Peng Zhou, Yan Bao, De-Hua Chang, Jun-Xiang Li, Tian-Zhi An, Ya-Ping Shen, Wen-Wu Cai, Lu Wen, Yu-Dong Xiao
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OS and RFS were also compared between the two groups in subgroups of tumor size smaller than 30 mm and tumor size 30–50 mm. The SMARS score classified 127 and 508 patients into predicted proliferative and nonproliferative HCCs, respectively. The predicted proliferative HCCs exhibited worse RFS but equivalent OS when compared with nonproliferative HCCs before (p < 0.001 for RFS; p = 0.166 for OS) and after (p < 0.001 for RFS; p = 0.456 for OS) matching. Regarding subgroups of tumor size smaller than 30 mm (p = 0.098) and tumor size 30–50 mm (p = 0.680), the OSs were similar between the two groups. However, predicted proliferative HCCs had worse RFS compared to nonproliferative HCCs in the subgroup of tumor size 30–50 mm (p < 0.001), while the RFS did not differ in the subgroup of tumor size smaller than 30 mm (p = 0.141). Predicted proliferative HCCs have worse RFS than nonproliferative ones after MWA, especially in tumor size larger than 30 mm. 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引用次数: 0
摘要
利用之前开发的基于成像的预测模型--SMARS评分,比较微波消融(MWA)术后预测增生性和非增生性肝细胞癌(HCC)的治疗效果。这项多中心回顾性研究纳入了 2013 年 8 月至 2020 年 9 月期间接受微波消融术的 635 例不可切除 HCC 患者。根据SMARS评分,患者被分为预测增殖和非增殖表型。比较了倾向评分匹配(PSM)前后预测增殖型和非增殖型HCC的总生存期(OS)和无复发生存期(RFS)。此外,还比较了肿瘤大小小于 30 毫米和肿瘤大小 30-50 毫米亚组两组患者的 OS 和 RFS。SMARS评分将127名和508名患者分别分为预测增殖性和非增殖性HCC。与匹配前(RFS p < 0.001;OS p = 0.166)和匹配后(RFS p < 0.001;OS p = 0.456)的非增殖性HCC相比,预测增殖性HCC的RFS较差,但OS相当。在肿瘤大小小于30毫米(p = 0.098)和肿瘤大小为30-50毫米(p = 0.680)的亚组中,两组的OS相似。然而,在肿瘤大小为 30-50 mm 的亚组中,预测增殖性 HCC 的 RFS 比非增殖性 HCC 更差(p < 0.001),而在肿瘤大小小于 30 mm 的亚组中,RFS 没有差异(p = 0.141)。预测增殖性 HCC 在 MWA 后的 RFS 比非增殖性 HCC 差,尤其是肿瘤大小大于 30 毫米的 HCC。不过,肿瘤的表型可能不会影响OS。在对肝细胞癌进行微波消融之前,应考虑肿瘤的表型,因为它可能会影响治疗效果。
Identification of proliferative hepatocellular carcinoma using the SMARS score and implications for microwave ablation
To compare therapeutic outcomes of predicted proliferative and nonproliferative hepatocellular carcinoma (HCC) after microwave ablation (MWA) using a previously developed imaging-based predictive model, the SMARS score. This multicenter retrospective study included consecutive 635 patients with unresectable HCC who underwent MWA between August 2013 and September 2020. Patients were stratified into predicted proliferative and nonproliferative phenotypes according to the SMARS score. Overall survival (OS) and recurrence-free survival (RFS) were compared between the predicted proliferative and nonproliferative HCCs before and after propensity score matching (PSM). OS and RFS were also compared between the two groups in subgroups of tumor size smaller than 30 mm and tumor size 30–50 mm. The SMARS score classified 127 and 508 patients into predicted proliferative and nonproliferative HCCs, respectively. The predicted proliferative HCCs exhibited worse RFS but equivalent OS when compared with nonproliferative HCCs before (p < 0.001 for RFS; p = 0.166 for OS) and after (p < 0.001 for RFS; p = 0.456 for OS) matching. Regarding subgroups of tumor size smaller than 30 mm (p = 0.098) and tumor size 30–50 mm (p = 0.680), the OSs were similar between the two groups. However, predicted proliferative HCCs had worse RFS compared to nonproliferative HCCs in the subgroup of tumor size 30–50 mm (p < 0.001), while the RFS did not differ in the subgroup of tumor size smaller than 30 mm (p = 0.141). Predicted proliferative HCCs have worse RFS than nonproliferative ones after MWA, especially in tumor size larger than 30 mm. However, the phenotype of the tumor may not affect the OS. Before performing microwave ablation for hepatocellular carcinoma, the tumor phenotype should be considered because it may affect the therapeutic outcome.
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