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Updated: Jan 20, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
A pilot study of first-line olaratumab, doxorubicin and ifosfamide in patients with metastatic soft tissue sarcoma
Olga Vornicova1, Nissim Haim2,3, Gil Bar-Sela4,5
1Cancer Center, Emek Medical Center, 21 Yitzhak Rabin Blvd, 1834111, Afula, Israel.
Introduction:
Olaratumab (O) is a monoclonal antibody that specifically binds PDGFRα. The addition of O to doxorubicin (D) has been approved by the regulatory authorities for metastatic soft tissue sarcoma (MSTS). Since the combination of D + ifosfamide (I) is commonly used in MSTS and is associated with a higher response rate than D alone, it seems reasonable to combine O with the combination of D + I (ODI). We report our preliminary experience with O + D+I in MSTS.
Methods:
Between 01/01/2015 and 30/05/2018, 15 patients (pts) with MSTS were treated with ODI as first-line therapy. The treatment protocol consisted of IV D 50 mg/m2 and I 5000 mg/m2, day 1 (3 pts), or D 37.5 mg/m2 and I 3000 mg/m2 days 1-2 (12 pts). O (15 mg/kg) was given IV on days 1, 8, and cycles were repeated every 21 days.
Results:
With a median follow up of 16 months, 63 cycles of ODI were given. Objective response was achieved in 4 pts (27%) (CR in 3, PR in 1); 5 pts (33%) remained with stable disease for ≥ 5 mo. Median overall survival was 22 months. Major hematological toxicities (grade 3-4) included: neutropenia-7 pts (47%), and neutropenic fever-3 pts (20%). Non-hematological toxicities included grade 3 diarrheas in 2 pts (13%) after the second cycle. There was no treatment-related mortality.
Conclusion:
According to our preliminary experience, adding olaratumab to doxorubicin and ifosfamide is active and its safety profile is comparable to that of doxorubicin and ifosfamide alone in MSTS.
Insights
Adding olaratumab to doxorubicin and ifosfamide shows activity in metastatic soft tissue sarcoma. This combination demonstrates a comparable safety profile to standard doxorubicin and ifosfamide treatments for MSTS.
Area of Science:
- Oncology
- Pharmacology
Background:
- Metastatic soft tissue sarcoma (MSTS) is a challenging diagnosis.
- Olaratumab (O), a PDGFRα-binding monoclonal antibody, is approved in combination with doxorubicin (D) for MSTS.
- Doxorubicin plus ifosfamide (D+I) is a common MSTS treatment with a higher response rate than D alone.
Purpose of the Study:
- To evaluate the preliminary efficacy and safety of combining olaratumab with doxorubicin and ifosfamide (ODI) in first-line MSTS treatment.
Main Methods:
- A total of 15 MSTS patients received first-line ODI therapy between January 2015 and May 2018.
- Two dosing regimens were used for D and I, with olaratumab administered intravenously on days 1 and 8 of each 21-day cycle.
Main Results:
- Objective response rate was 27% (3 complete responses, 1 partial response) with a median overall survival of 22 months.
- 33% of patients achieved stable disease for at least 5 months.
- Grade 3-4 neutropenia occurred in 47% of patients, and 20% experienced neutropenic fever. Grade 3 diarrhea was observed in 13% of patients, with no treatment-related mortality.
Conclusions:
- The combination of olaratumab, doxorubicin, and ifosfamide (ODI) demonstrates preliminary activity in MSTS.
- The safety profile of ODI appears comparable to that of doxorubicin and ifosfamide alone in MSTS patients.
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