MRI与[18F]FDG PET/CT联合确定FIGO分期对局部晚期宫颈癌患者的预后价值

IF 2.5 4区 医学 Q3 ONCOLOGY
Stefano Raffa , Francesco Lanfranchi , Camilla Satragno , Flavio Giannelli , Michela Marcenaro , Angela Coco , Sofia Elizabeth Cena , Luca Sofia , Cecilia Marini , Serafina Mammoliti , Alessia Levaggi , Alberto Stefano Tagliafico , Gianmario Sambuceti , Salvina Barra , Silvia Morbelli , Liliana Belgioia , Matteo Bauckneht
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引用次数: 0

摘要

最新版本的FIGO分类推荐影像学工具来完成宫颈癌患者的临床评估。然而,优选的成像方法仍不清楚。我们的目的是探讨磁共振成像(MRI)、对比增强计算机断层扫描(ceCT)和[18F]-氟脱氧葡萄糖正电子发射断层扫描([18F]FDG-PET)/CT在局部晚期宫颈癌(LACC, FIGO分期IB3-IVA)患者中的预后能力。回顾性纳入36例LACC患者(平均年龄55.47±14.01,范围31-82岁)。所有患者在接受同步放化疗前均行MRI、ceCT和[18F]FDG-PET/CT检查。中位剂量为45 Gy(范围42-50.4;25-28分,每周5分,每天1分)通过骨盆外束放射治疗(EBRT)给予,中位剂量为57.5 Gy(范围16-61.1;25-28份,每周5份,每天1份)给药于转移淋巴结。近距离放疗的中位剂量为28 Gy(范围28-30;4-5份,每隔一天1份)。每周给予顺铂或卡铂6个周期。研究终点为无复发生存期(RFS)和总生存期(OS)。MRI上盆腔淋巴结转移独立预测RFS (HR 13.271, 95% CI 1.730-101.805;P = 0.027),而FDG-PET/CT独立预测两种RFS (HR 11.734, 95% CI 3.200-43.026;P = 0.005)和OS (HR 13.799, 95% CI 3.378 ~ 56.361;P & lt;0.001)。MRI和[18F]FDG-PET/CT表现结合临床证据纳入FIGO分类。结合临床、MRI和ceCT数据,使用下一代成像(NGI)确定了10/36(27.7%)患者的分期迁移。不同的基于ngi的FIGO分类显示了显著不同的中位RFS(阶段IIB:未达到;第三阶段:44个月;IIIC2阶段:3个月;P & lt;0.001)和OS (IIB期:未达到;第三阶段:未达到;IIIC2阶段:14个月;P & lt;0.001)。基于MRI和[18F]FDG-PET/CT相结合的FIGO分级可以预测同步放化疗的LACC患者的RFS和OS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The prognostic value of FIGO staging defined by combining MRI and [18F]FDG PET/CT in patients with locally advanced cervical cancer

The last version of the FIGO classification recommended imaging tools to complete the clinical assessment of patients with cervical cancer. However, the preferable imaging approach is still unclear. We aimed to explore the prognostic power of Magnetic Resonance Imaging (MRI), contrast-enhanced Computed Tomography (ceCT), and [18F]-Fluorodeoxyglucose Positron Emission Tomography ([18F]FDG-PET)/CT in patients staged for locally advanced cervical cancer (LACC, FIGO stages IB3-IVA). Thirty-six LACC patients (mean age 55.47 ± 14.01, range 31-82) were retrospectively enrolled. All of them underwent MRI, ceCT and [18F]FDG-PET/CT before receiving concurrent chemoradiotherapy. A median dose of 45 Gy (range 42-50.4; 25-28 fractions, 5 fractions per week, 1 per day) was delivered through the external-beam radiation therapy (EBRT) on the pelvic area, while a median dose of 57.5 Gy (range 16-61.1; 25-28 fractions, 5 fractions per week, 1 per day) was administered on metastatic nodes. The median doses for brachytherapy treatment were 28 Gy (range 28-30; 4-5 fractions, 1 every other day). Six cycles of cisplatin or carboplatin were administered weekly. The study endpoints were recurrence-free survival (RFS) and overall survival (OS). Metastatic pelvic lymph nodes at MRI independently predicted RFS (HR 13.271, 95% CI 1.730-101.805; P = 0.027), while metastatic paraaortic lymph nodes at [18F]FDG-PET/CT independently predicted both RFS (HR 11.734, 95% CI 3.200-43.026; P = .005) and OS (HR 13.799, 95% CI 3.378-56.361; P < 0.001). MRI and [18F]FDG-PET/CT findings were incorporated with clinical evidences into the FIGO classification. With respect to the combination of clinical, MRI and ceCT data, the use of next-generation imaging (NGI) determined a stage migration in 10/36 (27.7%) of patients. Different NGI-based FIGO classes showed remarkably different median RFS (stage IIB: not reached; stage IIIC1: 44 months; stage IIIC2: 3 months; P < 0.001) and OS (stage IIB: not reached; stage IIIC1: not reached; stage IIIC2: 14 months; P < 0.001). A FIGO classification based on the combination of MRI and [18F]FDG-PET/CT might predict RFS and OS of LACC patients treated with concurrent chemoradiotherapy.

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来源期刊
Current Problems in Cancer
Current Problems in Cancer 医学-肿瘤学
CiteScore
5.10
自引率
0.00%
发文量
71
审稿时长
15 days
期刊介绍: Current Problems in Cancer seeks to promote and disseminate innovative, transformative, and impactful data on patient-oriented cancer research and clinical care. Specifically, the journal''s scope is focused on reporting the results of well-designed cancer studies that influence/alter practice or identify new directions in clinical cancer research. These studies can include novel therapeutic approaches, new strategies for early diagnosis, cancer clinical trials, and supportive care, among others. Papers that focus solely on laboratory-based or basic science research are discouraged. The journal''s format also allows, on occasion, for a multi-faceted overview of a single topic via a curated selection of review articles, while also offering articles that present dynamic material that influences the oncology field.
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