Literature DB >> 30470691

Concomitant Medications and Risk of Chemotherapy-Induced Peripheral Neuropathy.

Lara Sánchez-Barroso1,2, Maria Apellaniz-Ruiz1, Gerardo Gutiérrez-Gutiérrez3, María Santos1, Juan M Roldán-Romero1, Maria Curras1, Laura Remacha1, Bruna Calsina1, Isabel Calvo4,5, María Sereno6, María Merino6, Jesús García-Donas7, Beatriz Castelo8, Eva Guerra9, Rocio Letón1, Cristina Montero-Conde1, Alberto Cascón1,10, Lucía Inglada-Pérez1,10, Mercedes Robledo1,10, Cristina Rodríguez-Antona11,10.   

Abstract

BACKGROUND: Peripheral neuropathy is the dose-limiting toxicity of many oncology drugs, including paclitaxel. There is large interindividual variability in the neuropathy, and several risk factors have been proposed; however, many have not been replicated. Here we present a comprehensive study aimed at identifying treatment and physiopathology-related paclitaxel-induced neuropathy risk factors in a large cohort of well-characterized patients. PATIENTS AND METHODS: Analyses included 503 patients with breast or ovarian cancer who received paclitaxel treatment. Paclitaxel dose modifications caused by the neuropathy were extracted from medical records and patients self-reported neuropathy symptoms were collected. Multivariate logistic regression analyses were performed to identify concomitant medications and comorbidities associated with paclitaxel-induced neuropathy.
RESULTS: Older patients had higher neuropathy: for each increase of 1 year of age, the risk of dose modifications and grade 3 neuropathy increased 4% and 5%, respectively. Cardiovascular drugs increased the risk of paclitaxel dose reductions (odds ratio [OR], 2.51; p = .006), with a stronger association for beta-adrenergic antagonists. The total number of concomitant medications also showed an association with dose modifications (OR, 1.25; p = .012 for each concomitant drug increase). A dose modification predictive model that included the new identified factors gave an area under the curve of 0.74 (p = 1.07 × 10-10). Preexisting nerve compression syndromes seemed to increase neuropathy risk.
CONCLUSION: Baseline characteristics of the patients, including age and concomitant medications, could be used to identify individuals at high risk of neuropathy, personalizing chemotherapy treatment and reducing the risk of severe neuropathy. IMPLICATIONS FOR PRACTICE: Peripheral neuropathy is a common adverse effect of many cancer drugs, including chemotherapeutics, targeted therapies, and immune checkpoint inhibitors. About 40% of survivors of cancer have functional deficits caused by this toxicity, some of them irreversible. Currently, there are no effective treatments to prevent or treat this neuropathy. This study, performed in a large cohort of well-characterized patients homogenously treated with paclitaxel, identified concomitant medications, comorbidities, and demographic factors associated with peripheral neuropathy. These factors could serve to identify patients at high risk of severe neuropathy for whom alternative non-neurotoxic alternatives may be considered. © AlphaMed Press 2018.

Entities:  

Keywords:  Comorbidities; Concomitant medications; Paclitaxel; Peripheral neuropathy; Risk factors

Year:  2018        PMID: 30470691      PMCID: PMC6693699          DOI: 10.1634/theoncologist.2018-0418

Source DB:  PubMed          Journal:  Oncologist        ISSN: 1083-7159


  32 in total

1.  Pharmacogenomic characterization of US FDA-approved cytotoxic drugs.

Authors:  Eric J Peters; Alison Motsinger-Reif; Tammy M Havener; Lorraine Everitt; Nicholas E Hardison; Venita G Watson; Michael Wagner; Kristy L Richards; Mike A Province; Howard L McLeod
Journal:  Pharmacogenomics       Date:  2011-10       Impact factor: 2.533

2.  Validation and reduction of FACT/GOG-Ntx subscale for platinum/paclitaxel-induced neurologic symptoms: a gynecologic oncology group study.

Authors:  H Q Huang; M F Brady; D Cella; G Fleming
Journal:  Int J Gynecol Cancer       Date:  2007 Mar-Apr       Impact factor: 3.437

3.  Association between patient reported outcomes and quantitative sensory tests for measuring long-term neurotoxicity in breast cancer survivors treated with adjuvant paclitaxel chemotherapy.

Authors:  Dawn L Hershman; Louis H Weimer; Antai Wang; Grace Kranwinkel; Lois Brafman; Deborah Fuentes; Danielle Awad; Katherine D Crew
Journal:  Breast Cancer Res Treat       Date:  2010-12-03       Impact factor: 4.872

4.  Paclitaxel-induced peripheral neuropathy in patients receiving adjuvant chemotherapy for breast cancer.

Authors:  Yuko Tanabe; Kenji Hashimoto; Chikako Shimizu; Akihiro Hirakawa; Kenichi Harano; Mayu Yunokawa; Kan Yonemori; Noriyuki Katsumata; Kenji Tamura; Masashi Ando; Takayuki Kinoshita; Yasuhiro Fujiwara
Journal:  Int J Clin Oncol       Date:  2011-11-22       Impact factor: 3.402

5.  Statins and risk of polyneuropathy: a case-control study.

Authors:  D Gaist; U Jeppesen; M Andersen; L A García Rodríguez; J Hallas; S H Sindrup
Journal:  Neurology       Date:  2002-05-14       Impact factor: 9.910

Review 6.  Chemotherapy-induced peripheral neurotoxicity.

Authors:  Guido Cavaletti; Paola Marmiroli
Journal:  Nat Rev Neurol       Date:  2010-11-09       Impact factor: 42.937

7.  Statistical identification of predictors for paclitaxel-induced peripheral neuropathy in patients with breast or gynaecological cancer.

Authors:  Yuko Kanbayashi; Toyoshi Hosokawa; Jo Kitawaki; Tetsuya Taguchi
Journal:  Anticancer Res       Date:  2013-03       Impact factor: 2.480

8.  Psychometric evaluation of the Functional Assessment of Cancer Therapy/Gynecologic Oncology Group-Neurotoxicity (Fact/GOG-Ntx) questionnaire for patients receiving systemic chemotherapy.

Authors:  E A Calhoun; E E Welshman; C-H Chang; J R Lurain; D A Fishman; T L Hunt; D Cella
Journal:  Int J Gynecol Cancer       Date:  2003 Nov-Dec       Impact factor: 3.437

9.  Weekly paclitaxel in the adjuvant treatment of breast cancer.

Authors:  Joseph A Sparano; Molin Wang; Silvana Martino; Vicky Jones; Edith A Perez; Tom Saphner; Antonio C Wolff; George W Sledge; William C Wood; Nancy E Davidson
Journal:  N Engl J Med       Date:  2008-04-17       Impact factor: 91.245

10.  Randomized double-blind placebo-controlled trial of acetyl-L-carnitine for the prevention of taxane-induced neuropathy in women undergoing adjuvant breast cancer therapy.

Authors:  Dawn L Hershman; Joseph M Unger; Katherine D Crew; Lori M Minasian; Danielle Awad; Carol M Moinpour; Lisa Hansen; Danika L Lew; Heather Greenlee; Louis Fehrenbacher; James L Wade; Siu-Fun Wong; Gabriel N Hortobagyi; Frank L Meyskens; Kathy S Albain
Journal:  J Clin Oncol       Date:  2013-06-03       Impact factor: 44.544

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  5 in total

1.  Evaluation of risk factors associated with carboplatin and nab-paclitaxel treatment suspension in patients with non-small cell lung cancer.

Authors:  Yoshitaka Saito; Yoh Takekuma; Naofumi Shinagawa; Mitsuru Sugawara
Journal:  Support Care Cancer       Date:  2022-01-23       Impact factor: 3.603

Review 2.  Chemotherapy-induced peripheral neuropathy: where are we now?

Authors:  Lesley A Colvin
Journal:  Pain       Date:  2019-05       Impact factor: 7.926

Review 3.  The Method of Activating Blood and Dredging Collaterals for Reducing Chemotherapy-Induced Peripheral Neuropathy: A Systematic Review and Meta-Analysis.

Authors:  Zhaoyi Li; Huimin Jin; Qingying Yan; Leitao Sun; Harpreet S Wasan; Minhe Shen; Shanming Ruan
Journal:  Evid Based Complement Alternat Med       Date:  2019-06-03       Impact factor: 2.629

Review 4.  Targeting strategies for oxaliplatin-induced peripheral neuropathy: clinical syndrome, molecular basis, and drug development.

Authors:  Yang Yang; Bing Zhao; Xuejiao Gao; Jinbing Sun; Juan Ye; Jun Li; Peng Cao
Journal:  J Exp Clin Cancer Res       Date:  2021-10-22

5.  Risk Factors for Chemotherapy-Induced Peripheral Neuropathy Caused by Nanoparticle Albumin-Bound Paclitaxel in Advanced Breast Cancer.

Authors:  Qie Guo; Haonan Zhang; Xiao Li; Xianghua Quan
Journal:  Biomed Res Int       Date:  2022-09-13       Impact factor: 3.246

  5 in total

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