ACCURATE PREDICTION OF LONG-TERM RISK OF BIOCHEMICAL FAILURE AFTER SALVAGE RADIOTHERAPY INCLUDING THE IMPACT OF PELVIC NODE IRRADIATION.

Explainable models of long-term risk of biochemical failure (BF) after post-prostatectomy salvage radiotherapy (SRT) are lacking. A previously introduced radiobiology-based formula was adapted to incorporate the impact of pelvic nodes irradiation (PNI).

The risk of post-SRT BF may be expressed by a Poisson-based equation including pre-SRT PSA, the radiosensitivity α, the clonogen density C, the prescribed dose (in terms of EQD2, α/β=1.5Gy) and a factor (1-BxλxPSA) accounting for clonogens outside the irradiated volume, being λ the recovery due to PNI. Data of 795 pT2-pT3, pN0/pN1/pNx (n=627/94/74) patients with follow-up ≥5 years and pre-RT PSA ≤2ng/mL were randomly split into training (n=528) and validation (n=267) cohorts; the training cohort data were fitted by the least square method. Separate fits were performed for different risk groups. Model performances were assessed by calibration plots and tested in the validation group.

The median follow-up was 8.5y, median pre-SRT PSA and EQD2 were 0.43ng/mL and 71.3Gy respectively; 331/795 pts received PNI. The most clinically significant prognostic grouping was pT3b and/or ISUP4-5 versus pT2/3a and ISUP1-3. Best-fit parameters were αeff=0.26/0.23Gy-1, C=107/107, B=0.40/0.97, λ=0.87/0.41 for low/high-risk group. Performances were confirmed in the validation group (slope=0.89,R2=0.85). Results suggested optimal SRT dose at 70-74Gy. The estimated reduction of post-SRT BF due to PNI at these dose values was >5% for PSA >1/>0.15ng/mL for low/high-risk patients, being >10% for high-risk patients with pre-SRT PSA>0.25 ng/mL.

An explainable one-size-fits-all equation satisfactorily predicts long-term risk of post-SRT BF. The model was independently validated. A calculator tool was made available.

Radiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology. 2022 Aug 04 [Epub ahead of print]

Cesare Cozzarini, Michela Olivieri, Alessandro Magli, Domenico Cante, Barbara Noris Chiorda, Fernando Munoz, Adriana Faiella, Elisa Olivetta, Chiara De Antoni, Andrei Fodor, Marco Andrea Signor, Edoardo Petrucci, Barbara Avuzzi, Letizia Ferella, Alice Pastorino, Elisabetta Garibaldi, Marco Gatti, Luciana Rago, Teodora Statuto, Tiziana Rancati, Alberto Briganti, Francesco Montorsi, Riccardo Valdagni, Giuseppe Sanguineti, Nadia Gisella Di Muzio, Claudio Fiorino

IRCCS San Raffaele Scientific Institute, Milano, Italy., Azienda Ospedaliero Universitaria S. Maria della Misericordia, Udine, Italy., ASL TO4, Ospedale di Ivrea, Ivrea, Italy., Fondazione IRCCS Istituto Nazionale dei Tumori, MILANO, Italy., Ospedale Regionale Parini-AUSL Valle d'Aosta, Aosta, Italy., IRCCS Istituto Nazionale dei Tumori "Regina Elena", Roma, Italy., A.O.SS. Antonio e Biagio, Alessandria, Italy., Candiolo Cancer Institute - FPO,IRCCS Torino, Italy., Centro di Riferimento Oncologico della Basilicata (IRCCS - CROB), Rionero in Vulture (PZ)., Prostate Cancer Program, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy., San Raffaele Scientific Institute, Milano, Italy, Division of Experimental Oncology/Unit of Urology, URI, Urological Research Unit; Vita-Salute San Raffaele University, Milan, Italy., Fondazione IRCCS Istituto Nazionale dei Tumori, MILANO, Italy; Prostate Cancer Program, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy., IRCCS San Raffaele Scientific Institute, Milano, Italy; Vita-Salute San Raffaele University, Milan, Italy., IRCCS San Raffaele Scientific Institute, Milano, Italy. Electronic address: .

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