The efficacy of neoadjuvant chemotherapy in different histological types of cervical cancer

被引:123
作者
He, Lina [1 ]
Wu, Lanfang [1 ]
Su, Guidong [1 ]
Wei, Wenfei [1 ]
Liang, Li [2 ]
Han, Lingfei [3 ]
Kebria, Mehdi [4 ,5 ]
Liu, Ping [1 ]
Chen, Chunlin [1 ]
Yu, Yanhong [1 ]
Zhong, Mei [1 ]
Wang, Wei [1 ]
机构
[1] Southern Med Univ, Nanfang Hosp, Dept Obstet & Gynecol, Guangzhou 510515, Guangdong, Peoples R China
[2] Southern Med Univ, Nanfang Hosp, Dept Pathol, Guangzhou 510515, Guangdong, Peoples R China
[3] Tongji Univ, Sch Med, Shanghai Matern & Infant Hosp 1, Dept Minimally Invas Gynecol Surg, Shanghai 200040, Peoples R China
[4] Cleveland Clin, Dept Ob Gyn, Cleveland, OH 44120 USA
[5] Cleveland Clin, Womens Hlth Inst, Cleveland, OH 44120 USA
基金
中国国家自然科学基金;
关键词
Cervical cancer; Histological type; Neoadjuvant chemotherapy; SQUAMOUS-CELL-CARCINOMA; RADICAL HYSTERECTOMY; STAGE IB2; ADENOCARCINOMA; SURVIVAL; RADIOTHERAPY; CISPLATIN; OUTCOMES; SURGERY; CHEMORADIATION;
D O I
10.1016/j.ygyno.2014.06.001
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Objective. To determine whether the efficacy of neoadjuvant chemotherapy (NACT) is different among cervical cancer types, squamous cell carcinoma (SCC) and non-SCC, including adenocarcinoma of the cervix (ACC) and adenosquamous carcinoma (ASC). Methods. We searched PubMed, MEDLINE, ScienceDirect, Springerlink and CNKI for studies published between Jan 1987 and Sep 2012 and evaluated the studies published in English and Chinese on NACT and cervical carcinoma based on specific inclusion and exclusion criteria. Because there was a relative lack of relevant randomized controlled trials (RCTs), we included 2 RCTs and 9 observational studies in our analysis. Meta-analysis was applied to calculate the efficacy of NACT in different histological types of cervical cancer with 95% confidence intervals. The risk of bias was assessed by Begg's adjusted rank correlation test and Egger's regression asymmetry tests. Results. As many as 11 articles, 2 RCTs and 9 observational studies, were selected according to the eligibility criteria for a total of 1559 participants. For the short-term efficacy of NACT, either in terms of CR + PR or CR only, there was no difference between SCC and non-SCC when the data were pooled (P>0.05) in stratified studies based on the International Federation of Gynecology and Obstetrics (FIGO) stage (P>0.05) or histological type (P>0.05) or in observational studies (P>0.05). Nevertheless, SCC was associated with a higher short-term response rate than non-SCC in RCTs [6.57 (95%Cl 1.72-25.12) in CR + PR]. For the long-term outcome of NACT, patients with SCC experienced a significant 5-year overall survival (OS) and progress-free survival (PFS) when compared to patients with non-SCC in pooled [1.47 (95%Cl 1.06-2.06)] and observational studies [1.96 (95%CI 1.61-2.38)] other than RCTs (P>0.05). Moreover, this difference was especially obvious when the subgroup analysis was restricted to patients in stages above IIB [2.06 (95%CI 1.79-2.36)] rather than in stages IB-IIB [1.33 (95%C10.99-1.79)]. Conclusion. Although no significant differences exist in the short-term efficacy of NACT, the histological type may be used to predict the long-term efficacy of NACT in patients with cervical cancer, especially those with FIGO stages above IIB. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:419 / 425
页数:7
相关论文
共 43 条
[1]
[Anonymous], 1979, WHO OFFS PUBL
[2]
A comparison of prognoses of FIGO stage IB adenocarcinoma and squamous cell carcinoma [J].
Ayhan, A ;
Al, RA ;
Baykal, C ;
Demirtas, E ;
Yüce, K ;
Ayhan, A .
INTERNATIONAL JOURNAL OF GYNECOLOGICAL CANCER, 2004, 14 (02) :279-285
[3]
Does Histologic Type Correlate to Outcome after Pelvic Exenteration for Cervical and Vaginal Cancer? [J].
Baiocchi, Glauco ;
Guimaraes, Gustavo Cardoso ;
Faloppa, Carlos Chaves ;
Kumagai, Lillian Yuri ;
Rosa Oliveira, Renato Almeida ;
Begnami, Maria Dirlei ;
Soares, Fernando Augusto ;
Lopes, Ademar .
ANNALS OF SURGICAL ONCOLOGY, 2013, 20 (05) :1694-1700
[4]
OPERATING CHARACTERISTICS OF A BANK CORRELATION TEST FOR PUBLICATION BIAS [J].
BEGG, CB ;
MAZUMDAR, M .
BIOMETRICS, 1994, 50 (04) :1088-1101
[5]
Long-term survival following neoadjuvant chemotherapy and radical surgery in locally advanced cervical cancer [J].
Benedetti-Panici, P ;
Greggi, S ;
Scambia, G ;
Amoroso, M ;
Salerno, MG ;
Maneschi, F ;
Cutillo, G ;
Paratore, MP ;
Scorpiglione, N ;
Mancuso, S .
EUROPEAN JOURNAL OF CANCER, 1998, 34 (03) :341-346
[6]
Neoadjuvant chemotherapy for locally advanced cervical cancer:: a systematic review and meta-analysis of individual patient data from 21 randomised trials [J].
Benedetti-Panici, P ;
Bermudez, A ;
Blake, P ;
Cárdenas, J ;
Chang, TC ;
Chiara, S ;
Di Paola, G ;
Floquet, A ;
Guthrie, D ;
Kigawa, J ;
Kumar, L ;
Leborgne, F ;
Lodge, N ;
Poole, C ;
Sardi, J ;
Souhami, L ;
Sundfor, K ;
Symonds, P ;
Tattersall, M ;
Greggi, S ;
Guthrie, D ;
Parker, V ;
Parmar, MKB ;
Sardi, J ;
Stewart, LA ;
Tierney, JF .
EUROPEAN JOURNAL OF CANCER, 2003, 39 (17) :2470-2486
[7]
Randomized study of preoperative chemotherapy versus primary surgery for stage IB cervical cancer [J].
Cai, Hong-Bing ;
Chen, Hui-Zhen ;
Yin, Hou-Han .
JOURNAL OF OBSTETRICS AND GYNAECOLOGY RESEARCH, 2006, 32 (03) :315-323
[8]
Clinical efficacy of modified preoperative neoadjuvant chemotherapy in the treatment of locally advanced (stage IB2 to IIB) cervical cancer: A randomized study [J].
Chen, Huijun ;
Liang, Chuan ;
Zhang, Lei ;
Huang, Shuang ;
Wu, Xufeng .
GYNECOLOGIC ONCOLOGY, 2008, 110 (03) :308-315
[9]
Treatment of ("bulky") stage IB cervical cancer with or without neoadjuvant vincristine and cisplatin prior to radical hysterectomy and pelvic/para-aortic lymphadenectomy: A phase III trial of the gynecologic oncology group [J].
Eddy, Gary L. ;
Bundy, Brian N. ;
Creasman, William T. ;
Spirtos, Nick M. ;
Mannel, Robert S. ;
Hannigan, Edward ;
O'Connor, Dennis .
GYNECOLOGIC ONCOLOGY, 2007, 106 (02) :362-369
[10]
Bias in meta-analysis detected by a simple, graphical test [J].
Egger, M ;
Smith, GD ;
Schneider, M ;
Minder, C .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7109) :629-634