- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT00118352
Alemtuzumab, Fludarabine Phosphate, and Total-Body Irradiation Followed by Cyclosporine and Mycophenolate Mofetil in Treating Patients Who Are Undergoing Donor Stem Cell Transplant for Hematologic Cancer
Campath (Alemtuzumab) Dose Escalation, Low-Dose TBI and Fludarabine Followed by HLA Class II Mismatched Donor Stem Cell Transplantation for Patients With Hematologic Malignancies: A Multicenter Trial
Studieoversigt
Status
Betingelser
- Kronisk myelomonocytisk leukæmi
- Tilbagevendende akut myeloid leukæmi hos voksne
- Juvenil myelomonocytisk leukæmi
- Ekstranodal marginalzone B-celle lymfom i slimhinde-associeret lymfoidt væv
- Nodal Marginal Zone B-celle lymfom
- Tilbagevendende voksen Burkitt lymfom
- Tilbagevendende voksent diffust storcellet lymfom
- Tilbagevendende voksent diffust blandet celle lymfom
- Tilbagevendende, diffust, småcellet lymfom hos voksne
- Tilbagevendende voksen immunoblastisk storcellet lymfom
- Tilbagevendende voksenlymfoblastisk lymfom
- Tilbagevendende grad 1 follikulært lymfom
- Tilbagevendende grad 2 follikulært lymfom
- Tilbagevendende grad 3 follikulært lymfom
- Tilbagevendende kappecellelymfom
- Tilbagevendende marginalzone lymfom
- Milt Marginal Zone Lymfom
- Waldenström Makroglobulinæmi
- Voksen akut myeloid leukæmi i remission
- Akut myeloid leukæmi i barndom i remission
- Perifert T-celle lymfom
- Anaplastisk storcellet lymfom
- Angioimmunoblastisk T-celle lymfom
- Voksen akut lymfatisk leukæmi i remission
- Voksen Nasal Type Ekstranodal NK/T-celle lymfom
- Akut lymfoblastisk leukæmi i barndom i remission
- Kronisk myelogen leukæmi i barndommen
- Myelodysplastiske syndromer i barndommen
- Kronisk fase Kronisk myelogen leukæmi
- Kutant B-celle non-Hodgkin lymfom
- Hepatosplenisk T-celle lymfom
- Intraokulært lymfom
- Tidligere behandlede myelodysplastiske syndromer
- Tilbagevendende akut lymfatisk leukæmi hos voksne
- Tilbagevendende voksen grad III lymfomatoid granulomatose
- Tilbagevendende voksen Hodgkin-lymfom
- Tilbagevendende voksen T-celle leukæmi/lymfom
- Tilbagevendende akut lymfatisk leukæmi i barndommen
- Tilbagevendende akut myeloid leukæmi i barndommen
- Tilbagevendende kutan T-celle non-Hodgkin lymfom
- Tilbagevendende Mycosis Fungoides/Sezary Syndrom
- Tilbagevendende lille lymfocytisk lymfom
- Refraktær Myelom
- Recidiverende kronisk myelogen leukæmi
- Sekundære myelodysplastiske syndromer
- Tyndtarms lymfom
- Testikellymfom
- Refraktær kronisk lymfatisk leukæmi
- Ildfast hårcelleleukæmi
- Akut udifferentieret leukæmi
- Atypisk kronisk myeloid leukæmi, BCR-ABL1 negativ
- Mastcelleleukæmi
- Myelodysplastisk/myeloproliferativ neoplasma, uklassificerbar
- Diffust storcellet lymfom i barndommen
- Immunoblastisk storcellet lymfom hos børn
- Børnenæsetype Ekstranodal NK/T-celle lymfom
- Tilbagevendende anaplastisk storcellet lymfom i barndommen
- Tilbagevendende Childhood Grade III Lymphomatoid Granulomatosis
- Tilbagevendende storcellet lymfom i barndommen
- Tilbagevendende barndomslymfoblastisk lymfom
- Tilbagevendende barndoms små ikke-spaltede celle lymfom
- Tilbagevendende/refraktær Hodgkin-lymfom hos børn
- Burkitt lymfom i barndommen
- Ikke-kutan ekstranodal lymfom
Intervention / Behandling
- Andet: laboratoriebiomarkøranalyse
- Medicin: fludarabin fosfat
- Procedure: perifer blodstamcelletransplantation
- Medicin: mycophenolatmofetil
- Biologisk: alemtuzumab
- Stråling: bestråling af hele kroppen
- Medicin: cyclosporin
- Procedure: allogen hæmatopoietisk stamcelletransplantation
- Biologisk: graft versus host disease prophylaxis/therapy
Detaljeret beskrivelse
PRIMARY OBJECTIVES:
I. To determine which dose of Campath (alemtuzumab) allows related and unrelated human leukocyte antigen (HLA) class-II mismatched hematopoietic cell transplantation (HCT) with an incidence of grade III-IV acute graft-versus-host disease (GVHD) less than 40%.
SECONDARY OBJECTIVES:
I. Incidence of graft rejection.
II. Number of days of steroids >= 1mg/kg required before day 100 in each patient.
III. Incidence of non-relapse mortality.
IV. Risk/incidence of infections.
V. Immune reconstitution.
VI. Risk for disease progression and relapse.
OUTLINE: This is a dose-escalation study of alemtuzumab.
NONMYELOABLATIVE CONDITIONING REGIMEN: Patients receive alemtuzumab intravenously (IV) over 6 hours once daily on days -6, -5, and -4 OR days -5 and -4 and fludarabine phosphate IV over 30 minutes on days -4, -3, and -2. Patients also undergo low-dose total-body irradiation (TBI) on day 0.
ALLOGENEIC PERIPHERAL BLOOD STEM CELL TRANSPLANTATION (PBSCT): After completion of TBI, patients undergo allogeneic PBSCT on day 0.
IMMUNOSUPPRESSION: Patients receive cyclosporine orally (PO) or IV every 12 hours on days -3 to 180 followed by a taper until day 365 in the absence of GVHD. Beginning 4-6 hours after completion of allogeneic PBSCT, patients receive mycophenolate mofetil PO every 8 hours on days 0 to 100 followed by a taper until day 156 in the absence of GVHD.
After completion of study treatment, patients are followed up periodically for 12 months, at 18 months, and then annually for 5 years.
Undersøgelsestype
Tilmelding (Faktiske)
Fase
- Fase 2
Kontakter og lokationer
Studiesteder
-
-
Washington
-
Seattle, Washington, Forenede Stater, 98109
- Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium
-
-
-
-
-
Torino, Italien, 10126
- University of Torino
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- The patient must be not eligible for conventional transplants and must have disease expected to be stable for at least 100 days without chemotherapy
Patients with hematologic malignancies treatable with HCT will be included:
- Aggressive non-Hodgkin lymphomas (NHLs) and other histologies such as diffuse large B-cell NHL: not eligible for autologous HCT, not eligible for conventional myeloablative HCT, or after failed autologous HCT;
- Low grade NHL: with < 6 month duration of complete response (CR) between courses of conventional therapy;
- Mantle cell NHL: may be treated in first CR;
- Chronic lymphocytic leukemia (CLL): must have failed 2 lines of conventional therapy and must be refractory to fludarabine; this includes patients who fail to have a complete or partial response after therapy with a regimen containing fludarabine (or another nucleoside analog] or experience disease relapse within 12 months after completing therapy with a regimen containing fludarabine [or another nucleoside analog);
- Hodgkin's disease (HD): must have received and failed frontline therapy and have failed or were not eligible for autologous transplant;
- Multiple myeloma (MM): must have received prior chemotherapy or failed autografting; following a planned autologous transplant [tandem] is allowed;
- Acute myeloid leukemia (AML): must have < 5% marrow blasts at the time of transplant;
- Acute lymphocytic leukemia (ALL): must have < 5% marrow blasts at the time of transplant;
- Chronic myelogenous leukemia (CML): patients will be accepted beyond first clinical progression (CP1) if they have received previous myelosuppressive chemotherapy or HCT, and have < 5% marrow blasts at time of transplant;
- Myelodysplastic syndrome/myeloproliferative disease (MDS/MPD): must have failed previous myelosuppressive chemotherapy or HCT, and have < 5% marrow blasts at time of transplant;
- Waldenstrom's macroglobulinemia: must have failed 2 courses of therapy
- Patient refuses to be treated on a conventional transplant protocol; for this inclusion criteria, transplants must be approved by both the participating institution's patient review committee, such as the Patient Care Conference (PCC) at the Fred Hutchinson Cancer Research Center (FHCRC), and the FHCRC principal investigator
Patient with related or unrelated donors for whom:
- There is a likelihood of disease progression while HLA typing and results of a preliminary search and the donor pool suggest that a 10/10 HLA-A, B, C, DRB1 and DQB1 matched unrelated donor will not be found;
- Patient and donor must be matched for at least one DRB1 allele and one DQB1 allele;
- Best available matches are HLA class I HLA-A, -B, -C allele matched donors allowing for any one or two DRB1 and/or DQB1 antigen/allele mismatch;
- There is no indication for an autologous transplantation as a treatment option
- DONOR: For HLA matching inclusion criteria, see patient inclusion criteria
- DONOR: Only peripheral blood stem cells (PBSC) will be permitted as a HSC source on this protocol
Exclusion Criteria:
- Positive crossmatch between donor and recipients
- Patient's life expectancy is severely limited by diseases other than malignancy
- Patient has central nervous system (CNS) involvement with disease refractory to intrathecal chemotherapy
- Presence of circulating leukemic blasts (in the peripheral blood) detected by standard pathology for patients with AML, ALL or CML
- Patient is a fertile man or woman unwilling to use contraceptives during and for up to 12 months post treatment
- Patient is a female who is pregnant or breastfeeding
- Patient is human immunodeficiency virus (HIV) positive
- Patients with active non-hematologic malignancies (except non-melanoma skin cancers)
- Patients with a history of non-hematologic malignancies (except non-melanoma skin cancers) currently in a complete remission, who are less than 5 years from the time of complete remission, and have a > 20% risk of disease recurrence
- Patient has a fungal infection with radiological progression after receipt of amphotericin B or active triazole for greater than 1 month
Patient has the following organ dysfunction:
- Symptomatic coronary artery disease or ejection fraction < 35% or other cardiac failure requiring therapy; ejection fraction is required if age > 50 years or if the patient has a history of anthracyclines or history of cardiac disease;
- Diffusion capacity of the lung for carbon monoxide (DLCO) < 35% total lung capacity (TLC) < 35%, forced expiratory volume of the lung in one second (FEV1) < 35% and/or receiving supplementary continuous oxygen; the FHCRC study principal investigator (PI) must approve enrollment of all patients with pulmonary nodules;
- Liver function abnormalities: patient with clinical or laboratory evidence of liver disease will be evaluated for the cause of liver disease, its clinical severity in terms of liver function, bridging fibrosis, and the degree of portal hypertension; the patient will be excluded if he/she is found to have fulminant liver failure, cirrhosis of the liver with evidence of portal hypertension, alcoholic hepatitis, esophageal varices, a history of bleeding esophageal varices, hepatic encephalopathy, uncorrectable hepatic synthetic dysfunction evinced by prolongation of the prothrombin time, ascites related to portal hypertension, bacterial or fungal liver abscess, biliary obstruction, chronic viral hepatitis with total serum bilirubin > 3mg/dL, or symptomatic biliary disease
- Patient has poorly controlled hypertension and on multiple antihypertensives
- Karnofsky performance score < 70 for adult patients
- Lansky play-performance score < 70 for pediatric patients
- Patient received cytotoxic agents for "cytoreduction" within three weeks (or the interval in which a cycle of standard chemotherapy would be administered in a non-transplant setting) prior to initiating the nonmyeloablative transplant conditioning; (exceptions are hydroxyurea and imatinib mesylate)
- DONOR: Marrow donors
- DONOR: Positive crossmatch between donor and recipient
- DONOR: Donor is HIV-positive and/or has a medical condition that would result in increased risk for filgrastim (G-CSF) mobilization and harvest of PBSC
- DONOR: Donor age < 12 years
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: Treatment (chemotherapy, TBI, transplant)
NONMYELOABLATIVE CONDITIONING REGIMEN: Patients receive alemtuzumab IV over 6 hours once daily on days -6, -5, and -4 OR days -5 and -4 and fludarabine phosphate IV over 30 minutes on days -4, -3, and -2. Patients also undergo low-dose TBI on day 0. ALLOGENEIC PBSCT: After completion of TBI, patients undergo allogeneic PBSCT on day 0. IMMUNOSUPPRESSION: Patients receive cyclosporine PO or IV every 12 hours on days -3 to 180 followed by a taper until day 365 in the absence of GVHD. Beginning 4-6 hours after completion of allogeneic PBSCT, patients receive mycophenolate mofetil PO every 8 hours on days 0 to 100 followed by a taper until day 156 in the absence of GVHD. |
Korrelative undersøgelser
Givet IV
Andre navne:
Gennemgå PBSCT
Andre navne:
Givet PO
Andre navne:
Givet IV
Andre navne:
Gennemgå lavdosis TBI
Andre navne:
Givet PO eller IV
Andre navne:
Gennemgå allogen stamcelletransplantation
Undergo GVHD prophylaxis/therapy
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Incidence of Grade III-IV Acute GVHD
Tidsramme: 100 days after transplant
|
Severity of Individual Organ Involvement Liver: Stage 2 - bilirubin (3-5.9mg/100ml) Stage 3 - bilirubin (6-14.9mg/100ml) Stage 4 - bilirubin > 15mg/100ml Gut: Diarrhea is graded stage 1 to stage 4 in severity. Nausea and vomiting and/or anorexia caused by GVHD is assigned as stage 1 in severity. The severity of gut involvement is assigned to the most severe involvement noted. Patients with visible bloody diarrhea are at least stage 2 gut and grade 3 overall Severity of GVHD Grade III - Stage 2 to 4 gastrointestinal involvement and/or Stage 2 to 4 liver involvement with or without a rash Grade IV - Pattern and severity of GVHD similar to grade 3 with extreme constitutional symptoms or death |
100 days after transplant
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Incidence of Graft Rejection
Tidsramme: 84 days after transplant
|
Percentage patients that experienced graft rejection.
|
84 days after transplant
|
|
Incidence of High-dose Corticosteroid Utilization.
Tidsramme: 100 days after transplant
|
Percentage patients requiring steroids greater than 1 mg/kg.
|
100 days after transplant
|
|
Incidence of Non-relapse Mortality
Tidsramme: 100 days after transplant
|
Percentage patient deaths due to non-relapse mortality
|
100 days after transplant
|
|
Incidence of Infection
Tidsramme: Up to 5 years post-transplant
|
Percentage patients that experienced infection(s).
|
Up to 5 years post-transplant
|
|
Immune Reconstitution
Tidsramme: Up to 1 year post-transplant
|
The outcome of immune reconstitution was not analyzed by the collaborating laboratory because only a small number of patients were only enrolled in Dose Level 1 (no alemtuzumab).
The Dose Level 1 patients were going to be the baseline for which to compare the other patients on Dose Level 2 (and 3) who would have received alemtuzumab.
The collaborating investigator determined that the study was not worthwhile performing based on this information.
|
Up to 1 year post-transplant
|
|
Disease Progression/Relapse
Tidsramme: Up to 5 years
|
CML New cytogenetic abnormality and/or development of accelerated phase or blast crisis. The criteria for accelerated phase will be defined as unexplained fever greater than 38.3°C, new clonal cytogenetic abnormalities in addition to a single Ph-positive chromosome, marrow blasts and promyelocytes >20%. AML, ALL >5% marrow blasts by morphologic or flow cytometric, or appearance of extramedullary disease. CLL ≥1 of: Physical exam/Imaging studies (nodes, liver, and/or spleen) ≥50% increase or new, circulating lymphocytes by morphology and/or flow cytometry ≥50% increase, and lymph node biopsy w/ Richter's transformation. NHL >25% increase in the sum of the products of the perpendicular diameters of marker lesions, or the appearance of new lesions. MM ≥100% increase of the serum myeloma protein from its lowest level, or reappearance of myeloma peaks that had disappeared w/ treatment; or definite increase in the size or number of plasmacytomas or lytic bone lesions. |
Up to 5 years
|
Samarbejdspartnere og efterforskere
Sponsor
Samarbejdspartnere
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 (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Patologiske processer
- Hjerte-kar-sygdomme
- Karsygdomme
- Virussygdomme
- Infektioner
- Sygdomme i immunsystemet
- Neoplasmer, bindevæv og blødt væv
- Neoplasmer efter histologisk type
- Neoplasmer
- Lymfoproliferative lidelser
- Lymfesygdomme
- Immunproliferative lidelser
- Neoplasmer efter sted
- Sygdomsegenskaber
- Sygdom
- Knoglemarvssygdomme
- Hæmatologiske sygdomme
- Hæmoragiske lidelser
- Hæmostatiske lidelser
- Paraproteinæmier
- Blodproteinforstyrrelser
- DNA-virusinfektioner
- Bakterielle infektioner og mykoser
- Tumorvirusinfektioner
- Neoplasmer, Plasmacelle
- Forstadier til kræft
- Epstein-Barr-virusinfektioner
- Herpesviridae infektioner
- Leukæmi, B-celle
- Neoplasmer, bindevæv
- Øjeneoplasmer
- Lymfadenopati
- Mastocytose, systemisk
- Mastocytose
- Lymfom
- Lymfom, follikulært
- Lymfom, B-celle
- Lymfom, stor B-celle, diffus
- Syndrom
- Myelodysplastiske syndromer
- Myelomatose
- Leukæmi
- Leukæmi, myeloid
- Leukæmi, Myeloid, Akut
- Hodgkins sygdom
- Tilbagevenden
- Lymfom, Non-Hodgkin
- Præleukæmi
- Leukæmi, myelomonocytisk, akut
- Leukæmi, myelomonocytisk, kronisk
- Leukæmi, myelomonocytisk, juvenil
- Mykoser
- Burkitt lymfom
- Lymfom, kappecelle
- Lymfom, B-celle, marginalzone
- Precursorcelle lymfoblastisk leukæmi-lymfom
- Lymfom, storcellet, immunoblastisk
- Plasmablastisk lymfom
- Waldenstrom Makroglobulinæmi
- Leukæmi, lymfatisk, kronisk, B-celle
- Leukæmi, lymfoid
- Lymfom, T-celle
- Lymfom, T-celle, perifert
- Leukæmi, myelogen, kronisk, BCR-ABL positiv
- Leukæmi, myeloid, kronisk fase
- Lymfom, T-celle, kutan
- Leukæmi, T-celle
- Leukæmi-lymfom, voksen T-celle
- Mycosis Fungoides
- Sezary syndrom
- Lymfom, storcellet, anaplastisk
- Lymfomatoid granulomatose
- Lymfom, ekstranodal NK-T-celle
- Intraokulært lymfom
- Immunoblastisk lymfadenopati
- Myeloproliferative lidelser
- Myelodysplastisk-myeloproliferative sygdomme
- Leukæmi, hårcelle
- Leukæmi, Myeloid, Kronisk, Atypisk, BCR-ABL Negativ
- Leukæmi, mastcelle
- Lægemidlers fysiologiske virkninger
- Molekylære mekanismer for farmakologisk virkning
- Anti-infektionsmidler
- Enzymhæmmere
- Antirheumatiske midler
- Antimetabolitter, Antineoplastisk
- Antimetabolitter
- Antineoplastiske midler
- Immunsuppressive midler
- Immunologiske faktorer
- Dermatologiske midler
- Antibakterielle midler
- Antibiotika, antineoplastisk
- Antifungale midler
- Antituberkulære midler
- Antibiotika, Antituberkulær
- Calcineurin-hæmmere
- Antistoffer
- Immunoglobuliner
- Antistoffer, monoklonale
- Antineoplastiske midler, immunologiske
- Fludarabin
- Fludarabin phosphat
- Mycophenolsyre
- Cyclosporin
- Cyclosporiner
- Alemtuzumab
Andre undersøgelses-id-numre
- 1959.00 (Anden identifikator: Fred Hutchinson Cancer Research Center/University of Washington Cancer Consortium)
- P30CA015704 (U.S. NIH-bevilling/kontrakt)
- NCI-2009-01496 (Registry Identifier: CTRP (Clinical Trial Reporting Program))
- P01CA018029 (U.S. NIH-bevilling/kontrakt)
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