中华肿瘤杂志
中華腫瘤雜誌
중화종류잡지
CHINESE JOURNAL OF ONCOLOGY
2010年
1期
71-74
,共4页
顾爱琴%王慧敏%施春雷%熊丽纹%高志强%韩宝惠
顧愛琴%王慧敏%施春雷%熊麗紋%高誌彊%韓寶惠
고애금%왕혜민%시춘뢰%웅려문%고지강%한보혜
癌,非小细胞肺%靶向治疗%吉非替尼
癌,非小細胞肺%靶嚮治療%吉非替尼
암,비소세포폐%파향치료%길비체니
Carcinoma,non-small cell lung%Targeted therapy%Gefitinib
目的 探讨吉非替尼治疗晚期非小细胞肺癌(NSCLC)的疗效及安全性.方法 125例经化疗失败的或不能耐受化疗及不愿接受化疗的Ⅲb~Ⅳ期NSCLC患者,口服吉非替尼250 mg/d,直到病变进展或出现不可耐受的不良反应.结果 125例患者的总有效率为35.2%(44/125),疾病控制率为77.6%(97/125),中位无疾病进展生存时间(PFS)为5.8个月,中位生存时间(MST)为11.2个月,1年生存率为40.5%%.女性、腺癌、不吸烟患者的有效率明显高于男性、非腺癌、吸烟患者(P<0.05),ECOG评分和既往有无化疗对吉非替尼疗效无显著影响(P>0.05).体力状态ECOG评分0~1和吉非替尼治疗有效患者的中位PFS明显优于ECOG评分≥2和吉非替尼治疗无效的患者(P<0.01).腺癌、不吸烟、吉非替尼治疗有效患者的MST明显优于非腺癌、吸烟和吉非替尼治疗无效的患者(P<0.05).最常见的不良反应为皮疹(51.2%)和腹泻(34.4%),多为轻度.结论 吉非替尼治疗晚期NSCLC安全、有效.不良反应轻,患者可耐受.
目的 探討吉非替尼治療晚期非小細胞肺癌(NSCLC)的療效及安全性.方法 125例經化療失敗的或不能耐受化療及不願接受化療的Ⅲb~Ⅳ期NSCLC患者,口服吉非替尼250 mg/d,直到病變進展或齣現不可耐受的不良反應.結果 125例患者的總有效率為35.2%(44/125),疾病控製率為77.6%(97/125),中位無疾病進展生存時間(PFS)為5.8箇月,中位生存時間(MST)為11.2箇月,1年生存率為40.5%%.女性、腺癌、不吸煙患者的有效率明顯高于男性、非腺癌、吸煙患者(P<0.05),ECOG評分和既往有無化療對吉非替尼療效無顯著影響(P>0.05).體力狀態ECOG評分0~1和吉非替尼治療有效患者的中位PFS明顯優于ECOG評分≥2和吉非替尼治療無效的患者(P<0.01).腺癌、不吸煙、吉非替尼治療有效患者的MST明顯優于非腺癌、吸煙和吉非替尼治療無效的患者(P<0.05).最常見的不良反應為皮疹(51.2%)和腹瀉(34.4%),多為輕度.結論 吉非替尼治療晚期NSCLC安全、有效.不良反應輕,患者可耐受.
목적 탐토길비체니치료만기비소세포폐암(NSCLC)적료효급안전성.방법 125례경화료실패적혹불능내수화료급불원접수화료적Ⅲb~Ⅳ기NSCLC환자,구복길비체니250 mg/d,직도병변진전혹출현불가내수적불량반응.결과 125례환자적총유효솔위35.2%(44/125),질병공제솔위77.6%(97/125),중위무질병진전생존시간(PFS)위5.8개월,중위생존시간(MST)위11.2개월,1년생존솔위40.5%%.녀성、선암、불흡연환자적유효솔명현고우남성、비선암、흡연환자(P<0.05),ECOG평분화기왕유무화료대길비체니료효무현저영향(P>0.05).체력상태ECOG평분0~1화길비체니치료유효환자적중위PFS명현우우ECOG평분≥2화길비체니치료무효적환자(P<0.01).선암、불흡연、길비체니치료유효환자적MST명현우우비선암、흡연화길비체니치료무효적환자(P<0.05).최상견적불량반응위피진(51.2%)화복사(34.4%),다위경도.결론 길비체니치료만기NSCLC안전、유효.불량반응경,환자가내수.
Objective To evaluate the efficacy and safety of gefitinib for the treatment of advanced non-small cell lung cancer (NSCLC) . Methods 125 patients with advanced NSCLC who had failed or not tolerated or refused chemotherapy received 250 mg oral doses of gefitinib once daily until the disease progression or intolerable toxicity. Results A total of 125 NSCLC patients were studied,the overall response rate (RR) and the disease control rate ( DCR) after administration of gefitinib were 35. 2% (44/125) and 77. 6% (97/125), respectively. The median progression-free survival and the median survival time were 5.8 and 11.2 months, respectively. The one-year survival rate was 40. 5%. The response rate was significantly higher in females, adenocarcinoma and nonsmokers than that in males, non-adenocarcinoma and smokers (P<0.05).The response rate did not show significant differences regarding ECOG score or previous treatment. The median progression-free survival was significantly longer in ECOG PS 0-1 and gefitinib effective patients than that in ECOG PS ≥ 2 and gefitinib ineffective patients (P < 0. 01 ). The median survival time was significantly longer in adenocarcinoma,nonsmokers and gefitinib effective patients than that in non-adenocarcinoma, smokers and gefitinib ineffective patients (P < 0. 05). The most common side effects were rash (51.2% ) and diarrhea (34.4% ) ,but usually were mild. Conclusion Gefitinib is effective and safe in the treatment of advanced NSCLC patients.