Department of Obstetrics and Gynecology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Department of Gynecology, The Forth Hospital of Hebei Medical University, Shijiazhuang, China.
Acta Obstet Gynecol Scand. 2023 Aug;102(8):1045-1052. doi: 10.1111/aogs.14612. Epub 2023 Jun 20.
FIGO 2018 IIIC remains controversial for the heterogeneity of its prognoses. To ensure a better management of cervical cancer patients in Stage IIIC, a revision of the FIGO IIIC version classification is required according to local tumor size.
We retrospectively enrolled cervical cancer patients of FIGO 2018 Stages I-IIIC who had undergone radical surgery or chemoradiotherapy. Based on the tumor factors from the Tumor Node Metastasis staging system, IIIC cases were divided into IIIC-T1, IIIC-T2a, IIIC-T2b, and IIIC-(T3a+T3b). Oncologcial outcomes of all stages were compared.
A total of 63 926 cervical cancer cases were identified, among which 9452 fulfilled the inclusion criteria and were included in this study. Kaplan-Meier pairwise analysis showed that: the oncology outcomes of I and IIA were significantly better than of IIB, IIIA+IIIB, and IIIC; the oncology outcome of IIIC-(T1-T2b) was significantly better than of IIIA+IIIB and IIIC-(T3a+T3b); no significant difference was noted between IIB and IIIC-(T1-T2b), or IIIC-(T3a+T3b) and IIIA+IIIB. Multivariate analysis indicated that, compared with IIIC-T1, Stages T2a, T2b, IIIA+IIIB and IIIC-(T3a+T3b) were associated with a higher risk of death and recurrence/death. There was no significant difference in the risk of death or recurrence/death between patients with IIIC-(T1-T2b) and IIB. Also, compared with IIB, IIIC-(T3a+T3b) was associated with a higher risk of death and recurrence/death. No significant differences in the risk of death and recurrence/death were noted between IIIC-(T3a+T3b) and IIIA+IIIB.
In terms of oncology outcomes of the study, FIGO 2018 Stage IIIC of cervical cancer is unreasonable. Stages IIIC-T1, T2a, and T2b may be integrated as IIC, and it might be unnecessary for T3a/T3b cases to be subdivided by lymph node status.
FIGO 2018 分期的 IIIC 期存在预后异质性,仍颇具争议。为了更好地管理宫颈癌 IIIC 期患者,需要根据局部肿瘤大小对 FIGO IIIC 期进行修订。
我们回顾性纳入了接受根治性手术或放化疗的 FIGO 2018 分期的 I 期至 IIIC 期宫颈癌患者。基于肿瘤因素的肿瘤淋巴结转移分期系统,将 IIIC 病例分为 IIIC-T1、IIIC-T2a、IIIC-T2b 和 IIIC-(T3a+T3b)。比较所有分期的肿瘤学结局。
共纳入 63926 例宫颈癌患者,其中 9452 例符合纳入标准并纳入本研究。Kaplan-Meier 生存分析显示:I 期和 IIA 期的肿瘤学结局明显优于 IIB、IIIA+IIIB 和 IIIC 期;IIIC-(T1-T2b) 期的肿瘤学结局明显优于 IIIA+IIIB 期和 IIIC-(T3a+T3b) 期;IIB 期和 IIIC-(T1-T2b) 期之间,以及 IIIC-(T3a+T3b) 期和 IIIA+IIIB 期之间,差异均无统计学意义。多因素分析表明,与 IIIC-T1 期相比,T2a 期、T2b 期、IIIA+IIIB 期和 IIIC-(T3a+T3b) 期患者死亡和复发/死亡风险更高。IIIC-(T1-T2b) 期与 IIB 期患者死亡和复发/死亡风险无显著差异。此外,与 IIB 期相比,IIIC-(T3a+T3b) 期患者死亡和复发/死亡风险更高。IIIC-(T3a+T3b) 期与 IIIA+IIIB 期患者死亡和复发/死亡风险无显著差异。
从本研究的肿瘤学结局来看,FIGO 2018 分期的 IIIC 期不合理。IIIC-T1、T2a 和 T2b 期可整合为 IIC 期,T3a/T3b 期可能无需根据淋巴结状态进一步细分。