Abstract 567P
Background
Few information is available about the impact of concomitant medication (CM) on the tolerability of chemotherapy as well as on the outcome of cancer patients. Therefore, we evaluated the impact of CM on disease-free survival (DFS), overall survival (OS) as well as side effects under adjuvant chemotherapy in a large cohort of early colon cancer (CC) patients.
Methods
Patients of the phase III randomized trial PETACC8 had resection with curative intent of a stage II or III CC and were treated with standard adjuvant fluoropyrimidine and oxaliplatin (+/- cetuximab) over 6 months.Information on CM intake has been gathered by study visits at inclusion and during chemotherapy. We investigated the association between number of CM as well as the 5 most frequently applied CM categories according to the WHO ATC classification system (gastro-esophageal reflux disease (GERD) treatment, anticoagulants, aggregation inhibitors, cardiovascular sphere (CVS) treatment and antidiabetic drugs) with DFS, OS and grade 3/4 adverse events (AEs).
Results
Within 2537 patients eligible for this analysis, median number of CM intake was 8 (range 0 to 25), with only 22 patients (0.9%) without any CM. 1328 (51.9%) reported a GERD treatment, 452 (17.7%) an anticoagulant, 279 (10.9%) an anti-aggregant therapy, 1028 (40.2%) a CVS treatment and 236 (9.2%) an antidiabetic drug. Anticoagulation was the only CM category significantly and independently associated with a shorter DFS (HR 1.29, 95%CI 1.07-1.56, p=0.009) as well as OS (HR 1.29, 95%CI 1.03-1.61, p=0.027). No association of number of CM (<5, 5-10, >10) has been observed neither with DFS (ref.; HR 0.98; HR 1.17) nor OS (ref.; HR 0.98; HR 1.15) (p>0.05). Grade 3/4 AEs directly correlated with number of CM (p<0.001) and occurred significantly more frequently in patients with GERD treatment (78.8 vs 66.6%, p<0.001), anticoagulation (81.4 vs 71.1%, p<0.001) and anti-aggregants (79.2 vs 72.1%, p=0.001).
Conclusions
Early CC patients with a high CM intake did not generally exhibit an impaired outcome, even though tolerability of adjuvant chemotherapy was reduced. Anticoagulation was the only CM category associated with a shorter DFS and OS.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
J. Taieb: Financial Interests, Personal, Advisory Board: MSD, Astellas, Merck, Servier, Pierre Fabre, Amgen, Bristol Myers Squibb, Novartis, Pfizer; Financial Interests, Personal, Invited Speaker: Amgen, Bristol Myers Squibb, Merck, MSD, Novartis; Non-Financial Interests, Leadership Role, President of the scientific committee of the ARCAD foundation until end 2022: ARCAD Foundation; Non-Financial Interests, , Leadership Role, Chair of the ARCAD pancreas research group: ARCAD Foundation; Non-Financial Interests, Leadership Role, Member of the administrative council, the scientific committee, the executive board and responsible for the international relationships /partnership for FFCD in the prodige intergroup: Federation Francophone de Cancerologie Digestive (FFCD). All other authors have declared no conflicts of interest.
Resources from the same session
548P - Diffuse midline gliomas H3K27-altered in adults, the experience of an oncology center
Presenter: Carolina Trabulo
Session: Poster session 10
561P - Risk of colorectal cancer and premalignant lesions after kidney transplantation
Presenter: Koen Zwart
Session: Poster session 10
562P - Quantifying the effect of colonoscopy and polypectomy rates in stage shift of colorectal cancer and reduced need for adjuvant chemotherapy
Presenter: Mina Sarofim
Session: Poster session 10
563P - The impact of participation in colorectal cancer screening: A population-based results from Lithuania
Presenter: Tomas Poskus
Session: Poster session 10
564P - A large-scale real-world study for colorectal cancer screening
Presenter: Song LIU
Session: Poster session 10
565P - Real-world data of early-onset colon cancer (early-onset CC) from the AIO colopredict plus (CPP) registry: Clinical and molecular characteristics, treatment and outcome
Presenter: Doreen Gisder
Session: Poster session 10
566P - Long-term survivorship outcomes of adolescents and young adults (AYA) with cancer of the lower gastrointestinal tract
Presenter: Winette Van Der Graaf
Session: Poster session 10
568P - Single cell AI-based detection of DNA mismatch repair deficiency in 1,988 colorectal cancers reveals prognostic and predictive value in the SCOT trial
Presenter: Faiz Jabbar
Session: Poster session 10
569P - Artificial intelligence for detection of mismatch repair deficiency in colon carcinomas (alliance)
Presenter: Frank Sinicrope
Session: Poster session 10
570P - Subclasses of microsatellite-instability colorectal cancer with unique molecular features and immune cell infiltration patterns
Presenter: Kui Wu
Session: Poster session 10