PROGNOSTIC ASSESSMENT OF 1310 PATIENTS WITH NON-SMALL-CELL LUNG-CANCER WHO UNDERWENT COMPLETE RESECTION FROM 1980 TO 1993

Citation
K. Inoue et al., PROGNOSTIC ASSESSMENT OF 1310 PATIENTS WITH NON-SMALL-CELL LUNG-CANCER WHO UNDERWENT COMPLETE RESECTION FROM 1980 TO 1993, Journal of thoracic and cardiovascular surgery, 116(3), 1998, pp. 407-411
Citations number
14
Categorie Soggetti
Cardiac & Cardiovascular System",Surgery
ISSN journal
00225223
Volume
116
Issue
3
Year of publication
1998
Pages
407 - 411
Database
ISI
SICI code
0022-5223(1998)116:3<407:PAO1PW>2.0.ZU;2-M
Abstract
Objective: The TNM staging system of lung cancer is widely used as a g uide for estimating prognosis and selecting treatment modality. In 199 7, the International Union Against Cancer and the American Joint Commi ttee on Cancer have adopted a revised stage grouping for lung cancer, However, the validity of the new stage grouping has not been fully est ablished, We investigated the prognoses of patients who had resection of non-small-cell lung cancer to confirm the validity of the revised c lassification. Methods: A total of 1310 patients with non-small-cell l ung cancer underwent complete resection and pathologic staging of the disease in our hospitals from 1980 through 1993, A pulmonary resection was performed with a systematic nodal dissection. The survivals were calculated with the Kaplan-Meier method on the basis of overall deaths , and the survival curves were compared by log rank test. Results: The re were significant differences in survival between patients with T1 N 0 M0 and T2 N0 M0 disease and between those with T1 N1 M0 and T2 N1 M0 disease. However, there was no significant difference between patient s with T2 N0 M0 disease and those with T1 N1 M0 disease. No significan t difference in survival was observed among patients with T2 N1 M0, T3 N0 M0, and T3 N1 M0 cancer. Patients with different invaded organs of T3 subdivision (pleura, chest wall, pericardium, or diaphragm) had a different prognosis. There was no significant difference between patie nts with T3 N2 M0 disease and those with stage IIIB disease. Conclusio ns: We supported most of the revision, such as dividing stage I, divid ing stage II, and putting T3 N0 M0 to stage IIB, Furthermore, we found some candidates for a subsequent revision, such as putting T3 N1 M0 t o stage IIB, putting T2 N0 M0 and T1 N1 M0 together, regarding diaphra gm invasion as T4, and putting T3 N2 M0 to stage IIIB.