TY - JOUR
T1 - Liquid fiducial marker performance during radiotherapy of locally advanced non small cell lung cancer
AU - Rydhög, Jonas Scherman
AU - Mortensen, Steen Riisgaard
AU - Larsen, Klaus Richter
AU - Clementsen, Paul
AU - Jølck, Rasmus Irming
AU - Josipovic, Mirjana
AU - Aznar, Marianne Camille
AU - Specht, Lena
AU - Andresen, Thomas Lars
AU - Rosenschöld, Per Munck Af
AU - Persson, Gitte Fredberg
PY - 2016
Y1 - 2016
N2 - We analysed the positional and structural stability of a long-term biodegradable liquid fiducial marker (BioXmark) for radiotherapy in patients with locally advanced lung cancer. Markers were injected via endoscopic- or endobronchial ultrasound in lymph nodes and reachable primary tumours. Marker volume and Hounsfield Units (HU) changing rates were estimated using breath-hold CBCT. Inter-fraction variation in marker position relative to gross tumour volume (GTV) position was established, as well as the inter-fraction variation in mediastinal marker registration relative to a carina registration through the treatment. Fifteen patients were included and 29 markers analysed. All markers that were in situ at planning were visible through the treatment. Mean HU was 902±165HU for lymph node and 991±219HU for tumour markers. Volume degradation rates were -5% in lymph nodes and -23% in primary tumours. Three-dimensional inter-fraction variation for marker position relative to the GTV position was -0.1±0.7mm in lymph nodes and -1.5±2.3mm in primary tumours. Inter-fraction variations in marker registration relative to carina registration were -0.4±1.2mm in left-right, 0.2±2.0mm in anterior-posterior and -0.5±2.0mm in cranio-caudal directions. The liquid fiducial markers were visible and stable in size and position throughout the treatment course.
AB - We analysed the positional and structural stability of a long-term biodegradable liquid fiducial marker (BioXmark) for radiotherapy in patients with locally advanced lung cancer. Markers were injected via endoscopic- or endobronchial ultrasound in lymph nodes and reachable primary tumours. Marker volume and Hounsfield Units (HU) changing rates were estimated using breath-hold CBCT. Inter-fraction variation in marker position relative to gross tumour volume (GTV) position was established, as well as the inter-fraction variation in mediastinal marker registration relative to a carina registration through the treatment. Fifteen patients were included and 29 markers analysed. All markers that were in situ at planning were visible through the treatment. Mean HU was 902±165HU for lymph node and 991±219HU for tumour markers. Volume degradation rates were -5% in lymph nodes and -23% in primary tumours. Three-dimensional inter-fraction variation for marker position relative to the GTV position was -0.1±0.7mm in lymph nodes and -1.5±2.3mm in primary tumours. Inter-fraction variations in marker registration relative to carina registration were -0.4±1.2mm in left-right, 0.2±2.0mm in anterior-posterior and -0.5±2.0mm in cranio-caudal directions. The liquid fiducial markers were visible and stable in size and position throughout the treatment course.
KW - Image-guided radiotherapy
KW - Liquid fiducial marker
KW - Marker visibility
KW - NSCLC
U2 - 10.1016/j.radonc.2016.06.012
DO - 10.1016/j.radonc.2016.06.012
M3 - Journal article
C2 - 27443450
SN - 0167-8140
VL - 121
SP - 64
EP - 69
JO - Radiotherapy & Oncology
JF - Radiotherapy & Oncology
IS - 1
ER -