Cytokeratin 7 as a Predictive Factor for Response to Concommitant Radiochemotherapy for Locally Advanced Cervical Cancer: A Preliminary Study

被引:1
作者
Lambaudie, Eric [1 ,2 ]
Chereau, Elisabeth [1 ]
Pouget, Nicolas [1 ]
Thomassin, Jeanne [2 ,3 ]
Minsat, Mathieu [4 ]
Charafe-Jauffret, Emmanuelle [2 ,3 ]
Jacquemier, Jocelyne [2 ]
Houvenaeghel, Gilles [1 ,2 ]
机构
[1] Inst J Paoli I Calmettes, Dept Surg Oncol, CRCM, Inserm,UMR1068, F-13009 Marseille, France
[2] Inst J Paoli I Calmettes, Dept Mol Oncol, CRCM, Inserm,UMR1068, F-13009 Marseille, France
[3] Inst J Paoli I Calmettes, Dept Pathol, F-13009 Marseille, France
[4] Inst J Paoli I Calmettes, Dept Radiotherapy, F-13009 Marseille, France
关键词
Advanced cervical cancer; radiochemotherapy; biomarkers; CK7; survival; INDOLEAMINE 2,3-DIOXYGENASE; CHEMORADIATION THERAPY; STEM-CELLS; EXPRESSION; CARCINOMA; SURGERY; CHEMORADIOTHERAPY; SURVIVAL; DISEASE; TUMOR;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The role of completion surgery after concurrent radiochemotherapy (CCRC) for advanced cervical cancer remains controversial. Individual predictive factors of CCRC response and survival are mandatory for treatment adaptation and to determine a population who would take interest in completion surgery after CCRC. The aim of this study was to evaluate the ability of biomarkers to predict the response to CCRC. Patients and Methods: Between 1996 and 2008, in 58 patients with advanced cervical cancer for whom pre-therapeutic cone biopsy was available, we tested several biomarkers (ALDH1, CD44, CD24, IDO, Ki67, P63, CK7, p-Stat3, Foxp3 and IDO). Results: Residual disease was found in 49.1% of cases (n=26). We found a significant association between progression-free survival and residual disease on completion hysterectomy (p=0.044). Univariate analysis of the different factors showed that negativity for cytokeratin 7 expression was a strong predictor for the presence of residual tumor (p=0.001). Conclusion: These results are encouraging and CK7 could be used as a predictive factor of response to CCRC.
引用
收藏
页码:177 / 181
页数:5
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