eMedicine Specialties > Thoracic Surgery > Tumors
Carcinoid Lung Tumors: Follow-up
Updated: Oct 23, 2008
Outcome and Prognosis
Carcinoid tumors of the lung generally have a better prognosis than other forms of pulmonary malignancy. They possess an overall 5-year survival rate of 78-95% and a 10-year survival rate of 77-90%.
Typical carcinoid tumors have been found to have a much better prognosis than do the atypical variety. Atypical carcinoid tumors have been associated with a 5-year survival rate of 40-60% and a 10-year survival rate of 31-60%, depending on the series.
Regardless of the histologic type, the presence of lymph node metastases at the time of resection has a significant effect on prognosis in many series, producing 5-year survival rates of 37-80% and 10-year rates of 22-80%. This wide variation in survival rates is likely related to the percent of atypical carcinoid tumors present in each analyzed series.
The presence of tumorlets associated with the primary tumor appears to worsen the prognosis.
Whether or not tumor size is a prognostic risk factor is uncertain.
The presence of carcinoid syndrome or other paraneoplastic syndromes in the absence of lymph node or distant metastases does not seem to affect prognosis adversely.14,16,17,18,19
Future and Controversies
The exact determination of the specific histologic entities within the spectrum of pulmonary neuroendocrine tumors is an area of considerable controversy. Several authors have renamed the entire spectrum of pulmonary neuroendocrine neoplasms based on more advanced histologic study. One classification system labels typical carcinoid tumors as type 1 Kulchitsky cell carcinoma, atypical carcinoids as type 2 Kulchitsky cell carcinomas, and small cell carcinoma as type 3. Another defines these as well-differentiated, intermediate cell, and small cell neuroendocrine carcinomas.
Additional changes in tumor classification also have been proposed specifically regarding atypical carcinoid tumors. Recently, a number of subcategories of atypical carcinoid have been described based upon the identification of genetic molecular abnormalities. The addition of genetic marker identification to previous methods of tumor analysis has resulted in further subclassification for some of the more aggressive types of these neuroendocrine tumors. Large cell neuroendocrine and mixed small-large cell neuroendocrine carcinomas have been proposed as high-grade tumors more closely related to small cell carcinoma than to carcinoids, falling into the disease spectrum between atypical carcinoid and small cell carcinoma.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous author Jane M Eggerstedt, MD, to the development and writing of this article.
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Further Reading
Keywords
carcinoid lung tumor, bronchial adenomas, typical carcinoids, atypical carcinoids, neuroendocrine lung tumors, pulmonary neoplasms, bronchopulmonary carcinoid tumors, carcinoid syndrome, lung cancer, intrabronchial mass
Follow-up: Carcinoid Lung Tumors