Acalabrutinib, Venetoclax and Durvalumab for the Treatment of Richter Transformation From Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorMayo Clinic

About this trial

This phase II trial tests whether acalabrutinib, venetoclax, and durvalumab work in treating patients with Richter transformation from chronic lymphocytic leukemia or small lymphocytic lymphoma. Richter transformation is a rare condition in which chronic lymphocytic leukemia or small lymphocytic lymphoma changes into a fast-growing type of lymphoma. Acalabrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Venetoclax is in a class of medications called B-cell lymphoma-2 (BCL-2) inhibitors. It may stop the growth of cancer cells by blocking Bcl-2, a protein needed for cancer cell survival. Immunotherapy with monoclonal antibodies, such as durvalumab, may help the body's immune system attack the cancer, and may interfere with the ability of tumor cells to grow and spread. Giving acalabrutinib, venetoclax, and durvalumab may help improve survival in patients with Richter transformation.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age >= 18 years willing to provide consent and follow-up

Biopsy-proven SLL according to WHO 2008 criteria, or

Peripheral blood B cell count of >= 5 x 10^9/L consisting of small to moderate size lymphocytes (If there are enough evidence to document the prior diagnosis of CLL, it is not required to meet the criteria of peripheral blood B cell count more than 5 x 10^9/L )

The predominant population of lymphocytes share both B-cell antigens (CD19, CD20 [typically dim expression], or CD23) as well as CD5 in the absence of other pan-T-cell markers (CD3, CD2, etc.)

Disqualifiers

Symptomatic arrhythmias

Congestive heart failure

Myocardial infarction =< 3 months prior to registration

Any class 3 or 4 cardiac disease as defined by the New York Heart Association functional classification

Trial design

Design model

Single group

Treatments tested in this trial

  • Acalabrutinib

    Drug

    Given PO

  • Durvalumab

    Biological/Vaccine

    Given IV

  • Venetoclax

    Drug

    Given PO

  • Biospecimen Collection

    Procedure/Surgery

    Undergo blood sample collection

  • Bone Marrow Aspiration

    Procedure/Surgery

    Undergo bone marrow aspiration

  • Bone Marrow Biopsy

    Procedure/Surgery

    Undergo bone marrow biopsy

  • Positron Emission Tomography (PET)

    Procedure/Surgery

    Undergo PET/CT

  • Computed Tomography

    Procedure/Surgery

    Undergo PET/CT or CT

Treatment groups

27 Participants
are divided into 1 treatment group
Group A: Treatment (acalabrutinib, durvalumab, venetoclax)Experimental treatment 8 interventions

Trial outcomes

Primary outcomes

1

Progression free survival

Progression will be defined by Lugano positron emission tomography (PET)-computed tomography (CT) based criteria or chronic lymphocytic leukemia (CLL) criteria. The proportion of successes will be estimated by the number of successes divided by the total number of evaluable patients. Ninety-five percent confidence intervals for the true success proportion will be calculated according to the approach of Duffy and Santner. If patients are censored prior to 6 months, a Kaplan Meier estimate for progression-free survival at 6 months along with the 95% confidence intervals will be reported.

Time frame
At 6 months (end of cycle 6). Each cycle is 28 days.

Secondary outcomes

1

Overall response rate

Overall response rate (for both Richter transformation \[RT\] and CLL, calculated separately) will be estimated by the total number of patients who achieve a complete metabolic response (CMR)/partial metabolic response (PMR) or complete response (CR)/complete response with incomplete marrow recovery (CRi)/nodular partial response (nPR)/partial remission (PR) divided by the total number of evaluable patients. Exact binomial 95% confidence intervals for the true overall response rate will be calculated. The PR rate and CR rate will also be estimated.

Time frame
Up to 1 year
2

Overall survival

The distribution of overall survival will be estimated using the method of Kaplan-Meier.

Time frame
From registration to death due to any cause, assessed up to 5 years
3

Progression-free survival (PFS)

The distribution of progression-free survival will be estimated using the method of Kaplan-Meier. PFS estimates will be calculated at 3, 6, 12, and 24 months.

Time frame
From registration to progression or death due to any cause, assessed up to 2 years
4

Treatment-free survival

The distribution of treatment-free survival will be estimated using the method of Kaplan-Meier.

Time frame
From registration to subsequent treatment or death due to any cause, assessed up to 5 years

Other outcomes

Sponsors and contacts

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