Adherence, Patient Clinical Trial
Official title:
Observational Study to Assess Adherence of Oral Anticancer Therapies
Oral anticancer treatments are increasingly numerous. They represent an additional
alternative in the therapeutic arsenal of the clinician, and appear to satisfy patients who
prefer this route of administration over intravenous treatment. The objective of oral
therapies is twofold: to remove the constraints and risks associated with infusions and to
allow the patient to follow his treatment at home.
However, they have significant adverse effects that may affect patients, who are sometimes at
a disadvantage compared to how they are treated, and potentially lead to non-compliance with
the consequences.
This study will identify the factors associated with non-adherence and determine the impact
of this non-adherence in terms of treatment efficacy and tolerance.
The aim of this routine care study is to evaluate the adherence to oral anticancer therapies
during 3 months.
Primary objective
- To evaluate adherence to oral anti-cancer therapies at 3 months
Secondary objectives
- To evaluate the adherence to 3 months according to the age of the patients (less than 75
years versus 75 years and more)
- Evaluate compliance at 1 and 2 months
- Evaluate toxicity at 1, 2 and 3 months according to compliance according to criteria
CTCAE 4.03.
- Evaluate response to treatment at 3 months based on adherence
- Evaluate the factors associated with adherence and describe the reasons for
non-adherence.
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