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- Klinische proef NCT01757639
Ipilimumab in Treating Patients With Relapsed or Refractory High-Risk Myelodysplastic Syndrome or Acute Myeloid Leukemia
A Phase 1 Study of Ipilimumab in Relapsed and Refractory High Risk Myelodysplastic Syndrome and Acute Myeloid Leukemia With Minimal Residual Disease
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
PRIMARY OBJECTIVES:
I. Evaluate the safety and toxicity associated with the administration of ipilimumab in terms of dose limiting toxicities (DLT), and maximally-tolerated dose (MTD) in a cohort of patients with high risk myelodysplastic syndrome who failed hypomethylating therapy, and patients with acute myeloid leukemia (AML) who underwent induction therapy but are not planned for further intensive chemotherapy. (Dose-escalation) II. Determine the optimal dose of ipilimumab for the dose-expansion phase of the trial. (Dose-escalation) III. Better define immunologic profiles associated with ipilimumab use in terms of regulatory T-cells (T-regs) dynamic changes in 2 separate cohorts of myelodysplastic syndrome (MDS) and AML patients at the optimal dose level. (Dose-expansion) IV. Obtain preliminary efficacy data of ipilimumab in terms of complete response (CR), partial response (PR), and hematological improvement (HI) in both cohorts. (Dose-expansion)
SECONDARY OBJECTIVES:
I. Define immunologic profiles associated with ipilimumab use in terms of T-regs dynamic changes at different dose levels. (Dose-escalation) II. Define toxicity profiles of ipilimumab at the optimal dose in both patient cohorts. (Dose-expansion) III. Obtain preliminary data on potential correlations between noted ipilimumab-induced immunologic changes and observed toxicity and clinical responses. (Dose-expansion)
OUTLINE: This is a dose-escalation study.
INDUCTION: Patients receive ipilimumab intravenously (IV) on day 1. Treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity.
MAINTENANCE: Beginning 12 weeks after last dose of induction ipilimumab, patients receive ipilimumab IV on day 1. Treatment repeats every 12 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity.
After completion of study treatment, patients are followed up at least monthly for 6 months.
Studietype
Inschrijving (Werkelijk)
Fase
- Fase 1
Contacten en locaties
Studie Locaties
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Connecticut
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New Haven, Connecticut, Verenigde Staten, 06520
- Yale University
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North Haven, Connecticut, Verenigde Staten, 06473
- Yale-New Haven Hospital North Haven Medical Center
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Maryland
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Baltimore, Maryland, Verenigde Staten, 21287
- Johns Hopkins University/Sidney Kimmel Cancer Center
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Missouri
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Saint Louis, Missouri, Verenigde Staten, 63110
- Washington University School of Medicine
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New York
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New York, New York, Verenigde Staten, 10032
- Columbia University/Herbert Irving Cancer Center
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North Carolina
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Chapel Hill, North Carolina, Verenigde Staten, 27599
- UNC Lineberger Comprehensive Cancer Center
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Durham, North Carolina, Verenigde Staten, 27710
- Duke University Medical Center
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Texas
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Dallas, Texas, Verenigde Staten, 75246
- Baylor University Medical Center
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Irving, Texas, Verenigde Staten, 75061
- Texas Oncology at Baylor Irving Cancer Center
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- Patients must be able to understand and voluntarily sign an informed consent form
- Able to adhere to the study visit schedule and other protocol requirements
- Life expectancy of greater than 6 months
Must have one of the following diagnoses:
Pathologically confirmed chronic myelomonocytic leukemia (CMML) or myelodysplastic syndromes (MDS) with high risk features at the time of referral for trial as defined by:
- Intermediate (INT)-2 or high International Prognostic Scoring System (IPSS) score
- Secondary MDS (defined as MDS developing in a patient with an antecedent hematologic disorder or any patient with prior chemotherapy or radiation exposure)
- INT-1 MDS with excess blasts (>= 5% blasts in bone marrow [BM]) or red blood cell (RBC) transfusion-dependency
- MDS progressing to oligoblastic acute myeloid leukemia (AML) with 21-30% BM blasts
- CMML with >= 5% marrow blasts, or RBC or platelet transfusion-dependency, abnormal karyotype, or proliferative features (white blood cell count >=13,000/uL, splenomegaly on physical examination, or extramedullary disease)
- All patients are required to have failed to respond or relapsed after an initial response to hypomethylating agents 5-azacitidine or decitabine or have refused to receive hypomethylating therapy; failure to respond is defined as failing to achieve a CR, PR or HI after at least 4 cycles of hypomethylating therapy; these patients could have received other therapies or not, but must have received hypomethylating therapy or have refused to receive hypomethylating therapy
- Pathologically confirmed AML patients who have received one or two courses of induction chemotherapy or hypomethylating agent therapy AND no plans for further chemotherapy therapy, but remain with residual disease of < 5% blasts in BM, by morphology, cytogenetics, fluorescent in situ hybridization (FISH), polymerase chain reaction (PCR) or flow cytometry
- Patients must not have received any other treatment for their disease, including hematopoietic growth factors, within three weeks of beginning the trial, and should have recovered from all toxicities of prior therapy (to grade 0 or 1)
- Eastern Cooperative Oncology Group (ECOG) performance status of =< 2 at study entry ECOG, or Karnofsky >= 60%
- Calculated creatinine clearance by Modification of Diet in Renal Disease (MDRD) (CrCL) > 50 ml/min/1.73 squared meter
- Total bilirubin =< 2.0 mg/dL unless due to Gilbert's syndrome, hemolysis, or ineffective hematopoiesis
- Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT]) and alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 3 x upper limit of normal (ULN)
- Females of childbearing potential must have a negative serum or urine pregnancy test within 72 hours prior to start of ipilimumab
- Patients must have no clinical evidence of central nervous system (CNS) or pulmonary leukostasis, disseminated intravascular coagulation, or CNS leukemia
- Patients must have no serious or uncontrolled medical conditions
Exclusion Criteria:
- Any serious medical condition, uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, laboratory abnormality, or psychiatric illness/social situations that would limit compliance with study requirements or prevent the subject from signing the informed consent form
- Pregnant or breast feeding females (lactating females must agree not to breast feed while taking ipilimumab)
- Any condition, including the presence of laboratory abnormalities, which places the subject at unacceptable risk if he/she were to participate in the study or confounds the ability to interpret data from the study
- Use of any other experimental drug or therapy within 21 days of baseline
- Known hypersensitivity to ipilimumab or history of allergic reactions attributed to compounds of similar chemical or biologic composition to ipilimumab
- Prior use of ipilimumab, other cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) blocking therapies, anti-programmed cell death 1 (PD 1) antibody, cluster of differentiation (CD) 137 agonist or other immune activating therapy such as anti-CD 40 antibody within the last 3 months of enrollment in the study; if any of these of these agents were used more than 3 months earlier to enrollment in study, the patient should have recovered from all toxicity and at least 3 months had passed since last use to allow for clearance and observation of any other side effects from the previous therapy
- Concurrent use of other anti-cancer agents or treatments, including other investigational agents
- Autoimmune disease: patients with a history of inflammatory bowel disease, including ulcerative colitis and Crohn's disease, are excluded from this study, as are patients with a history of symptomatic disease (e.g., rheumatoid arthritis, systemic progressive sclerosis [scleroderma], systemic lupus erythematosus, autoimmune vasculitis [e.g., Wegener's granulomatosis]); CNS or motor neuropathy considered of autoimmune origin (e.g. Guillain-Barre syndrome and Myasthenia Gravis, multiple sclerosis)
- Patients with known immune impairment who may be unable to respond to anti-CTLA-4 antibody
- Patients with known evidence of active cancers, or other cancer under active treatment; exceptions include patients with no evidence of disease receiving adjuvant hormone-based therapy or either breast or prostate cancer
- Patients who have had chemotherapy or radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from adverse events due to agents administered more than 4 weeks earlier
- Patients with chronic human immunodeficiency virus (HIV), hepatitis B or hepatitis C infections should be excluded because of potential effects on immune function and/ or possible drug interactions
- Pregnant women are excluded from this study; breastfeeding should be discontinued if the mother is treated with ipilimumab
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: NVT
- Interventioneel model: Opdracht voor een enkele groep
- Masker: Geen (open label)
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
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Experimenteel: Treatment (ipilimumab)
INDUCTION: Patients receive ipilimumab IV on day 1. Treatment repeats every 21 days for up to 4 courses in the absence of disease progression or unacceptable toxicity. MAINTENANCE: Beginning 12 weeks after last dose of induction ipilimumab, patients receive ipilimumab IV on day 1. Treatment repeats every 12 weeks for up to 4 courses in the absence of disease progression or unacceptable toxicity. |
Correlatieve studies
IV gegeven
Andere namen:
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Incidence of DLT of ipilimumab by grading and tabulation using National Cancer Institute Common Terminology Criteria for Adverse Events version 4.0
Tijdsspanne: 42 days
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42 days
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Changes in percentages of T-regs
Tijdsspanne: Baseline to up to 6 months post-treatment
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Changes in T-regs percentages at designated time points will be correlated with clinical responses and toxicity after ipilimumab.
The response will be modeled as the vector for each individual from multiple measures of T-regs percentages as a function of time and group (MDS vs AML).
T-regs percentages will be transformed onto the log-scale, and t tests will be used to compare groups at specific time points.
Regression models that use generalized estimating equations will be implemented when all time points are considered to account for within-subject correlation of repeated measures.
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Baseline to up to 6 months post-treatment
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Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Efficacy as defined by the International working group 2006 criteria for CR, PR, HI
Tijdsspanne: Up to 6 months post-treatment
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The agreement between immunologic and clinical response will be evaluated with McNemar's test, separately by cohort.
Rates of CR, PR, and HI will be summarized separately by cohort and reported with an exact 95% confidence interval.
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Up to 6 months post-treatment
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Progression free survival (PFS)
Tijdsspanne: From start of study to progression or death, assessed up to 6 months post-treatment
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Median PFS will also be reported with a 95% confidence interval.
As an exploratory analysis, survival endpoints will be descriptively compared with a log-rank test between patients who do and do not have an immunologic response, separately by cohort.
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From start of study to progression or death, assessed up to 6 months post-treatment
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Overall survival (OS)
Tijdsspanne: From start of study to death, assessed up to 6 months post-treatment
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Median OS will also be reported with a 95% confidence interval.
As an exploratory analysis, survival endpoints will be descriptively compared with a log-rank test between patients who do and do not have an immunologic response, separately by cohort.
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From start of study to death, assessed up to 6 months post-treatment
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Rate of prior use of demethylating agents
Tijdsspanne: Up to 6 months post-treatment
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Will be descriptively compared between patients who have a clinical response and by toxicity with Fisher's exact tests.
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Up to 6 months post-treatment
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Rate of pre-treatment CR
Tijdsspanne: Up to 6 months post-treatment
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Will be descriptively compared between patients who have a clinical response and by toxicity with Fisher's exact tests.
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Up to 6 months post-treatment
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Lymphocyte counts
Tijdsspanne: Baseline
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Will be summarized and compared between response and toxicity groups with either t tests or Wilcoxon rank sum tests.
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Baseline
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T cell receptor diversity
Tijdsspanne: Baseline
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Will be summarized and compared between response and toxicity groups with either t tests or Wilcoxon rank sum tests.
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Baseline
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Medewerkers en onderzoekers
Sponsor
Onderzoekers
- Hoofdonderzoeker: B. Smith, Johns Hopkins University/Sidney Kimmel Cancer Center
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Primaire voltooiing (Werkelijk)
Studie voltooiing
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Schatting)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
- Pathologische processen
- Neoplasmata per histologisch type
- Neoplasmata
- Ziekte
- Beenmergziekten
- Hematologische ziekten
- Voorstadia van kanker
- Myelodysplastische-myeloproliferatieve ziekten
- Syndroom
- Myelodysplastische syndromen
- Leukemie
- Leukemie, myeloïde
- Leukemie, myeloïde, acuut
- Preleukemie
- Leukemie, myelomonocytische, chronische
- Leukemie, myelomonocytische, juveniele
- Moleculaire mechanismen van farmacologische werking
- Antineoplastische middelen
- Antineoplastische middelen, immunologisch
- Immuun Checkpoint-remmers
- Ipilimumab
Andere studie-ID-nummers
- NCI-2012-02990 (Register-ID: CTRP (Clinical Trial Reporting Program))
- P30CA006973 (Subsidie/contract van de Amerikaanse NIH)
- U01CA070095 (Subsidie/contract van de Amerikaanse NIH)
- UM1CA186691 (Subsidie/contract van de Amerikaanse NIH)
- UM1CA186704 (Subsidie/contract van de Amerikaanse NIH)
- NA_00076038
- J1276
- CDR0000744584
- 9214 (Andere identificatie: CTEP)
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
product vervaardigd in en geëxporteerd uit de V.S.
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