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立体定向体部放疗成功治疗多形性横纹肌肉瘤同步化疗耐药性肺转移:病例报告及文献复习。

Successful treatment of synchronous chemoresistant pulmonary metastasis from pleomorphic rhabdomyosarcoma with stereotaxic body radiation therapy: A case report and a review of the literature.

机构信息

Institut Jules Bordet-Université Libre de Bruxelles, Department of Radiation-Oncology, Brussels, Belgium.

Cancer Institute of Dakar Department of Radiation-Oncology, Dakar, Senegal.

出版信息

Cancer Treat Res Commun. 2021;26:100282. doi: 10.1016/j.ctarc.2020.100282. Epub 2020 Dec 11.

Abstract

BACKGROUND

Rhabdomyosarcoma (RMS) is a highly malignant soft tissue sarcoma (STS), usually of adults, displaying skeletal muscle differentiation. STS principally metastasize to the lungs with more than 50% of metastatic patients presenting with isolated pulmonary metastasis. Paradoxically, the majority of drugs prescribed to treat RMS are associated with multidrug resistance.

CASE REPORT

We report the case of a 53 year-old patient who developed three synchronous chemoresistant lung metastasis from pleomorphic RMS. Considering the poor prognosis, the patient's preference and the chemoresistance of her lung metastasis, we decided to perform two consecutive stereotactic body radiotherapy (SBRT) on two of these three lesions.

DISCUSSION

Initially, the patient was referred to our institute with a painful mass in the anterior part of the left thigh increasing in volume for 3 months. Biopsy revealed a high-grade pleomorphic RMS. The cancer being staged IB, she had neoadjuvant radiotherapy. After complete surgical excision, pathology examination revealed a 6 cm Grade II pleomorphic RMS, with clear margins. Six months later, she developed three synchronous lung metastases. She got 4 courses of doxorubicin-ifosfamide which were poorly supported. After two courses, a heterogeneous (morphological and metabolic) response was observed, hence SBRT was delivered with a Biologically Equivalent Dose (α/β10)> 100 Gray on the two more chemoresistant lesions. This SBRT was very well tolerated, no side effects were reported. The patient remained alive and achieved a complete response of these three metastases, which sustains after more than 3 years.

CONCLUSION

Early recognition and proper management of these oligometastatic patients may lead to motivating results in a poor prognosis disease.

摘要

背景

横纹肌肉瘤(RMS)是一种高度恶性的软组织肉瘤(STS),通常发生于成年人,具有骨骼肌分化特征。STS 主要向肺部转移,超过 50%的转移性患者表现为孤立性肺转移。矛盾的是,用于治疗 RMS 的大多数药物都与多药耐药有关。

病例报告

我们报告了一例 53 岁患者,该患者患有三种同步的化疗耐药性肺转移瘤,来自多形性 RMS。考虑到预后不良、患者的偏好以及肺转移瘤的化疗耐药性,我们决定对其中的两个病灶连续进行两次立体定向体部放射治疗(SBRT)。

讨论

最初,该患者因左大腿前部疼痛性肿块就诊,肿块体积在 3 个月内逐渐增大。活检显示高级别多形性 RMS。癌症分期为 IB 期,她接受了新辅助放疗。完全切除后,病理检查显示 6 厘米大小的 II 级多形性 RMS,切缘清晰。6 个月后,她出现了三个同步的肺转移。她接受了 4 个疗程的多柔比星-异环磷酰胺,但效果不佳。两个疗程后,观察到异质性(形态和代谢)反应,因此对两个化疗耐药性更强的病灶给予生物等效剂量(α/β10)> 100 戈瑞的 SBRT。SBRT 耐受性良好,无不良反应。患者仍然存活,并且这三个转移灶完全缓解,超过 3 年后仍持续缓解。

结论

早期识别和适当管理这些寡转移患者可能会为预后不良的疾病带来令人鼓舞的结果。

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