search
Back to results

TMC (Topotecan, Cyclophosphamide and Melphalan) for Multiple Myeloma

Primary Purpose

Myeloma

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Topotecan
Cyclophosphamide
Melphalan
Peripheral Blood Stem Cells
Sponsored by
M.D. Anderson Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Myeloma focused on measuring Myeloma, Topotecan, Hycamtin, Melphalan, Alkeran, Cyclophosphamide, Cytoxan, Neosar, Stem Cell Harvest, Peripheral Blood Stem Cells

Eligibility Criteria

undefined - 70 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patients with intermediate or high tumor mass multiple myeloma with responsive or primary refractory disease; and patients with responsive or refractory relapse.
  2. Physiological age </= 70.
  3. Zubrod performance status < 3.
  4. Life expectancy greater than 12 weeks.
  5. Left ventricular ejection fraction >/= 50%.
  6. No uncontrolled arrythmias or symptomatic cardiac disease.
  7. FEV1, FVC and DLCO >/= 50%.
  8. No symptomatic pulmonary disease.
  9. Serum creatinine < 1.5 mg/dL.
  10. Serum bilirubin < 2x upper limit of normal.
  11. No evidence of chronic or active hepatitis or cirrhosis.
  12. Patient is not pregnant.
  13. Patients or guardian able to sign informed consent.
  14. No active CNS disease.
  15. Platelet count > 100K.

Exclusion Criteria:

1) N/A

Sites / Locations

  • U.T. M.D. Anderson Cancer Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

TMC

Arm Description

Topotecan, Melphalan, and Cyclophosphamide

Outcomes

Primary Outcome Measures

Response Rate

Secondary Outcome Measures

Full Information

First Posted
December 23, 2009
Last Updated
November 6, 2018
Sponsor
M.D. Anderson Cancer Center
Collaborators
SmithKline Beecham
search

1. Study Identification

Unique Protocol Identification Number
NCT01039025
Brief Title
TMC (Topotecan, Cyclophosphamide and Melphalan) for Multiple Myeloma
Official Title
Phase II Study of High-Dose Topotecan, Cyclophosphamide and Melphalan for the Treatment of Multiple Myeloma
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
February 18, 2002 (Actual)
Primary Completion Date
May 19, 2006 (Actual)
Study Completion Date
May 19, 2006 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
M.D. Anderson Cancer Center
Collaborators
SmithKline Beecham

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
To determine the efficacy of high-dose topotecan, cyclophosphamide and melphalan in patients with Multiple Myeloma.
Detailed Description
Patients in this study will have a catheter (a tube) placed in the vein below the collarbone. Most of the drugs used in the study will be given through the catheter. Blood stem cells will be collected through this tube also. Before treatment starts, patients will have a complete physical exam, including blood and urine tests. A dentist will perform a dental exam either at M.D. Anderson or elsewhere. A chest x-ray and bone x-rays will be done. An EKG and a heart scan will be done to test heart function. A breathing test will be done. Patients will also be screened for HIV and Hepatitis. Blood stem cells will be collected from patients when white blood cell counts are normal. This will be after earlier chemotherapy or after a bone marrow growth factor (G-CSF) has been given. Collecting stem cells takes about 3 hours. It takes from 1 to 6 sessions to get the needed amount of cells. The process is called apheresis. A machine is attached to the catheter, and blood is drawn. The machine removes the stem cells from the blood and the blood is then returned to the body through the catheter. G-CSF is injected under the skin twice a day during the time the stem cells are collected. The stem cells are stored frozen and will be used later to help patients recover from the high-dose chemotherapy. After stem cells are collected, patients will receive high-dose chemotherapy. Cyclophosphamide is given over 2 hours on Days 1 - 3. Melphalan is given on Days 4 and 5. Topotecan is given over 30 minutes on Days 1 - 5, right after cyclophosphamide or melphalan. On Day 6, no drugs are given. On Day 7, some or all of the stem cells will be reinfused. G-CSF will be given once a day until blood counts return to normal. Patients must stay in the hospital for the high-dose drug treatment. The length of stay will be about 3 weeks. Blood tests will be done daily while in hospital, then once a week for the first month. A bone marrow sample will be taken on Day 30. Blood samples will be taken 4 times in the first year and once a year after that. Thyroid gland tests and a bone marrow test will be done once a year. This is an investigational study. Cyclophosphamide, melphalan, and topotecan are approved by the FDA. Their use together in this study is experimental. All participants will be enrolled at UTMDACC.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myeloma
Keywords
Myeloma, Topotecan, Hycamtin, Melphalan, Alkeran, Cyclophosphamide, Cytoxan, Neosar, Stem Cell Harvest, Peripheral Blood Stem Cells

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TMC
Arm Type
Experimental
Arm Description
Topotecan, Melphalan, and Cyclophosphamide
Intervention Type
Drug
Intervention Name(s)
Topotecan
Other Intervention Name(s)
Hycamtin
Intervention Description
After stem cells are collected, Topotecan 3.5 mg/m^2 intravenously given over 30 minutes on Days 1 - 5.
Intervention Type
Drug
Intervention Name(s)
Cyclophosphamide
Other Intervention Name(s)
Cytoxan, Neosar
Intervention Description
After stem cells are collected, Cyclophosphamide 1 g/m^2/day intravenously given over 2 hours on Days 1 - 3.
Intervention Type
Drug
Intervention Name(s)
Melphalan
Other Intervention Name(s)
Alkeran
Intervention Description
After stem cells are collected, Melphalan 70 mg/m^2/day intravenously given on Days 4 and 5.
Intervention Type
Other
Intervention Name(s)
Peripheral Blood Stem Cells
Intervention Description
On Day 7, some or all of the stem cells will be reinfused.
Primary Outcome Measure Information:
Title
Response Rate
Time Frame
Within 180 days after treatment

10. Eligibility

Sex
All
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with intermediate or high tumor mass multiple myeloma with responsive or primary refractory disease; and patients with responsive or refractory relapse. Physiological age </= 70. Zubrod performance status < 3. Life expectancy greater than 12 weeks. Left ventricular ejection fraction >/= 50%. No uncontrolled arrythmias or symptomatic cardiac disease. FEV1, FVC and DLCO >/= 50%. No symptomatic pulmonary disease. Serum creatinine < 1.5 mg/dL. Serum bilirubin < 2x upper limit of normal. No evidence of chronic or active hepatitis or cirrhosis. Patient is not pregnant. Patients or guardian able to sign informed consent. No active CNS disease. Platelet count > 100K. Exclusion Criteria: 1) N/A
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michelle Donato, MD
Organizational Affiliation
M.D. Anderson Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
U.T. M.D. Anderson Cancer Center
City
Houston
State/Province
Texas
ZIP/Postal Code
77030
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.clinicaltrials.org
Description
M.D. Anderson Cancer Center clinical trials web site

Learn more about this trial

TMC (Topotecan, Cyclophosphamide and Melphalan) for Multiple Myeloma

We'll reach out to this number within 24 hrs