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
581P - The effect of exercise intervention on defecation related symptoms of colorectal cancer patients a randomized controlled trial
Presenter: Justin Jeon
Session: Poster session 10
582P - High accuracy of a blood-based multimodal ctDNA test to detect advanced neoplasms in a FIT-positive screening population
Presenter: Joana Vidal Barrull
Session: Poster session 10
583P - A rapid blood test for the earlier detection of colorectal cancer
Presenter: Jennifer Nobes
Session: Poster session 10
584P - Two-year update of the prospective evaluation of ColonAiQ (PreC) study
Presenter: Yanbing Ding
Session: Poster session 10
585P - Fragmentomics early detection assay leading to potential clinical benefits in colorectal cancer
Presenter: Yuepeng Cao
Session: Poster session 10
586P - Minimal residual disease (MRD) detection using a tumour naïve circulating tumour DNA (ctDNA) assay in patients (pts) with resected colorectal cancer (CRC) in the phase III ASCOLT trial
Presenter: Daphne Day
Session: Poster session 10
588P - PLCRC-PROVENC3 study: Prognostic value of post-surgery liquid biopsy circulating tumor DNA in stage III colon cancer patients
Presenter: Carmen Rubio-Alarcón
Session: Poster session 10
589P - Impact of landmark point selection on molecular residual disease detection in stage I-IV resectable colorectal cancer
Presenter: Di Cao
Session: Poster session 10
590P - Assessment of circulating tumor (ct)DNA in patients (pts) with locally advanced rectal cancer (LARC) pts treated with neoadjuvant therapy (NAT)
Presenter: Chiara Molinari
Session: Poster session 10