Predictive factors for taxane acute pain syndrome determined by ordered logistic regression analysis.
Acute Pain
/ chemically induced
Adult
Aged
Albumins
/ administration & dosage
Analgesics
/ therapeutic use
Anti-Inflammatory Agents, Non-Steroidal
/ therapeutic use
Breast Neoplasms
/ drug therapy
Female
Humans
Logistic Models
Middle Aged
Paclitaxel
/ administration & dosage
Predictive Value of Tests
Quality of Life
Retrospective Studies
Risk Factors
Syndrome
Dexamethasone
Dose
Nanoparticle albumin-bound paclitaxel
TAPS
Taxanes
Journal
Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957
Informations de publication
Date de publication:
Jul 2019
Jul 2019
Historique:
received:
13
09
2018
accepted:
20
11
2018
pubmed:
28
11
2018
medline:
30
7
2019
entrez:
28
11
2018
Statut:
ppublish
Résumé
This retrospective study was undertaken to identify predictive factors for developing taxane acute pain syndrome (TAPS) and to determine new strategies for improving QoL in patients undergoing chemotherapy. Between November 2010 and May 2018, we enrolled 121 breast cancer patients at our outpatient chemotherapy center who were undergoing chemotherapy with nanoparticle albumin-bound paclitaxel (nab-PTX) every 3 weeks. Variables related to the development of TAPS were extracted from the patients' clinical records and used for regression analysis. The degree of TAPS was classified as grade 0 = not developed; grade 1 = developed but did not require analgesics; grade 2 = developed but alleviated by analgesics such as acetaminophen or non-steroidal anti-inflammatory drugs (NSAIDs); or grade 3 = syndrome developed, causing sleep problems or interfering with daily living activities, but not alleviated by analgesics such as acetaminophen or NSAIDs thus requiring opioids. Multivariate ordered logistic regression analysis was performed to identify predictive factors for the development of TAPS. Significant factors identified for the development of TAPS included dose of nab-PTX (odds ratio (OR) = 11.717, 95% confidence interval (CI) = 11.6161-11.8182; P = 0.0421) and the administration of dexamethasone for up to 3 days (OR = 0.133, 95% CI = 0.0235-0.7450; P = 0.0223). In conclusion, a high dose of nab-PTX and the lack of dexamethasone administration for up to 3 days were identified as significant predictors of the development of TAPS.
Identifiants
pubmed: 30478672
doi: 10.1007/s00520-018-4571-9
pii: 10.1007/s00520-018-4571-9
doi:
Substances chimiques
130-nm albumin-bound paclitaxel
0
Albumins
0
Analgesics
0
Anti-Inflammatory Agents, Non-Steroidal
0
Paclitaxel
P88XT4IS4D
Types de publication
Journal Article
Langues
eng
Pagination
2673-2677Références
Gynecol Oncol. 2001 May;81(2):333-4
pubmed: 11330975
J Clin Oncol. 2004 May 1;22(9):1767-9
pubmed: 15118009
Acta Paediatr. 2007 May;96(5):644-7
pubmed: 17376185
Curr Oncol. 2010 Aug;17(4):42-7
pubmed: 20697513
Nat Rev Drug Discov. 2010 Oct;9(10):790-803
pubmed: 20885410
J Clin Oncol. 2011 Apr 10;29(11):1472-8
pubmed: 21383290
Am J Hosp Palliat Care. 2012 Feb;29(1):70-9
pubmed: 21712306
Cancer. 2012 Oct 15;118(20):5171-8
pubmed: 22415454
Oncol Lett. 2012 Jun;3(6):1181-1185
pubmed: 22783414
Clin Cancer Res. 2012 Sep 15;18(18):5099-109
pubmed: 22843789
J Med Genet. 2013 Sep;50(9):599-605
pubmed: 23776197
Anticancer Drugs. 2014 May;25(5):593-8
pubmed: 24374330
Cancer Treat Rev. 2014 Jun;40(5):614-25
pubmed: 24560997
J Clin Oncol. 2014 Jun 1;32(16):1677-90
pubmed: 24799483
Oncol Lett. 2015 Apr;9(4):1822-1826
pubmed: 25789050
Mol Pain. 2015 Mar 11;11:10
pubmed: 25868824
Support Care Cancer. 2016 Apr;24(4):1583-94
pubmed: 26386706
Support Care Cancer. 2016 Aug;24(8):3633-50
pubmed: 27146496
Clin Genitourin Cancer. 2017 Feb;15(1):1-6
pubmed: 27554586
Ann Oncol. 2016 Sep;27(suppl 5):v119-v133
pubmed: 27664248
Support Care Cancer. 2018 Jan;26(1):203-211
pubmed: 28733699
Support Care Cancer. 2018 Sep;26(9):3073-3081
pubmed: 29564623
Gynecol Oncol. 1999 Jan;72(1):100-1
pubmed: 9889038