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恶性间皮瘤的化疗进展 被引量:2

Advances of chemotherapy for malignant mesothelioma
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摘要 本文对近20年来单药或联合化疗方案治疗恶性间皮瘤疗效的临床试验进行综述,但结果令人失望。罕有报告有效率>20%者,且均不能使中数生存期>10个月,新药培美曲赛类药物的出现使恶性间皮瘤治疗出现明显进展,与顺铂合用有效率可达45%,中数生存期超过12个月,以这2个药为基础的方案现已成为治疗恶性胸膜间皮瘤的标准一线方案。 It is reviewed that clinical trials of single agent or combined chemotherapy regiments treated malignant mesothelioma have been done in these 20 years. But their results were poor. The response rate of few agents was greater than 20%. None of drugs could improve median survival beyond 10 months. New drug-pemetrexed produced by recent year obtained encouraging result to treat malignant mesothelioma in phase I1 and phase 11 clinical trials. Specially, pemethrexed combined with cisplatin could obtain response rates of up to 45%, and improve median survival to over 12 months. The doublet - based chemotherapy regiment has become the first - line standard regiment of malignant pleural mesothelioma (MPM).
出处 《癌症进展》 2006年第6期534-539,共6页 Oncology Progress
关键词 恶性间皮瘤 化疗 malignant mesothelioma chemotherapy
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参考文献24

  • 1[1]Hassan R,Alexander R,et al.Nonpleural mesotheliomas:Mesothelioma of the peritoneum,tunica vaginalis,and pericardium.Hematol Oncol Clin North Am,2005,19 (6):1067
  • 2[2]Driscoll T,Nelson DI,Steenland K,et al.The global burden of disease due to occupational carcinogens.Am J Ind Med,2005,48 (6):419
  • 3[3]Steele JP.Prognostic factors for mesothelioma.Hematol Oncol Clin North Am,2005,19 (6):1041
  • 4[4]Maziak DE,Gagliardi A,Haynes AE,et al.Surgical management of malignant pleural mesothelioma:A systematic review and evidence summary.Lung Cancer,2005,48 (2):157
  • 5[5]Muers MF,Rudd RM,O' Brien ME,et al.BTS randomised feasibility study of active symptom control with or without chemotherapy in malignant pleural mesothelioma:ISRCTN54469112.Thorax,2004,59 (2):144
  • 6[6]Tomek S,Emri S,Krejcy K,et al.Chemotherapy for malignant pleural mesothelioma:past results and recent developments.Br J Cancer,2003,88:167
  • 7[7]Paul Baas.Chemotherapy for malignant mesothelioma.Lung Cancer,2005,49S:61
  • 8[8]Tomek S,ManegoldC.Chemotherapy for malignant pleuralmesothelioma:past resultsand recent developments.Lung Cancer,2004,45S:103
  • 9[9]Berghmans T,Lafitte JJ,Mascaux C,et al.Activity of chemotherapy and immunotherapy on malignant mesothelioma:A systematic review of the literature with meta-analysis.Cancer Ther,2003,1:245
  • 10[10]Kindler HL,van Meerbeeck JP.The role of gemcitabine in the treatment of malignant mesothelioma.Semin Oncol,2002,29 (1):70

同被引文献22

  • 1王东兴,高永良,恽榴红.高效液相色谱法测定大鼠血浆中雷替曲塞浓度[J].药物分析杂志,2005,25(7):778-780. 被引量:4
  • 2Waldman BC, Wang Y, Kilaru K, et al. Induction of intrachromosomal homologous recombination in human cells by raltitrexed, an inhibitor of thymidylate synthase[J]. DNA Repair(Amst) ,2008,7(10):1624-1635.
  • 3Wilson KS, Malfair Taylor SC. Raltitrexed: optimism and reality[J]. Expert Opin Drug Metab Toxicol, 2009,5 ( 11 ) :1447-1454.
  • 4Drake JC, Allegra CJ, Moran RG, et al. Resistance to tomudex (ZD1694) :muhifactorial in human breast and colon carcinoma cell lines[J]. Biochem Pharmacol, 1996,51(10) : 1349-1355.
  • 5Cunningham D, Zaleberg JR, Rath U, et al. Final results of a randomised trial comparing ' Tomudex' (rahitrexed) with 5fluorouracil plus leucovorin in advanced eolorectal cancer[J]. Ann Oneo1,1996,7 (9) :961-965.
  • 6Scheithauer W, Kornek GV, Raderer M, et al. Randomized multicenter phase Ⅱ trial of two different schedules of capecitabine plus oxaliplatin as first-line treatment in advanced colorectal cancer[J]. J Clin Oncol,2003,21(7):1307-1312.
  • 7Hind D,Tappenden P, Tumur I, et al. The use of irinotecan, oxaliplatin and raltitrexed for the treatment of advanced colorectal cancer: systematic review and economic evaluation [J]. Health Technol Assess,2008,12(15):iii-ix,xi-162.
  • 8Geurs F,Vandewaeter S, Ponette S, et al. Successful and welltolerated second line therapy with cetuximab, irinotecan, and raltitrexed in progressive liver disease due to metastatic colon cancer[J]. J Gastrointest Cancer,2008,39(1/4) :26-28.
  • 9Di Gennaro E, Bruzzese F, Pepe S, et al. Modulation of thymidilate synthase and p53 expression by HDAC inhibitor vorinostat resulted in synergistic antitumor effect in combination with 5FU or raltitrexed[J]. Cancer Biol Ther, 2009,8(9) : 782-791.
  • 10James RD, Botwood N, Vernon CC, et al. Raltitrexed plus radiotherapy for the treatment of unresectable/recurrent rectal cancer:aphase I study[J]. AnnOncol,2003,14(4):570-573.

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