RAD51 Foci as a Biomarker Predictive of Platinum Chemotherapy Response in Ovarian Cancer

被引:36
作者
Compadre, Amanda J. [1 ]
van Biljon, Lillian N. [1 ]
Valentine, Mark C. [1 ]
Llop-Guevara, Alba [2 ]
Graham, Emily [1 ]
Fashemi, Bisiayo [1 ]
Herencia-Ropero, Andrea [2 ,3 ]
Kotnik, Emilee N. [1 ]
Cooper, Isaac [1 ]
Harrington, Shariska P. [4 ]
Kuroki, Lindsay M. [1 ]
McCourt, Carolyn K. [1 ]
Hagemann, Andrea R. [1 ]
Thaker, Premal H. [1 ]
Mutch, David G. [1 ]
Powell, Matthew A. [1 ]
Sun, Lulu [5 ]
Mosammaparast, Nima [5 ]
Serra, Violeta [2 ]
Zhao, Peinan [6 ]
Lomonosova, Elena [1 ]
Khabele, Dineo [1 ]
Mullen, Mary M. [1 ,7 ]
机构
[1] Washington Univ, Dept Obstet & Gynecol, Div Gynecol Oncol, St Louis, MO USA
[2] Vall dHebron Inst Oncol, Expt Therapeut Grp, Barcelona, Spain
[3] Autonomous Univ Barcelona, Dept Biochem & Mol Biol, Barcelona, Spain
[4] Minnesota Oncol, St Paul, MN USA
[5] Washington Univ, Dept Pathol & Immunol, St Louis, MO USA
[6] Washington Univ, Ctr Reprod Hlth Sci, Dept Obstet & Gynecol, St Louis, MO USA
[7] Washington Univ, Sch Med, St Louis, MO 63122 USA
关键词
RECOMBINATION DEFICIENCY HRD; HOMOLOGOUS RECOMBINATION; NEOADJUVANT CHEMOTHERAPY; SOMATIC MUTATIONS; TUMOR; VALIDATION; CISPLATIN; THERAPY; SENSITIVITY; INHIBITION;
D O I
10.1158/1078-0432.CCR-22-3335
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the ability of RAD51 foci to predict platinum chemotherapy response in high-grade serous ovarian cancer (HGSOC) patient-derived samples.Experimental Design: RAD51 and yH2AX nuclear foci were evaluated by immunofluorescence in HGSOC patient-derived cell lines (n = 5), organoids (n = 11), and formalin-fixed, paraffin -embedded tumor samples (discovery n = 31, validation n = 148). Samples were defined as RAD51-High if >10% of geminin-positive cells had & GE;5 RAD51 foci. Associations between RAD51 scores, platinum chemotherapy response, and survival were evaluated.Results: RAD51 scores correlated with in vitro response to platinum chemotherapy in established and primary ovarian can-cer cell lines (Pearson r = 0.96, P = 0.01). Organoids from platinum-nonresponsive tumors had significantly higher RAD51 scores than those from platinum-responsive tumors (P < 0.001). In a discovery cohort, RAD51-Low tumors were more likely to have a pathologic complete response (RR, 5.28; P < 0.001) and to be platinum-sensitive (RR, .O; P = 0.05). The RAD51 score was predictive of chemotherapy response score [AUC, 0.90; 95% confidence interval (CI), 0.78-1.0; P < 0.001). A novel automatic quantification system accurately reflected the manual assay (92%). In a validation cohort, RAD51-Low tumors were more likely to be platinum-sensitive (RR, OO; P < 0.001) than RAD51-High tumors. Moreover, RAD51-Low status predicted platinum sensitivity with 100% positive predictive value and was associated with better progression-free (HR, 0.53; 95% CI, 0.33-0.85; P < 0.001) and overall survival (HR, 0.43; 95% CI, 0.25-0.75; P = 0.003) than RAD51-High status.Conclusions: RAD51 foci are a robust marker of platinum chemotherapy response and survival in ovarian cancer. The utility of RAD51 foci as a predictive biomarker for HGSOC should be tested in clinical trials.
引用
收藏
页码:2466 / 2479
页数:14
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