Table 2.

B cell–directed therapies effective in CAD

Study/publication referenceDrug(s) studiedStudy designPatients/courses of therapy, nOR, %CR, %Hb increase, g/dL*Median response duration, moToxicity
30  Rituximab Prospective, nonrandomized 27/37 54 4.0 11 (observed) Low 
12  Rituximab Prospective, nonrandomized 20/20 45 3.1 6.5 (observed) Low 
52  Fludarabine + rituximab Prospective, nonrandomized 29/29 76 21 3.1 >66 (estimated) Significant 
43  Bendamustine + rituximab Prospective, nonrandomized 45/45 71 40 4.0 >32 (observed) Relatively low, manageable 
53  Bortezomib Prospective, nonrandomized 19/19 32 16 2.9 16 (observed) Low 
1  Bendamustine + rituximab Follow-up, part of larger study 45/45 78 53 Not reevaluated >88 (estimated) Long-term: low 
Study/publication referenceDrug(s) studiedStudy designPatients/courses of therapy, nOR, %CR, %Hb increase, g/dL*Median response duration, moToxicity
30  Rituximab Prospective, nonrandomized 27/37 54 4.0 11 (observed) Low 
12  Rituximab Prospective, nonrandomized 20/20 45 3.1 6.5 (observed) Low 
52  Fludarabine + rituximab Prospective, nonrandomized 29/29 76 21 3.1 >66 (estimated) Significant 
43  Bendamustine + rituximab Prospective, nonrandomized 45/45 71 40 4.0 >32 (observed) Relatively low, manageable 
53  Bortezomib Prospective, nonrandomized 19/19 32 16 2.9 16 (observed) Low 
1  Bendamustine + rituximab Follow-up, part of larger study 45/45 78 53 Not reevaluated >88 (estimated) Long-term: low 

OR, overall response.

*

Median increase in responders.

Details provided in article text.

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