Suppr超能文献

12 基因复发评分对错配修复功能良好的 II/III 期结直肠癌辅助化疗处方的影响:系统评价和荟萃分析。

Impact of the 12-gene recurrence score in influencing adjuvant chemotherapy prescription in mismatch repair proficient stage II/III colonic carcinoma-a systematic review and meta-analysis.

机构信息

Department of Surgery, Galway University Hospitals, Galway, H91 YRY71, Ireland.

出版信息

Int J Colorectal Dis. 2023 Mar 13;38(1):71. doi: 10.1007/s00384-023-04364-2.

Abstract

INTRODUCTION

The 12-gene recurrence score (RS) is a clinically validated assay which predicts recurrence risk in patients with stage II/III colon cancer. Decisions regarding adjuvant chemotherapy may be guided using this assay or based on the judgement of tumour board.

AIMS

To assess the concordance between the RS and MDT decisions regarding adjuvant chemotherapy in colon cancer.

METHODS

A systematic review was performed in accordance with PRISMA guidelines. Meta-analyses were performed using the Mantel-Haenszel method using the Review Manager version 5.4 software.

RESULTS

Four studies including 855 patients with a mean age of 68 years (range: 25-90 years) met inclusion criteria. Overall, 79.2% had stage II disease (677/855) and 20.8% had stage III disease (178/855). For the entire cohort, concordant results between the 12-gene assay and MDT were more likely than discordant (odds ratio (OR): 0.38, 95% confidence interval (CI): 0.25-0.56, P < 0.001). Patients were more likely to have chemotherapy omitted than escalated when using the RS (OR: 9.76, 95% CI: 6.72-14.18, P < 0.001). For those with stage II disease, concordant results between the 12-gene assay and MDT were more likely than discordant (OR: 0.30, 95% CI: 0.17-0.53, P < 0.001). In stage II disease, patients were more likely to have chemotherapy omitted than escalated when using the RS (OR: 7.39, 95% CI: 4.85-11.26, P < 0.001).

CONCLUSIONS

The use of the 12-gene signature refutes the decision of tumour board in 25% of cases, with 75% of discordant decisions resulting in omission of adjuvant chemotherapy. Therefore, it is possible that a proportion of such patients are being overtreated when relying on tumour board decisions alone.

摘要

简介

12 基因复发评分 (RS) 是一种经过临床验证的检测方法,可预测 II/III 期结肠癌患者的复发风险。辅助化疗的决策可以使用该检测方法或根据肿瘤委员会的判断来指导。

目的

评估 RS 与肿瘤委员会关于结肠癌辅助化疗的决策之间的一致性。

方法

按照 PRISMA 指南进行系统综述。使用 Review Manager 版本 5.4 软件进行荟萃分析,采用 Mantel-Haenszel 方法。

结果

四项研究共纳入 855 例患者,平均年龄为 68 岁(范围:25-90 岁),符合纳入标准。总体而言,79.2%的患者为 II 期疾病(677/855),20.8%的患者为 III 期疾病(178/855)。对于整个队列,12 基因检测与 MDT 之间的一致结果比不一致结果更有可能(比值比 (OR):0.38,95%置信区间 (CI):0.25-0.56,P<0.001)。使用 RS 时,患者更有可能被排除化疗而非升级(OR:9.76,95% CI:6.72-14.18,P<0.001)。对于 II 期疾病患者,12 基因检测与 MDT 之间的一致结果比不一致结果更有可能(OR:0.30,95% CI:0.17-0.53,P<0.001)。在 II 期疾病中,使用 RS 时,患者更有可能被排除化疗而非升级(OR:7.39,95% CI:4.85-11.26,P<0.001)。

结论

在 25%的病例中,使用 12 基因特征否定了肿瘤委员会的决策,75%的不一致决策导致辅助化疗被排除。因此,仅依赖肿瘤委员会的决策,可能会使一部分此类患者过度治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6b4/10011316/95acad911c6a/384_2023_4364_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验