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pCR率は生存期間のサロゲートマーカーではないかもしれないという話

確かにpCR率が高い術前治療は良い治療と"信じ込まされている"けれど、冷静に考えてみると意外とその根拠は薄弱かもしれないなぁ。かと言って、他に代わりになってくれるサロゲート指標も無ければ、いちいちOSまで追跡する人的/資金的/時間的な余裕も無し…

Evaluation of pathological complete response as surrogate endpoint in neoadjuvant randomised clinical trials of early stage breast cancer: systematic review and meta-analysis
Objective To evaluate pathological complete response as a surrogate endpoint for disease-free survival and overall survival in regulatory neoadjuvant trials of early stage breast cancer. Design Systematic review and meta-analysis. Data sources Medline, Embase, and Scopus to 1 December 2020. Eligibility criteria for study selection Randomised clinical trials that tested neoadjuvant chemotherapy given alone or combined with other treatments, including anti-human epidermal growth factor 2 (anti-HER2) drugs, targeted treatments, antivascular agents, bisphosphonates, and immune checkpoint inhibitors. Data extraction and synthesis Trial level associations between the surrogate endpoint pathological complete response and disease-free survival and overall survival. Methods A weighted regression analysis was performed on log transformed treatment effect estimates (hazard ratio for disease-free survival and overall survival and relative risk for pathological complete response), and the coefficient of determination (R2) was used to quantify the association. The secondary objective was to explore heterogeneity of results in preplanned subgroups analysis, stratifying trials according treatment type in the experimental arm, definition used for pathological complete response (breast and lymph nodes v breast only), and biological features of the disease (HER2 positive or triple negative breast cancer). The surrogate threshold effect was also evaluated, indicating the minimum value of the relative risk for pathological complete response necessary to confidently predict a non-null effect on hazard ratio for disease-free survival or overall survival. Results 54 randomised clinical trials comprising a total of 32 611 patients were included in the analysis. A weak association was observed between the log(relative risk) for pathological complete response and log(hazard ratio) for both disease-free survival (R2=0.14, 95% confidence interval 0.00 to 0.29) and overall survival (R2 =0.08, 0.00 to 0.22). Similar results were found across all subgroups evaluated, independently of the definition used for pathological complete response, treatment type in the experimental arm, and biological features of the disease. The surrogate threshold effect was 5.19 for disease-free survival but was not estimable for overall survival. Consistent results were confirmed in three sensitivity analyses: excluding small trials (<200 patients enrolled), excluding trials with short median follow-up (<24 months), and replacing the relative risk for pathological complete response with the absolute difference of pathological complete response rates between treatment arms. Conclusion A lack of surrogacy of pathological complete response was identified at trial level for both disease-free survival and overall survival. The findings suggest that pathological complete response should not be used as primary endpoint in regulatory neoadjuvant trials of early stage breast cancer. Detailed data on the included studies are available on reasonable request to the corresponding author.
https://www.bmj.com/content/375/bmj-2021-066381.short

乳癌に関する54の臨床試験の32,000人あまりを組み込んだ統合解析で、pCR率とDFSやOSとの相関について検討したところ、その相関はあまり高くはなかったようだ。DFSについてはR^2=0.14、OSについてはR^2=0.08といずれも相関係数はかなり低かったとのこと。

Meta-analysis of 54 RCTs comprising a total of 32,611 pts with early stage #breastcancer finds only weak associations between pCR and DFS (R2=0.14) or OS (R2 =0.08), across all subgroups, suggesting a lack of surrogacy at the trial level: https://t.co/0LvMd10WPD #BCSM

— NatureRevClinOncol (@NatRevClinOncol) January 7, 2022

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更新日:2022-01-07 閲覧数:472 views.