The Applicability of a Predictive Index for Second- and Third-Line Treatment of Unselected Non-Small-Cell Lung Cancer Patients

被引:7
|
作者
Wojas-Krawczyk, Kamila [1 ]
Krawczyk, Pawel [1 ]
Mlak, Radoslaw [1 ]
Kucharczyk, Tomasz [1 ]
Kowalski, Dariusz M. [2 ,3 ]
Krzakowski, Maciej [2 ,3 ]
Milanowski, Janusz [1 ]
机构
[1] Med Univ Lublin, Dept Pneumonol Oncol & Allergol, PL-20954 Lublin, Poland
[2] Inst Oncol, Warsaw, Poland
[3] Maria Sklodowska Curie Mem Canc Ctr, Dept Lung Canc & Chest Tumours, Warsaw, Poland
关键词
Predictive index; Erlotinib; Non-small-cell lung cancer; EGFR gene mutation; FACTOR-RECEPTOR GENE; CLINICAL-OUTCOMES; COPY NUMBER; SENSITIVITY; MUTATIONS; GEFITINIB; CHEMOTHERAPY; DOCETAXEL; ERLOTINIB; PROTEIN;
D O I
10.1159/000322843
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Tyrosine kinase inhibitors of EGFR (TKI-EGFR) induced response in only 10% of Caucasian non-small-cell lung cancer patients in second- or third-line treatment. Independent predictive factors for qualification to TKI-EGFR treatment have not been assessed. In 2008, a prognostic index was reported for patients treated with erlotinib in the BR. 21 trial, but its application for real, unselected patients is limited. Objectives: Based on clinical and molecular factors of patients treated with erlotinib, we tried to create a predictive index which could be applied in real treatment practice. Methods: In a Cox regression model, we established 6 factors which affected overall survival for erlotinib treatment: performance status, erlotinib-induced rash, time from diagnosis to treatment, gender, weight loss and LDH level. We analyzed the risk factors of early progression and survival shorter than 6 months. In addition we included: time from first-line chemotherapy to erlotinib treatment, smoking status, mutation status in EGFR and anemia. Results: Our model consisted of 10 factors that were assigned points according to HR or chi(2) and p value. The score was used to separate patients into 4 risk categories of unfavorable disease course based on 10th, 50th and 90th percentiles: low risk (I), intermediate low risk (II), intermediate high risk (III) and high risk (IV). Survival probability was significantly higher for group I, intermediate for groups II and III, and significantly lower for group IV (chi(2) = 49.5, p < 0.0001). Based on the previously reported index we could not qualify our patients for the low risk group. Conclusions: Our model could be useful for qualification for erlotinib treatment of patients with numerous adverse factors and limited access to genetic examination. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:341 / 350
页数:10
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