Adjuvant Chemotherapy In Elderly With Colon Cancer Stage III

Colon Cancer Clinical Trial

— ACE  

Official title:

Adjuvant Chemotherapy In Elderly With Colon Cancer Stage III - Geriatric Assessment and Prognostic Gene Signatures

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT02978612
• Other study ID #: 2015/1252
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: June 2016
• Est. completion date: January 2032

Study information

• Verified date: April 2024
• Source: Oslo University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

Patients ≥ 75 years who have undergone surgery for colon cancer stage III, are eligible for inclusion in the study. Non-eligibility includes patients with obvious impaired cognitive or physical function or patients living in nursing homes. After signing informed consent, the patients first undergo geriatric assessment. Patients that are classified as having fit or intermediate function, and with no significant cardiovascular disease, are randomized with a 2:1 randomization process to either chemotherapy (Arm A: Capecitabine 1000 mg/m2 bid day 1-14 q3 weeks, 8 cycles) or no chemotherapy (Arm B: observation). The purpose of this study is to examine the tolerability of chemotherapy in elderly (> 75 years) patients operated on for colon cancer stage III. There is little evidence of benefit and tolerability of this therapy in the elderly; it is recommended individual consideration in elderly. In the study, a comprehensive geriatric a comprehensive geriatric assessment is performed first, to exclude frail patients or patients with serious comorbidities such as cardiovascular disease. Fit or intermediate patients will then be randomized so that 2/3 will receive chemotherapy with capecitabine tablets for 6 months, and 1/3 will not receive chemotherapy. A new geriatric assessment is performed after 6 and 12 months. The main objective of the study is to examine whether chemotherapy leads to significant loss of function, but secondary aims include survival, quality of life, and prognostic effect of biomarkers. The study may provide useful information on selection of patients who tolerate and benefit from adjuvant chemotherapy.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 170
• Est. completion date: January 2032
• Est. primary completion date: November 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 75 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Colon Cancer
• Colonic Neoplasms

Intervention

Drug:
• Capecitabine
Capecitabine is a prodrug to 5-fluorouracil. It is used for adjuvant chemotherapy after surgery for colon cancer. The tablets are either 150 mg or 500 mg

Locations

Country	Name	City	State
Norway	Oslo University Hospital	Oslo

Sponsors (1)

Lead Sponsor	Collaborator
Oslo University Hospital

Country where clinical trial is conducted

Norway, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Functional decline in instrumental activities of daily living (IADL) and/or activities of daily living (ADL)	Tolerance of adjuvant chemotherapy in elderly patients, measured as functional decline or independency, by ADL and IADL questionnaires.	1 year after surgery
Secondary	Relative dose intensity; i.e the percentage of planned chemotherapy dose the patient actually receives	Number of planned chemotherapy cycles given, total dose given	through study completion
Secondary	Toxicity of chemotherapy	Number of participants with treatment-related adverse events as assessed by CTCAE v4.0	During treatment and follow-up 1 year after surgery
Secondary	Disease-free survival	Follow-up, 3-year disease-free survival	3 years after surgery
Secondary	Quality of life questionnaire 1	EQ-5D-5L	Time of randomization, 6 months and 1 year after surgery
Secondary	Quality of life questionnaire 2	EORTC QLQ-C30	Time of randomization, 6 months and 1 year after surgery
Secondary	Quality of life questionnaire 3	QLQ-ELD14	Time of randomization, 6 months and 1 year after surgery
Secondary	Validation of the performance of prognostic biomarkers in estimating disease-free survival	Prognostic biomarkers validated for performance in estimating 3-year disease-free survival	3 years after surgery
Secondary	Overall survival	Follow-up, 5-year disease-free survival	5 years after surgery