Characteristics and outcomes of patients with HCC treated with atezolizumab/bevacizumab, stratified by second line therapy.
코호트
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
550 patients with uHCC in the US who initiated 1L atezo+bev between June 2020 and April 2023.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Patients who progressed after 1L atezo+bev benefited from additional systemic therapies. Future research analyzing the comparative effectiveness of 2L therapies is needed.
[BACKGROUND] Atezolizumab plus bevacizumab (atezo+bev) is a standard-of-care 1L treatment for unresectable hepatocellular carcinoma (uHCC).
- 연구 설계 cohort study
APA
Singal AG, Özgürdal K, et al. (2026). Characteristics and outcomes of patients with HCC treated with atezolizumab/bevacizumab, stratified by second line therapy.. Future oncology (London, England), 22(3), 349-357. https://doi.org/10.1080/14796694.2026.2614306
MLA
Singal AG, et al.. "Characteristics and outcomes of patients with HCC treated with atezolizumab/bevacizumab, stratified by second line therapy.." Future oncology (London, England), vol. 22, no. 3, 2026, pp. 349-357.
PMID
41550003 ↗
Abstract 한글 요약
[BACKGROUND] Atezolizumab plus bevacizumab (atezo+bev) is a standard-of-care 1L treatment for unresectable hepatocellular carcinoma (uHCC). Understanding its adoption and use, clinical outcomes, and subsequent therapies are needed.
[METHODS] This retrospective cohort study included 550 patients with uHCC in the US who initiated 1L atezo+bev between June 2020 and April 2023. Medical records were abstracted to describe treatment patterns and outcomes.
[RESULTS] Of 294 patients who discontinued 1L therapy, 176 patients initiated 2L therapy (2L cohort) and 48 patients didn't initiate 2L therapy after ≥8 weeks of follow-up (No 2L cohort). More of the No 2L cohort had Stage IVb tumors, BCLC stage D, ECOG-PS ≥2, ascites, and hepatic encephalopathy at baseline. The 2L cohort were more likely to discontinue atezo+bev due to disease progression (92.1% vs. 56.3%), and less likely due to toxicity/intolerability (4.0% vs. 10.4%) than the No 2L cohort. OS from 1L atezo+bev initiation was significantly longer in the 2L cohort vs. No 2L cohort (median 23.0 vs. 14.3 months; < 0.001]).
[CONCLUSIONS] 1L Atezo+bev was clinically active with 256 patients remaining on therapy at last follow-up. Patients who progressed after 1L atezo+bev benefited from additional systemic therapies. Future research analyzing the comparative effectiveness of 2L therapies is needed.
[METHODS] This retrospective cohort study included 550 patients with uHCC in the US who initiated 1L atezo+bev between June 2020 and April 2023. Medical records were abstracted to describe treatment patterns and outcomes.
[RESULTS] Of 294 patients who discontinued 1L therapy, 176 patients initiated 2L therapy (2L cohort) and 48 patients didn't initiate 2L therapy after ≥8 weeks of follow-up (No 2L cohort). More of the No 2L cohort had Stage IVb tumors, BCLC stage D, ECOG-PS ≥2, ascites, and hepatic encephalopathy at baseline. The 2L cohort were more likely to discontinue atezo+bev due to disease progression (92.1% vs. 56.3%), and less likely due to toxicity/intolerability (4.0% vs. 10.4%) than the No 2L cohort. OS from 1L atezo+bev initiation was significantly longer in the 2L cohort vs. No 2L cohort (median 23.0 vs. 14.3 months; < 0.001]).
[CONCLUSIONS] 1L Atezo+bev was clinically active with 256 patients remaining on therapy at last follow-up. Patients who progressed after 1L atezo+bev benefited from additional systemic therapies. Future research analyzing the comparative effectiveness of 2L therapies is needed.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Male
- Female
- Bevacizumab
- Liver Neoplasms
- Carcinoma
- Hepatocellular
- Middle Aged
- Retrospective Studies
- Aged
- Antibodies
- Monoclonal
- Humanized
- Antineoplastic Combined Chemotherapy Protocols
- Treatment Outcome
- Adult
- 80 and over
- Neoplasm Staging
- Atezolizumab
- bevacizumab
- cancer immunotherapy
- hepatocellular carcinoma
- real-world effectiveness
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