Table 1 Characteristics of the studies about panobinostat combined with other agents for patients with relapsed/refractory multiple myeloma.

From: Efficacy and Safety of Panobinostat in Relapsed or/and Refractory Multiple Myeloma: Meta Analyses of Clinical Trials and Systematic Review

Study

Year

Study design

Total No.

Female/Male (n)

Mean age (y)

ISS stage:1/2/3/unknown

Dose of panobinostat

Combined agents

ORR

Chari

2015

phase II

20

64

20 mg

Len&DXM

0.45

Berdeja

2015

phase I/II

42

25/17

66

20/14/5/5

20–30 mg

CFZ

0.67

San-Miguel

2014

phase III

387

185/202

63

156/104/77/50

20 mg

BTZ&DXM

0.61

Mangiacavalli

2014

phase II

15

20 mg

BTZ&DXM

0.67

Kaufman

2014

phase I

20

64.5

15–20 mg

CFZ

0.50

Berenson

2014

phase I/II

40

15/25

65.4

10–20 mg

Mel

0.09

San-Miguel

2013

phase Ib

62

19/43

62

25/15/20/2

10–20 mg

BTZ&DXM

0.52

Richardson

2013

phase II

55

26/29

61

18/23/13/1

20 mg

BTZ&DXM

0.35

Zangari

2012

phase I

11

58

5–15 mg

BTZ

0.36

Shah

2012

phase Ib

17

6/11

62

15 mg

CFZ

0.35

Offidani

2012

phase II

31

15/16

68

17/10/4/0

10–20 mg

Mel&PED&Tha

0.39

  1. ISS, International Staging System; Len, lenalidomide; BTZ, bortezomib; DXM, dexamethasone; CFZ, carfilzomib; Mel, melphalan; PED, prednisone; Tha, thalidomide.