Gronchi Alessandro, Strauss Dirk C, Miceli Rosalba, Bonvalot Sylvie, Swallow Carol J, Hohenberger Peter, Van Coevorden Frits, Rutkowski Piotr, Callegaro Dario, Hayes Andrew J, Honoré Charles, Fairweather Mark, Cannell Amanda, Jakob Jens, Haas Rick L, Szacht Milena, Fiore Marco, Casali Paolo G, Pollock Raphael E, Raut Chandrajit P
*Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy †Department of Surgery, Royal Marsden Hospital NHS Foundation Trust, London, United Kingdom ‡Department of Biostatistics, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy §Department of Surgery, Institute Gustave Roussy, Villejuif, France ¶Department of Surgical Oncology, Mount Sinai Hospital and Princess Margaret Cancer Centre, and Department of Surgery, University of Toronto, Toronto, Ontario, Canada ||Division of Surgical Oncology & Thoracic Surgery, Mannheim University Hospital, Mannheim, Germany **Department of Surgical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands ††Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie Memorial Cancer Center and Institute of Oncology, Warsaw, Poland ‡‡Department of Surgery, Division of Surgical Oncology, Brigham and Women's Hospital and Center for Sarcoma and Bone Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA §§Department of Radiation Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands ¶¶Department of Cancer Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy ||||Department of Surgery, Division of Surgical Oncology, Ohio State University Medical Center, Columbus, OH.
Ann Surg. 2016 May;263(5):1002-9. doi: 10.1097/SLA.0000000000001447.
Retroperitoneal sarcomas (RPS) are rare tumors composed of several well defined histologic subtypes. The aim of this study was to analyze patterns of recurrence and treatment variations in a large population of patients, treated at reference centers.
All consecutive patients with primary RPS treated at 6 European and 2 North American institutions between January 2002 and December 2011 were included. Five, 8, and 10-year overall survival (OS) and crude cumulative incidence (CCI) of local recurrence (LR) and distant metastasis (DM) were calculated. Multivariate analyses for OS, CCI of LR, and DM were performed.
In all, 1007 patients were included. Median follow-up was 58 months (first and third quartile range 36-90). The 5, 8, and 10-year OS were 67% [95% confidence interval (CI), 63, 70), 56% (95% CI, 52, 61), and 46% (95% CI, 40, 53). The 5, 8, and 10-year CCI of LR and DM were 25.9 (95% CI, 23.1, 29.1), 31.3 (95% CI, 27.8, 35.1), 35% (95% CI, 30.5, 40.1), and 21% (95% CI, 18.4, 23.8%), 21.6 (95% CI, 19.0, 24.6), and 21.6 (95% CI, 19.0, 24.6), respectively. Tumour size, histologic subtype, malignancy grade, multifocality, and completeness of resection were significant predictors of outcome. Patterns of recurrence varied depending on histologic subtype. Different treatment policies at participating institutions influenced LR of well differentiated liposarcoma without impacting OS, whereas discrepancies in adjuvant systemic therapies did not impact LR, DM, or OS of leiomyosarcoma.
Reference centers are critical to outcomes of RPS patients, as the management strategy requires specific expertise. Histologic subtype predicts patterns of recurrence and should inform management decision. A prospective international registry is under preparation, to further define our understanding of this disease.
腹膜后肉瘤(RPS)是由几种明确的组织学亚型组成的罕见肿瘤。本研究的目的是分析在参考中心接受治疗的大量患者的复发模式和治疗差异。
纳入2002年1月至2011年12月期间在6家欧洲机构和2家北美机构接受原发性RPS治疗的所有连续患者。计算5年、8年和10年总生存率(OS)以及局部复发(LR)和远处转移(DM)的粗累积发病率(CCI)。对OS、LR的CCI和DM进行多变量分析。
共纳入1007例患者。中位随访时间为58个月(第一和第三四分位数范围为36 - 90个月)。5年、8年和10年OS分别为67%[95%置信区间(CI),63, 70]、56%(95% CI,52, 61)和46%(95% CI,40, 53)。LR和DM的5年、8年和10年CCI分别为25.9(95% CI,23.1, 29.1)、31.3(95% CI,27.8, 35.1)、35%(95% CI,30.5, 40.1)和21%(95% CI,18.4, 23.8%)、21.6(95% CI,19.0, 24.6)和21.6(95% CI,19.0, 24.6)。肿瘤大小、组织学亚型、恶性程度、多灶性和切除完整性是预后的重要预测因素。复发模式因组织学亚型而异。参与机构不同的治疗策略影响高分化脂肪肉瘤的LR,但不影响OS,而辅助全身治疗的差异不影响平滑肌肉瘤的LR、DM或OS。
参考中心对RPS患者的治疗结果至关重要,因为管理策略需要特定的专业知识。组织学亚型可预测复发模式,并应为管理决策提供依据。一个前瞻性国际登记系统正在筹备中,以进一步明确我们对这种疾病的认识。