Schott Inna, Liffers Sven-Thorsten, Farzaliyev Farhad, Falkenhorst Johanna, Steinau Hans-Ulrich, Treckmann Jürgen-Walter, Podleska Lars Erik, Pöttgen Christoph, Schildhaus Hans-Ulrich, Ahrens Marit, Dirksen Uta, Murat Fatma-Zehra, Siveke Jens T, Bauer Sebastian, Hamacher Rainer
Department of Medical Oncology, Sarcoma Center, West German Cancer Center, University Hospital Essen, Essen, Germany.
Bridge Institute of Experimental Tumor Therapy, West German Cancer Center, University Hospital Essen, Essen, Germany.
Sarcoma. 2021 Sep 10;2021:9960085. doi: 10.1155/2021/9960085. eCollection 2021.
Angiosarcomas are rare and heterogeneous tumors with poor prognosis. The clinical subtypes are classified depending on the primary site and etiology.
We conducted a retrospective, monocentric study of 136 patients with localized AS between May 1985 and November 2018. Overall survival (OS), local recurrence-free survival (LRFS), and metastasis-free survival (MFS) were estimated using the Kaplan-Meier method. To identify prognostic factors, univariate and multivariate analyses were performed based on Cox regressions.
The median age was 67 years (19-72.8 years). Primary sites were cutaneous (27.2%), breast (38.2%), and deep soft tissue (34.6%). The majority was primary angiosarcomas (55.9%) followed by postradiation (40.4%) and chronic lymphedema angiosarcomas (2.9%). Prognosis significantly differed depending on the primary site and etiology. Shortest median OS and MFS were observed in deep soft tissue angiosarcomas, whereas cutaneous angiosarcomas, angiosarcomas of the breast, and radiation-associated angiosarcomas displayed worse median LRFS. Univariate analyses showed better OS for tumor size <10 cm ( = 0.009), negative surgical margins ( = 0.021), and negative lymph node status ( = 0.007). LRFS and MFS were longer for tumor size <10 cm ( = 0.012 and = 0.013). In multivariate analyses, age <70 years was the only independent positive prognostic factor for OS in all subgroups. For LRFS, secondary AS of the breast was a negative prognostic factor (HR: 2.35; = 0.035).
Different behaviors and prognoses depending on the primary site and etiology should be considered for the treatment of this heterogeneous disease. In cutaneous angiosarcomas of the head/neck and postradiation angiosarcomas of the breast, local recurrence seems to have a crucial impact on OS. Therefore, improved local therapies and local tumor staging may have to be implemented. However, in deep soft tissue angiosarcomas, distant recurrence seems to have a major influence on prognosis, which indicates a benefit of additional perioperative chemotherapy.
血管肉瘤是一种罕见的异质性肿瘤,预后较差。临床亚型根据原发部位和病因进行分类。
我们对1985年5月至2018年11月期间136例局限性血管肉瘤患者进行了一项回顾性单中心研究。采用Kaplan-Meier法估计总生存期(OS)、无局部复发生存期(LRFS)和无转移生存期(MFS)。为了确定预后因素,基于Cox回归进行单因素和多因素分析。
中位年龄为67岁(19 - 72.8岁)。原发部位为皮肤(27.2%)、乳腺(38.2%)和深部软组织(34.6%)。大多数为原发性血管肉瘤(55.9%),其次是放疗后血管肉瘤(40.4%)和慢性淋巴水肿性血管肉瘤(2.9%)。预后因原发部位和病因显著不同。深部软组织血管肉瘤的中位OS和MFS最短,而皮肤血管肉瘤、乳腺血管肉瘤和放疗相关血管肉瘤的中位LRFS较差。单因素分析显示,肿瘤大小<10 cm(P = 0.009)、手术切缘阴性(P = 0.021)和淋巴结状态阴性(P = 0.007)的患者OS较好。肿瘤大小<10 cm的患者LRFS和MFS更长(P = 0.012和P = 0.013)。多因素分析中,年龄<70岁是所有亚组中OS唯一独立的阳性预后因素。对于LRFS,乳腺继发性血管肉瘤是一个阴性预后因素(HR:2.35;P = 0.035)。
对于这种异质性疾病的治疗,应考虑根据原发部位和病因的不同行为和预后。在头颈部皮肤血管肉瘤和乳腺放疗后血管肉瘤中,局部复发似乎对OS有至关重要的影响。因此,可能需要实施改进的局部治疗和局部肿瘤分期。然而,在深部软组织血管肉瘤中,远处复发似乎对预后有重大影响,这表明围手术期辅助化疗有益。