- Pal T., Permuth-Wey J., Betts J.A. et al. BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases // Cancer. – 2005. – V. 104. – N 12. – P. 2807–16.
- Rooth C. Ovarian cancer: risk factors, treatment and management // Br J Nurs. – 2013. – V. 22. – N 17. – P. S23–30.
- Каприн А.Д., Старинский В.В., Шахзадова А.О. ред. Злокачественные новообразова-ния в России в 2021 г. (заболеваемость и смертность). М.: МНИОИ им. П.А. Герцена – филиал ФГБУ «НМИЦ радиологии» Минздрава России, 2022. 252 с.
- Ebell M.H., Culp M.B., Radke T.J. A Systematic Review of Symptoms for the Di-agnosis of Ovarian Cancer // Am J Prev Med. – 2016. – V. 50. – N 3. – P. 384–94.
- NCCN guidelines panel. Epithelial Ovarian Cancer (including Fallopian Tube Cancer and Primary Peritoneal Cancer). Version 1.2016 // published online: https://www.nccn.org/professionals/physician_gls/f_guidelines.asp#ovarian. – 2016. – P. OV1.
- Zhou Q., et al. Clinicopathological and prognostic significance of platelet count in pa-tients with ovarian cancer //Climacteric. – 2018. – Т. 21. – №. 1. – С. 60-68.
- Nomelini R.S. et al. Parameters of blood count and tumor markers: a retrospective analysis and relation to prognostic factors in ovarian cancer //Eur J Gynaecol Oncol. – 2017. – Т. 38. – С. 364-67.
- Ma X., et al. Prognostic significance of thrombocytosis, platelet parameters and aggre-gation rates in epithelial ovarian cancer //Journal of Obstetrics and Gynaecology Research. – 2014. – Т. 40. – №. 1. – С. 178-183.
- Qin Y., et al. The value of red cell distribution width in patients with ovarian cancer // Medicine. – 2017. – Т. 96. – №. 17.
- Slabuszewska-Jozwiak A., et al. The prognostic significance of thrombocytosis in ovar-ian cancer //Annals of Agricultural and Environmental Medicine. – 2015. – Т. 22. – №. 4.
- Yang Z., et al. Preoperative neutrophil-to-lymphocyte ratio is a predictor of survival of epithelial ovarian cancer: a systematic review and meta-analysis of observational studies // Oncotarget. – 2017. – Т. 8. – №. 28. – С. 46414.
- Schneider D., et al. Peritoneal fluid lactate dehydrogenase in ovarian cancer // Gynecologic oncology. – 1997. – Т. 66. – №. 3. – С. 399-404. DOI: 10.1006/gyno.1997.4792
- Gu P., et al. CA 125, PET alone, PET–CT, CT and MRI in diagnosing recurrent ovari-an carcinoma: a systematic review and meta-analysis //European journal of radiology. – 2009. – Т. 71. – №. 1. – С. 164–174.
- Ferraro S., et al. Serum human epididymis protein 4 vs carbohydrate antigen 125 for ovarian cancer diagnosis: a systematic review //Journal of clinical pathology. – 2013. – Т. 66. – №. 4. – С. 273-281.
- Stiekema A., Boldingh Q.J., Korse C.M., et al. Serum human epididymal protein 4 (HE4) as biomarker for the differentiation between epithelial ovarian cancer and ovarian metastases of gastrointestinal origin // Gynecol Oncol. – 2015. – V. 136. – N 3. – P. 562–6.
- Cui, Ranliang, et al. Clinical value of ROMA index in diagnosis of ovarian cancer: meta-analysis. Cancer management and research 28 Mar 2019; vol. 11: 2545–2551. doi:10.2147/CMAR.S199400
- Dochez V., Caillon H., Vaucel E., et al. Biomarkers and algorithms for diagnosis of ovarian cancer: CA125, HE4, RMI and ROMA, a review. J Ovarian Res 12, 28 (2019) doi:10.1186/s13048-019-0503-7
- Santotoribio J.D., Garcia-de la Torre A., Cañavate-Solano C., et al. Cancer antigens 19.9 and 125 as tumor markers in patients with mucinous ovarian tumors // Eur J Gynaecol Oncol. – 2016. – V. 37. – N 1. – P. 26–9.
- Colombo N., Peiretti M., Garbi A., et al. Non-Epithelial Ovarian Cancer: ESMO Clinical Practice Guidelines // Ann Oncol. – 2012. – V. 23 (Suppl 7). – P. vii20–vii26.
- Ledermann J.A., Raja F.A., Fotopoulou C., et al. Newly Diagnosed and Relapsed Epithelial Ovarian Carcinoma: ESMO Clinical Practice Guidelines // Ann Oncol. – 2013. – V. 24 (Suppl 6). – P. vi24–vi32. doi: 10.1093/annonc/mdt333.
- Zhong Q., et al. Effects of BRCA1-and BRCA2-related mutations on ovarian and breast cancer survival: a meta-analysis //Clinical Cancer Research. – 2015. – Т. 21. – №. 1. – P. 211-220.
- Sankaranarayanan R. Screening for cancer in low- and middle-income countries // Ann Glob Health. – 2014. – V. 80. – N 5. – P. 412–7.
- Holme Ø., et al. Effectiveness of flexible sigmoidoscopy screening in men and women and different age groups: pooled analysis of randomised trials // BMJ. – 2017. – Т. 356. – P. i6673.
- Roze J. F., et al. Positron emission tomography (PET) and magnetic resonance imaging (MRI) for assessing tumour resectability in advanced epithelial ovarian/fallopian tube/primary peritoneal cancer //Cochrane Database of Systematic Reviews. – 2018. – № 10.
- Nam E.J., et al. Diagnosis and staging of primary ovarian cancer: correlation between PET/CT, Doppler US, and CT or MRI //Gynecologic oncology. – 2010. – Т. 116. – №. 3. – С. 389–394.
- Fischerova D., et al. Ultrasound in preoperative assessment of pelvic and abdominal spread in patients with ovarian cancer: a prospective study //Ultrasound in Obstetrics & Gynecology. – 2017. – Т. 49. – №. 2. – P. 263-274.
- Yadav B.S., Sharma S.C., Robin T.P. Synchronous primary carcinoma of breast and ovary versus ovarian metastases. // Semin Oncol. – 2015. – V. 42. – N 2. – P. e13–24.
- Gøtzsche P.C., Jørgensen K.J. Screening for breast cancer with mammography // Cochrane database of systematic reviews. – 2013. – №. 6.
- Wubulihasimu M., Maimaitusun M., Xu X.-L., Liu X.-D., Luo B.-M. The added value of contrast-enhanced ultrasound to conventional ultrasound in differentiating benign and malignant solid breast lesions: a systematic review and meta-analysis. Clinical Radiology 2018. doi:10.1016/j.crad.2018.06.004
- Hu Q., Wang X.Y., Zhu, S.Y., Kang L.K., Xiao Y.J., Zheng H.Y. Meta-analysis of contrast-enhanced ultrasound for the differentiation of benign and malignant breast lesions. Acta Radiologica 2015; 56(1): 25–33. doi:10.1177/0284185113517115
- van de Vrie R., Rutten M.J., Asseler J., Leeflang M.M.G., Kenter G.G., Mol B.J., Buist M. Laparoscopy for diagnosing resectability of disease in women with advanced ovarian cancer. Cochrane Database of Systematic Reviews 2019, Issue 3. Art. No.: CD009786. doi: 10.1002/14651858.CD009786.pub3
- Stuart G., Kitchener H., Bacon M. et al. 2010 Gynecologic Cancer InterGroup (GCIG) Consensus Statement on Clinical Trials in Ovarian Cancer Int J Gynecol Cancer 2011;21: 750Y755.
- Trimbos J.B., Parmar M., Vergote I.. et al. International Collaborative Ovarian Ne-oplasm trial 1 and Adjuvant ChemoTherapy In Ovarian Neoplasm trial: two parallel random-ized phase III trials of adjuvant chemotherapy in patients with early-stage ovarian carcinoma. Journal of the National Cancer Institute, Volume 95, Issue 2, 15 January 2003, Pages 105–112, https://doi.org/10.1093/jnci/95.2.105
- Zhou M., et al. Tumor regression grading after neoadjuvant chemotherapy predicts long-term outcome of stage IIIC epithelial ovarian cancer // J Clin Oncol 2018 36:15_suppl, 5547–5547.
- AJCC. PART III: digestive systems. In: Edge S.B., Byrd D.R., Compton C.C., Fritz A.G., Greene F.L., Trotti A. III, eds. AJCC cancer staging manual. 7th ed. New York: Springer; 2010. P. 103–26.
- Elattar A., et al. Optimal primary surgical treatment for advanced epithelial ovarian cancer // Cochrane database of systematic reviews. – 2011. – № 8. 2А.
- Huo Y.R., et al. Hyperthermic intraperitoneal chemotherapy (HIPEC) and cytoreduc-tive surgery (CRS) in ovarian cancer: a systematic review and meta-analysis // European Journal of Surgical Oncology (EJSO). – 2015. – Т. 41. – №. 12. – С. 1578–1589.
- Cardenas-Goicoechea J., et al. Minimally invasive interval cytoreductive surgery in ovarian cancer: systematic review and meta-analysis //Journal of robotic surgery. – 2019. – Т. 13. – №. 1. – P. 23-33.
- Elattar A., et al. Optimal primary surgical treatment for advanced epithelial ovarian cancer // Cochrane database of systematic reviews. – 2011. – № 8. 2А.
- Huo Y.R., et al. Hyperthermic intraperitoneal chemotherapy (HIPEC) and cytoreduc-tive surgery (CRS) in ovarian cancer: a systematic review and meta-analysis // European Journal of Surgical Oncology (EJSO). – 2015. – Т. 41. – №. 12. – С. 1578-1589.
- Cardenas-Goicoechea J., et al. Minimally invasive interval cytoreductive surgery in ovarian cancer: systematic review and meta-analysis // Journal of robotic surgery. – 2019. – Т. 13. – №. 1. – С. 23-33.
- Young R.C., Walton L.A., Ellenberg S.S., et al. Adjuvant therapy in stage I and stage II epithelial ovarian cancer // N Engl J Med. – 1990. – V. 322. – P. 1021–7.
- Young R.C., Brady M.F., Nieberg R.M., et al. Adjuvant treatment for early ovarian cancer: a randomized phase III trial of intraperitoneal 32P or intravenous cyclophosphamide and cisplatin – A Gynecologic Oncology Group study // J Clin Oncol 2003. – V 21. – N 23. P. 4350–5.
- Bolis G., Colombo N., Pecorelli S., et al. Adjuvant treatment for early epithelial ovarian cancer: results of two randomized clinical trials comparing cisplatin to no further treatment or chromic phosphate (32P). GICOG: Gruppo Interregionale Collaborativo in Ginecologia Oncologica // Ann Oncol. – 1995. – V. 6, N 9. – P. 887–93.
- Elattar A., et al. Optimal primary surgical treatment for advanced epithelial ovarian cancer // Cochrane database of systematic reviews. – 2011. – №. 8. 2А.
- Vergote I., Trope C.G., Amant F., et al. Neoadjuvant chemotherapy or primary sur-gery in stage IIIC or IV ovarian cancer // N Engl J Med. – 2010. – V. 363. – P. 943–53.
- Yang L., et al. Neoadjuvant chemotherapy versus primary debulking surgery in ad-vanced epithelial ovarian cancer: A meta-analysis of peri-operative outcome // PloS One. – 2017. – Т. 12. – №. 10. – С. e0186725.
- Xiao Y., et al. Platinum-Based Neoadjuvant Chemotherapy versus Primary Surgery in Ovarian Carcinoma International Federation of Gynecology and Obstetrics Stages IIIc and IV: A Systematic Review and Meta-Analysis // Gynecologic and obstetric investigation. – 2018. – Т. 83. – №. 3. – С. 209–219.
- Harter P., Sehouli J., Lorusso D., et al. A Randomized Trial of Lymphadenectomy in Patients with Advanced Ovarian Neoplasms // N Engl J Med. – 2019. – V. 380. – P. 822–832.
- Zhou J., Shan G., Chen Y. The effect of lymphadenectomy on survival and recurrence in patients with ovarian cancer: a systematic review and meta-analysis // Japanese journal of clinical oncology. – 2016. – Т. 46. – №. 8. – С. 718–726.
- Lawrie T.A., et al. Adjuvant (post‐surgery) chemotherapy for early stage epithelial ovarian cancer // Cochrane Database of Systematic Reviews. – 2015. – № 12.
- Katsumata N., et al. Dose-dense paclitaxel once a week in combination with carboplatin every 3 weeks for advanced ovarian cancer: a phase 3, open-label, randomised con-trolled trial. Lancet. 2009 Oct 17;374(9698):1331-8. doi: 10.1016/S0140-6736(09)61157-0. Epub 2009 Sep 18.
- Kurman A., Hoskins P.J., Tinker A.V. Clinical oncology (Royal College of Radiologists (Great Britain)), 2015. Vol. 27, Issue 1, P. 40–7. doi: https://doi.org/10.1016/j.clon.2014.10.001.
- Armstrong D.K., et al. Intraperitoneal Cisplatin and Paclitaxel in Ovarian Cancer // N Engl J Med 2006; 354: 34-43 doi: 10.1056/NEJMoa052985
- Gorodnova T.V., Kotiv K.B., Ivantsov A.O., Mikheyeva O.N., Mikhailiuk G.I., Lisyanskaya A.S., et al. Efficacy of Neoadjuvant Therapy With Cisplatin Plus Mitomy-cin C in BRCA1-Mutated Ovarian Cancer. Int J Gynecol Cancer. 2018; 28(8): 1498–1506.
- Oza A.M., Cook A.D., Pfisterer J., et al. Standard chemotherapy with or without bevacizumab for women with newly diagnosed ovarian cancer (ICON7): overall survival re-sults of a phase 3 randomised trial // The Lancet Oncology. 2015. – V. 16, N 8. – P. 928–936.
- Li J., Zhou L., Chen X., Ba Y. Addition of bevacizumab to chemotherapy in patients with ovarian cancer: a systematic review and meta-analysis of randomized trials. Clinical and Translational Oncology 2015; 17(9): 673–683. doi:10.1007/s12094-015-1293-z.58. версия 1.
- версия 2 Ray-Coquard I, Leary A, Pignata S, Cropet C, González-Martín A, Marth C, Nagao S, Vergote I, Colombo N, Mäenpää J, Selle F, Sehouli J, Lorusso D, Guerra Alia EM, Bogner G, Yoshida H, Lefeuvre-Plesse C, Buderath P, Mosconi AM, Lortholary A, Burges A, Medioni J, El-Balat A, Rodrigues M, Park-Simon TW, Dubot C, Denschlag D, You B, Pujade-Lauraine E, Harter P; PAOLA-1/ENGOT-ov25 investigators. Olaparib plus bevacizumab first-line maintenance in ovarian cancer: final overall survival results from the PAOLA-1/ENGOT-ov25 trial. Ann Oncol. 2023 Aug;34(8):681-692. doi: 10.1016/j.annonc.2023.05.005. Epub 2023 May 19. PMID: 37211045.
- Gershenson D., Bodurka D., Coleman R. et al. Hormonal Maintenance Therapy for Women With Low-Grade Serous Cancer of the Ovary or Peritoneum // J Clin Oncol. – 2017. In print.
- Langdon S. P. et al. Endocrine therapy in epithelial ovarian cancer //Expert review of anticancer therapy. – 2017. – Т. 17. – №. 2. – С. 109-117.
- Chen H., et al. Maintenance chemotherapy for ovarian cancer // Cochrane database of systematic reviews. – 2013. – №. 6.
- Rustin G.J., Vergote I., Eisenhauer E., et al. Definitions for Response and Progression in Ovarian Cancer Clinical Trials Incorporating RECIST 1.1 and CA 125 Agreed by the Gynecological Cancer Intergroup (GCIG) // Int J Gynecol Cancer. – 2011. – V 21, N 2. – P. 419–23.
- Al Rawahi T., et al. Surgical cytoreduction for recurrent epithelial ovarian cancer // Cochrane Database of Systematic Reviews. – 2013. – №. 2.
- Rustin G.J., van der Burg M.E., Griffin C.L., et al. Early versus delayed treatment of relapsed ovarian cancer (MRC OV05/EORTC 55955): a randomised trial // Lancet. – 2010. – V. 376, N 9747. – P. 1155–63.
- Harter P., du Bois A., Hahmann M., et al. Surgery in recurrent ovarian cancer: the Arbeitsgemeinschaft Gynaekologische Onkologie (AGO) DESKTOP OVAR trial // Ann Surg Oncol. – 2006. – V. 13, N 12. – P. 1702–10.
- Harter P., Sehouli J., Reuss A., et al. Prospective validation study of a predictive score for operability of recurrent ovarian cancer: the Multicenter Intergroup Study DESKTOP II. A project of the AGO Kommission OVAR, AGO Study Group, NOGGO, AGO-Austria, and MITO // Int J Gynecol Cancer. – 2011. – V. 21, N 2. – P. 289–95.
- Al Rawahi T., et al. Surgical cytoreduction for recurrent epithelial ovarian cancer // Cochrane Database of Systematic Reviews. – 2013. – №. 2.
- Markman M., Rothman R., Hakes T., et al. Second-line platinum therapy in patients with ovarian cancer previously treated with cisplatin. J Clin Oncol 1991; 9: 389–393.
- Gore M., Fryatt I., Wiltshaw E., Dawson T. Treatment of relapsed carcinoma of the ovary with cisplatin or carboplatin following initial treatment with these components. Gynecol Oncol 36:207–211, 1990.
- Mahner S., Meier W., du Bois A., et al. Carboplatin and pegylated liposomal doxo-rubicin versus carboplatin and paclitaxel in very platinum-sensitive ovarian cancer patients: results from a subset analysis of the CALYPSO phase III trial. Eur J Cancer. 2015; 51(3): 352–8.
- The ICON and AGO Collaborators Paclitaxel plus platinum-based chemotherapy versus conventional platinum-based chemotherapy in women with relapsed ovarian cancer: the ICON4/AGO-OVAR-2.2 trial // Lancet. – 2003. – V. 361. – P. 2099–106.
- Lawrie TA, Bryant A, Cameron A, Gray E, Morrison J. Pegylated liposomal doxorubicin for relapsed epithelial ovarian cancer. Cochrane Database Syst Rev. 2013 Jul 9;2013(7):CD006910. doi: 10.1002/14651858.CD006910.pub2.
- Gershenson D.M., et al. A phase I study of a daily× 3 schedule of intravenous vi-norelbine for refractory epithelial ovarian cancer //Gynecologic oncology. – 1998. – Т. 70. – №. 3. – С. 404–409.
- Ray-Coquard I., et al. Gemcitabine-oxaliplatin combination for ovarian cancer resistant to taxane-platinum treatment: a phase II study from the GINECO group. Brit J Cancer 2009; 100(4): 601–7. doi: 10.1038/sj.bjc.6604878
- Recchia F., et al. Phase I study of liposomal doxorubicin and oxaliplatin as salvage chemotherapy in advanced ovarian cancer/Anticancer Drugs. 2003 Sep;14(8):633-8/DOI:10.1097/00001813-200309000-00008.
- Harnett P., et al. Phase II study of gemcitabine and oxaliplatin in patients with recur-rent ovarian cancer: an Australian and New Zealand Gynaecological Oncology Group study/Int J Gynecol Cancer. 2007 Mar-Apr;17(2):359–66. doi: 10.1111/j.1525-1438.2007.00763.x
- Wolf J.K., et al. A phase II trial of oral capecitabine in patients with platinum–and taxane–refractory ovarian, fallopian tube, or peritoneal cancer // Gynecol Oncol. – 2006. – Т. 102. – №. 3. – Р. 468–474. doi: 10.1016/j.ygyno.2005.12.040.
- Sugiyama T., et al. Irinotecan (CPT-11) combined with cisplatin in patients with refrac-tory or recurrent ovarian cancer/ Cancer Lett. 1998 Jun 19;128(2):211–8. doi: 10.1016/s0304-3835(98)00065-2.
- Conteduca V., Gurioli G., Rossi L., et al. Oxaliplatin plus leucovorin and 5-fluorouracil (FOLFOX-4) as a salvage chemotherapy in heavily-pretreated platinum-resistant ovarian cancer. BMC Cancer; 2018: 1267.
- Kumar A., et al. Chemotherapy is of Value in Second Line and Beyond, Relapsed High-grade, Serous Epithelial Ovarian Cancer: An Analysis of Outcomes Obtained With Oral Etoposide/Am J Clin Oncol. 2018 Apr;41(4):379-384. doi: 10.1097/COC.0000000000000281.
- Bajetta E., et al. Phase II study of vinorelbine in patients with pretreated advanced ovarian cancer: activity in platinum-resistant disease./ J Clin Oncol. 1996 Sep;14(9):2546–51. DOI: 10.1200/JCO.1996.14.9.2546
- Sehouli J., et al. Topotecan Weekly Versus Conventional 5-Day Schedule in Patients With Platinum-Resistant Ovarian Cancer: a randomized multicenter phase II trial of the North-Eastern German Society of Gynecological Oncology Ovarian Cancer Study Group // J Clin Oncol. 2011 Jan 10;29(2):242–8. doi: 10.1200/JCO.2009.27.8911. Epub 2010 Nov 29. doi: 10.1200/JCO.2009.27.8911
- Poveda A., et al. Phase II randomized study of PM01183 versus topotecan in patients with platinum-resistant/refractory advanced ovarian cancer. Ann Oncol 2017; 28(6): 1280–1287. doi: 10.1093/annonc/mdx111
- Gynecologic Oncology Group, Markman M, Blessing J et al. Phase II trial of weekly paclitaxel (80 mg/m2) in platinum and paclitaxel-resistant ovarian and primary peritone-al cancers: a Gynecologic Oncology Group study. Gynecol Oncol. 2006 Jun;101(3):436–40. doi:10.1016/j.ygyno.2005.10.036
- Vergote I., et al. A randomised, double-blind, phase II study of two doses of pemetrexed in the treatment of platinum-resistant, epithelial ovarian or primary peritoneal cancer. Еur J Cancer. 2009; 45(8): 1415–23. doi: 10.1016/j.ejca.2008.12.013.
- El-Husseiny K., et al. Continuous Low-Dose Oral Cyclophosphamide and Methotrexate as Maintenance Therapy in Patients With Advanced Ovarian Carcinoma After Complete Clinical Response to Platinum and Paclitaxel Chemotherapy. Int J Gynecol Cancer. 2016; 26(3): 437–42. doi: 10.1097/IGC.0000000000000647
- Langdon S.P., et al. Endocrine therapy in epithelial ovarian cancer./ Expert Rev Anti-cancer Ther. 2017 Feb;17(2):109-117. doi: 10.1080/14737140.2017.1272414. Epub 2016 Dec 24./ DOI:10.1080/14737140.2017.12724
- Aghajanian C., Goff B., Nycum L.R., et al. Final overall survival and safety analy-sis of OCEANS, a phase 3 trial of chemotherapy with or without bevacizumab in patients with platinum-sensitive recurrent ovarian cancer // Gynecol Oncol. – 2015. – V. 139, N 1. – P. 10–6. doi: 10.1016/j.ygyno.2015.08.004
- Pujade-Lauraine E., Hilpert F. Weber B. et al. Bevacizumab Combined With Chemotherapy for Platinum-Resistant Recurrent Ovarian Cancer: The AURELIA Open-Label Randomized Phase III Trial // J Clin Oncol. – 2014. – 32(13):1302-8 . doi: 10.1200/JCO.2013.51.4489
- Oza A.M., et al. Standart chemotherapy with or without bevacizumab for women with newly diagnosed ovarian cancer (ICON7): overall survival results of a phase3 randomised trial. V 16(8). P. 928–936. doi: 10.1016/S1470-2045(15)00086-8
- Gorodnova T.V., Sokolenko A.P., Kondratiev S.V., Kotiv K.B., Belyaev A.M., Berlev I.V., Imyanitov E.N. Mitomycin C plus cisplatin for systemic treatment of recurrent BRCA1-associated ovarian cancer. Invest New Drugs. 2020; 38(6): 1872–1878.
- Pujade-Lauraine E. et al. Olaparib tablets as maintenance therapy in patients with platinum-sensitive, relapsed ovarian cancer and a BRCA1/2 mutation (SOLO2/ENGOT-Ov21): a double-blind, randomised, placebo-controlled, phase 3 trial //The lancet oncology. – 2017. – Т. 18. – №. 9. – С. 1274-1284. doi: 10.1016/S1470-2045(17)30469-2.
- Pujade-Lauraine, et al. Presented at ESMO Virtual Congress 2021; 16–21 September (Oreo).
- Wagner, U., et al. Final overall survival results of phase III GCIG CALYPSO trial of pegylat-ed liposomal doxorubicin and carboplatin vs paclitaxel and carboplatin in platinum-sensitive ovarian cancer patients. Brit J Cancer vol. 2012; 107(4): 588–91. doi: 10.1038/bjc.2012.307
- Colombo N., et al. INOVATYON study: Randomized phase III international study compar-ing trabectedin/PLD followed by platinum at progression vs carboplatin/PLD in patients with recurrent ovarian cancer progressing within 6-12 months after last platinum line. Ann Oncol 2020; 31 (suppl_4): S1142–S1215.
- Hoskins P.J., Le N. Identifying patients unlikely to benefit from further chemo-therapy: A descriptive study of outcome at each relapse in ovarian cancer // Gynecol Oncol 2005. – V. 97. – P. 862–869.
- Ledermann J., Harter P., Gourley C., et al. Olaparib maintenance therapy in patients with platinum-sensitive relapsed serous ovarian cancer: a preplanned retrospective analysis of outcomes by BRCA status in a randomised phase 2 trial. Lancet Oncol. 2014 Jul;15(8):852–61.
- Wiggans A.J., et al. Poly (ADP‐ribose) polymerase (PARP) inhibitors for the treat-ment of ovarian cancer // Cochrane Database of Systematic Reviews. – 2015. – №. 5.
- Swenerton K.D., Santos J.L., Gilks C.B. et al. Histotype predicts the curative po-tential of radiotherapy: the example of ovarian cancers // Ann Oncol – 2011. – V. 22. – P. 341–347.
- Einhorn N. Ovarian Cancer. Acta Oncol 1996; 35(sup7): 86–92. doi:10.3109/02841869609101668
- Navari RM, Gray SE, Kerr AC. Olanzapine versus aprepitant for the prevention of chemotherapy-induced nausea and vomiting: a randomized phase III trial. J Support Oncol 2011; 9(5): 188–95.
- Владимирова Л. Ю., Гладков О. А., Королева И. А., Румянцев А. А., Семиглазова Т. Ю., Трякин А. А. Злокачественные опухоли: Практические рекомендации RUSSCO #3s2, 2021 (том 11). 37. https://www.rosoncoweb.ru/standarts/RUSSCO/2021/2021-37.pdf.
- Sonal Krishan, Nalinda Panditaratne, Rajeev Verma, Roderick Robertson. Incremental value of CT venography combined with pulmonary CT angiography for the detection of thromboembolic disease: systematic review and meta-analysis. AJR Am J Roentgenol 2011; 196(5): 1065–72.
- Wendy Lim, Grégoire Le Gal, Shannon M. Bates, et al. American Society of Hematol-ogy 2018 guidelines for management of venous thromboembolism: diagnosis of venous thromboembolism. Blood Adv 2018; 2(22): 3226–3256.
- Lyman G.H., Carrier M., Cihan A., et al. American Society of Hematology 2021 guidelines for management of venous thromboembolism: prevention and treatment in patients with cancer. Blood Adv 2021; 5(4): 927–974.
- Сомонова О. В., Антух Э. А., Долгушин Б. И., Елизарова А. Л., Сакаева Д. Д., Сельчук В. Ю., Трякин А. А., Черкасов В. А. Злокачественные опухоли: Практические рекомендации RUSSCO #3s2, 2021; (том 11): 47.
- NCCN Guidelines. Prevention and Treatment of Cancer-Related Infections. v.1, 2021. https://www.nccn.org/professionals/physician_gls/pdf/infections.pdf.
- Yoshimasa K., Yoshiaki R., Norikazu M., et al. Phase III placebo-controlled, double-blind, randomized trial of pegfilgrastim to reduce the risk of febrile neutropenia in breast cancer patients receiving docetaxel/cyclophosphamide chemother-apy. Support Care Cancer 2015; 23(4): 1137–43.
- Paul M., Yahav D., Fraser A., Leibovici L. Empirical antibiotic monotherapy for febrile neutropenia: systematic review and meta-analysis of random-ized controlled trials. Journal of Antimicrobial Chemotherapy, Vol 57, Issue 2, Feb 2006, P. 176–189.
- Сакаева Д. Д., Курмуков И. А., Орлова Р. В., Шабаева М. М Злокачественные опухоли: Практические рекомендации RUSSCO #3s2, 2021; (том 11): 39. https://www.rosoncoweb.ru/standarts/RUSSCO/2021/2021-39.pdf.
- Vincenzi B., Russo A., Terenzio A., et al. The use of SAMe in chemotherapy-induced liver injury. Crit Rev Oncol Hematol 2018 Oct;130: 70-77.
- Remash D., Prince D.S., McKenzie C., et al. Immune checkpoint inhibi-tor-related hepatotoxicity: A review. World J Gastroenterol 2021; 27(32): 5376–5391.
- Ткаченко П.Е., Ивашкин В.Т., Маевская М.В. Злокачественные опухоли: Практические рекомендации RUSSCO #3s2, 2021; (том 11): 40. https://www.rosoncoweb.ru/standarts/RUSSCO/2021/2021-40.pdf
- Mao Z., Shen K., Zhu L., et al. Comparisons of Cardiotoxicity and Efficacy of Anthracycline-Based Therapies in Breast Cancer: A Network Meta-Analysis of Randomized Clinical Trials. Oncol Res Treat 2019;42(7-8):405-413.
- Albakri A. Systolic heart failure: A review of clinical status and metaanalysis of di-agnosis and clinical management methods. Trends in Res, 2018, 1(4), doi: 10.15761/TR.1000124.
- Tromp J., Ouwerkerk W., van Veldhuisen D.J., et al. A Systematic Review and Network-Meta-Analysis of Pharmacological Treatment of Heart Failure With Re-duced Ejection Fraction. J Am Coll Cardiol HF. Dec 08, 2021.
- Kashif Kalam, Thomas H.Marwick. Role of cardioprotective therapy for prevention of cardiotoxicity with chemotherapy: A systematic review and meta-analysis. Eur J Cancer 2013; 49(13): 2900–9.
- Виценя М. В., Агеев Ф. Т., Гиляров М. Ю., Овчинников А. Г., Орлова Р. В., Полтавская М. Г. Злокачественные опухоли: Практические рекомендации RUSSCO #3s2, 2021; (том 11): 41. https://www.rosoncoweb.ru/standarts/RUSSCO/2021/2021-41.pdf
- Li J., Yan H. Skin toxicity with anti-EGFR monoclonal antibody in cancer patients: a meta-analysis of 65 randomized controlled trials. Cancer Chemother Pharmacol 2018; 82(4): 571–583.
- Королева И. А., Болотина Л. В., Гладков О. А., Горбунова В. А., Круглова Л. С., Манзюк Л. В. и соавт. Злокачественные опухоли: Практические рекомендации RUSSCO #3s2, 2021; (том 11): 42. https://www.rosoncoweb.ru/standarts/RUSSCO/2021/2021-42.pdf.
- http://cr.rosminzdrav.ru/#!/recomend/708.
- Silver J.A., Baima J. Cancer prehabilitation: an opportunity to decrease treatmen-trelated morbidity, increase cancer treatment options, and improve physical and psychological health outcomes. Am J Phys Med Rehabil 2103; 92: 715–727.
- Nilsson H., Angeras U., Bock D., Börjesson M., Onerup A., Fagevik Olsen M., et al. Is preoperative physical activity related to post-surgery recovery? BMJ Open. 2016; 6(1): e007997. doi: 10.1136/bmjopen-2015-007997
- Zhou Y., et al. Body mass index, physical activity, and mortality in women diag-nosed with ovarian cancer: results from the Women"s Health Initiative. Gynecol Oncol 2014; 133(1): 4–10.
- Hijazi Y., Gondal U., Aziz O. A systematic review of prehabilitation programs in abdominal cancer surgery. Int J Surg. 2017 Mar;39:156-162. doi: 10.1016/j.ijsu.2017.01.111. Epub 2017 Feb 2.
- Silver J.K., Baima J. Cancer prehabilitation: An opportunity to decrease treatment-related morbidity, increase cancer treatment options, and improve physical and psychological health outcomes. Am J Phys Med Rehabil. 2013;92:715–27.
- Tsimopoulou I., Pasquali S., Howard R., Desai A., Gourevitch D., Tolosa I., Vohra R. Psychological Prehabilitation Before Cancer Surgery: A Systematic Review. Ann Surg On-col. 2015 Dec;22(13):4117-23. DOI: 10.1245/s10434-015-4550-z. Epub 2015 Apr 14.
- Carter J. Fast-Track Surgery in Gynaecology and Gynaecologic Oncology: A Review of a Rolling Clinical Audit. ISRN Surgery. Vol. 2012, Article ID 368014, 19 p., 2012.
- Nelson G., Bakkum-Gamez J., Kalogera E., et al Guidelines for perioperative care in gynecologic/oncology: Enhanced Recovery After Surgery (ERAS) Society recommendations – 2019 update International Journal of Gynecologic Cancer Published Online First: 15 March 2019. doi: 10.1136/ijgc-2019-000356
- De Almeida E.P.M., De Almeida J.P., Landoni G., Galas F.R.B.G., Fukushima J.T., Fominskiy E., et al. Early mobilization programme improves functional capacity after major abdominal cancer surgery: A randomized controlled trial. Brit J Anaesth 2017; 119 (5): 900–907.
- Wren S.M., Martin M., Yoon J.K., Bech F. Postoperative pneumonia-prevention program for the inpatient surgical ward // Journal of the American College of Surgeons. – 2010. – Vol. 210, No. 4 – Pp. 491–495.
- Peedicayil A., Weaver A., Li X., Carey E., Cliby W., Mariani A. Incidence and timing of venous thromboembolism after surgery for gynecological cancer // Gynecol Oncol. – 2011. – Vol. 121, No. 1. – Pp. 64–69.
- Swarm R., Abernethy A.P., Anghelescu D.L. et al. NCCN Adult Cancer Pain. Adult cancer pain. J Natl Compr Canc Netw. 2010;8: 1046–1086.
- Ben-Arye E., Samuels N., Lavie O. Integrative Medicine for Female Patients with Gynecologic Cancer // The Journal of Alternative and Complementary Medicine. – Vol. 24, No. 9–10.
- Goerling U., Jaeger C., Walz A., et al. The efficacy of psycho-oncological interven-tions for women with gynaecological cancer: A randomized study // Oncology. 2014;87:114–124. Crossref, Medline.
- Smits A., Lopes A., Bekkers R., et al. Body mass index and the quality of life of endometrial cancer survivors – a systematic review and meta-analysis // Gynecol Oncol 2015;137:180–7. doi: 10.1016/j.ygyno.2015.01.540
- Schmitz K.H., Courneya K.S., Matthews C., et al. American College of Sports Medicine roundtable on exercise guidelines for cancer survivors. Med Sci Sports Exerc 2010; 42: 1409–26.
- Biglia N., Zanfagnin V., Daniele A., Robba E., Bounous V.E. Lower Body Lymphedema in Patients with Gynecologic Cancer. Anticancer Res. 2017; 37(8): 4005–15.
- Shaitelman S.F., Cromwell K.D., Rasmussen J.C., Stout N.L., Armer J.M., Lasinski B.B., Cormier J.N. Recent progress in the treatment and prevention of cancer-related lymphedema. CA Cancer J Clin. 2015 Jan-Feb;65(1):55-81. doi: 10.3322/caac.21253. Epub 2014 Nov 19. Erratum in: CA Cancer J Clin. 2015 May–Jun; 65(3): 252. PMID: 25410402.
- Borman Р. Lymphedema diagnosis, treatment, and follow-up from the view point of physical medicine and rehabilitation specialists. Turk J Phys Med Rehab 2018;64(3):179–197.
- Piller N., Douglass J., Heidenreich B., Moseley A. Placebo controlled trial of mild electrical stimulation. Journal of Lymphoedema. – 2010. – Vol 5, No 1. – P. 15–25.
- Грушина Т.И. Реабилитация в онкологии: физиотерапия. – М.: ГЭОТАР-Медиа, 2006. – 240 с.
- McNeely M.L., Peddle C.J., Yurick J.L., Dayes I.S., Mackey J.R. Conservative and dietary interventions for cancer‐related lymphedema: A Systematic review and meta‐analysis. Cancer. 2011 Mar 15;117(6):1136–48.
- Zhang Y.L., Huiling L., Yan L., Li H., Tian В. Effects of acupuncture on cancer-related fatigue: a meta-analysis // Supportive Care in Cancer. – 2018. – V. 26, Issue 2. – P. 415–425.
- Huffman L.B., Hartenbach E.M., Carter J., Rash J.K., Kushner D.M. Maintaining sexual health throughout gynecologic cancer survivorship: A comprehensive review and clini-cal guide. Gynecol Oncol. 2016 Feb;140(2):359-68. doi: 10.1016/j.ygyno.2015.11.010. Epub 2015 Nov 7. PubMed PMID: 26556768; PubMed Central PMCID: PMC4835814.
- Carmody J.F., Crawford S., Salmoirago-Blotcher E., Leung K., Churchill L., Olendzki N. Mindfulness training for coping with hot flashes: results of a randomized trial. Menopause. 2011 June;18(6):611–20. DOI: 10.1097/gme.0b013e318204a05c.
- Ferrandina G., Petrillo M., Mantegna G., Fuoco G., Terzano S., Venditti L., et al. Evaluation of quality of life and emotional distress in endometrial cancer patients: a 2-year prospective, longitudinal study. Gynecol Oncol. 2014 Jun;133(3):518-25. doi: 10.1016/j.ygyno.2014.03.015.
- Armbruster S.D., Song J., Bradford A. et al. Sexual health of endometrial cancer survivors before and after a physical activity intervention: A retrospective cohort analysis. Gynecol Oncol 2016;143:589–595. Crossref, Medline, Google Scholar.
- Lawvere, Silvana. (2002). The effect of massage therapy in ovarian cancer patients. doi: 10.1016/B978-0-7234-3217-3.50009-0
- Hu H., Xie Z.G., Qin W.L. Effect of electroacupuncture intervention at different phases of post-operation on bladder function in patients undergoing cervical cancer operation. Zhen Ci Yan Jiu 2013;38:64–67, 77. Medline, Google Scholar.
- Cannioto R.A., Moysich K.B. Epithelial ovarian cancer and recreational physical activity: A review of the epidemiological literature and implications for exercise prescription. Gynecol Oncol, 2015. 137(3): P. 559–73.
- Hu M., Lin W. Effects of exercise training on red blood cell production: implications for anemia. Acta Haematol. 2012;127(3):156–64. Epub 2012 Jan 31.
- Mustian K.M., Alfano C.M., Heckler C.. et al. Comparison of pharmaceutical, psy-chological, and exercise treatments for cancer-related fatigue: a meta-analysis. JAMA Oncol 2017;3:961–968.
- Kinkead B., Schettler P.J., Larson E.R., Carroll D., Sharenko M., Nettles J., et al. Massage therapy decreases cancer-related fatigue: Results from a randomized early phase trial. Cancer. 2018 Feb 1;124(3):546–554. DOI: 10.1002/cncr.31064.
- Streckmann F., Zopf E.M., Lehmann H.C. et al: Exercise intervention studies in patients with peripheral neuropathy: a systematic review. Sports Med 2014;44:1289–1304.
- Kleckner I.R., Kamen C., Gewandter J.S., et al. Effects of exercise during chemo-therapy on chemotherapy-induced peripheral neuropathy: a multicenter, randomized con-trolled trial. Support Care Cancer 2018;26:1019–1028.
- Rick O., von Hehn U., Mikus E., Dertinger H., Geiger G. Magnetic field therapy in patients with cytostatics-induced polyneuropathy: A prospective randomized pla-cebo-controlled phase-III study. Bioelectromagnetics 2016; 38(2): 85–94.
- Kılınç M., Livanelioğlu A., Yıldırım S.A., Tan E. Effects of transcutaneous electri-cal nerve stimulation in patients with peripheral and central neuropathic pain. J Rehabil Med. 2014 May;46(5):454-60. doi: 10.2340/16501977–1271
- Pearl M.L., et al. Transcutaneous electrical nerve stimulation as an adjunct for control-ling chemotherapy-induced nausea and vomiting in gynecologic oncology patients //Cancer nursing. – 1999. – Т. 22. – №. 4. – С. 307–311.
- Oberoi S., Zamperlini-Netto G., Beyene J., Treister N.S., Sung L. Effect of prophylactic low level laser therapy on oral mucositis: a systematic review and meta-analysis. Send to PLoS One. 2014 Sep 8;9(9):e107418. DOI: 10.1371/journal.pone.0107418. eCollec-tion 2014.
- Ross M., Fischer-Cartlidge E. Scalp Cooling: A Literature Review of Efficacy, Safety, and Tolerability for Chemotherapy-Induced Alopecia. Clin J Oncol Nurs. 2017 Apr 1;21(2):226-233. doi: 10.1188/17.CJON.226-233
- Avci P., Gupta G.K., Clark J., Wikonkal N., Hamblin M.R. Low-level la-ser (light) therapy (LLLT) for treatment of hair loss. Lasers in surgery and medicine 2013; 46(2): 144–51.
- Spence R.R., et al. Exercise and cancer rehabilitation: A systematic review. Cancer Treatment Reviews. – V. 36, Issue 2. – P. 185–194.
- Kew F., et al. Evaluation of follow‐up strategies for patients with epithelial ovarian cancer following completion of primary treatment //Cochrane Database of Systematic Reviews. – 2011. – №. 6.
- Oken M.M., Creech R.H., Tormey D.C., Horton J., Davis T.E., McFadden E.T., Carbone P.P. Toxicity and response criteria of the Eastern Cooperative Oncology Group. Am J Clin Oncol 1982;5(6):649−55.
- Karnofsky D.A., Burchenal J.H. The clinical evaluation of chemotherapeutic agents in cancer. In: MacLeod C. (ed.). Evaluation of chemotherapeutic agents. New York: Columbia University Press; 1949:191–205.
- Eisenhauer E.A., Therasse P., Bogaerts J., Schwartz L.H., Sargent D., Ford R., et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer 2009;45(2):228-47. doi: 10.1016/j.ejca.2008.10.026
- Hawker G.A., Mian S., Kendzerska T., French M. Measures of adult pain: Visual Analog Scale for Pain (VAS Pain), Numeric Rating Scale for Pain (NRS Pain), McGill Pain Questionnaire (MPQ), Short-Form McGill Pain Questionnaire (SF-MPQ), Chronic Pain Grade Scale (CPGS), Short Form-36 Bodily Pain Scale (SF-36 BPS), and Measure of Intermittent and Constant Osteoarthritis Pain (ICOAP). Arthritis Care Res (Hoboken) 2011;63(Suppl 11):S240–52.
167. ESUR guidelines: ovarian cancer staging and follow-up. Forstner R, Sala E, Kinkel K, Spencer JA; European Society of Urogenital Radiology.Eur Radiol. 2010 Dec;20(12):2773-80. doi: 10.1007/s00330-010-1886-4. Epub 2010 Sep 14. PMID: 20839002
168. O-RADS US Risk Stratification and Management System: A Consensus Guideline from the ACR Ovarian-Adnexal Reporting and Data System Committee// R. F. Andreotti et al., Radiology, 2019 (https://www.acr.org/Clinical-Resources/Reporting-and-Data-Systems/O-RADS)
169. Wang WH, Zheng CB, Gao JN, Ren SS, Nie GY, Li ZQ. Systematic review and meta-analysis of imaging differential diagnosis of benign and malignant ovarian tumors. Gland Surg. 2022 Feb;11(2):330-340. doi: 10.21037/gs-21-889. PMID: 35284306; PMCID: PMC8899432.
170. American College of Radiology. ACR Appropriateness Criteria®: Clinically Suspected Adnexal Mass. Available at: https://acsearch.acr.org/docs/69466/Narrative/. Accessed March 30, 3018.
171. ESUR recommendations for MR imaging of the sonographically indeterminate adnexal mass: an update. Forstner R, Thomassin-Naggara I, Cunha TM, Kinkel K, Masselli G, Kubik-Huch R, Spencer JA, Rockall A.Eur Radiol. 2017 Jun;27(6):2248-2257. doi: 10.1007/s00330-016-4600-3.Oct 21.PMID: 27770228
172. Michielsen K, Dresen R, Vanslembrouck R, et al. Diagnostic value of whole body diffusion-weighted MRI compared to computed tomography for pre-operative assessment of patients suspected for ovarian cancer. Eur J Cancer 2017;83:88–98.;
173.Vandecaveye V, Dresen R, De Keyzer F. Novel imaging techniques in gynaecological cancer. Curr Opin Oncol 2017;29:335–42;
174.ACR Appropriateness Criteria® Staging and Follow-Up of Ovarian Cancer. Expert Panel on Women’s Imaging:; Kang SK, Reinhold C, Atri M, Benson CB, Bhosale PR, Jhingran A, Lakhman Y, Maturen KE, Nicola R, Pandharipande PV, Salazar GM, Shipp TD, Simpson L, Small W Jr, Sussman BL, Uyeda JW, Wall DJ, Whitcomb BP, Zelop CM, Glanc P.J Am Coll Radiol. 2018 May;15(5S):S198-S207. doi: 10.1016/j.jacr.2018.03.015.PMID: 29724422
175. Lee E.Y.P., An H., Tse K.Y., Khong P.-L. Molecular Imaging of Peritoneal Carcinomatosis in Ovarian Carcinoma. Am. J. Roentgenol. 2020;215:305–312. doi: 10.2214/AJR.19.22621.
176. Prado J.G., Hernando C.G., Delgado D.V., Martínez R.S., Bhosale P., Sanchez J.B., Chiva L. Diffusion-weighted magnetic resonance imaging in peritoneal carcinomatosis from suspected ovarian cancer: Diagnostic performance in correlation with surgical findings. Eur. J. Radiol. 2019;121:108696. doi: 10.1016/j.ejrad.2019.108696.
177. Rizzo S., De Piano F., Buscarino V., Pagan E., Bagnardi V., Zanagnolo V., Colombo N., Maggioni A., Del Grande M., Del Grande F., et al. Pre-operative evaluation of epithelial ovarian cancer patients: Role of whole body diffusion weighted imaging MR and CT scans in the selection of patients suitable for primary debulking surgery. A single-centre study. Eur. J. Radiol. 2020;123:108786. doi: 10.1016/j.ejrad.2019.108786.
178. Yoshida Y, Kurokawa T, Tsuchida T et al (2004) The incremental benefits of FDG positron emission tomography over CT alone for the preoperative staging of ovarian cancer. AJR Am J Roentgenol 182:227–233 2779;
179. Kitajima K, Murakami K, Yamasaki E et al (2008) Diagnostic accuracy of integrated FDG-PET/contrast enhanced CT in staging ovarian cancer:comparison with enhanced CT. Eur J
Nucl Med Mol Imaging 35:1912–1920;
180. Expert Panel on Women"s Imaging, Kang SK, Reinhold C, et al. ACR Appropriateness Criteria((R)) Staging and Follow-Up of Ovarian Cancer. J Am Coll Radiol 2018;15:S198-S207]
181. Kitajima K, Murakami K, Yamasaki E et al (2008) Diagnostic accuracy of integrated FDG-PET/contrast enhanced CT in staging ovarian cancer:comparison with enhanced CT. Eur J Nucl Med Mol Imaging 35:1912–1920]
182. Franciszek Dłuski, D.; Mierzyński, R.; Poniedziałek-Czajkowska, E.; Leszczyńska-Gorzelak, B. Ovarian Cancer and Pregnancy—A Current Problem in Perinatal Medicine: A Comprehensive Review. Cancers 2020, 12, 3795. https://doi.org/10.3390/cancers12123795
183. NCCN Clinical Practice Guidelines in Oncology (NCCN Guidelines®) Ovarian Cancer Continue Including Fallopian Tube Cancer and Primary Peritoneal Cancer Version 1.2023, nccn.org)
184. ACR Appropriateness Criteria® Staging and Follow-Up of Ovarian Cancer. Expert Panel on Women’s Imaging:; Kang SK, Reinhold C, Atri M, Benson CB, Bhosale PR, Jhingran A, Lakhman Y, Maturen KE, Nicola R, Pandharipande PV, Salazar GM, Shipp TD, Simpson L, Small W Jr, Sussman BL, Uyeda JW, Wall DJ, Whitcomb BP, Zelop CM, Glanc P.J Am Coll Radiol. 2018 May;15(5S):S198-S207. doi: 10.1016/j.jacr.2018.03.015.PMID: 29724422;
185. Cengiz A, Koç ZP, Özcan Kara P, Yürekli Y. The Role of 18F-FDG PET/CT in Detecting Ovarian Cancer Recurrence in Patients with Elevated CA-125 Levels. Mol Imaging Radionucl Ther. 2019 Mar 19;28(1):8-14. doi: 10.4274/mirt.galenos.2018.00710. PMID: 30942056; PMCID: PMC6455098;
186. Gu P, Pan LL, Wu SQ et al (2009) CA125, PET alone, PET-CT. CT and MRI in diagnosing recurrent ovarian carcinoma A systematic review Eur J Radiol 71:164–174.
187. Тюляндина А. С. и др. Практические рекомендации по лекарственному лечению рака яичников, первичного рака брюшины и рака маточных труб //Злокачественные опухоли. – 2021. – Т. 11. – №. 3S2-1. – С. 158-171. DOI: 10.18027 / 2224-5057-2021-11-3s2-10