162P - Updated analysis: Phase II trial of irinotecan plus S-1 (IRIS) with cetuximab (IRIS/Cet) in pre-treated patients with KRAS wild type metastatic col...

Date 19 December 2015
Event ESMO Asia 2015 Congress
Session Poster presentation 1
Topics Anti-Cancer Agents & Biologic Therapy
Colon Cancer
Rectal Cancer
Presenter Ayumu Hosokawa
Citation Annals of Oncology (2015) 26 (suppl_9): 42-70. 10.1093/annonc/mdv523
Authors A. Hosokawa1, S. Yuki2, Y. Kawamoto3, T. Ando1, O. Muto4, M. Nakamura5, T. Kato6, I. Iwanaga7, K. Hatanaka8, Y. Tsuji9, A. Sato10, K. Eto11, K. Furukawa12, H. Okuda13, H. Hayashi14, K. Fujikawa15, M. Kudo16, T. Honda17, Y. Sakata18, Y. Komatsu3
  • 1Gastroenterology And Hematology, Toyama University Hospital, 930-0194 - Toyama/JP
  • 2Gastroenterology And Hepatology, Hokkaido University Hospital, 060-8638 - Sapporo/JP
  • 3Cancer Center, Hokkaido University Hospital, 060-8638 - Sapporo/JP
  • 4Medical Oncology, Japanese Red Cross Akita Hospital, Akita/JP
  • 5Gastroenterology, Sapporo City General Hospital, 060-8604 - Sapporo/JP
  • 6Internal Medicine, Hokkaido Gastroenterology Hospital, Sapporo/JP
  • 7Medical Oncology, Japanese Red Cross Kitami Hospital, Kitami/JP
  • 8Gastroenterology, Hakodate Municipal Hospital, Hakodate/JP
  • 9Medical Oncology, Tonan Hospital, 060-0001 - Sapporo/JP
  • 10Medical Oncology, Hirosaki University Graduate School of Medicine, Hirosaki/JP
  • 11Gastroenterology, Tomakomai City Hospital, Tomakomai/JP
  • 12Gastroenterology, Niigata City General Hospital, Niigata/JP
  • 13Medical Oncology, Keiyukai Sapporo Hospital, 003-0027 - Sapporo/JP
  • 14Gastroenterology, Abashiri Kosei General Hospital, Abashiri/JP
  • 15Gastroenterology, Hokkaido Cancer Center, Sapporo/JP
  • 16Gastroenterology, Sapporo Hokuyu Hospital, Sapporo/JP
  • 17Gastroenterology And Hepatology, Nagaski University Hospital, Nagasaki/JP
  • 18Ceo, Misawa City Hospital, 033-0022 - Misawa/JP

Abstract

Aim/Background

FIRIS trial reported that IRIS demonstrated the non-inferiority to FOLFIRI as second line treatment in mCRC. For the same setting, FOLFIRI/panitumumab significantly improved PFS as second-line treatment in patients with KRAS wild type mCRC (20050181 trial). Thus we conduct this study (HGCSG0902) to evaluate safety and efficacy combined IRIS and cetuximab (IRIS/Cet).

Methods

HGSCG0902 is a multicenter phase II study. Eligibility includes histologically confirmed colorectal cancer, previously received oxaliplatin-contained chemotherapy, PS: 0-1 and KRAS Exon2 wild type. Patients received S-1 80-120 mg/day p.o. on days 1-14 and irinotecan 100mg/m2 on days 1 and 15 repeated every 28 days. Cetuximab was administrated 400mg/m2 loading dose and continued 250mg/m2 every week or 500mg/m2 bi-weekly. The primary endpoint was response rate and the secondary endpoints were disease control rate, PFS, OS and safety. We estimated that a target sample size of 76 patients.

Results

Between Mar 2010 and September 2013, 58 pts were enrolled. One patient was not administered (57 pts were safety analysis set), and 3 pts were ineligible (54 pts were efficacy analysis set). Patients characteristics were as follows: median age 66 years (range 35-79), male: female 36:21, PS 0:1 38:19. Median number of cycles was 3. The main grade 3-4 AE were diarrhea (35.1%), neutropenia (26.8%), acne like rash (17.5%) and anorexia (15.8%). Response rate was 33.3% (95%CI 20.8-45.9%) and disease control rate was 79.6%. Median progression-free survival was 4.7 months (95%C.I. 3.3-6.1 months) and median survival time was 10.1 months (95%C.I. 7.8-12.4 months).

Conclusions

IRIS/Cet appeared to be highly effective with response rate of 33.3%, progression-free survival of 4.7 months, overall survival of 10.1 months, and had met the primary endpoint. Diarrhea as one of major adverse events could be manageable by appropriate dose reduction and supportive care. However, further control of diarrhea will be required for the future development of IRIS/Cet. This analysis had been presented at the European Cancer Congress 2015 (Nakamura M, et al. Abstract number was 2 096).

Clinical trial identification

Disclosure

A. Hosokawa: Research fund: Taiho Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd. Y. Sakata: Honoraria: Taiho Pharmaceutical Co., Ltd., Daiichi Sankyo Co., Ltd., Yakult Honsha Co., Ltd., Merck Serono Co., Ltd. Y. Komatsu: Honoraria and Research fund: Taiho Pharmaceutical Co., Ltd., Yakult Honsha Co., Ltd., Merck Serono Co., Ltd., Daiichi Sankyo Co., Ltd. All other authors have declared no conflicts of interest.