Correia Silvia da Silva, Pinto Carlos, Bernardo João
Serviço de Pneumologia. Unidade Local de Saúde. Guarda. Portugal.
Centro de Cirurgia Cardiotorácica. Centro Hospitalar e Universitário de Coimbra. Coimbra. Portugal.
Acta Med Port. 2014 Nov-Dec;27(6):749-54. Epub 2014 Dec 30.
Carcinoid tumors of the lung are rare neoplasms of neuroendocrine origin. According to the World Health Organization, they can be classified into typical carcinoids and atypical carcinoids. The outcome, when compared to other lung neoplasms is usually favorable.
To characterize the population of patients with a diagnosis of carcinoid tumor, treated in a single institution and analyze the prognostic factors.
Retrospective analysis including all the patients with histological diagnosis of lung carcinoid tumor during an 11 year period, in a single institution. The tumors were classified according to the World Health Organization classification of carcinoids tumors in 2004. Staging was made according to the TNM classification of 2009 for non-small lung cancer: T (Tumor); N (Node); M (metastasis).
59 patients were evaluated, including 53 with typical carcinoids and 6 with atypical carcinoid. 90% of the patients were submitted to surgery. The mean follow-up period was 57 months and the early post-operative mortality rate was 2% (one single case of palliative surgery). Histologic staging showed 49 patients in stage N0, one N1, eight N2 and one N3. The 5-year survival was 79.2%: 80.2% for typical carcinoids and 66.7% for atypical carcinoid (p < 0.05). The 5-year survival was 88.1%in T1 patients and 58.2% in T2-T4 patients (p < 0.01). In N0 patients, the 5-year survival was 89.7% while in N1-N3 it was 36% (p < 0.001). The 5-year survival was 85.9% in M0 disease and 0% in M1 disease (p < 0.01). Of the 11 patients who were submitted to adjuvant chemotherapy, 45.4% had atypical tumors.
In our sample, surgical treatment was safe, with a low postoperative complication rate. The prognosis was worse for atypical tumors, tumors with more than 3 cm, tumors with nodal involvement or metastasis. The five-year survival for typical carcinoid was excellent (80.2%), in agreement with the literature. For atypical carcinoid, the five-year was 66.7%, also similar to previous studies.
In our institution, most of the lung carcinoids are typical and have an excellent long term survival. The mainstay of treatment is surgical resection. The factors that were related to a poor prognosis were the histological subtype (typical carcinoids versus atypical carcinoids), the size of the tumor, the mediastinal lymphatic involvement and the presence of metastasis.
肺类癌是一种罕见的神经内分泌起源的肿瘤。根据世界卫生组织的分类,它们可分为典型类癌和非典型类癌。与其他肺肿瘤相比,其预后通常较好。
对在单一机构接受治疗的类癌患者群体进行特征描述,并分析预后因素。
对单一机构11年间所有经组织学诊断为肺类癌肿瘤的患者进行回顾性分析。肿瘤根据2004年世界卫生组织类癌肿瘤分类进行分类。分期按照2009年非小细胞肺癌的TNM分类进行:T(肿瘤);N(淋巴结);M(转移)。
共评估了59例患者,其中53例为典型类癌,6例为非典型类癌。90%的患者接受了手术治疗。平均随访期为57个月,术后早期死亡率为2%(仅1例姑息手术病例)。组织学分期显示49例患者为N0期,1例为N1期,8例为N2期,1例为N3期。5年生存率为79.2%:典型类癌为80.2%,非典型类癌为66.7%(p<0.05)。T1期患者的5年生存率为88.1%,T2 - T4期患者为58.2%(p<0.01)。N0期患者的5年生存率为89.7%,而N1 - N3期为36%(p<0.001)。M0期疾病的5年生存率为85.9%,M1期为0%(p<0.01)。在接受辅助化疗的11例患者中,45.4%患有非典型肿瘤。
在我们的样本中,手术治疗是安全的,术后并发症发生率低。非典型肿瘤、直径大于3 cm的肿瘤、有淋巴结受累或转移的肿瘤预后较差。典型类癌的5年生存率极佳(80.2%),与文献一致。对于非典型类癌,5年生存率为66.7%,也与先前研究相似。
在我们机构,大多数肺类癌为典型类癌,具有出色的长期生存率。治疗的主要方法是手术切除。与预后不良相关的因素是组织学亚型(典型类癌与非典型类癌)、肿瘤大小、纵隔淋巴结受累及转移的存在。