M. Roach et al., RADIATION PNEUMONITIS FOLLOWING COMBINED-MODALITY THERAPY FOR LUNG-CANCER - ANALYSIS OF PROGNOSTIC FACTORS, Journal of clinical oncology, 13(10), 1995, pp. 2606-2612
Purpose: To identify factors associated with radiation pneumonitis (RP
) resulting from combined modality therapy (CMT) for lung cancer. Mate
rials and Methods: Series published before 1994 that used CMT for the
treatment of lung cancer and explicitly reported the incidence of RP a
re the basis for this analysis. Factors evaluated included the radiati
on dose per fraction (Fx), total radiation dose, fractionation scheme
(split v continuous), type of chemotherapy and intended dose-intensity
, overall treatment time, histology (small-cell lung cancer [SCLC] v n
on-smell-cell lung cancer [NSCLC]), and treatment schedule (concurrent
v induction, sequential, or alternating CMT). Results: Twenty-four se
ries, including 27 treatment groups and 1,911 assessable patients, met
our criteria for inclusion in this analysis. The median total dose of
radiation used in the trials analyzed was 50 Gy (range, 25 to 63 Gy).
The median daily Fx used was 2.0 Gy (range, 1.5 to 4.0 Gy). Nineteen
series included 22 treatment groups and 1,745 patients treated with si
ngle daily fractions. Among these patients, 136 received a daily Fx gr
eeter than 2.67 Gy. Five series used twice-daily radiotherapy and incl
uded 166 patients (Fx, 1.5 to 1.7 Gy). The incidence of RP was 7.8%. I
n a multivariate analysis, only daily Fx, number of daily fractions, a
nd total dose were associated with the risk of RP (P < .0001, P < .018
, and P < .003, respectively). Conclusion: In this analysis, the use o
f Fx greater than 2.67 Gy was the most significant factor associated w
ith an increased risk of RP. High total dose also appears to be associ
ated with an increased risk, but twice-daily irradiation seems to redu
ce the risk expected if the same total daily dose is given as a single
fraction. High-Fx radiotherapy should be avoided in patients who rece
ive CMT with curative intent. (C) 1995 by American Society of Clinical
Oncology.