肝细胞癌的靶向免疫疗法: 临床病例

B. Kashakov, M. Akbarova
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摘要

相关性:肝细胞癌(HCC)是最常见的肝脏恶性肿瘤。由于肝细胞癌具有进展性、发现晚、存活率低和预后不良等特点,因此是哈萨克斯坦肿瘤服务领域最重要的问题之一。 本研究旨在以临床实例评估靶向免疫疗法在治疗肝细胞癌中的应用。 方法:本文介绍了克孜勒奥尔达地区肿瘤中心采用靶向免疫疗法联合阿特珠单抗1200毫克+贝伐单抗800毫克治疗肝细胞癌的临床病例,每3周一次。 治疗结果2018年首次出现肝损伤症状,当时发现了HCC。病毒性乙型肝炎于 2016 年确诊。 20 年 8 月 15 日的 MRI OBP:肝脏右叶 S5 - 9×7×6 厘米,S3 - 3.7 厘米,S7 - 3.0 厘米,S8 - 2.5 厘米。随访检查(2021 年 7 月)期间,酶免疫测定显示血管紧张素转换酶(ACE)水平较高,为 450.56 IU/ml;腹部 CT 扫描显示病情没有恶化。后来,尽管进行了治疗,但 ACE 还是迅速升高:2,595.3 IU/ml(2021 年 8 月)和 2,142.25 IU/ml(2021 年 9 月),治疗改为瑞戈非尼。ACE 继续上升至 4,405 IU/ml(2021 年 11 月)和 18,005 IU/ml(2021 年 12 月)。对照组腹部 CT 扫描显示肿瘤大小适度缩小。 考虑到 ACE 的稳定增长,2022 年 2 月,医生建议患者使用 Atezolizumab 和 Bevacizumab 治疗。2023 年 1 月,患者已经接受了 13 个疗程的治疗,ACE 继续下降:1,932 IU/ml(2023 年 1 月)、53.38 IU/ml(2023 年 2 月)、16.07 IU/ml(2023 年 3 月),腹部 CT 扫描显示出积极的动态变化。 结论靶向免疫疗法在上述无法手术的 HCC 病例中显示出其有效性,并使患者在超过 18 个月的时间里能够继续生活、工作和积极的生活方式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TARGETED IMMUNOTHERAPY FOR HEPATOCELLULAR CARCINOMA: A CLINICAL CASE
Relevance: Hepatocellular carcinoma (HCC) is the most common malignant tumor of the liver. HCC is one of the most important problems of the oncology service of Kazakhstan, as it has a progressive course, late detection, low survival, and unfavorable prognosis. The study aimed to evaluate the use of targeted immunotherapy in treating hepatocellular carcinoma in a clinical example. Methods: The paper presents a clinical case of targeted immunotherapy in combination with Atezolizumab 1200 mg + Bevacizumab 800 mg, once every 3 weeks, in treating HCC in the Regional Oncology Center in Kyzylorda. Results: The first symptoms of liver damage appeared in 2018, at which time HCC was discovered. Viral hepatitis B was diagnosed in 2016. MRI OBP from 15.08.20: a picture of the right lobe of the liver in S5 – 9×7×6 cm, in S3 – 3.7 cm, in S7 – 3.0 cm, in S8 – 2.5 cm. During the follow-up examination (July 2021), the enzyme immunoassay revealed a high angiotensin-converting enzyme (ACE) level of 450.56 IU/ml; the abdominal CT scan showed no deterioration. Later, despite the therapy, ACE increased rapidly: 2,595.3 IU/ml (August 2021) and 2,142.25 IU/ml (September 2021), and the therapy was changed to Regorafenib. ACE continued to rise to 4,405 IU/ml (November 2021) and 18,005 IU/ml (December 2021). A control abdominal CT scan showed a moderate reduction in the size of the tumor. Taking into account a steady ACE increase, in February 2022, the patient was recommended therapy with Atezolizumab and Bevacizumab. In January 2023, the patient has already received 13 courses, and ACE continued to decrease: 1,932 IU/ml (January 2023), 53.38 IU/ml (February 2023), 16.07 IU/ml (March 2023), and the abdominal CT scan showed positive dynamics. Conclusion: Targeted immunotherapy showed its effectiveness in the described case of inoperable HCC and allowed the patient to continue living, working, and leading an active lifestyle for more than 18 months.
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