Mu Xin-Lin, Li Long-Yun, Zhang Xiao-Tong, Wang Shu-Lan, Wang Meng-Zhao
Department of Respiratory Diseases, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
BMC Cancer. 2004 Aug 19;4:51. doi: 10.1186/1471-2407-4-51.
The gefitinib compassionate-use programme has enabled >39,000 patients worldwide to receive gefitinib ('Iressa', ZD1839) treatment. This paper reports the outcome of gefitinib treatment in Chinese patients who enrolled into the 'Iressa' Expanded Access Programme (EAP) at the Peking Union Medical College Hospital.
Thirty-one patients with advanced or metastatic non-small-cell lung cancer (NSCLC) that had progressed after prior systemic chemotherapy were eligible to receive oral gefitinib 250 mg/day as part of the EAP. Treatment was continued until disease progression or unacceptable toxicity occurred. The impact of treatment on disease-related symptoms and quality of life (QoL) was evaluated with the Chinese versions of European Organization for Research and Treatment of Cancer Quality of Life Questionnaires (EORTC QLQ-C30 and QLQ-LC13).
Gefitinib was well tolerated. Adverse events (AEs) were generally mild (grade 1 and 2) and reversible. The most frequent AEs were acneform rash and diarrhoea. Only one patient withdrew from the study due to a drug-related AE. The objective tumour response rate was 35.5% (95% confidence interval [CI]: 18.6-52.3); median progression-free survival was 5.5 months (95% CI, 1.6 to 9.4); median overall survival was 11.5 months (95% CI, 5.6 to 17.3). The QoL response rates for five functioning scales and global QoL varied from 56-88%. The main symptom response rates varied from 44-84%. QoL and symptom response were correlated with objective tumour response.
Gefitinib demonstrated safety and efficacy as monotherapy in this series of Chinese patients with advanced NSCLC and was also associated with remarkable symptom relief and improvement in QoL. Although clinical trials are needed to confirm these positive findings, the data suggest that treatment with gefitinib may be beneficial for some Chinese patients who do not respond to chemotherapy and have poor prognosis.
吉非替尼同情用药项目已使全球超过39000名患者接受吉非替尼(“易瑞沙”,ZD1839)治疗。本文报告了在北京协和医院参加“易瑞沙”扩大可及项目(EAP)的中国患者接受吉非替尼治疗的结果。
31例先前全身化疗后病情进展的晚期或转移性非小细胞肺癌(NSCLC)患者符合条件,作为EAP的一部分接受口服吉非替尼250毫克/天的治疗。治疗持续至疾病进展或出现不可接受的毒性反应。采用欧洲癌症研究与治疗组织生活质量问卷(EORTC QLQ-C30和QLQ-LC13)的中文版评估治疗对疾病相关症状和生活质量(QoL)的影响。
吉非替尼耐受性良好。不良事件(AE)一般为轻度(1级和2级)且可逆。最常见的AE是痤疮样皮疹和腹泻。仅有1例患者因与药物相关的AE退出研究。客观肿瘤缓解率为35.5%(95%置信区间[CI]:18.6 - 52.3);无进展生存期中位数为5.5个月(95% CI,1.6至9.4);总生存期中位数为11.5个月(95% CI,5.6至17.3)。五个功能量表和总体生活质量的QoL缓解率在56% - 88%之间。主要症状缓解率在44% - 84%之间。QoL和症状缓解与客观肿瘤缓解相关。
在这一系列中国晚期NSCLC患者中,吉非替尼作为单一疗法显示出安全性和有效性,并且还与显著的症状缓解和QoL改善相关。尽管需要临床试验来证实这些阳性结果,但数据表明,吉非替尼治疗可能对一些对化疗无反应且预后较差的中国患者有益。