Predictors of acute lymphopenia after radiotherapy for prostate cancer including pelvic node irradiation: results of a real-world prospective multi-centric study

Background: Acute lymphopenia (AL) is a clinically relevant concern in patients undergoing pelvic lymph-node irradiation (PNI) for prostate cancer (PCa) and reliable predictive models are not available.The purpose of the current analysis was to develop a predictive model of AL after PNI for PCa combining dosimetric and clinical information in a large, prospectively followed cohort.Materials and methods: Clinical/dosimetry/blood test data from a multi-centric prospective study were available, including absolute lymphocyte count (ALC) at baseline, mid-point and radiotherapy (RT) end.Dose-volume histograms (DVHs) of the body and of pelvic bones were extracted, as well as the integral dose (ID) to the body.Lymph-nodal planning target volume (LN-PTV) and its cranial limit were also recovered.The current analysis focused on acute CTCAEv4.03 grade 3 (G3+) lymphopenia (ALC < 500/l), defined as the lowest count between baseline and mid-point or RT end.The patient population was split into training and validation cohorts, and a multivariable logistic regression model combining DVHs and clinical information was trained and validated.Results: 700/887 patients with full 3D planning data and available baseline, mid-point and RT end counts were considered.290 patients (41.4%) experienced acute G3+ lymphopenia.Both ID and pelvic bone DVH parameters were significantly associated with the endpoint.The two best resulting models included baseline ALC (OR = 0.999, P < 0.001) and ID (Gy*l) (OR = 1.003,P = 0.012) or baseline ALC, cranial LN-PTV limit (OR = 1.019,P < 0.001) and EQD2 to LN-PTV (OR = 1.095,P = 0.002), when replacing ID with the cranial LN-PTV limit.Conclusions: Severe AL after PNI for PCa is largely modulated by baseline ALC, with an independent role of the LN-PTV cranial limit or, alternatively, of ID, with the risk increasing by 5%-10% per 10 2 Gy*l.

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Journal
ESMO Real World Data and Digital Oncology
Published
2026-01-30
DOI
https://doi.org/10.1016/j.esmorw.2025.100680
Primary Topic
Inflammatory Biomarkers in Disease Prognosis
Type
article
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article

Predictors of acute lymphopenia after radiotherapy for prostate cancer including pelvic node irradiation: results of a real-world prospective multi-centric study

Giuseppe Sanguineti, Alessandra Maggio, C. Cozzarini, B. Avuzzi et al.
ESMO Real World Data and Digital Oncology
Inflammatory Biomarkers in Disease Prognosis
article

Predictors of acute lymphopenia after radiotherapy for prostate cancer including pelvic node irradiation: results of a real-world prospective multi-centric study

Giuseppe Sanguineti, Alessandra Maggio, C. Cozzarini, B. Avuzzi, A. Cicchetti, N. Di Muzio, Stefania Aimonetto, Maddalena Pavarini, Valeria Landoni, B. Farina, T. Giandini, J.M. Waskiewicz, Lisa Alborghetti, Antonella Bianculli, Giuseppe Girelli, F. Muñoz, P. Salmoiraghi, Tiziana Rancati, E. Petrucci, E. Villa, L. Rago, B. Noris Chiorda, A. Magli, D. Cante, E. Moretti, P. Ferrari, C. Fiorino, V. Vavassori
article en

Abstract

Background: Acute lymphopenia (AL) is a clinically relevant concern in patients undergoing pelvic lymph-node irradiation (PNI) for prostate cancer (PCa) and reliable predictive models are not available.The purpose of the current analysis was to develop a predictive model of AL after PNI for PCa combining dosimetric and clinical information in a large, prospectively followed cohort.Materials and methods: Clinical/dosimetry/blood test data from a multi-centric prospective study were available, including absolute lymphocyte count (ALC) at baseline, mid-point and radiotherapy (RT) end.Dose-volume histograms (DVHs) of the body and of pelvic bones were extracted, as well as the integral dose (ID) to the body.Lymph-nodal planning target volume (LN-PTV) and its cranial limit were also recovered.The current analysis focused on acute CTCAEv4.03 grade 3 (G3+) lymphopenia (ALC < 500/l), defined as the lowest count between baseline and mid-point or RT end.The patient population was split into training and validation cohorts, and a multivariable logistic regression model combining DVHs and clinical information was trained and validated.Results: 700/887 patients with full 3D planning data and available baseline, mid-point and RT end counts were considered.290 patients (41.4%) experienced acute G3+ lymphopenia.Both ID and pelvic bone DVH parameters were significantly associated with the endpoint.The two best resulting models included baseline ALC (OR = 0.999, P < 0.001) and ID (Gy*l) (OR = 1.003,P = 0.012) or baseline ALC, cranial LN-PTV limit (OR = 1.019,P < 0.001) and EQD2 to LN-PTV (OR = 1.095,P = 0.002), when replacing ID with the cranial LN-PTV limit.Conclusions: Severe AL after PNI for PCa is largely modulated by baseline ALC, with an independent role of the LN-PTV cranial limit or, alternatively, of ID, with the risk increasing by 5%-10% per 10 2 Gy*l.

ESMO Real World Data and Digital OncologyVol. 11
Vita-Salute San Raffaele University (IT), Ospedale di Bolzano (IT), Ospedale degli Infermi (IT), Centro di Riferimento Oncologico della Basilicata (IT), Ospedale Civile Di Ivrea (IT), Humanitas Gavazzeni (IT), Ospedale Santa Maria della Misericordia di Udine (IT), Azienda USL della Valle d’Aosta (IT), Candiolo Cancer Institute (IT), Ospedale degli Infermi (IT), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Fondazione IRCCS Istituto Nazionale dei Tumori (IT), Fondazione Piemontese per la Ricerca sul Cancro Onlus (IT), Instituto Nazionale Tumori Regina Elena (IT)
Associazione Italiana per la Ricerca sul Cancro
Good health and well-being
Openalex Percentile: Top 73%
Inflammatory Biomarkers in Disease Prognosis
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