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. 2015 Oct 26;127(1):17–28. doi: 10.1182/blood-2015-07-657981

Table 1.

Baseline characteristics, prior treatment outcomes, and sirolimus response in ALPS patients.

Response
3 mo 6 mo 12 mo
Disorder Lineage cytopenia Lymphoproliferative disease Prior therapy Heme Lymphoproliferation Heme Lymphoproliferation Heme Lymphoproliferation Time on sirolimus
ALPS-FAS A+N+T Massive LAD splenomegaly Corticosteroid (RT) CR CR CR CR CR CR 8 y
IVIgG (PR)
MMF (NR)
Rituximab (RT)
ALPS-FAS T+N Massive LAD splenomegaly Corticosteroid (RT) CR CR* CR CR* CR CR* 6 y
MMF (NR)
ALPS-FAS A+N+T Massive LAD splenomegaly Corticosteroid (RT) CR* CR* CR* CR* CR* CR* 4.5 y
IVIgG (NR)
MMF (PR)
Rituximab (VTR)
ALPS-FAS A+N+T Massive LAD splenomegaly Corticosteroid (RT) CR CR CR CR CR CR 3 y
IVIgG (NR)
MMF (PR)
Rituximab (PR)
ALPS-FAS A+N+T Marked LAD splenomegaly Corticosteroid (NR) CR* CR* CR* CR* CR* CR* 2 y
IVIgG (NR)
G-CSF (NR)
ALPS-FAS A+T Marked splenomegaly Corticosteroid (RT) PR CR PR CR CR CR 1.5 y
IVIgG (RT)
ALPS-sFAS A+N+T Massive LAD and splenomegaly Corticosteroids (RT) CR CR CR CR CR CR 4.5 y
MMF (PR)
VCR (NR)
Pyrimethamine (NR)
ALPS-sFAS A+N+T Mild LAD and splenomegaly Corticosteroid (NR) CR CR CR CR CR CR 4 y
IVIgG (NR)
MMF (NR)
G-CSF (NR)
ALPS-sFAS A+N+T Massive LAD and splenomegaly Corticosteroid (RT) CR CR* CR CR CR CR 4 y
Depakote (PR)
ALPS-U A+N+T Massive LAD and splenomegaly Corticosteroid (RT) CR CR CR CR CR CR 3 y
IVIgG (NR)
MMF (PR)
6-MP (NR)
Methotrexate (NR)
ALPS-U A+N+T Massive LAD and splenomegaly Corticosteroid (NR) CR CR CR CR CR CR 3 y
IVIgG (NR)
ALPS-U A+N+T Lymphadenopathy Corticosteroid (RT) CR CR CR CR CR CR 3 y
IVIgG (PR)

A, anemia; G-CSF, granulocyte colony-stimulating factor; LAD, lymphadenopathy; N, neutropenia; 6-MP, mercaptopurine; T, thrombocytopenia; VCR, vincristine; VTR, very transient response. Prior therapy responses are listed in parentheses: CR, responds but toxicity (RT), PR, PR but relapse (PR-R), and no response (NR).

*

Designate the patients who remain in a durable CR but have occasional, mild, transient disease flares, manifested as dropping blood counts or the development of lymphadenopathy with viral illness. These “flares” are mild and do not require the use of additional immune suppression, as they self-resolve following the resolution of the infection