TY - JOUR
T1 - Efficacy of Second-Line Treatments After Atezolizumab and Bevacizumab in Advanced Hepatocellular Carcinoma and Related Prognostic Factors
T2 - A Multicenter Study by the Turkish Oncology Group (TOG)
AU - Majidova, Nargiz
AU - Yaslıkaya, Sendag
AU - Mıldanoglu, Maral Martin
AU - Coskun, Alper
AU - Uzundal, Duygu Ercan
AU - Sahin, Taha Koray
AU - Akyildiz, Arif
AU - Akbas, Sinem
AU - Camanlı, Ufuk
AU - Sahin, Elif
AU - Atacan, Huseyin
AU - Bayrakcı, Ismail
AU - Sakalar, Teoman
AU - Cicek, Ceren Mordag
AU - Gunenc, Damla
AU - İlhan, Nurullah
AU - Unal, Olcun Umit
AU - Alan, Ozkan
AU - Hamitoglu, Buket
AU - Engin, Esra Ozen
AU - Sever, Nadiye
AU - Guren, Ali Kaan
AU - Unsal, Ahmet
AU - Araz, Murat
AU - Erdogan, Bulent
AU - Aykan, Musa Barıs
AU - Selcukbiricik, Fatih
AU - Guven, Deniz Can
AU - Ozdemir, Nuriye
AU - Sahin, Ahmet Bilgehan
AU - Bilici, Ahmet
AU - Kara, Ismail Oguz
AU - Yalcın, Suayip
AU - Kostek, Osman
N1 - Publisher Copyright:
© 2025 AVES. All rights reserved.
PY - 2025/5
Y1 - 2025/5
N2 - Background/Aims: The treatment of hepatocellular carcinoma (HCC), which accounts for 90% of all liver cancers, is highly varied. The use of second-line treatments following progression on first-line atezolizumab and bevacizumab (Atez/Bev) for advanced HCC remains controversial. The aim of this study was to analyze the real-world clinical results of second-line treatments in progression after Atez/Bev and to determine the factors affecting prognosis. Materials and Methods: Fifty-eight patients treated with second-line sorafenib, regorafenib, and cabozantinib for progression after first-line Atez/Bev for advanced/metastatic HCC from 20 centers in Türkiye between October 2020 and June 2024 were retrospectively analyzed. Responses were evaluated by Response criteria, specifically Response Evaluation Criteria in Solid Tumors (RECIST v1.1) criteria. Median overall survival (OS) and progression-free survival (PFS) were computed with the Kaplan–Meier method. The Cox regression model was utilized to analyze multivariate analyses. Results: About 82.8% of the patients were male and the median age of the whole group was 62 (range, 18-78) years. All patients progressed after first-line Atez/Bev and were given second-line treatment. The most commonly used second-line treatment option was sorafenib (70.7%), followed by regorafenib (12.1%) and cabozantinib (10.3%). Both median PFS (4.1 months) and median OS (7.8 months) were longer in patients treated with sorafenib compared to other treatments. In univariate analyses, Child–Pugh score B, high alpha-fetoprotein (AFP) levels (>200 ng/mL), extrahepatic spread, and Prognostic Nutritional Index (PNI) < 47.6 substantially raised the risk of overall mortality. Multivariate analysis showed that extrahepatic spread (HR (Hazard ratio): 0.41, P = .012), PNI level (HR: 0.24, P = .005), and AFP level (HR:1.97, P = .049) were independent predictors of OS. Conclusion: Although second-line therapies after Atez/Bev show different degrees of efficacy, survival rates are consistent with the literature. Extrahepatic spread, AFP level, and PNI level are the main prognostic factors. In light of this information, personalized treatment strategies may improve outcomes for this challenging patient group.
AB - Background/Aims: The treatment of hepatocellular carcinoma (HCC), which accounts for 90% of all liver cancers, is highly varied. The use of second-line treatments following progression on first-line atezolizumab and bevacizumab (Atez/Bev) for advanced HCC remains controversial. The aim of this study was to analyze the real-world clinical results of second-line treatments in progression after Atez/Bev and to determine the factors affecting prognosis. Materials and Methods: Fifty-eight patients treated with second-line sorafenib, regorafenib, and cabozantinib for progression after first-line Atez/Bev for advanced/metastatic HCC from 20 centers in Türkiye between October 2020 and June 2024 were retrospectively analyzed. Responses were evaluated by Response criteria, specifically Response Evaluation Criteria in Solid Tumors (RECIST v1.1) criteria. Median overall survival (OS) and progression-free survival (PFS) were computed with the Kaplan–Meier method. The Cox regression model was utilized to analyze multivariate analyses. Results: About 82.8% of the patients were male and the median age of the whole group was 62 (range, 18-78) years. All patients progressed after first-line Atez/Bev and were given second-line treatment. The most commonly used second-line treatment option was sorafenib (70.7%), followed by regorafenib (12.1%) and cabozantinib (10.3%). Both median PFS (4.1 months) and median OS (7.8 months) were longer in patients treated with sorafenib compared to other treatments. In univariate analyses, Child–Pugh score B, high alpha-fetoprotein (AFP) levels (>200 ng/mL), extrahepatic spread, and Prognostic Nutritional Index (PNI) < 47.6 substantially raised the risk of overall mortality. Multivariate analysis showed that extrahepatic spread (HR (Hazard ratio): 0.41, P = .012), PNI level (HR: 0.24, P = .005), and AFP level (HR:1.97, P = .049) were independent predictors of OS. Conclusion: Although second-line therapies after Atez/Bev show different degrees of efficacy, survival rates are consistent with the literature. Extrahepatic spread, AFP level, and PNI level are the main prognostic factors. In light of this information, personalized treatment strategies may improve outcomes for this challenging patient group.
KW - Atezolizumab
KW - bevacizumab
KW - cabozantinib
KW - hepatocellular carcinoma
KW - overall survival
KW - progression-free survival
KW - regorafenib
KW - second-line treatment
KW - sorafenib
UR - https://www.scopus.com/pages/publications/105004932762
UR - https://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=performanshacettepe&SrcAuth=WosAPI&KeyUT=WOS:001487621300004&DestLinkType=FullRecord&DestApp=WOS_CPL
U2 - 10.5152/tjg.2025.24784
DO - 10.5152/tjg.2025.24784
M3 - Article
C2 - 40241388
AN - SCOPUS:105004932762
SN - 1300-4948
VL - 36
SP - 293
EP - 301
JO - Turkish Journal of Gastroenterology
JF - Turkish Journal of Gastroenterology
IS - 5
ER -