Literature DB >> 14528074

Docetaxel as neoadjuvant chemotherapy in patients with advanced cervical carcinoma.

Carlos T Vallejo1, Mario R Machiavelli, Juan E Pérez, Alberto O Romero, Fabrina Bologna, Hernán Vicente, Juan A Lacava, Eduardo H Ortiz, Alberto Cubero, Guillermo Focaccia, Guillermo Suttora, Mirna Scenna, José M Boughen, Bernardo A Leone.   

Abstract

The purpose of this study was to evaluate the efficacy and toxicity of docetaxel as single-agent neoadjuvant chemotherapy in locoregionally advanced cervical carcinoma. Between April 1998 and August 2000, 38 untreated patients with International Federation of Gynecology and Obstetrics stages IIB to IVA were entered onto this study. The median age was 44 years (range: 25-66 years). Stages: IIB 22 patients, IIIB 15 patients, and IVA 1 pt. Treatment consisted of docetaxel 100 mg/m2 IV infusion during 1 hour. Standard premedication with dexamethasone, diphenhydramine, and ranitidine was used. Cycles were repeated every 3 weeks for three courses, followed by radical surgery when it was judged appropriate, or definitive radiotherapy. Both staging and response assessment were performed by a multidisciplinary team. 106 cycles of therapy were administered; all patients were evaluable for TX, whereas 35 were evaluable for response (3 patients refused further treatment after the first cycle of therapy). Complete response (CR): 1 patient (3%); partial response: 11 patients (31%), for an overall objective response rate of 34% (95% CI: 15-53%); no change (NC): 16 patients (46%); and progressive disease: 7 patients (20%). Six patients (17%) underwent surgery and a pathologic CR was confirmed in 1 of them. The median time to treatment failure and the median survival have not been reached yet. The limiting toxicity was leukopenia in 25 patients (69%) (G1-G2: 14 patients, G3: 10 patients, and G4: 1 patient). Neutropenia: 28 patients (78%) (G1-G2: 10 patients, G3: 8 and G4: 10). Myalgias: 17 patients (47%) (G1-G2: 15 patients and G3: 2 patients). Emesis: 21 patients (55%) (G1-G2: 19 patients and G3: 2 patients). Alopecia G3: 13 patients (36%); rash cutaneous 26 patients (68%) (G1-G2: 22 patients and G3: 4 patients). There were no hypersensitivity reactions or fluid-retention syndrome. The received dose intensity was 91% of that projected. Docetaxel is an active drug against advanced cervical carcinoma with moderate toxicity. Further evaluation in association with other agents is clearly justified.

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Year:  2003        PMID: 14528074     DOI: 10.1097/01.coc.0000037109.12434.52

Source DB:  PubMed          Journal:  Am J Clin Oncol        ISSN: 0277-3732            Impact factor:   2.339


  3 in total

1.  Pharmacoethnicity of docetaxel-induced severe neutropenia: integrated analysis of published phase II and III trials.

Authors:  Ryoichi Yano; Aya Konno; Kyohei Watanabe; Hitoshi Tsukamoto; Yuichiro Kayano; Hiroaki Ohnaka; Nobuyuki Goto; Toshiaki Nakamura; Mikio Masada
Journal:  Int J Clin Oncol       Date:  2011-11-18       Impact factor: 3.402

2.  Glucose-regulated protein 94 modulates the therapeutic efficacy to taxane in cervical cancer cells.

Authors:  Cheng-Jeng Tai; Jin-Wun Wang; Hou-Yu Su; Chen-Jei Tai; Chien-Kai Wang; Chun-Te Wu; Yung-Chang Lien; Yu-Jia Chang
Journal:  Tumour Biol       Date:  2013-08-09

3.  A comparison of concurrent chemoradiotherapy and radiotherapy in Chinese patients with locally advanced cervical carcinoma: a multi-center study.

Authors:  Zhijie Li; Shuyan Yang; Lei Liu; Shiyu Han
Journal:  Radiat Oncol       Date:  2014-09-22       Impact factor: 3.481

  3 in total

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