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Table 5 Documented treatment-emergent all-grade adverse events in ≥ 10% of patients (safety population)

From: Observational study of lenalidomide in patients with mantle cell lymphoma who relapsed/progressed after or were refractory/intolerant to ibrutinib (MCL-004)

 

L (n = 13)

L + R (n = 11)

L + other (n = 34)

Overall (N = 58)

No.

%

No.

%

No.

%

No.

%

Hematologic

 Anemia

2

15

3

27

5

15

10

17

 Thrombocytopenia

1

8

1

9

7

21

9

16

 Neutropenia

1

8

1

9

6

18

8

14

 Pancytopenia

1

8

3

27

3

9

7

12

 Febrile neutropenia

0

0

0

0

6

18

6

10

Nonhematologic

 Fatigue

4

31

4

36

14

41

22

38

 Nausea

2

15

2

18

7

21

11

19

 Dizziness

2

15

2

18

7

21

11

19

 Dyspnea

2

15

3

27

6

18

11

19

 Peripheral edema

0

0

2

18

9

26

11

19

 Rash

2

15

1

9

7

21

10

17

 Cough

1

8

3

27

7

21

11

19

 Decreased appetite

2

15

0

0

5

15

7

12

 Diarrhea

0

0

1

9

7

21

8

14

 Headache

3

23

1

9

2

6

6

10

 Pyrexia

1

8

0

0

5

15

6

10

 Vomiting

0

0

2

18

4

12

6

10

 Constipation

0

0

0

0

6

18

6

10

Laboratory investigations

 Platelet count decreased

2

15

1

9

3

9

6

10

 White blood cell count decreased

1

8

1

9

4

12

6

10

  1. L lenalidomide, L + R lenalidomide plus rituximab