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High-dose continuous-infusion ifosfamide in advanced well-differentiated/dedifferentiated liposarcoma
Roberta Sanfilippo1, Rossella Bertulli1, Andrea Marrari1
1Adult Mesenchymal Tumor Medical Oncology Unit, Cancer Medicine Department, Fondazione IRCCS Istituto Nazionale dei Tumori, Via G. Venezian 1, 20133 Milano, Italy.
Continuous infusion high-dose ifosfamide (ciHDIFX) shows activity in dedifferentiated/well-differentiated liposarcoma, even after prior anthracycline and ifosfamide treatment. This regimen was better tolerated than standard high-dose ifosfamide.
Area of Science:
- Oncology
- Medical Oncology
- Pharmacology
Background:
- Liposarcomas are the most common soft-tissue sarcomas (STS), with WD/DD subtypes showing poor response to chemotherapy.
- Limited active agents exist for WD/DD liposarcoma, including anthracyclines, ifosfamide, and trabectedin.
- High-dose ifosfamide (HDIFX) is active but toxic; continuous infusion (ci) may mitigate toxicity.
Purpose of the Study:
- To evaluate the efficacy and tolerability of continuous infusion high-dose ifosfamide (ciHDIFX) in advanced liposarcoma.
- To assess activity in patients previously treated with standard chemotherapy regimens.
Main Methods:
- 28 patients with advanced WD/DD liposarcoma received ciHDIFX at 14 g/m2 over 14 days every 4 weeks.
- 86% of patients had prior chemotherapy, including anthracyclines and ifosfamide.
Main Results:
- Seven partial responses (PR) and two minor responses (MR) were observed, all in DDLPS.
- Six of nine patients with PR or MR had stable disease (SD) with prior anthracycline plus ifosfamide.
- Median progression-free survival was 7 months; manageable side effects included myelosuppression, nausea, and fatigue.
Conclusions:
- ciHDIFX demonstrates activity in WD/DDLPS, including in patients pre-treated with anthracyclines and ifosfamide.
- The ciHDIFX regimen appears better tolerated than previously reported HDIFX regimens.
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