Tansir Ghazal, Rastogi Sameer, Dhamija Ekta, Shamim Shamim Ahmed, Jain Deepali, Barwad Adarsh, Kumar Sunil, Pandey Rambha
Department of Medical Oncology, All India Institute of Medical Sciences, New Delhi 110029, India.
Department of Radiodiagnosis, All India Institute of Medical Sciences, New Delhi 110029, India.
Ecancermedicalscience. 2024 Sep 6;18:1757. doi: 10.3332/ecancer.2024.1757. eCollection 2024.
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.
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.
24 patients with a median age of 34.5 years (range 16-54) presented with chest pain ( = 11, 45.8%) and dyspnea ( = 10, 41.6%). Predominant primary sites of disease were the lung ( = 12, 50%) and mediastinum ( = 6, 25%). The stage at presentation was unresectable locally advanced ( = 10, 41.6%), localised ( = 8, 33.3%) and metastatic ( = 6, 25%) with pulmonary metastases ( = 10, 62.5%) and pleural effusion ( = 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 ( = 0.01) and treatment with surgical resection ( = 0.005) were significantly associated with OS on univariate analysis.
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.
Not applicable.
原发性胸段滑膜肉瘤(PTSS)是一种罕见的恶性肿瘤,临床表现多样。针对这一独特肿瘤亚型的数据较少,专门研究也不多。我们展示了在PTSS患者中开展的最大规模真实世界研究之一的结果。
这是一项针对2017年至2023年间纳入的PTSS患者的单中心真实世界研究。通过Kaplan-Meier法和Cox回归分析获得生存估计值。
24例患者,中位年龄34.5岁(范围16 - 54岁),表现为胸痛(n = 11,45.8%)和呼吸困难(n = 10,41.6%)。主要疾病原发部位为肺(n = 12,50%)和纵隔(n = 6,25%)。就诊时的分期为局部不可切除的晚期(n = 10,41.6%)、局限性(n = 8,33.3%)和转移性(n = 6,25%),伴有肺转移(n = 10,62.5%)和胸腔积液(n = 4,25%)。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例患者接受了NACT,分别有5例(50%)病情稳定,3例(30%)部分缓解,7例(70%)接受了手术。11例(62.5%)接受手术的患者实现了显微镜下完全切除,10例(41.6%)接受了术后放疗。一线治疗中23例(95.8%)患者使用了蒽环类药物,而帕唑帕尼分别是二线和三线治疗中最常用的药物。中位随访32个月(范围16.7 - 47.2个月),总体中位总生存期(OS)为41个月(95%CI:23.7 - 58.2),转移性疾病患者总体中位总生存期为8个月(95%CI:1 - 25.6)。单因素分析显示,出现转移(P = 0.01)和接受手术切除治疗(P = 0.005)与OS显著相关。
就诊时疾病的局部晚期性质表明需要早期诊断和技术上更优的确定性治疗。转移性疾病的生存结果仍然很差,目前晚期疾病对新疗法的需求仍未得到满足。
不适用。