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IDEA 协作研究结果对法国 III 期结肠癌患者临床实践的影响:一项法国 GERCOR-PRODIGE 调查。

Impact of the IDEA Collaboration Study Results on Clinical Practice in France for Patients With Stage III Colon Cancer: A National GERCOR - PRODIGE Survey.

机构信息

Medical Oncology Department, Saint-Antoine Hospital, AP-HP, Paris, France.

Medical Oncology Department, CHRU Lille, Lille, France.

出版信息

Clin Colorectal Cancer. 2021 Mar;20(1):79-83.e4. doi: 10.1016/j.clcc.2020.11.004. Epub 2020 Nov 14.

Abstract

BACKGROUND

The IDEA collaboration showed that the type and duration of adjuvant chemotherapy in stage III colon cancer (CC) could be adjusted according to the schedule of chemotherapy and the level of risk. We aimed at evaluating the implementation of IDEA's results in real-life practice for stage III CC.

MATERIAL AND METHODS

All clinicians registered in the French oncology cooperative groups GERCOR, FFCD, and UNICANCER GI mailing lists were invited to participate to an online anonymized nationwide survey from January 30, 2019 to March 31, 2019. Proportions were compared using the χ test.

RESULTS

A total of 213 physicians answered the survey. Of these, 173 (81%) considered that 3 months of adjuvant chemotherapy was the new standard of care for low-risk (pT1-3/N1) stage III CC, and 99% considered that 6 months remained the standard of care for high-risk (pT4 and/or pN2) stage III CC. In patients under 70 years, capecitabine and oxaliplatin (CAPOX) for 3 months was prescribed by 74% of the participants in low-risk CC, whereas 6 months of 5-fluorouracil, leucovorin, and oxaliplatin (FOLFOX) was preferred for high-risk CC in 94% of cases. For patients over 70 years with good performance status and no comorbidities, 172 (81%) physicians prescribed oxaliplatin-based chemotherapy for low-risk CC (3 months, 144 of 172%; 88%), and 200 (94%) physicians prescribed oxaliplatin-based adjuvant chemotherapy for high-risk CC (6 months, 199 of 200%; 99.5%).

CONCLUSIONS

The IDEA results have been practice-changing as French physicians have implemented 3 months of CAPOX for patients with low-risk stage III CC, substituting from 6 months of FOLFOX, which remains the preferred regimen for high-risk patients.

摘要

背景

IDEA 协作研究表明,可根据化疗方案和风险水平调整 III 期结直肠癌(CC)的辅助化疗类型和持续时间。我们旨在评估 IDEA 研究结果在 III 期 CC 真实世界实践中的实施情况。

材料与方法

邀请所有注册于法国肿瘤学合作组 GERCOR、FFCD 和 UNICANCER GI 邮件列表的临床医生参加 2019 年 1 月 30 日至 3 月 31 日的在线匿名全国性调查。使用 χ 检验比较比例。

结果

共有 213 名医生回答了调查。其中,173 名(81%)医生认为 3 个月的辅助化疗是低危(pT1-3/N1)III 期 CC 的新标准,99%的医生认为 6 个月仍然是高危(pT4 和/或 pN2)III 期 CC 的标准。对于 70 岁以下的患者,74%的参与者在低危 CC 中规定了 3 个月的卡培他滨联合奥沙利铂(CAPOX),而 94%的病例中,高危 CC 首选 6 个月的氟尿嘧啶、亚叶酸钙和奥沙利铂(FOLFOX)。对于身体状况良好且无合并症的 70 岁以上患者,172 名(81%)医生为低危 CC 开了奥沙利铂为基础的化疗(3 个月,144/172;88%),200 名(94%)医生为高危 CC 开了奥沙利铂为基础的辅助化疗(6 个月,199/200;99.5%)。

结论

IDEA 的研究结果改变了实践,法国医生用 CAPOX 替代了 6 个月的 FOLFOX,用于治疗低危 III 期 CC,而 6 个月的 FOLFOX 仍然是高危患者的首选方案。

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