Gaffney David K, Winter Kathryn, Dicker Adam P, Miller Brigitte, Eifel Patricia J, Ryu Janice, Avizonis Vilija, Fromm Mitch, Small William, Greven Kathryn
Department of Radiation Oncology, Huntsman Cancer Hospital, University of Utah, Salt Lake City, UT 84132, USA.
Int J Radiat Oncol Biol Phys. 2007 Sep 1;69(1):111-7. doi: 10.1016/j.ijrobp.2007.02.050. Epub 2007 May 4.
To determine the efficacy and patterns of initial failure for oral celecoxib, intravenous cisplatin, and 5-fluorouracil and concurrent pelvic radiotherapy in patients with locally advanced cancer of the cervix.
Patients were treated with concurrent 5-fluorouracil and cisplatin chemotherapy and pelvic radiotherapy and brachytherapy. Celecoxib was prescribed at a dose of 400 mg twice daily for 1 year beginning on the first day of radiotherapy. The overall and disease-free survival rates were determined.
A total of 84 patients were accrued, of whom 78 were eligible. The estimated 2-year disease-free survival and overall survival rate was 69% and 83%, respectively. Of the 78 patients, 24 had treatment failure: 3 with persistent local disease, 9 local only, 2 regional, 4 distant, 1 regional and distant, 1 local and distant, and 2 with local, regional, and distant disease, and 1 had died of cervical cancer without a reported site of first failure and 1 without evidence of disease.
At 2 years, the estimated disease-free survival and overall survival rate for patients with advanced cervical cancer who underwent a combination of chemoradiotherapy and celecoxib treatment was 69% and 83%, respectively. Recurrent disease developed in 24 patients, and, of those patients, 18 had a component of locoregional failure as a site of first failure. Thus, locoregional control continues to be problematic after chemoradiotherapy as delivered in our study. The identification of more active biologically targeted therapies is warranted for the treatment of advanced cancer of the cervix.
确定口服塞来昔布、静脉注射顺铂和5-氟尿嘧啶以及盆腔同步放疗用于局部晚期宫颈癌患者的疗效和初始失败模式。
患者接受5-氟尿嘧啶和顺铂同步化疗、盆腔放疗及近距离放疗。从放疗第一天开始,塞来昔布按每日两次,每次400mg的剂量给药,持续1年。测定总生存率和无病生存率。
共纳入84例患者,其中78例符合条件。估计2年无病生存率和总生存率分别为69%和83%。78例患者中,24例出现治疗失败:3例为局部病灶持续存在,9例仅为局部复发,2例为区域复发,4例为远处转移,1例为区域和远处转移,1例为局部和远处转移,2例为局部、区域和远处转移,1例死于宫颈癌但未报告首次失败部位,1例无疾病证据。
2年时,接受放化疗联合塞来昔布治疗的晚期宫颈癌患者估计无病生存率和总生存率分别为69%和83%。24例患者出现疾病复发,其中18例首次失败部位为局部区域复发。因此,在我们的研究中,放化疗后局部区域控制仍然存在问题。对于晚期宫颈癌的治疗,有必要确定更有效的生物靶向治疗方法。