Incidence of skeletal‐related events in patients with Ewing sarcoma: An observational retrospective study in Japan

Author:

Aiba Hisaki12ORCID,Kojima Yuki1,Shimoi Tatsunori1,Sudo Kazuki1,Yazaki Shu1ORCID,Imai Toru1,Yoshida Akihiko3,Iwata Shintaro4,Kobayashi Eisuke4ORCID,Kawai Akira4ORCID,Arakawa Ayumu5ORCID,Ogawa Chitose5,Kimura Hiroaki2,Yonemori Kan1

Affiliation:

1. Department of Medical Oncology National Cancer Center Hospital, National Cancer Center Hospital Tokyo Japan

2. Department of Orthopaedic Surgery Nagoya City University Nagoya Japan

3. Department of Diagnostic Pathology National Cancer Center Hospital, National Cancer Center Hospital Tokyo Japan

4. Department of Musculoskeletal Oncology and Rehabilitation National Cancer Center Hospital, National Cancer Center Hospital Tokyo Japan

5. Department of Pediatric Oncology National Cancer Center Hospital Tokyo Japan

Abstract

AbstractBackgroundSkeletal‐related events (SREs), including the pathological fracture, surgical treatment or radiation of bone lesions, malignant spinal cord compression, hypercalcemia, are important considerations when managing metastatic bone tumors; however, owing to their rarity, the incidence of SREs in patients with Ewing sarcoma remains unknown.MethodsWe retrospectively reviewed the clinical data from 146 patients with Ewing sarcoma treated at a single institution from 2005 to 2019. The median age at diagnosis was 22.7 years. Fifty patients (34.2%) had metastatic disease at diagnosis. The primary outcome was the SRE‐free rate among patients with Ewing sarcoma. Moreover, we identified the risk factors for SREs using univariate or multivariate analyses.ResultsDuring the observational period (median, 2.6 years), SREs occurred in 23 patients. Radiation to the bone, malignant spinal cord compression, and hypercalcemia were documented as the initial SREs in 12 patients (52.2%), 10 patients (43.5%), and one patient (4.3%), respectively. The SRE‐free rate was 94.2 ± 2.0, 87.3 ± 3.0, and 79.6 ± 3.8% at 1, 2, and 3 years after the initial visit, respectively. Multivariate analysis revealed bone metastasis at diagnosis (hazard ratio [HR] = 4.41, p = 0.007), bone marrow invasion (HR = 34.08, p < 0.001), and local progression or recurrence after definitive treatment (HR = 3.98, p = 0.012) as independent risk factors for SREs.ConclusionsSREs are non‐rare events that can occur during the treatment course for Ewing sarcoma, with an especially high incidence of malignant spinal cord compression. Patients with metastatic disease at diagnosis, especially in the bone or bone marrow, or with local progression or recurrence after definitive treatment, should be carefully monitored for the occurrence of SREs. The most effective methods to monitor the occurrence of SREs and new preventative therapies for SREs should be investigated in the future.

Publisher

Wiley

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