Clinical trial · Interventional
Adjuvant Chemotherapy In Elderly With Colon Cancer Stage III
Adjuvant Chemotherapy In Elderly With Colon Cancer Stage III - Geriatric Assessment and Prognostic Gene Signatures
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
This is a phase 2, randomized study where the aim of the study is to investigate the tolerance of adjuvant chemotherapy, measured by functional decline, after surgery for colon cancer stage III in elderly patients. Secondary aims are disease-free survival, toxicity, late functional outcome, quality of life, to establish a geriatric assessment for selection of patients, and to examine the prognostic value of gene signature tests / biomarkers for stage III colon cancer.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Colon Cancer | Malignant Colon Neoplasm | CURATED_EXACT | 0.92 |
Interventions
Interventions (1)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Capecitabine | Drug | Capecitabine | ALIAS |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Arm Capecitabine
- description
- Capecitabine 1000 mg/m2 bid day 1-14 q3 weeks, 8 cycles
- interventionNames
- Drug: Capecitabine
- type
- NO_INTERVENTION
- label
- Arm No treatment
- description
- no chemotherapy, observation
Primary outcomes (1)
- measure
- Functional decline in instrumental activities of daily living (IADL) and/or activities of daily living (ADL)
- timeFrame
- 1 year after surgery
- description
- Tolerance of adjuvant chemotherapy in elderly patients, measured as functional decline or independency, by ADL and IADL questionnaires.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: * Radical surgery (R0/R1) for colon cancer * Histologically verified adenocarcinoma of the colon * Histologically verified lymph node metastases (Stage III) * Age ≥ 75 years * Able to undergo ambulatory treatment (adequate physical and mental function) * Signed informed consent and expected cooperation of the patients for the treatment and follow up must be obtained and documented according to The International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH GCP) and national regulations. Exclusion Criteria: * Distant metastases (stage IV) * Frail according to geriatric assessment * Significant cardiovascular disease (congestive heart failure, symptomatic coronary artery disease and cardiac dysrhythmia) or myocardial infarction within the past 12 months * Previous treatment with chemotherapy for colorectal cancer * Metastatic disease from other cancer * Reduced cognitive function not enabling ability to give informed consent or compliance with the study * History of prior or concurrent malignant neoplasm other than colorectal adenocarcinoma within the past five years, except curatively treated non-melanoma skin cancer or in situ carcinoma of the cervix * Adverse reactions or hypersensitivity to capecitabine or related drugs and/or its excipients. Need to use medications contraindicated according to SmPC of the IMP(s), such as sorivudine, brivudin or chemically related compounds. Any other contraindication listed on the summary of product characteristics (SmPC) of the investigational medicinal Product (IMP) * Use of methotrexate or other cytotoxic drugs as treatment of rheumatoid arthritis or other inflammatory disease and where it is considered contraindicated to stop this medication * Known dihydropyrimidine dehydrogenase (DPD) deficiency * Any reason why, in the opinion of the investigator, the patient should not participate
References
Publications (0)
Data not yet available