Abstract 593P
Background
The incidence of patients with sporadic early-onset colorectal cancer (eoCRC) (<50 years) is increasing. Despite likely different tumor biology and suggestions of more aggressive disease, treatment is similar to older patients. The aim of this study was to investigate treatment response and survival in patients with eoCRC compared to matched data of older-onset (oo)CRC.
Methods
Clinicopathological data of all mismatch repair proficient (pMMR) eoCRC patients diagnosed between 2016 and 2022 were requested from the Netherlands Cancer Registry. Additionally matched data from patients between 50-70 and ≥70 years were requested. Matching was performed on tumor stage, RAS/BRAF mutation status, tumor sidedness and systemic therapy. To compare groups, two sided X2 tests and Fisher’s exact tests were used. Overall survival (OS) and progression free survival (PFS) was analyzed with Kaplan Meier and median survival times were compared with the log-rank test (R software). P-values < 0.05 were considered significant.
Results
In total 3412 patients with eoCRC (mean 43 years) and matched data from 3143 and 2624 ooCRC patients aged 50-70 (mean 60 years) and ≥70 (mean 75 years), respectively, were retrieved. The 5-year OS was 67%, 65% and 54% for patients <50, 50-70 and ≥70 years of age, respectively (p < 0.001). Median OS for patients with metastatic disease at diagnosis was 22, 22 and 19 months for patients <50, 50-70 and ≥70 years (p = 0.0013). Of eoCRC patients, 46% had a RAS mutation and 10% a BRAF mutation. Best response to first line treatment was 2% complete remission, 63% partial remission, 14% stable disease, 1% mixed response and 20% progressive disease (ns). Median PFS to first line treatment was 4 months for eoCRC patients and 5 months for ooCRC (ns). In total, 89%, 90% and 80% received oxaliplatin (ns), and 24%, 16% and 6% received irinotecan (p < 0.001) respectively. Anti-EGFR treatment was given in 21%, 9% and 3% of left-sided RAS/BRAF wildtype CRC patients, respectively (p = 0.035).
Conclusions
EoCRC patients have similar response rates and PFS to first line systemic treatment compared to matched ooCRC patients. Although eoCRC patients more often received irinotecan and anti-EGFR therapy compared to ooCRC, the OS for eoCRC was similar to patients aged 50-70.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
ZonMw.
Disclosure
L. Vermeulen: Other, Personal, Full or part-time Employment, Employee: Genentech Inc; Other, Personal, Stocks/Shares, Shareholder: Roche; Financial Interests, Speaker, Consultant, Advisor, These had no relation to the content of this abstract: Bayer, MSD, Genentech, Servier, Pierre Fabre. All other authors have declared no conflicts of interest.
Resources from the same session
489P - Interfering with the tumor microenvironment of glioblastoma: An in vitro study
Presenter: Serena Mastantuono
Session: Poster session 16
490P - Inhibiting glioma cells' migration: Exploring Rho-GTPases as a potential therapeutic target
Presenter: Irene Giulia Rolle
Session: Poster session 16
Resources:
Abstract
491P - SRSF7 promotes glioblastoma progression via CDK1-mediated G2/M phase arrest of GBM cells
Presenter: Ya qin Hu
Session: Poster session 16
Resources:
Abstract
492P - Linking cellular drug responses to corresponding metabolomic tissue signatures in gliomas
Presenter: Stefanie Stanzer
Session: Poster session 16
493P - The usefulness of pre-radiotherapy MRI in assessing pseudo-progression in patients with glioblastoma included in first-line clinical trials
Presenter: Kreina Vega Cano
Session: Poster session 16
494P - Effect of a new method for operating electric field patches on scalp reactions in glioblastoma patients receiving tumor treating fields
Presenter: Jinghui Liu
Session: Poster session 16
Resources:
Abstract
495P - Clinicopathological risk factors for prognosis and therapeutic response of primary central nervous system lymphoma in China: A single-center retrospective analysis of 118 cases
Presenter: Feng Chen
Session: Poster session 16
496P - Association of brain metastasis and peritumoral edema volume with the neurological symptom burden in lung cancer patients
Presenter: Ariane Steindl
Session: Poster session 16
497P - Does the primary location and metastatic timing of colorectal cancer influence the survival of patients with brain metastasis? A meta-analysis
Presenter: Junmin Song
Session: Poster session 16