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Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
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ICE Regimen for Relapsed/Refractory Bone and Soft Tissue Sarcomas in Children
Burca Aydin1, Canan Akyuz1, Ali Varan1
1Hacettepe University Cancer Institute, Department of Pediatric Oncology, Ankara, Turkey.
Reviews on Recent Clinical Trials
|January 26, 2018
Summary
The ifosfamide, etoposide, and carboplatin (ICE) regimen shows promise for treating relapsed bone and soft tissue sarcomas in children. Patients without metastases at relapse experienced significantly better outcomes with ICE therapy.
Area of Science:
- Pediatric Oncology
- Sarcoma Research
- Chemotherapy Regimens
Background:
- Relapsed bone and soft tissue sarcomas (BST) have a poor prognosis with limited treatment options.
- The ifosfamide, etoposide, and carboplatin (ICE) regimen has shown promising responses in BST.
- Survival rates for relapsed BST are often less than 39%.
Purpose of the Study:
- To evaluate the demographic features, treatment response, and outcomes of children with recurrent or refractory BST treated with the ICE regimen.
- To assess the efficacy of ICE as a second-line treatment for pediatric sarcomas.
Main Methods:
- Retrospective evaluation of patient files for children diagnosed with BST and treated with ICE at relapse or progression.
- Inclusion criteria: primary BST diagnosis, treated with ICE for relapse, progression, or unresponsive disease.
Main Results:
- Overall response rate (ORR) to ICE was 43%, with median 5 cycles administered.
- First and second-year overall survival (OS) rates were 83% and 62%, respectively.
- Significantly higher survival rates (event-free survival [EFS] and OS) were observed in good responders and patients without metastases at relapse.
Conclusions:
- The ICE combination regimen improves outcomes for relapsed or refractory pediatric sarcomas.
- ICE may serve as an effective second-line treatment option.
- Patients with non-metastatic disease at relapse benefit more significantly from ICE therapy compared to those with metastatic disease.
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