Prediction of radiation pneumonitis using the effective α/β of lungs and heart in NSCLC patients treated with proton beam therapy


Prediction of radiation pneumonitis using the effective α/β of lungs and heart in NSCLC patients treated with proton beam therapy

Weiß, A.; Löck, S.; Xu, T.; Liao, Z.; Hoffmann, A. L.; Troost, E. G. C.

Purpose: Radiation pneumonitis (RP) remains a major complication in non-small cell lung cancer (NSCLC) pa-
tients undergoing radiochemotherapy (RCHT). Traditionally, the mean lung dose (MLD) and the volume of the
total lung receiving at least 20 Gy (V20Gy) are used to predict RP in patients treated with normo-fractionated
photon therapy.
However, other models, including the actual dose-distribution in the lungs using the effective α/β model or a
combination of radiation doses to the lungs and heart, have been proposed for predicting RP. Moreover, the
models established for photons may not hold for patients treated with passively-scattered proton therapy (PSPT).
Therefore, we here tested and validated novel predictive parameters for RP in NSCLC patient treated with PSPT.
Methods: Data on the occurrence of RP, structure files and dose-volume histogram parameters for lungs and heart
of 96 NSCLC patients, treated with PSPT and concurrent chemotherapy, was retrospectively retrieved from
prospective clinical studies of two international centers. Data was randomly split into a training set (64 patients)
and a validation set (32 patients). Statistical analyses were performed using binomial logistic regression.
Results: The biologically effective dose (BED) of the’lungs - GTV’ significantly predicted RP ≥ grade 2 in the
training-set using both a univariate model (p = 0.019, AUCtrain = 0.72) and a multivariate model in combination
with the effective α/β parameter of the heart (pBED = 0.006, pα/βeff = 0.043, AUCtrain = 0.74). However, these
results did not hold in the validation-set (AUCval = 0.52 andAUCval = 0.50, respectively). Moreover, these models
were found to neither outperform a model built with the MLD (p = 0.015, AUCtrain = 0.73, AUCval = 0.51), nor a
multivariate model additionally including the V20Gy of the heart (pMLD = 0.039, pV20Gy,heart = 0.58, AUCtrain =
0.74, AUCval = 0.53).
Conclusion: Using the effective α/β parameter of the lungs and heart we achieved similar performance to
commonly used models built for photon therapy, such as MLD, in predicting RP ≥ grade 2. Therefore, prediction
models developed for photon RCHT still hold for patients treated with PSPT.

Keywords: NTCP; NSCLC; PSPT; Radiation pneumonitis; Effective α/β

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