It was suggested that SNPs in the XRCC1

gene may alter the ability of XRCC1 to repair damaged DNA, especially SNPs at codon 399 [7]. Some studies have shown that genetic polymorphisms of the XRCC1 gene are associated with response to platinum-based chemotherapy in non-small-cell lung cancer, colorectal cancer, and breast cancer [8, 9], but few studies have investigated the association of XRCC1 SNPs with response to chemotherapy in locally advanced cervical carcinoma. Only one study has analyzed XRCC1 SNPs at codon 399, and another study has analyzed SNPs at codon 194 recently, the results have shown that the XRCC1 Arg399Trp polymorphism or the XRCC1 Arg194Trp polymorphism is associated with the response selleck chemicals to platinum-based NAC in cervical cancer, but the number of cases were all small (36 patients and 66 patients respectively) [10, 11]. No results Compound C in vitro of this two SNPs in the same patients were showed. To clarify the influence of the XRCC1 gene polymorphisms on the response to NAC, in the present study, we examined the association of the different genotypes (at codons 194 and 399), as well as protein expression

with NAC response in patients with locally advanced cervical carcinoma. Methods Patient enrollment From June 2003 to June 2007, a total of 109 patients with histologically confirmed locally advanced cervical carcinoma (FIGO stage IB2-IIA at least 4 cm in diameter) underwent NAC and subsequent radical hysterectomy in Women’s Hospital School of Medicine, Zhejiang University. Of those, 70 patients who had complete clinical data, peripheral blood samples, and cervical carcinoma next tissures by biopsy just before chemotherapy were enrolled in the study. Each patient signed a form to indicate informed consent before

chemotherapy. Chemotherapy NAC regimens consisted of cisplatinum-based combined chemotherapy. The regimens included BVP (blemycin 15 mg/m2, on d1, d7; cisplatin 60 mg/m2 on d1; vindesine 4 mg/m2 on d1–d2) in 47 patients, BIP (blemycin 15 mg/m2 on d1; ifosfamide 1 g/m2 on d1–d5; cisplatin 50 mg/m2 on d1) in 15 patients, TP (taxol 60 mg/m2 d1; cisplatin 60 mg/m2 on d1) in 8 patients. NAC was administered every 3 to 4 weeks, for one to three cycles: one cycle in 15 patients, two cycles in 49 patients, and three cycles in 6 patients. All of the chemotherapeutic agents were administered intravenously. Evaluation of chemotherapy response The chemotherapy response was evaluated two weeks after completion of the final cycle according to WHO criteria, if no obvious response occurred after two cycles, the patient would not accept another cycle of chemotherapy. Tumor size was measured by pelvic examination and colposcopy as the product of the maximal perpendicular Selleck Selonsertib diameter of the tumor.