Successful Complete Response of Tumor Thrombus after Combined with Chemotherapy and Irradiation for Ewing Sarcoma
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Updated: Feb 12, 2026

Establishment of a Primary Culture of Patient-derived Soft Tissue Sarcoma
Published on: April 11, 2018
Yusuke Minami1, Seiichi Matsumoto1, Keisuke Ae1
1Department of Orthopedic Surgery, The Cancer Institute Hospital of the Japanese Foundation for Cancer Research, Tokyo, Japan.
Insights
Pelvic Ewing sarcoma with inferior vena cava (IVC) tumor thrombus is challenging. This case shows successful treatment with chemotherapy and irradiation, leading to long-term remission.
Area of Science:
- Oncology
- Pediatric Oncology
- Surgical Oncology
Background:
- Pelvic Ewing sarcoma presents a poor prognosis.
- Thromboembolic events are common in pediatric cancer patients, including sarcomas.
- Inferior vena cava (IVC) tumor thrombus complicates management.
Observation:
- A pediatric patient with left iliac bone Ewing sarcoma had an IVC tumor thrombus.
- The tumor extended into the sacral bone, complicating surgical resection.
- MRI and CT scans confirmed tumor extent and IVC involvement.
Findings:
- Combined chemotherapy (VCR, Act-D, IFM, ADR) and irradiation (31.2 Gy) achieved complete tumor response.
- The IVC tumor thrombus completely resolved.
- A lung metastasis 4 years post-treatment was resected, with no recurrence at 14 years.
Implications:
- This case highlights the efficacy of multimodal therapy for pelvic Ewing sarcoma with IVC tumor thrombus.
- Successful management can lead to long-term survival.
- It underscores the importance of considering surgical and oncological interventions in complex cases.
Abstract:
Pelvic Ewing sarcoma is associated with a worse prognosis. Thromboembolic events are relatively common in pediatric patients with cancers including sarcomas. We have presented a case of Ewing sarcoma arising from the left iliac bone with tumor thrombus of inferior vena cava (IVC) which was obtained complete response by both chemotherapy and irradiation. Magnetic resonance imaging (MRI) scan demonstrated that the tumor arising from the left iliac bone extended into the left side of sacral bone, suggesting the difficulty of surgical resection. Computed tomography (CT) revealed the existence of the tumor thrombus of IVC. We performed irradiation (31.2 Gy) and chemotherapy (combination of VCR, Act-D, IFM, and ADR). The tumor was controlled successfully, and the tumor thrombus of IVC has completely vanished. Four years after the treatment, coin lesion in the left upper lung appeared. Suspected of metastasis, segmental resection of the left upper lung was performed. Fourteen years after the surgery, the patient has been remained free of recurrence. It is clinically significant for surgeons to treat pelvic Ewing sarcoma with tumor thrombus.
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