Abstract 119P
Background
To conduct a comparative analysis of the effectiveness of hypofractional and classical radiotherapy regimens in neoadjuvant chemoradiotherapy for locally advanced rectal cancer (LARC).
Methods
This study based on a retrospective analysis of a database in patients with LARC who underwent a course of neoadjuvant chemoradiotherapy followed by surgery. The patients were divided into two groups: the first (main) group, 104 patients who underwent a course of hypofractionated chemotherapy (4 Gy x 40 Gy 3 fractions per week) in combination with capecitabine 1650 mg/m2 in two doses. The second group (control group) included 120 patients who underwent a course of CRT in the classical fractionation regimen (2 Gy x 50-58 Gy 5 fractions per week) in combination with capecitabine 1650 mg/m2 in two doses. The main evaluated indicators are the frequency of pCR and cCR. Additional assessed indicators are the severity of early radiation toxicity, the frequency of local relapses, overall and disease-free survival.
Results
The study included 224 patients. The average duration of the CRT course in the study group was 22.56 (95% CI from 21.94 to 23.18) days, in the control group - 38.84 (95% CI from 38.12 to 39.54), p=0.0001. Radiation toxicity grade III and IV was registered in 5.75% of patients in the study group and in 6.41% of patients in the control group. pCR in the study groups was achieved in 19.23% and 15.83% of cases, respectively, p=0.504. The cCR in the studied groups was achieved in 25% and 18.3% of cases, respectively, p=0.226. The median time without progression was 37.6 months. In the main and control groups, local control rates were 91.34% and 88.3% respectively, p=0.954, HR=1.05 (95% CI 0.21 to 5.22). Five-year disease-free survival in the main group was 71.1% and in the control group 60.8%, respectively, p=0.353, HR=0.79 (95% CI 0.42 to 1.35). Five-year overall survival in the main and control groups were 81.7% and 79.2%, respectively, p=0.743, HR=0.87 (95% CI 0.39 to 1.92).
Conclusions
Thus, the hypofractionation regimen showed high antitumor efficacy and can be considered as an alternative and not inferior to the classical regimen in neoadjuvant CRT in patients with LARC.
Clinical trial identification
N/A
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
561P - Mechanisms of osimertinib resistance using circulating tumor DNA analyses for EGFR-mutated non-small cell lung cancer, results from ELUCIDATOR: A prospective observational multicenter study
Presenter: Daijiro Harada
Session: Poster Display
Resources:
Abstract
562P - First-line (1L) osimertinib (osi) ± platinum-pemetrexed in patients (pts) with EGFRm advanced NSCLC: FLAURA2 China cohort
Presenter: Yan Yu
Session: Poster Display
Resources:
Abstract
563P - Real-world effectiveness and safety of first-line osimertinib for EGFR-mutated advanced NSCLC in China (FLOURISH study)
Presenter: Jianya Zhou
Session: Poster Display
Resources:
Abstract
564P - Co-occurring EGFR p.E709X mutation affects the treatment response to the third-generation EGFR-TKIs in EGFR p.G719X-mutant patients with advanced NSCLC
Presenter: Wen Feng Fang
Session: Poster Display
Resources:
Abstract
565P - Genome-guided targeted therapy combination improves survival in patients with advanced EGFR mutation positive NSCLC failing osimertinib
Presenter: Molly Li
Session: Poster Display
Resources:
Abstract
566P - Safety of tepotinib + osimertinib in EGFR-mutant NSCLC with MET amplification after first-line osimertinib
Presenter: Chong Kin Liam
Session: Poster Display
Resources:
Abstract
567P - Furmonertinib in combination with bevacizumab and intrathecal chemotherapy as later-line re-challenge treatment in EGFR –mutated NSCLC patients with leptomeningeal metastasis after third-generation EGFR-TKIs treatment failure
Presenter: Fang Cun
Session: Poster Display
Resources:
Abstract
568P - First-line (1L) osimertinib + platinum-pemetrexed in EGFR-mutated (EGFRm) advanced NSCLC: Updated FLAURA2 safety run-in (SRI) results
Presenter: David Planchard
Session: Poster Display
Resources:
Abstract
569P - Whole-transcriptome sequencing of transformed small-cell lung cancer from EGFR-mutated lung adenocarcinoma reveals LUAD–like and SCLC–like subsets
Presenter: Chan-Yuan Zhang
Session: Poster Display
Resources:
Abstract
570P - First-line osimertinib for patients with advanced NSCLC harboring EGFR mutations: A real-world study
Presenter: Wenxiang Ji
Session: Poster Display
Resources:
Abstract