Ipilimumab or Nivolumab in Treating Patients With Relapsed Hematologic Malignancies After Donor Stem Cell Transplant

Sponsor

National Cancer Institute (NCI) (NIH)

Overall Status

Completed

CT.gov ID

NCT01822509

Collaborator

(none)

Enrollment

Locations

Arm

96.8

Actual Duration (Months)

5.5

Patients Per Site

0.1

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

This phase I/Ib trial studies the side effects and best dose of ipilimumab or nivolumab in treating patients with cancers of the blood and blood-forming tissues (hematologic cancers) that have returned after a period of improvement (relapsed) after donor stem cell transplant. Immunotherapy with monoclonal antibodies, such as ipilimumab and nivolumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread.

Condition or Disease	Intervention/Treatment	Phase
Allogeneic Hematopoietic Stem Cell Transplant Recipient Myeloproliferative Neoplasm Recurrent Acute Lymphoblastic Leukemia Recurrent Acute Myeloid Leukemia Recurrent Chronic Lymphocytic Leukemia Recurrent Chronic Myelogenous Leukemia, BCR-ABL1 Positive Recurrent Hematologic Malignancy Recurrent Hodgkin Lymphoma Recurrent Myelodysplastic Syndrome Recurrent Non-Hodgkin Lymphoma Recurrent Plasma Cell Myeloma	Biological: Ipilimumab Other: Laboratory Biomarker Analysis Biological: Nivolumab	Phase 1

Detailed Description

PRIMARY OBJECTIVES:

To determine the maximum-tolerated dose (MTD) of ipilimumab or nivolumab administered to patients with relapsed hematologic malignancies following allogeneic stem cell transplantation. (Phase I) II. To characterize the toxicity of ipilimumab or nivolumab administered at the MTD in this patient population. (Phase Ib)

SECONDARY OBJECTIVES:

To assess response rate. II. To assess progression free and overall survival.

EXPLORATORY OBJECTIVE:

To assess the phenotypic and functional effects of ipilimumab or nivolumab on immune cells.

OUTLINE: This is a dose-escalation study.

INDUCTION PHASE: Patients receive ipilimumab intravenously (IV) over 90 minutes on day 1. Treatment repeats every 21 days for 4 cycles in the absence of disease progression or unacceptable toxicity. Patients also receive nivolumab IV over 30 minutes on day 1. Treatment repeats every 14 days for 8 cycles in the absence of disease progression or unacceptable toxicity.

MAINTENANCE PHASE: Patients receive ipilimumab IV over 90 minutes. Treatment repeats every 12 weeks beginning at cycle 5 (24 weeks after the first dose of ipilimumab) for up to 4 cycles in the absence of disease progression or unacceptable toxicity. Patients achieving clinical benefit will have the option to continue with ongoing maintenance dosing every 12 weeks in the absence of disease progression or unacceptable toxicity. Patients also receive nivolumab IV over 30 minutes every 2 weeks in the absence of disease progression or unacceptable toxicity. Treatment repeats every 14 days for up to a total of 60 weeks (including Induction) in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up for 1 year.

Study Design

Study Type:

Interventional

Actual Enrollment :

71 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

A Phase I/IB Study of Ipilimumab or Nivolumab in Patients With Relapsed Hematologic Malignancies After Allogeneic Hematopoietic Cell Transplantation

Actual Study Start Date :

May 16, 2013

Actual Primary Completion Date :

Dec 31, 2018

Actual Study Completion Date :

Jun 10, 2021

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Treatment (ipilimumab, nivolumab) See Detailed Description.	Biological: Ipilimumab Given IV Other Names: Anti-Cytotoxic T-Lymphocyte-Associated Antigen-4 Monoclonal Antibody BMS-734016 Ipilimumab Biosimilar CS1002 MDX-010 MDX-CTLA4 Yervoy Other: Laboratory Biomarker Analysis Correlative studies Biological: Nivolumab Given IV Other Names: BMS-936558 CMAB819 MDX-1106 NIVO Nivolumab Biosimilar CMAB819 ONO-4538 Opdivo

Arm

Intervention/Treatment

Experimental: Treatment (ipilimumab, nivolumab)

See Detailed Description.

Biological: Ipilimumab

Given IV

Other Names:

Anti-Cytotoxic T-Lymphocyte-Associated Antigen-4 Monoclonal Antibody

BMS-734016

Ipilimumab Biosimilar CS1002

MDX-010

MDX-CTLA4

Yervoy

Other: Laboratory Biomarker Analysis

Correlative studies

Biological: Nivolumab

Given IV

Other Names:

BMS-936558

CMAB819

MDX-1106

NIVO

Nivolumab Biosimilar CMAB819

ONO-4538

Opdivo

Outcome Measures

Primary Outcome Measures

Maximum tolerated dose (MTD) of ipilimumab according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 (Phase I) [At 12 weeks]
Dose-limiting toxic (DLT) effects were defined as grade III or IV acute graft versus host disease (GVHD), grade 4 hematologic toxic effects unrelated to the underlying disease, or grade 3 nonhematologic toxic effects that did not improve to grade 1 with a 3-week dose delay. Immune-related adverse events that resolved to grade 1 or lower with the use of glucocorticoids were not considered to be dose-limiting toxic effects. We designated the observation period for toxic effects to be 12 weeks to capture delayed immunologic toxic effects.
Maximum tolerated dose (MTD) of nivolumab according to the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 (Phase I) [At 12 weeks]
Dose-limiting toxic (DLT) effects are defined as grade III or IV acute GVHD, grade 4 hematologic toxic effects unrelated to the underlying disease, or grade 3 nonhematologic toxic effects that did not improve to grade 1 with a 3-week dose delay. Immune-related adverse events that resolved to grade 1 or lower with the use of glucocorticoids were not considered to be dose-limiting toxic effects. We designated the observation period for toxic effects to be 12 weeks to capture delayed immunologic toxic effects.
Incidence of adverse events as assessed by National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) version 5.0 (Phase Ib) [Up to 1 year after completion of study treatment]
A serious adverse event (SAE) is any adverse event, occurring at any dose and regardless of causality that 1) Results in death, 2) Is life-threatening, 3) Requires or prolongs inpatient hospitalization, 4) Results in persistent or significant disability/incapacity, 5) Is an important medical event when, based upon appropriate medical judgment, it may jeopardize the participant and require medical or surgical intervention to prevent one of the outcomes listed above.

Secondary Outcome Measures

Clinical response [Up to 1 year]
Summarized by simple descriptive summary statistics delineating complete, partial, and best overall response, stable and progressive disease.
Progression-free survival (PFS) [From start of treatment to time of objective disease progression, assessed up to 1 year]
Using the Kaplan-Meier method. Will be analyzed and reported both for the entire cohort and within each disease group if feasible.
Overall survival (OS) [From the start of treatment to time of death, assessed up to 1 year]
Using the Kaplan-Meier method. Will be analyzed and reported both for the entire cohort and within each disease group if feasible.

Other Outcome Measures

Change in immune cell numbers [Baseline to up to 1 year]
Laboratory studies will be performed to characterize the effects of ipilimumab and nivolumab in the post allogeneic stem cell transplantation (alloSCT) setting on B cells, NK, cells, or dendritic cells, both in terms of pre and post alloSCT changes in cell numbers.
Change in cytokine production [Baseline to up to 1 year]
Laboratory studies will be performed to characterize the effects of ipilimumab and nivolumab in the post alloSCT setting on B cells, NK, cells, or dendritic cells, both in terms of pre and post alloSCT changes in cell numbers.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically or cytologically confirmed hematologic malignancy
The following malignancies will be considered eligible if progressive or persistent:
Chronic lymphocytic leukemia (CLL)
Non-Hodgkin lymphoma (NHL)
Hodgkin lymphoma (HL)
Multiple myeloma (MM)
Acute leukemia (acute myeloid leukemia [AML], acute lymphoblastic leukemia [ALL])
Myelodysplastic syndrome (MDS)
Myeloproliferative neoplasms (MPN)
Chronic myeloid leukemia (CML)
Life expectancy of greater than 3 months
Must have undergone allogeneic hematopoietic stem cell transplantation (HSCT) (regardless of stem cell source)
Must have baseline donor T cell chimerism of >= 20%
Eastern Cooperative Oncology Group (ECOG) performance status =< 2
Total bilirubin =< 1.5 x institutional upper limit of normal (ULN) (unless due to Gilbert's disease or disease-related hemolysis, then =< 3.0 x ULN)
Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase [SGPT]) =< 3.0 x institutional ULN
Creatinine =< 1.5 x institutional ULN
Prednisone dose =< 5 mg/day and off all other systemic immunosuppressive medications for at least 4 weeks prior to study entry
Ability to understand and the willingness to sign a written informed consent document

Exclusion Criteria:

Participants who have had anti-tumor therapy or other investigational agents within 4 weeks prior to registration (6 weeks for nitrosoureas or mitomycin C), or those who have not recovered from adverse events due to agents administered more than 4 weeks prior to registration
Patients with prior history of or active severe (grade 3 or 4) acute graft-versus-host disease (GVHD)
Patients with a history of prior treatment with ipilimumab, anti-programmed cell death protein 1 (PD 1) antibody, or cluster of differentiation (CD)137 agonist therapy are ineligible for the ipilimumab arm, but are eligible for the nivolumab arm
Patients who have had donor lymphocyte infusion (DLI) within 8 weeks prior to registration
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]) and motor neuropathy considered of autoimmune origin (e.g. Guillain-Barre syndrome and myasthenia gravis); patients with Hashimoto's thyroiditis are eligible to go on study
Patients with known chronic human immunodeficiency virus (HIV), hepatitis B or hepatitis C infections should be excluded
Uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
Pregnant women are excluded from this study because ipilimumab and nivolumab are immunomodulatory agents with the potential for teratogenic or abortifacient effects; the effects of ipilimumab and nivolumab on the developing human fetus are unknown; for this reason and because immunomodulatory agents are known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study or within 23 weeks after the last dose of study drug, she should inform her treating physician immediately; men treated or enrolled on this protocol must also agree to use adequate contraception prior to the study, for the duration of study participation, and for at least 31 weeks after completion of ipilimumab or nivolumab administration

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	City of Hope Comprehensive Cancer Center	Duarte	California	United States	91010
2	UC San Diego Moores Cancer Center	La Jolla	California	United States	92093
3	City of Hope South Pasadena	South Pasadena	California	United States	91030
4	Colorado Blood Cancer Institute	Denver	Colorado	United States	80218
5	Moffitt Cancer Center-International Plaza	Tampa	Florida	United States	33607
6	Moffitt Cancer Center	Tampa	Florida	United States	33612
7	Northside Hospital	Atlanta	Georgia	United States	30342
8	Eastern Maine Medical Center	Bangor	Maine	United States	04401
9	Lafayette Family Cancer Center-EMMC	Brewer	Maine	United States	04412
10	Massachusetts General Hospital Cancer Center	Boston	Massachusetts	United States	02114
11	Beth Israel Deaconess Medical Center	Boston	Massachusetts	United States	02215
12	Dana-Farber Cancer Institute	Boston	Massachusetts	United States	02215
13	Massachusetts General Hospital	Charlestown	Massachusetts	United States	02129