Cappuzzo Federico, Gregorc Vanesa, Rossi Elisa, Cancellieri Alessandra, Magrini Elisabetta, Paties Carlo Terenzio, Ceresoli Giovanni, Lombardo Laura, Bartolini Stefania, Calandri Cesare, de Rosa Marisa, Villa Eugenio, Crino Lucio
Bellaria Hospital, Division of Medical Oncology, Via Altura 3, 40139 Bologna, Italy.
J Clin Oncol. 2003 Jul 15;21(14):2658-63. doi: 10.1200/JCO.2003.01.039.
To evaluate the correlation between HER2 expression and gefitinib (ZD 1839, Iressa; AstraZeneca, London, United Kingdom) efficacy in terms of response rate, time to progression (TTP), and overall survival (OS) time.
Patients with pretreated advanced non-small-cell lung cancer (NSCLC) received gefitinib at a daily dose of 250 mg until disease progression. Tumor tissue specimens obtained at the time of primary diagnosis were collected to determine HER2/epidermal growth factor receptor (EGFR) status by immunohistochemistry.
From February 2001 to June 2002, 63 consecutive patients were enrolled onto the study. The overall disease control rate was 58.7% (partial response [PR], 15.9%; stable disease [SD], 42.8%), median TTP was 3.3 months, and median OS was 4.1 months. Among the 43 patients in whom EGFR/HER2 status was determined, we observed six PRs (14%) and 18 SDs (42%). Disease control, including PR and SD, was 40% in the 15 patients overexpressing HER2 and 64.3% in the 28 patients not overexpressing HER2 (P =.126). No difference was found between the two groups in terms of TTP (3.5 v 3.7 months, respectively) and OS (5.7 v 6.8 months, respectively). In addition, we did not find any difference in TTP, OS, toxicity, and symptom outcome in the group of patients overexpressing both HER2 and EGFR compared with patients who had no overexpression of HER2
According to these data, efficacy, toxicity, and symptom outcome in patients with NSCLC treated with gefitinib do not seem to be related to HER2 expression.
从缓解率、疾病进展时间(TTP)和总生存期(OS)方面评估HER2表达与吉非替尼(ZD 1839,易瑞沙;阿斯利康公司,英国伦敦)疗效之间的相关性。
接受过预处理的晚期非小细胞肺癌(NSCLC)患者每日服用250 mg吉非替尼,直至疾病进展。收集初次诊断时获取的肿瘤组织标本,通过免疫组织化学确定HER2/表皮生长因子受体(EGFR)状态。
2001年2月至2002年6月,连续63例患者纳入本研究。总体疾病控制率为58.7%(部分缓解[PR],15.9%;疾病稳定[SD],42.8%),中位TTP为3.3个月,中位OS为4.1个月。在确定了EGFR/HER2状态的43例患者中,我们观察到6例PR(14%)和18例SD(42%)。HER2过表达的15例患者中疾病控制(包括PR和SD)为40%,HER2未过表达的28例患者中为64.3%(P = 0.126)。两组在TTP(分别为3.5个月和3.7个月)和OS(分别为5.7个月和6.8个月)方面未发现差异。此外,与未过表达HER2的患者相比,HER2和EGFR均过表达的患者组在TTP、OS、毒性和症状结果方面未发现任何差异。
根据这些数据,接受吉非替尼治疗的NSCLC患者的疗效、毒性和症状结果似乎与HER2表达无关。