Abstract 279P
Background
The moderated hypofractionation (MoHF) radiotherapy (RT) protocols offer an alternative treatment (Tx) that solves both the workload issue as well as the duration of Tx for prostate cancer (PC) patients while delivering a more adapted dose to the tumor cells. Therefore, the MoHF protocol has been implemented in our department using the Volumetric Arc Modulated Therapy (VMAT) with Image Guided Radiation Therapy (IGRT) for our PC patients.
Methods
From May 24th 2021 to June 30th 2023, there were totally 23 patients who were applied the MoHF protocols. Initially, we implemented protocol of 60Gy in 20 fractions (60Gy/20fx) for intermediate-risk PC patients. Since December 2022, the protocol of 68Gy in 25 fractions (68Gy/25fx) was implemented for high-risk PC patients based on the new data of PCS5 trial. All patients were treated accordingly to institutional protocol for Tx of PC. A weekly consultation during RT course was also held for each patient to follow up with the possible acute side effects.
Results
The average duration to complete Tx planning was 7 days. For dose constraint achievement, 100% of planning had D2% < 107% of dose prescription while 21/23 plans (91.30%) achieved the criteria of planning target volum (PTV) coverage as well as organs at risk (OARs) protection. 2/23 plans (8.70%) were validated with a minor deviation in either target coverage or OARs constraints. The most common acute toxicity was dysuria which happened on 21/23 cases (91.30%) with grade 1 or 2. This side effect was resolutive in 100% of patients within 1 month after completion of Tx. No grade 3 or higher acute or late toxicity was reported. The cost-effectiveness of the MoHF protocols, was compared to a normo-fractionated protocol in 8 weeks (80Gy/40fx). The cost of RT was reduced by 25% going from more than 7000USD for the 8-weeks protocol to 5800USD for the 68Gy/25fx protocol and to 4900USD for the 60Gy/20fx protocol. The entire treatment costs were further reduced due to lower accommodation and transportation fees in the shorter protocols.
Conclusions
For PC patients indicated with definitive RT, the MoHF is a more convenient and safer alternative with manageable side effects and a reduction of treatment direct and indirect cost.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The author.
Funding
Has not received any funding.
Disclosure
The author has declared no conflicts of interest.
Resources from the same session
613P - Differences in the interactions with pharmaceutical companies between medical oncologists and infectious diseases physicians
Presenter: Hui Ling Yeoh
Session: Poster Display
Resources:
Abstract
614P - The role of PD-L1 expression in prognosis of osteosarcoma patients: A systematic review and meta-analysis
Presenter: Alexander Purnomo
Session: Poster Display
Resources:
Abstract
615P - Pulmonary resectable metastases of osteosarcoma with apatinib and chemotherapy (PROACH): An open-label, single-arm phase II clinical trial
Presenter: Qiyuan Bao
Session: Poster Display
Resources:
Abstract
616P - Incidence of cardiotoxicity after high cumulative dose of anthracyclines in adult patients with advanced soft tissue sarcomas: A systematic review and meta-analysis
Presenter: Paula Franco
Session: Poster Display
Resources:
Abstract
617P - The risk of acute myeloid leukaemia in patients with Ewing's sarcoma and trend analysis: A SEER-based study 2000-2020
Presenter: Mohamed Abdalla
Session: Poster Display
Resources:
Abstract
618P - Adult renal Ewing’s sarcoma/primitive neuroectodermal tumor: A 20-year retrospective review of molecular histopathological profiles, and clinical outcomes
Presenter: Josh Thomas Georgy
Session: Poster Display
Resources:
Abstract
619P - Single-cell and bulk RNA-seq analyses decode the renal microenvironment induced by polystyrene microplastics in mice receiving high-fat diet
Presenter: Wangrui Liu
Session: Poster Display
Resources:
Abstract
620P - A unique circulating microRNA pairs signature serves as a superior tool for early diagnosis of pan-cancer
Presenter: Dongyu Li
Session: Poster Display
Resources:
Abstract
621P - Effective identification of primary liver cancer from cirrhosis or chronic hepatitis virus infection using eight methylated plasma DNA markers: Marker discovery, phase I pilot, and phase II clinical validation
Presenter: Tian Yang
Session: Poster Display
Resources:
Abstract
622P - A prognostic and immune infiltration analysis of CCL26 in pan-cancer
Presenter: Mengyue Li
Session: Poster Display
Resources:
Abstract