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

Recurrent Adult Hodgkin Lymphoma Clinical Trial

— LEBEN  

Official title:

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT01412307
• Other study ID #: LEBEN-HL
• Secondary ID: 2011-002810-35
• Status: Active, not recruiting
• Phase: Phase 1/Phase 2
• First received: August 3, 2011
• Last updated: August 8, 2015
• Start date: July 2011
• Est. completion date: July 2016

Study information

• Verified date: August 2015
• Source: Fondazione Giovanni Pascale
• Contact: n/a
• Is FDA regulated: No
• Health authority: Italy: The Italian Medicines Agency
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 36
• Est. completion date: July 2016
• Est. primary completion date: July 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

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

Study Design

Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Hodgkin Disease
• Lymphoma
• Recurrent Adult Hodgkin Lymphoma

Intervention

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

Other:
• Bio-specimen Retention
Samples with DNA and without DNA

Locations

Country	Name	City	State
Italy	Hematology Oncology and Stem Cell Transplantation Unit , IRCCS Fondazione "G.Pascale"	Naples

Sponsors (1)

Lead Sponsor	Collaborator
Fondazione Giovanni Pascale

Country where clinical trial is conducted

Italy, 

References & Publications (1)

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

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dose finding, as best trade-off between toxicity and efficacy according to the Bayesian phase I/II dose finding method of Thall and Cook	According to the Bayesian phase I/II dose finding method of Thall and Cook,a target efficacy-toxicity trade-off contour has been constructed by fitting a curve to target values of pE (probability ofEfficacy) and pT (probability of Toxicity) of 0.30 and 0.40, respectively and probability cut-offs pE (for Efficacy)and pT (for Toxicity) set at 0.10 and 0.10,respectively.The area underneath the target contour has desirable pE, pT pairs. Up to 36 patients can be treated in cohorts of size 3. The 'best' dose is defined as that giving the largest response-toxicity trade-off.	Evaluation at day +56, i.g. after two cycles.	Yes
Secondary	AE/SAE rate at completion of treatment		After course 6. i.g. about 6 months	Yes
Secondary	Overall Rate Response		After 2, 4 and 6 cycles	No
Secondary	Event Free Survival		From the time from study entry to any treatment failure including disease progression, or discontinuation of treatment for any reason	No
Secondary	Time to Progression		From entry until documented lymphoma progression or death as a result of lymphoma.	No
Secondary	Response Duration		From the time when criteria for response (i.g. CR or PR) are met, for which the event is the first documentation of relapse or progression.	No