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. Author manuscript; available in PMC: 2013 Sep 20.
Published in final edited form as: Sci Transl Med. 2013 Mar 20;5(177):177ra38. doi: 10.1126/scitranslmed.3005930

Table 1. Patient Characteristics and Response Summary.

Cy indicates cyclophosphamide; Vinc, vincristine; Pred, prednisone; Etop, Etoposide; Peg, pegylated asparaginase; Mito, mitoxantrone; CR1, first complete remission; MRD, minimal residual disease as assessed by deep sequencing (see Supplemental Data); Allo-SCT, allogeneic stem cell transplant. All patients were treated with cyclophosphamide before T cell infusion, either 1.5 gm/m2 (MSK-ALL04, MSKALL05, MSK-ALL06) or 3.0 gm/m2 (MSK-ALL01, MSK-ALL03).

Patient
ID*
Age FISH/Cyto
genetics
Initial therapy Duration
of CR1
Salvage
therapy
Disease response
to Salvage
therapy**
Disease
Response
Steroids Outcome
MSK-
ALL01
66 Normal
karyotype
Mito/Cy →
Vinc/Pred →
Cy→ Etop/Cy
27 weeks Vinc/Pred/Peg MRD+ MRD− N Allo-SCT
MSK-
ALL03
56 Normal
karyotype
HyperCVAD 45 weeks Inotuzumab
ozogamicin →
Vinc/Pred/Peg
MRD− MRD− N Allo-SCT
MSK-
ALL04
59 t(9;11), 9p21
deletion
ECOG2993(24) 5 weeks Vinc/Pred Refractory disease,
63% blasts in BM
MRD− Y Ineligible for
Allo-SCT,
relapse 90 days
MSK-
ALL05***
58 9p21
deletion
ECOG2993 28 weeks HIDAC/Mito Refractory disease,
70% blasts in BM
MRD− Y Allo-SCT
MSK-
ALL06
23 Normal
karyotype
NYII
ref (25)
34
months
Modified NYII
Consolidation I
ref (25)
MRD+ MRD− N Allo-SCT
*

MSK-ALL02 patient was removed from the study prior to the planned T cell infusion because they deferred T cell infusion for an allo-SCT.

**

Disease status within 1 week of infusion with CD19-targeted T cells

***

This patient’s T cells were harvested while in remission. All other patients listed had their T cells harvested while they had relapsed disease.