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Is the Concurrent Use of Sorafenib and External Radiotherapy Feasible for Advanced Hepatocellular Carcinoma? A Meta-Analysis

SIMPLE SUMMARY: Concurrent chemotherapy and external radiation is a commonly used method for cancer treatment. However, concurrent application of sorafenib and external radiotherapy has not been commonly used in clinical practice due to the possible risk of excessive complication. The results of thi...

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Detalles Bibliográficos
Autores principales: Rim, Chai Hong, Park, Sunmin, Shin, In-Soo, Yoon, Won Sup
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8230463/
https://www.ncbi.nlm.nih.gov/pubmed/34200809
http://dx.doi.org/10.3390/cancers13122912
Descripción
Sumario:SIMPLE SUMMARY: Concurrent chemotherapy and external radiation is a commonly used method for cancer treatment. However, concurrent application of sorafenib and external radiotherapy has not been commonly used in clinical practice due to the possible risk of excessive complication. The results of this meta-analysis suggest that concurrent treatment might be a feasible option, and treatment targeting metastatic lesion or vessel involvement is particularly recommended. ABSTRACT: We evaluate the feasibility of a concurrent application of sorafenib and external beam radiation therapy (EBRT) for advanced hepatocellular carcinoma (HCC). PubMed, Embase, Medline, and Cochrane Library were searched up to 9 April 2021. The primary endpoint was grade ≥3 complications, and the secondary endpoint was overall survival (OS). Subgroup analyses were performed for studies with the EBRT targets, intrahepatic vs. non-intrahepatic lesions (e.g., extrahepatic metastases or malignant vessel involvement only). Eleven studies involving 512 patients were included in this meta-analysis. Pooled rates of gastrointestinal, hepatologic, hematologic, and dermatologic grade ≥3 toxicities were 8.1% (95% confidence interval (CI): 4.8–13.5, I(2) = ~0%), 12.9% (95% CI: 7.1–22.1, I(2) = 22.4%), 9.1% (95% CI: 3.8–20.3, I(2) = 51.3%), and 6.8% (95% CI: 3.8–11.7, I(2) = ~0%), respectively. Pooled grade ≥3 hepatologic and hematologic toxicity rates were lower in studies targeting non-intrahepatic lesions than those targeting intrahepatic lesions (hepatologic: 3.3% vs. 17.1%, p = 0.041; hematologic: 3.3% vs. 16.0%, p = 0.078). Gastrointestinal and dermatologic grade ≥3 complications were not significantly different between the subgroups. Regarding OS, concurrent treatment was more beneficial than non-concurrent treatment (odds ratio: 3.3, 95% CI: 1.3–8.59, p = 0.015). One study reported a case of lethal toxicity due to tumor rupture and gastrointestinal bleeding. Concurrent treatment can be considered and applied to target metastatic lesions or local vessel involvement. Intrahepatic lesions should be treated cautiously by considering the target size and hepatic reserve.