Risk of death from intercurrent disease is not excessively increased by modern postoperative radiotherapy for high-risk resected non-small-cell lung carcinoma
M. Machtay et al., Risk of death from intercurrent disease is not excessively increased by modern postoperative radiotherapy for high-risk resected non-small-cell lung carcinoma, J CL ONCOL, 19(19), 2001, pp. 3912-3917
Purpose : Some studies report a high risk of death from intercurrent diseas
e (DID) after postoperative radiotherapy (XRT) for non-small-cell lung canc
er (NSCLC). This study determines the risk of DID after modern-technique po
stoperative XRT.
Patients and Methods: A total of 202 patients were treated with surgery and
postoperative XRT for NSCLC. Most patients (97%) had pathologic stage II o
r III disease. Many patients (41%) had positive/close/uncertain resection m
argins. The median XRT dose was 55 Gy with fraction size of 1.8 to 2 Gy. Th
e risk of DID was calculated actuarially and included patients who died of
unknown/uncertain causes. Median follow-up was 24 months for all patients a
nd 62 months for survivors.
Results: A total of 25 patients (12.5%) died from intercurrent disease, 16
from confirmed noncancer causes and nine from unknown causes. The 4-year ac
tuarial rate of DID was 13.5%. This is minimally increased compared with th
e expected rate for a matched population (approximately 10% at 4 years). On
multivariate analysis, age and radiotherapy dose were borderline significa
nt factors associated with a higher risk of DID (P = .06). The crude risk o
f DID for patients receiving less than greater than or equal to 54 Gy was 2
% (4-year actuarial risk 0%) versus 17% for XRT dose a 54 Gy The 4-year act
uarial overall survival was 34%; local control was 84%; and freedom from di
stant metastases was 37%.
Conclusion: Modern postoperative XRT for NSCLC does not excessively increas
e the risk of intercurrent deaths. Further study of postoperative XRT, part
icularly when using more sophisticated treatment planning and reasonable to
tal doses, for carefully selected high-risk resected NSCLC is warranted. (C
) 2001 by American Society of Clinical Oncology.