Concomitant chemoradiation treatment in selected Stage I endometrioid endometrial cancers

被引:16
作者
Rossetti, D. [1 ]
Vitale, S. G. [2 ]
Gulino, F. A. [3 ]
Cignini, P. [4 ]
Rapisarda, A. M. C. [2 ]
Biondi, A. [3 ]
Frigerio, L. [1 ]
机构
[1] Papa Giovanni XXIII Hosp, Dept Obstet & Gynecol, Bergamo, Italy
[2] Univ Catania, Dept Med Surg Specialties, Gynaecol & Obstet Sect, Via Santa Sofia 78, I-95123 Catania, Italy
[3] Univ Catania, Dept Surg, Catania, Italy
[4] ALTAMED Fetal Maternal Med Ctr, Dept Gynecol Ultrasound Imaging, Rome, Italy
关键词
Endometrial cancer; Radiotherapy; Adjuvant chemotherapy; Toxicity; RADIATION-THERAPY; INDEPENDENT-PREDICTOR; SPACE INVOLVEMENT; DISTANT-FAILURE; FIELD RADIATION; TUMOR DIAMETER; CARCINOMA; PACLITAXEL; CHEMOTHERAPY; RADIOTHERAPY;
D O I
10.12892/ejgo3125.2016
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose of investigation: To evaluate chemotherapy with concomitant radiotherapy (RT) in "high risk" endometrial cancer (EC) patients. Furthermore to develop a new algorithm for management and treatment. Materials and Methods: The study included 182 Stage I endometrioid EC patients who underwent definitive surgery after a first treatment. Stage, grade, ploidy DNA index, lymphovascular space involvement (LVSI), tumor diameter (TD), and p53 were considered to identify "high-risk" patients. Twenty-seven women received adjuvant concomitant chemoradiation (CR). Toxicity related to the CR treatment, disease free interval (DFI), and status of the patients were considered. Results: Twenty-seven patients according to the present algorithm treatment were considered at "high risk". Median follow up was 43 months (range 16-68). Twenty-five (92%) patients completed CR treatment. Overall, grade 3/4 hematological toxicity was 18% while gastrointestinal toxicity was 15%. Four patients relapsed with a five-year rate of 14% of recurrences. Conclusions: Adjuvant concomitant CR is well tolerated and is a feasible regimen in "high risk" patients. The authors' new algorithm treatment could be used for management and further clinical studies.
引用
收藏
页码:657 / 661
页数:5
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