- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT01416246
Fractionated Stem Cell Infusions in Myeloma Patients Undergoing Autologous Stem Cell Transplant
Pilot Trial of Fractionated Stem Cell Infusions in Myeloma Patients Undergoing Autologous Stem Cell Transplant
Multiple myeloma is difficult to treat with only anti-cancer medicine (called chemotherapy) or radiation alone. Sometimes higher doses of chemotherapy are used but when used can also lower blood counts. Using own cells (special cells called stem cells) to help increase the blood counts after high doses of chemotherapy is called autologous stem cell transplantation (ASCT).
Using own stem cells to restore blood counts and other advances in supportive measures (antibiotics and growth factors that increase blood counts) has improved the safety of ASCT. However, blood counts still decrease for a period of days after high doses of chemotherapy. During that time, patients are at greater risk for infections. Studies have shown that the faster the blood counts recover after ASCT, the less at risk there is for developing unwanted side effects after ASCT.
Typically during an ASCT, a patient's stem cells are given back to them all at once on a single day. In this study, the investigators plan to see what happens when smaller amounts of own stem cells are given back to the patient over multiple days. The investigators want to find out what effects good and/or bad this will have on the patient and there multiple myeloma. Some studies have shown that giving back stem cells over a period of days helps to increase bone marrow activity and decrease the time it takes for blood counts to recover after ASCT. It is our hope that this new approach may lower a patient's risk of side effects and infections, decrease the number of blood transfusions that a patient needs during this process, reduce the time a patient has to spend in the hospital, and lower overall treatment costs.
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Ikke anvendelig
Kontakter og lokationer
Studiesteder
-
-
New York
-
New York, New York, Forenede Stater, 10065
- Memorial Sloan-Kettering Cancer Center
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Age ≥18 and < than or = to 75
- Histologic and serologic findings, reviewed at MSKCC, confirming the diagnosis of multiple myeloma. Standard diagnostic criteria for multiple myeloma will be used, as per the International Myeloma Foundation consensus guidelines (Durie et al, 2003) .
Patients must have symptomatic multiple myeloma who have responded to prior induction or salvage chemotherapy (i.e. chemosensitive disease):
- Patients who are receiving high-dose melphalan and ASCT as part of their initial therapy require at least minor response to their last line of therapy to document chemosensitive disease (Anderson et al. 2008)
- Patients who are receiving high-dose melphalan and ASCT as part of salvage therapy require at least a minor response to their last line of therapy to document chemosensitive disease (Anderson et al. 2008).
There is no limit on the number of prior regimens received by the patient.
- Patients must have at least 7 x 10^6 (+/- 0.5 x 10^6) CD34+ stem cells/kg frozen if he/she is being treated as part of a salvage (second) transplant strategy; patients must have 10 x 10^6 (+/- 0.5 x 10^6) CD34+ stem cells/kg frozen if ASCT is being performed as part of initial therapy.
- Adequate organ function is required, defined as follows:
- Serum bilirubin ≤ 2.0 mg/dl
- AST, ALT and alkaline phosphatase < 3 times the upper limit of laboratory normal
Creatinine clearance > or = to 40 ml/min (24 hour urine collection or calculated*)
*To be calculated by the Cockroft-Gault method: (140-Age) x Mass (kg) x [0.85 if female] (72 x Creatinine (mg/dL)
- LVEF > or = to 45% by MUGA or rest ECHO
- Diffusing capacity > or = to 45% (adjusted for hemoglobin) predicted by pulmonary function testing
- Performance status KPS > or = to 70%.
Exclusion Criteria:
- Unstable angina or myocardial infarction within 4 months of initiating therapy on trial, NYHA Class III or IV heart failure, uncontrolled angina, severe uncontrolled ventricular arrhythmias, sick sinus syndrome, or electrocardiographic evidence of acute ischemia or Grade 3 conduction system abnormalities unless subject has a pacemaker
- Pregnant or lactating females
- Nonhematologic malignancy within the past 3 years with the exception of a) adequately treated basal cell carcinoma, squamous cell skin cancer, or thyroid cancer; b) carcinoma in situ of the cervix or breast; c) prostate cancer of Gleason Grade 6 or less with stable prostate-specific antigen levels; or d) cancer considered cured by surgical resection or unlikely to impact survival during the duration of the study, such as localized transitional cell carcinoma of the bladder or benign tumors of the adrenal or pancreas
- Contraindication to melphalan or any of the required supportive treatments, including hypersensitivity to G-CSF or pegfilgrastim
- Any other medical condition or laboratory evaluation that, in the treating physician's or principal investigator's opinion, makes the patient unsuitable to participate in this clinical trial
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: N/A
- Interventionel model: Enkelt gruppeopgave
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Fractionated Stem Cell Infusions
A single arm, open-label, single institution pilot trial is planned.
Patients with chemosensitive MM and at least 7 x 10^6 CD34+ stem cells/kg (+/- 0.5 x 10^6 CD34+ stem cells/kg)available for use will be enrolled following initial induction or salvage therapy.
|
Following enrollment patients will be treated with melphalan intravenously (IV) through a central venous catheter (CVC) over 30 minutes at 200mg/m2 or 140mg/m2 (if creatinine clearance is < or = to 50 and/or age > 70 years) on day -2.
Following 24 hours of rest, the first dose of CD34+ stem cell will be administered on day 0 (2.5-5 x 106 CD 34+ stem cells/kg)+/- 0.5 x 106 CD34+ stem cells/kg), followed by 3 additional doses of CD 34+ stem cells (1.5-2.5 x 106 CD 34+ stem cells/kg)+/- 0.5 x 106 CD34+ stem cells/kg) on days +2, +4, and +6.
Pegfilgrastim 6μg will be administered on day +1.
Filgrastim 5μg/kg will be 12-24 hours after the 2nd-4th stem cell infusions.
There will be a +/- 1 day window for the Day +2, +4, and +6 infusions to accommodate infusions that occur over the weekend or on holidays.
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
engraftment kinetics
Tidsramme: 2 years
|
as measured by duration of neutropenia in patients with MM undergoing high-dose melphalan followed by fractionated CD34+ stem cell infusions.
|
2 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
safety and toxicity profile
Tidsramme: 2 years
|
of high-dose melphalan therapy followed by multiple doses of CD34+ stem cell rescue in patients with MM.
Whenever possible, the Common Terminology Criteria for Adverse Events (CTCAE) version 4.0 should be used to describe the event and for assessing the severity of AEs.
|
2 years
|
|
neutrophil and platelet recovery rates.
Tidsramme: 2 years
|
Duration of neutropenia will be defined as the number of days ANC< 500x106/L.
Time until platelet recovery (defined as platelets>=30x109/L), the number of units of red blood cells and platelets.
|
2 years
|
|
incidence of infection
Tidsramme: 3 months post-SCT
|
The incidence of infection by three months after re-infusion will be calculated.
|
3 months post-SCT
|
|
red cell and platelet transfusion requirements
Tidsramme: 2 years
|
will be evaluated using the Spearman rank correlation coefficient
|
2 years
|
|
duration of hospital admission
Tidsramme: 2 years
|
length of hospital stay in days will be summarized using descriptive statistics.
|
2 years
|
|
To assess symptom burden
Tidsramme: 2 years
|
using the MSK Modified M.D. Anderson Symptom Inventory (MDASI).
|
2 years
|
|
Multiple Myeloma response rates
Tidsramme: at 3 months
|
at 3 months post-transplant according to standard response criteria.
Response rates will be evaluated based on International Myeloma Working Group Uniform Response Criteria at 3 months following ASCT.
|
at 3 months
|
|
correlation between engraftment kinetics and symptom burden
Tidsramme: 2 years
|
in patients with MM who receive high-dose melphalan and fractionated CD34+ stem cell infusions
|
2 years
|
|
the number of CD34+ cells/Kg present
Tidsramme: 2 years
|
at the time of infusion.
The difference between the number of CD34+ cells/kg given at each stem cell infusion time point and the number of CD34+ cells/kg before cryopreservation will be calculated as both a simple difference and percentage change.
|
2 years
|
|
To correlate the number CD34+ cells/Kg given
Tidsramme: 2 years
|
at the time of transplant with engraftment kinetics.
The difference between the number of CD34+ cells/kg given at each stem cell infusion time point and the number of CD34+ cells/kg before cryopreservation will be calculated as both a simple difference and percentage change.
|
2 years
|
Samarbejdspartnere og efterforskere
Publikationer og nyttige links
Hjælpsomme links
Datoer for undersøgelser
Studer store datoer
Studiestart
Primær færdiggørelse (Faktiske)
Studieafslutning (Faktiske)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Hjerte-kar-sygdomme
- Karsygdomme
- Sygdomme i immunsystemet
- Neoplasmer efter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Immunproliferative lidelser
- Hæmatologiske sygdomme
- Hæmoragiske lidelser
- Hæmostatiske lidelser
- Paraproteinæmier
- Blodproteinforstyrrelser
- Myelomatose
- Neoplasmer, Plasmacelle
- Antibakterielle midler
- Anti-infektionsmidler
Andre undersøgelses-id-numre
- 11-105
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Myelomatose
-
Guangzhou Bio-gene Technology Co., LtdTrukket tilbageMultiple myeloma -ildfast
-
University Health Network, TorontoIkke rekrutterer endnuMyelom i tilbagefald | Multiple myeloma -ildfastCanada
-
Hebei Senlang Biotechnology Inc., Ltd.Peking University People's Hospital; Institute of Hematology & Blood Diseases...Ikke rekrutterer endnuMyelom i tilbagefald | Multiple myeloma -ildfast
-
Baskent UniversityIkke rekrutterer endnuMULTIPL SKLEROSETyrkiet (Türkiye)
-
Minsk Scientific-Practical Center for Surgery,...RekrutteringAnti-BCMA CAR-T-celleterapi for voksne med tilbagevendende eller refraktær myelomatose (MSTH-CAR001)Multiple myeloma -ildfastHviderusland
-
HuniLife Biotechnology, Inc.Tilmelding efter invitationMultiple myeloma -ildfastTaiwan
-
CHU de Quebec-Universite LavalRekrutteringRecidiverende myelomatose | Multiple myeloma -ildfastCanada
-
PETHEMA FoundationRekrutteringDe novo multiple myeloma | Anitocabtagene AutoleucelSpanien
-
CellCentric Ltd.RekrutteringMyelom i tilbagefald | Multiple myeloma -ildfastForenede Stater, Det Forenede Kongerige
-
Asan Medical CenterAfsluttetAkut leukæmi, myelodysplastisk syndrom, myeloproliferative neoplasmer, lymfom, multiple myelomaSydkorea
Kliniske forsøg med Fractionated Stem Cell Infusions
-
PETHEMA FoundationRekrutteringHøj risiko ulmende myelomatoseSpanien
-
University of NebraskaBristol-Myers SquibbAktiv, ikke rekrutterendeFollikulært lymfom | Refraktær non-Hodgkin lymfom | Højgradigt B-celle lymfom | DLBCL - Diffust storcellet B-celle lymfom | Recidiverende non-Hodgkin lymfom | Mediastinalt stort B-cellet lymfom | Indolent B-celle non-Hodgkin lymfomForenede Stater