Chemoradiotherapy followed by consolidation chemotherapy involving paclitaxel and carboplatin and in FIGO stage IIIB/IVA cervical cancer patients

被引:37
作者
Mabuchi, Seiji [1 ]
Isohashi, Fumiaki [2 ]
Okazawa, Mika [1 ]
Kitada, Fuminori [3 ]
Maruoka, Shintaro [4 ]
Ogawa, Kazuhiko [2 ]
Kimura, Tadashi [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Obstet & Gynecol, Osaka, Japan
[2] Osaka Univ, Grad Sch Med, Dept Radiat Oncol, Osaka, Japan
[3] Suita Tokusyukai Hosp, Dept Obstet & Gynecol, Osaka, Japan
[4] Suita Tokusyukai Hosp, Dept Radiol, Osaka, Japan
关键词
Uterine Cervical Neoplasms; Chemoradiotherapy; Consolidation Chemotherapy; Prognosis; MODULATED PELVIC RADIOTHERAPY; CONCURRENT CHEMOTHERAPY; RADIATION-THERAPY; PLUS CISPLATIN; ONCOLOGY-GROUP; PHASE-I; IVA CARCINOMA; OPEN-LABEL; ADJUVANT; TRIAL;
D O I
10.3802/jgo.2017.28.e15
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To evaluate the efficacy and toxicity of paclitaxel plus carboplatin (TC)-based concurrent chemoradiotherapy (CCRT) followed by consolidation chemotherapy in the International Federation of Gynecology and Obstetrics (FIGO) stage IIIB/IVA cervical cancer patients. Methods: We reviewed the medical records of FIGO stage IIIB/IVA cervical cancer patients (n=30) who had been intended to be treated with TC-based CCRT followed by consolidation chemotherapy (TC-CCRT-group) from April 2012-May 2016. Patients who had been treated with CCRT involving a single platinum agent (CCRT-group; n=52) or definitive radiotherapy alone (RT-group; n=74) from January 1997-September 2012 were also identified and used as historical controls. Survival was calculated using the Kaplan-Meier method and compared using the log-rank test. Results: Of the 30 patients included in the TC-CCRT-group, 22 patients (73.3%) completed the planned TC-based CCRT. The most frequently observed acute grade 3/4 hematological toxicities were leukopenia and neutropenia, and diarrhea was the most common acute grade 3/4 non-hematological toxicity. After a median follow-up of 35 months, 9 patients (30.0%) had developed recurrent disease. The patients' estimated 3-year progression-free survival (PFS) and overall survival (OS) rates were 67.9% and 90.8%, respectively. In comparisons with historical control groups, the survival outcomes of TC-CCRT-group was significantly superior to CCRT-group in terms of OS (p=0.011) and significantly superior to RT-group in terms of both PFS (p=0.009) and OS (p<0.001). Conclusion: TC-based CCRT followed by consolidation chemotherapy is safe and effective. A randomized controlled study needs to be conducted to further evaluate the efficacy of this multimodal approach in this patient population.
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页数:13
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