MRI-based morphological and spatial characteristics of leptomeningeal metastasis: prognostic value in non-small cell lung cancer.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
환자: LM, whose prognostic relevance remains poorly defined
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
The mixed morphology, extensive brain involvement (>3 regions), and invasions of specific location such as the tempoarl lobe is associated with poorer survival outcomes. These findings support the use of MRI phenotyping for risk-adapted clinical management in NSCLC-LM.
[BACKGROUND] Leptomeningeal metastasis (LM) represents a devastating complication of non-small cell lung cancer (NSCLC), with limited survival and poorly defined imaging-based prognostic markers.
- 표본수 (n) 41
- p-value p<0.001
- p-value p=0.016
- 95% CI 1.01-1.03
- HR 1.02
APA
Chen X, He X, et al. (2026). MRI-based morphological and spatial characteristics of leptomeningeal metastasis: prognostic value in non-small cell lung cancer.. Frontiers in oncology, 16, 1764407. https://doi.org/10.3389/fonc.2026.1764407
MLA
Chen X, et al.. "MRI-based morphological and spatial characteristics of leptomeningeal metastasis: prognostic value in non-small cell lung cancer.." Frontiers in oncology, vol. 16, 2026, pp. 1764407.
PMID
42038376
Abstract
[BACKGROUND] Leptomeningeal metastasis (LM) represents a devastating complication of non-small cell lung cancer (NSCLC), with limited survival and poorly defined imaging-based prognostic markers.
[PURPOSE] This study evaluated the combined prognostic value of MRI-based morphological and spatial patterns in NSCLC patients with LM, whose prognostic relevance remains poorly defined.
[METHODS] We retrospectively reviewed 71 NSCLC patients with LM confirmed by 3.0T black-blood MRI, selected from 109 initially screened after applying exclusion criteria. Patients were classified into linear (n=41) and mixed (n=30) morphological subtypes based on MRI, and stratified by the number of involved brain regions (>3 vs. ≤3). Clinical, imaging, and survival data were analyzed using Kaplan-Meier estimates and multivariate Cox regression to identify independent prognostic factors.
[RESULTS] The mixed subtype exhibited a significantly higher lesion burden than the linear subtype (26.86 ± 26.72 vs. 7.25 ± 10.95, p<0.001). Involvement of more than three brain regions was associated with significantly shorter median overall survival (14 vs. 24 months, p=0.016). Multivariate analysis identified several independent adverse prognostic factors: increased lesion number (HR = 1.02, 95% CI: 1.01-1.03, p<0.01), temporal lobe invasion (HR = 1.96, 95% CI: 1.07-3.58, p=0.029), Regionsinvolved (HR = 0.52, p=0.020).
[CONCLUSION] MRI-based morphological subtyping and spatial distribution provide significant prognostic value in NSCLC-LM. The mixed morphology, extensive brain involvement (>3 regions), and invasions of specific location such as the tempoarl lobe is associated with poorer survival outcomes. These findings support the use of MRI phenotyping for risk-adapted clinical management in NSCLC-LM.
[PURPOSE] This study evaluated the combined prognostic value of MRI-based morphological and spatial patterns in NSCLC patients with LM, whose prognostic relevance remains poorly defined.
[METHODS] We retrospectively reviewed 71 NSCLC patients with LM confirmed by 3.0T black-blood MRI, selected from 109 initially screened after applying exclusion criteria. Patients were classified into linear (n=41) and mixed (n=30) morphological subtypes based on MRI, and stratified by the number of involved brain regions (>3 vs. ≤3). Clinical, imaging, and survival data were analyzed using Kaplan-Meier estimates and multivariate Cox regression to identify independent prognostic factors.
[RESULTS] The mixed subtype exhibited a significantly higher lesion burden than the linear subtype (26.86 ± 26.72 vs. 7.25 ± 10.95, p<0.001). Involvement of more than three brain regions was associated with significantly shorter median overall survival (14 vs. 24 months, p=0.016). Multivariate analysis identified several independent adverse prognostic factors: increased lesion number (HR = 1.02, 95% CI: 1.01-1.03, p<0.01), temporal lobe invasion (HR = 1.96, 95% CI: 1.07-3.58, p=0.029), Regionsinvolved (HR = 0.52, p=0.020).
[CONCLUSION] MRI-based morphological subtyping and spatial distribution provide significant prognostic value in NSCLC-LM. The mixed morphology, extensive brain involvement (>3 regions), and invasions of specific location such as the tempoarl lobe is associated with poorer survival outcomes. These findings support the use of MRI phenotyping for risk-adapted clinical management in NSCLC-LM.
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