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阿替利珠单抗/贝伐珠单抗联合治疗获得完全缓解的晚期肝细胞癌患者的特征和预后。

Characteristics and Prognosis of Patients with Advanced Hepatocellular Carcinoma Treated with Atezolizumab/Bevacizumab Combination Therapy Who Achieved Complete Response.

机构信息

Department of Gastroenterology and Hepatology, Fujita Health University, Toyoake 470-1192, Japan.

Department of Gastroenterology and Hepatology, Fujita Health University Bantane Hospital, Nagoya 454-8509, Japan.

出版信息

Curr Oncol. 2024 Oct 16;31(10):6218-6231. doi: 10.3390/curroncol31100463.

Abstract

AIM

To investigate the characteristics and prognosis of patients with advanced hepatocellular carcinoma (HCC) treated with atezolizumab and bevacizumab (Atz/Bev) who achieved a complete response (CR) according to the modified Response Evaluation Criteria in Solid Tumors (mRECIST).

METHODS

A total of 120 patients with Eastern Cooperative Oncology Group performance status (PS) 0 or 1 and Child-Pugh A at the start of Atz/Bev treatment were included. Barcelona Clinic Liver Cancer stage C was recorded in 59 patients.

RESULTS

The CR rate with Atz/Bev alone was 15.0%. The median time to CR was 3.4 months, and the median duration of CR was 15.6 months. A significant factor associated with achieving CR with Atz/Bev alone was an AFP ratio of 0.34 or less at 3 weeks. Adding transarterial chemoembolization (TACE) in the six patients who achieved a partial response increased the overall CR rate to 20%. Among the 24 patients who achieved CR, the median progression-free survival was 19.3 months, the median overall survival was not reached, and 14 patients (58.3%) were able to discontinue Atz/Bev and achieve a drug-free status. Twelve of these patients developed progressive disease (PD), but eleven successfully received post-PD treatments and responded well.

CONCLUSIONS

Achieving CR by mRECIST using Atz/Bev alone or with additional TACE can be expected to offer an extremely favorable prognosis.

摘要

目的

研究根据改良实体瘤疗效评价标准(mRECIST)达到完全缓解(CR)的接受阿替利珠单抗联合贝伐珠单抗(Atz/Bev)治疗的晚期肝细胞癌(HCC)患者的特征和预后。

方法

共纳入 120 例在开始 Atz/Bev 治疗时东部肿瘤协作组体力状态(PS)0 或 1 级和 Child-Pugh A 级的患者。59 例患者记录为巴塞罗那临床肝癌分期 C 期。

结果

单用 Atz/Bev 的 CR 率为 15.0%。CR 的中位时间为 3.4 个月,CR 的中位持续时间为 15.6 个月。单用 Atz/Bev 达到 CR 的显著相关因素是第 3 周 AFP 比值为 0.34 或更低。在 6 例达到部分缓解的患者中添加肝动脉化疗栓塞(TACE),将总 CR 率提高到 20%。在 24 例达到 CR 的患者中,无进展生存期的中位值为 19.3 个月,中位总生存期未达到,14 例(58.3%)患者能够停用 Atz/Bev 并达到无药物状态。其中 12 例患者出现疾病进展(PD),但 11 例成功接受了 PD 后治疗且反应良好。

结论

通过 mRECIST 单用或联用 TACE 达到 CR 有望带来极其有利的预后。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/17ca/11506828/190ef0407bea/curroncol-31-00463-g001.jpg

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