Clinical outcome of leiomyosarcomas of vascular origin: comparison with leiomyosarcomas of other origin

被引:43
作者
Italiano, A. [1 ]
Toulmonde, M. [1 ]
Stoeckle, E. [2 ]
Kind, M. [3 ]
Kantor, G. [4 ]
Coindre, J. -M. [5 ]
Bui, B. [1 ]
机构
[1] Inst Bergonie, Dept Med Oncol, F-33076 Bordeaux, France
[2] Inst Bergonie, Dept Surg, F-33076 Bordeaux, France
[3] Inst Bergonie, Dept Radiol, F-33076 Bordeaux, France
[4] Inst Bergonie, Dept Radiotherapy, F-33076 Bordeaux, France
[5] Inst Bergonie, Dept Pathol, F-33076 Bordeaux, France
关键词
chemotherapy; leiomyosarcoma of vascular origin; INFERIOR VENA-CAVA; SOFT-TISSUE; ARTERY; DEFINITION; SARCOMAS;
D O I
10.1093/annonc/mdq039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: There are no data about the natural history of leiomyosarcoma of vascular origin (vLMS) in comparison with leiomyosarcoma (LMS) of other origin and about the management of advanced disease. Methods: Among 1472 patients diagnosed with sarcoma from January 1980 to December 2008 at our institution, 195 patients (13%) had LMS. LMS had a vascular origin in 14 cases (7%). Results: Patients with vLMS had a significantly worse median metastasis-free survival (MFS) (0.25 versus 9.6 years, P = 0.001) and overall survival (OS; 2.1 versus 7 years, P < 0.0001) than patients with LMS of other origin. On multivariate analysis, grade and vascular origin were the sole independent adverse prognostic factors for OS. Eight metastatic patients with vLMS received a first-line anthracycline chemotherapy regimen. Two patients had partial response, four had stable disease and two had progressive disease. OS of patients with metastatic vLMS was not significantly different from that observed in patients with metastatic LMS of other origin (22.1 versus 16.5 months, P = 0.84). Conclusions: Vascular origin is an independent adverse prognostic factor for MFS and OS in patients with LMS. Patients with metastatic vLMS had a similar outcome than patients with metastatic LMS of other origin.
引用
收藏
页码:1915 / 1921
页数:7
相关论文
共 19 条
  • [1] PRIMARY VENOUS LEIOMYOSARCOMA - A RARE BUT LETHAL DISEASE
    DZSINICH, C
    GLOVICZKI, P
    VANHEERDEN, JA
    NAGORNEY, DM
    PAIROLERO, PC
    JOHNSON, CM
    HALLETT, JW
    BOWER, TC
    CHERRY, KJ
    [J]. JOURNAL OF VASCULAR SURGERY, 1992, 15 (04) : 595 - 603
  • [2] ENZINGER FM, 2007, SOFT TISSUE TUMORS
  • [3] Fletcher C DM., 2002, World Health Organisation Classification of tumours: Tumours of Soft Tissue and Bone, V3rd
  • [4] Comparative study of the National Cancer Institute and French Federation of Cancer Centers Sarcoma Group grading systems in a population of 410 adult patients with soft tissue sarcoma
    Guillou, L
    Coindre, JM
    Bonichon, F
    Bui, NB
    Terrier, P
    Collin, F
    Vilain, MO
    Mandard, AM
    LeDoussal, V
    Leroux, A
    Jacquemier, J
    Duplay, H
    SastreGarau, X
    Costa, J
    [J]. JOURNAL OF CLINICAL ONCOLOGY, 1997, 15 (01) : 350 - 362
  • [5] Hines OJ, 1999, CANCER-AM CANCER SOC, V85, P1077, DOI 10.1002/(SICI)1097-0142(19990301)85:5<1077::AID-CNCR10>3.3.CO
  • [6] 2-S
  • [7] Gain-of-function mutations of c-kit in human gastrointestinal stromal tumors
    Hirota, S
    Isozaki, K
    Moriyama, Y
    Hashimoto, K
    Nishida, T
    Ishiguro, S
    Kawano, K
    Hanada, M
    Kurata, A
    Takeda, M
    Tunio, GM
    Matsuzawa, Y
    Kanakura, Y
    Shinomura, Y
    Kitamura, Y
    [J]. SCIENCE, 1998, 279 (5350) : 577 - 580
  • [8] Leiomyosarcoma of the inferior vena cava: Survival after aggressive management
    Ito, Hiromichi
    Hornick, Jason L.
    Bertagnolli, Monica M.
    George, Suzanne
    Morgan, Jeffrey A.
    Baldini, Elizabeth H.
    Wagner, Andrew J.
    Demetri, George D.
    Raut, Chandrajit P.
    [J]. ANNALS OF SURGICAL ONCOLOGY, 2007, 14 (12) : 3534 - 3541
  • [9] KEVORKIAN J, 1973, SURGERY, V73, P390
  • [10] Gastrointestinal stromal tumors - definition, clinical, histological, immunohistochemical, and molecular genetic features and differential diagnosis
    Miettinen, M
    Lasota, J
    [J]. VIRCHOWS ARCHIV, 2001, 438 (01) : 1 - 12