Hepatic response after high-dose melphalan and stem cell transplantation in patients with AL amyloidosis associated liver disease

1 Department of Medicine 2 Stem Cell Transplantation Program of the Section of Hematology-Oncology and 3 Amyloid Treatment and Research Program, Department of Medicine; 4 Department of Pathology and Laboratory Medicine, Boston University School of Medicine and 5 Department of Biostatistics, Boston U...

Full description

Saved in:
Bibliographic Details
Published inHaematologica (Roma) Vol. 94; no. 7; pp. 1029 - 1032
Main Authors Girnius, Saulius, Seldin, David C, Skinner, Martha, Finn, Kathleen T, Quillen, Karen, Doros, Gheorghe, Sanchorawala, Vaishali
Format Journal Article
LanguageEnglish
Published Pavia Ferrata Storti Foundation 01.07.2009
Subjects
Online AccessGet full text
ISSN0390-6078
1592-8721
1592-8721
DOI10.3324/haematol.2008.001925

Cover

Abstract 1 Department of Medicine 2 Stem Cell Transplantation Program of the Section of Hematology-Oncology and 3 Amyloid Treatment and Research Program, Department of Medicine; 4 Department of Pathology and Laboratory Medicine, Boston University School of Medicine and 5 Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA Correspondence: Vaishali Sanchorawala, MD, Section of Hematology/Oncology, FGH 1007, 820 Harrison Avenue, Boston, MA 02118, USA. E-mail: vaishali.sanchorawala{at}bmc.org High-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation has been shown to result in durable hematologic response and prolonged overall survival in systemic AL amyloidosis. In this retrospective study, we evaluated clinical and hematologic responses in 69 patients with predominant liver involvement who were treated with high-dose intravenous melphalan and autologous stem cell transplantation from 1998 to 2006. Nine patients (13%) died from treatment-related mortality, similar to patients without hepatic involvement. The overall survival was 81% at one year and 61% at five years, by Kaplan-Meier estimates. A hematologic complete response was achieved by 53% (31/58) of patients at one year. A hepatic response occurred in 57% (33/58) at one year after high-dose intravenous melphalan and autologous stem cell transplantation and 63% (19/30) at two years after high-dose intravenous melphalan and autologous stem cell transplantation. In conclusion, hepatic disease improves in almost 2/3 patients treated with high-dose intravenous melphalan and autologous stem cell transplantation who have a complete or partial hematologic response to treatment. Key words: AL amyloidosis, stem cell transplantation, liver disease.
AbstractList In patients with AL amyloidosis and liver involvement, treatment with high-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation resulted in 61% overall survival at 5 years. Moreover, the transplant-related mortality (13%) was similar to that of patients with AL amyloidosis without associated liver disease. High-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation has been shown to result in durable hematologic response and prolonged overall survival in systemic AL amyloidosis. In this retrospective study, we evaluated clinical and hematologic responses in 69 patients with predominant liver involvement who were treated with high-dose intravenous melphalan and autologous stem cell transplantation from 1998 to 2006. Nine patients (13%) died from treatment-related mortality, similar to patients without hepatic involvement. The overall survival was 81% at one year and 61% at five years, by Kaplan-Meier estimates. A hematologic complete response was achieved by 53% (31/58) of patients at one year. A hepatic response occurred in 57% (33/58) at one year after high-dose intravenous melphalan and autologous stem cell transplantation and 63% (19/30) at two years after high-dose intravenous melphalan and autologous stem cell transplantation. In conclusion, hepatic disease improves in almost 2/3 patients treated with high-dose intravenous melphalan and autologous stem cell transplantation who have a complete or partial hematologic response to treatment.
High-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation has been shown to result in durable hematologic response and prolonged overall survival in systemic AL amyloidosis. In this retrospective study, we evaluated clinical and hematologic responses in 69 patients with predominant liver involvement who were treated with high-dose intravenous melphalan and autologous stem cell transplantation from 1998 to 2006. Nine patients (13%) died from treatment-related mortality, similar to patients without hepatic involvement. The overall survival was 81% at one year and 61% at five years, by Kaplan-Meier estimates. A hematologic complete response was achieved by 53% (31/58) of patients at one year. A hepatic response occurred in 57% (33/58) at one year after high-dose intravenous melphalan and autologous stem cell transplantation and 63% (19/30) at two years after high-dose intravenous melphalan and autologous stem cell transplantation. In conclusion, hepatic disease improves in almost 2/3 patients treated with high-dose intravenous melphalan and autologous stem cell transplantation who have a complete or partial hematologic response to treatment.
1 Department of Medicine 2 Stem Cell Transplantation Program of the Section of Hematology-Oncology and 3 Amyloid Treatment and Research Program, Department of Medicine; 4 Department of Pathology and Laboratory Medicine, Boston University School of Medicine and 5 Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA Correspondence: Vaishali Sanchorawala, MD, Section of Hematology/Oncology, FGH 1007, 820 Harrison Avenue, Boston, MA 02118, USA. E-mail: vaishali.sanchorawala{at}bmc.org High-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation has been shown to result in durable hematologic response and prolonged overall survival in systemic AL amyloidosis. In this retrospective study, we evaluated clinical and hematologic responses in 69 patients with predominant liver involvement who were treated with high-dose intravenous melphalan and autologous stem cell transplantation from 1998 to 2006. Nine patients (13%) died from treatment-related mortality, similar to patients without hepatic involvement. The overall survival was 81% at one year and 61% at five years, by Kaplan-Meier estimates. A hematologic complete response was achieved by 53% (31/58) of patients at one year. A hepatic response occurred in 57% (33/58) at one year after high-dose intravenous melphalan and autologous stem cell transplantation and 63% (19/30) at two years after high-dose intravenous melphalan and autologous stem cell transplantation. In conclusion, hepatic disease improves in almost 2/3 patients treated with high-dose intravenous melphalan and autologous stem cell transplantation who have a complete or partial hematologic response to treatment. Key words: AL amyloidosis, stem cell transplantation, liver disease.
High-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation has been shown to result in durable hematologic response and prolonged overall survival in systemic AL amyloidosis. In this retrospective study, we evaluated clinical and hematologic responses in 69 patients with predominant liver involvement who were treated with high-dose intravenous melphalan and autologous stem cell transplantation from 1998 to 2006. Nine patients (13%) died from treatment-related mortality, similar to patients without hepatic involvement. The overall survival was 81% at one year and 61% at five years, by Kaplan-Meier estimates. A hematologic complete response was achieved by 53% (31/58) of patients at one year. A hepatic response occurred in 57% (33/58) at one year after high-dose intravenous melphalan and autologous stem cell transplantation and 63% (19/30) at two years after high-dose intravenous melphalan and autologous stem cell transplantation. In conclusion, hepatic disease improves in almost 2/3 patients treated with high-dose intravenous melphalan and autologous stem cell transplantation who have a complete or partial hematologic response to treatment.High-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation has been shown to result in durable hematologic response and prolonged overall survival in systemic AL amyloidosis. In this retrospective study, we evaluated clinical and hematologic responses in 69 patients with predominant liver involvement who were treated with high-dose intravenous melphalan and autologous stem cell transplantation from 1998 to 2006. Nine patients (13%) died from treatment-related mortality, similar to patients without hepatic involvement. The overall survival was 81% at one year and 61% at five years, by Kaplan-Meier estimates. A hematologic complete response was achieved by 53% (31/58) of patients at one year. A hepatic response occurred in 57% (33/58) at one year after high-dose intravenous melphalan and autologous stem cell transplantation and 63% (19/30) at two years after high-dose intravenous melphalan and autologous stem cell transplantation. In conclusion, hepatic disease improves in almost 2/3 patients treated with high-dose intravenous melphalan and autologous stem cell transplantation who have a complete or partial hematologic response to treatment.
Author Finn, Kathleen T
Seldin, David C
Quillen, Karen
Sanchorawala, Vaishali
Girnius, Saulius
Doros, Gheorghe
Skinner, Martha
AuthorAffiliation 2 Stem Cell Transplantation Program of the Section of Hematology-Oncology and
4 Department of Pathology and Laboratory Medicine, Boston University School of Medicine and
3 Amyloid Treatment and Research Program, Department of Medicine
5 Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA
1 Department of Medicine
AuthorAffiliation_xml – name: 3 Amyloid Treatment and Research Program, Department of Medicine
– name: 1 Department of Medicine
– name: 2 Stem Cell Transplantation Program of the Section of Hematology-Oncology and
– name: 4 Department of Pathology and Laboratory Medicine, Boston University School of Medicine and
– name: 5 Department of Biostatistics, Boston University School of Public Health, Boston, MA, USA
Author_xml – sequence: 1
  fullname: Girnius, Saulius
– sequence: 2
  fullname: Seldin, David C
– sequence: 3
  fullname: Skinner, Martha
– sequence: 4
  fullname: Finn, Kathleen T
– sequence: 5
  fullname: Quillen, Karen
– sequence: 6
  fullname: Doros, Gheorghe
– sequence: 7
  fullname: Sanchorawala, Vaishali
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21748784$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/19454500$$D View this record in MEDLINE/PubMed
BookMark eNqFkk1vEzEQhi1URNPAP0DIF7ht8PojXnNAqiqglSJxgbM1sb1ZV971Ym8a9cg_x0vSQrlwsjx-55kZz3uBzoY4OIRe12TFGOXvO3A9TDGsKCHNipBaUfEMLWqhaNVIWp-hBWGKVGsim3N0kfMtIZQoJV-g81pxwQUhC_Tz2o0weYOTy2McssPQTi7hzu-6ysZy710YOwgwYBgszpPrsXEh4CnBkMcSn0p-HLAf8Exyw5TxwU8dvtxg6O9D9AXjM4aco_EwOYuDvyslrM8OsnuJnrcQsnt1Opfo--dP366uq83XLzdXl5vKCMamSgCrW1m6BtkItVWCU0Mpc41YW9a6EmCg1kRIVUvWKlIzIQxXAoBtraSCLdHNkWsj3Oox-R7SvY7g9e9ATDsNqfxEcLoxkppSrFWw5VbUqiHSKuqosdwaygrr45E17re9s6YMnSA8gT59GXynd_FOU0k4Kw0u0bsTIMUfe5cn3fs8fysMLu6zXkvOuZCz8M3flR5LPGywCN6eBJANhLZsxfj8qKO15I1seNHxo86kmHNy7R8U0bOh9IOh9GwofTRUSfvwT5rxx4WXuXz4X_JpytlNB5-czj2EUEah-nA4KK5lAVDFfgFGweL9
CitedBy_id crossref_primary_10_1016_j_jceh_2022_10_011
crossref_primary_10_1016_j_bbmt_2015_04_001
crossref_primary_10_1038_s41375_020_1006_7
crossref_primary_10_1159_000506498
crossref_primary_10_1177_2324709618760079
crossref_primary_10_3109_13506129_2010_543443
crossref_primary_10_1111_bjh_16143
crossref_primary_10_1002_ajh_23242
crossref_primary_10_1080_07853890_2022_2069281
crossref_primary_10_3390_diagnostics14020226
crossref_primary_10_2169_internalmedicine_2864_19
crossref_primary_10_1111_pin_13041
crossref_primary_10_1136_bcr_2019_231563
crossref_primary_10_1038_s41572_018_0034_3
crossref_primary_10_1016_j_hoc_2014_08_013
crossref_primary_10_1016_S1665_2681_19_31450_4
ContentType Journal Article
Copyright 2009 INIST-CNRS
Copyright© Ferrata Storti Foundation
Copyright_xml – notice: 2009 INIST-CNRS
– notice: Copyright© Ferrata Storti Foundation
DBID AAYXX
CITATION
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
DOA
DOI 10.3324/haematol.2008.001925
DatabaseName CrossRef
Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList


MEDLINE
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Anatomy & Physiology
EISSN 1592-8721
EndPage 1032
ExternalDocumentID oai_doaj_org_article_8c72cf75f9ab4d519807d92e2cd4dc23
PMC2704317
19454500
21748784
10_3324_haematol_2008_001925
www94_7_1029
Genre Journal Article
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NHLBI NIH HHS
  grantid: P01 HL68705
– fundername: NHLBI NIH HHS
  grantid: P01 HL068705
GroupedDBID -
29I
2WC
53G
5GY
5RE
5VS
ABFLS
ADACO
ADBBV
AENEX
AGCAB
ALMA_UNASSIGNED_HOLDINGS
BAWUL
BCNDV
C1A
CS3
DIK
E3Z
EBS
EJD
F5P
FRP
GROUPED_DOAJ
H13
HYE
KQ8
M~E
O0-
OK1
P2P
RHF
RHI
RNS
RPM
SJN
TFS
WOQ
WOW
ZA5
---
AAFWJ
AAYXX
AFPKN
AOIJS
BTFSW
CITATION
OVT
TR2
W8F
IQODW
UDS
CGR
CUY
CVF
ECM
EIF
NPM
SV3
7X8
5PM
ID FETCH-LOGICAL-c533t-5a31f7545a7859b9542c223e856d3feb953a960579173f901355c495aa3bd7253
IEDL.DBID DOA
ISSN 0390-6078
1592-8721
IngestDate Wed Aug 27 01:31:38 EDT 2025
Thu Aug 21 14:03:35 EDT 2025
Thu Jul 10 23:42:17 EDT 2025
Thu Jan 02 22:14:13 EST 2025
Mon Jul 21 09:14:32 EDT 2025
Thu Apr 24 22:58:14 EDT 2025
Tue Jul 01 01:44:20 EDT 2025
Tue Jan 05 20:16:30 EST 2021
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 7
Keywords Antineoplastic agent
Human
AL amyloidosis
Hematology
liver disease
Digestive system
Stem cell
Liver
stem cell transplantation
Hematopoietic cell
Hepatic disease
Dose activity relation
Alkylating agent
Nitrogen mustard
Melphalan
Digestive diseases
Graft
High dose
Language English
License CC BY 4.0
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c533t-5a31f7545a7859b9542c223e856d3feb953a960579173f901355c495aa3bd7253
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
OpenAccessLink https://doaj.org/article/8c72cf75f9ab4d519807d92e2cd4dc23
PMID 19454500
PQID 67444577
PQPubID 23479
PageCount 4
ParticipantIDs doaj_primary_oai_doaj_org_article_8c72cf75f9ab4d519807d92e2cd4dc23
pubmedcentral_primary_oai_pubmedcentral_nih_gov_2704317
proquest_miscellaneous_67444577
pubmed_primary_19454500
pascalfrancis_primary_21748784
crossref_primary_10_3324_haematol_2008_001925
crossref_citationtrail_10_3324_haematol_2008_001925
highwire_smallpub2_www94_7_1029
ProviderPackageCode RHF
RHI
CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2009-07-01
PublicationDateYYYYMMDD 2009-07-01
PublicationDate_xml – month: 07
  year: 2009
  text: 2009-07-01
  day: 01
PublicationDecade 2000
PublicationPlace Pavia
PublicationPlace_xml – name: Pavia
– name: Italy
PublicationTitle Haematologica (Roma)
PublicationTitleAlternate Haematologica
PublicationYear 2009
Publisher Ferrata Storti Foundation
Publisher_xml – name: Ferrata Storti Foundation
References 17968927 - Arthritis Rheum. 2007 Nov;56(11):3858-68
11329232 - Ann Intern Med. 2001 May 1;134(9 Pt 1):746-53
16862166 - Bone Marrow Transplant. 2006 Sep;38(5):339-43
17968685 - Amyloid. 2007 Dec;14(4):261-9
17272986 - Curr Opin Oncol. 2007 Mar;19(2):136-41
9302305 - N Engl J Med. 1997 Sep 25;337(13):898-909
3389383 - Am J Med. 1988 Jul;85(1):73-80
9110907 - N Engl J Med. 1997 Apr 24;336(17):1202-7
1916751 - Hum Pathol. 1991 Sep;22(9):904-7
7878478 - Semin Hematol. 1995 Jan;32(1):45-59
15044325 - Circ Res. 2004 Apr 30;94(8):1008-10
8629674 - Am J Med. 1996 Mar;100(3):290-8
14734330 - Ann Intern Med. 2004 Jan 20;140(2):85-93
15572585 - Blood. 2005 Apr 1;105(7):2949-51
20536404 - Amyloid. 2009;16(2):103-7
9920856 - Blood. 1999 Feb 1;93(3):1062-6
17673601 - Blood. 2007 Nov 15;110(10):3561-3
17855669 - N Engl J Med. 2007 Sep 13;357(11):1083-93
14530778 - Medicine (Baltimore). 2003 Sep;82(5):291-8
6353084 - Mayo Clin Proc. 1983 Oct;58(10):665-83
16044444 - Am J Hematol. 2005 Aug;79(4):319-28
15070667 - Blood. 2004 Apr 15;103(8):2936-8
References_xml – reference: 17673601 - Blood. 2007 Nov 15;110(10):3561-3
– reference: 16862166 - Bone Marrow Transplant. 2006 Sep;38(5):339-43
– reference: 17968685 - Amyloid. 2007 Dec;14(4):261-9
– reference: 15070667 - Blood. 2004 Apr 15;103(8):2936-8
– reference: 20536404 - Amyloid. 2009;16(2):103-7
– reference: 6353084 - Mayo Clin Proc. 1983 Oct;58(10):665-83
– reference: 1916751 - Hum Pathol. 1991 Sep;22(9):904-7
– reference: 8629674 - Am J Med. 1996 Mar;100(3):290-8
– reference: 9110907 - N Engl J Med. 1997 Apr 24;336(17):1202-7
– reference: 9920856 - Blood. 1999 Feb 1;93(3):1062-6
– reference: 3389383 - Am J Med. 1988 Jul;85(1):73-80
– reference: 9302305 - N Engl J Med. 1997 Sep 25;337(13):898-909
– reference: 15572585 - Blood. 2005 Apr 1;105(7):2949-51
– reference: 17855669 - N Engl J Med. 2007 Sep 13;357(11):1083-93
– reference: 14530778 - Medicine (Baltimore). 2003 Sep;82(5):291-8
– reference: 11329232 - Ann Intern Med. 2001 May 1;134(9 Pt 1):746-53
– reference: 16044444 - Am J Hematol. 2005 Aug;79(4):319-28
– reference: 14734330 - Ann Intern Med. 2004 Jan 20;140(2):85-93
– reference: 7878478 - Semin Hematol. 1995 Jan;32(1):45-59
– reference: 17968927 - Arthritis Rheum. 2007 Nov;56(11):3858-68
– reference: 15044325 - Circ Res. 2004 Apr 30;94(8):1008-10
– reference: 17272986 - Curr Opin Oncol. 2007 Mar;19(2):136-41
SSID ssj0020997
Score 2.045466
Snippet 1 Department of Medicine 2 Stem Cell Transplantation Program of the Section of Hematology-Oncology and 3 Amyloid Treatment and Research Program, Department of...
High-dose melphalan chemotherapy and autologous peripheral blood stem cell transplantation has been shown to result in durable hematologic response and...
In patients with AL amyloidosis and liver involvement, treatment with high-dose melphalan chemotherapy and autologous peripheral blood stem cell...
SourceID doaj
pubmedcentral
proquest
pubmed
pascalfrancis
crossref
highwire
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 1029
SubjectTerms Adult
Aged
Amyloidosis - drug therapy
Amyloidosis - therapy
Biological and medical sciences
Brief Reports
Female
Hematologic and hematopoietic diseases
Humans
Liver - pathology
Liver Diseases - complications
Liver Diseases - drug therapy
Male
Medical sciences
Melphalan - therapeutic use
Middle Aged
Myeloablative Agonists - therapeutic use
Retrospective Studies
Stem Cell Transplantation - methods
Treatment Outcome
Title Hepatic response after high-dose melphalan and stem cell transplantation in patients with AL amyloidosis associated liver disease
URI http://www.haematologica.org/cgi/content/abstract/94/7/1029
https://www.ncbi.nlm.nih.gov/pubmed/19454500
https://www.proquest.com/docview/67444577
https://pubmed.ncbi.nlm.nih.gov/PMC2704317
https://doaj.org/article/8c72cf75f9ab4d519807d92e2cd4dc23
Volume 94
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV1Nb9QwELVQD4gLgpaPlNL6gLhFDf6I4-MWUa0Q5USl3iLHdtSVsglqtlr1yD9nxnaWDULqhduuk13HeS_KG3v8hpAPRVtqxzwgYFkDAYrkudYeohTbctdaURmBG5yvvpfLa_H1Rt7slfrCnLBoDxxv3HllFbOtkq02jXCgN6pCOc08s044y4LPZ6GLKZhKoRbuBw3rBxq6hbdg3DTHQT2c3xo0Qx26KY8SJI6cvZSCd_-eXzCmS5oR7lgbS138S4v-nVK59466fEGeJ3FJF3FQL8kT3x-So0UPF7J-oB9pSPcM8-iH5OlVWlU_Ir-WHvOqLb2LCbOehsrhFC8tdwN8X3vcktuZnpreUfR-pjjjTzfBGh3a44I-XfU0GbWOFGd46eIbNeuHbljB36xGahIZvKMdJoTQtD70ilxffvnxeZmn0gy5BX24yaXhnwAUIY2qpG60FIA1476SpeOthwZuIDaSCqJB3oLmAFljIRYzhjdOMclfk4N-6P1bQlUJcJaN8gqowT1IQvhk0BVLeFBnIiN8wqa2ybccy2d0NcQviGg9IZpKagZEM5LvfvUz-nY8cv4Fwr47F123QwNwsU5crB_jYkbOJtLU49p0HXCC1dvtVotaQfdMZ-R0xqVdfxgZVqqC0Z5N5KrhQUcsTe-H-7EulRBCKpWRN5Fqf8alBSBRFBlRMxLOBjM_0q9ug5U4U2iupI7_x-jfkWdxqQ1zmU_Iwebu3r8HxbZpTsPD-RtlckCM
linkProvider Directory of Open Access Journals
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Hepatic+response+after+high-dose+melphalan+and+stem+cell+transplantation+in+patients+with+AL+amyloidosis+associated+liver+disease&rft.jtitle=Haematologica+%28Roma%29&rft.au=Girnius%2C+Saulius&rft.au=Seldin%2C+David+C&rft.au=Skinner%2C+Martha&rft.au=Finn%2C+Kathleen+T&rft.date=2009-07-01&rft.issn=0390-6078&rft.eissn=1592-8721&rft.volume=94&rft.issue=7&rft.spage=1029&rft_id=info:doi/10.3324%2Fhaematol.2008.001925&rft_id=info%3Apmid%2F19454500&rft.externalDBID=n%2Fa&rft.externalDocID=www94_7_1029
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0390-6078&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0390-6078&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0390-6078&client=summon