30 Fujigaoka, Aoba-ku, Yokohama, Kanagawa, 227-8501, Japan.
Br J Cancer ; 123(10): 1490-1495, 2020 11.
Article em En | MEDLINE | ID: mdl-32863385
ABSTRACT

BACKGROUND:

Regorafenib or trifluridine/tipiracil as third-line treatment have limited efficacy in metastatic colorectal cancer (mCRC).

METHODS:

This Phase 2 trial evaluated the efficacy and safety of irinotecan plus cetuximab rechallenge as third-line treatment in KRAS wild-type mCRC patients who achieved clinical benefit with first-line cetuximab-containing therapy. The primary endpoint was 3-month progression-free survival (PFS) rate. A sample size was calculated; 30 patients with a 3-month PFS rate of 45% deemed promising and 15% unacceptable. Patients with greater and less than the cut-off value of cetuximab-free intervals (CFIs) were classified into the long and short CFI groups, respectively, in subgroup analyses.

RESULTS:

Among 34 eligible patients who received treatment at least once, 3-month PFS rate was 44.1% (95% confidence interval, 27.4-60.8%). The median PFS and overall survival (OS) were 2.4 and 8.2 months, respectively. The response and disease control rates were 2.9 and 55.9%, respectively. PFS and OS were significantly longer in the long- than in the short CFI group.

CONCLUSIONS:

Irinotecan plus cetuximab rechallenge as third-line treatment for KRAS wild-type mCRC was safe and had promising activity, especially in those with a long CFI, warranting further investigation in a Phase 3 randomised trial. CLINICAL TRIAL REGISTRATION UMIN000010638.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Cetuximab / Irinotecano Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Adenocarcinoma / Protocolos de Quimioterapia Combinada Antineoplásica / Cetuximab / Irinotecano Tipo de estudo: Clinical_trials Limite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2020 Tipo de documento: Article