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Authors Liu L, Yu H, Huang L, Shao F, Bai J, Lou D, Chen F
Published Date April 2015 Volume 2015:8 Pages 921—928
DOI http://dx.doi.org/10.2147/OTT.S82365
Received 6 February 2015, Accepted 10 March 2015, Published 22 April 2015
Background: The
correlation between overall survival (OS) and progression-free survival (PFS)
has been evaluated in patients with metastatic or advanced gastric cancer who
have received first-line and/or second-line chemotherapy. However, no
corresponding analysis has been done for patients who have undergone third-line
or later-line chemotherapy.
Methods: A total of 303
patients from the Phase II/III studies of apatinib were pooled (the Phase II
study as a training data set, the Phase III study as a testing data set).
Landmark analyses of PFS at 2 months from randomization were performed to
minimize lead time bias. The Cox proportional hazard model was used to test for
the significance effect of PFS rate at 2 months in predicting OS. Additionally,
the PFS/OS correlations were evaluated by the normal induced copula (National
Institute for Health and Care Excellence) estimation model.
Results: The median OS was
3.37 months (95% confidence interval 2.63–3.80) in patients who
experienced progression at 2 months and 5.67 months in patients who
did not (95% confidence interval 4.83–6.67; P <0.0001).
Compared with patients who did not progress at 2 months, the adjusted
hazard ratio for death was 3.39 (95% confidence interval 1.79–6.41; P <0.0001) for patients who experienced
progression at 2 months. Moreover, the correlation of PFS/OS was 0.84 (95%
confidence interval 0.74–0.90). Similar results were found in the testing data
set.
Conclusion: These results
indicate that PFS correlates strongly with OS, suggesting PFS may be a useful
early endpoint for patients with advanced gastric cancer who have undergone
third-line or later-line chemotherapy. These observations require prospective
validation.
Keywords: gastric cancer,
surrogate endpoint, progression-free survival, overall survival