Switching to Bortezomib may Improve Recovery From Severe Vincristine Neuropathy in Pediatric Acute Lymphoblastic Leukemia

The purpose of this study was to evaluate the impact of switching patients being treated for acute lymphoblastic leukemia (ALL) from vincristine to bortezomib. A total of 20 patients with ALL were switched from vincristine to bortezomib (1.3 mg/m/dose) because of worsening neuropathy despite physica...

Celý popis

Uložené v:
Podrobná bibliografia
Vydané v:Journal of pediatric hematology/oncology Ročník 41; číslo 6; s. 457
Hlavní autori: Joshi, Jaitri, Tanner, Lynn, Gilchrist, Laura, Bostrom, Bruce
Médium: Journal Article
Jazyk:English
Vydavateľské údaje: United States 01.08.2019
Predmet:
ISSN:1536-3678, 1536-3678
On-line prístup:Zistit podrobnosti o prístupe
Tagy: Pridať tag
Žiadne tagy, Buďte prvý, kto otaguje tento záznam!
Abstract The purpose of this study was to evaluate the impact of switching patients being treated for acute lymphoblastic leukemia (ALL) from vincristine to bortezomib. A total of 20 patients with ALL were switched from vincristine to bortezomib (1.3 mg/m/dose) because of worsening neuropathy despite physical therapy interventions (n=18) or at increased risk of neuropathy (n=2). Relapse rates were compared with 56 vincristine-only patients matched by prognostic factors. Maintenance blood counts in bortezomib patients were compared with cooperative group data using vincristine during maintenance. In addition, 6 evaluable patients were assessed for neuropathy using the pediatric-modified total neuropathy score. Neuropathy scores were collected during treatment with vincristine and after switching to bortezomib. After a median follow-up of 3.5 years the relapse rate in patients switched to bortezomib was nonsignificantly different than those remaining on vincristine. Patients on monthly bortezomib had statistically significantly lower platelet counts that did not require transfusions or dose adjustment. Total neuropathy for all 6 cases decreased significantly when switched to bortezomib from vincristine (P=0.015), with motor neuropathy declines in 5 of 6 subjects. Bortezomib substitution for vincristine in ALL treatment is a potential strategy to mitigate severe vincristine neuropathy. These findings should be confirmed in a randomized clinical trial to further assess benefits and risks of this approach.
AbstractList The purpose of this study was to evaluate the impact of switching patients being treated for acute lymphoblastic leukemia (ALL) from vincristine to bortezomib. A total of 20 patients with ALL were switched from vincristine to bortezomib (1.3 mg/m/dose) because of worsening neuropathy despite physical therapy interventions (n=18) or at increased risk of neuropathy (n=2). Relapse rates were compared with 56 vincristine-only patients matched by prognostic factors. Maintenance blood counts in bortezomib patients were compared with cooperative group data using vincristine during maintenance. In addition, 6 evaluable patients were assessed for neuropathy using the pediatric-modified total neuropathy score. Neuropathy scores were collected during treatment with vincristine and after switching to bortezomib. After a median follow-up of 3.5 years the relapse rate in patients switched to bortezomib was nonsignificantly different than those remaining on vincristine. Patients on monthly bortezomib had statistically significantly lower platelet counts that did not require transfusions or dose adjustment. Total neuropathy for all 6 cases decreased significantly when switched to bortezomib from vincristine (P=0.015), with motor neuropathy declines in 5 of 6 subjects. Bortezomib substitution for vincristine in ALL treatment is a potential strategy to mitigate severe vincristine neuropathy. These findings should be confirmed in a randomized clinical trial to further assess benefits and risks of this approach.
The purpose of this study was to evaluate the impact of switching patients being treated for acute lymphoblastic leukemia (ALL) from vincristine to bortezomib.PURPOSEThe purpose of this study was to evaluate the impact of switching patients being treated for acute lymphoblastic leukemia (ALL) from vincristine to bortezomib.A total of 20 patients with ALL were switched from vincristine to bortezomib (1.3 mg/m/dose) because of worsening neuropathy despite physical therapy interventions (n=18) or at increased risk of neuropathy (n=2). Relapse rates were compared with 56 vincristine-only patients matched by prognostic factors. Maintenance blood counts in bortezomib patients were compared with cooperative group data using vincristine during maintenance. In addition, 6 evaluable patients were assessed for neuropathy using the pediatric-modified total neuropathy score. Neuropathy scores were collected during treatment with vincristine and after switching to bortezomib.PATIENTS AND METHODSA total of 20 patients with ALL were switched from vincristine to bortezomib (1.3 mg/m/dose) because of worsening neuropathy despite physical therapy interventions (n=18) or at increased risk of neuropathy (n=2). Relapse rates were compared with 56 vincristine-only patients matched by prognostic factors. Maintenance blood counts in bortezomib patients were compared with cooperative group data using vincristine during maintenance. In addition, 6 evaluable patients were assessed for neuropathy using the pediatric-modified total neuropathy score. Neuropathy scores were collected during treatment with vincristine and after switching to bortezomib.After a median follow-up of 3.5 years the relapse rate in patients switched to bortezomib was nonsignificantly different than those remaining on vincristine. Patients on monthly bortezomib had statistically significantly lower platelet counts that did not require transfusions or dose adjustment. Total neuropathy for all 6 cases decreased significantly when switched to bortezomib from vincristine (P=0.015), with motor neuropathy declines in 5 of 6 subjects.RESULTSAfter a median follow-up of 3.5 years the relapse rate in patients switched to bortezomib was nonsignificantly different than those remaining on vincristine. Patients on monthly bortezomib had statistically significantly lower platelet counts that did not require transfusions or dose adjustment. Total neuropathy for all 6 cases decreased significantly when switched to bortezomib from vincristine (P=0.015), with motor neuropathy declines in 5 of 6 subjects.Bortezomib substitution for vincristine in ALL treatment is a potential strategy to mitigate severe vincristine neuropathy. These findings should be confirmed in a randomized clinical trial to further assess benefits and risks of this approach.CONCLUSIONSBortezomib substitution for vincristine in ALL treatment is a potential strategy to mitigate severe vincristine neuropathy. These findings should be confirmed in a randomized clinical trial to further assess benefits and risks of this approach.
Author Bostrom, Bruce
Joshi, Jaitri
Tanner, Lynn
Gilchrist, Laura
Author_xml – sequence: 1
  givenname: Jaitri
  surname: Joshi
  fullname: Joshi, Jaitri
  organization: Children's Hospitals and Clinics of Minnesota, Minneapolis, MN
– sequence: 2
  givenname: Lynn
  surname: Tanner
  fullname: Tanner, Lynn
– sequence: 3
  givenname: Laura
  surname: Gilchrist
  fullname: Gilchrist, Laura
– sequence: 4
  givenname: Bruce
  surname: Bostrom
  fullname: Bostrom, Bruce
BackLink https://www.ncbi.nlm.nih.gov/pubmed/31233464$$D View this record in MEDLINE/PubMed
BookMark eNpNkEtLw0AUhQdR7EP_gcgs3aRmnkmWtVhbiFqsug2T6a0dzWTiJFHirzdghZ7FPWfxceGcETouXQkIXZBwQsIkur5fLSbhgYigyREaEsFkwGQUHx_kARrV9XvPRIzTUzRghDLGJR-ibv1tGr0z5RtuHL5xvoEfZ02Orerw0lbefQF-At2b7_DcO4vX0GfAr6bU3tSNKQE_QOtdpZpdh02JV7AxqvFG46luG8BpZ6udywvVwxqn0H6ANeoMnWxVUcP53sfoZX77PFsE6ePdcjZNA82ETAKa04jLLZe6P4QlYpurhGgRUxrTMBQ8iblmNGTACFFMUxJFXAvFNypiIEM6Rld_f_suny3UTWZNraEoVAmurTNKuUxCwSLRo5d7tM0tbLLKG6t8l_3PRX8BiOVvYA
CitedBy_id crossref_primary_10_3389_fphar_2025_1661493
crossref_primary_10_1007_s12288_025_02047_2
crossref_primary_10_1093_bmb_ldaa045
crossref_primary_10_1002_pbc_28115
crossref_primary_10_3389_fonc_2021_710163
ContentType Journal Article
DBID CGR
CUY
CVF
ECM
EIF
NPM
7X8
DOI 10.1097/MPH.0000000000001529
DatabaseName Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 7X8
  name: MEDLINE - Academic
  url: https://search.proquest.com/medline
  sourceTypes: Aggregation Database
DeliveryMethod no_fulltext_linktorsrc
Discipline Medicine
EISSN 1536-3678
ExternalDocumentID 31233464
Genre Journal Article
GroupedDBID ---
.-D
.3C
.55
.GJ
.XZ
.Z2
0R~
4Q1
4Q2
4Q3
53G
5GY
5RE
5VS
8L-
AAAAV
AAHPQ
AAIQE
AARTV
AASCR
AAYEP
ABASU
ABBUW
ABDIG
ABJNI
ABOCM
ABPPZ
ABVCZ
ABXVJ
ABZAD
ABZZY
ACCJW
ACDDN
ACEWG
ACGFO
ACILI
ACNWC
ACWDW
ACWRI
ACXJB
ACXNZ
ADFPA
ADGGA
ADHPY
ADNKB
AE3
AE6
AEETU
AENEX
AFBFQ
AFDTB
AFFNX
AFUWQ
AGINI
AHQNM
AHRYX
AHVBC
AINUH
AJCLO
AJIOK
AJNWD
AJNYG
AJZMW
AKCTQ
ALKUP
ALMA_UNASSIGNED_HOLDINGS
ALMTX
AMJPA
AMKUR
AMNEI
AOHHW
AOQMC
BQLVK
BS7
C45
CGR
CS3
CUY
CVF
DIWNM
DU5
DUNZO
E.X
EBS
ECM
EEVPB
EIF
EJD
EX3
F2K
F2L
F5P
FCALG
FL-
GNXGY
GQDEL
H0~
HLJTE
HZ~
IKREB
IN~
IPNFZ
JF9
JG8
JK3
JK8
K8S
KD2
KMI
L-C
N9A
NPM
N~M
O9-
OAG
OAH
OCUKA
ODA
OL1
OLG
OLV
OLZ
OPUJH
ORVUJ
OUVQU
OVD
OVDNE
OWU
OWV
OWW
OWX
OWY
OWZ
OXXIT
P-K
P2P
R58
RIG
RLZ
S4R
S4S
T8P
TEORI
TSPGW
V2I
VVN
W3M
WOQ
WOW
X3V
X3W
X7M
XXN
XYM
YFH
YOC
ZFV
ZGI
ZXP
ZZMQN
7X8
ABPXF
ACBKD
ADKSD
ID FETCH-LOGICAL-c3569-2b2746f46c6f41395fba91c5822820054984c3203e311a3c21774c5a4da73e602
IEDL.DBID 7X8
ISICitedReferencesCount 6
ISICitedReferencesURI http://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestLinkType=CitingArticles&DestApp=WOS_CPL&KeyUT=000479116100019&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
ISSN 1536-3678
IngestDate Sun Nov 09 10:59:44 EST 2025
Thu Apr 03 07:09:46 EDT 2025
IsPeerReviewed true
IsScholarly true
Issue 6
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c3569-2b2746f46c6f41395fba91c5822820054984c3203e311a3c21774c5a4da73e602
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 31233464
PQID 2246905375
PQPubID 23479
ParticipantIDs proquest_miscellaneous_2246905375
pubmed_primary_31233464
PublicationCentury 2000
PublicationDate 2019-08-00
20190801
PublicationDateYYYYMMDD 2019-08-01
PublicationDate_xml – month: 08
  year: 2019
  text: 2019-08-00
PublicationDecade 2010
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Journal of pediatric hematology/oncology
PublicationTitleAlternate J Pediatr Hematol Oncol
PublicationYear 2019
SSID ssj0017342
Score 2.259602
Snippet The purpose of this study was to evaluate the impact of switching patients being treated for acute lymphoblastic leukemia (ALL) from vincristine to bortezomib....
The purpose of this study was to evaluate the impact of switching patients being treated for acute lymphoblastic leukemia (ALL) from vincristine to...
SourceID proquest
pubmed
SourceType Aggregation Database
Index Database
StartPage 457
SubjectTerms Adolescent
Adult
Antineoplastic Agents - therapeutic use
Antineoplastic Agents, Phytogenic - adverse effects
Bortezomib - therapeutic use
Child
Child, Preschool
Drug Substitution - statistics & numerical data
Female
Follow-Up Studies
Humans
Male
Nervous System Diseases - chemically induced
Nervous System Diseases - pathology
Nervous System Diseases - prevention & control
Precursor Cell Lymphoblastic Leukemia-Lymphoma - drug therapy
Precursor Cell Lymphoblastic Leukemia-Lymphoma - pathology
Prognosis
Retrospective Studies
Vincristine - adverse effects
Young Adult
Title Switching to Bortezomib may Improve Recovery From Severe Vincristine Neuropathy in Pediatric Acute Lymphoblastic Leukemia
URI https://www.ncbi.nlm.nih.gov/pubmed/31233464
https://www.proquest.com/docview/2246905375
Volume 41
WOSCitedRecordID wos000479116100019&url=https%3A%2F%2Fcvtisr.summon.serialssolutions.com%2F%23%21%2Fsearch%3Fho%3Df%26include.ft.matches%3Dt%26l%3Dnull%26q%3D
hasFullText
inHoldings 1
isFullTextHit
isPrint
link http://cvtisr.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1JS8NAFB7UinhxX-rGCF6DbWfrnKSIpYe2FKrSW5mZvECQJrWLEn-9b5LU3kQwhyGXwDD53v7mfYTcGUCYSKsDFVkZcOVEoJlvXFOhlVADxDTPySZUv98cjfSgTLjNy7bKlU7MFXWYOp8jv_eDz7QfPiIepu-BZ43y1dWSQmOTVBi6Ml4w1WhdRVAsJ89BoZYBQ628ujqn1X1v0ClGF5YPmrFfnMzc2LT3_7vNA7JXupm0VeDikGxAckR2emUh_Zhkw894kbdR0kVKPac6fKWT2NKJyWiRaADqQ1NEekbbs3RCh4DvQF_jxOWKIQGaT_bwnMYZjRP6w_pBW265ANrNECmpRfccN0G7sHyDSWxOyEv76fmxE5QsDIFjQuqgYTFwlRGXDhc8ZBFZo-tOoGfR9CkprpvcsUbNZ1PrhjmMcRR3wvDQKAay1jglW0mawDmhzrN6GGaFxaDSgrDcRgatdBRqEKGpV8nt6lDHiHJfujAJpMv5eH2sVXJW_JnxtBjHMWZofBmX_OIPX1-SXfR4dNHBd0UqEco4XJNt97GI57ObHD649ge9b9xez0w
linkProvider ProQuest
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=Switching+to+Bortezomib+may+Improve+Recovery+From+Severe+Vincristine+Neuropathy+in+Pediatric+Acute+Lymphoblastic+Leukemia&rft.jtitle=Journal+of+pediatric+hematology%2Foncology&rft.au=Joshi%2C+Jaitri&rft.au=Tanner%2C+Lynn&rft.au=Gilchrist%2C+Laura&rft.au=Bostrom%2C+Bruce&rft.date=2019-08-01&rft.eissn=1536-3678&rft.volume=41&rft.issue=6&rft.spage=457&rft_id=info:doi/10.1097%2FMPH.0000000000001529&rft_id=info%3Apmid%2F31233464&rft_id=info%3Apmid%2F31233464&rft.externalDocID=31233464
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1536-3678&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1536-3678&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1536-3678&client=summon