Stereotactic Body Radiation Therapy With Continued First-Line PD-1 Inhibitor-based Therapy as a Resistance-Overcoming Strategy in Oligoprogressive Hepatocellular Carcinoma: A Prospective Phase 2 Clinical Study.
2/5 보강
TL;DR
SBRT augmentation of frontline PD-1 inhibitor-based therapy enabled significant prolongation of PFS in oligoprogressive HCC with a favorable safety profile, suggesting this strategy may overcome acquired ICI-based therapy resistance through localized immunomodulation while preserving the continuity of systemic treatment.
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
환자: oligoprogressive hepatocellular carcinoma (HCC)
I · Intervention 중재 / 시술
tumor-directed SBRT (biologically effective dose ≥ 60 Gy) to all oligoprogressive sites while continuing their original therapy
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] SBRT augmentation of frontline PD-1 inhibitor-based therapy enabled significant prolongation of PFS in oligoprogressive HCC with a favorable safety profile. This strategy may overcome acquired immune checkpoint inhibitor-based therapy resistance through localized immunomodulation while preserving the continuity of systemic treatment.
OpenAlex 토픽 ·
Hepatocellular Carcinoma Treatment and Prognosis
Cancer Immunotherapy and Biomarkers
Cholangiocarcinoma and Gallbladder Cancer Studies
SBRT augmentation of frontline PD-1 inhibitor-based therapy enabled significant prolongation of PFS in oligoprogressive HCC with a favorable safety profile, suggesting this strategy may overcome acqui
- p-value P < .05
- 추적기간 24.4 months
APA
Shu-Jung Hsu, Yen-cheng Chao, et al. (2026). Stereotactic Body Radiation Therapy With Continued First-Line PD-1 Inhibitor-based Therapy as a Resistance-Overcoming Strategy in Oligoprogressive Hepatocellular Carcinoma: A Prospective Phase 2 Clinical Study.. International journal of radiation oncology, biology, physics, 124(5), 1388-1398. https://doi.org/10.1016/j.ijrobp.2025.12.049
MLA
Shu-Jung Hsu, et al.. "Stereotactic Body Radiation Therapy With Continued First-Line PD-1 Inhibitor-based Therapy as a Resistance-Overcoming Strategy in Oligoprogressive Hepatocellular Carcinoma: A Prospective Phase 2 Clinical Study.." International journal of radiation oncology, biology, physics, vol. 124, no. 5, 2026, pp. 1388-1398.
PMID
41520893 ↗
Abstract 한글 요약
[PURPOSE] This prospective phase 2 trial (NCT06870942) aimed to evaluate whether stereotactic body radiation therapy (SBRT) combined with continued first-line PD-1 inhibitor-based therapy could overcome acquired resistance and prolong progression-free survival (PFS) in patients with oligoprogressive hepatocellular carcinoma (HCC).
[METHODS AND MATERIALS] Patients with oligoprogressive HCC (≤5 lesions, ≤3 organs) of first-line PD-1 inhibitor therapy (camrelizumab/sintilimab) combined with lenvatinib were enrolled. Participants received tumor-directed SBRT (biologically effective dose ≥ 60 Gy) to all oligoprogressive sites while continuing their original therapy. The primary endpoint was PFS.
[RESULTS] Thirty-five eligible patients were recruited between July 2022 and March 2023, with a median follow-up of 24.4 months. The primary endpoint was met, with a median PFS of 11.3 months (95% confidence interval, 5.6-17.0). The overall response rate (ORR) and disease control rate were 74.3% and 91.4%, respectively. The 2-year overall survival (OS) rate was 84.9%. According to the European Society for Radiotherapy and Oncology and European Organisation for Research and Treatment of Cancer (ESTRO-EORTC) classification, repeat oligoprogression demonstrated significantly higher median PFS (16.6 vs 8.9 vs 8.9 months; P < .05) and ORR (81.5% vs 40.0% vs 33.3%) compared with metachronous/induced subtypes. Grade 3-4 toxicities occurred in 8.5% (3/35) of patients, although these adverse events were reversible and manageable.
[CONCLUSIONS] SBRT augmentation of frontline PD-1 inhibitor-based therapy enabled significant prolongation of PFS in oligoprogressive HCC with a favorable safety profile. This strategy may overcome acquired immune checkpoint inhibitor-based therapy resistance through localized immunomodulation while preserving the continuity of systemic treatment.
[METHODS AND MATERIALS] Patients with oligoprogressive HCC (≤5 lesions, ≤3 organs) of first-line PD-1 inhibitor therapy (camrelizumab/sintilimab) combined with lenvatinib were enrolled. Participants received tumor-directed SBRT (biologically effective dose ≥ 60 Gy) to all oligoprogressive sites while continuing their original therapy. The primary endpoint was PFS.
[RESULTS] Thirty-five eligible patients were recruited between July 2022 and March 2023, with a median follow-up of 24.4 months. The primary endpoint was met, with a median PFS of 11.3 months (95% confidence interval, 5.6-17.0). The overall response rate (ORR) and disease control rate were 74.3% and 91.4%, respectively. The 2-year overall survival (OS) rate was 84.9%. According to the European Society for Radiotherapy and Oncology and European Organisation for Research and Treatment of Cancer (ESTRO-EORTC) classification, repeat oligoprogression demonstrated significantly higher median PFS (16.6 vs 8.9 vs 8.9 months; P < .05) and ORR (81.5% vs 40.0% vs 33.3%) compared with metachronous/induced subtypes. Grade 3-4 toxicities occurred in 8.5% (3/35) of patients, although these adverse events were reversible and manageable.
[CONCLUSIONS] SBRT augmentation of frontline PD-1 inhibitor-based therapy enabled significant prolongation of PFS in oligoprogressive HCC with a favorable safety profile. This strategy may overcome acquired immune checkpoint inhibitor-based therapy resistance through localized immunomodulation while preserving the continuity of systemic treatment.
🏷️ 키워드 / MeSH 📖 같은 키워드 OA만
- Humans
- Carcinoma
- Hepatocellular
- Liver Neoplasms
- Radiosurgery
- Male
- Female
- Middle Aged
- Aged
- Antibodies
- Monoclonal
- Humanized
- Prospective Studies
- Immune Checkpoint Inhibitors
- Quinolines
- Programmed Cell Death 1 Receptor
- Progression-Free Survival
- Adult
- Disease Progression
- Drug Resistance
- Neoplasm
- 80 and over
- Phenylurea Compounds
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