TY - JOUR
T1 - Pathological stage grouping of patients with resected carcinoma of the lung
AU - Shields, T. W.
AU - Humphrey, E. W.
AU - Matthews, M.
AU - Eastridge, C. E.
AU - Keehn, R. J.
PY - 1980
Y1 - 1980
N2 - Data from a series of 569 patients with 'curative' resection of non-oat cell tumors were analyzed by the life-table method to evaluate the validity of the postresection pathological staging classification suggested by the American Joint Committee. The cell types were as follows: squamous, 305; adenocarcinoma, 172; large cell, 73; and mixed, 19. Each patient was assigned a pathological TN classification on examination of the resected specimen (all patients were judged clinically to have no distant metastases - MO). There were 173 lesions classified as T1 No. 37 as T1 N1, 212 as T2 NO, 115 as T2, N1, and 32 as either T3 with any N or N2 with any T. In analyzing the data, we identified a subset of lesions (25), initially staged as T2 NO, which were small central lesions, 3 cm or less, located distal to a lobar takeoff. Regardless of the presence of atelectasis or pneumonitis to the hilar area, patients with these lesions had a survival rate similar to that of patients with lesions larger than 3 cm, which could be classified as T2 NO regardless of their location. When lymph nodes were affected (N1), patients with small central lesions (20) had a better survival rate than the patients with either T1 N1 or other T2 N1 lesions. It is therefore suggested that all small central lesions, 3 cm or less, distal to a lobar takeoff be considered T1 lesions. Patients with T1 N1 lesions had a 3 year survival rate of only 36.7%, which is similar to the 39.8% 3-year survival rate of those with T2 N1 lesions. The other patients in Stage 1 had a much better survival rate: Patients with T1 NO lesions had 3 and 5 year survival rates of 68.5% and 54.4%, and those with T2 NO lesions, 53.6% and 40.0%, respectively. Therefore, it would appear more appropriate to classify these patients as having Stage II rather than Stage I disease.
AB - Data from a series of 569 patients with 'curative' resection of non-oat cell tumors were analyzed by the life-table method to evaluate the validity of the postresection pathological staging classification suggested by the American Joint Committee. The cell types were as follows: squamous, 305; adenocarcinoma, 172; large cell, 73; and mixed, 19. Each patient was assigned a pathological TN classification on examination of the resected specimen (all patients were judged clinically to have no distant metastases - MO). There were 173 lesions classified as T1 No. 37 as T1 N1, 212 as T2 NO, 115 as T2, N1, and 32 as either T3 with any N or N2 with any T. In analyzing the data, we identified a subset of lesions (25), initially staged as T2 NO, which were small central lesions, 3 cm or less, located distal to a lobar takeoff. Regardless of the presence of atelectasis or pneumonitis to the hilar area, patients with these lesions had a survival rate similar to that of patients with lesions larger than 3 cm, which could be classified as T2 NO regardless of their location. When lymph nodes were affected (N1), patients with small central lesions (20) had a better survival rate than the patients with either T1 N1 or other T2 N1 lesions. It is therefore suggested that all small central lesions, 3 cm or less, distal to a lobar takeoff be considered T1 lesions. Patients with T1 N1 lesions had a 3 year survival rate of only 36.7%, which is similar to the 39.8% 3-year survival rate of those with T2 N1 lesions. The other patients in Stage 1 had a much better survival rate: Patients with T1 NO lesions had 3 and 5 year survival rates of 68.5% and 54.4%, and those with T2 NO lesions, 53.6% and 40.0%, respectively. Therefore, it would appear more appropriate to classify these patients as having Stage II rather than Stage I disease.
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U2 - 10.1016/s0022-5223(19)37765-7
DO - 10.1016/s0022-5223(19)37765-7
M3 - Article
C2 - 7412343
AN - SCOPUS:0019214705
SN - 0022-1120
VL - 80
SP - 400
EP - 405
JO - Unknown Journal
JF - Unknown Journal
IS - 3
ER -