Published June 2014 | Version v1
Journal article

SU-D-16A-03: A Radiation Pneumonitis Dose-Response Model Incorporating Non- Local Radiation-Induced Bystander Effect

  • 1. Henry Ford Health System, Dept. Radiation Oncology, Detroit, MI (United States)

Description

Purpose: Dose-response models that can reliably predict radiation pneumonitis (RP) to guide radiation therapy (RT) for lung cancer presently do not exist. A model is proposed that incorporates non-local radiationinduced bystander effect (RIBE). Methods: A single sigmoid response function, derived from published data for whole lung irradiation, relates RP probability to cumulative lung damage, regardless of fractionation scheme. Lung damage is assumed to be caused by direct local radiation damage, quantified via the linear-quadratic (LQ) model, and RIBE. Based on published data, RIBE is assumed to be activated when per-fraction dose rises above ∼0.6 Gy, but is constant with dose above that threshold. Integral RIBE damage is assumed proportional to lung volume irradiated above ∼0.6 Gy per fraction. Key model parameters include LQ α and β, and two RIBE parameters: the single-fraction probability δ of damage, and a proportionality parameter κ that relates the potential for RIBE damage to irradiated lung volume. All parameters are tentatively fitted from published data, the RIBE parameters from published RP rates for conventionally fractionated RT (CFRT) and stereotactic body RT (SBRT). Results: The model predicts dose-response curves that are consistent with clinical experience. It provides a tentative explanation for why V20 (33 fractions), V13 (20 fractions) and V5 (<10 fractions) are observed to be correlated with RP. It also provides a plausible explanation for the success of SBRT — RIBE damage increases with the number of fractions, so penalizes CFRT relative to SBRT. Conclusion: The proposed model is relatively simple, extrapolates from published data, plausibly explains several clinical observations, and produces dose-response curves that are consistent with clinical experience. While capable of elaboration, its ability to explain doseresponse experience with different fractionation schemes using a small number of assumptions and parameters is an advantage

Additional details

Identifiers

Publishing Information

Journal Title
Medical Physics
Journal Volume
41
Journal Issue
6
Journal Page Range
p. 108
ISSN
0094-2405
CODEN
MPHYA6

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46040250
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
BIOLOGICAL RADIATION EFFECTS; FRACTIONATION; IRRADIATION; LUNGS; NEOPLASMS; PNEUMONITIS; RADIATION DOSES; RADIOTHERAPY; RESPONSE FUNCTIONS
Descriptors DEC
BIOLOGICAL EFFECTS; BODY; DISEASES; DOSES; FUNCTIONS; MEDICINE; NUCLEAR MEDICINE; ORGANS; RADIATION EFFECTS; RADIOLOGY; RESPIRATORY SYSTEM; SEPARATION PROCESSES; THERAPY

Optional Information

Notes
(c) 2014 American Association of Physicists in Medicine