Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy

November 6, 2019 updated by: Fatiha Tasmin Jeenia, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh

Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy: A Randomized, Double Blind, Placebo Controlled, Multi Center Trial

This study will be conducted to evaluate the effect of vitamin B12 and vitamin B6 in delaying the onset and reducing the incidence and severity of Vincristine Induced Peripheral Neuropathy (VIPN) in Acute Lymphoblastic Leukemia (ALL) patient.

Study Overview

Detailed Description

Acute Lymphoblastic Leukemia (ALL) is an emerging health burden for Bangladesh. It is anticipated that about 20 million people are going to be affected annually by 2025 in countries currently on developmental transition. Good prognostic outcome of ALL relies on uninterrupted and complete course of chemotherapy. About 85% of adult patients and 98% of children attain complete recovery with full course of treatment. One of the crucial chemotherapeutic agents used to treat ALL is vincristine. It is needed to complete vincristine with adequate dose in order to get a better prognostic outcome. About 45% of the patients getting vincristine develop a deleterious side effect called Vincristine Induced Peripheral Neuropathy (VIPN). Unfortunately, development of VIPN results in dose reduction, protocol deviation and even abandonment of treatment with vincristine in some ALL patients. Better prognostic outcome becomes an arcadia. So far, many researches have been conducted to explore a way to prevent or treat VIPN. But still no conclusive recommendation can be made. Therefore, VIPN has become an important issue need to be addressed. This study will be a small effort to identify the potential of vitamin B12 and vitamin B6 as probable preventive measures of VIPN. Evidence suggests that, vitamin B12 and vitamin B6 two water soluble, non toxic vitamins well recognized for the treatment of peripheral neuropathy. Vitamin B12 plays a very fundamental role in neurological function. It exerts its physiological effects through mediating two principal enzymatic pathways by which it maintains the integrity of neuronal membrane. On the other hand, vitamin B6 or pyridoxine is an essential co- factor in various synthesis pathways including synthesis of myelin sheath. Patients will be randomly allocated into two arms by using online research randomizer and newly diagnosed ALL patients will be enrolled in this research. From the day of starting chemotherapy, patients on arm A (Intervention arm) will be concurrently administered with vitamin B12 and vitamin B6. Vitamin B12 will be given 500 μg three times a week intravenously on a basis of every alternate day except the day of receiving vincristine and vitamin B6 will be given 50 mg thrice daily orally during the induction period (5 weeks) of chemotherapy cycle. On the other hand, patients on arm B (Placebo arm) will be given placebo pill and intravenous placebo injection at same interval. Prior to initiation of induction chemotherapy each participant will undergo neuropathy evaluation per National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI-CTCAE) v.4.0 scale and will be interviewed according to the neurotoxicity subscale of Functional Assessment of Cancer Therapy (FACT) -GOG- Ntx quality of life assessment questionnaire. The participants will be re-evaluated once weekly on the outset of 2nd week, 3rd week, 4th and 5th week of vincristine chemotherapy during induction period. They will be assessed per NCI-CTCAE v.4.0 scale for severity of neuropathy and by FACT- GOG- Ntx by answering specific questions regarding the presence of tingling, numbness, pain, muscle weakness and motor activities. As neuropathy and neuropathic pain are mostly subjective issue rather than objective and reflected more comprehensively by the particular person encountering with, so patient based measures will be used in this study. Incidence, onset and severity of peripheral neuropathy will be compared on both arms.

Study Type

Interventional

Enrollment (Actual)

88

Phase

  • Phase 4

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Dhaka, Bangladesh
        • Dhaka Medical College Hospital
      • Dhaka, Bangladesh
        • Bangabandhu Sheikh Mujib Medical University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 90 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. All patients, 18 years of age or older with newly diagnosed ALL going to start induction chemotherapy with Vincristine
  2. Patients with good performance status (ECOG 0- 3)
  3. Patients with no preexisting peripheral neuropathy
  4. Patients with grade 0 neuropathy on admission
  5. Patients with normal renal function (Serum creatinine <1.5 mg/dl)
  6. Patients agree to participate in the study signing an informed written consent

Exclusion Criteria:

  1. Pregnant women and nursing mothers
  2. Patients with clinical neuropathy due to diabetes mellitus or other causes
  3. Patients with head neck tumors
  4. Patients taking anticonvulsants, antidepressants, opioids, vitamin E and other neuropathic pain medication agents

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Quadruple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Experimental

Intervention: Injection Mecobalamin (500mcg) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks.

Intervention: Tablet Pyridoxine hydrochloride (25 mg) 2 tablets thrice daily for 5 weeks.

Injection Mecobalamin (500mcg) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks.
Other Names:
  • Vitamin B12
Tab. Pyridoxine hydrochloride (25 mg) 2 tablets thrice daily for 5 weeks
Other Names:
  • Vitamin B6
Placebo Comparator: Placebo

Intervention: Injection normal saline (1 ml) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks.

Intervention: Oral placebo pill 2 tablets thrice daily for 5 weeks.

Normal saline 1 ml three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks
Other Names:
  • Normal saline
Placebo pill orally thrice daily for 5 weeks
Other Names:
  • Placebo

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Time Frame
Time of onset of Vincristine Induced Peripheral Neuropathy
Time Frame: 0 weeks (baseline), change in neuropathy status on the outset 2nd week, 3rd week, 4th week and 5th week of vincristine chemotherapy
0 weeks (baseline), change in neuropathy status on the outset 2nd week, 3rd week, 4th week and 5th week of vincristine chemotherapy
Severity of Vincristine Induced Peripheral Neuropathy
Time Frame: On the outset of 1st week change in the severity of neuropathy on the outset of 2nd week, 3rd week, 4th week, 5th week of vincristine chemotherapy
On the outset of 1st week change in the severity of neuropathy on the outset of 2nd week, 3rd week, 4th week, 5th week of vincristine chemotherapy
Incidence of Vincristine Induced Peripheral Neuropathy
Time Frame: Cumulative incidence at 5th week of vincristine chemotherapy
Cumulative incidence at 5th week of vincristine chemotherapy

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2016

Primary Completion (Actual)

June 1, 2018

Study Completion (Actual)

July 1, 2018

Study Registration Dates

First Submitted

August 31, 2016

First Submitted That Met QC Criteria

October 3, 2016

First Posted (Estimate)

October 4, 2016

Study Record Updates

Last Update Posted (Actual)

November 8, 2019

Last Update Submitted That Met QC Criteria

November 6, 2019

Last Verified

November 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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