A 3-Tier Chemotherapy Response Score for Ovarian/Fallopian Tube/Peritoneal High-grade Serous Carcinoma

B. Lawson, E. Euscher, R. Bassett, Jinsong Liu, P. Ramalingam, Y. Zhong, N. Fleming, A. Malpica
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引用次数: 9

Abstract

The chemotherapy response score (CRS) is used to score histopathologic response to neoadjuvant chemotherapy (NACT) of patients with extrauterine high-grade serous carcinoma. This study was undertaken to determine if the CRS in the omentum, adnexa or when combined correlates with (1) progression-free survival (PFS) or overall survival (OS), (2) laparoscopic score of abdominal disease, (3) Cancer antigen 125 levels, (4) BRCA status, and (5) platinum-resistant disease. A total of 158 cases were retrospectively collected that received NACT between April 2013 and February 2018 at a single institution. The 3-tier Böhm CRS system was applied to the omentum and adnexa. Survival outcomes between scored subgroups were analyzed using Cox proportional hazards regression. Spearman rank correlation analyses were used to assess CRS and clinical data. A total of 119 cases were treated only with carboplatin/paclitaxel. Omental CRS was: 1 (23 cases, 19.3%), 2 (65 cases, 54.6%), and 3 (31 cases, 26.1%), whereas adnexal CRS was: 1 (50 cases, 42%), 2 (48 cases, 40.3%) and 3 (21 cases, 17.6%). The omental CRS was significantly associated with PFS as a 2-tier score (hazard ratio [HR]=0.612, 95% confidence interval [CI]: 0.378-0.989, P=0.045) but not associated with the PFS using the 3-tier score or with OS using either system. Adnexal CRS was not associated with OS but was significantly associated with PFS using the 3-tier (HR=0.49, 95% CI: 0.263-0.914, P=0.025) and 2-tier scores (HR=0.535, 95% CI: 0.297-0.963, P=0.037). The combined score was not associated with OS but was significantly associated with PFS using the 3-tier (HR=0.348, 95% CI: 0.137-0.88, P=0.026) and 2-tier scores (HR=0.364, 95% CI: 0.148-0.896, P=0.028). No CRS system used associated with laparoscopic assessment of disease. CRS in the omentum had no significant association with platinum resistance; however, the adnexal CRS 1/2 were 3 times as likely to develop platinum resistance compared with CRS 3 (relative risk=3.94, 95% CI: 1.03-15.09, P=0.046). The CRS, when used on the omentum, adnexa, and as a combined score, was significantly associated with PFS but not with OS. Adnexal CRS 1/2 are more likely to develop platinum-resistant disease. Therefore, the use of this pathology parameter may be useful for clinical management.
卵巢/输卵管/腹膜高级别浆液性癌的3级化疗反应评分
化疗反应评分(CRS)用于评价子宫外高级别浆液性癌患者对新辅助化疗(NACT)的组织病理反应。本研究旨在确定大网膜、附件或合并CRS是否与(1)无进展生存期(PFS)或总生存期(OS)、(2)腹腔疾病腹腔镜评分、(3)癌抗原125水平、(4)BRCA状态和(5)铂耐药疾病相关。回顾性收集了2013年4月至2018年2月在同一家机构接受NACT治疗的158例患者。网膜和附件采用3层Böhm CRS系统。采用Cox比例风险回归分析评分亚组间的生存结局。采用Spearman秩相关分析评估CRS和临床资料。总共有119例患者只接受卡铂/紫杉醇治疗。大网膜CRS分别为1例(23例,19.3%)、2例(65例,54.6%)、3例(31例,26.1%),附件CRS分别为1例(50例,42%)、2例(48例,40.3%)、3例(21例,17.6%)。网膜CRS与2级评分的PFS显著相关(风险比[HR]=0.612, 95%可信区间[CI]: 0.378-0.989, P=0.045),但与3级评分的PFS或两种评分的OS无相关性。附件CRS与OS无相关性,但与PFS有显著相关性,采用3级评分(HR=0.49, 95% CI: 0.263-0.914, P=0.025)和2级评分(HR=0.535, 95% CI: 0.297-0.963, P=0.037)。综合评分与OS无相关性,但与PFS有显著相关性,采用3层评分(HR=0.348, 95% CI: 0.137-0.88, P=0.026)和2层评分(HR=0.364, 95% CI: 0.148-0.896, P=0.028)。没有CRS系统用于腹腔镜疾病评估。网膜CRS与铂电阻无显著相关性;然而,与CRS 3相比,附件CRS 1/2发生铂耐药的可能性是CRS 3的3倍(相对风险=3.94,95% CI: 1.03-15.09, P=0.046)。CRS,当用于网膜、附件和作为综合评分时,与PFS显著相关,但与OS无关。附件CRS 1/2更容易发生铂耐药疾病。因此,使用该病理参数可能对临床管理有用。
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