Division of Surgical Oncology, Department of Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.
Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ann Surg Oncol. 2023 Sep;30(9):5743-5753. doi: 10.1245/s10434-023-13697-9. Epub 2023 Jun 9.
The AJCC 8th edition stratifies stage IV disseminated appendiceal cancer (dAC) patients based on grade and pathology. This study was designed to externally validate the staging system and to identify predictors of long-term survival.
A 12-institution cohort of dAC patients treated with CRS ± HIPEC was retrospectively analyzed. Overall survival (OS) and recurrence-free survival (RFS) were analyzed by using Kaplan-Meier and log-rank tests. Univariate and multivariate cox-regression was performed to assess factors associated with OS and RFS.
Among 1009 patients, 708 had stage IVA and 301 had stage IVB disease. Median OS (120.4 mo vs. 47.2 mo) and RFS (79.3 mo vs. 19.8 mo) was significantly higher in stage IVA compared with IVB patients (p < 0.0001). RFS was greater among IVA-M1a (acellular mucin only) than IV M1b/G1 (well-differentiated cellular dissemination) patients (NR vs. 64 mo, p = 0.0004). Survival significantly differed between mucinous and nonmucinous tumors (OS 106.1 mo vs. 41.0 mo; RFS 46.7 mo vs. 21.2 mo, p < 0.05), and OS differed between well, moderate, and poorly differentiated (120.4 mo vs. 56.3 mo vs. 32.9 mo, p < 0.05). Both stage and grade were independent predictors of OS and RFS on multivariate analysis. Acellular mucin and mucinous histology were associated with better OS and RFS on univariate analysis only.
AJCC 8 edition performed well in predicting outcomes in this large cohort of dAC patients treated with CRS ± HIPEC. Separation of stage IVA patients based on the presence of acellular mucin improved prognostication, which may inform treatment and long-term, follow-up strategies.
AJCC 第 8 版根据分级和病理将 IV 期播散性阑尾癌(dAC)患者分为不同的分期。本研究旨在对该分期系统进行外部验证,并确定长期生存的预测因素。
回顾性分析了 12 家机构接受 CRS ± HIPEC 治疗的 dAC 患者的队列。采用 Kaplan-Meier 和对数秩检验分析总生存期(OS)和无复发生存期(RFS)。采用单因素和多因素 cox 回归分析评估与 OS 和 RFS 相关的因素。
在 1009 例患者中,708 例为 IVA 期,301 例为 IVB 期。与 IVB 期患者相比,IVA 期患者的中位 OS(120.4 个月 vs. 47.2 个月)和 RFS(79.3 个月 vs. 19.8 个月)显著提高(p < 0.0001)。IVA-M1a(无细胞黏蛋白)患者的 RFS 高于 IV M1b/G1(分化良好的细胞播散)患者(NR 与 64 个月,p = 0.0004)。黏液性和非黏液性肿瘤的生存差异显著(OS 为 106.1 个月 vs. 41.0 个月;RFS 为 46.7 个月 vs. 21.2 个月,p < 0.05),OS 在分化良好、中度和低度之间也存在差异(120.4 个月 vs. 56.3 个月 vs. 32.9 个月,p < 0.05)。在多变量分析中,分期和分级均为 OS 和 RFS 的独立预测因素。在单因素分析中,无细胞黏蛋白和黏液组织学与更好的 OS 和 RFS 相关。
AJCC 第 8 版在预测接受 CRS ± HIPEC 治疗的大量 dAC 患者的预后方面表现良好。根据有无无细胞黏蛋白对 IVA 期患者进行分层,可改善预后,这可能为治疗和长期随访策略提供信息。