m+Medelevator.RU
← Поиск публикаций
PloS one · 2025

Efficacy and safety of Atezolizumab plus Bevacizumab and Lenvatinib as first-line systemic therapies for hepatocellular carcinoma: A real-world study.

СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

История · было → стало

Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.

Boonkaya Sangdao, Pattarawongpaiboon Chidkamon, Thaimai Panarat, Ananchuensook Prooksa, Sriphoosanaphan Supachaya, Tanasanvimon Suebpong, Teeyapun Nattaya, Pakvisal Nussara, Siripon Nipaporn, Treeprasertsuk Sombat, Komolmit Piyawat, Thanapirom Kessarin

Аннотация

Atezolizumab plus bevacizumab (ATEZO/BEV) and Lenvatinib (LEN) have demonstrated efficacy as first-line systemic therapies for unresectable hepatocellular carcinoma (HCC). This study aimed to compare the efficacy, safety, and outcomes of these two treatments. Data were retrospectively collected from 163 patients with unresectable HCC receiving first-line Lenvatinib (LEN) (n = 85) or ATEZO/BEV (n = 78) between 2020 and 2023 at Chulalongkorn University Hospital in Bangkok, Thailand. The primary outcome was overall survival (OS) following treatment. Propensity score matching (PSM) was used for analysis. The median patient age was 60.6 (SD 11.8) years; 82.2% were male. Most had hepatitis B/C (66.9%), BCLC stage C (73%), and Child-Pugh class A cirrhosis (63.8%). After PSM analysis, overall survival (OS) was significantly longer in the ATEZO/BEV group (12.7 vs. 7.5 months; p = 0.016, HR = 0.618, 95% CI: 0.417-0.916). However, there was no significant difference in progression-free survival (PFS) between ATEZO/BEV and LEN groups (10.8 vs. 7.8 months; p = 0.26, HR = 0.73, 95% CI: 0.431-1.255). Assessed by mRECIST, neither objective response rate (ORR: 23.7% vs. 19.7%, p = 0.555) nor disease control rate (DCR: 36.8% vs. 38.2%, p = 0.867) differed significantly. Multivariate analysis revealed alpha-fetoprotein ≥500 ng/mL (HR = 1.881, 95% CI: 1.028-3.443, p = 0.04), tumor size (HR = 1.833, 95% CI: 1.010-3.327, p = 0.046) and ATEZO/BEV therapy (HR = 0.604, 95%CI: 0.373-0.977, p = 0.04) were independently associated with OS. Adverse event rates were comparable (ATEZO/BEV 43.7% vs. LEN 56.3%; p = 0.08). In conclusion, the study demonstrates that ATEZO/BEV significantly improves OS compared to LEN in patients with unresectable HCC, despite similar PFS, ORR, and DCR. Both treatments have comparable safety profiles.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты