Management of advanced uterine leiomyosarcoma

被引:11
作者
Hyman, David M. [1 ,2 ]
Grisham, Rachel N. [1 ,2 ]
Hensley, Martee L. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Gynecol Med Oncol Serv, New York, NY 10065 USA
[2] Weill Cornell Med Coll, New York, NY USA
关键词
advanced leiomyosarcoma; treatment; uterine leiomyosarcoma; PHASE-II TRIAL; PROGESTERONE-RECEPTOR EXPRESSION; GEMCITABINE PLUS DOCETAXEL; SOFT-TISSUE SARCOMAS; SURGICAL RESECTION; IMMUNOHISTOCHEMICAL EXPRESSION; INTRAOPERATIVE RADIOTHERAPY; PULMONARY METASTASECTOMY; EUROPEAN ORGANIZATION; RADIATION-THERAPY;
D O I
10.1097/CCO.0000000000000094
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of review The purpose of this article is to review current evidence-based management strategies for patients with recurrent and metastatic uterine leiomyosarcoma (LMS). We will focus on treatment of advanced multifocal disease as well as new developments in targeted cancer therapies. Recent findings The management of patients with advanced uterine LMS is divided between those with localized and those with disseminated disease. Selected patients with localized or single-organ oligometastatic disease may benefit from surgical resection. For patients with disseminated disease, fixed-dose-rate gemcitabine plus docetaxel is an appropriate first-line chemotherapy regimen. Other active cytotoxic agents include doxorubicin, ifosfamide, and dacarbazine. The role of trabectedin (approved by the European Medicine Agency to be marketed for advanced or metastatic soft tissue sarcoma) is being explored. Trials are also underway for targeted therapy in uterine LMS. Currently, the only approved targeted therapy for advanced soft tissue sarcoma is pazopanib. In patients with small volume and slowly progressive estrogen receptor/progesterone receptor-positive disease, antiestrogen therapy with an aromatase inhibitor is a reasonable alternative to observation alone. Summary Despite recent advances, overall survival for advanced disease remains poor and identification of novel agents with activity in LMS is clearly needed.
引用
收藏
页码:422 / 427
页数:6
相关论文
共 72 条
[1]   Temozolomide in uterine leiomyosarcomas [J].
Anderson, S ;
Aghajanian, C .
GYNECOLOGIC ONCOLOGY, 2005, 98 (01) :99-103
[2]   Pulmonary metastases from uterine malignancies: Results of surgical resection in 133 patients [J].
Anraku, M ;
Yokoi, K ;
Nakagawa, K ;
Fujisawa, T ;
Nakajima, J ;
Akiyama, H ;
Nishimura, Y ;
Kobayashi, K .
JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 2004, 127 (04) :1107-1112
[3]   Long-Term Outcomes With Intraoperative Radiotherapy as a Component of Treatment for Locally Advanced or Recurrent Uterine Sarcoma [J].
Barney, Brandon M. ;
Petersen, Ivy A. ;
Dowdy, Sean C. ;
Bakkum-Gamez, Jamie N. ;
Haddock, Michael G. .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2012, 83 (01) :191-197
[4]   The role of surgery and treatment trends in uterine sarcoma [J].
Benoit, L ;
Arnould, L ;
Cheynel, N ;
Goui, S ;
Collin, F ;
Fraisse, J ;
Cuisenier, J .
EJSO, 2005, 31 (04) :434-442
[5]  
Bodner K, 2003, ANTICANCER RES, V23, P729
[6]  
Boyar Michelle S., 2008, Sarcoma, V2008, P412503, DOI 10.1155/2008/412503
[7]   Pazopanib and the treatment palette for soft-tissue sarcoma [J].
Bramwell, Vivien H. C. .
LANCET, 2012, 379 (9829) :1854-1856
[8]   HIGH-DOSE DTIC IN ADVANCED SOFT-TISSUE SARCOMAS IN THE ADULT - A PHASE II STUDY OF THE EORTC SOFT-TISSUE AND BONE-SARCOMA-GROUP [J].
BUESA, JM ;
MOURIDSEN, HT ;
VANOOSTEROM, AT ;
VERWEIJ, J ;
WAGENER, T ;
STEWARD, W ;
POVEDA, A ;
VESTLEV, PM ;
THOMAS, D ;
SYLVESTER, R .
ANNALS OF ONCOLOGY, 1991, 2 (04) :307-309
[9]   Repeated and Aggressive Pulmonary Resections for Leiomyosarcoma Metastases Extends Survival [J].
Burt, Bryan M. ;
Ocejo, Santiago ;
Mery, Carlos M. ;
Dasilva, Marcelo ;
Bueno, Raphael ;
Sugarbaker, David J. ;
Jaklitsch, Michael T. .
ANNALS OF THORACIC SURGERY, 2011, 92 (04) :1202-1207
[10]  
CASSON AG, 1992, CANCER, V69, P662, DOI 10.1002/1097-0142(19920201)69:3<662::AID-CNCR2820690311>3.0.CO