Shinji Miwa, Katsuhiro Hayashi, Yuta Taniguchi, Hirotaka Yonezawa, Sei Morinaga, Yohei Asano, Norio Yamamoto, Satoru Demura
{"title":"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。","authors":"Shinji Miwa, Katsuhiro Hayashi, Yuta Taniguchi, Hirotaka Yonezawa, Sei Morinaga, Yohei Asano, Norio Yamamoto, Satoru Demura","doi":"10.1007/s10147-025-02807-0","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":13869,"journal":{"name":"International Journal of Clinical Oncology","volume":" ","pages":"1650-1658"},"PeriodicalIF":2.8000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Prognostic factors and the impact of neoadjuvant chemotherapy on the development of metastasis in patients with undifferentiated pleomorphic sarcoma of soft tissue.\",\"authors\":\"Shinji Miwa, Katsuhiro Hayashi, Yuta Taniguchi, Hirotaka Yonezawa, Sei Morinaga, Yohei Asano, Norio Yamamoto, Satoru Demura\",\"doi\":\"10.1007/s10147-025-02807-0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>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.</p><p><strong>Methods: </strong>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.</p><p><strong>Results: </strong>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).</p><p><strong>Conclusions: </strong>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.</p>\",\"PeriodicalId\":13869,\"journal\":{\"name\":\"International Journal of Clinical Oncology\",\"volume\":\" \",\"pages\":\"1650-1658\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"International Journal of Clinical Oncology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10147-025-02807-0\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/6/11 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q3\",\"JCRName\":\"ONCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Clinical Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10147-025-02807-0","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
Prognostic factors and the impact of neoadjuvant chemotherapy on the development of metastasis in patients with undifferentiated pleomorphic sarcoma of soft tissue.
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.
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.