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EGFR-TKI治疗晚期非小细胞肺癌的临床疗效和安全性观察 被引量:1

The clinical efficacy and tolerability of EGFR-TKI in locally advanced or metastatic NSCLC patients
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摘要 目的 评价表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)对局部晚期或转移性非小细胞肺癌(NSCLC)患者临床疗效与安全性.方法 对经病理确诊的初治或经治的29例晚期NSCLC的患者,予吉非替尼250mg/d或厄洛替尼150mg/d 口服,至肿瘤进展或发生不可耐受的毒副作用.结果 29例患者的总有效率为48.3%,疾病控制率为72.4%,中位疾病进展时间为7.7个月;随访结束时11例患者死亡,死亡患者的中位生存期为8个月;主要的的毒副作用是皮疹和腹泻,均可耐受.结论 EGFR-TKI制剂治疗NSCLC,具有较好的疗效和耐受性. Objective Gefitinib and erlotinib are small molecule tyrosine kinase inhibitors of the epidermal growth factor receptor (EGFR-TKI). EGFR-TKI is a valid treatment for advanced non-small-cell lung cancer (NSCLC). Increased likelihood of responding to small-molecule therapy is associated with Asian race, female gender, never smoking and adenocarcinoma. To evaluate the clinical efficacy and toterability of EGFR-TKI in locally advanced or metastatic NSCLC patients. Methods Twenty-nine pathologically verified, locally advanced or metastatic NSCLC patients were treated with gefitinib 250 mg/d or erlotinib 150mg/d, until disease progression or unacceptable toxicity. Results Overall response rate (RR) of 29 patients was 48.3%, and the disease control rate (DCR) was 72.4%. The median progession-free survival (PFS) was 7.7 month. At the end of follow-up, eleven patients died of lung cancer. The median overall survival of these dead patients was 8 months. The most common drug-related adverse events were skin rashes and diarrhea, but generally mild and tolerant. Conclusion EGFR-TKI is effective and safe in the treatment of patients with locally advanced or metastatic NSCLC
出处 《浙江医学》 CAS 2010年第7期1028-1030,共3页 Zhejiang Medical Journal
关键词 非小细胞肺癌 EGFR—TKI 吉非替尼 厄洛替尼 NSCLC EGFR-TKI Gefitinib Erlotinib
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参考文献6

  • 1Yang C H,Yu C J,Shih J Y,et al.Specific EGFR mutations predict treatment outcome of stage ⅢB/Ⅳ patients with chemotherapy-naive non-small-cell lung cancer receiving first-line gefitinib monotherapy[J].J Clin Oncol 2008,26(16):2745-2753.
  • 2Fukuoka M,Yano S,Giaccone G,et al.Multi-institutional randomized phase Ⅱ trial of getinib for previously treated patients with advanced non-small-celllungcancer[J].J Clin Oncol,2003,21:2237.
  • 3Thatcher N,Chang A,Parikh P,et al.Gefitinib plus best supportive care in previously treated patients with refractory advanced non small cell lung cancer results from a randomized placebo controlled multicentre study (Iressa Survival Evaluation In Lung Cancer)[J].Lancet,2005,366:1527-1537.
  • 4Mok T,Wu Y L,Thongprasent S,et al.Phase Ⅲ randomized open-label first-line study of gefitinib versus carboplatin /paclitaxel in clinically selected patients with advanced non-small-cell lung cancer (IPASS)[J].Ann Oncol,2008,19:2302.
  • 5Takamochi K,Suzuki K,Sugimura H,et al.Surgical resection after getinib treatment in patients with lung adenocarcinoma harboring epidermal growth factor receptor genemutation[J].Lung Cancer,2007,58:149-155.
  • 6Hida T,Okamoto I,Kashii T,et al.Randomized phase Ⅲ study of platinum-doublet chemotherapy followed by gefitinib versus continued platinum-doublet chemotherapy in patients with advanced non-small cell lung cancer:results of west japan thoracic oncology group trial (WJTOG 0203)[J].J Clin Oncol,2008,26:42.

同被引文献18

  • 1周春辉,王华新,李晓楠,孙雷,宋波,郑仁恕,李连宏.肺癌中p63与p53、E-cadherin、Ki-67表达的比较[J].临床与实验病理学杂志,2004,20(4):432-435. 被引量:11
  • 2王红梅,周小鸽.TTF-1在肺癌诊断及鉴别诊断中的应用价值[J].诊断病理学杂志,2005,12(6):441-443. 被引量:35
  • 3Khayyata S, Yun S, Pasha T, et al. Value of P63 and CK5/6 in distinguishing squamous cell carcinoma from adenocarcinoma in lung fine-needle aspiration specimens [ J]. Diagn Cytopathol, 2009, 37 (13) : 178-183.
  • 4Terry J, Leung S, Laskin J, et al. Optimal Immunohistochemieal markers for distinguishing lung adenoearcinomas from squamous cell carcinomas in small tumor samples[ J]. Am J Surg Pathol, 2010, 34(12) : 1805-1811.
  • 5Reis-Filho JS, Torio B, Albergaria A, et al. p63 expression in normal skin and usual cutaneous carcinoma [ J]. Cutan Pathol, 2002, 29 (9) : 517-523.
  • 6Parsa R, Yang A, McKeon F, et al. Association of p63 with proliferative potential in normal and neoplastic human keratinocytes[ J]. J Invest Dermatol, 1999, 113(6): 1099-1105.
  • 7Wang BY, Gil J, Kaufman D, et al. P63 in pulmonary epithelium, pulmonary squamous neoplasms, and other pulmonary tumors [ J ]. Hum Pathol, 2002, 33(9): 921-926.
  • 8Loo PS, Thomas SC, Nicolson MC, et al. Subtyping of undifferentiated non-small cell carcinomas in bronchial biopsy specimens [ J ]. J Thorac Oncol, 2010, 5(4): 442-447.
  • 9Nicholson AG, Gonzalez D, Shah P, et al. Refining the diagnosis and EGFR status of non-small cell lung carcinoma in biopsy and cytologic material, using a panel of mucin staining, TIT-1,cytokeratin 5/6, and P63, and EGFR mutation analysis [ J]. J Thorae Oncol, 2010, 5(4): 436-441.
  • 10Camilo R, Capelozzi VL, Siqueira SA, et al. Expression of p63, keratin 5/6, keratin 7, and surfaetant-A in non-small cell lung carcinomas[J]. Hum Pathol, 2006, 37(5): 542-546.

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