Natural History of Familial Carcinoid Tumor

家族性类癌的自然史

• 批准号: 8349916
• 负责人: Stephen Wank
• 金额: $ 53.03万
• 依托单位: NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES
• 依托单位国家: 美国
• 资助国家: 美国
• 起止时间: 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8349916
• 关键词: Affect; Age of Onset; Biochemical; Carcinoid Tumor; Clinical; Collection; Colonoscopy; Consultations; DNA; Development; Diagnosis; Diagnostic; Diagnostic tests; Disease; Endoscopy; Esophagogastroduodenoscopy; Evaluation; Excision; Family; Family Study; Family member; Gastrointestinal Carcinoid Tumor; Gene Mutation; Genes; Genetic; Genotype; Hereditary Malignant Neoplasm; Histologic; Histology; Incidence; Intention; Knowledge; Location; Magnetic Resonance Imaging; Metabolic; Metastatic Carcinoid Tumor; Modality; Morbidity - disease rate; Mutate; Natural History; Newly Diagnosed; Operative Surgical Procedures; Patients; Population; Prognostic Factor; Recruitment Activity; Relative (related person); Scanning; Screening procedure; Sensitivity and Specificity; Specimen; Staging; Survival Rate; Susceptibility Gene; Symptoms; Syndrome; Testing; X-Ray Computed Tomography; capsule; effective therapy; follow-up; genetic analysis; imaging modality; improved; indexing; kindred; lifetime risk; member; mortality; oncology; peripheral blood; proband; somatostatin analog; treatment planning; tumor

Carcinoid tumors are rare and cause either no or few nonspecific symptoms. Therefore, patients with carcinoid tumors most often present late in the course of their illness when there is already progression to an incurable state as a result of metastatic disease. At present there are neither practical population screening tests nor effective therapies and hence the 5 year survival rate is low. Due to the rareness of sporadic carcinoid tumors, large scale genetic analysis and development of sensitive and specific diagnostic tests have not been successful. While kindreds with familial carcinoid tumors that are not ascribable to known genetic syndromes are exceedingly rare, they provide a unique opportunity to facilitate the identification of the responsible gene mutation. In addition, the mutated gene in the rare familial form may also underlie the origin of the more common sporadic occurrence of carcinoid tumors. We propose to study families in which there are at least two known affected members with carcinoid tumors. We aim to diagnose patients with early and therefore potentially curable occult disease. Therefore, family members who have up to a 50% lifetime risk of harboring a carcinoid tumor will undergo an intensive diagnostic evaluation using biochemical, endoscopic and imaging modalities at initial and subsequent two year follow up encounters. Early phenotypic assignment of affected family members and collection of germline and tumoral DNA from multiple kindreds should also facilitate the genetic analysis leading to the identity of the disease gene. Evaluation of affected family members at varying stages of disease will contribute to our understanding of the natural history of carcinoid tumors and the relative utility of a variety of diagnostic and surveillance tests. Hopefully, such knowledge gained will also be applicable to patients with carcinoid tumors occurring sporadically or in the setting of other familial cancer syndromes. There is no planned treatment for patients with existing or newly diagnosed primary or metastatic carcinoid tumors. However, these patients may be evaluated by consultation with oncology and surgery for potential treatment.

类癌瘤是罕见的，并导致要么没有或很少非特异性症状。 因此，患有类癌肿瘤的患者通常在其疾病过程的后期出现，此时由于转移性疾病已经进展到不可治愈的状态。 目前，既没有实用的人群筛查试验，也没有有效的治疗方法，因此5年生存率很低。 由于散发性类癌的罕见性，大规模的基因分析和敏感性和特异性诊断测试的开发尚未成功。 虽然与家族性类癌肿瘤，不归因于已知的遗传综合征是非常罕见的，他们提供了一个独特的机会，以促进责任基因突变的鉴定。 此外，罕见的家族性形式中的突变基因也可能是更常见的散发性类癌发生的起源的基础。 我们建议研究家族中至少有两个已知的受影响的成员与类癌肿瘤。我们的目标是早期诊断患者，因此有可能治愈隐匿性疾病。因此，具有高达50%的携带类癌肿瘤的终生风险的家庭成员将在初始和随后的两年随访中使用生化，内窥镜和成像方式进行强化诊断评估。 受影响的家庭成员的早期表型分配和生殖系和肿瘤DNA的收集，从多个激酶也应该促进遗传分析，导致疾病基因的身份。 在疾病的不同阶段评估受影响的家庭成员将有助于我们了解类癌肿瘤的自然史和各种诊断和监测测试的相对效用。希望这些知识也能应用于偶发性类癌或其他家族性癌症综合征的患者。 对于患有现有或新诊断的原发性或转移性类癌的患者，没有计划的治疗。 然而，这些患者可能会通过与肿瘤科和手术咨询进行评估，以寻求潜在的治疗。