Radiotherapy with Targeted Therapy or Immune Checkpoint Inhibitors for Hepatocellular Carcinoma with Hepatic Vein and/or Inferior Vena Cava Tumor Thrombi.

IF 4.2 3区 医学 Q2 ONCOLOGY Journal of Hepatocellular Carcinoma Pub Date : 2024-08-05 eCollection Date: 2024-01-01 DOI:10.2147/JHC.S464140
Zhuoran Li, Yirui Zhai, Fan Wu, Dayong Cao, Feng Ye, Yan Song, Shulian Wang, Yueping Liu, Yongwen Song, Yuan Tang, Hao Jing, Hui Fang, Shunan Qi, Ningning Lu, Ye-Xiong Li, Jianxiong Wu, Bo Chen
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Abstract

Purpose: This study evaluated the clinical outcomes of patients with hepatocellular carcinoma (HCC) with hepatic vein tumor thrombus (HVTT) and/or inferior vena cava tumor thrombus (IVCTT) receiving radiotherapy (RT) combined with systemic therapies.

Patients and methods: Patients with HCC with HVTT and/or IVCTT who received RT were identified at our institution. The prescription doses were 30-65 Gy for planning target volume and 40-65 Gy for the gross tumor volume. Targeted therapy and immune checkpoint inhibitors were used concurrently if patients were at a high risk of or already had distant metastasis. After RT completion, follow-up was performed at 1, 3, 6, and 12 months, and 3 to 6 months thereafter. The objective response rate (ORR), overall survival (OS), progression-free survival (PFS) and toxicity were recorded.

Results: Thirty-four patients were retrospectively enrolled between January 2016 and September 2021. Most patients received concurrent targeted therapy (70.6%) and/or post-RT (79.4%). The in-field ORR and disease control rates were 79.4% and 97.1%, respectively. The OS rates were 77.6% at 1 year and 36.3% at 2 years (median OS, 15.8 months). The median PFS and median in-field PFS were 4.2 months and not reached, respectively. The PFS and in-field PFS rates were 24.6% and 79.2% at 1 year, 19.7% and 72.0% at 2 years, respectively. An alpha-fetoprotein level >1000 ng/mL was a significant prognostic factor for worse OS (HR, 5.674; 95% CI, 1.588-20.276; p=0.008); in-field complete/partial response was a significant prognostic factor for better OS (HR, 0.116; 95% CI, 0.027-0.499; p=0.004). The most common site of first failure was the lungs (13/34 patients, 38.2%), followed by the liver (7/34 patients, 20.6%). No patients developed radiation-induced liver disease or pulmonary embolism during follow-up.

Conclusion: Combining RT and systemic therapy was safe and effective in treating patients with HCC with HVTT and IVCTT.

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放疗联合靶向治疗或免疫检查点抑制剂治疗伴有肝静脉和/或下腔静脉瘤栓的肝细胞癌。
目的:本研究评估了肝静脉瘤栓(HVTT)和/或下腔静脉瘤栓(IVCTT)肝细胞癌(HCC)患者接受放疗(RT)联合全身治疗的临床疗效:本院确定了接受 RT 的 HVTT 和/或 IVCTT HCC 患者。计划靶体积的处方剂量为30-65 Gy,肿瘤总体积的处方剂量为40-65 Gy。如果患者有远处转移的高风险或已经出现远处转移,则同时使用靶向治疗和免疫检查点抑制剂。RT 结束后,在 1、3、6 和 12 个月时进行随访,此后 3 至 6 个月进行随访。记录客观反应率(ORR)、总生存期(OS)、无进展生存期(PFS)和毒性:34名患者于2016年1月至2021年9月期间回顾性入组。大多数患者同时接受了靶向治疗(70.6%)和/或RT后治疗(79.4%)。现场ORR和疾病控制率分别为79.4%和97.1%。1年的OS率为77.6%,2年的OS率为36.3%(中位OS为15.8个月)。中位 PFS 和中位现场 PFS 分别为 4.2 个月和未达标。1年的PFS和现场PFS率分别为24.6%和79.2%,2年的PFS和现场PFS率分别为19.7%和72.0%。甲胎蛋白水平>1000 ng/mL是OS较差的重要预后因素(HR,5.674;95% CI,1.588-20.276;P=0.008);场内完全/部分反应是OS较好的重要预后因素(HR,0.116;95% CI,0.027-0.499;P=0.004)。首次衰竭最常见的部位是肺(13/34 例患者,38.2%),其次是肝(7/34 例患者,20.6%)。在随访期间,没有患者出现辐射诱发的肝病或肺栓塞:结论:在治疗HVTT和IVCTT的HCC患者时,将RT和全身治疗相结合是安全有效的。
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来源期刊
CiteScore
0.50
自引率
2.40%
发文量
108
审稿时长
16 weeks
期刊最新文献
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