PREDICTORS OF CHEMORESISTANCE TO PLATINUM-CONTAINING NEOADJUVANT CHEMOTHERAPY IN ADVANCED OVARIAN CANCER
##article.numberofdownloads## 51
##article.numberofviews## 238
PDF (Русский)

Keywords

OVARIAN CANCER
ASCITES
CHEMORESISTANCE

How to Cite

Dolgova, D., Gening, S., Abakumova, T., Antoneeva, I., Gening, T., & Fedotova, A. (2019). PREDICTORS OF CHEMORESISTANCE TO PLATINUM-CONTAINING NEOADJUVANT CHEMOTHERAPY IN ADVANCED OVARIAN CANCER. Voprosy Onkologii, 65(3), 422–426. https://doi.org/10.37469/0507-3758-2019-65-3-422-426

Abstract

Chemoresistance is one of the main causes of treatment failure in advanced ovarian cancer (OC). In order to identify predictors of chemoresistance, 30 patients with ascitic form of OC, who received neoadjuvant chemotherapy (NACT) according to AP regimen, were examined. In the epithelial cells of ascites and in tumor tissue after NACT, expression of the VEGFa, ABCB1 and ERCC1 genes was assessed by PCR-RT. The effectiveness of NACT was assessed using the criteria of therapeutic pathomorphosis, survival - using the Kaplan-Meier criterion, the relationship of clinical and molecular parameters - using the Mann-Whitney criterion. Results. We established that in 43% of patients the response to NACT was absent (CRS1), the significant response (CRS2) was in 35% of cases, and the complete response (CRS3) was in 21% of cases. VEGFa expression was increased in ascites in 17% of cases, in tumor tissue - in 33% in the CRS1 group. In groups with CRS 2,3, overexpression of VEGFa in ascites was detected in 25% of cases, in tumor tissue in 37.5%. ABCB1 mRNA expression was increased after NACT in 50% of cases in the CRS1 group and in 25% of cases in the CRS 2,3 group. Thus, platinum-based NACT initiates an increase in the expression of VEGFa and ABCB1 in tumor tissue. We established that in case of high expression (ERCC + / VEGF + / ABCB1 +) in ascites, there is a statistically significant increase in relapse-free survival compared with the group with low or absent expression (p = 0.012). The overall survival rate was 41.8 months in patients with overexpression of the studied genes in the tissue of the primary tumor after NACT and 25.3 months in patients with low expression (p = 0.058). Conclusion. The levels of ERCC1, VEGFa and ABCB1 mRNA in ascitic cells before NACT and in the primary tumor after NACT according to the AP scheme can serve as a predictor of the effectiveness of this treatment in ascitic OC.

https://doi.org/10.37469/0507-3758-2019-65-3-422-426
##article.numberofdownloads## 51
##article.numberofviews## 238
PDF (Русский)

References

Литвяков Н.В., Гарбуков Е.Ю., Слонимская Е.М., и др. Связь безметастатической выживаемости больных раком молочной железы и вектора изменения экспрессии генов множественной лекарственной устойчивости в опухоли при проведении неоадъювантной химиотерапии // Вопросы онкологии. - 2013. - Т. 59. - № 3. - С. 334-340.

Ставровская A.A., Стромская Т.П. Транспортные белки семейства АВС и множественная лекарственная устойчивость опухолевых клеток (обзор) // Биохимия. - 2008. - Т 73. - №5. - С.735-750. [Stavrovskaya A.A., Stromskaya T.P. Transport proteins of the ABC family and multidrug resistance of tumor cells. Biochemistry (Moscow). 2008; 73(5):592-604. (In Russ).] DOI: 10.1134/S0006297908050118

Ahmed N, Abubaker K, Findlay J, Quinn M. Cancerous ovarian stem cells: obscure targets for therapy but relevant to chemoresistance. J Cell Biochem. 2013; 114(1):21-34. DOI: 10.1002/jcb.24317

Arora S, Kothandapani A, Tillison K, et al. Downregulation of XPF-ERCC1 enhances cisplatin efficacy in cancer cells. DNA Repair (Amst). 2010; 9(7):745-53. DOI: 10.1016/j.dnarep.2010.03.010

B hm St. Chemotherapy Response Score: Development and Validation of a System to Quantify Histopathologic Response to Neoadjuvant Chemotherapy in Tubo-Ovarian High-Grade Serous Carcinoma. Journal of Clinical Oncology. 2015; 33(22): 2457-2463. DOI: 10.1200/JC0.2014.60.5212

Goler-Baron V, Assaraf YG. Overcoming multidrug resistance via photodestruction of ABCG2-rich extracellular vesicles sequestering photosensitive chemotherapeutics. PLoS One. 2012, 7(4): e35487. DOI: 10.1371/journal.pone.0035487

Kim S, Gwak H, Kim HS, et al. Malignant ascites enhances migratory and invasive properties of ovarian cancer cells with membrane bound IL-6R in vitro. Oncotarget. 2016; 7(50):83148-83159. DOI: 10.18632/oncotarget.13074

Kolomeyevskaya NV, Lele SB, Miller A, et al. Oxaliplatin is a safe alternative option for patients with recurrent gynecologic cancers after hypersensitivity reaction to Carboplatin. Int J Gynecol Cancer. 2015; 25(1):42-8. DOI: 10.1097/IGC.0000000000000307

Lane D, Matte I, Garde-Granger P, et al. Inflammation-regulating factors in ascites as predictive biomarkers of drug resistance and progression-free survival in serous epithelial ovarian cancers. BMC Cancer. 2015; 15:492. DOI: 10.1186/s12885-015-1511-7

Litviakov NV, Cherdyntseva NV, Tsyganov MM, et al. Changing the expression vector of multidrug resistance genes is related to neoadjuvant chemotherapy response. Cancer Chemotherapy and Pharmacology. 2013; 71(1): 153-163. DOI: 10.1007/s00280-012-1992-x

Matte I, Lane D, Laplante C, Rancourt C, Pich A. Profiling of cytokines in human epithelial ovarian cancer ascites. Am J Cancer Res. 2012; 2(5):566-80.

Ren F, Shen J, Shi H., et al. Novel mechanisms and approaches to overcome multidrug resistance in the treatment of ovarian cancer. Biochim Biophys Acta. 2016; 1866(2):266-275. DOI: 10.1016/j.bbcan.2016.10.001

Sedl kov I., Laco J., Caltov K., et al. Clinical significance of the resistance proteins LRP, Pgp, MRP1, MRP3, and MRP5 in epithelial ovarian cancer. Int J Gynecol Cancer. 2015; 25(2):236-43. DOI: 10.1097/IGC.0000000000000354

Sun Y Guan Z, Liang L, et al. NF-B signaling plays irreplaceable roles in cisplatin-induced bladder cancer chemoresistance and tumor progression. Int J Oncol. 2016; 48(1):225-34. DOI: 10.3892/ijo.2015.3256

Xu X, Wang X Guo W, et al. The significance of the alteration of 8-OHdG in serous ovarian carcinoma. J Ovarian Res. 2013; 6(1):74. DOI: 10.1186/1757-2215-6-74

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.

© АННМО «Вопросы онкологии», Copyright (c) 2019