CHildren Treated With Vincristine: A Trial Regarding Pharmacokinetics, DNA And Toxicity of Targeted Therapy In Pediatric Oncology Patients.

Pediatric Cancer Clinical Trial

— CHAPATI  

Official title:

CHildren Treated With Vincristine: A Trial Regarding Pharmacokinetics, DNA And Toxicity of Targeted Therapy In Pediatric Oncology Patients.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05844670
• Other study ID #: V314092022
• Status: Recruiting
• Phase: Phase 4
• Start date: April 20, 2023
• Est. completion date: November 1, 2024

Study information

• Verified date: April 2023
• Source: Moi University
• Contact: Aniek Uittenboogaard, MD
• Phone: +31631293157
• Email: a.uittenboogaard[@]amsterdamumc.nl
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical trial is to individualize the dosage of vincristine, a chemotherapy drug, in children with cancer. The main question it aims to answer is: can vincristine dosage be optimized while carefully monitoring toxicity.

The following will happen:

• Participants will receive vincristine according to the institutional treatment protocol.

• After receiving vincristine, blood samples will be taken at three time points.

• The amount of vincristine in the blood samples will be determined.

• If the amount of vincristine in the blood samples is lower than the reference and the participants do not experience toxicity due to vincristine, the dose of vincristine may be increased.

• Toxicity will be carefully monitored.

Description:

Vincristine is among the most widely used and potentially effective chemotherapeutic agents in pediatric oncology patients. However, in black African children it may be sub optimally dosed due to genetic differences in the metabolism of vincristine. This study aims to optimize the dosing regimen of vincristine while carefully monitoring toxicity.

This will be a prospective cohort study consisting of two parts: a feasibility study and the rest of the study. In the feasibility study, 15 children aged 5-14 years who are scheduled to receive at least 2 vincristine administrations can be included. After the administration of vincristine, venous blood samples and finger prick blood samples will be taken to determine the vincristine concentrations. The samples will be shipped to and analyzed in the Netherlands to determine the vincristine concentration in each sample. Based on this, a dose advise will be given for subsequent vincristine administrations. This cycle will be repeated maximum 2 times but maximum 1 dose advice is given. Toxicity will be monitored by determination of the bilirubin, by questionnaires and by physical examination to check for signs of peripheral neuropathy. In the rest of the study, in which 85 children will be included, only finger prick samples will be taken.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 100
• Est. completion date: November 1, 2024
• Est. primary completion date: August 1, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 14 Years

Eligibility

Feasibility study:

Inclusion Criteria:

• Black patients aged 5-14 years with a malignancy for which they are scheduled to receive a minimum of two VCR administrations as part of their treatment protocol: acute lymphoblastic leukemia, non-Hodgkin's lymphoma, rhabdomyosarcoma, neuroblastoma, nephroblastoma, retinoblastoma.

• Written informed consent

Exclusion Criteria:

• Severe malnutrition

• Total bilirubin >3 times upper limit of normal

• Pre-existent severe mental retardation e.g. Down syndrome

• Pre-existent peripheral neuropathy (CTCAE constipation, peripheral sensory neuropathy, peripheral motor neuropathy, or neuralgia = 2 or ped-mTNS = 5)

Rest of the study:

Inclusion Criteria:

• Black patients aged 2-14 years with a malignancy for which they are scheduled to receive a minimum of four VCR administrations as part of their treatment protocol: acute lymphoblastic leukemia, non-Hodgkin's lymphoma, rhabdomyosarcoma, neuroblastoma, nephroblastoma, retinoblastoma.

• Written informed consent

Exclusion Criteria:

• Severe malnutrition

• Total bilirubin >3 times upper limit of normal

• Pre-existent severe mental retardation e.g. Down syndrome

• Pre-existent peripheral neuropathy (CTCAE constipation, peripheral sensory neuropathy, peripheral motor neuropathy, or neuralgia = 2 or ped-mTNS = 5)

Related Conditions & MeSH terms

• Neoplasms
• Pediatric Cancer

Intervention

Drug:
• Vincristine
The initial vincristine dosage will be according to institutional treatment protocol. After vincristine administration, three blood samples will be taken at T=1, T=1.5 and T=4 hours. The concentration of vincristine will be analyzed in the samples. If the concentration of 2 or more samples is lower than the reference concentration and there is no toxicity, an advice will be given to increase dosage by 20%. Whether or not a dosage is given, vincristine concentrations will be measured again for the next dose administration. For the feasibility study, both venous blood samples and finger prick blood samples using Mitra tips will be taken. The cycle can be repeated maximum 2 times. For the rest of the study, finger prick blood samples using Mitra tips will be taken. The cycle can be repeated maximum 3 times. Toxicity will be monitored through physical exam and questionnaire, bilirubin levels and clinical status of the patient.

Locations

Country	Name	City	State
Kenya	Moi Teaching and Referral Hospital	Eldoret	Rift Valley

Sponsors (3)

Lead Sponsor	Collaborator
Moi University	Amsterdam UMC, location VUmc, Princess Maxima Center for Pediatric Oncology

Country where clinical trial is conducted

Kenya, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Adapting vincristine dosage	The number of patients in whom it is possible to adapt vincristine dosage based on vincristine concentrations in the blood at three time points and the presence of side-effects.	Through study completion, an average of four months per patient (depending on treatment protocol).
Secondary	Vincristine-induced peripheral neuropathy	The number of patients who develop vincristine-induced peripheral neuropathy (VIPN) and the degree of VIPN. VIPN is measured using the CTCAE v5 items peripheral sensory neuropathy, peripheral motor neuropathy, neuralgia and constipation. In children aged 5 or above, VIPN will also be assessed with the ped-mTNS.	Through study completion, an average of four months per patient (depending on treatment protocol).
Secondary	Genetics	The association between pharmacogenomic parameters and the concentration of vincristine at three time points (T=60 minutes, T=90 minutes and T=240 minutes after vincristine administration) and vincristine-induced peripheral neuropathy using CTCAE v5 and ped-mTNS.	Through study completion, an average of four months per patient (depending on treatment protocol).
Secondary	Vincristine pharmacokinetics	The median vincristine concentrations and interquartile ranges (IQR) on three time points (T=60 minutes, T=90 minutes and T=240 minutes after vincristine administration).	Through study completion, an average of four months per patient (depending on treatment protocol).