Phase I study of primary treatment with 5-FU, oxaliplatin, irinotecan, levofolinate, and panitumumab combination chemotherapy in patients with advanced/recurrent colorectal cancer involving the wild-type RAS gene: the JACCRO CC-14 study

International Journal of Clinical Oncology - Tập 23 - Trang 490-496 - 2018
Hironaga Satake1, Akihito Tsuji2, Masato Nakamura3, Masaaki Ogawa4, Takeshi Kotake1, Yukimasa Hatachi1, Hisateru Yasui1, Akinori Takagane5, Yoshihiro Okita2, Kumi Nakamura3, Toshihide Onikubo3, Masahiro Takeuchi6, Masashi Fujii7
1Department of Medical Oncology, Kobe City Medical Center General Hospital, Kobe, Japan
2Department of Clinical Oncology, Kagawa University Faculty of Medicine–Kagawa University Hospital, Kita-gun, Japan
3Aizawa Comprehensive Cancer Center, Aizawa Hospital, Matsumoto, Japan
4Department of Surgery, Kazuno Kosei Hospital, Kazuno, Japan
5Department of Surgery, Hakodate Goryoukaku Hospital, Hakodate, Japan
6Department of Clinical Medicine (Biostatistics), Kitasato University School of Pharmacy, Tokyo, Japan
7Japan Clinical Cancer Research Organization, Tokyo, Japan

Tóm tắt

FOLFOXIRI is now regarded as the chemotherapy regimen that offers the best platform for the treatment of colorectal cancer. However, the safety and efficacy of FOLFOXIRI + panitumumab has not been demonstrated. We conducted a phase I study to determine the recommended dose of FOLFOXIRI + panitumumab as first-line treatment for RAS wild-type metastatic colorectal cancer (mCRC). Patients received combination therapy consisting of panitumumab (6 mg/kg on day 1) + FOLFOXIRI [irinotecan (CPT-11), oxaliplatin (L-OHP) 85 mg/m2, and folinate (LV) 200 mg/m2] on day 1, followed by fluorouracil (5-FU) 3200 mg/m2 infused as a 46-h continuous infusion starting on day 1) repeated every 2 weeks as first-line treatment of RAS wild-type mCRC patients. A decrease in CPT-11 dose was planned (started at level 1: CPT-11 165 mg/m2). Seven patients were enrolled, and six were assessed for safety and efficacy. Maximum tolerated dose was not reached at level 1; all patients were treated at these levels. The common Grade 3 or 4 relevant toxicities were diarrhea (50%), hypokalemia (33%) and stomatitis (33%). No treatment-related deaths occurred. Of the six patients assessed four had partial response and the two others had stable disease; hence, the response rate was 66.7% (95% confidence interval 28.9–100%) and the disease control rate was 100%. Time to protocol treatment failure was 7.2 (1.4–7.3) months. The FOLFOXIRI + panitumumab chemotherapy regimen was well tolerated by our patients with mCRC and showed promising anti-tumor activity. The recommended phase II dose was determined to be the same as the standard doses of this regimen used worldwide.

Tài liệu tham khảo

Cancer information service projected cancer statistics, 2014. http://ganjoho.jp/en/public/statistics/short_pred.html. Accessed 16 Oct 2014 Grothey A, Sargent D (2005) Overall survival of patients with advanced colorectal cancer correlates with availability of fluorouracil, irinotecan, and oxaliplatin regardless of whether doublet or single-agent therapy is used first line. J Clin Oncol 23(36):9441–9442 Falcone A, Ricci S, Brunetti I et al (2007) Phase III trial of infusional fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFOXIRI) compared with infusional fluorouracil, leucovorin, and irinotecan (FOLFIRI) as first-line treatment for metastatic colorectal cancer: the Gruppo Oncologico Nord Ovest. J Clin Oncol 25(13):1670–1676 Loupakis F, Cremolini C, Masi G et al (2014) Initial therapy with FOLFOXIRI and bevacizumab for metastatic colorectal cancer. N Engl J Med 371(17):1609–1618 Satake H, Tsuji A, Kotake T et al (2015) First report of a Japanese phase I study of triplet plus bevacizumab for chemotherapy-naive metastatic colorectal cancer (J1-TRIBE study). Cancer Treat Commun 4:75–80 Fornaro L, Lonardi S, Masi G et al (2013) FOLFOXIRI in combination with panitumumab as first-line treatment in quadruple wild-type (KRAS, NRAS, HRAS, BRAF) metastatic colorectal cancer patients: a phase II trial by the Gruppo Oncologico Nord Ovest (GONO). Ann Oncol 24(8):2062–2067 Saridaki Z, Androulakis N, Vardakis N et al (2012) A triplet combination with irinotecan (CPT-11), oxaliplatin (LOHP), continuous infusion 5-fluorouracil and leucovorin (FOLFOXIRI) plus cetuximab as first-line treatment in KRAS wt, metastatic colorectal cancer: a pilot phase II trial. Br J Cancer 107(12):1932–1937 Assenat E, Desseigne F, Thezenas S et al (2011) Cetuximab plus FOLFIRINOX (ERBIRINOX) as first-line treatment for unresectable metastatic colorectal cancer: a phase II trial. Oncologist 16(11):1557–1564 Sunakawa Y, Fujita K, Ichikawa W et al (2012) A phase I study of infusional 5-fluorouracil, leucovorin, oxaliplatin and irinotecan in Japanese patients with advanced colorectal cancer who harbor UGT1A1*1/*1,*1/*6 or *1/*28. Oncology 82(4):242–248 Douillard JY, Siena S, Cassidy J et al (2010) Randomized, phase III trial of panitumumab with infusional fluorouracil, leucovorin, and oxaliplatin (FOLFOX4) versus FOLFOX4 alone as first-line treatment in patients with previously untreated metastatic colorectal cancer: the PRIME study. J Clin Oncol 28(31):4697–4705 Schutz FA, Jardim DL, Je Y et al (2011) Haematologic toxicities associated with the addition of bevacizumab in cancer patients. Eur J Cancer 47(8):1161–1174