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Oxaliplatin,Fluorouracil and Leucovorin (FOLFOX) as First-line Chemotherapy for Metastatic or Recurrent Colorectal Cancer Patients 被引量:2

Oxaliplatin,Fluorouracil and Leucovorin (FOLFOX) as First-line Chemotherapy for Metastatic or Recurrent Colorectal Cancer Patients
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摘要 OBJECTIVE To investigate the efficiency and safety of the oxaliplatin, fluorouracil(5-FU)and leucovorin regimen(FOLFOX)in previously untreated patients with metastatic or recurrent colorectal cancer. METHODS Previously untreated patients with metastatic or recurrent colorectal cancer received 100 mg/m2 of oxaliplatin intravenously(IV)over 2 h on day 1,and IV 400 mg/m2 of leucovorin over 2 h followed by a bolus of 400 mg/m2 of 5-FU.Then 2,600~3,000 mg/m2 of 5-FU was administered by continuous infusion over 46 h. RESULTS An evaluated response rate was determined for 97 of 105 treated patients.The overal response rate was 35.1%,9 patients(9.3%) had a complete response and 25 patients(25.8%)a partial response.Thirty-two patients(33.0%)developed stable disease and 32.0%of the patients progressed.The median time to progression(TTP)was 7.7 months and the median overal survival 20.5 months.One and 2-year survival rates were 68%and 32%.Toxic effects based on the National Cancer Institute-Common Toxicity Criteria(NCI-CTC),reaching grade 3/4 were:neutropenia 12.3%, anemia 11.3%,vomiting 4.1%and diarrhea 7.2%.Grade 3 neuropathy was 5.1%.The overall survival rate of patients who had received a radical resection was superior to the patients who had not received a operation,or had received a pal iative resection(P=0.0658).The serum levels of CEA,ALP and LDH had no relationship with survival(P>0.05). CONCLUSION The FOLFOX regimen containing oxaliplatin,5-FU plus leucovorin was an efficacious regimen with good tolerability in previously untreated metastatic or recurrent colorectal cancer patients. OBJECTIVE To investigate the efficiency and safety of the oxaliplatin, fluorouracil (5-FU) and leucovorin regimen (FOLFOX)in previously untreated patients with metastatic or recurrent colorectal cancer. METHODS Previously untreated patients with metastatic or recurrent colorectal cancer received 100 mg/m^2 of oxaliplatin intravenously (Ⅳ) over 2 h on day 1, and Ⅳ 400 mg/m^2 of leucovorin over 2 h followed by a bolus of 400 mg/m^2 of 5-FU. Then 2,600-3,000 mg/m^2 of 5-FU was administered by continuous infusion over 46 h. RESULTS An evaluated response rate was determined for 97 of 105 treated patients. The overall response rate was 35.1%, 9 patients (9.3%) had a complete response and 25 patients (25.8%) a partial response. Thirtytwo patients (33.0%) developed stable disease and 32.0% of the patients progressed. The median time to progression (TTP) was 7.7 months and the median overall survival 20.5 months. One and 2-year survival rates were 68% and 32%. Toxic effects based on the National Cancer Institute-Common Toxicity Criteria (NCI-CTC), reaching grade 3/4 were: neutropenia 12.3%, anemia 11.3%, vomiting 4.1% and diarrhea 7.2%. Grade 3 neuropathy was 5.1%. The overall survival rate of patients who had received a radical resection was superior to the patients who had not received a operation, or had received a palliative resection (P=0.0658). The serum levels of CEA, ALP and LDH had no relationship with survival (P〉0.05). CONCLUSION The FOLFOX regimen containing oxaliplatin, 5-FU plus leucovorin was an efficacious regimen with good tolerability in previously untreated metastatic or recurrent colorectal cancer patients.
出处 《Chinese Journal of Clinical Oncology》 CSCD 2007年第6期397-400,共4页 中国肿瘤临床(英文版)
关键词 奥克赛铂 氟尿嘧啶 抗癌药 甲酰四氢叶酸 chemotherapy, fluorouracil, leucovorin, colorectal cancer.
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参考文献10

  • 1Gil-delgado MA,Khayat D,Taieb J.Cancer of the Co-lon and Rectum[].UICC manual of clinical oncology.2004
  • 2Levi F,Misser JL,Brienza S,et al.A chronopharmaco-logic phase II clinical trial with 5 fluorouracil,flolinicacid,and oxaliplatin using an ambulatory multichan-nel programmable pump,high antitumor effectivenessagainst metastatic colorectal cancer[].Cancer.1992
  • 3Wan DS,Pan ZZ.Carcinoma of Large Intestine[].Clinical Oncology.2005
  • 4Cohen AM,Minsky BD,Schilsky RL.Cancer of the Co-lon[].Principles and Practice of Oncology.1997
  • 5Piedbois P,Buyse M,Rustum Y,et al.AdvancedColorectal Cancer Meta-Analysis Project:Modulationof fluorouracil by leucovorin in patients with advancedcolorectal cancer:Evidence in terms of response rate[].Journal of Clinical Oncology.1992
  • 6Lo Bello L,Pistone G,Restuccia S,et al.5-fluoroura-cil alone versus 5-fluorouracil plus folinic acid in thetreatment of colorectal carcinoma:Meta-analysis[].International Journal of Clinical Pharmacology and Therapeutics.2000
  • 7Goldberg RM,Sargent DJ,Morton RF,et al.A random-ized controlled trial of fluorouracil plus leucovorin,irinotecan,and oxaliplatin combinations in patientswith previously untreated metastatic colorectal cancer[].Journal of Clinical Oncology.2004
  • 8Colucci G,Gebbia V,Paoletti G,et al.Phase III ran-domized trial of FOLFIRI versus FOLFOX4 in the treat-ment of advanced colorectal cancer:a multicenterstudy of the Gruppo Oncologico Dell‘Italia Meridionale[].Journal of Clinical Oncology.2005
  • 9Tournigand C,Andre T,Achille E,et al.FOLFIRI fol-lowed by FOLFOX6 or the reverse sequence in ad-vanced colorectal cancer.A randomized GERCORstudy[].Journal of Clinical Oncology.2004
  • 10Mathe G,Kidani Y,Segiguchi M,et al.Oxalato-plati-num or L-OHP,a third generation platinum complex:An experimental and clinical appraisal and preliminarycomparison with cis-platinum and carboplatinum[].Biomedicine and Pharmacotherapy.1989

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  • 1江昱,李有明,严朝明.FAM和EAP方案治疗进展期胃癌的临床研究[J].疾病控制杂志,2002,6(z1):53-54. 被引量:1
  • 2Kindler HL, Shulman KL. Metastatic colorectal caneer [ J ]. Curr Treat Options Oncol, 2001,2 (6) :459-471.
  • 3Choti MA, Sitzmann JV, Tiburi MF, et al. Trends in long- term survival following liver resection for hepatic colorectal metastases [J]. Ann Surg, 2002, 235 (6) : 759 -66.
  • 4Adam R, Pascal G, Azoulay D, et al. Liver resection for colorectal metastases: the third hepatectomy [J]. Ann Surg, 2003,238 ( 6 ) : 871-883.
  • 5Vauthey JN, Pawlik TM, Abdalla EK, eta. 1. Is ex- tended hepatectomy for hepatobiliarymalignancy justified [ J ] ? Ann Surg, 2004,239 (5) :722-730.
  • 6Kokudo N, Miki Y, Sugai S, et al. Genetic and histo- logical assessment of surgicalmargins in resected liver- metastases from colorectal carcinoma: minimum surgi- calmargins for successful resection [J].Arch Surg, 2002, 137(7): 833-840.
  • 7Zorzi D, Mullen JT, Abdalla EK, et al. Comparisonbetween hepaticwedge resection and anatomic resection for eolorectal liver metastases[J]. J Gastroin/est Surg, 2006, 10( 1 ) : 86-94.
  • 8Adam R, Wieherts DA, de ttaas RJ, eta]. Complete pathologic response after preoperative ehemotherapy |br coloreetal liver metastases: myth or reality [J].? J Clin Onco1,2008,26(10) :1635-41.
  • 9Gruenberger B, Scheithauer W, Punzengruber R,et al. Importance of response to neoadjuvant chemotherapy in potentially curable eolorectal eancer liver metastases[J]. BMC Caneer,2008,8 : 120.
  • 10Nordlinger B, Sorbye H, Glimelius B, et al. Periopera- tire chemotherapy with FOLFOX4 and surgery versus surgery alone for resectable liver metastases from color- ectal cancer (EORTC Intergrouptrial 40983 ): a ran- domised controlled trial [J].l.ancet,2008,371 (9617 ) : 1007-1016.

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