Objectives: This study aims to evaluate oncological outcomes in women affected by locally advanced cervical cancer (LACC) treated by neoadjuvant chemotherapy before radical surgery (NACT + RS) or concurrent chemo-radiotherapy (CCRT). Methods: This was a multicenter retrospective analysis of data related to women with LACC (FIGO stage IB2-IVA), who were treated by NACT + RS or CCRT between November 2006 and January 2018. The first endpoints were the evaluation of disease-free survival (DFS) and overall survival (OS); univariate and multivariate analyses were performed for identifying the prognostic factors independently associated with these oncological outcomes. Results: Overall, 106 women were included in the analysis; 55 of them (51.9%) u...
Objective In this meta-analysis, we aimed to evaluate the oncological outcomes of preoperative neoad...
Purpose: Neoadjuvant chemotherapy followed by surgery (NACT + S) has been compared with definitive c...
Objectives: This is a protocol for a Cochrane Review (intervention). The objectives are as follows:....
Objectives: This study aims to evaluate oncological outcomes in women affected by locally advanced c...
Background. This study was to compare the efficacy and safety between neoadjuvant chemotherapy follo...
Purpose: The aim of this Phase II, non-randomized study was to assess activity and safety of neoadju...
Background: In recent years, before radical hysterectomy, neoadjuvant chemotherapy (NACT) has been a...
Xue Tian,1,* Feiyue Yang,2,* Fenghu Li,1 Li Ran,1 Jianying Chang,1 Jiehui Li,1 Wei Hong,3 La...
Objective: The purpose of this study was to determine if a survival advantage may exist from neoadju...
Cervical cancer is a major global health problem for women. Despite the screening and vaccines avail...
In 1984 the first pilot study on neoadjuvant chemotherapy in cervical cancer was reported. Since the...
Background: To compare the treatment outcomes of different treatment modalities for International Fe...
Abstract Background Currently, the standard treatment for locally advanced cervical cancer is concur...
Concurrent cisplatin-based chemotherapy and radiotherapy (CCRT) plus brachytherapy is standard treat...
Objectives: To evaluate the efficacy, in terms of safety, overall survival and progression free surv...
Objective In this meta-analysis, we aimed to evaluate the oncological outcomes of preoperative neoad...
Purpose: Neoadjuvant chemotherapy followed by surgery (NACT + S) has been compared with definitive c...
Objectives: This is a protocol for a Cochrane Review (intervention). The objectives are as follows:....
Objectives: This study aims to evaluate oncological outcomes in women affected by locally advanced c...
Background. This study was to compare the efficacy and safety between neoadjuvant chemotherapy follo...
Purpose: The aim of this Phase II, non-randomized study was to assess activity and safety of neoadju...
Background: In recent years, before radical hysterectomy, neoadjuvant chemotherapy (NACT) has been a...
Xue Tian,1,* Feiyue Yang,2,* Fenghu Li,1 Li Ran,1 Jianying Chang,1 Jiehui Li,1 Wei Hong,3 La...
Objective: The purpose of this study was to determine if a survival advantage may exist from neoadju...
Cervical cancer is a major global health problem for women. Despite the screening and vaccines avail...
In 1984 the first pilot study on neoadjuvant chemotherapy in cervical cancer was reported. Since the...
Background: To compare the treatment outcomes of different treatment modalities for International Fe...
Abstract Background Currently, the standard treatment for locally advanced cervical cancer is concur...
Concurrent cisplatin-based chemotherapy and radiotherapy (CCRT) plus brachytherapy is standard treat...
Objectives: To evaluate the efficacy, in terms of safety, overall survival and progression free surv...
Objective In this meta-analysis, we aimed to evaluate the oncological outcomes of preoperative neoad...
Purpose: Neoadjuvant chemotherapy followed by surgery (NACT + S) has been compared with definitive c...
Objectives: This is a protocol for a Cochrane Review (intervention). The objectives are as follows:....