Clinical Drug Experience Knowledgebase

Criteria

Inclusion Criteria:

Clinicopathological diagnosis of WM as defined by consensus panel one of the Second International Workshop on WM. Pathological diagnosis has to occur before study inclusion and randomization. In addition, pathological specimens have to be sent to the national pathological reference center at study inclusion and randomization. The positivity for CD20 can be assumed from any previous bone marrow immunohistochemistry or flow cytometry analysis performed up to 6 months prior to enrollment. Inclusion in the study will be based on morphological and immunological criteria. Immunophenotyping will be performed in each center and saved locally. Flow cytometry of bone marrow and blood cells will include at least one double staining and assess the expression of the following antigens: surface immunoglobulin, CD19, CD20, CD5, CD10 and CD23. Patients are eligible if tumor cells express the following antigens: CD19, CD20, and if they are negative for CD5, CD10 and CD23 expression. Patients with tumor cells positive for CD5 and/or CD23 and morphologically similar to WM cells may be included after ruling out other low grade B-cell malignancies.

Presence of at least one criterion for initiation of therapy, according to the 2nd Workshop on WM:

Recurrent fever, night sweats, weight loss, fatigue
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
Cold agglutinin anemia
IgM related immune hemolytic anemia and/or thrombocytopenia
Nephropathy related to WM
Amyloidosis related to WM
Hemoglobin ≤10g/dL
Platelet count <100x10^9/L
Serum monoclonal protein >5g/dL, even with no overt clinical symptoms Cumulative illness rating scale (CIRS) score less than 6
World Health Organization (WHO)/ECOG performance status 0 to 2.

Other criteria:

Age ≥ than 18 years
Life expectancy >3 months.
Baseline platelet count ≥ 50 ×10^9/L, absolute neutrophil count ≥ 0.75×10^9/L (if not due to BM infiltration by the lymphoma).

Meet the following pretreatment laboratory criteria at the Screening visit conducted within 28 days of study enrollment:

ASAT (SGOT): ≤3 times the upper limit of institutional laboratory normal value
ALAT (SGPT): ≤3 times the upper limit of institutional laboratory normal value
Total Bilirubin: ≤20 mg/L or 2 times the upper limit of institutional laboratory normal value, unless clearly related to the disease (except if due to Gilbert's syndrome)
Serum creatinine: ≤ 2mg/dl
Premenopausal fertile females must agree to use a highly effective method of birth control for the duration of the therapy up to 6 months after end of therapy. A highly effective method of birth control is defined as those which result in a low failure rate (i.e. less than 1% per year) when used consistently and correctly such as implants, injectables, combined oral contraceptives, some IUDs, sexual abstinence or vasectomised partner.
Men must agree not to father a child for the duration of therapy and 6 months after and must agree to advice a female partner to use a highly effective method of birth control.
Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care.

Exclusion criteria:

Prior systemic treatment of the WM (plasmapheresis and short- term administration of corticosteroids < 4 weeks administered at a dose equivalent to < 20 mg/day prednisone is allowed)
Patient with hypersensitivity to dexamethasone.
Serious medical or psychiatric illness likely to interfere with participation in this clinical study.
Uncontrolled bacterial, viral or fungal infection
Active HIV, HBV or HCV infection
Known interstitial lung disease
Prior allergic reaction or severe anaphylactic reaction related to humanized or murine monoclonal antibody.
Central Nervous System involvement by lymphoma

Prior history of malignancies unless the subject has been free of the disease for ≥ 5 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).

Uncontrolled illness including, but not limited to:

Uncontrolled diabetes mellitus mellitus (as indicated by metabolic derangements and/or severe diabetes mellitus related uncontrolled organ complications)
Chronic symptomatic congestive heart failure (Class NYHA III or IV).
Unstable angina pectoris, angioplasty, stenting, or myocardial infarction within 6 months
Clinically significant cardiac arrhythmia that is symptomatic or requires treatment, or asymptomatic sustained ventricular tachycardia.
Known pericardial disease
Subjects with ≥ Grade 2 neuropathy.
Women who are pregnant as well as women who are breastfeeding and do not consent to discontinue breast-feeding.
Participation in another clinical trial within four weeks before randomization in this study
No consent for registration, storage and processing of the individual disease-characteristics and course as well as information of the family physician about study participation.