Neoadjuvant and adjuvant nivolumab associated with irreversible electroporation in patients with BCLC a hepatocellular carcinoma and high risk of recurrence (NIVOLEP trial).
기술보고
2/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
43 patients (mean age: 71 y, 88% male, 81% cirrhosis) were considered.
I · Intervention 중재 / 시술
two neoadjuvant nivolumab infusions, IRE with curative intent, and 12 monthly adjuvant nivolumab infusions
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSION] Neoadjuvant and adjuvant nivolumab in BCLC A HCC patients eligible for IRE lead to pathological response related to immune activation and show anti-tumoral effect. [CLINICALTRIALSGOV IDENTIFIER] NCT03630640.
OpenAlex 토픽 ·
Microbial Inactivation Methods
Hepatocellular Carcinoma Treatment and Prognosis
Ultrasound and Hyperthermia Applications
[BACKGROUND] Irreversible electroporation (IRE) is a non-thermal ablation technique suited for difficult-to-treat hepatocellular carcinoma (HCC) with one-year local recurrence (LR) rates above 50.
APA
Pierre Nahon, M. Ziol, et al. (2026). Neoadjuvant and adjuvant nivolumab associated with irreversible electroporation in patients with BCLC a hepatocellular carcinoma and high risk of recurrence (NIVOLEP trial).. Hepatology (Baltimore, Md.). https://doi.org/10.1097/HEP.0000000000001764
MLA
Pierre Nahon, et al.. "Neoadjuvant and adjuvant nivolumab associated with irreversible electroporation in patients with BCLC a hepatocellular carcinoma and high risk of recurrence (NIVOLEP trial).." Hepatology (Baltimore, Md.), 2026.
PMID
41950497 ↗
Abstract 한글 요약
[BACKGROUND] Irreversible electroporation (IRE) is a non-thermal ablation technique suited for difficult-to-treat hepatocellular carcinoma (HCC) with one-year local recurrence (LR) rates above 50.
[OBJECTIVE] We hypothesized that peri-procedural immunotherapy could synergize with IRE to decrease local recurrence.
[DESIGN] NIVOLEP is a multicenter phase 2 trial evaluating nivolumab combined with IRE in patients with BCLC A HCC. Patients received two neoadjuvant nivolumab infusions, IRE with curative intent, and 12 monthly adjuvant nivolumab infusions. Tumor biopsies were performed at baseline and during IRE. Primary endpoint was 1-year local recurrence-free survival (LRFS).
[RESULTS] 62 HCC nodules (mean size: 30.0 mm) from 43 patients (mean age: 71 y, 88% male, 81% cirrhosis) were considered. All patients received neoadjuvant nivolumab, 35 underwent curative IRE (8 others: 4 IRE failures, 3 HCC progressions, 1 death). After neoadjuvant nivolumab, radiological or pathological response were observed in 24.2% and 26.3% nodules respectively. One-year LRFS was 70.6% (95% CI: [55.3 - 85.9]), two-year overall survival was 74.2% in intention-to-treat analysis. Grade 3 or 4 adverse events related to nivolumab occurred in 2 patients, 1 patient died due to nivolumab. RNA sequencing analysis of tumor after neoadjuvant nivolumab showed an enrichment of pathways associated with leukocyte migration, T cell activation or CD8+ T and B cell infiltration associated with pathological response. Circulating protein variations were associated with pathological or radiological responses and local recurrence.
[CONCLUSION] Neoadjuvant and adjuvant nivolumab in BCLC A HCC patients eligible for IRE lead to pathological response related to immune activation and show anti-tumoral effect.
[CLINICALTRIALSGOV IDENTIFIER] NCT03630640.
[OBJECTIVE] We hypothesized that peri-procedural immunotherapy could synergize with IRE to decrease local recurrence.
[DESIGN] NIVOLEP is a multicenter phase 2 trial evaluating nivolumab combined with IRE in patients with BCLC A HCC. Patients received two neoadjuvant nivolumab infusions, IRE with curative intent, and 12 monthly adjuvant nivolumab infusions. Tumor biopsies were performed at baseline and during IRE. Primary endpoint was 1-year local recurrence-free survival (LRFS).
[RESULTS] 62 HCC nodules (mean size: 30.0 mm) from 43 patients (mean age: 71 y, 88% male, 81% cirrhosis) were considered. All patients received neoadjuvant nivolumab, 35 underwent curative IRE (8 others: 4 IRE failures, 3 HCC progressions, 1 death). After neoadjuvant nivolumab, radiological or pathological response were observed in 24.2% and 26.3% nodules respectively. One-year LRFS was 70.6% (95% CI: [55.3 - 85.9]), two-year overall survival was 74.2% in intention-to-treat analysis. Grade 3 or 4 adverse events related to nivolumab occurred in 2 patients, 1 patient died due to nivolumab. RNA sequencing analysis of tumor after neoadjuvant nivolumab showed an enrichment of pathways associated with leukocyte migration, T cell activation or CD8+ T and B cell infiltration associated with pathological response. Circulating protein variations were associated with pathological or radiological responses and local recurrence.
[CONCLUSION] Neoadjuvant and adjuvant nivolumab in BCLC A HCC patients eligible for IRE lead to pathological response related to immune activation and show anti-tumoral effect.
[CLINICALTRIALSGOV IDENTIFIER] NCT03630640.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
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