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Table 1 Patients’ clinical characteristics and treatment response

From: Semi-quantitative measurements of chemokine receptor 4-targeted 68Ga-pentixafor PET/CT in response assessment of Waldenström macroglobulinemia/lymphoplasmacytic lymphoma

Patient

Age/sex

ISS-WM*

M-protein type

IgM (g/L)

M-protein (g/L)

β2-MG (mg/L)

Involvement at baseline

Chemotherapy regimensa (cycles)

Clinical response

1

61/M

Intermediate

IgMκ

30.49

18.5

6.13

BM, LN, PMD, nerve root

R-FC(5) + R-DC(1)

CR

2

72/M

High

IgMκ

5.78

2.1

8.93

BM, LN

DRC(7)

PR

3

72/M

Intermediate

IgMλ

15.2

10.5

3.27

BM

DRC(6)

VGPR

4

64/M

Intermediate

IgMλ

23.69

10.6

5.71

BM, LN

BRD(6)

CR

5

64/M

Intermediate

IgMκ

53.3

32.5

5.27

BM, LN

DRC(8)

VGPR

6

48/F

N/A

IgDκ

6.67(IgD)

6.67

N/A

BM, LN

DRC(6)

PR

7

55/F

Low

IgMκ

82.49

35.6

2.93

BM, LN

DRC(1) + BRD(4) + BD(1)

PR

8

52/F

Intermediate

IgMκ

38.13

21.6

3.34

BM, spleen

DRC(6)

PR

9

58/M

Intermediate

IgMκ

43.48

27.9

12.6

BM, LN, liver, pancreas, PMD

R2(5)

PR

10

48/M

Intermediate

IgMλ

50.9

32.5

6

BM, LN, liver, PMD

DRC(6)

PD

11

62/M

High

IgMκ

33.42

23.7

6

BM, LN

DRC(4)

VGPR

12

76/M

High

IgMλ

96.02

62.8

3.6

BM, LN

BRD(8)

PR

13

53/M

Intermediate

IgMλ

79.89

56.5

3.5

BM, LN, spleen

Chlorambucil(2) + BCD(5)

MR

14

64/M

Intermediate

IgMλ

52.73

30.6

5.9

BM, LN

BRD(4) + DRC(2)

PR

15

64/M

Intermediate

IgMκ

7.57

3.6

3.5

BM

Chlorambucil(5)

PD

  1. β2-MG β2-microglobulin, BM bone marrow, LN lymph node, PMD paramedullary disease
  2. *International Staging System for WM (ISS-WM) prognostic scoring includes age of > 65 y, ß2-microglobulin level of > 3 mg/L, hemoglobin level of ≤ 11.5 g/dL, platelet count of ≤ 100 × 109/L, and IgM level of > 7 g/dL
  3. Serum IgD level was measured as IgD-type M-protein level
  4. CR complete response, VGPR very good partial response, PR partial response, MR minimal response, SD stable disease, PD progressive disease
  5. aR rituximab, D dexamethasone, C cyclophosphamide, B bortezomib, F fludarabine, R2 lenalidomide plus rituximab