Nitecki Wilke Roni, Liu Jinsong, Westin Shannon Neville, Fellman Bryan M, Sims Travis T, Pham Melissa, Rangel Kelly, Sey Esther, Rauh-Hain Jose Alejandro, Lu Karen H, Sood Anil K, Fleming Nicole D
Department of Gynecologic Oncology and Reproductive Medicine, University of Texas MD Anderson Cancer Center, Houston, Texas, USA
Department of Pathology, University of Texas MD Anderson Cancer Center, Houston, Teaxs, USA.
Int J Gynecol Cancer. 2025 Jan 6. doi: 10.1136/ijgc-2024-005893.
In patients undergoing interval tumor reductive surgery, a good response to neoadjuvant chemotherapy may limit available tumor for homologous recombination deficiency testing. The objective of this study was to assess whether the chemotherapy response score predicts homologous recombination status.
We identified patients with advanced epithelial ovarian cancer (diagnosed January 2019 to 20 June 2023) who received neoadjuvant chemotherapy, underwent interval surgery, and for whom a chemotherapy response score was reported (1=no or minimal tumor response, 2=appreciable tumor response, 3=complete or near complete response with no residual tumor). Comparisons were made using ANOVAs or Kruskal-Wallis test for continuous variables and χ or Fisher's exact test for categorical variables.
The cohort consisted of 234 patients with advanced ovarian cancer who underwent interval surgery following neoadjuvant chemotherapy. Of those who underwent germline genetic testing, 22% (51/232) had a pathogenic or mutation and of those with tumors sent for testing, 65% were found to have homologous recombination deficiency (66/146). With increasing chemotherapy response scores, a higher likelihood of a complete gross resection was observed (50% (chemotherapy response score, CRS 1) vs 77% (CRS 2) vs 88% (CRS 3), p<0.001). On multivariable analysis, CRS 2 (adjusted odds ratio=3.28, 95% CI 1.12 to 9.60, p=0.03) and CRS 3 (5.83, 1.79 to 18.93, p=0.003) were independently associated with homologous recombination deficiency compared with CRS 1.
A positive response to chemotherapy at the time of interval tumor reductive surgery defined by the chemotherapy response score was associated with homologous recombination status and the likelihood of achieving a complete gross resection.
在接受间歇性肿瘤减瘤手术的患者中,对新辅助化疗的良好反应可能会限制用于同源重组缺陷检测的可用肿瘤。本研究的目的是评估化疗反应评分是否能预测同源重组状态。
我们确定了2019年1月至2023年6月20日期间接受新辅助化疗、进行间歇性手术且报告了化疗反应评分的晚期上皮性卵巢癌患者(1 =无或最小肿瘤反应,2 =明显肿瘤反应,3 =完全或接近完全反应且无残留肿瘤)。连续变量采用方差分析或Kruskal-Wallis检验进行比较,分类变量采用χ²检验或Fisher精确检验进行比较。
该队列包括234例晚期卵巢癌患者,他们在新辅助化疗后接受了间歇性手术。在接受种系基因检测的患者中,22%(51/232)有致病性或疑似致病性突变,在送检肿瘤检测的患者中,65%被发现存在同源重组缺陷(66/146)。随着化疗反应评分的增加,观察到完全大体切除的可能性更高(化疗反应评分1为50%,化疗反应评分2为77%,化疗反应评分3为88%,p<0.001)。多变量分析显示,与化疗反应评分1相比,化疗反应评分2(调整比值比=3.28,95%CI 1.12至9.60,p=0.03)和化疗反应评分3(5.83,1.79至18.93,p=0.003)与同源重组缺陷独立相关。
根据化疗反应评分定义的间歇性肿瘤减瘤手术时对化疗的阳性反应与同源重组状态以及实现完全大体切除的可能性相关。