Εμφανίζονται 1 - 2 Αποτελέσματα από 2 για την αναζήτηση '"тотальная неоадъювантная терапия"', χρόνος αναζήτησης: 0,43δλ Περιορισμός αποτελεσμάτων
  1. 1
    Academic Journal

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

    Πηγή: Malignant tumours; Том 14, № 2 (2024); 65-74 ; Злокачественные опухоли; Том 14, № 2 (2024); 65-74 ; 2587-6813 ; 2224-5057

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    Relation: https://www.malignanttumors.org/jour/article/view/1328/945; Злокачественные новообразования в России в 2018 году (заболеваемость и смертность). Под ред. А.Д. Каприна, В.В. Старинского, Г.В. Петровой. М.: МНИОИ им. П.А. Герцена – филиал ФГБУ «НМИЦ радиологии» Минздрава России, 2019.250 с.; The Beyond TME Collaborative. Consensus statement on the multidisciplinary management of patients with recurrent and primary rectal cancer beyond total mesorectal excision planes. Br J Surg 2013;100(8):1009–1014. doi:10.1002/bjs.9192; Zwart W.H., Hotca A., Hospers G.A.P., et al. The multimodal management of locally advanced rectal cancer: making sense of the new data. Am Soc Clin Oncol Educ Book 2022;42:1–14. doi:10.1200/EDBK_351411; Mendis S., Hang To Y., Tie J. Biomarkers in locally advanced rectal cancer : a review. Clin Colorectal Cancer 2022;21(1):36–44. doi:10.1016/j.clcc.2021.11.002; Van Gijn W., Marijnen C.A.M., Nagtegaal I.D., et al. Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer: 12-year follow-up of the multicentre, randomised controlled TME trial. Lancet Oncol. 2011;12(6):575–582. doi:10.1016/S1470-2045(11)70097-3; Erlandsson J., Holm T., Pettersson D., et al. Optimal fractionation of preoperative radiotherapy and timing to surgery for rectal cancer (Stockholm III): a multicentre, randomised, non-blinded, phase 3, non-inferiority trial. Lancet Oncol 2017;18(3):336–346. doi:10.1016/S1470-2045(17)30086-4; Cionini L., Sainato A., De Paoli A., et al. Final results of randomized trial on adjuvant chemotherapy after preoperative chemoradiation in rectal cancer. Radiother Oncol 2010;96: S113-S114.; Breugom A.J., Swets M., Bosset J.F., et al. Adjuvant chemotherapy after preoperative (chemo) radiotherapy and surgery for patients with rectal cancer : a systematic review and meta-analysis of individual patient data. Lancet Oncol 2015;16(2):200–207. doi:10.1016/S1470-2045(14)71199-4; Morris M.C., Winer L.K., Lee T.C., et al. Omission of adjuvant chemotherapy in rectal cancer patients with pathologic complete response: a national analysis. J Gastrointest Surg 2021;25(7):1857–1865. doi:10.1007/s11605-020-04749-6; Bahadoer R.R., Dijkstra E.A., Van Etten B., et al. Short-course radiotherapy followed by chemotherapy before total mesorectal excision (TME) versus preoperative chemoradiotherapy, TME, and optional adjuvant chemotherapy in locally advanced rectal cancer (RAPIDO): a randomised, open-label, phase 3 trial. Lancet Oncol 2020;22(1):29–42. doi:10.1016/S1470-2045(20)30555-6; Conroy T., Bosset J.-F., Etienne P-L., et al. Neoadjuvant chemotherapy with FOLFIRINOX and preoperative chemoradiotherapy for patients with locally advanced rectal cancer (UNICANCER-PRODIGE 23): a multicentre, randomised, open-label, phase 3 trial; Lancet Oncol 2021;22(5):702–715. doi: /10.1016/S1470-2045(21)00079-6; Jin J., Tang Y., Hu C., et al. Multicenter, randomized, phase III trial of short-term radiotherapy plus chemotherapy versus long-term chemoradiotherapy in locally advanced rectal cancer (STELLAR). J Clin Oncol 2022;40(15):1681–1692. doi:10.1200/JCO.21.01667; Liao C.-K., Kuo Y.-T., Lin Y.-C. et. al. Neoadjuvant short-course radiotherapy followed by consolidation chemotherapy before surgery for treating locally advanced rectal cancer : a systematic review and meta-analysis. Curr Oncol 2022;29(5):3708–3727. doi:10.3390/curroncol29050297; Sauer R., Liersch T., Merkel S., et al. Preoperative versus postoperative chemoradiotherapy for locally advanced rectal cancer: results of the German CAO/ARO/AIO-94 randomized phase III trial after a median follow-up of 11 years. J Clin Oncol 2012;30(16):1926–1933. doi:10.1200/JCO.2011.40.1836; Gao Y.-H., Lin J.-Z., An X., et al. Neoadjuvant sandwich treatment with oxaliplatin and capecitabine administered prior to, concurrently with, and following radiation therapy in locally advanced rectal cancer: a prospective phase 2 trial. Int J Radiat Oncol Biol Phys 2014;90(5):1153–1160. doi:10.1016/j.ijrobp.2014.07.021; Fernandez-Martos C., Garcia-Albeniz X., Pericay C., et al. Chemoradiation, surgery and adjuvant chemotherapy versus induction chemotherapy followed by chemoradiation and surgery: long-term results of the Spanish GCR-3 phase II randomized trial. Ann Oncol 2015;26(8):1722–1728. doi:10.1093/annonc/mdv223; Bujko K., Wyrwicz L., Rutkowski A., et al. Long-course oxaliplatin-based preoperative chemoradiation versus 5 × 5 Gy and consolidation chemotherapy for cT4 or fixed cT3 rectal cancer: results of a randomized phase III study. Ann Oncol 2016;27(5):834–842. doi:10.1093/annonc/mdw062; Fokas E., Allgäuer M., Polat B., et al. Randomized phase ii trial of chemoradiotherapy plus induction or consolidation chemotherapy as total neoadjuvant therapy for locally advanced rectal cancer: CAO/ARO/AIO-12. J Clin Oncol 2019;37(34):3212–3222. doi:10.1200/JCO.19.00308.; Dijkstra E.A., Nilsson P.J., Hospers G.A.P., et al. Locoregional failure during and after short-course radiotherapy followed by chemotherapy and surgery compared with long-course chemoradiotherapy and surgery. A 5-year follow-up of the RAPIDO trial. Ann Surg 2023;278(4):e766-e772. doi:10.1097/SLA.0000000000005799; Romesser P.B., Park B.K., Nemirovsky D., et al. Organ preservation and total neoadjuvant therapy for rectal cancer: Investigating long course chemoradiation versus short course radiation therapy. Meeting Abstract 2023 ASCO Annual Meeting I GASTROINTESTINAL CANCER—COLORECTAL AND ANAL. doi:10.1200/JCO.2023.41.4_suppl.10; Garcia-Aguilar J., Patil S., Gollub M.J., et al. Organ preservation in patients with rectal adenocarcinoma treated with total neoadjuvant therapy. J Clin Oncol 2022:40(23):2546–2556. doi:10.1200/JCO.22.00032; Petrelli F., Trevisan F., Cabiddu M., et al. Total neoadjuvant therapy in rectal cancer : a systematic review and meta-analysis of treatment outcomes. Ann Surg 2020;271(3):440–448. doi:10.1097/SLA.0000000000003471; Liu S., Jiang T., Xiao L., et al. Total neoadjuvant therapy (TNT) versus standard neoadjuvant chemoradiotherapy for locally advanced rectal cancer : a systematic review and meta-analysis. Oncologist 2021;26(9):e1555-e1566. doi:10.1002/onco.13824; Kong J.C., Soucisse M., Michael M., et al. Total neoadjuvant therapy in locally advanced rectal cancer : a systematic review and metaanalysis of oncological and operative outcomes. Ann Surg Oncol 2021;28(12):7476–7486. doi:10.1245/s10434-021-09837-8; Wu Q., Zhou J., Huang J., et al. Total neoadjuvant therapy versus chemoradiotherapy for locally advanced rectal cancer: Bayesian network meta-analysis. Br J Surg 2023;110(7):784–796. doi:10.1093/bjs/znad120; Habr-Gama A., Perez R.O., Nadalin W., et al. Operative versus nonoperative treatment for stage 0 distal rectal cancer following chemoradiation therapy: long-term results. Ann Surg 2004;240(4):711–717. doi:10.1097/01.sla.0000141194.27992.32; Garcia-Aguilar J., Chow O.S., Smith D.D., et al. Effect of adding mFOLFOX6 after neoadjuvant chemoradiation in locally advanced rectal cancer: a multicentre, phase 2 trial. Lancet Oncol 2015;16(8):957–966. doi:10.1016/S1470-2045(15)00004-2; Markovina S., Youssef F., Roy A., et al. Improved metastasis- and disease-free survival with preoperative sequential short-course radiation therapy and FOLFOX chemotherapy for rectal cancer compared with neoadjuvant long-course chemoradiotherapy: results of a matched pair analysis. Int J Radiat Oncol Biol Phys 2017;99(2):417–426. doi:10.1016/j.ijrobp.2017.05.048; Glynne-Jones R., Counsell N., Quirke P., et al. Chronicle: results of a randomised phase III trial in locally advanced rectal cancer after neoadjuvant chemoradiation randomising postoperative adjuvant capecitabine plus oxaliplatin (XELOX) versus control. Ann Oncol 2014;25(7):1356–62. doi:10.1093/annonc/mdu147; Breugom A.J., van Gijn W., Muller E.W., et al. Adjuvant chemotherapy for rectal cancer patients treated with preoperative (chemo) radiotherapy and total mesorectal excision: a Dutch Colorectal Cancer Group (DCCG) randomized phase III trial. Ann Oncol 2015;26(4):696–701. doi:10.1093/annonc/mdu560; Hong Y.S., Kim S.Y., Lee J.S., et al. Oxaliplatin-based adjuvant chemotherapy for rectal cancer after preoperative chemoradiotherapy (ADORE): long-term results of a randomized controlled trial. J Clin Oncol 2019;37(33):3111–3123. doi:10.1200/JCO.19.00016; Dijkstra E.A., Hospers G.A., Kranenbarg E.M.-K., et al. Quality of life and late toxicity after short-course radiotherapy followed by chemotherapy or chemoradiotherapy for locally advanced rectal cancer–The RAPIDO trial. Radiother Oncol 2022;171:69–76. doi:10.1016/j.radonc.2022.04.013.; https://www.malignanttumors.org/jour/article/view/1328

  2. 2
    Academic Journal

    Πηγή: Surgery and Oncology; Том 14, № 1 (2024); 21-31 ; Хирургия и онкология; Том 14, № 1 (2024); 21-31 ; 2949-5857

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    Relation: https://www.onco-surgery.info/jour/article/view/687/451; Sakamoto T., Shimura M., Kitano S. et al. Extramural depth of tumor invasion at thin-section MR in patients with rectal cancer: results of the MERCURY study. Radiology 2007;243(1):132–9. DOI:10.1148/radiol.2431051825; Engstrom P.F., Arnoletti J.P., Benson A.B. 3rd et al. Rectal cancer. J Natl Compr Canc Netw 2009:7(8):838–81. DOI:10.6004/jnccn.2009.0057; De Caluwé L., Van Nieuwenhove Y., Ceelen W.P. Preoperative chemoradiation versus radiation alone for stage II and III resectable rectal cancer. Cochrane Database Syst Rev 2013(2):CD006041. DOI:10.1002/14651858.CD006041.pub3; Bahadoer R.R., Dijkstra E.A., van Etten B. et al. Short-course radiotherapy followed by chemotherapy before total mesorectal excision (TME) versus preoperative chemoradiotherapy, TME, and optional adjuvant chemotherapy in locally advanced rectal cancer (RAPIDO): a randomised, open-label, phase 3 trial. Lancet Oncol 2021;22(1):29–42. 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Selective approach for upper rectal cancer treatment: total mesorectal excision and preoperative chemoradiation are seldom necessary. Dis Colon Rectum 2015;58(6):556–65. DOI:10.1097/DCR.0000000000000349; Rosenberg R., Maak M., Schuster T. et al. Does a rectal cancer of the upper third behave more like a colon or a rectal cancer? Dis Colon Rectum 2010;53(5):761–70. DOI:10.1007/DCR.0b013e3181cdb25a; Folkesson J., Birgisson H., Pahlman L. et al. Swedish Rectal Cancer Trial: long lasting benefits from radiotherapy on survival and local recurrence rate. J Clin Oncol 2005;23(24):5644–50. DOI:10.1200/JCO.2005.08.144; Sebag-Montefiore D., Stephens R.J., Steele R. et al. Preoperative radiotherapy versus selective postoperative chemoradiotherapy in patients with rectal cancer (MRC CR07 and NCIC-CTG C016): a multicentre, randomised trial. Lancet 2009;373(9666):811–20. DOI:10.1016/S0140-6736(09)60484-0; Van Gijn W., Marijnen C.A., Nagtegaal I.D. et al. Preoperative radiotherapy combined with total mesorectal excision for resectable rectal cancer: 12-year follow-up of the multicentre, randomised controlled TME trial. Lancet Oncol 2011;12(6):575–82. DOI:10.1016/S1470-2045(11)70097-3; Morton D., Seymour M., Magill L. et al. Preoperative chemotherapy for operable colon cancer: mature results of an international randomized controlled trial. J Clin Oncol 2023;41(8):1541. DOI:10.1200/JCO.22.00046; Hu H., Huang M., Li Y. et al. Perioperative chemotherapy with mFOLFOX6 or CAPOX for patients with locally advanced colon cancer (OPTICAL): A multicenter, randomized, phase 3 trial. J Clin Oncol 2022;40(16_suppl). DOI:10.1200/JCO.2022.40.16_suppl.3500; Jensen L.H., Kjaer M.L., Holländer N.H., Larsen F.O. Phase III randomized clinical trial comparing the efficacy of neoadjuvant chemotherapy and standard treatment in patients with locally advanced colon cancer: The NeoCol trial. J Clin Oncol 2023;41(17_suppl):LBA3503. DOI:10.1200/JCO.2023.41.17_suppl.LBA3503; Karoui M., Rullier A., Piessen G. et al. Perioperative FOLFOX 4 versus FOLFOX 4 plus cetuximab versus immediate surgery for high-risk stage II and III colon cancers: a phase II multicenter randomized controlled trial (PRODIGE 22). Ann Surg 2020;271(4):637–45. DOI:10.1097/SLA.0000000000003454; Ngan S.Y., Burmeister B., Fisher R.J. et al. Randomized trial of short-course radiotherapy versus long-course chemoradiation comparing rates of local recurrence in patients with T3 rectal cancer: Trans-Tasman Radiation Oncology Group trial 01.04. J Clin Oncol 2012;30(31):3827–33. DOI:10.1200/JCO.2012.42.9597; Cisel B., Pietrzak L., Michalski W. et al. Long-course preoperative chemoradiation versus 5 × 5 Gy and consolidation chemotherapy for clinical T4 and fixed clinical T3 rectal cancer: long-term results of the randomized Polish II study. Ann Oncol 2019;30(8):1298–303. DOI:10.1093/annonc/mdz186; Dijkstra E.A., Hospers G.A.P., Kranenbarg E.M. et al. 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Neoadjuvant chemotherapy with CAPOX versus Chemoradiation for Locally Advanced Rectal Cancer with Uninvolved Mesorectal Fascia (CONVERT): initial results of a phase III trial. Ann Surg 2023;277(4):557–64. DOI:10.1097/SLA.0000000000005780; Hazen S.-M.J., Sluckin T.C., Intven M.P.W. et al. Abandonment of Routine Radiotherapy for Nonlocally Advanced Rectal Cancer and Oncological Outcomes. JAMA Oncol 2024;10(2):202–11. DOI:10.1001/jamaoncol.2023.5444; Sychev S., Ponomarenko A., Chernyshov S. et al. Total neoadjuvant therapy in rectal cancer: a network meta-analysis of randomized trials. Ann Coloproctol 2023;39(4):289–300. DOI:10.3393/ac.2022.00920.0131; Verheij F.S., Omer D.M., Williams H. et al. Long-Term Results of Organ Preservation in Patients With Rectal Adenocarcinoma Treated With Total Neoadjuvant Therapy: The Randomized Phase II OPRA Trial. J Clin Oncol 2023:42(5):500–6. DOI:10.1200/JCO.23.01208; Liao C.-K., Kuo Y.T., Lin Y.C. et al. 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Long-term outcomes of clinical complete responders after neoadjuvant treatment for rectal cancer in the International Watch & Wait Database (IWWD): an international multicentre registry study. Lancet 2018;391(10139):2537–45. DOI:10.1016/S0140-6736(18)31078-X; Ellis C.T., Cole A.L., Sanoff H.K. et al. Evaluating surveillance patterns after Chemoradiation-only compared with conventional Management for Older Patients with rectal cancer. J Am Coll Surg 2019;228(5):782–91. DOI:10.1016/j.jamcollsurg.2019.01.010; Giordano P., Efron J., Vernava A.M. 3rd et al. Strategies of followup for colorectal cancer: a survey of the American Society of Colon and Rectal Surgeons. Tech Coloproctol 2006;10(3):199–207. DOI:10.1007/s10151-006-0280-3; Федянин М., Гладков О., Гордеев С. и др. Рак ободочной кишки, ректосигмоидного соединения и прямой кишки. Злокачественные опухоли 2023;13(3s2-1):425–82. DOI:10.18027/2224-5057-2023-13-3s2-1-425-482; Федянин М., Трякин А.А., Буланов А.А. и др. К вопросу о числе лимфатических узлов, необходимых к изучению при раке толстой кишки II стадии. Тазовая хирургия и онкология 2019;9(1):42–50. DOI:10.17650/2220-3478-2019-9-1-42-50; Jeon J., Shen L., Kim Y. et al. The number of lymph nodes examined as a poor prognosis factor in stage II and stage III colon cancer patients undergoing curative surgery. J Clin Oncol 2023;41(16_suppl). DOI:10.1200/JCO.2023.41.16_suppl.3612; Ahmed F., Selfridge J., Kakishet H. et al. SO-19 The outcome of resected stage II colon cancer patients with deficient mismatch repair T4 tumors: A National Cancer Database analysis. Ann Oncol 2023;34(1_suppl):S170. DOI:10.1016/j.annonc.2023.04.491; Fleming P., Chen Ch., Moore D.F. et al. High-risk MSI-H stage II colon cancer: Treatment patterns and outcomes. J Clin Oncol 2022;40(16_suppl). DOI:10.1200/JCO.2022.40.16_suppl.e15588; Oki E., Kotani D., Nakamura Y. et al. 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