Prognostic factors and the impact of neoadjuvant chemotherapy on the development of metastasis in patients with undifferentiated pleomorphic sarcoma of soft tissue.

IF 2.8 3区 医学 Q3 ONCOLOGY
Shinji Miwa, Katsuhiro Hayashi, Yuta Taniguchi, Hirotaka Yonezawa, Sei Morinaga, Yohei Asano, Norio Yamamoto, Satoru Demura
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引用次数: 0

Abstract

Background: Although undifferentiated pleomorphic sarcoma (UPS), previously termed as malignant fibrous histiocytoma (MFH), is one of the most common soft tissue sarcomas, the number of studies focusing on UPS remains limited. This retrospective study aimed to identify prognostic factors and assess the clinical impact of chemotherapy on the development of metastasis in patients with UPS.

Methods: This study included 147 patients with UPS who underwent tumor resection. The associations of various parameters with oncological outcomes were investigated. Furthermore, the efficacy of chemotherapy against the development of metastatic disease has been investigated in patients with localized UPS.

Results: 5-year disease-specific and local recurrence-free survival rates were 71.7% and 61.6%, respectively. Metastatic disease at diagnosis (hazard ratio [HR], 16.7; P < 0.001) and trunk involvement (HR, 2.6; P = 0.015) were independently associated with disease-specific survival. R1/R2 resection (HR, 2.3; P = 0.008) and metastatic disease at diagnosis (HR, 5.2; P = 0.003) were independently associated with local recurrence-free survival. Among 39 patients who underwent neoadjuvant chemotherapy, 10 (25.6%) showed a good response (tumor necrosis ≥ 90%) to the neoadjuvant chemotherapy, and the responders showed a significantly higher metastasis-free survival rate than non-responders (P = 0.034).

Conclusions: This study showed that metastatic disease at diagnosis, trunk involvement, and incomplete resection are risk factors for poor oncological outcomes in patients with UPS, and that effective neoadjuvant chemotherapy decreases metastatic disease. The development of effective anticancer agents and methods for predicting of the chemotherapeutic effects is warranted to improve the clinical outcomes in patients with UPS.

预后因素及新辅助化疗对软组织未分化多形性肉瘤转移发展的影响。
背景:虽然未分化多形性肉瘤(undifferentiated pleomorphic sarcoma, UPS),以前被称为恶性纤维组织细胞瘤(malignant fibrohistiocytoma, MFH),是最常见的软组织肉瘤之一,但关注UPS的研究数量仍然有限。本回顾性研究旨在确定预后因素并评估化疗对UPS患者转移发展的临床影响。方法:本研究纳入147例行肿瘤切除术的UPS患者。研究了各种参数与肿瘤预后的关系。此外,化疗对局部UPS患者转移性疾病发展的疗效已经进行了研究。结果:5年疾病特异性生存率为71.7%,局部无复发生存率为61.6%。诊断时的转移性疾病(危险比[HR], 16.7;结论:本研究表明,诊断时的转移性疾病、躯干受累和不完全切除是UPS患者肿瘤预后不良的危险因素,有效的新辅助化疗可减少转移性疾病。开发有效的抗癌药物和预测化疗效果的方法是改善UPS患者临床预后的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.80
自引率
3.00%
发文量
175
审稿时长
2 months
期刊介绍: The International Journal of Clinical Oncology (IJCO) welcomes original research papers on all aspects of clinical oncology that report the results of novel and timely investigations. Reports on clinical trials are encouraged. Experimental studies will also be accepted if they have obvious relevance to clinical oncology. Membership in the Japan Society of Clinical Oncology is not a prerequisite for submission to the journal. Papers are received on the understanding that: their contents have not been published in whole or in part elsewhere; that they are subject to peer review by at least two referees and the Editors, and to editorial revision of the language and contents; and that the Editors are responsible for their acceptance, rejection, and order of publication.
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