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横纹肌肉瘤的其他部位。

The Other Site of Rhabdomyosarcoma.

机构信息

Department of Pediatric Hematology and Oncology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.

出版信息

Cancer Med. 2024 Oct;13(20):e70348. doi: 10.1002/cam4.70348.

Abstract

BACKGROUND

Rhabdomyosarcoma (RMS) is a rare malignant soft tissue sarcoma (STS), accounting for almost 50% of pediatric STSs. Due to its heterogeneity, RMS presents challenges in diagnosis and treatment, with prognosis varying depending on multiple factors. Tumors localized in the other site (OTH)-including the paraspinal, perianal, thoracic, abdominal, pelvic, and perineal regions-are generally classified as unfavorable. This study assesses the clinical features and prognoses of RMS in OTH locations depending on its site of origin.

METHODS

An explorative analysis of RMS cases from the SEER 17 database 2000-2020 was conducted. Patients of all ages with histologically confirmed RMS as primary malignant disease classified under OTH, were included. OTH was categorized in four granular site classifications. Overall survival (OS) and disease-specific survival (DSS) were analyzed using Kaplan-Meier estimators. Factors independently influencing survival, including a site classification model presented in this study, were identified through Cox regression analysis.

RESULTS

Out of 4168 patients with RMS, 990 cases of RMS with the OTH site met the inclusion criteria. The median age was 16 years. The predominant histological subtypes were embryonal (33.0%) and alveolar (25.5%). Most tumors were ≥ 5 cm (median 9 cm) and located primarily in the pelvic region (41.5%). The 3-, 5-, and 10-year OS rates were 45.4% ± 3.332 (95% CI), 40.7 ± 3.332, and 38.6% ± 3.332, respectively, while DSS rates were 43.3% ± 3.136 (95% CI), 38.3% ± 3.136, and 35.1% ± 3.332. In the multivariate analysis age, histological type, site in a granular categorization, stage, regional lymph node examination, and regional lymph node involvement (pathologically proven) were independently associated with survival. Through both univariate and multivariate analyses, an OTH favorable group could be established. The OTH favorable group consists of the anal region, gallbladder and biliary tract, and breast.

CONCLUSION

RMS in OTH shows significant differences in prognosis, putting the current categorization as unfavorable into question and making a more detailed classification necessary. Furthermore, pathological regional lymph node assessment is specifically in the OTH localization recommended.

摘要

背景

横纹肌肉瘤(RMS)是一种罕见的恶性软组织肉瘤(STS),占小儿 STS 的近 50%。由于其异质性,RMS 在诊断和治疗方面存在挑战,预后因多种因素而异。局部位于其他部位(OTH)的肿瘤-包括脊柱旁、肛门周围、胸部、腹部、骨盆和会阴区域-通常被归类为不利。本研究根据起源部位评估 OTH 部位 RMS 的临床特征和预后。

方法

对 2000 年至 2020 年 SEER17 数据库中的 RMS 病例进行探索性分析。纳入所有年龄组、经组织学证实为原发性恶性疾病的 RMS 患者,分类为 OTH。OTH 分为四个颗粒状部位分类。使用 Kaplan-Meier 估计值分析总生存期(OS)和疾病特异性生存期(DSS)。通过 Cox 回归分析确定通过单因素和多因素分析独立影响生存的因素,包括本研究提出的部位分类模型。

结果

在 4168 例 RMS 患者中,990 例 OTH 部位 RMS 病例符合纳入标准。中位年龄为 16 岁。主要组织学亚型为胚胎型(33.0%)和肺泡型(25.5%)。大多数肿瘤≥5cm(中位数 9cm),主要位于骨盆区(41.5%)。3、5 和 10 年 OS 率分别为 45.4%±3.332(95%CI)、40.7%±3.332 和 38.6%±3.332,而 DSS 率分别为 43.3%±3.136(95%CI)、38.3%±3.136 和 35.1%±3.332。多因素分析显示,年龄、组织学类型、颗粒状分类部位、分期、区域淋巴结检查和区域淋巴结受累(病理证实)与生存独立相关。通过单因素和多因素分析,可建立 OTH 有利组。OTH 有利组包括肛门区域、胆囊和胆道以及乳房。

结论

OTH 中的 RMS 在预后方面存在显著差异,这对当前的不利分类提出了质疑,并需要进行更详细的分类。此外,建议在 OTH 定位中特别进行病理性区域淋巴结评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b46/11513437/99eadf1b82a6/CAM4-13-e70348-g001.jpg

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