Doherty Mark K, O'Connor Emer, Hannon David, O'Reilly Aine, Yen Daphne, Redmond Maeve, Grogan Liam M, Hennessy Bryan T, Breathnach Oscar S, Morris Patrick G
Cancer Clinical Trials and Research Unit, Beaumont Hospital, Dublin, Ireland.
Department of Pathology, Beaumont Hospital, Dublin, Ireland.
Ir J Med Sci. 2019 Feb;188(1):69-74. doi: 10.1007/s11845-018-1839-5. Epub 2018 Jun 9.
Adenocarcinoma is the commonest histologic subtype of lung cancer and is often identified by immunohistochemical staining for thyroid transcription factor-1 (TTF-1). However, up to 20% of lung adenocarcinomas do not express TTF-1, and there is uncertainty regarding the significance of this. We aimed to evaluate the prognostic effect of TTF-1 expression status on survival in patients treated with pemetrexed-based chemotherapy for advanced adenocarcinoma of the lung.
This retrospective study included patients treated with pemetrexed-based chemotherapy for stage IIIB/IV lung adenocarcinoma, who had known TTF-1 expression status. Clinical and demographic data were obtained from medical records. Overall survival (OS) was estimated using the Kaplan-Meier method, and differences in survival between groups assessed using the Cox proportional hazards model.
Forty-four patients were identified with documented TTF-1 expression: 35 with TTF-1-positive and 9 with TTF-1-negative disease. Patients in the TTF-1-negative group had poorer performance scores than those in the TTF-1-positive group (ECOG 2: 67 vs 20%, p = 0.008), and received less chemotherapy (median cycles 2 vs 4, p = 0.009), and were fewer in treatment with doublet regimens (22 vs 69%, p = 0.013). OS was significantly shorter in the TTF-1-negative group than in the TTF-1-positive group (2.4 vs 11.5 months, HR 8.38, p < 0.0001).
In this group of patients treated with pemetrexed-based chemotherapy for advanced pulmonary adenocarcinoma, absence of TTF-1 expression was associated with an aggressive tumor phenotype, poorer performance status, and poor survival. This subgroup of patients should be recognized as having a distinct clinical course, with limited benefit from standard chemotherapy.
腺癌是肺癌最常见的组织学亚型,通常通过甲状腺转录因子-1(TTF-1)免疫组化染色来识别。然而,高达20%的肺腺癌不表达TTF-1,其意义尚不确定。我们旨在评估TTF-1表达状态对接受培美曲塞为基础的化疗的晚期肺腺癌患者生存的预后影响。
这项回顾性研究纳入了接受培美曲塞为基础的化疗治疗的IIIB/IV期肺腺癌患者,这些患者已知TTF-1表达状态。临床和人口统计学数据从病历中获取。采用Kaplan-Meier方法估计总生存期(OS),并使用Cox比例风险模型评估组间生存差异。
确定了44例记录有TTF-1表达的患者:35例TTF-1阳性和9例TTF-1阴性疾病。TTF-1阴性组患者的体能状态评分比TTF-1阳性组差(东部肿瘤协作组2级:67%对20%,p = 0.008),接受的化疗较少(中位周期2对4,p = 0.009),接受双联方案治疗的患者较少(22%对69%,p = 0.013)。TTF-1阴性组的OS明显短于TTF-1阳性组(2.4对11.5个月,风险比8.38,p < 0.0001)。
在这组接受培美曲塞为基础的化疗治疗晚期肺腺癌的患者中,TTF-1表达缺失与侵袭性肿瘤表型、较差的体能状态和不良生存相关。这一亚组患者应被视为具有独特的临床病程,从标准化疗中获益有限。