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Table 2 Modeling on risk of progression on ibrutinib

From: Predictive factors and outcomes for ibrutinib in relapsed/refractory marginal zone lymphoma: a multicenter cohort study

Variable

PP versus CR/PR

SD versus CR/PR

RR

95% CI

p value

RR

95% CI

p value

Age at diagnosis

1.02

0.96–1.08

0.61

0.99

0.96–1.03

0.65

Gender

 Male

Referent

     

 Female

1.05

0.34–3.22

0.93

1.22

0.54–2.78

0.63

BMI

  < 30

Referent

     

  ≥ 30

0.95

0.22–4.04

0.94

1.14

0.43–3.01

0.79

ECOG PS at diagnosis

 0

Referent

     

 1

0.39

0.10–1.46

0.16

0.66

0.25–1.73

0.40

  ≥ 2

1.04

0.09–11.61

0.97

1.28

0.19–8.75

0.80

MZL subtype

 NMZL

Referent

     

 SMZL

1.32

0.31–5.63

0.71

0.78

0.27–2.19

0.63

 EMZL

1.40

0.38–5.20

0.61

0.69

0.26–1.79

0.44

Stage at diagnosis

 1–2

Referent

     

 3–4

1.18

0.23–6.06

0.84

0.92

0.31–2.75

0.88

B symptoms at diagnosis

 No

Referent

     

 Yes

0.58

0.15–2.30

0.44

0.65

0.24–1.76

0.40

LDH higher than institutional baseline

 No

Referent

     

 Yes

1.37

0.35–5.28

0.65

0.84

0.30–2.33

0.73

Monoclonal protein at diagnosis

 No

Referent

     

 Yes

3.46

0.64–18.84

0.15

0.41

0.14–1.19

0.10

BM involvement at diagnosis

 No

Referent

     

 Yes

0.60

0.16–2.15

0.43

0.85

0.33–2.20

0.74

TP53 mutation/17p deletion

 No

      

 Yes

0.76

0.08–7.25

0.81

0.81

0.15–4.48

0.81

Complex cytogenetics

 No

      

 Yes

4.63

0.81–26.35

0.08

1.63

0.32–8.21

0.55

Primary refractory disease*

 No

      

 Yes

3.77

1.15–12.33

0.03

1.72

0.66–4.47

0.26

Line of ibrutinib therapy

 Second line

      

 Third line

0.82

0.23–2.90

0.76

0.65

0.24–1.70

0.38

 Fourth line and beyond

1.21

0.26–5.54

0.81

1.76

0.62–5.04

0.29

  1. CR complete response, PR partial response, SD stable disease, PD progressive disease, BMI body mass index, ECOG PS Eastern Cooperative Oncology Group performance status, MZL marginal zone lymphoma, LDH lactate dehydrogenase, BM bone marrow
  2. *Primary refractory disease: defined as progression of disease at the end of induction therapy or within 6 months of treatment completion