Calcium and Magnesium in Preventing Peripheral Neuropathy Caused by Ixabepilone in Patients With Breast Cancer

Mayo Clinic

Status and phase: Terminated; Phase 3

Conditions: Recurrent Breast Carcinoma; Neuropathy; Pain; Stage IV Breast Cancer

Treatments: Drug: Ixabepilone; Other: Quality-of-Life Assessment; Drug: Magnesium Sulfate; Other: Placebo; Other: Questionnaire Administration; Drug: Calcium Gluconate

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00998738

NCI-2009-01229 (Registry Identifier)

P30CA015083 (U.S. NIH Grant/Contract)

RC08CC (Other Identifier)

Details and patient eligibility

About

This randomized phase III trial studies calcium and magnesium to see how well they work in preventing peripheral neuropathy caused by ixabepilone in patients with breast cancer. Giving calcium together with magnesium may stop or delay the development of peripheral neuropathy in patients with cancer who are receiving treatment with ixabepilone. It is not yet known whether calcium and magnesium are effective in preventing peripheral neuropathy caused by ixabepilone.

Full description

PRIMARY OBJECTIVES:

I. To compare ixabepilone-induced peripheral neuropathy (sensory) as measured by European Organization for Research and Treatment of Cancer (EORTC) Quality of life Questionnaire (QLQ)-Chemotherapy-Induced Peripheral Neuropathy (CIPN)20 sensory subscale between calcium (Ca) Magnesium (Mg) and placebo arms.

SECONDARY OBJECTIVES:

I. To compare the incidence of CTCAE measured grade 2+ and/or grade 3+ peripheral neuropathy between CaMg and placebo arms.

II. To compare the times to onset of CTCAE measured grade 2+ and/or grade 3+ peripheral neuropathy between CaMg and placebo arms.

III. To compare the proportion of patients requiring ixabepilone dose reductions and/or stopping ixabepilone secondary to peripheral neuropathy (sensory) between CaMg and placebo arms.

IV. To assess the toxicity of CaMg in this situation. V. To document the incidence and severity of the acute pain syndrome (APS, commonly known as arthralgias/myalgias) induced by ixabepilone.

VI. To evaluate whether CaMg will decrease the acute pain syndrome (APS). VII. To evaluate the incidence and characteristics of, and change in, ixabepilone-APS over several cycles.

VIII. To evaluate the association between the ixabepilone-APS and eventual chemotherapy-induced neuropathy.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

ARM I: Patients receive calcium gluconate and magnesium sulfate IV over 30 minutes immediately before and after each ixabepilone administration.

ARM II: Patients receive placebo IV over 30 minutes immediately before and after each ixabepilone administration.

After completion of study treatment, patients are followed up monthly for 12 months.

Enrollment: 1 patient

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Scheduled to undergo cancer treatment for metastatic breast cancer (weekly or once every three weeks) with ixabepilone with no prior exposure to ixabepilone and no more than 2 prior chemotherapy regimens for metastatic disease
• Serum calcium =< 1.2 x upper normal limit (UNL)
• Serum magnesium =< UNL
• Serum creatinine =< 1.5 x UNL
• Ability to sign informed consent and understand the nature of a placebo-controlled trial
• Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0, 1, or 2
• Ability to complete questionnaire(s) by themselves or with assistance
• Life expectancy >= 4 months
• Presence of a central line

Exclusion criteria

• Pre-existing history of peripheral neuropathy >= grade 2 (National Cancer Institute [NCI] CTCAE Active Version) due to any cause (chemotherapy, diabetes, alcohol, toxin, hereditary, etc.)

• Concurrent treatment with anticonvulsants, tricyclic antidepressants, or other neuropathic pain medications agents such as carbamazepine, phenytoin, valproic acid, gabapentin, lamotrigine, topical lidocaine patch, capsaicin cream, etc., or any other treatments specifically for prevention or treatment of neuropathy

• Other medical conditions, which in the opinion of the treating physician/allied health professional would make this protocol unreasonably hazardous for the patient

• Any of the following:

  • Pregnant women
  • Nursing women
  • Women of childbearing potential (per physician judgment)

• Diagnosed diabetes requiring insulin or oral hypoglycemic medications

• Receiving digoxin or digitoxin

• History of heart block (any degree)

• Current treatment for arrhythmias

• Concurrent treatment with other neuropathic chemotherapy agents

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

---

1 participants in 2 patient groups, including a placebo group

Arm I (calcium gluconate, magnesium sulfate)

Experimental group

Description:

Patients receive calcium gluconate and magnesium sulfate IV over 30 minutes immediately before and after each ixabepilone administration.

Treatment:

Drug: Calcium Gluconate

Other: Questionnaire Administration

Drug: Ixabepilone

Other: Quality-of-Life Assessment

Drug: Magnesium Sulfate

Arm II (placebo)

Placebo Comparator group

Description:

Patients receive placebo IV over 30 minutes immediately before and after each ixabepilone administration.

Treatment:

Other: Questionnaire Administration

Other: Placebo

Drug: Ixabepilone

Other: Quality-of-Life Assessment