Purpose: To evaluate whether proton MR spectroscopy (1H-MRS) improves the differentiation of tumoral from non-tumoral intracranial lesions beyond conventional MRI, and to quantify its effect on diagnostic confidence, in a consecutive real-world bicentric cohort of diagnostically ambiguous lesions. Methods: This retrospective, bicentric observational study screened 122 consecutive patients who underwent brain MRI with 1H-MRS at two imaging centers, of whom 99 were eligible for final analysis after excluding 23 patients due to insufficient follow-up (<12 months) or incomplete reference standard. The reference standard was histopathological confirmation in 43 cases (43.4%) and structured clinico-radiological follow-up of at least 12 months in 56 cases (56.6%). The reporting radiologist’s binary diagnostic impression and confidence score were recorded before and after 1H-MRS. Conventional MRI alone was compared to MRI plus 1H-MRS using the exact McNemar test; Cho/NAA discrimination was assessed by ROC analysis with bootstrap confidence intervals, and confidence change by the Wilcoxon signed-rank test. Secondary analyses comprised an intention-to-diagnose analysis of all 99 examinations, counting non-diagnostic spectra as test failures, and an evaluable-case sensitivity analysis restricted to histopathologically confirmed patients with interpretable spectra. Results: Of 99 examinations, 89 (89.9%) yielded interpretable spectra. In the primary analysis, qualitative MRS interpretation demonstrated sensitivity of 76.0% (95% CI: 61.8–86.9), specificity of 94.9% (95% CI: 82.7–99.4), and accuracy of 84.3% (CI: 75.0–91.1), compared with 54.0%, 89.7% and 69.7% (59.0–79.0) for conventional MRI alone (exact McNemar p = 0.024). ROC analysis of the Cho/NAA ratio (n = 89) yielded an AUC of 0.858 (0.774–0.931); the exploratory, cohort-specific Youden-optimal cut-off was 1.41 (sensitivity 78.0%, specificity 87.2%). In the intention-to-diagnose analysis including all 99 examinations, accuracy was 78.8% (69.4–86.4). Diagnostic confidence increased significantly after 1H-MRS (median 1 to 2; Wilcoxon p < 0.001; effect size r = 0.81), with moderate or major added value in 71 of 99 examinations (71.7%). Conclusions: In a diagnostically heterogeneous real-world cohort, 1H-MRS significantly improved the accuracy achievable with conventional MRI alone and substantially increased reported diagnostic confidence, with high specificity but only moderate sensitivity. A zone-based Cho/NAA interpretative framework better reflects biological overlap than rigid binary thresholds. As this study assessed diagnostic accuracy and reported confidence rather than therapeutic decisions or patient outcomes, 1H-MRS should be regarded as an adjunctive decision-support modality rather than a standalone classifier in routine neuro-oncologic workflows.
Laura Maria Georgescu, Alexandru Șerbănoiu, A. Costache et al.· Diagnostics· 0 citations
Background CDK4/6 inhibitors are standard-of-care for HR+/HER2− advanced breast cancer, but grade 3/4 neutropenia occurs in up to 60% of patients. Germline polymorphisms in ABCB1, encoding the P-glycoprotein efflux transporter, have been investigated as predictors of CDK4/6 inhibitor–induced neutropenia, with conflicting results across populations. No meta-analysis has previously pooled these findings. Methods PubMed, Scopus, and Web of Science were systematically searched. Studies reporting genotype-stratified grade 3/4 neutropenia in CDK4/6 inhibitor–treated patients were eligible. Four SNPs were analyzed: ABCB1 rs1128503, ABCB1 rs1045642, ERCC1 rs11615, and ERCC1 rs3212986. Odds ratios were pooled using Mantel-Haenszel weighting with random-effects (rs1128503, rs11615) or fixed-effect (rs1045642, rs3212986) models under dominant genetic models, stratified by ancestry. The protocol was registered in PROSPERO (CRD420261379298). Results Four studies (1,138 patients) were included. No SNP showed a significant overall association. However, significant ancestry-dependent heterogeneity was detected for two ABCB1 SNPs. For rs1045642, T-carrier status was significantly associated with increased neutropenia in European/Caucasian patients (pooled OR 1.62, 95% CI 1.05–2.52, p = 0.03, I2 = 0%) but decreased risk in East Asians (OR 0.31, 95% CI 0.13–0.74, p = 0.009; subgroup difference p = 0.0009). For rs1128503, a concordant European trend was observed (OR 1.87, 95% CI 0.87–4.00, p = 0.11) with reversed direction in North African/Middle Eastern patients (OR 0.33, 95% CI 0.12–0.92, p = 0.03; subgroup difference p = 0.02). For ERCC1 rs11615, the inclusion of Wang 2024 nullified the previously borderline European signal (pooled OR 0.99, 95% CI 0.42–2.33, p = 0.98, I2 = 75%), with subgroup differences no longer significant (p = 0.17). ERCC1 rs3212986 showed no association (OR 1.07, 95% CI 0.53–2.17, I2 = 0%). Conclusion These preliminary findings suggest that ABCB1 rs1045642 T-carrier status may be associated with CDK4/6 inhibitor–induced neutropenia in European/Caucasian patients, with a concordant trend for rs1128503 findings. Both associations appear ancestry-dependent, although the limited number of studies and single-study ancestry subgroups preclude definitive conclusions. ERCC1 rs11615, previously borderline in a single study, was not confirmed upon independent replication. Prospective validation in adequately powered, ancestry-stratified cohorts incorporating ABCB1 haplotype analysis and pharmacokinetic sampling is warranted. Systematic Review Registration identifier CRD420261379298.
Marina-Daniela Dimulescu, C. Lungulescu, A. Riza et al.· Frontiers in Pharmacology· 0 citations
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