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Completed

NCT Number: NCT01682499

Calcium and Magnesium Infusion for the Prevention of Taxane Induced Neuropathy

This is a pilot study evaluating the feasibility of intravenous calcium and magnesium (Ca/Mg) infusion for prevention of taxane induced neuropathy in patients with early stage breast cancer receiving adjuvant or neo-adjuvant paclitaxel, either given every 2 weeks for 4 cycles or every week for 12 weeks.

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Key information

Age range

21 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Beth Israel Comprehensive Cancer Center, New York, United States

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About this study

Chemotherapy induced peripheral neuropathy (CIPN) is a major dose limiting side effect of many cytotoxic chemotherapy, and can be extremely disabling, causing significant loss of functional abilities. Calcium and magnesium infusions were shown to decreased the incidence and intensity of neuropathy symptoms related to oxaliplatin.

There are currently no effective drugs or treatment modalities for the prevention or treatment of taxane related neuropathy. Given the morbidity of taxane induced neuropathy and the safety of Ca/Mg infusion, it is reasonable to assess the feasibility of this intervention in woman with stage I-III breast cancer receiving adjuvant or neo-adjuvant paclitaxel treatment, either given every 2 weeks for 4 cycles or every week for 12 weeks. Calcium gluconate and magnesium sulfate, 1 g of each agent in 100 ml D5W will be infused over 30 minutes, immediately before and after each dose of paclitaxel. The Ca/Mg infusion will be given through the same line used for giving chemotherapy.

The primary aim of this study is to assess paclitaxel-related neuropathy (grade 2 or greater) as measured by NCI Common Terminology Criteria Version 3 in patients receiving Ca/Mg infusion during paclitaxel chemotherapy and compare it with historical controls. Secondary endpoints will include other measures of neuropathy and quality of life such as the FACT-Tax score, taxane-related neuropathy pain as measured by the Brief Pain Inventory-Short Form (BPI-SF), and measure of cognitive impairment using FACT-cog score.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 21 years
  • History of stage I-III breast cancer
  • Patient scheduled to be receiving adjuvant or neo-adjuvant paclitaxel given every week for 12 weeks or given every two weeks for 4 cycles
  • Serum magnesium level ≤ UNL
  • Serum calcium level ≤ UNL
  • Serum creatinine ≤ 1.5 x UNL
  • Signed informed consent

Exclusion criteria

  • Pre-existing peripheral neuropathy of any grade
  • Current treatment for arrhythmias
  • Concurrent treatment with anticonvulsants, tricyclic antidepressants, or other neuropathic medications such as carbamazepine, phenytoin, gabapentin, lamotrigine, or concurrent treatment with other neuropathic chemotherapy agents
  • Current narcotic use

Treatment and study plan

calcium gluconate and magnesium sulfate

Drug

Intravenous calcium gluconate and magnesium sulfate, 1g each agent in 100 ml D5W over 30 minutes, immediately before and after each dose of paclitaxel

Other names: Ca, Mg, Calcium, Magnesium

Primary outcomes

  1. to assess paclitaxel-related neuropathy (grade 2 or greater)

    Time frame: 2 years

    The primary aim of this study is to assess paclitaxel-related neuropathy (grade 2 or greater) as measured by NCI Common Terminology Criteria Version 3 in patients receiving Ca/Mg infusion during paclitaxel chemotherapy and compare it with historical controls

Secondary outcomes

  1. Other measures of neuropathy and quality of life

    Time frame: 2 years

    The secondary endpoints will include other measures of neuropathy and quality of life such as the FACT-TAX score

  2. Taxane-related neuropathic pain

    Time frame: 2 years

    Taxane-related neuropathic pain as measured by the Brief Pain Inventory-Short Form (BPI-SF)

  3. Measure of cognitive impairment

    Time frame: 2 years

    Measurement of cognitive impairment using FACT-Cog score

Sponsors and collaborators

Lead sponsor

Beth Israel Medical Center

Other

Collaborators

  • St. Luke's-Roosevelt Hospital Center

Registry information

Official study title

Calcium and Magnesium Infusion for the Prevention of Taxane Induced Neuropathy in Earlier Stage Breast Cancer

Important dates

Study start
2012
Primary completion
2014
Study completion
2014
First posted
Sep 11, 2012
Registry last updated
Sep 25, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.