Acupuncture for Chemo-Induced Peripheral Neuropathy

Lymphoma Clinical Trial

Official title:

Acupuncture for Chemo-induced Peripheral Neuropathy in Multiple Myeloma and Lymphoma Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00891618
• Other study ID #: 2006-0679
• Status: Completed
• Phase: Phase 2
• First received: April 30, 2009
• Last updated: April 9, 2013
• Start date: April 2009

Study information

• Verified date: April 2013
• Source: M.D. Anderson Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Interventional

Clinical Trial Summary

The goal of this clinical research study is to learn if giving acupuncture to patients with lymphoma or a plasma cell dyscrasia can help to relieve numbness and/or tingling of the feet and/or hands that is related to chemotherapy.

Description:

Acupuncture:

Acupuncture involves the insertion of small, solid, sterile needles into specific points on the skin. In this study, the needles are placed in areas that are intended to help relieve numbness and tingling of the feet and hands. Weak electrical stimulation is also applied to the needles to try to improve the treatment effects of the acupuncture.

Acupuncture Sessions:

Your first acupuncture session will be on the same day as the tests described above, if possible. (If not, it will be scheduled for another day that will be no more than about 10 days after the screening visit.)

You will have an acupuncture session 3 times per week for 4 weeks (Weeks 1-4). You will then have 1 week off (Week 5). After that, you will have an acupuncture session twice per week for 4 more weeks (Weeks 6-10). This is a total of 20 sessions. In addition to the 20 planned sessions, you may also choose to receive an optional 21st acupuncture session at the end-of-study visit that is scheduled for Week 13.

For each session, you will be placed in a comfortable position and the study doctor/acupuncturist will find points on your body where the needles will be placed. All study participants will have the needles placed at the same points on the body (the hands, feet, legs, abdomen, and scalp).

Very thin, solid, sterile, stainless steel needles will be used. All of the needles are specially made for acupuncture. The depth of the needle in the skin and the number of needles used is based on standard acupuncture procedures. The needles will remain in place for about 20-30 minutes.

Electrical stimulation will be added to some of the needles on the feet and hands. This involves placing wires on the needles, which are connected to a machine that delivers a weak electrical current through the wires. The strength of the electrical current will be changed slowly until it is at a comfortable level for you.

Study Procedures:

At each session, before you receive the acupuncture, the following procedures will be performed:

• Your vital signs will be measured.

• You will be asked about any drugs you may be taking and any side effects you may be experiencing.

• The color and coating of your tongue and the quality of your pulse will be recorded.

Once a week, you will also be asked to complete the same 3 questionnaires as you did at the beginning of the study.

Most study visits will last about 1 hour. On the weeks that you complete the questionnaires, it may add about 15-20 minutes.

During the study, you may still receive your regular pain treatments. If you are receiving Neurontin (gabapentin), Cymbalta (duloxetine), and/or Lyrica (pregabalin), you must stay on the same drug(s) until you go off this study. Minor changes in the doses of your pain treatments are allowed, but if there is a large change, you will be taken off study early.

Length of Study Participation:

You may receive up to 21 acupuncture sessions over 13 weeks. If intolerable side effects or symptoms occur, you will be taken off study early.

End-of-Study Visit:

At Week 13, or if you go off study early for any reason, you will have an end-of-study visit. If the doctor thinks it is necessary, the following procedures will be performed:

• Your medical history will be recorded.

• Your vital signs will be measured.

• You will be asked about any drugs you may be taking and any side effects you may have experienced.

• You will complete the same 3 questionnaires as before.

• The 4 nerve tests will be repeated in order to learn if there have been any changes in your nerve function.

• Your tongue and pulse will be evaluated.

After the end-of-study visit, your participation in this study will be over.

This is an investigational study. The acupuncture needles used in this study are commercially available and FDA approved. It is considered experimental, however, to use acupuncture to treat numbness and/or tingling in the feet and/or hands that is related to chemotherapy.

Up to 30 patients will take part in this study. All will be enrolled at M. D. Anderson.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 27
• Est. primary completion date: April 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Patients, or the legal guardians of patients, must have the ability to understand English, sign a written informed consent document, and be willing to follow protocol requirements.

2. Age > 18 years and have a diagnosis of a plasma cell dyscrasia or lymphoma.

3. Patients must have neuropathy greater or equal to 2 according to CTCAE v 3.0 scale (Appendix A) in spite of previous treatment with Neurontin, Cymbalta and/or Lyrica. Patients receiving any of these drugs must remain on the same medications throughout the study period; however, minor adjustments in dosage are allowed. Patients will be removed from the study if a change in type of medication is necessary. All patients will receive treatment to both upper and lower extremities, regardless of whether or not they are experiencing symptoms in all four extremities - see Section 7.0 Treatment Plan.)

4. The patient's previous chemotherapy treatment must have included thalidomide and/or bortezomib and/or any derivatives.

5. ECOG Performance Status of 0, 1, or 2 (Appendix B).

6. If the patient is a woman of child-bearing potential, she must have a negative urine pregnancy test and agree to use contraception.

Exclusion Criteria:

1. Current active treatment with thalidomide and/or bortezomib.

2. Local infection at or near the acupuncture site. (Although acupuncture is a minimally invasive procedure, patients will be excluded if there is an indication of infection.)

3. Deformities that could interfere with accurate acupuncture point location or out of energy pathway as defined by traditional acupuncture theory.

4. Concurrent use of other alternative medicines such as herbal agents, high dose vitamins and anticoagulation agents.

5. Known coagulopathy and taking heparin (including low molecular weight heparin) or Coumadin at any dose. Patients on aspirin or non-steroidal anti-inflammatories will be allowed to participate.

6. Platelets < 50 H K/UL.

7. WBCs < 3.0 K/UL.

8. Active CNS disease. (The action for acupuncture may be associated with central nervous system activity, and patients with CNS pathology may respond differently to treatment than the general population.)

9. Cardiac pacemaker.

10. Mental incapacitation or significant emotional or psychological disorder that, in the opinion of the investigators, precludes study entry. (These patients may not be able to cooperate with this slightly invasive procedure or with the data collection process.)

11. Currently pregnant or lactating females. (Certain acupuncture applications have been reported to stimulate uterine contractions and may alter lactation.)

12. Chronic alcohol use as clinically estimated by the patient's physician.

13. History of diabetic neuropathy or neuropathy related to HIV.

14. Previous acupuncture treatment for any indication within 30 days of enrollment.

15. Active treatment for lymphoma, non-Hodgkin's lymphoma or multiple myeloma.

16. Planned or actual changes in type of medications that could affect symptoms related to PN. Note: Minor adjustments in current medications at the time of enrollment is allowed.

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Lymphoma
• Myeloma
• Peripheral Nervous System Diseases
• Peripheral Neuropathy

Intervention

Other:
• Acupuncture
3 acupuncture sessions per week for 4 weeks (Weeks 1-4), 1 week off (Week 5), then 2 per week for 4 more weeks (Weeks 6-10), total of 20 sessions. Each session lasts 20-30 minutes.

Locations

Country	Name	City	State
United States	UT MD Anderson Cancer Center	Houston	Texas

Sponsors (2)

Lead Sponsor	Collaborator
M.D. Anderson Cancer Center	Millennium Pharmaceuticals, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Neuropathy Severity (FACT-GOG-Ntx Total Score Assessment)		At baseline, once per week during two treatment phases of study, and one month (week 13) after last acupuncture treatment.	Yes

External Links

•   UT MD Anderson Cancer Center website