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淋巴结阳性(N1)肺泡横纹肌肉瘤患者的融合状态是预后的有力预测指标:欧洲儿科软组织肉瘤研究组(EpSSG)的经验。

Fusion status in patients with lymph node-positive (N1) alveolar rhabdomyosarcoma is a powerful predictor of prognosis: Experience of the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG).

机构信息

Pediatric Oncology and Hematology, Children's Hospital Vall d'Hebron, Barcelona, Spain.

Padova University Hospital, Padova, Italy.

出版信息

Cancer. 2018 Aug 1;124(15):3201-3209. doi: 10.1002/cncr.31553. Epub 2018 May 24.

Abstract

BACKGROUND

Alveolar rhabdomyosarcoma (aRMS) with lymph node involvement (N1 classification) accounts for up to 10% of all cases of RMS. The prognosis is poor, and is comparable to that of distant metastatic disease. In the European Paediatric Soft Tissue Sarcoma Study Group (EpSSG) RMS2005 protocol, patients with a histologic diagnosis of aRMS/N1 received intensified chemotherapy with systematic locoregional treatment.

METHODS

Patients with aRMS/N1 were enrolled prospectively after primary surgery/biopsy and fusion status was assessed in tumor samples. All patients received 9 cycles of induction chemotherapy and 6 months of maintenance therapy. Local treatment included radiotherapy to the primary site and lymph nodes with or without secondary surgical resection.

RESULTS

A total of 103 patients were enrolled. The clinical characteristics of the patients were predominantly unfavorable: 90% had macroscopic residual disease after initial surgery/biopsy, 63% had locally invasive tumors, 77% had a tumor measuring >5 cm, and 81% had disease at unfavorable sites. Fusion genes involving forkhead box protein O1 (FOXO1) were detected in 56 of 84 patients. Events occurred in 52 patients: 43 developed disease recurrence, 7 had disease that was refractory to treatment, and 2 patients developed second neoplasms. On univariate analysis, unfavorable disease site, tumor invasiveness, Intergroup Rhabdomyosarcoma Study group III, and fusion-positive status correlated with worse prognosis. The 5-year event-free survival rate of patients with fusion-positive tumors was 43% compared with 74% in patients with fusion-negative tumors (P = .01). On multivariate analysis, fusion positivity and tumor invasiveness proved to be unfavorable prognostic markers.

CONCLUSIONS

Fusion status and tumor invasiveness appear to have a strong impact on prognosis in patients with aRMS/N1. Fusion status will be used to stratify these patients in the next EpSSG RMS study, and treatment will be intensified in patients with fusion-positive tumors. Cancer 2018. © 2018 American Cancer Society.

摘要

背景

具有淋巴结受累(N1 分类)的肺泡横纹肌肉瘤(aRMS)占 RMS 总病例的 10%。预后较差,与远处转移性疾病相当。在欧洲儿科软组织肉瘤研究组(EpSSG) RMS2005 方案中,组织学诊断为 aRMS/N1 的患者接受强化化疗和系统性局部治疗。

方法

患者在初次手术/活检后进行前瞻性入组,并在肿瘤样本中评估融合状态。所有患者均接受 9 个周期的诱导化疗和 6 个月的维持治疗。局部治疗包括对原发部位和淋巴结进行放疗,可辅以二次手术切除。

结果

共入组 103 例患者。患者的临床特征主要为不良:初始手术/活检后 90%有肉眼残留病灶,63%有局部侵袭性肿瘤,77%肿瘤>5cm,81%疾病发生在不利部位。84 例患者中有 56 例检测到涉及叉头框蛋白 O1(FOXO1)的融合基因。52 例患者发生事件:43 例发生疾病复发,7 例发生难治性疾病,2 例发生第二肿瘤。单因素分析显示,不良疾病部位、肿瘤侵袭性、Intergroup Rhabdomyosarcoma Study group III 和融合阳性状态与预后不良相关。融合阳性肿瘤患者的 5 年无事件生存率为 43%,而融合阴性肿瘤患者为 74%(P=0.01)。多因素分析显示,融合阳性和肿瘤侵袭性是预后不良的标志物。

结论

融合状态和肿瘤侵袭性似乎对 aRMS/N1 患者的预后有很大影响。在未来的 EpSSG RMS 研究中,融合状态将用于分层这些患者,融合阳性肿瘤患者的治疗将加强。癌症 2018。© 2018 美国癌症协会。

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