Cappuzzo Federico, Ligorio Claudia, Jänne Pasi A, Toschi Luca, Rossi Elisa, Trisolini Rocco, Paioli Daniela, Holmes Alison J, Magrini Elisabetta, Finocchiaro Giovanna, Bartolini Stefania, Cancellieri Alessandra, Ciardiello Fortunato, Patelli Marco, Crino Lucio, Varella-Garcia Marileila
Department of Hematology-Oncology, Istituto Clinico Humanitas IRCCS, Rozzano, Italy.
J Clin Oncol. 2007 Jun 1;25(16):2248-55. doi: 10.1200/JCO.2006.09.4300.
In non-small-cell lung cancer (NSCLC), clinical and biologic predictors for epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor sensitivity have been identified in retrospective studies, and there is urgent need to validate these results in prospective trials. The ONCOBELL trial is a prospective phase II study evaluating gefitinib sensitivity in NSCLC patients who never smoked or have increased EGFR gene copy number or activation of the antiapoptotic protein Akt.
EGFR gene copy number was evaluated using fluorescence in situ hybridization (FISH), and presence of phospho-Akt was evaluated using immunohistochemistry. Additional tests included immunohistochemistry analysis of EGFR, FISH analysis of HER2, and mutation analysis of EGFR, HER2, and K-ras.
From November 2004 to February 2006, 183 patients were screened, and 42 patients were enrolled onto the trial. We observed one complete and 19 partial responses, for an overall response rate (RR) of 47.6% (95% CI, 32.5% to 62.7%). Median duration of response was 6.1 months, median time to progression (TTP) was 6.4 months, 1-year survival rate was 64.3%, and median survival time was not reached. EGFR FISH-positive patients, compared with negative patients, had higher RR (68.0% v 9.1%, respectively; P < .001), longer TTP (7.6 v 2.7 months, respectively; P = .02), and a trend for longer survival (median survival not reached v 7.4 months, respectively; P = .3). Therapy was well tolerated, and there were no drug-related deaths. Median follow-up time was too short for significance tests of differences in survival outcomes.
Gefitinib is active and well tolerated in patients with trial characteristics, and EGFR FISH analysis is an accurate predictor for such therapy.
在非小细胞肺癌(NSCLC)中,回顾性研究已确定了表皮生长因子受体(EGFR)酪氨酸激酶抑制剂敏感性的临床和生物学预测指标,迫切需要在前瞻性试验中验证这些结果。ONCOBELL试验是一项前瞻性II期研究,旨在评估吉非替尼对从不吸烟或EGFR基因拷贝数增加或抗凋亡蛋白Akt激活的NSCLC患者的敏感性。
使用荧光原位杂交(FISH)评估EGFR基因拷贝数,使用免疫组织化学评估磷酸化Akt的存在情况。其他检测包括EGFR的免疫组织化学分析、HER2的FISH分析以及EGFR、HER2和K-ras的突变分析。
2004年11月至2006年2月,共筛查了183例患者,42例患者入组该试验。我们观察到1例完全缓解和19例部分缓解,总缓解率(RR)为47.6%(95%CI,32.5%至62.7%)。中位缓解持续时间为6.1个月,中位疾病进展时间(TTP)为6.4个月,1年生存率为64.3%,中位生存时间未达到。与EGFR FISH阴性患者相比,阳性患者的RR更高(分别为68.0%和9.1%;P<.001),TTP更长(分别为7.6个月和2.7个月;P=.02),且生存时间有延长趋势(中位生存时间未达到和7.4个月,分别;P=.3)。治疗耐受性良好,无药物相关死亡。中位随访时间过短,无法进行生存结局差异的显著性检验。
吉非替尼对具有试验特征的患者有效且耐受性良好,EGFR FISH分析是此类治疗的准确预测指标。