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吉非替尼治疗老年非小细胞肺癌的临床分析 被引量:3

Clinical analysis of gefitinib in treatment of elderly patients with non-small cell lung cancer
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摘要 为了观察吉非替尼治疗老年非小细胞肺癌(non-small celllung cancer,NSCLC)的有效性和毒副反应,回顾性研究32例经病理学或细胞学确诊的老年NSCLC,应用吉非替尼(250mg,口服1次/d)治疗,直到病情进展或出现严重不良反应。32例患者,PR8例(25.0%),SD17例(53.1%),PD7例(21.9%),有效率(CR+PR)为25%,疾病控制率(CR+PR+SD)为78.1%。女性有效率优于男性,P=0.013。病理、分期及吸烟史等各亚组之间疗效对比均差异无统计学意义,P>0.05。中位生存时间(MST)10.1个月,中位疾病进展时间(MTTP)5.7个月。腺癌和肺泡癌患者的中位生存时间及中位疾病进展时间优于鳞癌及大细胞癌患者,P值分别为0.037和0.024。吉非替尼最主要的毒副反应是皮疹(62.5%)、腹泻(30%)、皮肤干燥(46.9%)及食欲减退(25%)。3例因严重皮疹和腹泻而中断治疗。初步研究结果提示,吉非替尼单药治疗老年NSCLC疗效肯定,毒副反应相对较小,患者耐受性好。 The objective of this study was to analysis the efficacy and side effects of gefitinb in the elderly patients with non-small lung cancer (NSCLC).A retrospective research of 32 elderly patients who were histologically or cytologically diagnosed as NSCLC and were treated with gefitinib orally 250 mg daily.Then the efficacy and side-effects of gefitinib were evaluated.All the 32 patients were evaluated.PR,SD and PD were 25.0%(8/32),53.1%(17/32) and 21.9%(7/32),respectively.The effective rate (CR+PR) was 25% and the disease control rate (CR+PR+SD) was 78.1%.The response rate had a significant difference between the female and the male (P=0.013).No significant difference was found in the age,pathology,stage and smoking history among the different subtypes (P〉0.05).The median survival time (MST) and median time to tumor progression (MTTP) were 10.1 and 5.7 months,respectively.MST and MTTP were signigicantly longer in the patients of bronchioloalveolar carcinoma and adenocarcinoma than in the patients of squamous carcinoma and large cell carcinoma (P were 0.037 and 0.024).The main toxicities of gefitinib were skin rash (62.5%),diarrhea (30%),asteatosis cutis (46.9%),and anorexia (25%).Three patients quitted the treatment because of severe rash and diarrhea.In conclusion,monotherapy with gefttinib in elderly NSCLC patients is effiective and tolerated with adverse events.
出处 《中华肿瘤防治杂志》 CAS 2010年第15期1223-1225,共3页 Chinese Journal of Cancer Prevention and Treatment
关键词 非小细胞肺 药物疗法 治疗结果 carcinoma non-small cell lung drug therapy treatment outcome
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参考文献14

  • 1谢晓冬,郑振东.分子靶点药物吉非替尼治疗复发难治性非小细胞肺癌的现状[J].中国实用内科杂志,2005,25(8):688-690. 被引量:9
  • 2Salomon D S, Brandt R, Ciardiello F, et al. Epidermal growth factor-related peptides and their receptor and tis ligands in primary non small cell lung cancers and adjacent benign lung[J]. Crit Rev Oncol Hematol, 1995,19(3), 183-232.
  • 3Rusch V, Bselga J, Cordon-Cardo C, er al. Differential expression of the epidermal growth factor receptor and tis ligands in primary non-small cell lung cancers and adjacent benigh lung[J]. Cancer Res,1993, 53(10 Suppl) :2379-2385.
  • 4Chang A, Parikh P, Thongprasert S, et al. Gefitinib in patients of Asian origin with refractory adbanced non-small cell lung cancer:subset analysis from the ISEL study[J]. Thorac Oncol, 2006, 1(8) :847-855.
  • 5Kris M G, Natale R B, Herbst R S, et al. A phase Ⅱ trial of um-and docetaxel based regimens(IDAEL2)[J]. Proc Am Soc Clin Oncol, 2002, 21:292a.
  • 6Curer T, Vrdoljak E, Gaafar R, et al. Phase Ⅱ , open label, randomaize study (SIGN) of single agent gefitinib(IRESSA) or docetaxel as second-line therapy in patients with advanced (stage [Ⅲbor Ⅳ ) non small cell lung cancer[J]. Anticancer Drugs, 2006,17(4):401- 109.
  • 7Quoix E, Breton J L, Ducolone A, et al. First line chemothera py with gemcitabine in advanced non-small cell lung cancer elderly patients: a randomized phase I1 study of 3 week versus 4-week schedule[J]. Lung Cancer, 2005, 47(3) :405- 412.
  • 8Dan L, Zhu B, Chen Z, Meta analysisi of the literature: Neoad- juvant chemotherapy versus surgery alone in non-small lung cancer (NSCLC)[J]. J Clin Oncol, 2008, 26:a7580.
  • 9穆新林,张永香,韩亚静,魏海东.晚期肺癌患者诊断延迟的原因分析[J].中华肿瘤防治杂志,2009,16(5):384-385. 被引量:3
  • 10Marinis F De, Raftopoulos H, Bria E, et al. Should 3 weekly docetaxel (3WD) remain the standard for second line therapy of advanced non-small cell lung cancer (ANSCL C) Meta analysis of comparator arms[J]. J ClinOncol, 2008, 26:a8087.

二级参考文献15

  • 1吴一龙,杨学宁,杨衿记,黄玉娟.中国的非小细胞肺癌Gefitinib分子靶向治疗[J].中国肺癌杂志,2004,7(4):318-320. 被引量:15
  • 2吕梅君,陈子丹,施海燕,周彩存.肺癌患者就诊及治疗延迟对预后的影响[J].中华肿瘤防治杂志,2006,13(19):1499-1501. 被引量:1
  • 3Jemal A, Siegel R, Ward E, et al. Cancer Statistics, 2008[J]. CA Cancer J Clin, 2008, 58(2): 71-96.
  • 4Spiro S G, Gould M K, Colice G L. Initial Evaluation of the Patient With Lung Cancer: Symptoms, Signs, Laboratory Tests, and Paraneoplastic Syndromes: ACCP Evidenced-Based Clinical Practice Guidelines (2nd Edition)[J]. Chest, 2007, 132(3 Suppl): 149-160.
  • 5Jensen A R, Mainz J, Overgaard J. Impact of Delay on Diagnosis and Treatment of Primary Lung Cancer[J]. Acta Oncol, 2002, 41(2):147-152.
  • 6Koyi H, Hillerdal G, Branden E. A prospective study of a total material of lung cancer from a county in Sweden 1997-1999[J]. Lung Cancer, 2002, 36(1):9-14.
  • 7Comer J, Hopkinson J, Fitzsimmons D, et al. Is late diagnosis of lung cancer inevitable? Interview study of patients' recollections of symptoms before diagnosis[J]. Thorax, 2005, 60(4): 314-319.
  • 8Hamilton W, Peters T J, Round A, et al. What are the clinical features of lung cancer before the diagnosis is made? A population based case-control study[J]. Thorax, 2005, 60(12): 1059-1065.
  • 9Bjerager M. Delay in diagnosis of lung cancer in general practice [J]. BrJ Gen Praet, 2006, 56(532): 863-868.
  • 10Koyi H, Hillerdal G, Branden E. Patient's and doctors' delays in the diagnosis of chest tumors[J]. Lung cancer, 2002, 35(1) :53-57.

共引文献10

同被引文献36

  • 1Ginsberg MS. Epidemiology of lung cancer[J]. Semin Roentgenol, 2005,40 (2) : 83-89.
  • 2Janssen HL,Haustermans KM,Balm AJ,et al. Hypoxia in head and neck cancer: how much, how important? [J]. Head Neck, 2005,27(7) : 622-638.
  • 3Sohda M, Ishikawa H, Masuda N, et al. Pretreatrnent evaluation of combined HIF Jalpha,p53 and p21 expression is a useful and sensitive indicator of response to radiation and chemotherapy in esophageal cancer[J]. Int J Cancer, 2004,110(6) : 838-844.
  • 4Greijer AE,van der Wall E. The role of hypoxia inducible factor1 (HIF-1) in hypoxia induced apoptosis[J].J Clin Pathol,2004, 57(10) :1009- 1014.
  • 5Lee MJ, Kim JY, Suk K, et al. Identification of the hypoxia-inducible factor 1 alpha-responsive HGTD-P gene as a mediator in the mito- chondrial apoptotic pathway[J]. Mol Cell Biol, 2004,24(9) : 3918- 3927.
  • 6Erler JT, Cawthorne CJ, Williams KJ, et al. Hypoxia-mediated down-regulation of Bid and Bax in tumors occurs via hypoxia in- ducible factor 1-dependent and -independent mechanisms and contributes to drug resistance[J ]. Mol Cell Biol, 2004,24 ( 7 ) 2875-2889.
  • 7Moeller BJ,Dreher MR,Rabbani ZN,et al. Pleiotropic effects of HIF-1 blockade on tumor radiosensitivity[J]. Cancer Ce11,2005, 8(2) :99-110.
  • 8Goda N,Ryan HE,Khadivi B, et al. Hypoximinducible factor 1alpha is essential for cell cycle arrest during hypoxia[J]. Mol Cell Biol, 2003,23(1) :359-369.
  • 9Garcia-Barros M,Paris F Cordon-Cardo C, et ak Tumor response to radiotherapy regulated by endothelial cell apoptosis[J]. Science, 2003,300(5622) : 1155-1159.
  • 10Moeller BJ,Dewhirst MW. HIF-1 and tumour radiosensitivity[J]. Br J Cancer,2006,95(1) :1-5.

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