原发性胸部滑膜肉瘤:一家三级医疗中心处理的罕见病例的临床概况和治疗效果。

IF 1.2 Q4 ONCOLOGY ecancermedicalscience Pub Date : 2024-09-06 eCollection Date: 2024-01-01 DOI:10.3332/ecancer.2024.1757
Ghazal Tansir, Sameer Rastogi, Ekta Dhamija, Shamim Ahmed Shamim, Deepali Jain, Adarsh Barwad, Sunil Kumar, Rambha Pandey
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引用次数: 0

摘要

简介:原发性胸部滑膜肉瘤(PTSS)是一种罕见的恶性肿瘤,临床表现各不相同。专门针对这一独特肿瘤亚群的研究数据极少。我们介绍了对 PTSS 患者进行的最大规模真实世界研究的结果:这是一项单中心、真实世界研究,研究对象为2017年至2023年间的PTSS患者。结果:24 名患者的中位年龄为 34.5 岁(16-54 岁不等),出现胸痛(11 人,45.8%)和呼吸困难(10 人,41.6%)。主要原发部位为肺(12 人,50%)和纵隔(6 人,25%)。发病阶段为无法切除的局部晚期(10 例,41.6%)、局部晚期(8 例,33.3%)和转移期(6 例,25%),其中肺转移(10 例,62.5%)和胸腔积液(4 例,25%)。16例(66.6%)患者接受了手术切除,其中7例(43.8%)接受了新辅助化疗(NACT)。10名患者接受了新辅助化疗(NACT),其中5人(50%)病情稳定,3人(30%)部分应答,7人(70%)接受了手术。11例(62.5%)手术患者在显微镜下进行了完整切除,10例(41.6%)术后接受了放疗。23例(95.8%)一线患者接受了蒽环类药物治疗,而帕唑帕尼分别是二线和三线最常见的治疗药物。中位随访时间为32个月(16.7-47.2),中位总生存期(OS)分别为41个月(95% CI:23.7-58.2)和8个月(95% CI:1-25.6)。在单变量分析中,出现转移灶(p = 0.01)和手术切除治疗(p = 0.005)与OS显著相关:解释:这种疾病在发病时属于局部晚期,因此需要早期诊断和技术上更优越的明确疗法。临床试验注册:临床试验注册:不适用。
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Primary thoracic synovial sarcomas: clinical profile and treatment outcomes of a rare entity managed at a tertiary care centre.

Introduction: Primary thoracic synovial sarcoma (PTSS) is a rare malignancy presenting with varying clinical manifestations. There is a paucity of data with few studies dedicated to this unique subset of neoplasms. We present our findings from one of the largest real-world studies among patients with PTSS.

Methods: This is a single-centre, real-world study in patients with PTSS included between 2017 and 2023. Survival estimates were obtained by the Kaplan-Meier method and Cox regression analysis.

Results: 24 patients with a median age of 34.5 years (range 16-54) presented with chest pain (n = 11, 45.8%) and dyspnea (n = 10, 41.6%). Predominant primary sites of disease were the lung (n = 12, 50%) and mediastinum (n = 6, 25%). The stage at presentation was unresectable locally advanced (n = 10, 41.6%), localised (n = 8, 33.3%) and metastatic (n = 6, 25%) with pulmonary metastases (n = 10, 62.5%) and pleural effusion (n = 4, 25%). 16 (66.6%) patients underwent surgical resection including 7 (43.8%) who received neoadjuvant chemotherapy (NACT). NACT was given in ten patients producing stable disease in 5 (50%) and partial response in 3 (30%) patients, respectively, with surgery performed in 7 (70%). 11 (62.5%) operated patients had a microscopically complete resection and 10 (41.6%) received postoperative radiotherapy. Anthracyclines were given in 23 (95.8%) patients in the first line, while pazopanib was the most common therapy in the second and third lines, respectively. At a median follow-up of 32 months (range 16.7-47.2), the median overall survival (OS) was 41 months (95% CI: 23.7-58.2) and 8 months (95% CI: 1-25.6) overall and in metastatic disease, respectively. Presentation with metastases (p = 0.01) and treatment with surgical resection (p = 0.005) were significantly associated with OS on univariate analysis.

Interpretation: The locally advanced nature of the disease at presentation signifies the need for early diagnosis and technically superior definitive therapies. The survival outcomes for metastatic disease remain poor and the need for novel therapies for advanced disease remains unmet so far.

Clinical trial registration: Not applicable.

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