风险分层工具用于辅助已切除软组织肉瘤的辅助化疗决策:爱尔兰肉瘤中心十年经验回顾。

IF 2.1 Q3 ONCOLOGY World Journal of Oncology Pub Date : 2024-08-01 Epub Date: 2024-06-17 DOI:10.14740/wjon1863
Catherine S Weadick, Caitriona Goggin, Rachel J Keogh, Jake F Murphy, Linda Feeley, Michael W Bennett, Seamus O'Reilly, H Paul Redmond, Jason Kelly, Deirdre O'Mahony, Sinead Noonan, A James P Clover, Richard M Bambury
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引用次数: 0

摘要

背景:软组织肉瘤(STS)包括约 80 种亚型,在欧洲的发病率为每年每 10 万人中 4-5 例。美国国家综合癌症网络(NCCN)指南建议,根据美国癌症联合委员会(AJCC)的分期,复发风险高的肿瘤应考虑新辅助/辅助化疗。另外,Sarculator 是一种风险预测工具,它确定了一个风险阈值,超过该阈值,化疗可能会带来总生存期(OS)的获益。使用该提名图,10年预测OS<60%的患者被归类为高风险患者,应考虑接受化疗。本研究旨在评估这两种风险预测方法在爱尔兰人群中的预后准确性:方法:确定科克大学医院 STS 肿瘤委员会在 2012 年 1 月至 2021 年 12 月期间讨论的所有新诊断的 STS 切除患者。收集临床病理数据。使用 AJCC 和 Sarculator 提名图对所有肢体/躯干肉瘤患者进行风险评估。采用 Kaplan-Meier 法对事件发生时间进行分析,计算 OS:结果:共对200例STS患者进行了复查,其中134例为躯干或四肢肿瘤。对其中的 60 例进行了 Sarculator 评分(不包括分化良好的脂肪肉瘤、类苔藓瘤和原发性皮纤维肉瘤)。使用 Sarculator 提名图计算 10 年预测 OS,19 例患者被归类为高风险,41 例被归类为低风险。使用AJCC分期,25名患者被归为高风险,35名被归为低风险。Sarculator 高风险组的 5 年 OS 率为 60.2%,而低风险组为 87.1%(P = 0.009)。AJCC高风险组的5年OS率为67.6%,低风险组为86.3%(P = 0.083):结论:我们的队列在广泛的组织学亚型中具有代表性。在我们的人群中,Sarculator评分结果与国际结果相关,评分越高,死亡率越高。Sarculator 比 AJCC 分期更能预测临床结果,使用 Sarculator 可以降低考虑辅助化疗的患者比例,从而减轻毒性,这在临床疗效不确定的情况下非常重要。
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Risk Stratification Tools to Aid Decisions on Adjuvant Chemotherapy Usage in Resected Soft Tissue Sarcomas: A Ten-Year Review of an Irish Sarcoma Center Experience.

Background: Soft tissue sarcoma (STS) is comprised of approximately 80 subtypes, with an incidence of 4 - 5 per 100,000 annually in Europe. The National Comprehensive Cancer Network (NCCN) guidelines recommend consideration of neoadjuvant/adjuvant chemotherapy in tumors at high risk of recurrence based on the American Joint Committee on Cancer (AJCC) staging. Alternatively, the Sarculator is a risk prediction tool that has identified a threshold of risk, above which chemotherapy may provide an overall survival (OS) benefit. Using this nomogram, patients with a 10-year predicted OS < 60% are classified as high risk and should be considered for chemotherapy. The aim of this study was to assess the prognostic accuracy of these two risk prediction methods in an Irish population.

Methods: All newly diagnosed patients with resected STS discussed in the STS tumor board in Cork University Hospital between January 2012 and December 2021 were identified. Clinicopathological data were collected. Risk assessment using AJCC and Sarculator nomogram was performed on all patients with an extremity/trunk sarcoma. The OS was calculated including Kaplan-Meier method for time to event analysis.

Results: In total, 200 STS patients were reviewed, of whom 134 had truncal or extremity tumors. Sarculator score was calculated for 60 of these (well differentiated liposarcomas, desmoid tumors and dermatofibrosarcoma protuberans were excluded). Using the Sarculator nomogram to calculate 10-year predicted OS, 19 patients were categorized as high risk and 41 were categorized as low risk. Using AJCC staging, 25 patients were categorized as high risk and 35 as low risk. The 5-year OS rate in the Sarculator high-risk group was 60.2%, compared with 87.1% in the low-risk group (P = 0.009). The 5-year OS rate in the AJCC high-risk group was 67.6%, compared with 86.3% in the low-risk group (P = 0.083).

Conclusions: Our cohort is representative of the broad histological subtypes expected. In our population, Sarculator score results correlate with international outcomes and higher scores were associated with increased mortality. The Sarculator was more predictive of clinical outcome than AJCC staging, and its use would lower the proportion of patients being considered for adjuvant chemotherapy thereby sparing toxicity, which is important in the setting of uncertain clinical benefit.

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期刊介绍: World Journal of Oncology, bimonthly, publishes original contributions describing basic research and clinical investigation of cancer, on the cellular, molecular, prevention, diagnosis, therapy and prognosis aspects. The submissions can be basic research or clinical investigation oriented. This journal welcomes those submissions focused on the clinical trials of new treatment modalities for cancer, and those submissions focused on molecular or cellular research of the oncology pathogenesis. Case reports submitted for consideration of publication should explore either a novel genomic event/description or a new safety signal from an oncolytic agent. The areas of interested manuscripts are these disciplines: tumor immunology and immunotherapy; cancer molecular pharmacology and chemotherapy; drug sensitivity and resistance; cancer epidemiology; clinical trials; cancer pathology; radiobiology and radiation oncology; solid tumor oncology; hematological malignancies; surgical oncology; pediatric oncology; molecular oncology and cancer genes; gene therapy; cancer endocrinology; cancer metastasis; prevention and diagnosis of cancer; other cancer related subjects. The types of manuscripts accepted are original article, review, editorial, short communication, case report, letter to the editor, book review.
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