Table 2 Patient characteristics during combined imatinib/IFN-α therapy

From: Efficacy and safety of imatinib mesylate (Glivec™) in combination with interferon-α (IFN-α) in Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL)

Patient

Disease status at IFN-α start

Interval imatinib start to IFN-α addition (months)

DFS (mo.) since imatinib start

Site of relapse

Relapse therapy

Duration of combination (months)

OS (mo.) since imatinib start

Outcome

1

MRD+

3.4

21.4+

18+

21.4+

Ongoing CHR, MRD decline

2

MRD+

4.8

20.81+

16+

20.8+

Ongoing CHR, MRD−

3

MRD+

3.5

9

Isolated CNS relapse

i.t. therapy, CNS-irr., imatinib+IFN-α

17+*

20.5+

Ongoing CHR, MRD−

4

MRD+

3.8

6.4

Isolated CNS relapse

i.t. therapy, CNS-irr., imatinib+IFN-α

15.3+**

19.1+

Ongoing CMR, MRD−

5

MRD+

4

5

BM relapse

6-MP, MTX, imatinib

1

10.5

Dead

6

Refractory first relapse, imatinib failure

0.5

5.4

BM relapse

Second auto-SCT, MUD-SCT

5

14.3

Dead

Median (range)

 

3.7 (0.5–4.8)

8 (5–21.4+)

  

15.7 (1–18+)

20 (10.5–21.4+)

 
  1. MRD=minimal residual disease by TaqMan-PCR; DFS=disease-free survival calculated from start of imatinib; CMR=complete marrow response; CHR=complete hematologic response; +=ongoing; *=4 weeks interruption; **=2 weeks interruption; OS=overall survival.