Efficacy and safety of cetuximab-based versus platinum-based chemoradiation in HNSCC: evidence from a meta-analysis of 10 randomized controlled trials.
메타분석
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
557 patients).
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
While CxRT may be an option for cisplatin-ineligible patients, platinum-based therapy appears to be the standard. Future research should optimize cetuximab's role through biomarker-driven selection.
[BACKGROUND] Platinum-based chemoradiotherapy (CTRT) is the standard treatment for head and neck squamous cell carcinoma (HNSCC).
- 표본수 (n) 2,557
- 95% CI 1.07-2.10
- 연구 설계 meta-analysis
APA
Kumar T, Kesh N, et al. (2026). Efficacy and safety of cetuximab-based versus platinum-based chemoradiation in HNSCC: evidence from a meta-analysis of 10 randomized controlled trials.. Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 28(3), 963-973. https://doi.org/10.1007/s12094-025-04044-3
MLA
Kumar T, et al.. "Efficacy and safety of cetuximab-based versus platinum-based chemoradiation in HNSCC: evidence from a meta-analysis of 10 randomized controlled trials.." Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, vol. 28, no. 3, 2026, pp. 963-973.
PMID
40884618 ↗
Abstract 한글 요약
[BACKGROUND] Platinum-based chemoradiotherapy (CTRT) is the standard treatment for head and neck squamous cell carcinoma (HNSCC). While cetuximab-based radiotherapy (CxRT) has been proposed as an alternative, its efficacy remains controversial. Multiple meta-analyses have compared CxRT with CTRT for HNSCC though they combined randomized controlled trials (RCTs) with lower-evidence studies, compromising result validity. This study presents the first meta-analysis using exclusively RCT data, providing the highest level of evidence for clinical decision-making.
[METHODS] We systematically searched MEDLINE, Embase, Cochrane, and SCOPUS, identifying 10 RCTs (n = 2,557 patients). Primary outcomes included overall survival (OS), disease-free survival (DFS), and all-cause mortality; secondary outcomes were Grade ≥ 3 toxicities. Hazard ratios (HRs) and odds ratios (ORs) were pooled using random effect models.
[RESULTS] CxRT was associated with a 50% higher recurrence risk (HR 1.50, 95% CI 1.07-2.10) and 27% increased all-cause mortality (OR 1.27, 95% CI 1.05-1.55) compared to CTRT. OS did not differ significantly (HR 1.33, 95% CI 0.79-2.22). Toxicity profiles varied: CxRT had higher mucositis (OR 1.17, 95% CI 1.04-1.32) and skin rash (OR 3.46, 95% CI 1.28-9.36), while CTRT showed more anemia (OR 0.15, 95% CI 0.05-0.52) and nausea/vomiting (OR 0.31, 95% CI 0.19-0.53).
[CONCLUSION] CxRT is inferior to CTRT in HNSCC, with poorer disease control and survival outcomes. The lack of biomarker (EGFR/RAS) stratification in trials may have contributed to suboptimal patient selection. While CxRT may be an option for cisplatin-ineligible patients, platinum-based therapy appears to be the standard. Future research should optimize cetuximab's role through biomarker-driven selection.
[METHODS] We systematically searched MEDLINE, Embase, Cochrane, and SCOPUS, identifying 10 RCTs (n = 2,557 patients). Primary outcomes included overall survival (OS), disease-free survival (DFS), and all-cause mortality; secondary outcomes were Grade ≥ 3 toxicities. Hazard ratios (HRs) and odds ratios (ORs) were pooled using random effect models.
[RESULTS] CxRT was associated with a 50% higher recurrence risk (HR 1.50, 95% CI 1.07-2.10) and 27% increased all-cause mortality (OR 1.27, 95% CI 1.05-1.55) compared to CTRT. OS did not differ significantly (HR 1.33, 95% CI 0.79-2.22). Toxicity profiles varied: CxRT had higher mucositis (OR 1.17, 95% CI 1.04-1.32) and skin rash (OR 3.46, 95% CI 1.28-9.36), while CTRT showed more anemia (OR 0.15, 95% CI 0.05-0.52) and nausea/vomiting (OR 0.31, 95% CI 0.19-0.53).
[CONCLUSION] CxRT is inferior to CTRT in HNSCC, with poorer disease control and survival outcomes. The lack of biomarker (EGFR/RAS) stratification in trials may have contributed to suboptimal patient selection. While CxRT may be an option for cisplatin-ineligible patients, platinum-based therapy appears to be the standard. Future research should optimize cetuximab's role through biomarker-driven selection.
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