Modeling Bilateral Lymphatic Head and Neck Tumour Progression for Personalized Elective Target Volume Definition

Fuente: arXiv
Saved in:
Bibliographic Details
Main Authors: Moos, Kristoffer, Holm, Anne Ivalu Sander, Haas, Yoel Perez, Ludwig, Roman, Eriksen, Jesper Grau, Korreman, Stine Sofia
Format: Preprint
Published: 2025
Subjects:
Online Access:
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866909814770106368
author Moos, Kristoffer
Holm, Anne Ivalu Sander
Haas, Yoel Perez
Ludwig, Roman
Eriksen, Jesper Grau
Korreman, Stine Sofia
author_facet Moos, Kristoffer
Holm, Anne Ivalu Sander
Haas, Yoel Perez
Ludwig, Roman
Eriksen, Jesper Grau
Korreman, Stine Sofia
contents Objective: Large irradiated volumes are a major contributor to severe side-effects in patients with head and neck cancer undergoing curatively intended radiotherapy. We propose a data-driven approach for defining the elective clinical target volume (CTV-E) on a patient-specific basis, with the potential to reduce irradiated volumes compared to standard guidelines. Approach: We introduce a bilateral Bayesian Network (BN), trained on a large cohort, to estimate the patient-specific risk of undetected nodal involvement for both ipsilateral and contralateral lymph node levels (LNLs) I, II, III, and IV, using clinical features, such as patterns of nodal involvement, T-stage, tumour location. By applying risk thresholds, we generated individualized, risk-dependent CTV-E's for representative patient scenarios and compared the resulting treatment volumes and residual risk to those recommended by standard clinical guidelines. Main results: We computed the risks for a set of representative patient scenarios including 1) N0 (T1 and T2 tumour stage), 2) N+ in ipsilateral LNL II (T1 and T2 tumour stage), 3) N+ in ipsilateral LNL II and III (T1 and T2 tumour stage), and 4) N+ of both ipsilateral and contralateral LNL II (T3 and T4 tumour stage). Depending on the chosen risk threshold, the bilateral BN allowed for reductions in irradiated volumes relative to standard clinical protocols. For every patient scenario considered, the CTV-E's defined by the applied risk thresholds were associated with a low estimated probability of undetected nodal involvement in any excluded LNL. Significance: We present a data-driven framework for personalized CTV-E definition, encouraging the discussion of more patient-specific elective nodal target volumes, with potential for de-escalation of irradiated elective volumes.
format Preprint
id arxiv_https___arxiv_org_abs_2509_24911
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Modeling Bilateral Lymphatic Head and Neck Tumour Progression for Personalized Elective Target Volume Definition
Moos, Kristoffer
Holm, Anne Ivalu Sander
Haas, Yoel Perez
Ludwig, Roman
Eriksen, Jesper Grau
Korreman, Stine Sofia
Medical Physics
Objective: Large irradiated volumes are a major contributor to severe side-effects in patients with head and neck cancer undergoing curatively intended radiotherapy. We propose a data-driven approach for defining the elective clinical target volume (CTV-E) on a patient-specific basis, with the potential to reduce irradiated volumes compared to standard guidelines. Approach: We introduce a bilateral Bayesian Network (BN), trained on a large cohort, to estimate the patient-specific risk of undetected nodal involvement for both ipsilateral and contralateral lymph node levels (LNLs) I, II, III, and IV, using clinical features, such as patterns of nodal involvement, T-stage, tumour location. By applying risk thresholds, we generated individualized, risk-dependent CTV-E's for representative patient scenarios and compared the resulting treatment volumes and residual risk to those recommended by standard clinical guidelines. Main results: We computed the risks for a set of representative patient scenarios including 1) N0 (T1 and T2 tumour stage), 2) N+ in ipsilateral LNL II (T1 and T2 tumour stage), 3) N+ in ipsilateral LNL II and III (T1 and T2 tumour stage), and 4) N+ of both ipsilateral and contralateral LNL II (T3 and T4 tumour stage). Depending on the chosen risk threshold, the bilateral BN allowed for reductions in irradiated volumes relative to standard clinical protocols. For every patient scenario considered, the CTV-E's defined by the applied risk thresholds were associated with a low estimated probability of undetected nodal involvement in any excluded LNL. Significance: We present a data-driven framework for personalized CTV-E definition, encouraging the discussion of more patient-specific elective nodal target volumes, with potential for de-escalation of irradiated elective volumes.
title Modeling Bilateral Lymphatic Head and Neck Tumour Progression for Personalized Elective Target Volume Definition
topic Medical Physics
url https://arxiv.org/abs/2509.24911