Skip to content

Author

I. Gheonea

2 papers indexed here

We haven’t gathered this author’s papers yet. Follow them and we’ll fetch their work.

Not the right person? Other researchers publish under this name.

Open access Aug 2026

1H-MR Spectroscopy as a Decision-Support Tool in the Differential Diagnosis of Intracranial Lesions: A Real-World Bicentric Retrospective Cohort

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. · 0 citations
Review Open access Aug 2026

Association of germline ABCB1 and ERCC1 polymorphisms with CDK4/6 inhibitor-induced neutropenia in patients with breast cancer: a systematic review and meta-analysis

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. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.