N-acetyl Cysteine Effect in Peripheral Neuropathy in Cancer Patients
Primary Purpose
Peripheral Neuropathy Due to Chemotherapy
Status
Completed
Phase
Phase 1
Locations
Egypt
Study Type
Interventional
Intervention
low dose N-acetylcysteine
high dose N-acetylcysteine
Paclitaxel
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Neuropathy Due to Chemotherapy focused on measuring paclitaxel, peripheral neuropathy, N-acetyl cysteine
Eligibility Criteria
Inclusion Criteria:
- Adult patients (>18 years old).
- Breast cancer patients who will receive adjuvant weekly paclitaxel for 12 cycles.
- ECOG performance status 0-2
- Adequate bone marrow function (white blood count ≥4,000/mm3, platelet count ≥100,000/mm3), liver function (serum total bilirubin <1.5 mg/dl), renal function (creatinine <1.5 mg/dl).
Exclusion Criteria:
Patients who have any of the following:
- Clinical neuropathy.
- Diabetes mellitus.
- Patients receiving vitamin B1, B6, B12,or other vitamin supplemental therapy.
- Patients receiving antidepressants, opioids, adjuvant analgesic agents (eg, anticonvulsants, clonazepam, or mexiletine), topical analgesics, and amifostine.
- Hypersensitivity to NAC.
Sites / Locations
- AinShams University Hospitals
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Experimental
Experimental
Arm Label
control
high dose N-acetyl cysteine
low dose N-acetyl cysteine
Arm Description
they will receive paclitaxel 80 mg/m2 once per week for 12 weeks only
they will receive paclitaxel 80 mg/m2 once per week for 12 weeks and high dose N-acetylcysteine (1200 mg twice daily) for the paclitaxel treatment period
they will receive paclitaxel 80 mg/m2 once per week for 12 weeks and low dose N-acetylcysteine (600mg twice daily) for the paclitaxel treatment period.
Outcomes
Primary Outcome Measures
Incidence of chemotherapy induced-peripheral neuropathy
Number of patients reported neuropathy from paclitaxel
Secondary Outcome Measures
severity of chemotherapy induced-peripheral neuropathy
severity of paclitaxel induced peripheral neuropathy using NCI-CTCAE criteria
Adverse effects
any adverse/ side effect will be evaluated
severity of chemotherapy induced-peripheral neuropathy
severity of chemotherapy induced-peripheral neuropathy using modified total neuropathy score ,Each neuropathy item is scored by a physician on a 0-4 scale the scores are summed to obtain a total score, modified total neuropathy score score ranges from 0-24 with higher total scores indicate more severe neuropathy.
Full Information
NCT ID
NCT03492047
First Posted
March 2, 2018
Last Updated
February 25, 2020
Sponsor
Ain Shams University
Collaborators
Nasser Institute For Research and Treatment
1. Study Identification
Unique Protocol Identification Number
NCT03492047
Brief Title
N-acetyl Cysteine Effect in Peripheral Neuropathy in Cancer Patients
Official Title
Evaluation of The Effect of N-AcetylCysteine in The Prevention of Paclitaxel-Induced Peripheral Neuropathy in Cancer Patients
Study Type
Interventional
2. Study Status
Record Verification Date
February 2020
Overall Recruitment Status
Completed
Study Start Date
April 1, 2018 (Actual)
Primary Completion Date
April 1, 2019 (Actual)
Study Completion Date
June 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ain Shams University
Collaborators
Nasser Institute For Research and Treatment
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of the study is to evaluate the effect of N-acetyl cysteine in combination with paclitaxel on the clinical outcomes of patients with peripheral neuropathy, paclitaxel-induced peripheral neuropathy affect quality of life in cancer patients.
new therapeutic approches such as the antioxidant N-acetyl cysteine, showed to has neuroprotective effect, the aim of the study is to evaluate the effect of N- acetylcysteine(NAC) administration in the prevention of paclitaxel-Induced peripheral neuropathy.
Detailed Description
Paclitaxel is a first-line chemotherapeutic treatment of solid tumors. Neuronal damage also seems to have a major role in paclitaxel-induced neuropathic pain, paclitaxel contributes to ROS formation (superoxide, hydroxyl radical, nitric oxide and hydrogen peroxide) in neuronal mitochondria that are involved in nerve injury-induced.
N-acetylcysteine (NAC) is a cysteine pro-drug and glutathione (GSH) precursor which is a protective agent and detoxifies and scavenges reactive oxygen species (ROS), which seems to help normalize the oxidative status.
It has been reported that high dose of N-acetylcysteine shown to Prevent retrograde motor neuron death after neonatal peripheral nerve injury and significantly increases motor neuron survival, which may improve functional outcomes after obstetrical brachial plexus injury in rats.
Also, it has been reported that NAC significantly inhibited CCI-induced microglia activation but elicited no notable effects on astrocytes. These results demonstrate an effective and safe approach that has been used clinically to alleviate neuropathic pain via the powerful inhibition of the activation of MMPs in rats.
N-acetylcysteine has been shown to have neuroprotective effects against oxaliplatin-based adjuvant chemotherapy in colon cancer patients with Oral administration of N-acetylcysteine1,200 mg) was given one and a half hours before each oxaliplatin administration.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Neuropathy Due to Chemotherapy
Keywords
paclitaxel, peripheral neuropathy, N-acetyl cysteine
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
75 (Actual)
8. Arms, Groups, and Interventions
Arm Title
control
Arm Type
Active Comparator
Arm Description
they will receive paclitaxel 80 mg/m2 once per week for 12 weeks only
Arm Title
high dose N-acetyl cysteine
Arm Type
Experimental
Arm Description
they will receive paclitaxel 80 mg/m2 once per week for 12 weeks and high dose N-acetylcysteine (1200 mg twice daily) for the paclitaxel treatment period
Arm Title
low dose N-acetyl cysteine
Arm Type
Experimental
Arm Description
they will receive paclitaxel 80 mg/m2 once per week for 12 weeks and low dose N-acetylcysteine (600mg twice daily) for the paclitaxel treatment period.
Intervention Type
Dietary Supplement
Intervention Name(s)
low dose N-acetylcysteine
Intervention Description
N-acetylcysteine 600mg twice daily
Intervention Type
Dietary Supplement
Intervention Name(s)
high dose N-acetylcysteine
Intervention Description
N-acetylcysteine 1200mg twice daily
Intervention Type
Drug
Intervention Name(s)
Paclitaxel
Intervention Description
Paclitaxel 80mg /m2 IV
Primary Outcome Measure Information:
Title
Incidence of chemotherapy induced-peripheral neuropathy
Description
Number of patients reported neuropathy from paclitaxel
Time Frame
up to 12 week
Secondary Outcome Measure Information:
Title
severity of chemotherapy induced-peripheral neuropathy
Description
severity of paclitaxel induced peripheral neuropathy using NCI-CTCAE criteria
Time Frame
at baseline and before each cycle up to 12 week
Title
Adverse effects
Description
any adverse/ side effect will be evaluated
Time Frame
at baseline and each cycle up to 12 week
Title
severity of chemotherapy induced-peripheral neuropathy
Description
severity of chemotherapy induced-peripheral neuropathy using modified total neuropathy score ,Each neuropathy item is scored by a physician on a 0-4 scale the scores are summed to obtain a total score, modified total neuropathy score score ranges from 0-24 with higher total scores indicate more severe neuropathy.
Time Frame
at baseline, at the end of 6 cycle and at the end of 12 cycles
Other Pre-specified Outcome Measures:
Title
the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity(FACT-GOG-NTX) subscale
Description
measures quality of life related to signs and symptoms of paclitaxel induced peripheral neuropathy
Time Frame
weekly up to 12 week
Title
serum nerve growth factor
Description
measuring serum level of nerve growth factor using ELISA KIT
Time Frame
at baseline and after 12 week
Title
serum malionaldehyde
Description
measuring serum level of maliomaldehyde using spectrophometric kit
Time Frame
at baseline and after 12 week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients (>18 years old).
Breast cancer patients who will receive adjuvant weekly paclitaxel for 12 cycles.
ECOG performance status 0-2
Adequate bone marrow function (white blood count ≥4,000/mm3, platelet count ≥100,000/mm3), liver function (serum total bilirubin <1.5 mg/dl), renal function (creatinine <1.5 mg/dl).
Exclusion Criteria:
Patients who have any of the following:
Clinical neuropathy.
Diabetes mellitus.
Patients receiving vitamin B1, B6, B12,or other vitamin supplemental therapy.
Patients receiving antidepressants, opioids, adjuvant analgesic agents (eg, anticonvulsants, clonazepam, or mexiletine), topical analgesics, and amifostine.
Hypersensitivity to NAC.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hadeer G Khalefa, master
Organizational Affiliation
Nassar institute for research and treatment hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
AinShams University Hospitals
City
Cairo
ZIP/Postal Code
11566
Country
Egypt
12. IPD Sharing Statement
Citations:
PubMed Identifier
32601973
Citation
Khalefa HG, Shawki MA, Aboelhassan R, El Wakeel LM. Evaluation of the effect of N-acetylcysteine on the prevention and amelioration of paclitaxel-induced peripheral neuropathy in breast cancer patients: a randomized controlled study. Breast Cancer Res Treat. 2020 Aug;183(1):117-125. doi: 10.1007/s10549-020-05762-8. Epub 2020 Jun 29.
Results Reference
derived
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N-acetyl Cysteine Effect in Peripheral Neuropathy in Cancer Patients
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