Veliparib, Bendamustine Hydrochloride, and Rituximab in Treating Patients With Advanced Lymphoma, Multiple Myeloma, or Solid Tumors

This study is currently recruiting participants.
Verified February 2014 by National Cancer Institute (NCI)
Sponsor:
Information provided by (Responsible Party):
National Cancer Institute (NCI)
ClinicalTrials.gov Identifier:
NCT01326702
First received: March 30, 2011
Last updated: April 21, 2014
Last verified: February 2014

March 30, 2011
April 21, 2014
July 2011
November 2015   (final data collection date for primary outcome measure)
  • MTD of veliparib and bendamustine hydrochloride combination based on the incidence of dose-limiting toxicity (DLT) graded using the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCATE) version 4.0 (Phase I) [ Time Frame: 28 days ] [ Designated as safety issue: Yes ]
  • Adverse event profile as assessed by NCI CTCAE v. 4.0 (Phase I) [ Time Frame: Up to 30 days post-treatment ] [ Designated as safety issue: Yes ]
  • Response rate (best response at any point on therapy) in patients with non-Hodgkin lymphoma treated with veliparib, bendamustine hydrochloride and rituximab using Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 (Phase II) [ Time Frame: Up to 30 days post-treatment ] [ Designated as safety issue: No ]
  • Adverse event profile as assessed by NCI CTCAE v. 4.0 (phase I) [ Designated as safety issue: Yes ]
  • Safety of veliparib in combination with bendamustine hydrochloride and rituximab [ Designated as safety issue: Yes ]
  • MTD of veliparib in combination with bendamustine (phase I) [ Designated as safety issue: No ]
  • Complete response rate (phase II) [ Designated as safety issue: No ]
Complete list of historical versions of study NCT01326702 on ClinicalTrials.gov Archive Site
  • Pharmacokinetic parameters of veliparib (Phase I) [ Time Frame: Baseline; at 30 minutes; and at 1, 1.5, 2, 3, 4, 6, 8, and 24 hours on day 2 of course1 ] [ Designated as safety issue: No ]
  • Complete response (CR) to study treatment (Phase II) [ Time Frame: Up to 30 days post-treatment ] [ Designated as safety issue: No ]
    Summary statistics will be used for CR.
  • Progression-free survival using RECIST version 1.1 (Phase II) [ Time Frame: From start of treatment to time of progression or death, whichever occurs first, assessed up to 30 days post-treatment ] [ Designated as safety issue: No ]
    Kaplan-Meier estimates will be calculated and log-rank tests will be employed when certain comparisons are needed.
  • Duration of remission (Phase II) [ Time Frame: From the first documented response to the first documented progression or death, assessed up to 30 days post-treatment ] [ Designated as safety issue: No ]
  • Overall survival (Phase II) [ Time Frame: Up to 30 days post-treatment ] [ Designated as safety issue: No ]
    Kaplan-Meier estimates will be calculated and log-rank tests will be employed when certain comparisons are needed.
  • Pharmacokinetic parameters of veliparib [ Designated as safety issue: No ]
  • Pharmacodynamic parameters of veliparib [ Designated as safety issue: No ]
  • Response rates and survival (phase II) [ Designated as safety issue: No ]
  • Progression-free survival (phase II) [ Designated as safety issue: No ]
  • Duration of remission (phase II) [ Designated as safety issue: No ]
Not Provided
Not Provided
 
Veliparib, Bendamustine Hydrochloride, and Rituximab in Treating Patients With Advanced Lymphoma, Multiple Myeloma, or Solid Tumors
A Phase 1b/2a Study of ABT-888 in Combination With Bendamustine +/- Rituximab in Lymphoma, Multiple Myeloma and Solid Tumors

This phase I/II trial studies the side effects and the best dose of veliparib when given together with bendamustine hydrochloride and rituximab and to see how well it works in treating patients with advanced lymphoma, multiple myeloma, or solid tumors. Veliparib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Drugs used in chemotherapy, such as bendamustine hydrochloride, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as rituximab, can block cancer growth in different ways. Some find cancer cells and help kill them or carry cancer-killing substances to them. Others interfere with the ability of cancer cells to grow and spread. Giving veliparib together with bendamustine hydrochloride and rituximab may kill more cancer cells.

PRIMARY OBJECTIVES:

I. To determine the maximum-tolerated dose (MTD) of veliparib (ABT-888) in combination with bendamustine hydrochloride in patients with solid tumors, lymphoma, or multiple myeloma. (Phase I) II. To establish the safety of ABT-888 in combination with bendamustine hydrochloride and rituximab in an expansion cohort of patients with non-Hodgkin lymphoma (NHL). (Phase I) III. To assess the toxicity profile of this regimen in the above patients. (Phase I) IV. To determine the complete response (CR) rate in patients with indolent NHL or mantle cell lymphoma (MCL) treated with ABT-888, bendamustine, and rituximab. (Phase II)

SECONDARY OBJECTIVES:

I. To assess response rates and survival parameters of patients treated with ABT-888, bendamustine hydrochloride, and with or without rituximab. (Phase I) II. To assess pharmacokinetic parameters of ABT-888 in this regimen. (Phase I) III. To assess progression-free survival, overall survival, and duration of remission of patients with indolent NHL and MCL treated with ABT-888, bendamustine, and rituximab. (Phase II)

OUTLINE: This is a dose-escalation, phase I study of veliparib followed by an expansion cohort and phase II study.

Patients receive veliparib orally (PO) twice daily (BID) on days 1-7 and bendamustine hydrochloride intravenously (IV) over 30-60 minutes on days 1-2. Treatment repeats every 28 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Once the maximum-tolerated dose is determined, a cohort of patients receives veliparib and bendamustine hydrochloride as above and rituximab IV on day 1. Treatment repeats every 28 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

After completion of study therapy, patients are followed up for 30 days.

Interventional
Phase 1
Phase 2
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Adult Nasal Type Extranodal NK/T-cell Lymphoma
  • Anaplastic Large Cell Lymphoma
  • Angioimmunoblastic T-cell Lymphoma
  • B-cell Adult Acute Lymphoblastic Leukemia
  • B-cell Chronic Lymphocytic Leukemia
  • Cutaneous B-cell Non-Hodgkin Lymphoma
  • Extranodal Marginal Zone B-cell Lymphoma of Mucosa-associated Lymphoid Tissue
  • Hepatosplenic T-cell Lymphoma
  • Intraocular Lymphoma
  • Nodal Marginal Zone B-cell Lymphoma
  • Noncutaneous Extranodal Lymphoma
  • Peripheral T-cell Lymphoma
  • Recurrent Adult Acute Lymphoblastic Leukemia
  • Recurrent Adult Burkitt Lymphoma
  • Recurrent Adult Diffuse Large Cell Lymphoma
  • Recurrent Adult Diffuse Mixed Cell Lymphoma
  • Recurrent Adult Diffuse Small Cleaved Cell Lymphoma
  • Recurrent Adult Grade III Lymphomatoid Granulomatosis
  • Recurrent Adult Hodgkin Lymphoma
  • Recurrent Adult Immunoblastic Large Cell Lymphoma
  • Recurrent Adult Lymphoblastic Lymphoma
  • Recurrent Adult T-cell Leukemia/Lymphoma
  • Recurrent Cutaneous T-cell Non-Hodgkin Lymphoma
  • Recurrent Grade 1 Follicular Lymphoma
  • Recurrent Grade 2 Follicular Lymphoma
  • Recurrent Grade 3 Follicular Lymphoma
  • Recurrent Mantle Cell Lymphoma
  • Recurrent Marginal Zone Lymphoma
  • Recurrent Mycosis Fungoides/Sezary Syndrome
  • Recurrent Small Lymphocytic Lymphoma
  • Refractory Chronic Lymphocytic Leukemia
  • Refractory Hairy Cell Leukemia
  • Refractory Multiple Myeloma
  • Small Intestine Lymphoma
  • Splenic Marginal Zone Lymphoma
  • T-cell Adult Acute Lymphoblastic Leukemia
  • T-cell Large Granular Lymphocyte Leukemia
  • Testicular Lymphoma
  • Unspecified Adult Solid Tumor, Protocol Specific
  • Waldenström Macroglobulinemia
  • Drug: bendamustine hydrochloride
    Given IV
    Other Names:
    • bendamustin hydrochloride
    • bendamustine
    • cytostasan hydrochloride
    • Treanda
  • Drug: veliparib
    Given PO
    Other Name: ABT-888
  • Biological: rituximab
    Given IV
    Other Names:
    • IDEC-C2B8
    • IDEC-C2B8 monoclonal antibody
    • Mabthera
    • MOAB IDEC-C2B8
    • Rituxan
  • Other: pharmacological study
    Correlative studies
    Other Name: pharmacological studies
Experimental: Treatment (bendamustine hydrochloride, veliparib, rituximab)

Patients receive veliparib PO BID on days 1-7 and bendamustine hydrochloride IV over 30-60 minutes on days 1-2. Treatment repeats every 28 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Once the maximum-tolerated dose is determined, a cohort of patients receives veliparib and bendamustine hydrochloride as above and rituximab IV on day 1. Treatment repeats every 28 days for up to 6 courses in the absence of disease progression or unacceptable toxicity.

Interventions:
  • Drug: bendamustine hydrochloride
  • Drug: veliparib
  • Biological: rituximab
  • Other: pharmacological study
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
81
Not Provided
November 2015   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patients must have a histologically confirmed solid malignancy, lymphoma, or multiple myeloma for which standard curative or palliative measures do not exist, are no longer effective, or for which the patient is not eligible or refuses (Phase I)

    • Patients must have a histologically confirmed cluster of differentiation (CD)-20 positive B-cell non-Hodgkin lymphoma for which standard curative or palliative measures do not exist, are no longer effective, or for which the patient is not eligible or refuses (Phase Ib cohort expansion)
  • Patients must have histologically or cytologically confirmed marginal zone B-cell lymphoma, small lymphocytic lymphoma, lymphoplasmacytic lymphoma, or mantle cell lymphoma, and must have at least one measurable site of disease (phase II)
  • For lymphoma and multiple myeloma patients: patients who have relapsed or are refractory to at least one prior chemotherapeutic regimen or biologic agent; patients must either be ineligible for or have refused curative options for treatment, including stem cell transplant, if applicable
  • For solid tumor patients: relapsed or refractory to at least one prior chemotherapeutic regimen or biologic agent; patients must either be ineligible for or have refused curative options for treatment
  • Patients must have had a rest period of at least 3 weeks since prior chemotherapy or radiation therapy, 6 weeks if the last regimen included BCNU or mitomycin C; there must be a rest period of at least 3 months if the last therapy was immunotherapy or radioimmunotherapy (unless the disease has progressed since treatment)
  • Eastern Cooperative Oncology Group (ECOG) performance status =< 2 (Karnofsky >= 60%)
  • Life expectancy of greater than 3 months
  • Absolute neutrophil count (ANC) >= 1,000/mcL
  • Platelet count >= 100,000/mcL unsupported by transfusion within the prior 2 weeks
  • Hemoglobin >= 8.0 g/dL unsupported by transfusion within the prior 2 weeks
  • Total bilirubin =< 2 x upper normal institutional limits; in patients with Gilbert's disease or documented liver metastases, total bilirubin up to 3 x upper limits of normal (ULN) will be allowed
  • Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT) (serum glutamic pyruvate transaminase [SGPT]) =< 2.5 X institutional upper limit of normal
  • Creatinine within normal institutional limits OR creatinine clearance >= 60 mL/min for patients with creatinine levels above institutional normal
  • Patients with prior stem cell transplant will be eligible as long as they have not relapsed or progressed within 100 days post-transplant and they meet the above inclusion criteria
  • Women of child-bearing potential and men must agree to use adequate contraception (hormonal, barrier method of birth control, or 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, she should inform her treating physician immediately
  • Ability to understand and the willingness to sign a written informed consent document
  • Toxicities from prior therapies must have resolved to baseline, or be =< grade 2 and stable for at least one month
  • Patient must be able to swallow pills
  • Patients with central nervous system (CNS) metastases must be stable after therapy for > 3 months and off steroid treatment prior to study enrollment

Exclusion Criteria:

  • Patients who have had chemotherapy or radiotherapy within 3 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered to baseline (or are not at stable grade =< 2) from adverse events due to agents administered more than 3 weeks earlier; patients who have received immunotherapy or radioimmunotherapy within 3 months, unless disease has progressed since treatment; patients who have been administered ABT-888 as part of a single or limited dosing study, such as a phase 0 study, will not be excluded from participating in this study solely because of receiving prior ABT-888
  • Patients may not be receiving any other investigational agents
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to ABT-888, bendamustine or mannitol; patients enrolling in the cohort expansion or phase 2 portions of the study who have been intolerant of repeated doses of rituximab in the past will be excluded (patients who have had infusion reactions to their initial dose of rituximab will not 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; breastfeeding should be discontinued if the mother is treated with ABT-888
  • Human immunodeficiency virus (HIV)-positive patients on combination antiretroviral therapy are eligible if their HIV is under adequate control with an antiretroviral regimen that has been stable for >= 4 weeks, as long as the CD4 count is > 300; appropriate studies will be undertaken in patients receiving combination antiretroviral therapy when indicated; due to toxicity issues, patients on zidovudine or stavudine would not be eligible
  • Patients with active seizure or a history of seizure are not eligible
  • Patients with uncontrolled CNS metastasis are not eligible
  • Patients with unrelated prior malignancies must have undergone potentially curative therapy for their prior malignancy, have no evidence of that disease for three years, or be deemed at low risk for recurrence of their prior malignancy by her/his treating physician; patients with dermal squamous cell carcinoma, basal cell carcinoma or melanoma in situ that has been completely excised will be eligible following excision
Both
18 Years and older
No
Not Provided
United States
 
NCT01326702
NCI-2011-02583, NCI-2011-02583, CDR0000697580, 10-174, 8818, U01CA069856, P30CA008748
Not Provided
National Cancer Institute (NCI)
National Cancer Institute (NCI)
Not Provided
Principal Investigator: John Gerecitano Memorial Sloan-Kettering Cancer Center
National Cancer Institute (NCI)
February 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP