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Phase 2 N=30 Treatment

Alemtuzumab and Rituximab in Treating Patients With High-Risk, Early-Stage Chronic Lymphocytic Leukemia

Leukemia

Enrolled (actual)
30
Serious AEs
3.3%
Results posted
Oct 2011
Primary outcome: Primary: Confirmed Response, Defined as Objective Complete Remission or Partial Remission for a Duration of at Least 2 Months — 27 participants

Study Design & Population

Study type
Interventional
Phase
Phase 2
Interventions
Alemtuzumab (Drug); Rituximab (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Mayo Clinic
Primary completion
Jul 2008

Outcome Measures

OutcomeResultp-value
PRIMARY
Confirmed Response, Defined as Objective Complete Remission or Partial Remission for a Duration of at Least 2 Months
27
PRIMARY
Number of Participants With Treatment Related Adverse Events
11; 3
SECONDARY
Time to Response
8
SECONDARY
Duration of Response
14.4
SECONDARY
Survival
SECONDARY
Time to Disease Progression
12.5

Summary

RATIONALE: Monoclonal antibodies, such as alemtuzumab and rituximab, can block cancer growth in different ways. Some block the ability of cancer cells to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them. Giving alemtuzumab together with rituximab may kill more cancer cells. PURPOSE: This phase II trial is studying the side effects and how well giving alemtuzumab together with rituximab works in treating patients with high-risk, early-stage chronic lymphocytic leukemia.

Eligibility Criteria

DISEASE CHARACTERISTICS:

  • Diagnosis of B-cell chronic lymphocytic leukemia (CLL)
  • Early-stage, biologically high-risk disease defined by the following criteria:
  • Rai stage 0-II (does not meet standard NCI-sponsored Working Group criteria for treatment)
  • Clinical and phenotypic features manifested in the peripheral blood, including the following:
  • Minimum threshold peripheral blood lymphocyte count of > 5,000/mm³
  • Small-to-moderate peripheral blood lymphocytes with ≤ 55% prolymphocytes
  • Monoclonality of B lymphocytes by immunophenotypic evaluation, demonstrating co-expression of CD19, CD5, and CD23 antigens, surface expression of CD20 and CD52, and B-cell monoclonal population defined by light-chain exclusions
  • Poor prognosis demonstrated by ≥ 1 of the following high-risk parameters:
  • Unmutated human immunoglobulin variable region heavy chain (IgVH) gene and CD38 expression (≥ 30% cells positive on flow cytometry) OR unmutated IgVH ZAP-70 expression (≥ 20% cells positive on flow cytometry) = 11q- = 17p-

PATIENT CHARACTERISTICS:

  • ECOG performance status 0-2
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • Creatinine ≤ 1.5 times upper limit of normal (ULN)
  • Total bilirubin ≤ 3.0 times ULN OR direct bilirubin ≤ 1.5 times ULN
  • AST ≤ 3.0 times ULN (unless due to hemolysis or CLL)
  • Hemoglobin ≥ 9.0 g/dL
  • No New York Heart Association class III-IV heart disease
  • No myocardial infarction within the past month
  • No uncontrolled infection
  • No active HIV infection
  • No evidence of autoimmune hemolytic anemia, immune thrombocytopenia, or pure red blood cell aplasia
  • No other active primary malignancy requiring treatment or limiting survival to less than 2 years

PRIOR CONCURRENT THERAPY:

  • No prior treatment for CLL
  • Prior corticosteroids allowed
  • No prior radiotherapy
  • More than 4 weeks since prior major surgery
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00436904). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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