A Phase 1/2 Study of Lenalidomide in Combination With Bendamustine in Relapsed and Primary Refractory Hodgkin Lymphoma

NCT ID: NCT01412307

Last Updated: 2015-08-11

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 36 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-07-31
• Study Completion Date: 2016-07-31

Brief Summary

Management of patients with recurring Hodgkin lymphoma (HL) after stem cell transplantation failure represents a typical unmet medical need prompting active development and validation of new agents and treatment strategies. The LEBEN protocol combines two agents, lenalidomide and bendamustine, framing different targets on both tumor and microenvironmental cells of HL. These agents, while showing a low risk of overlapping extrahematologic toxicities, may hit the proliferation machinery of H-RS cells and/or their progenitors, synergistically inhibit tumor-related angiogenesis and interfere on cytokine-mediate circuitries operating in the microenvironment to support tumor cell survival.

A weekly schedule of bendamustine, at 60 mg/m2, is combined with the continuous administration of increasing dose of lenalidomide (10, 15, 20 e 25 mg dose levels in a 28-day cycle). Such schedule of Bendamustine is aimed at enhancing the antiangiogenic and immunomodulatory activity of continuous Lenalidomide, as studies have shown that low and protracted doses of alkylators induce a decrease in microvascular density of tumor tissues and inhibit mobilization and viability of circulating endothelial progenitors.

The Bayesian phase 1/2 dose finding method of Thall and Cook was employed. This method chooses doses based-on both response and toxicity, and accounts for the trade-off between these two outcomes.

Conditions

Recurrent Adult Hodgkin Lymphoma

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

lenalidomide plus bendamustine

Group Type: EXPERIMENTAL

Lenalidomide

Intervention Type: DRUG

10, 15, 20 or 25 mg orally per cohort day 1-28 in a 28 days cycle

Bendamustine

Intervention Type: DRUG

intravenous on days 1, 8 and 15 of each 28-days cycle at fixed dose of 60 mg/m2, as a 30-60 min i.v. infusion

Bio-specimen Retention

Intervention Type: OTHER

Samples with DNA and without DNA

Interventions

Lenalidomide

10, 15, 20 or 25 mg orally per cohort day 1-28 in a 28 days cycle

Intervention Type: DRUG

Bendamustine

intravenous on days 1, 8 and 15 of each 28-days cycle at fixed dose of 60 mg/m2, as a 30-60 min i.v. infusion

Intervention Type: DRUG

Bio-specimen Retention

Samples with DNA and without DNA

Intervention Type: OTHER

Other Intervention Names

CC-5013; IMiD-1; Revlimid; SDX-105; Ribomustin; Treanda; Cytostasan

Eligibility Criteria

Inclusion Criteria

• Patients must have histologically confirmed classical Hodgkin lymphoma (HL).
• Patients must have failed an autologous stem cell transplant or be ineligible for high-dose therapy due to chemorefractory disease (as defined as <50% response to standard salvage chemotherapy), age or comorbidity.
• Patients must have at least one target PET-avid bidimensionally measurable lesion,
• Age >18 years
• Life expectancy of greater than 3 months
• ECOG performance status <2
• Patients must have adequate organ and marrow function as defined below: absolute neutrophil count >1,000/mL; platelets >75,000/mL; total bilirubin < 2.0 mg/dl in the absence of a history of Gilbert's disease (or pattern consistent with Gilbert's disease); however dose reduction is recommended for Bendamustine in patients with 30 - 70 % tumour involvement of the liver and moderately diminished liver function (serum bilirubin 1.2 - 3.0 mg/dl); AST(SGOT)/ALT(SGPT) <3 X institutional upper limit of normal; creatinine within normal institutional limits OR creatinine clearance >50 mL/min/1.73 m2
• Patients must have echocardiogram or gated blood pool scan (MUGA) with an ejection fraction > or = to 50%
• If patients have a history of malignancy other than cutaneous basal cell or squamous cell carcinoma, they must be disease-free for ~ 5 years at the time of enrolment
• Patients must accept contraception measures until 4 weeks after the completion of chemotherapy, and up to 6 months for male patients.
• Women of child-bearing must have a medically supervised negative pregnancy test even if had been using effective contraception.
• Patients agree not to share study medication with another person and to return all unused study drug to the investigator
• Patients or their guardians must be capable to understand and must be willing to sign a written informed consent document.

Exclusion Criteria

• Treatment with chemotherapy or external radiotherapy within 6 weeks, or monoclonal antibodies within 8 weeks or radioimmunoconjugates in the previous 12 weeks prior to entering the study
• Treatment with any other investigational agent
• Parenchymal brain or leptomeningeal HL involvement
• History of allergic reactions attributed to compounds of similar chemical or biologic composition to the agents used in the study
• Known HIV positivity or active infectious hepatitis, type A, B, or C
• Clinically significant cardiac disease (NYHA Class III or IV)
• Abnormal QTcF interval prolonged (> 459 msec)
• Known pregnancy or breastfeeding.
• Jaundice
• Yellow fever vaccination
• Medical illness unrelated to HL, which in the opinion of the attending physician and principal investigator will preclude safe administration of lenalidomide and bendamustine
• Corticoid treatment different from low dose prednisone or methylprednisone (up to 16 mg), used for B symptoms control.
• Contraindications for receiving prophylaxis against deep vein thrombosis
• Thromboembolic disease grade 3-4 in the last 6 months
• More than one month between staging procedures and the start of the treatment
• Major surgical procedures less than 30 days before the start of treatment

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Istituto Nazionale Tumori IRCCS - Fondazione G. Pascale

NETWORK

Sponsor Role: lead

Responsible Party

Antonio Pinto

Director of Hematology Oncology and Stem Cell Transplant Unit at National Tumor Institute 'Fondazione G. Pascale', Naples - Italy

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Antonio Pinto, MD

Role: PRINCIPAL_INVESTIGATOR

Hematology Oncology and Stem Cell Transplantation Unit , IRCCS Fondazione "G.Pascale" - Naples, Italy

Gaetano Corazzelli, MD

Role: PRINCIPAL_INVESTIGATOR

Hematology Oncology and Stem Cell Transplantation Unit , IRCCS Fondazione "G.Pascale" - Naples, Italy

Locations

Hematology Oncology and Stem Cell Transplantation Unit , IRCCS Fondazione "G.Pascale"

Naples, , Italy

Countries

Italy

References

http://meetinglibrary.asco.org/content/132091-144

Reference Type: RESULT

Other Identifiers

2011-002810-35

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

LEBEN-HL

Identifier Type: -

Identifier Source: org_study_id