Comparable survival outcome with anti-EGFR therapy in any treatment line in left-sided metastatic colorectal cancer.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 3/4)
유사 논문P · Population 대상 환자/모집단
300 patients with wt left-sided mCRC patients receiving anti-EGFR mAb, 32% of the patients (98 of 300) were treated in the first-line, while 15% and 51% were treated in the second- and third- to later-line, respectively.
I · Intervention 중재 / 시술
anti-EGFR mAb in all treatment lines between 2008 and 2023
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] While earlier line use confers longer PFS, OS remains similar regardless of the timing of anti-EGFR therapy. These findings support the introduction of anti-EGFR agents at any line when feasible, highlighting that ensuring access may be more important than timing in treatment sequencing.
[BACKGROUND] Anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (mAbs) are the standard first-line treatment in wild-type (wt) left-sided metastatic colorectal cancer (mCRC), but the
- p-value P<0.001
- 95% CI 4.16-7.35
- 추적기간 30.4 months
APA
Archwamety A, Akewanlop C, Korphaisarn K (2026). Comparable survival outcome with anti-EGFR therapy in any treatment line in left-sided metastatic colorectal cancer.. Journal of gastrointestinal oncology, 17(1), 14. https://doi.org/10.21037/jgo-2025-811
MLA
Archwamety A, et al.. "Comparable survival outcome with anti-EGFR therapy in any treatment line in left-sided metastatic colorectal cancer.." Journal of gastrointestinal oncology, vol. 17, no. 1, 2026, pp. 14.
PMID
41816577 ↗
Abstract 한글 요약
[BACKGROUND] Anti-epidermal growth factor receptor (EGFR) monoclonal antibodies (mAbs) are the standard first-line treatment in wild-type (wt) left-sided metastatic colorectal cancer (mCRC), but the benefit of later treatment is unclear. This study aimed to assess whether the timing of anti-EGFR mAb therapy influences survival outcomes in this population.
[METHODS] We conducted a retrospective study in patients diagnosed with wt mCRC who received anti-EGFR mAb in all treatment lines between 2008 and 2023. The impact of line of anti-EGFR mAb on progression-free survival (PFS) and overall survival (OS) was determined using the Kaplan-Meier method and compared with the log-rank test.
[RESULTS] Of 300 patients with wt left-sided mCRC patients receiving anti-EGFR mAb, 32% of the patients (98 of 300) were treated in the first-line, while 15% and 51% were treated in the second- and third- to later-line, respectively. Anti-vascular growth factors were used in 34% of patients. Median follow-up time was 30.4 months. Patients receiving anti-EGFR mAb in the first-line setting exhibited a significantly longest median PFS [11.87 months; 95% confidence interval (CI): 5.28-18.46; P<0.001]. The median PFS in the second- and third- to later-line settings were 5.75 months (95% CI: 4.16-7.35; P<0.001), and 5.06 months (95% CI: 3.86-6.27; P<0.001), respectively. There were no significant differences in terms of OS among treatment lines (P=0.29).
[CONCLUSIONS] While earlier line use confers longer PFS, OS remains similar regardless of the timing of anti-EGFR therapy. These findings support the introduction of anti-EGFR agents at any line when feasible, highlighting that ensuring access may be more important than timing in treatment sequencing.
[METHODS] We conducted a retrospective study in patients diagnosed with wt mCRC who received anti-EGFR mAb in all treatment lines between 2008 and 2023. The impact of line of anti-EGFR mAb on progression-free survival (PFS) and overall survival (OS) was determined using the Kaplan-Meier method and compared with the log-rank test.
[RESULTS] Of 300 patients with wt left-sided mCRC patients receiving anti-EGFR mAb, 32% of the patients (98 of 300) were treated in the first-line, while 15% and 51% were treated in the second- and third- to later-line, respectively. Anti-vascular growth factors were used in 34% of patients. Median follow-up time was 30.4 months. Patients receiving anti-EGFR mAb in the first-line setting exhibited a significantly longest median PFS [11.87 months; 95% confidence interval (CI): 5.28-18.46; P<0.001]. The median PFS in the second- and third- to later-line settings were 5.75 months (95% CI: 4.16-7.35; P<0.001), and 5.06 months (95% CI: 3.86-6.27; P<0.001), respectively. There were no significant differences in terms of OS among treatment lines (P=0.29).
[CONCLUSIONS] While earlier line use confers longer PFS, OS remains similar regardless of the timing of anti-EGFR therapy. These findings support the introduction of anti-EGFR agents at any line when feasible, highlighting that ensuring access may be more important than timing in treatment sequencing.
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