Deep Learning-Derived Sarcopenia Marker Predicts Benefit from Anti-EGFR Therapy in Patients with RAS Wild-type Metastatic Colorectal Cancer.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: mCRC from the prospective PanaMa study and a real-world validation cohort
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
[CONCLUSIONS] The benefit of anti-EGFR therapy in mCRC is confined to patients with a high MBR. Automated sarcopenia assessment holds promise for personalized treatment intensification in mCRC.
[PURPOSE] The benefit of treatment intensification in metastatic colorectal cancer (mCRC) may be influenced by host-related factors that are not accounted for in clinical trials or standard care.
- p-value P = 0.002
- p-value P = 0.006
- 95% CI 0.21-0.77
APA
Keyl J, Hosch R, et al. (2026). Deep Learning-Derived Sarcopenia Marker Predicts Benefit from Anti-EGFR Therapy in Patients with RAS Wild-type Metastatic Colorectal Cancer.. Clinical cancer research : an official journal of the American Association for Cancer Research, 32(5), 938-946. https://doi.org/10.1158/1078-0432.CCR-25-3080
MLA
Keyl J, et al.. "Deep Learning-Derived Sarcopenia Marker Predicts Benefit from Anti-EGFR Therapy in Patients with RAS Wild-type Metastatic Colorectal Cancer.." Clinical cancer research : an official journal of the American Association for Cancer Research, vol. 32, no. 5, 2026, pp. 938-946.
PMID
41489691
Abstract
[PURPOSE] The benefit of treatment intensification in metastatic colorectal cancer (mCRC) may be influenced by host-related factors that are not accounted for in clinical trials or standard care. We investigated the prognostic and predictive value of the muscle/bone ratio (MBR), a sarcopenia marker automatically derived from computed tomography (CT) images, in patients with mCRC from the prospective PanaMa study and a real-world validation cohort.
[EXPERIMENTAL DESIGN] PanaMa (AIO KRK 0212; NCT01991873) randomized patients with RAS wild-type mCRC, following induction therapy, to maintenance therapy with fluorouracil and folinic acid (FU/FA) with or without panitumumab (Pmab). MBR was automatically calculated from baseline CT images using a validated deep learning model, and patients were stratified by MBR tertiles. Associations with progression-free survival (PFS) and overall survival (OS) were studied using Kaplan-Meier and Cox regression analyses. A retrospective real-world cohort of patients with mCRC treated with cetuximab was used for validation.
[RESULTS] Premaintenance CT images were available for 189 of 248 randomized patients (76.2%) from PanaMa. In patients receiving FU/FA + Pmab, high MBR was associated with longer PFS [HR, 0.43; 95% confidence interval (CI), 0.25-0.73; P = 0.002] and OS (HR, 0.41; 95% CI, 0.21-0.77; P = 0.006), whereas no association was observed in patients receiving FU/FA alone. Pmab provided a PFS benefit only in patients with high MBR (HR, 0.42; 95% CI, 0.24-0.73; P = 0.002). The association of high MBR with superior PFS (P = 0.002) and OS (P < 0.001) was confirmed in the real-world cohort.
[CONCLUSIONS] The benefit of anti-EGFR therapy in mCRC is confined to patients with a high MBR. Automated sarcopenia assessment holds promise for personalized treatment intensification in mCRC.
[EXPERIMENTAL DESIGN] PanaMa (AIO KRK 0212; NCT01991873) randomized patients with RAS wild-type mCRC, following induction therapy, to maintenance therapy with fluorouracil and folinic acid (FU/FA) with or without panitumumab (Pmab). MBR was automatically calculated from baseline CT images using a validated deep learning model, and patients were stratified by MBR tertiles. Associations with progression-free survival (PFS) and overall survival (OS) were studied using Kaplan-Meier and Cox regression analyses. A retrospective real-world cohort of patients with mCRC treated with cetuximab was used for validation.
[RESULTS] Premaintenance CT images were available for 189 of 248 randomized patients (76.2%) from PanaMa. In patients receiving FU/FA + Pmab, high MBR was associated with longer PFS [HR, 0.43; 95% confidence interval (CI), 0.25-0.73; P = 0.002] and OS (HR, 0.41; 95% CI, 0.21-0.77; P = 0.006), whereas no association was observed in patients receiving FU/FA alone. Pmab provided a PFS benefit only in patients with high MBR (HR, 0.42; 95% CI, 0.24-0.73; P = 0.002). The association of high MBR with superior PFS (P = 0.002) and OS (P < 0.001) was confirmed in the real-world cohort.
[CONCLUSIONS] The benefit of anti-EGFR therapy in mCRC is confined to patients with a high MBR. Automated sarcopenia assessment holds promise for personalized treatment intensification in mCRC.
🏷️ 키워드 / MeSH
- Humans
- Male
- Female
- Sarcopenia
- Colorectal Neoplasms
- ErbB Receptors
- Aged
- Middle Aged
- Antineoplastic Combined Chemotherapy Protocols
- Deep Learning
- Prognosis
- Panitumumab
- Leucovorin
- Cetuximab
- Retrospective Studies
- Biomarkers
- Tumor
- Fluorouracil
- ras Proteins
- Tomography
- X-Ray Computed
- Prospective Studies
- Neoplasm Metastasis