Table 2 Prespecified subgroup analysis of progression-free survival.

From: Lenalidomide and dexamethasone with or without clarithromycin in patients with multiple myeloma ineligible for autologous transplant: a randomized trial

Subgroup

Clarithromycin Group

Control Group

Clarithromycin Group

Control Group

Hazard ratio (95% CI)

 

no. of progression events or deaths/total no.

median progression-free survival (mo)

  

Sex

 Male

37/71

32/64

23

26

1.24 (0.77–1.98)

 Female

33/71

29/79

35

39

1.38 (0.84–2.27)

Age

 <75yr

26/64

26/59

NR

33

1.02 (0.59–1.75)

 ≥75yr

44/78

35/84

19

28

1.56 (1.00–2.42)

ISS

 I

10/36

11/33

NR

33

0.90 (0.38–2.13)

 II

32/52

31/59

15

25

1.35 (0.82–2.20)

 III

28/54

19/51

17

NR

1.67 (0.94–2.98)

Baseline creatinine clearance

 >60 ml/min

63/131

56/132

23

29

View full size image

1.29 (0.90–1.84)

 ≤60 ml/min

7/11

5/11

9

NR

1.65 (0.52–5.20)

Type of MM

 IgG

29/74

32/84

35

39

1.06 (0.64–1.74)

 Non-IgG

41/68

29/59

16

28

1.50 (0.93–2.40)

Cytogenetic profile

 High risk

17/25

9/22

12

NR

2.16 (0.96–4.86)

 Standard risk

48/106

43/108

27

33

1.22 (0.81–1.84)

ECOG score

 0

11/32

18/41

39

33

0.60 (0.28–1.27)

 1

30/64

22/61

26

NR

1.36 (0.79–2.36)

 ≥2

29/46

21/41

11

29

1.99 (1.13–3.51)

R-ISS

 I

3/15

6/17

NR

29

0.68 (0.17–2.74)

 II

42/79

36/83

23

29

1.21 (0.77–1.88)

 III

16/23

5/18

7

NR

3.89 (1.41–10.7)

     

 
  1. Shown are the results of an analysis of progression-free survival in prespecified subgroups of the intention-to-treat population that were defined according to baseline characteristics. The experimental group was treated with clarithromycin, lenalidomide and dexamethasone; the control group received lenalidomide and dexamethasone. The International Staging System (ISS) has three stages defined as follows: I (serum β2-microglobulin level < 3.5 mg/L and albumin level ≥ 3.5 g/dL; stage II, neither stage I nor III; and stage III serum β2-microglobulin level ≥ 5.5 mg/L. A high-risk cytogenetic profile was defined by a funding of t(4;14), t(14;16), or del17p on fluorescence in situ hybridization testing. The R-ISS is obtained on the basis of the combination of ISS, chromosomal abnormalities (CA) detected by interphase fluorescent in situ hybridization after CD138 plasma cell purification and serum lactate dehydrogenase (LDH). R-ISS I includes ISS stage I, no high-risk CA [del(17p) and/or t(4;14) and/or t(14;16)], and normal LDH level (less than the upper limit of normal range); R-ISS III including ISS stage III and high-risk CA or high LDH level; and R-ISS II, including all other possible combinations. Eastern Cooperative Oncology Group (ECOG) performance status is scored on a scale from 0 to 5, with higher scores indicating increasing disability.