Department of Lung Cancer, Tianjin Medical University Cancer Institute and Hospital, Tianjin Lung Cancer Center, Tianjin Key Laboratory of Cancer Prevention and Therapy, National Clinical Research Center for Cancer, Tianjin, People's Republic of China; Georgetown University, Washington, District of Columbia.
Georgetown University, Washington, District of Columbia.
J Thorac Oncol. 2018 Feb;13(2):237-245. doi: 10.1016/j.jtho.2017.10.010. Epub 2017 Oct 31.
SCLC accounts for 15% and 20% of all lung cancers, with combined SCLC (CSCLC) comprising 2% to 5%. Little is known about the clinical characteristics and molecular changes associated with the various histologic components.
A total of 205 SCLC cases were resected between 2005 and 2015. Clinical and pathologic features were analyzed. All CSCLC cases were confirmed by histologic examination and immunohistochemistry. The individual components were microdissected using a novel automated dissection system, and DNA was extracted and subjected to targeted exome sequencing.
A total of 10 cases of CSCLC were identified out of 170 cases with adequate histologic material; squamous cell carcinoma comprised the second component in half of these (n = 5). There were no significant differences between CSCLC and pure SCLC with respect to clinical features. The median follow-up time was 36 months. The median survival times of patients with pure SCLC and CSCLC were 58 months and 26 months, respectively (p = 0.030). The different components of three cases of CSCLC were deemed adequate for microdissection and sequencing. Approximately 75% of the identified somatic mutations were present in both components. There were also 15 gene mutations or six amplifications unique to only one of the components.
We identified no significant clinical or pathologic differences between pure SCLC and CSCLC; CSCLC was associated with decreased overall survival compared with pure SCLC. The histologic components of CSCLC had high genetic concordance but also showed divergent genotypes. These findings may suggest a common precursor with subsequent acquisition of oncogenic changes in CSCLC.
小细胞肺癌占所有肺癌的 15%和 20%,其中包括 2%至 5%的小细胞肺癌合并症(CSCLC)。对于与各种组织学成分相关的临床特征和分子变化,人们知之甚少。
在 2005 年至 2015 年间共切除了 205 例小细胞肺癌病例。分析了临床和病理特征。所有 CSCLC 病例均通过组织学检查和免疫组织化学证实。使用新型自动化解剖系统对个别成分进行微解剖,提取 DNA 并进行靶向外显子组测序。
在有足够组织学材料的 170 例病例中,共发现 10 例 CSCLC;其中一半(n=5)的鳞癌为第二成分。CSCLC 与纯小细胞肺癌在临床特征方面无显著差异。中位随访时间为 36 个月。纯小细胞肺癌和 CSCLC 患者的中位生存时间分别为 58 个月和 26 个月(p=0.030)。三个 CSCLC 病例的不同成分被认为足以进行微解剖和测序。约 75%的已识别体细胞突变存在于两个成分中。还有 15 个基因突变或 6 个扩增仅存在于一个成分中。
我们未发现纯小细胞肺癌和 CSCLC 之间存在显著的临床或病理差异;CSCLC 与纯小细胞肺癌相比,总体存活率降低。CSCLC 的组织学成分具有较高的遗传一致性,但也表现出不同的基因型。这些发现可能表明 CSCLC 存在共同的前体,随后获得致癌变化。