TY - JOUR
T1 - Exploration of potential prognostic biomarkers in aflibercept plus FOLFIRI in Japanese patients with metastatic colorectal cancer
AU - Hamaguchi, Tetsuya
AU - Denda, Tadamichi
AU - Kudo, Toshihiro
AU - Sugimoto, Naotoshi
AU - Ura, Takashi
AU - Yamazaki, Kentaro
AU - Fujii, Hirofumi
AU - Kajiwara, Takeshi
AU - Nakajima, Takako Eguchi
AU - Takahashi, Shin
AU - Otsu, Satoshi
AU - Komatsu, Yoshito
AU - Nagashima, Fumio
AU - Moriwaki, Toshikazu
AU - Esaki, Taito
AU - Sato, Takeo
AU - Itabashi, Michio
AU - Oki, Eiji
AU - Sasaki, Toru
AU - Chiron, Marielle
AU - Yoshino, Takayuki
N1 - Funding Information:
The authors would like to thank all patient participants. This study was sponsored by Sanofi writing assistance by Michelle L. Jones, PhD, ELS, and funded by Sanofi. Yoshinori Sunaga, Sanofi K. K., Tokyo, Japan analyzed the data and contributed to interpretation of the study.
Funding Information:
T.H. received honoraria from Taiho, Chugai, Takeda, Yakult, and Merck Serono; a consulting fee from NanoCarrier; and research funding from MSD, Ono, Sanofi, Daiichi‐Sankyo, Sumitomo Dainippon Pharma, Taiho, Teijin, and NanoCarrier. T.K. received research finding from Yakult. N.S. received honoraria from Chugai and Eli Lilly, and research funding from Chugai, Eli Lilly, Dainippon Sumitomo, Taiho, MSD, Ono, Daiichi‐Sankyo, and Sanofi. T.U. received honoraria from Merck Serono, Taiho, Chugai, and Takeda, and research funding from Sanofi. K.Y. received honoraria from Chugai, Takeda, Yakult, Daiichi‐Sankyo, Merck Serono, Bristol, Bayer, Eli Lilly, and Taiho, and research funding from BMS and Sanofi. H.F. received research funding from Sanofi. S.T. received honoraria from Asahikasei and research funding from Merck Serono, Ono, and Sanofi. Y.K. received honoraria from BMS and Sanofi, and research funding from Eli Lilly, BMS, and Sanofi. T.E. received honoraria from Eli Lilly, and research funding from Boehringer, Daiichi‐Sankyo, Dainippon Sumitomo, Eli Lilly, Merck Serono, MSD, Novartis, Ono, and Taiho, and scholarship from Ono. S.T. received honoraria from Asahikasei, and research funding from Merck Serono, Ono and Sanofi. E.O. received honoraria from Bayer, Chugai, Eli Lilly, Merck Serono, Taiho, Takeda, and Yakult. T.Y. received honoraria from Chugai, Eli Lilly, Merck Serono, Sanofi, and Taiho, and research funding from Boehringer Ingelheim, Chugai, Dainippon Sumitomo, GlaxoSmithKline, MSD, Novartis, and Sanofi. The affiliated medical institutions of physician authors received study funding from Sanofi. T.S. and M.C. are employees of Sanofi. Funding for this research was provided by Sanofi.
Publisher Copyright:
© 2019 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association.
PY - 2019/11/1
Y1 - 2019/11/1
N2 - Aflibercept plus 5-fluorouracil/levofolinate/irinotecan (FOLFIRI) is a second-line treatment for metastatic colorectal cancer. This ancillary exploratory analysis of data in Japanese people was aimed at exploring the relationship between a set of potential prognostic biomarkers and efficacy endpoints following aflibercept plus FOLFIRI therapy. Sixty-two patients with metastatic colorectal cancer received aflibercept (4 mg/kg) plus FOLFIRI every 2 weeks. Seventy-eight potential protein biomarkers were chosen for analysis based on their roles in angiogenesis, tumor progression, and tumor-stroma interaction. Plasma levels of biomarkers at baseline and at pre-dose 3 (day 1 of treatment cycle 3) were measured in all patients by ELISA. Relationships between these levels and efficacy endpoints were assessed. Ten potential biomarkers had a ±30% change from baseline to pre-dose 3 (adjusted P <.001), with the greatest changes occurring in placental growth factor (median: +4716%) and vascular endothelial growth factor receptor 1 (+2171%). Baseline levels of eight potential biomarkers correlated with overall survival in a univariate Cox regression analysis: extracellular newly identified receptor for advanced glycation end-products binding protein, insulin-like growth factor-binding protein 1, interleukin-8, kallikrein 5, pulmonary surfactant-associated protein D, tissue inhibitor of metalloproteinases 1, tenascin-C, and tumor necrosis factor receptor 2. None correlated with progression-free survival or maximum tumor shrinkage. Pre-dose 3 levels did not correlate with any efficacy endpoints. Preliminary data show that these eight biomarkers could be associated with overall survival. ClinicalTrials.gov identifier: NCT01882868.
AB - Aflibercept plus 5-fluorouracil/levofolinate/irinotecan (FOLFIRI) is a second-line treatment for metastatic colorectal cancer. This ancillary exploratory analysis of data in Japanese people was aimed at exploring the relationship between a set of potential prognostic biomarkers and efficacy endpoints following aflibercept plus FOLFIRI therapy. Sixty-two patients with metastatic colorectal cancer received aflibercept (4 mg/kg) plus FOLFIRI every 2 weeks. Seventy-eight potential protein biomarkers were chosen for analysis based on their roles in angiogenesis, tumor progression, and tumor-stroma interaction. Plasma levels of biomarkers at baseline and at pre-dose 3 (day 1 of treatment cycle 3) were measured in all patients by ELISA. Relationships between these levels and efficacy endpoints were assessed. Ten potential biomarkers had a ±30% change from baseline to pre-dose 3 (adjusted P <.001), with the greatest changes occurring in placental growth factor (median: +4716%) and vascular endothelial growth factor receptor 1 (+2171%). Baseline levels of eight potential biomarkers correlated with overall survival in a univariate Cox regression analysis: extracellular newly identified receptor for advanced glycation end-products binding protein, insulin-like growth factor-binding protein 1, interleukin-8, kallikrein 5, pulmonary surfactant-associated protein D, tissue inhibitor of metalloproteinases 1, tenascin-C, and tumor necrosis factor receptor 2. None correlated with progression-free survival or maximum tumor shrinkage. Pre-dose 3 levels did not correlate with any efficacy endpoints. Preliminary data show that these eight biomarkers could be associated with overall survival. ClinicalTrials.gov identifier: NCT01882868.
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U2 - 10.1111/cas.14198
DO - 10.1111/cas.14198
M3 - Article
C2 - 31520559
AN - SCOPUS:85074221951
SN - 1347-9032
VL - 110
SP - 3565
EP - 3572
JO - Cancer Science
JF - Cancer Science
IS - 11
ER -