Meloxicam vs Placebo for Mobilization

Multiple Myeloma Clinical Trial

Official title:

Non-steroidal Anti-inflammatory Drugs (Meloxicam) to Mobilize Hematopoietic Stem Cells: A Phase II Randomized Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02003625
• Other study ID #: 13-195
• Status: Completed
• Phase: Phase 2
• Start date: October 2013
• Est. completion date: April 2019

Study information

• Verified date: May 2020
• Source: Massachusetts General Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This research study is evaluating a drug called meloxicam to see if it provides a benefit to people receiving Autologous Hematopoietic Stem Cell Transplantation (AHSCT).

The participant is currently scheduled to receive an AHSCT, which is a procedure that removes blood-forming stem cells (cells from which all blood cells develop) from the body. These stem cells are stored and later given back to the participant by a process called apheresis. This is a standard procedure to treat certain blood diseases such as lymphoma and multiple myeloma. However the use of meloxicam with this procedure is considered investigational.

Meloxicam is a non-steroidal anti-inflammatory drug (NSAID) which is given to decrease fever, swelling and pain that may come with inflammation. It has been approved by the FDA for the treatment of arthritis however it has not been approved for use in people receiving AHSCT.

This study will compare the combination of meloxicam with a drug called G-CSF (also called neupogen), to the combination of G-CSF with an agent that has no medicine (placebo). G-CSF is a substance that causes blood stem cells to change or increase in number when given to people undergoing AHSCT. The researchers would like to learn if giving meloxicam in combination with G-CSF to people before they undergo AHSCT will increase the number of stem cells available in the blood to collect and make the collection process easier.

Description:

After the screening procedures confirm that the participant is eligible to participate in the research study:

Because no one knows which of the study options is best, the participant will be "randomized" into one of the study groups:

• G-CSF with meloxicam

• G-CSF with placebo (pills with no medicine)

Randomization means that the participants are put into a group by chance. It is like flipping a coin. Neither the participant nor the research doctor will choose what group the participant will be in. The participant will have an equal chance of being placed in any group.

• Study Drug (meloxicam or placebo): If the participant takes part in this research study, the participant will be given a study drug-dosing diary. The study drug will come as a pill that the participant will take by mouth daily for 5 days, starting 6 days (Day -6) before the participant is scheduled to undergo the first apheresis procedure (Day 0) and continuing until 2 days before apheresis (Day -2). The participant will take meloxicam or placebo for a total of 5 days. The diary will also include special instructions for taking the study drug(s).

-G-CSF: All participants receive G-CSF as an injection under the skin (subcutaneous) in the clinic, daily starting 4 days (Day -4) before the first apheresis procedure (Day 0). The participant will continue to receive G-CSF for 3 days after apheresis.

• Apheresis: The participant may receive up to 4 apheresis procedures, depending on how their body reacts to the stem cell mobilization. The participant will receive either meloxicam or placebo in combination with G-CSF on Days -6 to -2 as described above.

Clinical Exams: While the participant is receiving this procedure, the participant will have regular physical exams and they will be asked specific questions about any problems that they might be having. The participant will also have blood tests every day to look at how their bone marrow is recovering, to give possible transfusional support, and how to see how their liver and kidneys are functioning.

Planned Follow-up: The investigators would like to keep track of the participant's medical condition for the rest of their life. The investigators would like keep track of the participant's medical condition for 6 months after the study to see how they are doing.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: April 2019
• Est. primary completion date: February 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Participants must meet the following criteria on screening examination to be eligible to participate in the study:

• Patients with hematologic malignancies for whom autologous stem cell transplantation is deemed clinically appropriate. Patients participating in this study are patients who are going for their first attempt at stem cell mobilization.

• Non-Hodgkin's lymphoma, or Hodgkin's lymphoma: refractory/relapsed but chemosensitive disease. Patients with CR or PR will be eligible for this protocol.

The designation of PR requires all of the following:

• At least a 50% decrease in sum of the product of the diameters (SPD) of up to six of the largest dominant nodes or nodal masses. These nodes or masses should be selected according to all of the following: they should be clearly measurable in at least 2 perpendicular dimensions; if possible they should be from disparate regions of the body; and they should include mediastinal and retroperitoneal areas of disease whenever these sites are involved.

• No increase should be observed in the size of other nodes, liver, or spleen.

• Splenic and hepatic nodules must regress by = 50% in their SPD or, for single nodules, in the greatest transverse diameter.

• With the exception of splenic and hepatic nodules, involvement of other organs is usually assessable and no measurable disease should be present.

• Bone marrow assessment is irrelevant for determination of a PR if the sample was positive before treatment. However, if positive, the cell type should be specified (eg, large-cell lymphoma or small neoplastic B cells). Patients who achieve a CR by the above criteria, but who have persistent morphologic bone marrow involvement will be considered partial responders. Multiple myeloma in first or second remission. Patients with CR or VGPR will be eligible for this protocol. [VGPR: Serum and urine M-protein detectable by immunofixation only but not on electrophoresis or 90% or greater reduction in serum M-protein plus urine M-protein level <100mg per 24 h]

• Ages 18-75 years

• ECOG performance status of 0, 1, or 2.

• Ability to understand and the willingness to sign a written informed consent

• Patients on NSAIDs will be eligible only when they are off NSAIDs for a month.

Exclusion Criteria:

• Participants who exhibit any of the following conditions at screening will not be eligible for admission into the study.

• Cardiac disease: symptomatic congestive heart failure or RVG or echocardiogram determined left ventricular ejection fraction of < 45%, active angina pectoris, or uncontrolled hypertensionParticipants may not be receiving any other study agents.

• Pulmonary disease: severe chronic obstructive lung disease, or symptomatic restrictive lung disease, or corrected DLCO of < 50% of predicted.

• Renal disease: serum creatinine > 2.0 mg/dl.

• Hepatic disease: SGOT or SGPT > 3 x normal; serum bilirubin >2.0 mg/dl that is not due to Gilbert's syndrome or hemolysis

• Uncontrolled infection.

• Pregnancy or lactation

• Patients with NSAIDs allergies, including patients who have experienced a prior GI bleed due to NSAIDs will be excluded. Patients who have had a recent GI bleed less than 2 weeks ago will be excluded. Patients who are on therapeutic dose anticoagulants will be excluded from this protocol.

Related Conditions & MeSH terms

• Hematopoietic Stem Cells
• Hodgkin Disease
• Hodgkin's Lymphoma
• Lymphoma
• Lymphoma, Non-Hodgkin
• Multiple Myeloma
• Non-Hodgkin's Lymphoma

Intervention

Drug:
• GCSF

• meloxicam

• Placebo

Locations

Country	Name	City	State
United States	Massachusetts General Hospital	Boston	Massachusetts

Sponsors (2)

Lead Sponsor	Collaborator
Massachusetts General Hospital	The Leukemia and Lymphoma Society

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Numbers of Circulating CD34+ Cells on the First Day of Apheresis	Numbers of circulating CD34+ cells on the first day of apheresis	3 days after starting treatment (or 9 days for multiple myeloma patients that received cyclophosphamide)
Primary	Number of Apheresis Sessions Required to Collect = 4 x 10^6 CD34+ Cells/kg for Multiple Myeloma Patients and = 2 x 10^6 CD34+ Cells/kg for Lymphoma Patients		Up to 6 days after the start of treatment or up to 12 days for multiple myeloma patients that received cyclophosphamide
Primary	Time to Neutrophil Engraftment After AHSCT	The median to neutrophil engraftment (absolute neutrophil counts above 0.5/mcl for 3 consecutive days) .	Up to 6 months after transplantation ( up to 66-72 days after the start of treatment)
Primary	Time to Platelet Engraftment After AHSCT	The median to platelet engraftment (platelet count above 20,000/mcl for 3 consecutive days)	Up to 6 months after transplantation ( up to 66-72 days after the start of treatment)
Secondary	Number of Patients With Grade 3+ Treatment Related Adverse Events	Adverse events were assessed using Common Terminology Criteria for Adverse Events (CTCAE v4). Related adverse events were defined as adverse events that were deemed to be possibly, probably, or definitely related to study treatment.	Up to 30 days after the last apheresis session (up to 36 days after the start of treatment or 42 days for multiple myeloma patients that received cyclophosphamide)
Secondary	Number of Participants That Received Red Blood Cell and Platelet Transfusions Prior to Engraftment		Up to 6 months after transplantation ( up to 66-72 days after the start of treatment)
Secondary	Number of Patients That Failed to Achieve Stem Cell Mobilization.	The number of patients that did not achieve CD34+ count of = 4 x 10^6 CD34+ cells/kg for multiple myeloma patients or = 2 x 10^6 CD34+ cells/kg for lymphoma patients.	Up to 6 days after the start of treatment or up to 12 days for multiple myeloma patients that received cyclophosphamide