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268 источников, процитированных на этой странице. Ссылки ведут к первоисточнику.

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  22. US Food and Drug Administration. Supplement approval letter, Camptosar (irinotecan hydrochloride injection), NDA 20-571/S-008, Pharmacia & Upjohn; letter dated 22 October 1998 (date stamp on the scanned letter; the letter also gives 22 October 1998 as the user-fee goal date). Источник
  23. International Multicentre Pooled Analysis of B2 Colon Cancer Trials (IMPACT B2) Investigators. Efficacy of adjuvant fluorouracil and folinic acid in B2 colon cancer. J Clin Oncol. 1999;17(5):1356-63. PubMedDOI
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  24. de Gramont A, Figer A, Seymour M, Homerin M, Hmissi A, Cassidy J, et al. Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer. J Clin Oncol. 2000;18(16):2938-47. PubMedDOI
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  25. Douillard JY, Cunningham D, Roth AD, Navarro M, James RD, Karasek P, et al. Irinotecan combined with fluorouracil compared with fluorouracil alone as first-line treatment for metastatic colorectal cancer: a multicentre randomised trial. Lancet. 2000;355(9209):1041-7. PubMedDOI
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  26. US Food and Drug Administration. Supplement approval letter, Camptosar (irinotecan hydrochloride injection), NDA 20-571/S-009, Pharmacia & Upjohn; letter dated 20 April 2000. Источник
  27. Giacchetti S, Perpoint B, Zidani R, Le Bail N, Faggiuolo R, Focan C, et al. Phase III multicenter randomized trial of oxaliplatin added to chronomodulated fluorouracil-leucovorin as first-line treatment of metastatic colorectal cancer. J Clin Oncol. 2000;18(1):136-47. PubMedDOI
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  28. Mandel JS, Church TR, Bond JH, Ederer F, Geisser MS, Mongin SJ, et al. The effect of fecal occult-blood screening on the incidence of colorectal cancer. N Engl J Med. 2000;343(22):1603-7. PubMedDOI
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  30. US Food and Drug Administration. Approval letter, Eloxatin (oxaliplatin) for Injection, NDA 21-492, Sanofi-Synthelabo, Inc.; electronically signed 9 August 2002. Источник
  31. Jørgensen OD, Kronborg O, Fenger C. A randomised study of screening for colorectal cancer using faecal occult blood testing: results after 13 years and seven biennial screening rounds. Gut. 2002;50(1):29-32. PubMedDOI
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  32. Longley DB, Harkin DP, Johnston PG. 5-fluorouracil: mechanisms of action and clinical strategies. Nat Rev Cancer. 2003;3(5):330-8. PubMedDOI
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  33. Ribic CM, Sargent DJ, Moore MJ, Thibodeau SN, French AJ, Goldberg RM, et al. Tumor microsatellite-instability status as a predictor of benefit from fluorouracil-based adjuvant chemotherapy for colon cancer. N Engl J Med. 2003;349(3):247-57. PubMedDOI
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  34. André T, Boni C, Mounedji-Boudiaf L, Navarro M, Tabernero J, Hickish T, et al. Oxaliplatin, fluorouracil, and leucovorin as adjuvant treatment for colon cancer. N Engl J Med. 2004;350(23):2343-51. PubMedDOI
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  35. Clinical Outcomes of Surgical Therapy Study Group, Nelson H, Sargent DJ, Wieand HS, Fleshman J, Anvari M, et al. A comparison of laparoscopically assisted and open colectomy for colon cancer. N Engl J Med. 2004;350(20):2050-9. PubMedDOI
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  36. Cunningham D, Humblet Y, Siena S, Khayat D, Bleiberg H, Santoro A, et al. Cetuximab monotherapy and cetuximab plus irinotecan in irinotecan-refractory metastatic colorectal cancer. N Engl J Med. 2004;351(4):337-45. PubMedDOI
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  37. US Food and Drug Administration. Approval letter, Avastin (bevacizumab), STN BL 125085/0, Genentech, Incorporated; letter dated 26 February 2004 (scanned document, read by optical character recognition). Источник
  38. U.S. Food and Drug Administration. Supplement approval letter, NDA 21-492/S-004 and S-005, Eloxatin (oxaliplatin). Signed 4 November 2004. Источник
  39. US Food and Drug Administration. Supplement approval letter, Eloxatin (oxaliplatin) for Injection, NDA 21-492/S-002, Sanofi-Synthelabo, Inc.; electronically signed 9 January 2004. Источник
  40. US Food and Drug Administration. Biologics licence letter, Erbitux (cetuximab), STN BL 125084/0, ImClone Systems, Incorporated; letter dated 12 February 2004 (scanned document, read by optical character recognition). Источник
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  44. European Medicines Agency. Xeloda: EPAR, procedural steps taken and scientific information after the authorisation. Variation II/0009, extension of indication to the adjuvant treatment of patients following surgery of stage III (Dukes' stage C) colon cancer: opinion 17/02/2005, Commission decision 30/03/2005 (column order confirmed from the table header). PDF read 22 October 2026. Источник
  45. U.S. Food and Drug Administration. Supplement approval letter, NDA 20-896/S-016, Xeloda (capecitabine), Hoffmann-La Roche Inc. Electronic signature dated 15 June 2005. Источник
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  49. US Food and Drug Administration. Biologics licence letter, Vectibix (panitumumab), STN BL 125147/0, Amgen, Incorporated; letter dated 27 September 2006. Источник
  50. Lièvre A, Bachet JB, Le Corre D, Boige V, Landi B, Emile JF, et al. KRAS mutation status is predictive of response to cetuximab therapy in colorectal cancer. Cancer Res. 2006;66(8):3992-5. PubMedDOI
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  51. Tournigand C, Cervantes A, Figer A, Lledo G, Flesch M, Buyse M, et al. OPTIMOX1: a randomized study of FOLFOX4 or FOLFOX7 with oxaliplatin in a stop-and-Go fashion in advanced colorectal cancer--a GERCOR study. J Clin Oncol. 2006;24(3):394-400. PubMedDOI
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  52. Falcone A, Ricci S, Brunetti I, Pfanner E, Allegrini G, Barbara C, et al. Phase III trial of infusional fluorouracil, leucovorin, oxaliplatin, and irinotecan (FOLFOXIRI) compared with infusional fluorouracil, leucovorin, and irinotecan (FOLFIRI) as first-line treatment for metastatic colorectal cancer: the Gruppo Oncologico Nord Ovest. J Clin Oncol. 2007;25(13):1670-6. PubMedDOI
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  53. US Food and Drug Administration. Supplement approval letter, Erbitux (cetuximab), STN BL 125084/103, ImClone Systems, Incorporated; letter dated 2 October 2007 (scanned document, read by optical character recognition). Источник
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  62. US Food and Drug Administration. Supplement approval letter, Vectibix (panitumumab), STN BL 125147/26, Amgen, Incorporated; letter dated 23 June 2008. The letter restates the accelerated-approval (Subpart E) status of the 27 September 2006 approval. Источник
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  83. US Food and Drug Administration. Supplement approval letter, Erbitux (cetuximab), BLA 125084/225, ImClone LLC; electronically signed 6 July 2012. Subpart E fulfilment and K-ras mutation-negative indication. Источник
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  92. Nordlinger B, Sorbye H, Glimelius B, Poston GJ, Schlag PM, Rougier P, et al. Perioperative FOLFOX4 chemotherapy and surgery versus surgery alone for resectable liver metastases from colorectal cancer (EORTC 40983): long-term results of a randomised, controlled, phase 3 trial. Lancet Oncol. 2013;14(12):1208-15. PubMedDOI
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