PS-067 Peripheral neuropathy induced by oxaliplatin: risk factors
BackgroundOxaliplatin is widely used in the treatment of solid cancers. The main limit of use is the occurrence of peripheral neuropathy (PN). The principal predisposing risk factors (RF) are: diabetes, chronic alcoholism, cumulative dose, malnutrition, history of gastrointestinal surgery (malabsorp...
Saved in:
Published in | European journal of hospital pharmacy. Science and practice Vol. 22; no. Suppl 1; p. A163 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group LTD
01.03.2015
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | BackgroundOxaliplatin is widely used in the treatment of solid cancers. The main limit of use is the occurrence of peripheral neuropathy (PN). The principal predisposing risk factors (RF) are: diabetes, chronic alcoholism, cumulative dose, malnutrition, history of gastrointestinal surgery (malabsorption of neuroprotectors such as the vitamin B12), anaemia, kidney failure and concomitant neurotoxic drugs.PurposeTo analyse these RFs and to determine a relationship between the number of RFs and the average cumulative dose (ACD) of oxaliplatin.Material and methodsRetrospective 2-year study (2011–2012), n = 96 patients. The RFs mentioned above were identified from patients’ records. From the chemotherapy software Asclepios we identified the total cumulative dose and the threshold dose for occurrence of PN for each patient. The tests used were the Pearson correlation coefficient and Student’s significance test.ResultsThe incidence of PN in our sample was 46%. 3 groups were identified: 0–1 RF (59%), 2 RF (27%), 3 RF or more (11%). The proportion for each RF was: anaemia (48%), malnutrition and antecedents of gastrointestinal surgery (40%), diabetes (16%), administration of neurotoxic drugs before or during chemotherapy (16%) and chronic alcoholism (13%). The ACD at the onset of clinical signs was 331 mg/m². According to the Summary of Product Characteristics the cumulative dose is 850 mg/m². In our sample it was 2.6 times smaller (p < 0). For each group it was 360 mg/m² in the 0–1 RF group, 250 mg/m²0 in the 2 RFs group and 215 mg/m² in the 3 RFs or more. It was inversely proportional to the number of RFs (r = -0.930) (p = 0.069).ConclusionIt has been shown that the greater the number of RFs, the lower the ACD at which PN occurs. According to the literature these RFs do not contraindicate the use of oxaliplatin and in practice the reducing or stopping of oxaliplatin is dictated by the clinical appearance of NP.References and/or acknowledgementsNo conflict of interest. |
---|---|
AbstractList | Background Oxaliplatin is widely used in the treatment of solid cancers. The main limit of use is the occurrence of peripheral neuropathy (PN). The principal predisposing risk factors (RF) are: diabetes, chronic alcoholism, cumulative dose, malnutrition, history of gastrointestinal surgery (malabsorption of neuroprotectors such as the vitamin B12), anaemia, kidney failure and concomitant neurotoxic drugs. Purpose To analyse these RFs and to determine a relationship between the number of RFs and the average cumulative dose (ACD) of oxaliplatin. Material and methods Retrospective 2-year study (2011-2012), n = 96 patients. The RFs mentioned above were identified from patients' records. From the chemotherapy software Asclepios we identified the total cumulative dose and the threshold dose for occurrence of PN for each patient. The tests used were the Pearson correlation coefficient and Student's significance test. Results The incidence of PN in our sample was 46%. 3 groups were identified: 0-1 RF (59%), 2 RF (27%), 3 RF or more (11%). The proportion for each RF was: anaemia (48%), malnutrition and antecedents of gastrointestinal surgery (40%), diabetes (16%), administration of neurotoxic drugs before or during chemotherapy (16%) and chronic alcoholism (13%). The ACD at the onset of clinical signs was 331 mg/m². According to the Summary of Product Characteristics the cumulative dose is 850 mg/m². In our sample it was 2.6 times smaller (p < 0). For each group it was 360 mg/m² in the 0-1 RF group, 250 mg/m²0 in the 2 RFs group and 215 mg/m² in the 3 RFs or more. It was inversely proportional to the number of RFs (r = -0.930) (p = 0.069). Conclusion It has been shown that the greater the number of RFs, the lower the ACD at which PN occurs. According to the literature these RFs do not contraindicate the use of oxaliplatin and in practice the reducing or stopping of oxaliplatin is dictated by the clinical appearance of NP. References and/or acknowledgements No conflict of interest. BackgroundOxaliplatin is widely used in the treatment of solid cancers. The main limit of use is the occurrence of peripheral neuropathy (PN). The principal predisposing risk factors (RF) are: diabetes, chronic alcoholism, cumulative dose, malnutrition, history of gastrointestinal surgery (malabsorption of neuroprotectors such as the vitamin B12), anaemia, kidney failure and concomitant neurotoxic drugs.PurposeTo analyse these RFs and to determine a relationship between the number of RFs and the average cumulative dose (ACD) of oxaliplatin.Material and methodsRetrospective 2-year study (2011–2012), n = 96 patients. The RFs mentioned above were identified from patients’ records. From the chemotherapy software Asclepios we identified the total cumulative dose and the threshold dose for occurrence of PN for each patient. The tests used were the Pearson correlation coefficient and Student’s significance test.ResultsThe incidence of PN in our sample was 46%. 3 groups were identified: 0–1 RF (59%), 2 RF (27%), 3 RF or more (11%). The proportion for each RF was: anaemia (48%), malnutrition and antecedents of gastrointestinal surgery (40%), diabetes (16%), administration of neurotoxic drugs before or during chemotherapy (16%) and chronic alcoholism (13%). The ACD at the onset of clinical signs was 331 mg/m². According to the Summary of Product Characteristics the cumulative dose is 850 mg/m². In our sample it was 2.6 times smaller (p < 0). For each group it was 360 mg/m² in the 0–1 RF group, 250 mg/m²0 in the 2 RFs group and 215 mg/m² in the 3 RFs or more. It was inversely proportional to the number of RFs (r = -0.930) (p = 0.069).ConclusionIt has been shown that the greater the number of RFs, the lower the ACD at which PN occurs. According to the literature these RFs do not contraindicate the use of oxaliplatin and in practice the reducing or stopping of oxaliplatin is dictated by the clinical appearance of NP.References and/or acknowledgementsNo conflict of interest. |
Author | Henault, S Ekoume, I Malaurie, E Poullain, S Rusu, T |
Author_xml | – sequence: 1 givenname: T surname: Rusu fullname: Rusu, T organization: CHI de Creteil, Oncology, Creteil, France – sequence: 2 givenname: I surname: Ekoume fullname: Ekoume, I organization: CHI de Creteil, Oncology, Creteil, France – sequence: 3 givenname: S surname: Henault fullname: Henault, S organization: CHI de Creteil, Oncology, Creteil, France – sequence: 4 givenname: E surname: Malaurie fullname: Malaurie, E organization: CHI de Creteil, Oncology, Creteil, France – sequence: 5 givenname: S surname: Poullain fullname: Poullain, S organization: CHI de Creteil, Oncology, Creteil, France |
BookMark | eNp9kM1KAzEUhYNUsNa-Q8D11Jv_xp0UtULBgroOSZphUqczY2YG7M6NL-qTOKXq0tU9cD_Oge8cjaq6CghhAjNCmLwK26IpbNplFIjIAEAyPWOanqAxBa4yrSUf_WUhz9C0baMDwdhcc6bHaLF-ykCqr4_PdUixKUKyJa5Cn-rGdsUex2rT-7DBbo_rd1vGprRdrK5xiu0rzq3v6tReoNPclm2Y_twJerm7fV4ss9Xj_cPiZpU5AiAyOWduY4UMIbcA2hNFh2bHvfcQfG5JbmWwTCsv5pxIzYT1angrUEKC02yCLo-9Tarf-tB2Zlv3qRomDRWCKsEJEf9SwLWgoKgcKHak3G5rmhR3Nu0NAXPQan61moNWc9RqBq3sG9-ubtI |
ContentType | Journal Article |
Copyright | 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions Copyright: 2015 © 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions 2015 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions |
Copyright_xml | – notice: 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions – notice: Copyright: 2015 © 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions – notice: 2015 2015, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions |
DBID | 3V. 7X7 7XB 8FI 8FJ 8FK ABUWG AFKRA BENPR BTHHO CCPQU FYUFA GHDGH K9. PQEST PQQKQ PQUKI PRINS |
DOI | 10.1136/ejhpharm-2015-000639.392 |
DatabaseName | ProQuest Central (Corporate) Health & Medical Collection ProQuest Central (purchase pre-March 2016) Hospital Premium Collection Hospital Premium Collection (Alumni Edition) ProQuest Central (Alumni) (purchase pre-March 2016) ProQuest Central (Alumni) ProQuest Central UK/Ireland ProQuest Central BMJ Journals ProQuest One Community College Health Research Premium Collection Health Research Premium Collection (Alumni) ProQuest Health & Medical Complete (Alumni) ProQuest One Academic Eastern Edition (DO NOT USE) ProQuest One Academic ProQuest One Academic UKI Edition ProQuest Central China |
DatabaseTitle | ProQuest One Academic Eastern Edition ProQuest Health & Medical Complete (Alumni) ProQuest Central (Alumni Edition) ProQuest One Community College ProQuest Hospital Collection Health Research Premium Collection (Alumni) ProQuest Central China ProQuest Hospital Collection (Alumni) ProQuest Central ProQuest Health & Medical Complete Health Research Premium Collection ProQuest One Academic UKI Edition BMJ Journals ProQuest One Academic ProQuest Central (Alumni) |
DatabaseTitleList | ProQuest One Academic Eastern Edition ProQuest One Academic Eastern Edition |
Database_xml | – sequence: 1 dbid: 7X7 name: Health & Medical Collection url: https://search.proquest.com/healthcomplete sourceTypes: Aggregation Database |
DeliveryMethod | fulltext_linktorsrc |
EISSN | 2047-9964 |
EndPage | A163 |
GroupedDBID | 0R~ 3V. 53G 7X7 8FI 8FJ AAYAA ABKRM ABUWG ABVAJ ABWEH ADBBV ADMRH AFKRA AHMBA AHQMW AJYBZ ALMA_UNASSIGNED_HOLDINGS AOIJS BAWUL BENPR BPHCQ BTHHO C45 CCPQU CXRWF EBS EJD FYUFA H13 HAJ HMCUK HYE OK1 OVD PQQKQ PROAC RHI RMJ RPM TEORI UKHRP 7XB 8FK K9. PQEST PQUKI PRINS |
ID | FETCH-LOGICAL-b1005-683bda56eefa009c172cedb4ccc0ecfa1fa6ea397c58416935ac7b4c707560b93 |
IEDL.DBID | 7X7 |
ISSN | 2047-9956 |
IngestDate | Thu Oct 10 17:52:17 EDT 2024 Thu Oct 10 20:13:17 EDT 2024 Wed Aug 21 03:28:42 EDT 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | Suppl 1 |
Language | English |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-b1005-683bda56eefa009c172cedb4ccc0ecfa1fa6ea397c58416935ac7b4c707560b93 |
PQID | 2049520726 |
PQPubID | 2040966 |
ParticipantIDs | proquest_journals_2552754115 proquest_journals_2049520726 bmj_primary_10_1136_ejhpharm_2015_000639_392 |
PublicationCentury | 2000 |
PublicationDate | 20150300 20150301 |
PublicationDateYYYYMMDD | 2015-03-01 |
PublicationDate_xml | – month: 03 year: 2015 text: 20150300 |
PublicationDecade | 2010 |
PublicationPlace | London |
PublicationPlace_xml | – name: London |
PublicationTitle | European journal of hospital pharmacy. Science and practice |
PublicationYear | 2015 |
Publisher | BMJ Publishing Group LTD |
Publisher_xml | – name: BMJ Publishing Group LTD |
SSID | ssib053389439 ssj0000605265 ssib018287486 |
Score | 1.9714477 |
Snippet | BackgroundOxaliplatin is widely used in the treatment of solid cancers. The main limit of use is the occurrence of peripheral neuropathy (PN). The principal... Background Oxaliplatin is widely used in the treatment of solid cancers. The main limit of use is the occurrence of peripheral neuropathy (PN). The principal... |
SourceID | proquest bmj |
SourceType | Aggregation Database Publisher |
StartPage | A163 |
SubjectTerms | Alcoholism Anemia Chemotherapy Diabetes Drug dosages Gastrointestinal surgery Malnutrition Neurotoxicity Peripheral neuropathy Risk factors |
Title | PS-067 Peripheral neuropathy induced by oxaliplatin: risk factors |
URI | http://dx.doi.org/10.1136/ejhpharm-2015-000639.392 https://www.proquest.com/docview/2049520726 https://www.proquest.com/docview/2552754115 |
Volume | 22 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1RS8MwEA5ue_FFFBWnc-TBR6Nt06atLzJlYwiOoQ72FposRYZ21U1w_967NN0eFOlj0kLvLrnvcpfvCLnggQfLOVdM2Ss5EKEwzC4xgLpKgUfJY9u94XEkhpPwYRpN3YHb0pVV1nui3ahnC41n5BCkA5QPvDgQt-UHw65RmF11LTQapOXDGLZuiKcbd-pbMvctPRogG2QbTzdnMJ5AthOscgyQsAAvedbFPlxcm_lrifTRYEh-xCpnfsUxZ9pQ7_Nfe7d1SIN9sueQJO1Vqj8gO6Y4JL3xMwPPQMdgWJYw4I1axkpsPLymEH-DJmdUreniGwB4iYVwxQ3F-nLqOu8ckcmg_3I_ZK5LAlM-0oiKhKtZFglj8gwAkwZEAl9SodbaMzrP_DwTJgPYoSNMMaY8ynQMwzGABeGplB-TZrEozAmhAJ6EzoM4iVId8hzmw2Q_8SAITBQ8bXIJfy7LigdD2viBC1kLSqKgZCUoCYJqk04tIulWxlJu9fj3MDLCRSHg1NP_3z4ju5VesBysQ5qrzy9zDvhgpbrWCLqkddcfjZ9-ANegszA |
link.rule.ids | 315,783,787,12070,21402,27938,27939,31733,33758,43324,43819,74081,74638 |
linkProvider | ProQuest |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1RS8MwEA5uPuiLKCpOp-bBR6Nt06atLzLEMXUbAzfYW2iyFBmzq26C-_fepe32oEgfkxZ6l9x9l7t8R8gV9xzYzqliyl7JgQiFYXaJAdRVCjxKGtruDb2-6Iz853EwLg_cFmVZZWUTraGezDWekUOQDlDec0JP3OcfDLtGYXa1bKFRI9vIw4Xc-eF47U5dS-a-oUcDZINs4_H6DMYRyHaCVY4eEhbgJc-q2IeLWzN9y5E-GhaSG7DCmd9wzJnW1Pv0l-22Dqm9T_ZKJElbheoPyJbJDklr8MrAM9ABLCxLGDCjlrESGw-vKMTfoMkJVSs6_wYAnmMhXHZHsb6clp13jsio_Th86LCySwJTLtKIioirSRIIY9IEAJMGRAJfUr7W2jE6Tdw0ESYB2KEDTDHGPEh0CMMhgAXhqJgfk3o2z8wJoQCehE69MApi7fMU5sNkN3IgCIwUPA1yDX8u84IHQ9r4gQtZCUqioGQhKAmCapBmJSJZ7oyF3Ojx72FkhAt8wKmn_799SXY6w15Xdp_6L2dkt9ARloY1SX35-WXOASss1YVdED_Hh7SG |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV1NSwMxEA22gngRRcVq1Rw8Gruf2V0vUtRSv0pBC72FTZogRdvVVrD_3plstj0ossdkF3YyybxJXt4QchYGHkxnI5m0V3IgQ2F4usQA6koJEcUktnrDU493B9H9MB46_tPM0SqrNdEu1KOpwj1ySNIBygdeEvCWcbSI_k3nqvhgWEEKT1pdOY0aWU8iCHTg28lwGVp9K-y-kkoDlIPK49lyP8bjqHyCjMcAxQvwwmdF_Al5S49fC5SSBqfyY1YG9osQz09r8n38ax23wamzTbYcqqTt0g12yJqe7JJ2_5lBlKB9cDIrHvBGrXolFiFeUMjFYVRHVC7o9BvAeIGkuMklRa45dVV49sigc_ty3WWuYgKTPkqK8jSUozzmWpscwJMCdAJfkpFSytPK5L7Juc4BgqgYjxuzMM5VAs0JAAfuySzcJ_XJdKIPCAUgxZUJkjTOVBQa6A-d_dSDhDCV8DTIOfy5KEpNDGFziZCLylACDSVKQwkwVIM0KxMJN0tmYjWmfzejOlwcAWY9_P_tU7IBviAe73oPR2SzHCJkiTVJff75pY8BNszlifWHH3CVuLs |
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=PS-067+Peripheral+neuropathy+induced+by+oxaliplatin%3A+risk+factors&rft.jtitle=European+journal+of+hospital+pharmacy.+Science+and+practice&rft.au=Rusu%2C+T&rft.au=Ekoume%2C+I&rft.au=Henault%2C+S&rft.au=Malaurie%2C+E&rft.date=2015-03-01&rft.pub=BMJ+Publishing+Group+LTD&rft.issn=2047-9956&rft.eissn=2047-9964&rft.volume=22&rft.spage=A163&rft_id=info:doi/10.1136%2Fejhpharm-2015-000639.392&rft.externalDBID=HAS_PDF_LINK |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2047-9956&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2047-9956&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2047-9956&client=summon |