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免疫治疗肝细胞癌患者的预后——CRAFITY 评分的建立和验证。

Prognosis of patients with hepatocellular carcinoma treated with immunotherapy - development and validation of the CRAFITY score.

机构信息

Division of Gastroenterology and Hepatology, Department of Internal Medicine III, Medical University of Vienna, Vienna, Austria; Liver Cancer (HCC) Study Group Vienna, Medical University of Vienna, Vienna, Austria.

Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Hannover, Germany; Department of Medicine I, University Medical Center Schleswig-Holstein, Lübeck, Germany.

出版信息

J Hepatol. 2022 Feb;76(2):353-363. doi: 10.1016/j.jhep.2021.09.035. Epub 2021 Oct 12.

Abstract

BACKGROUND & AIMS: Immunotherapy with atezolizumab plus bevacizumab represents the new standard of care in systemic front-line treatment of hepatocellular carcinoma (HCC). However, biomarkers that predict treatment success and survival remain an unmet need.

METHODS

Patients with HCC put on PD-(L)1-based immunotherapy were included in a training set (n = 190; 6 European centers) and a validation set (n = 102; 8 European centers). We investigated the prognostic value of baseline variables on overall survival using a Cox model in the training set and developed the easily applicable CRAFITY (CRP and AFP in ImmunoTherapY) score. The score was validated in the independent, external cohort, and evaluated in a cohort of patients treated with sorafenib (n = 204).

RESULTS

Baseline serum alpha-fetoprotein ≥100 ng/ml (hazard ratio [HR] 1.7; p = 0.007) and C-reactive protein ≥1 mg/dl (HR, 1.7; p = 0.007) were identified as independent prognostic factors in multivariable analysis and were used to develop the CRAFITY score. Patients who fulfilled no criterion (0 points; CRAFITY-low) had the longest median overall survival (27.6 (95% CI 19.5-35.8) months), followed by those fulfilling 1 criterion (1 point; CRAFITY-intermediate; 11.3 (95% CI 8.0-14.6) months), and patients meeting both criteria (2 points; CRAFITY-high; 6.4 (95% CI 4.8-8.1) months; p <0.001). Additionally, best radiological response (complete response/partial response/stable disease/progressive disease) was significantly better in patients with lower CRAFITY score (CRAFITY-low: 9%/20%/52%/20% vs. CRAFITY-intermediate: 3%/25%/36%/36% vs. CRAFITY-high: 2%/15%/22%/61%; p = 0.003). These results were confirmed in the independent validation set and in different subgroups, including Child-Pugh A and B, performance status 0 and ≥1, and first-line and later lines. In the sorafenib cohort, CRAFITY was associated with survival, but not radiological response.

CONCLUSIONS

The CRAFITY score is associated with survival and radiological response in patients receiving PD-(L)1 immunotherapy. The score may help with patient counseling but requires prospective validation.

LAY SUMMARY

The immunotherapy-based regimen of atezolizumab plus bevacizumab represents the new standard of care in systemic first-line therapy of hepatocellular carcinoma (HCC). Biomarkers to predict treatment outcome are an unmet need in patients undergoing immunotherapy for HCC. We developed and externally validated a score that predicts outcome in patients with HCC undergoing immunotherapy with immune checkpoint blockers.

摘要

背景与目的

阿替利珠单抗联合贝伐珠单抗的免疫治疗代表了肝细胞癌(HCC)系统一线治疗的新标准。然而,预测治疗效果和生存的生物标志物仍然是一个未满足的需求。

方法

将接受 PD-(L)1 为基础的免疫治疗的 HCC 患者纳入训练集(n=190;6 个欧洲中心)和验证集(n=102;8 个欧洲中心)。我们使用 Cox 模型在训练集中研究基线变量对总生存期的预后价值,并开发了易于应用的 CRAFITY(免疫治疗中的 CRP 和 AFP)评分。该评分在独立的外部队列中进行了验证,并在接受索拉非尼治疗的患者队列(n=204)中进行了评估。

结果

多变量分析确定基线时血清甲胎蛋白≥100ng/ml(风险比[HR]1.7;p=0.007)和 C 反应蛋白≥1mg/dl(HR,1.7;p=0.007)是独立的预后因素,并用于开发 CRAFITY 评分。不符合任何标准的患者(0 分;CRAFITY-低)中位总生存期最长(27.6(95%CI 19.5-35.8)个月),其次是符合 1 个标准的患者(1 分;CRAFITY-中值;11.3(95%CI 8.0-14.6)个月),符合 2 个标准的患者(2 分;CRAFITY-高;6.4(95%CI 4.8-8.1)个月;p<0.001)。此外,较低 CRAFITY 评分的患者最佳影像学反应(完全缓解/部分缓解/稳定疾病/进展性疾病)明显更好(CRAFITY-低:9%/20%/52%/20%vs.CRAFITY-中值:3%/25%/36%/36%vs.CRAFITY-高:2%/15%/22%/61%;p=0.003)。这些结果在独立的验证集和不同的亚组中得到了证实,包括 Child-Pugh A 和 B、表现状态 0 和≥1 以及一线和二线治疗。在索拉非尼队列中,CRAFITY 与生存相关,但与影像学反应无关。

结论

CRAFITY 评分与接受 PD-(L)1 免疫治疗的患者的生存和影像学反应相关。该评分可能有助于患者咨询,但需要前瞻性验证。

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