Department of Pathology, University of Southern California, Los Angeles, CA.
Transl Oncol. 2012 Dec;5(6):469-74. doi: 10.1593/tlo.12265. Epub 2012 Dec 1.
The use of neoadjuvant chemotherapy followed by tumor reduction surgery, also called interval debulking surgery (IDS), is considered an alternative therapeutic regimen for selected patients with advanced stage epithelial ovarian cancer (EOC). Although minimal residual disease has been proven to be a prognostic factor in traditional cytoreduction for advanced stage EOC, predictive factors after IDS still remain unexplored. The aim of this study was to determine the prognostic value of post-neoadjuvant histologic changes with clinical outcome. Three pathologists evaluated 67 cases for the following parameters: fibrosis, necrosis, residual tumor, and inflammation. The Cohen's kappa statistic was used to measure agreement among pathologists. Univariate and multivariate Cox proportional hazards models were used to determine the association between histologic parameters and recurrence-free survival (RFS) and overall survival (OS). There was substantial to almost perfect agreement among the three pathologists in all four histologic parameters (k ranged from 0.65 to 0.97). Fibrosis was associated with longer RFS (P = 0.0257) with a median of 20 months for tumors with fibrosis (3+) versus 12 months for tumors with fibrosis (1+, 2+) and longer OS (P = 0.0249) with a median of 51 months for tumors with fibrosis (3+) versus 32 months for tumors with fibrosis (1+, 2+). Our results revealed that patients with tumors exhibiting fibrosis (1+, 2+), as well as necrosis (0, 1+), had significant shorter RFS and OS (P = 0.059 and P = 0.0234, respectively). We suggest that the assessment of fibrosis and necrosis should be implemented in pathologic evaluation and prospectively validated in future studies.
新辅助化疗后肿瘤缩小手术(也称为间隔减瘤术,IDS),被认为是一种选择治疗方案,适用于特定的晚期上皮性卵巢癌(EOC)患者。虽然在传统的晚期 EOC 肿瘤细胞减灭术中,微小残留病灶已被证明是预后因素,但 IDS 后的预测因素仍有待探索。本研究旨在确定新辅助化疗后组织学变化与临床结果之间的预后价值。三位病理学家评估了 67 例患者的以下参数:纤维化、坏死、残留肿瘤和炎症。采用 Cohen's kappa 统计量来衡量病理学家之间的一致性。采用单因素和多因素 Cox 比例风险模型来确定组织学参数与无复发生存(RFS)和总生存(OS)之间的关联。在所有四个组织学参数中,三位病理学家之间的一致性很高,达到几乎完全一致(κ值范围为 0.65 至 0.97)。纤维化与 RFS 延长相关(P = 0.0257),纤维化(3+)肿瘤的中位 RFS 为 20 个月,而纤维化(1+、2+)肿瘤的中位 RFS 为 12 个月;纤维化与 OS 延长相关(P = 0.0249),纤维化(3+)肿瘤的中位 OS 为 51 个月,而纤维化(1+、2+)肿瘤的中位 OS 为 32 个月。我们的结果表明,纤维化(1+、2+)和坏死(0、1+)的肿瘤患者的 RFS 和 OS 显著缩短(P = 0.059 和 P = 0.0234)。我们建议在病理评估中实施纤维化和坏死的评估,并在未来的研究中进行前瞻性验证。