TY - JOUR
T1 - Alpha-fetoprotein kinetics in patients with hepatocellular carcinoma receiving ramucirumab or placebo
T2 - An analysis of the phase 3 REACH study
AU - Chau, Ian
AU - Park, Joon Oh
AU - Ryoo, Baek Yeol
AU - Yen, Chia Jui
AU - Poon, Ronnie
AU - Pastorelli, Davide
AU - Blanc, Jean Frédéric
AU - Kudo, Masatoshi
AU - Pfiffer, Tulio
AU - Hatano, Etsuro
AU - Chung, Hyun Cheol
AU - Kopeckova, Katerina
AU - Phelip, Jean Marc
AU - Brandi, Giovanni
AU - Ohkawa, Shinichi
AU - Li, Chung Pin
AU - Okusaka, Takuji
AU - Hsu, Yanzhi
AU - Abada, Paolo B.
AU - Zhu, Andrew X.
N1 - Funding Information:
This study was funded by Eli Lilly and Company. We thank the patients, their families and the study personnel across all sites for participating in this study. Yihuan Xu of Eli Lilly and Company (Bridgewater, NJ) provided statistical expertise. Nathalie Godinot of Eli Lilly and Company (Indianapolis, IN) provided writing assistance. I.C. would like to thank the National Health Service for funding to the National Institute for Health Research Biomedical Research Centre at the Royal Marsden NHS Foundation Trust and The Institute of Cancer Research.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/7/3
Y1 - 2018/7/3
N2 - Background: Post-hoc analyses of AFP response and progression and their relationship with objective measures of response and survival were performed in patients from REACH. Methods: Serum AFP was measured at baseline and every 3 cycles (2 weeks/cycle). Associations between AFP and radiographic progression and efficacy end points were analysed. Results: Median percent AFP increase from baseline was smaller in the ramucirumab than in the placebo arm throughout treatment. Time to AFP progression (HR 0.621; P < 0.0001) and to radiographic progression (HR 0.613; P < 0.0001) favoured ramucirumab. Association between AFP and radiographic progression was shown at 6 (OR 6.44, 95% CI 4.03, 10.29; P < 0.0001) and 12 weeks (OR 2.28, 95% CI 1.47, 3.53; P = 0.0002). AFP response was higher with ramucirumab compared with placebo (P < 0.0001). More patients in the ramucirumab arm experienced tumour shrinkage and AFP response compared with placebo. Survival was longer in patients with AFP response (13.6 months) than in patients without (6.2 months), irrespective of treatment (HR 0.457, P < 0.0001). Conclusions: Treatment with ramucirumab prolonged time to AFP progression, slowed AFP increase and was more likely to induce AFP response. Similar benefits in radiographic progression and response correlated with AFP changes.
AB - Background: Post-hoc analyses of AFP response and progression and their relationship with objective measures of response and survival were performed in patients from REACH. Methods: Serum AFP was measured at baseline and every 3 cycles (2 weeks/cycle). Associations between AFP and radiographic progression and efficacy end points were analysed. Results: Median percent AFP increase from baseline was smaller in the ramucirumab than in the placebo arm throughout treatment. Time to AFP progression (HR 0.621; P < 0.0001) and to radiographic progression (HR 0.613; P < 0.0001) favoured ramucirumab. Association between AFP and radiographic progression was shown at 6 (OR 6.44, 95% CI 4.03, 10.29; P < 0.0001) and 12 weeks (OR 2.28, 95% CI 1.47, 3.53; P = 0.0002). AFP response was higher with ramucirumab compared with placebo (P < 0.0001). More patients in the ramucirumab arm experienced tumour shrinkage and AFP response compared with placebo. Survival was longer in patients with AFP response (13.6 months) than in patients without (6.2 months), irrespective of treatment (HR 0.457, P < 0.0001). Conclusions: Treatment with ramucirumab prolonged time to AFP progression, slowed AFP increase and was more likely to induce AFP response. Similar benefits in radiographic progression and response correlated with AFP changes.
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U2 - 10.1038/s41416-018-0103-0
DO - 10.1038/s41416-018-0103-0
M3 - Article
C2 - 29808014
AN - SCOPUS:85047663920
SN - 0007-0920
VL - 119
SP - 19
EP - 26
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 1
ER -