Everolimus and Brentuximab Vedotin in Treating Patients With Relapsed or Refractory Hodgkin Lymphoma

NCT ID: NCT02254239

Last Updated: 2019-12-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

TERMINATED

Clinical Phase

PHASE1

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-02-04

Study Completion Date

2018-12-12

Brief Summary

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This phase I trial studies the side effects and the best dose of everolimus when given together with brentuximab vedotin in treating patients with Hodgkin lymphoma that has come back (relapsed) or is not responding to treatment (refractory). Everolimus may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Brentuximab vedotin may interfere with the ability of cancer cells to grow and spread by binding to a protein on the surface of cancer cells and then releasing a cancer-killing substance to them. Giving everolimus together with brentuximab vedotin may be a better treatment for Hodgkin lymphoma.

Detailed Description

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PRIMARY OBJECTIVES:

I. To determine the safety and optimal dose of everolimus given in combination with brentuximab vedotin in relapsed or refractory Hodgkin lymphoma patients.

SECONDARY OBJECTIVES:

I. To determine the efficacy of everolimus in combination with brentuximab vedotin in relapsed or refractory Hodgkin lymphoma.

II. To evaluate duration of response, progression free survival, and overall survival.

III. To evaluate response by positron emission tomography (PET)-computed tomography (CT) based response criteria.

TERTIARY OBJECTIVES:

I. To assess cytokines and free light chain before and after therapy.

OUTLINE: This is a dose-escalation study of everolimus.

Patients receive brentuximab vedotin intravenously (IV) over 30 minutes on day 1 and everolimus orally (PO) once daily (QD) or every other day (QOD) on days 1-21. Treatment repeats every 21 days for up to 15 courses in the absence of disease progression or unacceptable toxicity. Patients then receive brentuximab vedotin IV over 30 minutes on day 1 and everolimus PO QD or every other day on days 1-84 for 1 course.

MAINTENANCE THERAPY: Beginning on course 17, patients receive everolimus PO QD, QOD, twice weekly, or thrice weekly on days 1-84. Courses repeat every 84 days in the absence of disease progression and unacceptable toxicity.

After completion of study treatment, patients are followed up every 6 months for 1 year.

Conditions

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Recurrent Hodgkin Lymphoma Refractory Hodgkin Lymphoma

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Treatment (everolimus, brentuximab vedotin)

Patients receive brentuximab vedotin IV over 30 minutes on day 1 and everolimus PO QD or QOD on days 1-21. Treatment repeats every 21 days for up to 15 courses in the absence of disease progression or unacceptable toxicity. Patients then receive brentuximab vedotin IV over 30 minutes on day 1 and everolimus PO QD or every other day on days 1-84 for 1 course.

MAINTENANCE THERAPY: Beginning on course 17, patients receive everolimus PO QD, QOD, twice weekly, or thrice weekly on days 1-84. Courses repeat every 84 days in the absence of disease progression and unacceptable toxicity.

Group Type EXPERIMENTAL

Brentuximab Vedotin

Intervention Type DRUG

Given IV

Everolimus

Intervention Type DRUG

Given PO

Laboratory Biomarker Analysis

Intervention Type OTHER

Correlative studies

Pharmacological Study

Intervention Type OTHER

Correlative studies

Interventions

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Brentuximab Vedotin

Given IV

Intervention Type DRUG

Everolimus

Given PO

Intervention Type DRUG

Laboratory Biomarker Analysis

Correlative studies

Intervention Type OTHER

Pharmacological Study

Correlative studies

Intervention Type OTHER

Other Intervention Names

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ADC SGN-35 Adcetris Anti-CD30 Antibody-Drug Conjugate SGN-35 Anti-CD30 Monoclonal Antibody-MMAE SGN-35 Anti-CD30 Monoclonal Antibody-Monomethylauristatin E SGN-35 cAC10-vcMMAE SGN-35 42-O-(2-Hydroxy)ethyl Rapamycin Afinitor Certican RAD 001 RAD001 Votubia Zortress

Eligibility Criteria

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Inclusion Criteria

* Biopsy-proven relapsed (response to last treatment \> 6 months duration), refractory (no response to last treatment or response duration \< 6 months) or residual Hodgkin lymphoma; NOTE: re-biopsy is necessary unless the patient has had a previous biopsy \< 180 days prior to registration on this protocol with no intervening therapy and tissue is available for translational research studies
* Eligible to receive standard brentuximab vedotin for relapsed Hodgkin lymphoma
* Measurable disease by CT or magnetic resonance imaging (MRI) or the CT portion of the PET/CT: must have at least one lesion that has a single diameter of \>= 2 cm
* Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0, 1, or 2
* Absolute neutrophil count (ANC) \>= 1000/uL
* Hemoglobin (Hgb) \>= 9 g/dl
* Platelet (PLT) \>= 75,000/uL
* Serum total bilirubin within normal range (or =\< 1.5 x upper limit of normal \[ULN\] if liver metastases are present; or total bilirubin =\< 3.0 x ULN with direct bilirubin within normal range in patients with well documented Gilbert syndrome)
* Aspartate aminotransferase (AST) =\< 1.5 x ULN
* Alkaline phosphatase =\< 1.5 x ULN
* Serum creatinine =\< 1.5 x ULN
* Negative serum pregnancy test done =\< 7 days prior to registration, for women of childbearing potential only
* Provide informed written consent
* Willing to return to Mayo Clinic for follow-up
* Willing to provide blood and tissue samples for correlative research purposes
* Willingness to take everolimus orally and maintain a pill diary

Exclusion Criteria

* Any of the following

* Pregnant women
* Nursing women
* Women of childbearing potential who are unwilling to employ highly effective contraception while on study treatment and for 6 months after the final dose of treatment; NOTE: women of childbearing potential are defined as all women physiologically capable of becoming pregnant
* Men of childbearing potential who are unwilling to employ highly effective contraception while on study treatment and for 6 months after the final dose of treatment and should not father a child during this time; NOTE: men of childbearing potential are defined as all males physiologically capable of conceiving offspring
* Candidate for known standard therapy for the patient's disease that is potentially curative
* Therapy with myelosuppressive chemotherapy or biologic therapy \< 21 days prior to registration unless the patient has recovered from the nadir of the previous treatment to a level that meets the inclusion eligibility criteria of this protocol
* Patients who have received any continuous or intermittent small molecule therapeutics (excluding monoclonal antibodies) =\< 5 effective half-lives prior to registration or who have not recovered from side effects of such therapy
* Received wide field radiotherapy =\< 28 days or limited field radiation for palliation =\< 14 days prior to registration or who have not recovered from side effects of such therapy
* Receiving corticosteroids \> 20 mg of prednisone per day (or equivalent); Note: the dose should be noted on the medication record each cycle
* Persistent toxicities \>= grade 2 from prior chemotherapy or biological therapy regardless of interval since last treatment
* Patients who have any severe and/or uncontrolled medical conditions or other conditions that could affect their participation in the study such as:

* Symptomatic congestive heart failure of New York Heart Association class III or IV
* Unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction within 6 months prior to registration, serious uncontrolled cardiac arrhythmia or any other clinically significant cardiac disease
* Severely impaired lung function as defined as spirometry and diffusion capacity of carbon monoxide (DLCO) that is less than 50% of the normal predicted value and/or oxygen (O2) saturation that is 88% or less at rest on room air
* Uncontrolled diabetes as defined by fasting serum glucose \> 1.5 x ULN (Note: optimal glycemic control should be achieved before starting everolimus)
* Active (acute or chronic) or uncontrolled severe infections
* Other concurrent chemotherapy, immunotherapy, radiotherapy, or any ancillary therapy considered investigational (utilized for a non-Food and Drug Administration \[FDA\]-approved indication and in the context of a research investigation)
* Known positivity for human immunodeficiency virus (HIV); Note: baseline testing for HIV is not required
* Active hepatitis B or C with uncontrolled disease

* Note: a detailed assessment of hepatitis B/C medical history and risk factors must be done at screening for all patients; hepatitis B virus surface antigen (HBsAg) and hepatitis C virus (HCV) ribonucleic acid (RNA) polymerase chain reaction (PCR) testing are required at screening for all patients with a positive medical history based on risk factors and/or confirmation of prior hepatitis B virus (HBV) infection
* Other active malignancy requiring treatment that would interfere with the assessments of response of the lymphoma to protocol treatment
* Inability to swallow or impairment of gastrointestinal function or gastrointestinal disease that may significantly alter the absorption of the drugs (e.g., ulcerative disease, uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome or small bowel resection) that would preclude use of oral medications
* Major surgery =\< 14 days prior to registration or have not recovered from side effects of such therapy
* Treated with any hematopoietic colony-stimulating growth factors (e.g., granulocyte-colony stimulating factor \[G-CSF\], granulocyte-macrophage colony-stimulating factor \[GM-CSF\]) =\< 2 weeks prior to study registration; NOTE: erythropoietin or darbepoetin therapy, if initiated at least 2 weeks prior to study registration, may be continued
* Pre-existing neuropathy of \>= grade 2
* Patients receiving strong inhibitors of cytochrome P450 family 3, subfamily A, polypeptide 4 (CYP3A4)

* Use of the following strong or moderate inhibitors are prohibited =\< 7 days prior to registration

* Boceprevir (Victrelis \[TM\])
* Clarithromycin (Biaxin, Biaxin XL)
* Conivaptan (Vaprisol)
* Itraconazole (Sporanox)
* Ketoconazole (Nizoral)
* Nefazodone (Serzone)
* Posaconazole (Noxafil)
* Telithromycin (Ketek)
* Voriconazole (Vfend)
* Use of the following inducers are prohibited =\< 12 days prior to registration

* Bosentan (Tracleer)
* Carbamazepine (Carbatrol, Epitol, Equetro \[TM\], Tegretol, Tegretol-XR)
* Modafinil (Provigil)
* Phenobarbital (Luminal)
* Phenytoin (Dilantin, Phenytek)
* Rifabutin (Mycobutin)
* Rifampin (Rifadin)
* St. John's wort
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Cancer Institute (NCI)

NIH

Sponsor Role collaborator

Mayo Clinic

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Patrick Johnston

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

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Mayo Clinic

Rochester, Minnesota, United States

Site Status

Countries

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United States

Other Identifiers

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NCI-2014-01804

Identifier Type: REGISTRY

Identifier Source: secondary_id

MC1387

Identifier Type: OTHER

Identifier Source: secondary_id

P30CA015083

Identifier Type: NIH

Identifier Source: secondary_id

View Link

MC1387

Identifier Type: -

Identifier Source: org_study_id