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  1. 1
    Academic Journal

    Contributors: The article was prepared without sponsorship., Статья подготовлена без спонсорской поддержки.

    Source: Malignant tumours; Том 14, № 4 (2024); 50-57 ; Злокачественные опухоли; Том 14, № 4 (2024); 50-57 ; 2587-6813 ; 2224-5057

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    Relation: https://www.malignanttumors.org/jour/article/view/1425/1024; Banerjee S., Moore K.N., Colombo N., et al. Maintenance olaparib for patients with newly diagnosed advanced ovarian cancer and a BRCA mutation (SOLO1/GOG 3004): 5-year follow-up of a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Oncol 2021;22(12):1721–1731. https://doi.org/10.1016/S1470-2045(21)00531-3; DiSilvestro P., Banerjee S., Colombo N., et al. Overall survival with maintenance olaparib at a 7-year follow-up in patients with newly diagnosed advanced ovarian cancer and a BRCA mutation: The SOLO1/GOG 3004 trial. J Clin Oncol Off J Am Soc Clin Oncol 2023;41(3):609–617. https://doi.org/10.1200/JCO.22.01549; Wu X., Liu J., Wang J., et al. Senaparib as first-line maintenance therapy in advanced ovarian cancer: a randomized phase 3 trial. Nat Med 2024;30(6):1612–1621. https://doi.org/10.1038/s41591-024-03003-9; González-Martín A., Pothuri B., Vergote I., et al. Progression-free survival and safety at 3.5 years of follow-up: results from the randomised phase 3 PRIMA/ENGOT-OV26/GOG-3012 trial of niraparib maintenance treatment in patients with newly diagnosed ovarian cancer. Eur J Cancer 2023;189:112908. https://doi.org/10.1016/j.ejca.2023.04.024; Monk B.J., Parkinson C., Lim M.C., et al. A randomized, phase III trial to evaluate rucaparib monotherapy as maintenance treatment in patients with newly diagnosed ovarian cancer (ATHENA–MONO/GOG-3020/ENGOT-ov45). J Clin Oncol 2022;40(34):3952–3964. https://doi.org/10.1200/JCO.22.01003; Dias M.P., Moser S.C., Ganesan S., Jonkers J. Understanding and overcoming resistance to PARP inhibitors in cancer therapy. Nat Rev Clin Oncol 2021;18(12):773–791. https://doi.org/10.1038/s41571-021-00532-x; Frenel J.S., Kim J.W., Aryal N., et al. Efficacy of subsequent chemotherapy for patients with BRCA1/2-mutated recurrent epithelial ovarian cancer progressing on olaparib versus placebo maintenance: post-hoc analyses of the SOLO2/ ENGOT Ov-21 trial. Ann Oncol 2022;33(10):1021–1028. https://doi.org/10.1016/j.annonc.2022.06.011; Ho D.E., Imai K., King G., Stuart E.A. MatchIt: Nonparametric Preprocessing for Parametric Causal Inference. J Stat Softw 2011;42(8). https://doi.org/10.18637/jss.v042.i08; Fortin S.P., Johnston S.S., Schuemie M.J. Applied comparison of large-scale propensity score matching and cardinality matching for causal inference in observational research. BMC Med Res Methodol 2021;21(1):109. https://doi.org/10.1186/s12874-021-01282-1; Harter P., Mouret-Reynier M.A., Lorusso D., et al. Efficacy of subsequent therapies in patients (pts) with advanced ovarian cancer (AOC) in the phase III PAOLA-1/ENGOT-ov25 trial according to whether disease progression occurred during or after the end of olaparib (ola) maintenance. J Clin Oncol 2023;41(16_suppl):5550–5550. https://doi.org/10.1200/JCO.2023.41.16_suppl.5550.; https://www.malignanttumors.org/jour/article/view/1425

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    Academic Journal

    Source: Siberian journal of oncology; Том 22, № 4 (2023); 14-21 ; Сибирский онкологический журнал; Том 22, № 4 (2023); 14-21 ; 2312-3168 ; 1814-4861

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    Relation: https://www.siboncoj.ru/jour/article/view/2673/1133; Astaras C., Bornand A., Koessler T. Squamous rectal carcinoma: a rare malignancy, literature review and management recommendations. ESMO Open. 2021; 6(4). doi:10.1016/j.esmoop.2021.100180.; Sturgeon J.D., Crane C.H., Krishnan S., Minsky B.D., Skibber J.M., Rodriguez-Bigas M.A., Chang G.J., You Y.N., Eng C., Das P. Defnitive Chemoradiation for Squamous Cell Carcinoma of the Rectum. Am J Clin Oncol. 2017; 40(2): 163–6. doi:10.1097/COC.0000000000000126.; Malakhov N., Kim J.K., Adedoyin P., Albert A., Schreiber D., Lee A. Patterns of Care and Outcomes of Low-Lying Adenocarcinoma and Squamous Cell Carcinoma of the Rectum. J Gastrointest Cancer. 2022; 53(1): 105–12. doi:10.1007/s12029-020-00552-3.; Клинические рекомендации «Рак прямой кишки». М: 2022. 78 с.; Guerra G.R., Kong C.H., Warrier S.K., Lynch A.C., Heriot A.G., Ngan S.Y. Primary squamous cell carcinoma of the rectum: An update and implications for treatment. World J Gastrointest Surg. 2016; 8(3): 252–65. doi:10.4240/wjgs.v8.i3.252.; Дудаев З.А., Худоеров Д.Х., Мамедли З.З., Алиев В.А., Гордеев С.С., Мышляков В.С. Тактика «watch and wait» (активное динамическое наблюдение) в лечении больных раком прямой кишки с клиническим полным ответом. Тазовая хирургия и онкология. 2022; 12(1): 35–40. doi:10.17650/2686-9594-2022-12-1-35-40.; Дудаев З.А., Худоеров Д.Х., Мамедли З.З., Алиев В.А., Гордеев С.С., Магаррамова З.Н. Непосредственные и отдаленные результаты лечения пациентов с раком средне- и нижнеампулярного отделов прямой кишки с клиническим и патоморфологическим полным ответом после комбинированной терапии. Тазовая хирургия и онкология. 2022; 12(1): 41–8. doi:10.17650/2686-9594-2022-12-1-41-48.; Dyson T., Draganov P.V. Squamous cell cancer of the rectum. World J Gastroenterol. 2009; 15(35): 4380–6. doi:10.3748/wjg.15.4380.; Jeong B.G., Kim D.Y., Kim S.Y. Concurrent chemoradiotherapy for squamous cell carcinoma of the rectum. Hepatogastroenterology. 2013; 60(123): 512–6. doi:10.5754/hge11293.; Dutta S.W., Alonso C.E., Waddle M.R., Khandelwal S.R., Janowski E.M., Trifletti D.M. Squamous cell carcinoma of the rectum: Practice trends and patient survival. Cancer Med. 2018; 7(12): 6093–103. doi:10.1002/cam4.1893.; Musio D., De Felice F., Manfrida S., Balducci M., Meldolesi E., Gravina G.L., Tombolini V., Valentini V. Squamous cell carcinoma of the rectum: The treatment paradigm. Eur J Surg Oncol. 2015; 41(8): 1054–8. doi:10.1016/j.ejso.2015.03.239.; Glynne-Jones R., Sebag-Montefore D., Meadows H.M., Cunningham D., Begum R., Adab F., Benstead K., Harte R.J., Stewart J., Beare S., Hackshaw A., Kadalayil L.; ACT II study group. Best time to assess complete clinical response after chemoradiotherapy in squamous cell carcinoma of the anus (ACT II): a post-hoc analysis of randomised controlled phase 3 trial. Lancet Oncol. 2017; 18(3): 347–56. doi:10.1016/S1470-2045(17)30071-2. Erratum in: Lancet Oncol. 2017; 18(4). Erratum in: Lancet Oncol. 2020; 21(11).; Id Said B., Buchan D., Liu Z., Kim J., Hosni A., Brierley J.D., Chadi S., Grant R.C., Kalimuthu S., Liu Z.A., Lukovic J. Demographics, pattern of practice and clinical outcomes in rectal squamous cell carcinoma. Colorectal Dis. 2023; 25(4): 608–15. doi:10.1111/codi.16417.; Loganadane G., Servagi-Vernat S., Schernberg A., Schlienger M., Touboul E., Bosset J.F., Huguet F. Chemoradiation in rectal squamous cell carcinoma: Bi-institutional case series. Eur J Cancer. 2016; 58: 83–9. doi:10.1016/j.ejca.2016.02.005.; Péron J., Bylicki O., Laude C., Martel-Lafay I., Carrie C., Racadot S. Nonoperative management of squamous-cell carcinoma of the rectum. Dis Colon Rectum. 2015; 58(1): 60–4. doi:10.1097/DCR.0000000000000218.; Steinemann D.C., Müller P.C., Billeter A.T., Bruckner T., Ulrich A., Müller-Stich B.P. Surgery is essential in squamous cell cancer of the rectum. Langenbecks Arch Surg. 2017; 402(7): 1055–62. doi:10.1007/s00423-017-1614-5.; Yang Y., Yu J., Hu J., Zhou C., Niu J., Ma H., Han J., Fan S., Liu Y., Zhao Y., Zhao L., Wang G. A systematic and comprehensive analysis of colorectal squamous cell carcinoma: Implication for diagnosis and treatment. Cancer Med. 2022; 11(12): 2492–502. doi:10.1002/cam4.4616.; Astaras C., De Vito C., Chaskar P., Bornand A., Khanfr K., Sciarra A., Letovanec I., Corro C., Dietrich P.Y., Tsantoulis P., Koessler T. The frst comprehensive genomic characterization of rectal squamous cell carcinoma. J Gastroenterol. 2023; 58(2): 125–34. doi:10.1007/s00535-022-01937-w.; Daling J.R., Madeleine M.M., Johnson L.G., Schwartz S.M., Shera K.A., Wurscher M.A., Carter J.J., Porter P.L., Galloway D.A., McDougall J.K. Human papillomavirus, smoking, and sexual practices in the etiology of anal cancer. Cancer. 2004; 101(2): 270–80. doi:10.1002/cncr.20365.; Alemany L., Saunier M., Alvarado-Cabrero I., Quirós B., Salmeron J., Shin H.R., Pirog E.C., Guimerà N., Hernandez-Suarez G., Felix A., Clavero O., Lloveras B., Kasamatsu E., Goodman M.T., Hernandez B.Y., Laco J., Tinoco L., Geraets D.T., Lynch C.F., Mandys V., Poljak M., Jach R., Verge J., Clavel C., Ndiaye C., Klaustermeier J., Cubilla A., Castellsagué X., Bravo I.G., Pawlita M., Quint W.G., Muñoz N., Bosch F.X., de Sanjosé S.; HPV VVAP Study Group. Human papillomavirus DNA prevalence and type distribution in anal carcinomas worldwide. Int J Cancer. 2015; 136(1): 98–107. doi:10.1002/ijc.28963.; André F., Ciruelos E.M., Juric D., Loibl S., Campone M., Mayer I.A., Rubovszky G., Yamashita T., Kaufman B., Lu Y.S., Inoue K., Pápai Z., Takahashi M., Ghaznawi F., Mills D., Kaper M., Miller M., Conte P.F., Iwata H., Rugo H.S. Alpelisib plus fulvestrant for PIK3CAmutated, hormone receptor-positive, human epidermal growth factor receptor-2-negative advanced breast cancer: fnal overall survival results from SOLAR-1. Ann Oncol. 2021; 32(2): 208–17. doi:10.1016/j.annonc.2020.11.011.; Kalinsky K., Hong F., McCourt C.K., Sachdev J.C., Mitchell E.P., Zwiebel J.A., Doyle L.A., McShane L.M., Li S., Gray R.J., Rubinstein L.V., Patton D., Williams P.M., Hamilton S.R., Conley B.A., O'Dwyer P.J., Harris L.N., Arteaga C.L., Chen A.P., Flaherty K.T. Efect of Capivasertib in Patients With an AKT1 E17K-Mutated Tumor: NCI-MATCH Subprotocol EAY131-Y Nonrandomized Trial. JAMA Oncol. 2021; 7(2): 271–8. doi:10.1001/jamaoncol.2020.6741. Erratum in: JAMA Oncol. 2021.; Yap T.A., Tan D.S.P., Terbuch A., Caldwell R., Guo C., Goh B.C., Heong V., Haris N.R.M., Bashir S., Drew Y., Hong D.S., Meric-Bernstam F., Wilkinson G., Hreiki J., Wengner A.M., Bladt F., Schlicker A., Ludwig M., Zhou Y., Liu L., Bordia S., Plummer R., Lagkadinou E., de Bono J.S. Firstin-Human Trial of the Oral Ataxia Telangiectasia and RAD3-Related (ATR) Inhibitor BAY 1895344 in Patients with Advanced Solid Tumors. Cancer Discov. 2021; 11(1): 80–91. doi:10.1158/2159-8290.CD-20-0868.; https://www.siboncoj.ru/jour/article/view/2673

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    Academic Journal

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  5. 5
    Academic Journal

    Source: Cancer Urology; Том 16, № 3 (2020); 126-134 ; Онкоурология; Том 16, № 3 (2020); 126-134 ; 1996-1812 ; 1726-9776

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    Relation: https://oncourology.abvpress.ru/oncur/article/view/1308/1199; https://oncourology.abvpress.ru/oncur/article/view/1308/1238; Babjuk M., Burger M., Comperat E.M. et al. European Association of Urology Guidelines on Nonmuscle-invasive Bladder Cancer (TaT1 and Carcinoma In Situ): 2019 update. Eur Urol 2019;76(5):639-57. DOI:10.1016/j.eururo.2019.08.016.; Chang S.S., Boorjian S.A., Chou R. et al. Diagnosis and treatment of non-muscle invasive bladder Cancer: AUA/SUO guideline. J Urol 2016;196 (4):1021-9. DOI:10.1016/j.juro.2016.06.049.; Злокачественные опухоли (спецвыпуск журнала): практические рекомендации Российского общества клинической онкологии. Лекарственное лечение злокачественных опухолей. Поддерживающая терапия в онкологии. Под ред. В.М. Моисеенко. М.: Общероссийская общественная организация «Российское общество клинической онкологии», 2018. 704 с.; Bohle A., Jocham D., Bock P.R. Intravesical bacillus Calmette-Guerin versus mitomycin C for superficial bladder cancer: a formal meta-analysis of comparative studies on recurrence and toxicity. J Urol 2003;169(1):90-5. DOI:10.1097/01.ju.0000039680.90768.b3.; Sylvester R.J., Brausi M.A., Kirkels W.J. et al. Long-term efficacy results of EORTC Genito-Urinary Group randomized phase 3 study 30911 comparing intravesical instillations of epirubicin, bacillus Calmette-Guerin, and bacillus Calmette-Guerin plus isoniazid in patients with intermediate- and high-risk stage Ta T1 urothelial carcinoma of the bladder. Eur Urol 2010;57(5):766-73. DOI:10.1016/j.eururo.2009.12.024.; Fernandez-Gomez J., Madero R., Solsona E. et al. Predicting nonmuscle invasive bladder cancer recurrence and progression in patients treated with bacillus Calmette-Guerin: the CUETO scoring model. J Urol 2009;182(5):2195-203. DOI:10.1016/j.juro.2009.07.016.; Солодова А.А. БЦЖ-терапия в России: инстинкт самосохранения и министерские документы. Урология сегодня 2019;2(52). Доступно по: http://www.urotoday.ru/article/id-171.; Davies B.J., Hwang T.J., Kesselheim A.S. Ensuring access to injectable generic drugs: the case of intravesical BCG for bladder cancer. N Engl J Med 2017;376(15):1401-3. DOI:10.1056/NEJMp1615697.; Зорина М.М., Кульчавеня Е.В., Холто-бин Д.П. Правовые основы BCG-терапии для лечения рака мочевого пузыря в условиях муниципальных поликлиник. Туберкулез и болезни легких 2016;94(10):55-61.; Oddens J., Brausi M., Sylvester R. et al. Final results of an EORTC-GU cancers group randomized study of maintenance bacillus Calmette-Guerin in intermediate- and high risk Ta, T1 papillary carcinoma of the urinary bladder: one-third dose versus full dose and 1 year versus 3 years of maintenance. Eur Urol 2013;63(3):462-72. DOI:10.1016/j.eururo.2012.10.039.; Sylvester R.J., Oosterlinck W., van der Meijden A.P. A single immediate postoperative instillation of chemotherapy decreases the risk of recurrence in patients with stage Ta T1 bladder cancer: a metaanalysis of published results of randomized clinical trials. J Urol 2004;171 (6 Pt 1):2186-90. DOI:10.1097/01.ju.0000125486.92260.b2.; Friedrich M.G., Pichlmeier U., Schwaibold H. et al. Long-term intravesical adjuvant chemotherapy further reduces the recurrence rate compared with shortterm intravesical chemotherapy and shortterm therapy with bacillus Calmette-Guerin (BCG) in patients with non-muscle-invasive bladder carcinoma. Eur Urol 2007;52(4):1123-29. DOI:10.1016/j.eururo.2007.02.063.; Veeratterapillay R., Heer R., Johnson M.I. et al. High-risk non-muscle-invasive bladder cancer-therapy options during intravesical BCG shortage. Curr Urol Rep 2016;17(9):68. DOI:10.1007/s11934-016-0625-z.; Новые технологии в медицине. Тизоль: сборник научных статей. Под ред. В.И. Шилко. Екатеринбург: УГМА, 2003. 152 с. [New technologies in medicine. Tizol: collection of research articles. Ed.: V.I. Shilko. Yekaterinburg: UGMA, 2003. 152 p. (In Russ.)].; Высокоэффективные технологии в медицине. Тизоль: сборник материалов межобластной конференции (15 марта 2001 г.). Екатеринбург: УГМА. 80 c.; Замятин А.В., Магер В.О., Орлов А.С. и др. Отдаленные результаты адъювантной внутрипузырной химиотерапии с аквакомплексом глицеросольвата титана у больных немышечно-инвазив-ным раком мочевого пузыря высокого риска. Онкоурология 2019;15(1): 92-100.; Rosenbaum P.R., Rubin D.B. The central role of the propensity score in observational studies for causal effects. Biometrika 1983;70(1):41-55.; Гржибовский А.М., Иванов С.В., Горбатова М.А., Дюсупов А.А. Псевдорандомизация (propensity score matching) как современный статистический метод устранения систематических различий сравниваемых групп при анализе количественных исходов в обсервационных исследованиях. Экология человека 2016;(7):51-60.; EAU Guidelines. Edn. presented at the EAU Annual Congress Amsterdam 2020.; Flaig T.W., Spiess P.E., Agarwal N. et al. NCCN Clinical Practice Guidelines in Oncology Bladder Cancer Version 3, 2019. Available at: https://www.nccn.org/professionals/physician_gls/PDF/bladder.pdf. Accessed July, 2019.; Martmez-Pineiro J.A., Leon J. J., Martmez-Pineiro L. Jr et al. Bacillus Calmette-Guerin versus doxorubicin versus thiotepa: a randomized prospective study in 202 patients with superficial bladder cancer. J Urol 1990;143(3):502-6. DOI:10.1016/s0022-5347(17)40002-4.; Chou R., Selph S., Buckley D. et al. Intravesical therapy for the treatment of nonmuscle invasive bladder cancer: a systematic review and meta-analysis. J Urol 2017;197(5):1189-99. DOI:10.1016/j.juro.2016.12.090.; Malmstrom P.U., Sylvester R.J., Crawford D.E. et al. An individual patient data meta-analysis of the long-term outcome of randomised studies comparing intravesical mitomycin C versus bacillus Calmette-Guerin for non-muscleinvasive bladder cancer. Eur Urol 2009;56(2):247-56. DOI:10.1016/j.eururo.2009.04.038.; Arends T.J., van der Heijden A.G., Witjes J.A. Combined chemohyperthermia: 10-year single center experience in 160 patients with nonmuscle invasive bladder cancer. J Urol 2014;192 (3):708-13. DOI:10.1016/j.juro.2014.03.101.; Di Stasi S.M., Valenti M., Verri C. et al. Electromotive instillation of mitomycin immediately before transurethral resection for patients with primary urothelial nonmuscle invasive bladder cancer: a randomised controlled trial. Lancet Oncol 2011;12(9):871-9. DOI:10.1016/S1470-2045(11)70190-5.; Bendary L., Khalil S., Shahin A., Nawar N. 1655 intravesical gemcitabine versus bacillus Calmette-Guerin (BCG) in treatment of nonmuscle invasive bladder cancer: short term comparative study. J Urol 2011;185:e664-5.; Barlow L.J., Mckiernan J.M., Benson M.C. Longterm survival outcomes with intravesical docetaxel for recurrent nonmuscle invasive bladder cancer after previous bacillus Calmette-Guerin therapy. J Urol 2013;189(3):834-9. DOI:10.1016/j.juro.2012.10.068.; Kamat A.M., Colombel M., Sundi D. et al. BCG-unresponsive non-muscle-invasive bladder cancer: definition, treatment options and management recommendations from the International Bladder Cancer Group (IBCG). Nat Rev Urol 2017;14(4):244-55. DOI:10.1038/nrurol.2017.16.; https://oncourology.abvpress.ru/oncur/article/view/1308

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