Literature DB >> 22707405

Ten-year survival after autologous stem cell transplantation for immunoglobulin light chain amyloidosis.

Stefan Cordes1, Angela Dispenzieri, Martha Q Lacy, Suzanne R Hayman, Francis K Buadi, David Dingli, Shaji K Kumar, William J Hogan, Morie A Gertz.   

Abstract

BACKGROUND: The current study was conducted to determine characteristics distinguishing the 10-year survivor group in patients with systemic immunoglobulin light chain (AL) amyloidosis who underwent autologous stem cell transplantation (SCT).
METHODS: The study group included all 74 patients with AL amyloidosis who underwent high-dose melphalan treatment supported by autologous SCT since the beginning of the Mayo Clinic's SCT program until prior to August 2001.
RESULTS: A total of 32 patients (43%) patients survived for > 10 years. Statistically significant baseline differences in the 10-year survivor group included: 1) the number of organs involved; 2) septal thickness; 3) total cholesterol; and 4) urine total protein. The number of organs involved was the only predictor found on multivariable analysis. Depth of the response to therapy, as measured by the lowest posttransplantation serum free light chain level, was found to be the most significant indicator of durability of response.
CONCLUSIONS: Autologous SCT can offer durable benefit for patients with AL amyloidosis. The number of organs involved offers the greatest pretreatment prognostic value, whereas the lowest posttransplantation serum free light chain level offers the best posttreatment prognostic value.
Copyright © 2012 American Cancer Society.

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Year:  2012        PMID: 22707405     DOI: 10.1002/cncr.27660

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  13 in total

1.  Extended follow up of high-dose melphalan and autologous stem cell transplantation after vincristine, doxorubicin, dexamethasone induction in amyloid light chain amyloidosis of the prospective phase II HOVON-41 study by the Dutch-Belgian Co-operative Trial Group for Hematology Oncology.

Authors:  Bouke P C Hazenberg; Alexandra Croockewit; Bronno van der Holt; Sonja Zweegman; Gerard M J Bos; Michel Delforge; Reinier A P Raymakers; Pieter Sonneveld; Edo Vellenga; Pierre W Wijermans; Peter A von dem Borne; Marinus H van Oers; Okke de Weerdt; Fokje M Spoelstra; Henk M Lokhorst
Journal:  Haematologica       Date:  2015-02-06       Impact factor: 9.941

2.  Revisiting conditioning dose in newly diagnosed light chain amyloidosis undergoing frontline autologous stem cell transplant: impact on response and survival.

Authors:  N Tandon; E Muchtar; S Sidana; A Dispenzieri; M Q Lacy; D Dingli; F K Buadi; S R Hayman; R Chakraborty; W J Hogan; W Gonsalves; R Warsame; T V Kourelis; N Leung; P Kapoor; S K Kumar; M A Gertz
Journal:  Bone Marrow Transplant       Date:  2017-04-10       Impact factor: 5.483

3.  Stringent patient selection improves outcomes in systemic light-chain amyloidosis after autologous stem cell transplantation in the upfront and relapsed setting.

Authors:  Christopher P Venner; Julian D Gillmore; Sajitha Sachchithanantham; Shameem Mahmood; Thirusha Lane; Darren Foard; Murielle Roussel; Lisa Rannigan; Simon Dj Gibbs; Jennifer H Pinney; Carol J Whelan; Helen J Lachmann; Philip N Hawkins; Ashutosh D Wechalekar
Journal:  Haematologica       Date:  2014-09-05       Impact factor: 9.941

4.  A matched comparison of cyclophosphamide, bortezomib and dexamethasone (CVD) versus risk-adapted cyclophosphamide, thalidomide and dexamethasone (CTD) in AL amyloidosis.

Authors:  C P Venner; J D Gillmore; S Sachchithanantham; S Mahmood; T Lane; D Foard; L Rannigan; S D J Gibbs; J H Pinney; C J Whelan; H J Lachmann; P N Hawkins; A D Wechalekar
Journal:  Leukemia       Date:  2014-07-16       Impact factor: 11.528

Review 5.  Stem Cell Mobilization and Autologous Transplant for Immunoglobulin Light-Chain Amyloidosis.

Authors:  Morie A Gertz; Stefan Schonland
Journal:  Hematol Oncol Clin North Am       Date:  2020-09-12       Impact factor: 3.722

6.  Immunoparesis status in immunoglobulin light chain amyloidosis at diagnosis affects response and survival by regimen type.

Authors:  Eli Muchtar; Angela Dispenzieri; Shaji K Kumar; David Dingli; Martha Q Lacy; Francis K Buadi; Suzanne R Hayman; Prashant Kapoor; Nelson Leung; Rajshekhar Chakraborty; Stephen Russell; John A Lust; Yi Lin; Ronald S Go; Steven Zeldenrust; Robert A Kyle; S Vincent Rajkumar; Morie A Gertz
Journal:  Haematologica       Date:  2016-06-16       Impact factor: 9.941

Review 7.  Daratumumab for the treatment of AL amyloidosis.

Authors:  M Hasib Sidiqi; Morie A Gertz
Journal:  Leuk Lymphoma       Date:  2018-07-22

Review 8.  Heart transplantation in cardiac amyloidosis.

Authors:  Matthew Sousa; Gregory Monohan; Navin Rajagopalan; Alla Grigorian; Maya Guglin
Journal:  Heart Fail Rev       Date:  2017-05       Impact factor: 4.214

9.  Coexistent multiple myeloma or increased bone marrow plasma cells define equally high-risk populations in patients with immunoglobulin light chain amyloidosis.

Authors:  Taxiarchis V Kourelis; Shaji K Kumar; Morie A Gertz; Martha Q Lacy; Francis K Buadi; Suzanne R Hayman; Steven Zeldenrust; Nelson Leung; Robert A Kyle; Stephen Russell; David Dingli; John A Lust; Yi Lin; Prashant Kapoor; S Vincent Rajkumar; Arleigh McCurdy; Angela Dispenzieri
Journal:  J Clin Oncol       Date:  2013-10-21       Impact factor: 44.544

Review 10.  Immunoglobulin light chain amyloidosis diagnosis and treatment algorithm 2021.

Authors:  M Hasib Sidiqi; Morie A Gertz
Journal:  Blood Cancer J       Date:  2021-05-15       Impact factor: 11.037

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