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Salvage therapy with lenalidomide and dexamethasone in patients with advanced AL amyloidosis refractory to melphalan, bortezomib, and thalidomide

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Abstract

The increasing number of effective agents allows rescue therapy of patients with light-chain (AL) amyloidosis refractory to ≥2 previous treatments. Lenalidomide is effective in this disease and its toxicity profile encourages its use in salvage regimens. All the patients with AL amyloidosis refractory to both melphalan and bortezomib referred to our center between July 2007 and July 2009 were treated with the combination of lenalidomide and dexamethasone. Twenty-four consecutive patients were enrolled. Seventy-nine percent were also refractory to thalidomide. Two patients died before evaluation of response, and 50% experienced severe adverse events. Survival was significantly shorter in subjects with troponin I >0.1 ng/mL and in patients diagnosed <18 months before treatment initiation. Hematologic response was observed in 41% of patients and prolonged survival (median 10 months vs. not reached, P = 0.005) independently from troponin I concentration and from pre-treatment disease duration. Salvage therapy beyond second line of treatment can improve survival in AL amyloidosis and lenalidomide plus dexamethasone is a valuable option in this setting.

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References

  1. Merlini G, Stone M (2006) Dangerous small B-cell clones. Blood 108:2520–2530

    Article  PubMed  CAS  Google Scholar 

  2. Palladini G, Lavatelli F, Russo P et al (2006) Circulating amyloidogenic free light chains and serum N-terminal natriuretic peptide type B decrease simultaneously in association with improvement of survival in AL. Blood 107:3854–3858

    Article  PubMed  CAS  Google Scholar 

  3. Palladini G, Merlini G (2011) Transplantation vs. conventional-dose therapy for amyloidosis. Curr Opin Oncol 23:214–220

    Article  PubMed  CAS  Google Scholar 

  4. Dispenzieri A, Lacy M, Zeldenrust S et al (2007) The activity of lenalidomide with or without dexamethasone in patients with primary systemic amyloidosis. Blood 109:465–470

    Article  PubMed  CAS  Google Scholar 

  5. Sanchorawala V, Wright D, Rosenzweig M et al (2007) Lenalidomide and dexamethasone in the treatment of AL amyloidosis: results of a phase 2 trial. Blood 109:492–496

    Article  PubMed  CAS  Google Scholar 

  6. Moreau P, Jaccard A, Benboubker L et al. (2010) Lenalidomide in combination with melphalan and dexamethasone in patients with newly diagnosed AL amyloidosis: a multicenter phase 1/2 dose-escalation study. Blood 116:4777–4782.

    Article  PubMed  CAS  Google Scholar 

  7. Gertz M, Comenzo R, Falk R et al (2005) Definition of organ involvement and treatment response in immunoglobulin light chain amyloidosis (AL): a consensus opinion from the 10th International Symposium on Amyloid and Amyloidosis, Tours, France, 18–22 April 2004. Am J Hematol 79:319–328

    Article  PubMed  Google Scholar 

  8. Palladini G, Barassi A, Klersy C et al (2010) The combination of high-sensitivity cardiac troponin T (hs-cTnT) at presentation and changes in N-terminal natriuretic peptide type B (NT-proBNP) after chemotherapy best predicts survival in AL amyloidosis. Blood 116:3426–3430

    Article  PubMed  CAS  Google Scholar 

  9. Palladini G, Russo P, Zenone Bragotti L et al (2009) A phase II trial of cyclophosphamide, lenalidomide and dexamethasone (CLD) in previously treated patients with AL amyloidosis. Blood 114:1117–1118 [ASH annu Meet Abstr]

    Google Scholar 

  10. Gibbs S, De Cruz M, Sattianayagam P et al (2009) Transient post chemotherapy rise in NT Pro-BNP in AL amyloidosis: implications for organ response assessment. Blood 114:712 [ASH annu Meet Abstr]

    Google Scholar 

  11. Dispenzieri A, Dingli D, Kumar S et al (2010) Discordance between serum cardiac biomarker and immunoglobulin-free light-chain response in patients with immunoglobulin light-chain amyloidosis treated with immune modulatory drugs. Am J Hematol 85:757–759

    Article  PubMed  CAS  Google Scholar 

  12. Tapan U, Seldin DC, Finn KT et al (2010) Increases in B-type natriuretic peptide (BNP) during treatment with lenalidomide in AL amyloidosis. Blood 116:5071–5072

    Article  PubMed  CAS  Google Scholar 

  13. Specter R, Sanchorawala V, Seldin DC et al (2011) Kidney dysfunction during lenalidomide treatment for AL amyloidosis. Nephrol Dial Transplant 26:881–886

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

The authors would like to thank Dr. Leda Roggeri for the data management.

Funding

This work was supported by grants from the, Ministry of Health (Ricerca Finalizzata Malattie Rare), “Istituto Superiore di Sanità” (526D/63); Ministry of Research and University (2007AESFX2_003); and “Associazione Italiana per la Ricerca sul Cancro” Program “Harnessing tumor cell/microenvironment cross talk to treat mature B cell tumors”.

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Correspondence to Giampaolo Merlini.

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Palladini, G., Russo, P., Foli, A. et al. Salvage therapy with lenalidomide and dexamethasone in patients with advanced AL amyloidosis refractory to melphalan, bortezomib, and thalidomide. Ann Hematol 91, 89–92 (2012). https://doi.org/10.1007/s00277-011-1244-x

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  • DOI: https://doi.org/10.1007/s00277-011-1244-x

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