Division of Thoracic Surgery, Department of General Surgery and Surgical Specialties, University of Modena and Reggio Emilia, Modena, Italy.
J Thorac Oncol. 2010 Jun;5(6):830-6. doi: 10.1097/jto.0b013e3181d60ff5.
Prognostic evaluation of bronchioloalveolar carcinoma (BAC) from a homogenous population of Caucasian patients.
Retrospective analysis of resected BAC reclassified according to the 2004 World Health Organization classification of lung tumors. Analyzed variables are clinicoradiologic presentation, histologic subtypes, stage, epidermal growth factor receptor (EGFR) and HER2/neu immunohistochemical expression, EGFR exons 18, 19, and 21 mutations, K-RAS exon 2 mutation. Univariate and multivariate analyses of survival were performed.
Of 40 patients analyzed, EGFR and HER2/neu expression were detected in 72% and 20%, respectively. HER2/neu expression significantly characterized mucinous BAC (46% versus 7%; p = 0.014). EGFR mutations were identified in 17% (30% in nonmucinous BAC and none in mucinous BAC; p = 0.083). K-RAS mutations were found in 42.5% (92% in mucinous BAC versus 18% in other types; p 0.0001). Early stages (IA+IB) nonmucinous BAC had excellent prognosis: 5 years overall survival of 91% (100% for stage IA). Sixty six percent (4 of 6) of patients with multifocal disease died (two mucinous BAC and one nonmucinous BAC with recurrent disease). Seventy one percent (5 of 7) of patients with pneumonic-like tumor (all mucinous BAC) died of recurrent/progressive disease. Stage (p = 0.004) and histologic classifications (p = 0.035) resulted as independent prognostic factors at multivariate analysis.
Early stage nonmucinous BAC has excellent prognosis, whereas mucinous BAC presents a poor prognosis. Locally advanced nonmucinous BAC has a poor prognosis: the diagnosis of nonmucinous BAC in large tumors should be interpreted with caution given the possible presence of invasive areas in incompletely sampled tumor. Coexpression of EGFR and HER2/neu in mucinous BAC could be considered for future trials on target therapies even in Caucasian population.
从同质的白种人群中对细支气管肺泡癌(BAC)进行预后评估。
对根据 2004 年世界卫生组织肺癌分类重新分类的切除 BAC 进行回顾性分析。分析的变量是临床放射学表现、组织学亚型、分期、表皮生长因子受体(EGFR)和 HER2/neu 免疫组化表达、EGFR 外显子 18、19 和 21 突变、K-RAS 外显子 2 突变。进行单变量和多变量生存分析。
在 40 例分析患者中,分别有 72%和 20%检测到 EGFR 和 HER2/neu 的表达。HER2/neu 的表达显著特征性地出现在黏液性 BAC 中(46%与 7%;p=0.014)。在 17%(非黏液性 BAC 中 30%,黏液性 BAC 中无;p=0.083)中发现了 EGFR 突变。在 42.5%(黏液性 BAC 中 92%,其他类型中 18%;p<0.0001)中发现了 K-RAS 突变。早期(IA+IB)非黏液性 BAC 具有极好的预后:5 年总生存率为 91%(IA 期为 100%)。66%(6 例中的 4 例)多灶性疾病患者死亡(2 例黏液性 BAC 和 1 例非黏液性 BAC 复发)。71%(7 例中的 5 例)类肺炎性肿瘤(均为黏液性 BAC)患者死于疾病复发/进展。在多变量分析中,分期(p=0.004)和组织学分类(p=0.035)是独立的预后因素。
早期非黏液性 BAC 具有极好的预后,而黏液性 BAC 则预后不良。局部晚期非黏液性 BAC 预后不良:在大型肿瘤中诊断非黏液性 BAC 时应谨慎,因为在未完全取样的肿瘤中可能存在侵袭区域。即使在白种人群中,黏液性 BAC 中 EGFR 和 HER2/neu 的共表达也可考虑用于靶向治疗的未来试验。