TY - JOUR
T1 - Radiotherapy quality assurance of the prospective randomised EORTC-1219/DAHANCA-29 trial
T2 - an individual case review analysis
AU - Alyamani, Najlaa
AU - Abrunhosa-Branquinho, André
AU - Corning, Coreen
AU - Sharabiani, Marjan
AU - Castadot, Pierre
AU - Giralt, Jordi
AU - Kazmierska, Joanna
AU - Grant, Warren
AU - Christiaens, Melissa
AU - Tomsej, Milan
AU - Bar-Deroma, Raquel
AU - Monti, Angelo F.
AU - Stelmes, Jean Jacques
AU - Clementel, Enrico
AU - Fortpied, Catherine
AU - Collette, Sandra
AU - Hurkmans, Coen W.
AU - Grégoire, Vincent
AU - Overgaard, Jens
AU - Weber, D. C.
AU - Andratschke, Nicolaus
N1 - Publisher Copyright:
© 2025
PY - 2025/12
Y1 - 2025/12
N2 - Background: The EORTC-1219/DAHANCA-29 trial investigated whether adding nimorazole to accelerated radiotherapy (RT) and chemotherapy improves locoregional control of locally advanced head and neck cancer. As part of the trial's RT quality assurance (RTQA) program, individual case review (ICR) of RT plans was performed to assess protocol compliance and treatment planning quality. Materials and methods: Nineteen centers submitted RT plans for central review. The trial mandated prospective ICR (p-ICR) for the first five patients per institution, with subsequent plans reviewed retrospectively or as optional p-ICR. Plans were reviewed by radiation oncologists and medical physicists. Plans deemed unacceptable in p-ICR were resubmitted for review, whereas retrospective ICR (r-ICR) cases were reviewed once. Plans were categorized as “Acceptable as per protocol,” “Acceptable variation,” or “Unacceptable variation.”. Results: RT plans for all 194 randomized patients were reviewed, with 174p-ICRs and 44 r-ICRs. The delineation acceptability rate for p-ICR improved from 69% at the first submission to 93% at final review. p-ICR had an 18% higher acceptance rate (90%) compared to r-ICR (73%). Dose and plan acceptability remained high (97%) at both first and final submission, with minimal differences between p-ICR and r-ICR. Conclusion: P-ICR significantly improved CTV delineation quality, ensuring higher protocol compliance and treatment planning accuracy. p-ICRs are recommended for complex treatments, tailored to the performance of individual sites.
AB - Background: The EORTC-1219/DAHANCA-29 trial investigated whether adding nimorazole to accelerated radiotherapy (RT) and chemotherapy improves locoregional control of locally advanced head and neck cancer. As part of the trial's RT quality assurance (RTQA) program, individual case review (ICR) of RT plans was performed to assess protocol compliance and treatment planning quality. Materials and methods: Nineteen centers submitted RT plans for central review. The trial mandated prospective ICR (p-ICR) for the first five patients per institution, with subsequent plans reviewed retrospectively or as optional p-ICR. Plans were reviewed by radiation oncologists and medical physicists. Plans deemed unacceptable in p-ICR were resubmitted for review, whereas retrospective ICR (r-ICR) cases were reviewed once. Plans were categorized as “Acceptable as per protocol,” “Acceptable variation,” or “Unacceptable variation.”. Results: RT plans for all 194 randomized patients were reviewed, with 174p-ICRs and 44 r-ICRs. The delineation acceptability rate for p-ICR improved from 69% at the first submission to 93% at final review. p-ICR had an 18% higher acceptance rate (90%) compared to r-ICR (73%). Dose and plan acceptability remained high (97%) at both first and final submission, with minimal differences between p-ICR and r-ICR. Conclusion: P-ICR significantly improved CTV delineation quality, ensuring higher protocol compliance and treatment planning accuracy. p-ICRs are recommended for complex treatments, tailored to the performance of individual sites.
KW - Chemo-radiation therapy
KW - EORTC-1219
KW - Head and Neck cancer
KW - Individual Case Review
KW - Radiotherapy quality assurance
UR - https://www.scopus.com/pages/publications/105018696550
U2 - 10.1016/j.radonc.2025.111141
DO - 10.1016/j.radonc.2025.111141
M3 - Article
C2 - 40987385
AN - SCOPUS:105018696550
SN - 0167-8140
VL - 213
JO - Radiotherapy and Oncology
JF - Radiotherapy and Oncology
M1 - 111141
ER -