172P - Updated analysis: observational cohort study of 1st line bevacizumab combined with chemotherapy in metastatic colorectal cancer (HGCSG0802): Compar...

Date 19 December 2015
Event ESMO Asia 2015 Congress
Session Poster presentation 1
Topics Anticancer agents
Colon and Rectal Cancer
Biological Therapy
Presenter Yoshito Komatsu
Citation Annals of Oncology (2015) 26 (suppl_9): 42-70. 10.1093/annonc/mdv523
Authors Y. Komatsu1, S. Yuki2, H. Nakatsumi1, K. Sawada2, K. Hatanaka3, T. Kato4, T. Meguro4, M. Nakamura5, I. Iwanaga6, M. Uebayashi6, M. Tateyama7, K. Eto8, M. Kudo9, K. Kato10, H. Okuda11, S. Sogabe12, T. Miyagishima12, K. Miyashita13, N. Sakamoto2, Y. Sakata14
  • 1Cancer Center, Hokkaido University Hospital, 060-8638 - Sapporo/JP
  • 2Gastroenterology And Hepatology, Hokkaido University Hospital, 060-8638 - Sapporo/JP
  • 3Gastroenterology, Hakodate Municipal Hospital, Hakodate/JP
  • 4Internal Medicine, Hokkaido Gastroenterology Hospital, Sapporo/JP
  • 5Gastroenterology, Sapporo City General Hospital, 060-8604 - Sapporo/JP
  • 6Medical Oncology, Japanese Red Cross Kitami Hospital, Kitami/JP
  • 7Internal Medicine, Tomakomai Nisshou Hospital, Tomakomai/JP
  • 8Gastroenterology, Tomakomai City Hospital, Tomakomai/JP
  • 9Gastroenterology, Sapporo Hokuyu Hospital, Sapporo/JP
  • 10Gastroenterology, Iwamizawa Municipal General Hospital, Iwamizawa/JP
  • 11Medical Oncology, Keiyukai Sapporo Hospital, 003-0027 - Sapporo/JP
  • 12Medical Oncology, Kushiro Rosai Hospital, Kushiro/JP
  • 13Gastroenterology, Aiiku Hospital, Sapporo/JP
  • 14Ceo, Misawa City Hospital, 033-0022 - Misawa/JP



Some studies had reported that oral FU/Oxaliplatin (OX) was non-inferior to infusional FU/OX as 1st line treatment for metastatic colorectal cancer (mCRC). We conducted observational cohort study (HGCSG0802) which investigated Japanese patients (pts) treated with bevacizumab (BV) containing regimen. Therefore, we had performed analysis in order to investigate whether there was a difference in safety and efficacy of infusional FU/OX (mFOLFOX6 + BV: iFU) and oral FU/OX (CapeOX/SOX + BV: oFU) using the HGCSG0802 database.


The key eligibility criteria of HGCSG0802 were with evaluable lesions, older than 20 years, ECOG PS 0-2, and this analysis used the cohort treated with OX-based regimens. In this analysis, pts characteristics, RR and safety were compared using Fisher's exact test. PFS, TTF and OS were compared using log-rank test for comparison of the iFU and oFU.


Of 108 pts (the full analysis set), 95 pts were evaluable for treated with OX-based regimens. Forty-eight pts (50.5%) were treated with iFU and 47 pts (49.5%) were treated with oFU (CapeOX + BV 42 pts/SOX + BV 5 pts). The pts characteristics between those were generally balanced except for PS 0-1 (72.9% in iFU/93.6% in oFU; p = 0.012) and synchronous liver metastases (93.8% in iFU/78.8% in oFU; p = 0.040). Adverse events ≥ Grade 3 were balanced except for leucopenia (25.0% in iFU versus 2.1% in oFU; p = .002) and neutropenia (43.5% in iFU and 10.9% in oFU; p = .001). Hand-foot skin reaction was not different between two cohorts. RR was 62.5% in iFU versus 71.1% in oFU (p = 0.835). The median PFS was 8.3 months in iFU versus 8.2 months in oFU (p = 0.970) and median OS was 18.3 months in iFU versus 23.5 months in oFU (p = 0.247).


As a result of this analysis, in Japanese daily practice, efficacy was no significant difference between iFU and oFU, and the profiles of adverse events varied from each regimens. This analysis had been presented at the European Cancer Congress 2015 (Nakatsumi H, et al. Abstract number was 2 092).

Clinical trial identification


Y. Komatsu: Honoraria: Yakult Honsha Co., Ltd., Daiichi Sankyo Co., Ltd., Takeda Pharmaceutical Co., Ltd. Research fund: Yakult Honsha Co., Ltd., Daiichi Sankyo Co., Ltd., Takeda Pharmaceutical Co., Ltd. Y. Sakata: Honoraria: Daiichi Sankyo Co., Ltd., Yakult Honsha Co., Ltd. All other authors have declared no conflicts of interest.