Department of Surgery, Galway University Hospitals, Galway, H91 YRY71, Ireland.
Int J Colorectal Dis. 2023 Mar 13;38(1):71. doi: 10.1007/s00384-023-04364-2.
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.
To assess the concordance between the RS and MDT decisions regarding adjuvant chemotherapy in colon cancer.
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.
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).
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.
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。
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。
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。
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)。
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。