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Amyloid
The Journal of Protein Folding Disorders
Volume 25, 2018 - Issue 4
323
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Original Article

Efficacy of lenalidomide as salvage therapy for patients with AL amyloidosis

ORCID Icon, ORCID Icon, , , , , , , , , , , , , , , , & ORCID Icon show all
Pages 234-241 | Received 01 Jul 2018, Accepted 18 Oct 2018, Published online: 20 Jan 2019
 

Abstract

We retrospectively evaluated 55 consecutive patients who received at least one dose of lenalidomide for relapsed/refractory AL amyloidosis. Their median age was 63 years; 72% had heart and 75% kidney involvement and 13% were on dialysis; while 20%, 46% and 34% had Mayo stage -1, -2 and -3 disease, respectively. Median time from start of primary therapy to lenalidomide was 15 months (range 2–100) and median number of prior therapies was 1 (range 1–4); 73% of the patients had prior bortezomib and 42% were bortezomib-refractory. On intent to treat, haematologic response rate was 51% (5.5% CRs, 20% VGPRs) and was 56% versus 40% for patients with and without prior bortezomib and 47% versus 62.5% for bortezomib refractory versus non-refractory patients (p = .351). Organ response was achieved by 16% of evaluable patients (22% renal, 7% liver and 3% cardiac); however, 10 (21%) patients progressed to dialysis. Median survival post lenalidomide was 25 months. Bortezomib-refractory patients had worse outcome (median survival of 10.5 versus 25 months for bortezomib-sensitive patients versus not reached for bortezomib-naive patients, p = .011). Median lenalidomide dose was 10 mg and no patient received the 25 mg dose; however, in 60% a dose reduction was required. Median duration of lenalidomide therapy was 7.2 months and 46% discontinued lenalidomide before completion of planned therapy, mainly due to toxicity (26%) or disease progression/no response (13%). We conclude that although lenalidomide is a major salvage option for patients with relapsed/refractory AL amyloidosis, its toxicity in patients with AL amyloidosis is significant and doses should be adjusted for optimal tolerability.

Disclosure statement

EK has received honoraria form Amgen, Genesis Pharma, Janssen, Prothena and Takeda, ET has received honoraria form Amgen, Genesis Pharma, Janssen and Takeda MAD has received honoraria form Amgen, BMS, Celgene, Janssen and Takeda

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