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Impact of a Multidisciplinary Consultation Program on Drug Adherence in First Oral Anticancer Treatment

Impact of a Multidisciplinary Consultation Program on Drug Adherence in First Oral Anticancer Treatment

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04797143
Acronym
IMPAM
Enrollment
300
Registered
2021-03-15
Start date
2021-03-11
Completion date
2026-03-31
Last updated
2025-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adherence to Oral Anticancer Treatment, Drug Related Toxicity, Multidisciplinary Consultation Program, Securing Medication Management

Keywords

Multidisciplinary consultation program, adherence to oral anticancer treatment, drug related toxicity, securing medication management

Brief summary

Oncology management has changed dramatically over the last decade with the approval and rapid adoption of newly targeted oral oncology medications. The movement to oral oncology medications has altered the balance of risks and adverse effects (AEs) in the treatment of cancer care. These treatments are associated with a different constellation of AEs and drug interactions. Patients receiving treatment with oral anticancer treatment (OAT) encounter several barriers to adherence, which may include limited access to specialty medications, severe adverse effects, complex medication regimens, and special handling precautions. Medication nonadherence not only reduces the efficacy of drug therapy but also has the potential to increase healthcare expenditures due to disease-related hospitalizations. The purpose of this study is to evaluate the drug adherence in cancer patients, using the medication possession ratio (MPR), before and after the implementation of a multidisciplinary consultation program (MCP), on initiation of OAT.

Interventions

DEVICEmultidisciplinary consultation program

The multidisciplinary consultation program (MCP) was divided into 3 steps: the first step involved a consultation with an oncologist, the second step involved a consultation with an oncology pharmacist, and the third step involved a meeting with a coordinating nurse (CN). The CN put in place a regular telephone follow-up with the patient, a few days later (7 to 15 days), to ensure adherence and tolerance of the oral anticancer treatment (OAT).

Sponsors

Centre Hospitalier Universitaire, Amiens
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* French speaking patients with a newly diagnosed or relapsed cancer, regardless of location and introduction of oral anticancer treatment

Exclusion criteria

* patients treated with hormone therapy only * Patient with severe psychiatric disorders * patient who does not speak the French language

Design outcomes

Primary

MeasureTime frameDescription
medication possession ratio (MPR)two monthsThe MPR makes it possible to determine the percentage of days of treatment covered by pharmacy dispensing. A patient is generally considered observant if MPR is greater than or equal to 80%.

Countries

France

Contacts

Primary ContactAurélie terrier-lenglet, DR
terrier-lenglet.aurelie@chu-amiens.fr0322087173

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026