Outcomes of Patients with Advanced Non-Small Cell Lung Cancer Treated in a Phase I Clinic

被引:7
作者
Janku, Filip [1 ]
Tsimberidou, Apostolia M.
Wang, Xuemei [2 ]
Hong, David S.
Naing, Aung
Gong, Jing
Garrido-Laguna, Ignacio
Parsons, Henrique A.
Zinner, Ralph G. [3 ]
Kurzrock, Razelle
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Invest Canc Therapeut, Phase Clin Trials Program 1, Unit 455, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
关键词
Phase I; Non-small cell lung cancer; Survival; VINORELBINE PLUS CISPLATIN; ENDOTHELIAL GROWTH-FACTOR; PROGNOSTIC-FACTORS; RANDOMIZED-TRIAL; ONCOLOGY TRIALS; III TRIAL; SAFETY; CHEMOTHERAPY; DOCETAXEL; COMBINATION;
D O I
10.1634/theoncologist.2010-0308
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background. The outcomes of patients with advanced non-small cell lung cancer (NSCLC) treated in phase I clinical trials have not been systematically analyzed. Methods. We reviewed the records of consecutive patients with advanced/metastatic NSCLC who were treated in the Phase I Clinical Trials Program at MD Anderson from August 2004 to May 2009. Results. Eighty-five patients (51 men, 34 women) treated on various phase I protocols were identified. The median age was 62 years (range, 30-85). The median number of previous systemic therapies was two (range, 0-5). A partial response was observed in eight patients (9.5%) and stable disease lasting > 4 months was observed in 16 patients (19%). The median overall survival time was 10.6 months and median progression-free survival (PFS) time was 2.8 months, which was 0.6 months shorter than the median PFS of 3.4 months following prior second-line therapy. Factors predicting longer survival in the univariate analysis were an Eastern Cooperative Oncology Group performance status (PS) score of 0-1, no prior smoking, two or fewer organ systems involved, a hemoglobin level > 12 g/dL, liver metastases, a history of thromboembolism, and a platelets count > 440 x 10(9)/L. In the multivariate analysis, a PS score of 0-1 and history negative for smoking predicted longer survival. Sixty-two (73%) patients had grade <= 2 toxicity, and there were no treatment-related deaths. Conclusion. Phase I clinical trials were well tolerated by selected patients with advanced NSCLC treated at M. D. Anderson. Nonsmokers and patients with a good PS survived longer. PFS in our population was shorter in smokers/ex-smokers and patients with a PS score of 2. It is reasonable to refer pretreated patients with a good PS to phase I clinical trials. The Oncologist 2011; 16: 327-335
引用
收藏
页码:327 / 335
页数:9
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