Table 4

Subsequent therapies for AL amyloidosis

Subsequent therapy for AL, n (%)*Bortezomib dose groupsTotal (n = 70)
1.6 mg/m2 QW (n = 18)1.3 mg/m2 BIW (n = 34)Lower doses QW/BIW (n = 18)
Any subsequent therapy for AL 7 (39) 21 (62) 12 (67) 40 (57) 
Median (95% CI) time to subsequent therapy, months 50.1 (11.4-NE) 17.2 (12.7-30.4) 29.0 (13.9-45.4) 22.7 (16.9-40.6) 
Agents received in any subsequent line     
 Dexamethasone 6 (33) 13 (38) 9 (50) 28 (40) 
 Bortezomib 5 (28) 10 (29) 4 (22) 19 (27) 
 Lenalidomide 2 (11) 9 (26) 7 (39) 18 (26) 
 Cyclophosphamide 4 (22) 3 (9) 2 (11) 9 (13) 
 Melphalan 2 (11) 3 (9) 3 (17) 8 (11) 
 Thalidomide 3 (17) 1 (3) 3 (17) 7 (10) 
 Prednisone 1 (6) 3 (9) 4 (6) 
 Investigational drug 2 (6) 1 (6) 3 (4) 
 Bendamustine 1 (6) 1 (3) 2 (3) 
 Cisplatin 1 (6) 1 (3) 2 (3) 
 Doxorubicin 1 (6) 1 (3) 2 (3) 
 Etoposide 1 (6) 1 (3) 2 (3) 
 HDM-SCT 2 (11) 2 (3) 
Subsequent therapy for AL, n (%)*Bortezomib dose groupsTotal (n = 70)
1.6 mg/m2 QW (n = 18)1.3 mg/m2 BIW (n = 34)Lower doses QW/BIW (n = 18)
Any subsequent therapy for AL 7 (39) 21 (62) 12 (67) 40 (57) 
Median (95% CI) time to subsequent therapy, months 50.1 (11.4-NE) 17.2 (12.7-30.4) 29.0 (13.9-45.4) 22.7 (16.9-40.6) 
Agents received in any subsequent line     
 Dexamethasone 6 (33) 13 (38) 9 (50) 28 (40) 
 Bortezomib 5 (28) 10 (29) 4 (22) 19 (27) 
 Lenalidomide 2 (11) 9 (26) 7 (39) 18 (26) 
 Cyclophosphamide 4 (22) 3 (9) 2 (11) 9 (13) 
 Melphalan 2 (11) 3 (9) 3 (17) 8 (11) 
 Thalidomide 3 (17) 1 (3) 3 (17) 7 (10) 
 Prednisone 1 (6) 3 (9) 4 (6) 
 Investigational drug 2 (6) 1 (6) 3 (4) 
 Bendamustine 1 (6) 1 (3) 2 (3) 
 Cisplatin 1 (6) 1 (3) 2 (3) 
 Doxorubicin 1 (6) 1 (3) 2 (3) 
 Etoposide 1 (6) 1 (3) 2 (3) 
 HDM-SCT 2 (11) 2 (3) 
*

Therapies listed are not mutually exclusive; patients could have received >1 agent or combination of agents.

27 patients with subsequent therapy had discontinued initial bortezomib treatment in CAN2007 prior to disease progression.

Patients received their first HDM-SCT as a subsequent therapy.

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