Efficacy of Venetoclax in combination with Rituximab in Waldenström’s Macroglobulinemia

Phase 2

Recruiting

• Conditions: Waldenström’s Macroglobulinemia

• Registration Number: 2022-500574-34-00
• Lead Sponsor: University Hospital Of Ulm AöR

Brief Summary

The primary objective of the study is to explore the efficacy of Venetoclax in combination with Rituximab compared to Dexamethasone/ Rituximab/ Cyclophosphamide in patients with de novo WM.

Detailed Description

In Waldenström's macroglobulinemia (WM) chemotherapy induces only low CR/VGPR rates and response duration is limited. In addition, WM patients are often elderly, partly not tolerating chemotherapy related toxicities. Thus, innovative approaches are needed which combine excellent activity and tolerability in WM. Chemotherapy-free approaches are highly attractive for this patient group. Based on its high activity and favorable toxicity profile in indolent B-NHL such as CLL, Venetoclax was approved for the treatment of this diseases by the FDA and the European Medicines Agency (EMA). First data in relapsed/refractory WM have documented high activity and low toxicity of Venetoclax also in WM, including patients with prior Ibrutinib treatment or patients carrying CXCR4 mutations. Ibrutinib itself has high activity and a relatively low toxicity profile in WM, but has also major disadvantages: the main disadvantage is the need to apply this drug continuously. Furthermore, Ibrutinib efficacy depends largely on the genotype with a substantial drop in major responses and PFS in the presence of CXCR4 mutations and non-mutated MYD88. In particular the need of continuous treatment for Ibrutinib has prevented that Ibrutinib has become the standard of care outcompeting conventional Rituximab/chemotherapy. This is reflected in current guidelines such as the NCCN and the ESMO guidelines, which still see immunochemotherapy as a backbone of treatment, largely because of the advantage of a timely fixed application. Data in CLL in the relapsed as well as in the first line setting have convincingly shown that in contrast to Ibrutinib Venetoclax is highly efficient also when used in a timely defined application scheme over 12 months in combination with the anti-CD20 antibody Rituximab. Data documented deep responses including molecular responses and a highly significant advantage over immunochemotherapy in large international Phase III trials, changing the standard of care in this disease.

Based on this the hypothesis is that timely fixed application of the combination of Venetoclax and Rituximab induces significantly superior treatment outcomes compared to chemotherapy and Rituximab (DRC) in patients with treatment naïve WM, regardless of the genotype. A first indication for this assumption in the proposed trial will allow the performance of confirmatory phase 3 trials that might change the standard of care in WM.

This study is an International phase II explorative, multicenter, open label, and randomized trial.

The study will consist of an open labeled, stratified 1:1 randomization between Arm A and Arm B for de novo WM patients in need of treatment (phase II). Stratification factors are MYD88 and CXCR4 status (positive vs. negative). A stratified central block randomization will be used. The central randomization service will be used to avoid predictability of the treatment arm.

The primary goal of this study is to explore the efficacy of Venetoclax plus Rituximab versus Dexamethasone/Cyclophosphamide/Rituximab in the treatment of de novo WM patients (Arm A vs. Arm B).

80 patients are planned to be recruited for this study at approcimately 30 sites in Germany, Greece and France.

Study Timeline

• Study First Posted: 2024-11-19
• Last Update Posted: 2024-11-20

Recruitment & Eligibility

• Status: Ongoing, recruiting
• Sex: Not specified
• Target Recruitment: 55

Inclusion Criteria

Proven clinicopathological diagnosis of WM as defined by consensus panel one of the second International Workshop on WM (IWWM). Histopathology has to be performed before randomization but within the last 4 months before start of treatment. In addition, pathological specimens have to be sent to the central pathological reference center prior to randomization for the determination of the mutational status of MYD88 and CXCR4 prior to randomization if the mutational status hasn’t been determined before. Additionally, TP53 mutation will be examined. Pathological reference center must confirm the diagnosis of WM.

Women of childbearing potential (WCBP), i.e. fertile, following menarche and until becoming postmenopausal must have negative results for pregnancy test and must agree to use a highly effective method of birth control for the duration of the therapy up to 12 months after end of therapy.

Men must agree not to father a child for the duration of therapy and 12 months after and must agree to advice their female partner to use a highly effective method of birth control. Males must refrain from sperm donation for the duration of treatment and at least 12 months after the last dose of study medication.

Each patient must voluntarily date and sign an informed consent form in the native language of the patient indicating that he or she understands the purpose of and procedures required for the study and are willing to participate in the study. Patients must be willing and able to adhere to the prohibitions and restrictions specified in this protocol.

Affiliation to a social security scheme (relevant for France only).

De novo WM independent of the genotype in need of treatment.

Patients must have at least one of the following criteria to start study treatment as partly defined by consensus panel criteria from the Seventh IWWM and ESMO Guideline: Recurrent fever, night sweats, weight loss, fatigue (at least one of them); Hyperviscosity; Lymphadenopathy which is either symptomatic or bulky (≥ 5 cm in maximum diameter); Symptomatic hepatomegaly and / or splenomegaly; Symptomatic organomegaly and / or organ or tissue infiltration; Peripheral neuropathy due to WM; Symptomatic cryoglobulinemia; Symptomatic Cold agglutinin anemia; Autoimmun hemolytic anemia and/or thrombocytopenia; Nephropathy related to WM; Amyloidosis related to WM; Hemoglobin ≤ 10 g/dL (patients should not have received red blood cells transfusions for at least 7 days prior to obtaining the screening hemoglobin); Platelet count < 100 x 10^9/L (caused by bone marrow [BM] infiltration of the lymphoma); IgM serum concentration > 6 g/dL and other WM associated relevant symptoms.

Subject must be ≥ 18 years of age.

Life expectancy > 3 months.

World Health Organization (WHO) / ECOG performance status ≤ 2.

Baseline platelet count ≥ 50x10^9/L, absolute neutrophil count ≥ 0.75x109/L (if not due to BM infiltration by the lymphoma).

Adequate hepatic function per local laboratory reference range as follows: Aspartate transaminase (AST) and alanine transaminase (ALT) ≤ 3.0 x ULN; Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert’s syndrome or of nonhepatic origin).

Subject must have adequate renal function as demonstrated by a creatinine clearance ≥ 30 mL/min; calculated by the Cockcroft Gault formula or measured by 24 hours urine collection.

Exclusion Criteria

Serious medical or psychiatric illness (especially undergoing treatment) likely to interfere with participation in this clinical study.

Unstable angina pectoris, angioplasty, stenting, or myocardial infarction within 6 months prior to start therapy.

Clinically significant cardiac arrhythmia that is symptomatic or requires treatment, or asymptomatic sustained ventricular tachycardia.

Subject has a cardiovascular disability status of New York Heart Association Class > 2. Class 2 is defined as cardiac disease in which patients are comfortable at rest but ordinary physical activity results in fatigue, palpitations, dyspnea, or anginal pain.

Known pericardial disease.

History of stroke or intracranial haemorrhage within 6 months prior start of treatment.

Known interstitial lung disease.

Infiltrative pulmonary disease, known pulmonary hypertension.

Prior history of malignancies unless the subject has been free of the disease for ≥ 3 years. Exceptions include the following: Basal cell carcinoma of the skin; Squamous cell carcinoma of the skin; Carcinoma in situ of the cervix; Carcinoma in situ of the breast; Incidental histologic finding of prostate cancer (TNM stage of T1a or T1b).

Known cirrhosis (meeting child-pugh stage C).

Chemotherapy with approved or investigational anticancer therapeutic within 21 days prior to start of therapy.

Subject is known to be positive for HIV.

Glucocorticoid therapy within 14 days prior to therapy that exceeds a cumulative dose of 160 mg of dexamethasone or equivalent dose of other corticosteroids given for antineoplastic intent.

Treatment with any of the following within 7 days prior to the first dose of study drug: moderate or strong cytochrome P450 3A (CYP3A) inhibitors (such as fluconazole, ketoconazole, and clarithromycin); moderate or strong CYP3A inducers (such as rifampin, carbamazepine, phenytoin, St. John's wort).

Contraindication to the active substances or any of the other excipients of the Investigational Medicinal Products as well as to any of the required concomitant drugs or supportive treatments, including hypersensitivity to antiviral drugs.

Vaccination with live attenuated vaccines within 4 weeks prior to start of therapy.

History or evidence of any other clinically significant disorder, condition or disease (with the exception of those outlined above) that, in the opinion of the investigator or sponsor, if consulted, would pose a risk to subject safely or interfere with the study evaluation, procedures or completion.

Women who are pregnant as well as women who are breast-feeding and do not consent to discontinue breast-feeding.

Participation in another clinical trial within four weeks before start of therapy in this study.

No consent for registration, storage and processing of the individual diseasecharacteristics.

Administration or consumption of any of the following within 3 days prior to the first dose of study drug: grapefruit or grapefruit products; Seville oranges (including marmalade containing Seville oranges); star fruit.

Person of legal age who is incapable of comprehending the nature, significance and implications of the clinical trial and of determining his/her will in the light of these facts.

Active severe infection.

Congenital or acquired severe immunodeficiency not attributed to lymphoma (clinical appearance: recurrent infections, necessity of immunoglobulin substitution therapy, patients after transplantation).

Evidence of other clinically significant uncontrolled condition(s) including, but not limited to: Uncontrolled systemic infection (viral, bacterial or fungal); Chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infection requiring treatment. Note: subjects with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface (HBs) antigen negative-, anti-HBs antibody positive and antihepatitis B core (HBc) antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate.

Adequate pulmonary function as demonstrated by DLCO ≤ 65% or FEV1 ≤ 65%.

Uncontrolled diabetes mellitus (as indicated by metabolic derangements and / or severe diabetes mellitus related uncontrolled organ complications).

Uncontrolled hypertension.

Cardiac history of CHF requiring treatment or Ejection Fraction ≤ 50% or chronic stable angina.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Rate of complete remission (CR) or very good partial remission (VGPR) 12 months after randomization using the modified response criteria updated at the Sixth IWWM (CR/VGPR).		Rate of complete remission (CR) or very good partial remission (VGPR) 12 months after randomization using the modified response criteria updated at the Sixth IWWM (CR/VGPR).

Secondary Outcome Measures

Name	Time	Method
Interim Response (C4D1; C7D1 (arm A) / 28 days after C6D1 (arm B); C10D1 (arm A) / post treatment staging 1 (arm B)		Interim Response (C4D1; C7D1 (arm A) / 28 days after C6D1 (arm B); C10D1 (arm A) / post treatment staging 1 (arm B)
Response and response rate: Overall response rate (CR, VGPR, PR, MR) 12 months after randomization; Major Response rate (CR, VGPR, PR) 12 months from randomization		Response and response rate: Overall response rate (CR, VGPR, PR, MR) 12 months after randomization; Major Response rate (CR, VGPR, PR) 12 months from randomization
Best response from randomization up to 24 months		Best response from randomization up to 24 months
Time to first overall response within 24 months from start of treatment		Time to first overall response within 24 months from start of treatment
Time to first major response within 24 months from start of treatment		Time to first major response within 24 months from start of treatment
Event free survival (EFS)		Event free survival (EFS)
Response duration (RD)		Response duration (RD)
Progression free survival (PFS)		Progression free survival (PFS)
Lymphoma specific survival (LSS)		Lymphoma specific survival (LSS)
Overall survival (OS)		Overall survival (OS)
Safety		Safety
Quality of life		Quality of life
Comparison of response rates between CXCR4 mutated and CXCR4 wildtype patients		Comparison of response rates between CXCR4 mutated and CXCR4 wildtype patients

Trial Locations

Locations (12)

Universitaetsklinikum Ulm AöR; 🇩🇪 Ulm, Germany

Gesellschaft Zur Forderung Des Wissenschaftlich Medizinischen Erkenntnisgewinns In Der Hamatologie Und Oncologie; 🇩🇪 Muenster, Germany

Onkologische Schwerpunktpraxis Bielefeld; 🇩🇪 Bielefeld, Germany

Dr. Vehling-Kaiser MVZ GmbH; 🇩🇪 Landshut, Germany

Universitaet Muenster; 🇩🇪 Muenster, Germany

Klinikverbund Allgaeu gGmbH; 🇩🇪 Kempten (Allgau), Germany

Kliniken Maria Hilf GmbH Moenchengladbach; 🇩🇪 Moenchengladbach, Germany

Klinikum Chemnitz gGmbH; 🇩🇪 Chemnitz, Germany

Haematologie und Onkologie Muenchen-Pasing MVZ GmbH; 🇩🇪 Munich, Germany

Universitaetsklinikum Schleswig-Holstein AöR; 🇩🇪 Kiel, Germany

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Universitaetsklinikum Ulm AöR

🇩🇪Ulm, Germany

Christian Buske

Site contact

004973150065801

christian.buske@uni-ulm.de