Prognostic Value of Clinical and CT Features in Camrelizumab Plus Apatinib Treatment for Unresectable Hepatocellular Carcinoma.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
109 patients, the median OS was 20 months, median PFS was 9 months, and the ORR was 43.
I · Intervention 중재 / 시술
camrelizumab plus Apatinib treatment from June 2019 to August 2021
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] Clinical and contrast-enhanced show significant prognostic value in patients receiving Camrelizumab plus Apatinib. The developed models may assist in identifying responsive patients and personalizing treatment strategies.
[BACKGROUND] Immunotherapy combined with targeted therapy is a key approach for patients with unresectable hepatocellular carcinoma (HCC).
- OR 6.31
- HR 2.04
APA
Che J, Chen Y, et al. (2025). Prognostic Value of Clinical and CT Features in Camrelizumab Plus Apatinib Treatment for Unresectable Hepatocellular Carcinoma.. Journal of hepatocellular carcinoma, 12, 2279-2293. https://doi.org/10.2147/JHC.S527624
MLA
Che J, et al.. "Prognostic Value of Clinical and CT Features in Camrelizumab Plus Apatinib Treatment for Unresectable Hepatocellular Carcinoma.." Journal of hepatocellular carcinoma, vol. 12, 2025, pp. 2279-2293.
PMID
41089334 ↗
Abstract 한글 요약
[BACKGROUND] Immunotherapy combined with targeted therapy is a key approach for patients with unresectable hepatocellular carcinoma (HCC). This study aimed to evaluate the prognostic value of clinical and CT features in Camrelizumab plus Apatinib treatment for these patients.
[MATERIALS AND METHODS] A retrospective study was conducted on unresectable HCC patients who received camrelizumab plus Apatinib treatment from June 2019 to August 2021. Clinical and contrast-enhanced CT features were analyzed. Logistic regression identified predictors of objective response, and Cox regression assessed prognostic factors for progression-free survival (PFS) and overall survival (OS). Nomograms were constructed based on independent predictors.
[RESULTS] Among 109 patients, the median OS was 20 months, median PFS was 9 months, and the ORR was 43.1%. Independent predictors of objective response included AFP ≥ 400 ng/mL (OR = 6.31), NLR ≥ 3.2 (OR = 3.72), tumor numbers ≥ 3 (OR = 3.93), and ΔAER < 15% (OR = 10.99), the AUC for objective response model was 0.874. Independent factors for PFS included AFP ≥ 400 ng/mL (HR = 2.04) and ΔAER < 15% (HR = 2.57), resulting in a model AUC of 0.859. Independent factors for OS were NLR ≥ 3.2 (HR = 2.07), Tumor numbers ≥ 3 (HR = 2.68), and extrahepatic metastasis (HR = 2.32), with an AUC of 0.848 and 0.866 for 1- and 2-year survival, respectively.
[CONCLUSION] Clinical and contrast-enhanced show significant prognostic value in patients receiving Camrelizumab plus Apatinib. The developed models may assist in identifying responsive patients and personalizing treatment strategies.
[MATERIALS AND METHODS] A retrospective study was conducted on unresectable HCC patients who received camrelizumab plus Apatinib treatment from June 2019 to August 2021. Clinical and contrast-enhanced CT features were analyzed. Logistic regression identified predictors of objective response, and Cox regression assessed prognostic factors for progression-free survival (PFS) and overall survival (OS). Nomograms were constructed based on independent predictors.
[RESULTS] Among 109 patients, the median OS was 20 months, median PFS was 9 months, and the ORR was 43.1%. Independent predictors of objective response included AFP ≥ 400 ng/mL (OR = 6.31), NLR ≥ 3.2 (OR = 3.72), tumor numbers ≥ 3 (OR = 3.93), and ΔAER < 15% (OR = 10.99), the AUC for objective response model was 0.874. Independent factors for PFS included AFP ≥ 400 ng/mL (HR = 2.04) and ΔAER < 15% (HR = 2.57), resulting in a model AUC of 0.859. Independent factors for OS were NLR ≥ 3.2 (HR = 2.07), Tumor numbers ≥ 3 (HR = 2.68), and extrahepatic metastasis (HR = 2.32), with an AUC of 0.848 and 0.866 for 1- and 2-year survival, respectively.
[CONCLUSION] Clinical and contrast-enhanced show significant prognostic value in patients receiving Camrelizumab plus Apatinib. The developed models may assist in identifying responsive patients and personalizing treatment strategies.
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