Hoberger, Michael; Zuber, Romy L.; Burkhard-Meier, Anton; Di Gioia, Dorit; Jurinovic, Vindi; Völkl, Michael; Güler, Sinan E.; Albertsmeier, Markus; Klein, Alexander; Dürr, Hans Roland; Schmidt-Hegemann, Nina-Sophie; Knösel, Thomas; Kunz, Wolfgang G.; Bergwelt-Baildon, Michael von; Lindner, Lars H.; Berclaz, Luc M. (2026): Long-term benefit from high-dose ifosfamide in sarcoma depends on sustained prior control and timely intervention: a machine learning analysis. Journal of Cancer Research and Clinical Oncology, 152: 34. ISSN 1432-1335
Veröffentlichte Publikation
s00432-025-06410-8.pdf
Abstract
Purpose
High-dose ifosfamide (HD-IFO) remains an effective regimen for advanced bone and soft tissue sarcomas, but predictors of long-term benefit are poorly defined. This study evaluated clinical outcomes and prognostic factors using machine learning-assisted modeling in sarcoma patients treated with HD-IFO at a high-volume academic center.
Methods
We retrospectively analyzed 26 patients with histologically confirmed bone or soft tissue sarcoma who received HD-IFO (≥ 12 g/m 2 per cycle) between 2015 and 2025. Progression-free survival (PFS) and overall survival (OS) were estimated by the Kaplan–Meier method and compared across RECIST response categories using log-rank testing. Prognostic factors were identified using Least Absolute Shrinkage and Selection Operator (LASSO) logistic regression with leave-one-out cross-validation. The top three variables were entered into multivariable logistic regression to estimate odds ratios (ORs) for OS > 24 months.
Results
Median PFS and OS from start of HD-IFO was 6.6 months (95% CI 4.4–9.8) and 24.7 months (95% CI, 14.7–34.2), respectively. Patients with progressive disease (PD) had significantly shorter OS than those with partial response (PR; p = 0.0047) or stable disease (SD; p = 0.0485). LASSO identified intervention prior to progression, prior tumor control ≥ 12 months, and absence of metastases as the strongest predictors for OS > 24 months. In multivariable analysis, intervention prior to progression (OR 24.18, 95% CI 1.81–1001.27, p = 0.037) and prior tumor control ≥ 12 months (OR 25.39, 95% CI 2.1–1008.9, p = 0.030) independently predicted OS > 24 months.
Conclusion
HD-IFO provides durable disease control in selected sarcoma patients, particularly those with sustained prior tumor control and intervention prior to progression.
| Dokumententyp: | Artikel (Klinikum der LMU) |
|---|---|
| Organisationseinheit (Fakultäten): | 07 Medizin > Klinikum der LMU München > Medizinische Klinik und Poliklinik III (Onkologie) |
| DFG-Fachsystematik der Wissenschaftsbereiche: | Lebenswissenschaften |
| Veröffentlichungsdatum: | 07. Jul 2026 13:27 |
| Letzte Änderung: | 07. Jul 2026 13:27 |
| URI: | https://oa-fund.ub.uni-muenchen.de/id/eprint/2541 |
| DFG: | Gefördert durch die Deutsche Forschungsgemeinschaft (DFG) - 491502892 |
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