Impact of the PRISM-care Multidisciplinary Oncology Program Versus Usual Care on Secured Drug Intake of Patients With Kidney Cancer, Through Self-management of Adverse Events Related to Oral Targeted Therapies, Control of Drug Interactions, and Sharing of the Information Between Ambulatory and Hospital Settings.
试验速览
- 阶段
- 不适用
- 入组人数
- 190
- 试验地点
- 13
- 主要终点
- Relative dose intensity of oral chemotherapy
研究概览
简要总结
The rise of oral targeted therapies favors outpatient care of cancer patients but exposes them to new risks compared to the injectable chemotherapy in the hospital: non-adherence to treatment, inappropriate management of side effects and interactions with other co-prescribed drugs. The clinical consequences (reduced efficacy and potentialized toxicity) are all the more important that ambulatory monitoring of treatments prescribed at the hospital remains underdeveloped due to default of coordination between these two settings.
Adverse drug reactions are a major concern, as such, and because they involve prescription changes (dose reduction, treatment interruption). This results in a decrease in the dose taken and a risk of loss of efficacy.
In the context of metastatic renal cell carcinoma, the risk of iatrogenicity is even higher because the oral targeted therapies available in this indication have a safety profile marked by potentially serious toxicities (hematologic and cardiac toxicity) or are known to reduce the treatment adherence (digestive and skin toxicities). In addition, these molecules are metabolized by the CYP3A4 hepatic cytochrome, which leads to avoid associating them with drugs inducing and / or inhibiting the CYP3A4, because of the risk of toxicity and / or loss of efficacy.
The investigators propose to assess a program set up to secure drug taking by enhancing self-management of side effects and control of drug interactions by the patient. This program includes pharmaceutical visits and involves inpatient and outpatient (doctor, referent pharmacist and liberal nurse) professionals.
The hypothesis of the study is that the PRISM care program will improve self-management of side effects by the patient, resulting in a relative dose intensity of oral chemotherapy improved compared to usual care.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Patient aged 18 years old or more
- •With metastatic renal cell carcinoma
- •With an initiation or change of oral targeted therapy, especially: tyrosine kinase inhibitor (sunitinib, sorafenib, pazopanib, axitinib) or mTor inhibitor (everolimus)
- •With ambulatory status (not hospitalized for the management and treatment of its metastatic renal cell carcinoma)
- •Without either cognitive disorders or major psychiatric disorders
- •With a sufficient autonomy for the management of medication at home
- •Having declared an outpatient doctor
- •Having declared a usual pharmacy
- •Having given his written consent to participate in the study
排除标准
- •Significant cognitive and psychiatric disorders
- •Management of medication at home exclusively performed by the family caregiver
- •Patient in an institution or under guardianship, major protected by law
- •Patient refusing to participate in the study
结局指标
主要结局
Relative dose intensity of oral chemotherapy
时间窗: 6 months from the treatment initiation
Relative dose intensity will be computed by the ratio between the overall dose delivered and the overall dose prescribed during the 6 months of follow-up.
次要结局
- Adherence to the oral chemotherapy measured with the prescription renewal rate(6 months from the treatment initiation)
- Cause of changes dose relative intensity: number of reduction of dosage(6 months from the treatment initiation)
- Number of unplanned hospitalizations related to the oral chemotherapy(6 months from the treatment initiation)
- Number of emergency admissions related to the oral chemotherapy(6 months from the treatment initiation)
- Adherence to the oral chemotherapy measured with the Girerd questionnaire(6 months from the treatment initiation)
- Drug interactions (for patients included in the interventional group)(6 months from the treatment initiation)
- Cause of changes dose relative intensity: number of interruption or discontinuation of treatment(6 months from the treatment initiation)
- Consumption of health care resources: number and nature of consultations with GPs and / or medical specialists(6 months from the treatment initiation)
- Satisfaction with treatment with medicines, measured with the SAT-MED Q questionnaire(Inclusion and 6 months from the treatment initiation)
- Health locus of control, measured with the Therapeutic Self Care Toll (TSCT) scale(Inclusion and 6 months from the treatment initiation)
- Grade 3 and 4 adverse events related to the oral chemotherapy(6 months from the treatment initiation)
- Consumption of health care resources: number of acts of imagery(6 months from the treatment initiation)
- Consumption of health care resources: number of prescribed drugs and self-medication and other health products(6 months from the treatment initiation)
- Quality of life, measured with the EORTC QLQ-C30 questionnaire (version 3.0)(Inclusion and 6 months from the treatment initiation)
- Consumption of health care resources: number of acts of biology(6 months from the treatment initiation)
- Patient's perception of its illness, measured with the Brief Illness Perception Questionnaire (B-IPQ)(Inclusion and 6 months from the treatment initiation)
- Rate of patients presenting satisfying knowledge about adverse effects of their oral chemotherapy, according to the hospital pharmacists and measured with a 4-items Likert scale(2 months and 6 months from the treatment initiation)
- Involvement of outpatient caregivers (doctors, pharmacists and liberal nurses) in the PRISM care program(During the 6 months of follow-up)
- Satisfaction of outpatient caregivers (doctors, pharmacists and liberal nurses) relative to the PRISM care program, measured with a rating out of 10(6 months of follow-up)