ABSTRACT: BACKGROUND: Breast cancer is the most common malignancy in women in the United States and is second only to lung cancer as a cause of cancer death. Worldwide, breast cancer is the most frequently diagnosed cancer and the chief cause of cancer death among females. The National Comprehensive Cancer Network Guidelines recommend taxanes for the treatment of early-stage and metastatic breast cancer. Peripheral neuropathy is a common non-hematological side effect of taxanes, which may result in chemotherapy delays, reductions, discontinuations and poor quality of life. Taxane-induce peripheral nerve damage can lead motor and sensory symptoms. Initial detection of peripheral neuropathy simplifies complete regression since an acute taxane induce peripheral neuropathy is both reversible and mild to moderate in severity. Till now, there are no accepted preventive procedures or expectable parameters for chemotherapy induced peripheral neuropathy including taxanes, however duloxetine 60mg was official in large randomized phase 3 trials for treatment of chemotherapy induce peripheral neuropathy. PATIENTS AND METHOD: Single institution retrospective study started between November 2019 to December 2020, was conducted in Babil Oncology Center/Babil/Iraq which included 60 randomly selected patients with breast cancer, receiving chemotherapy including Taxane group and had undergone nerve conduction study. A collected multiple demographic parameters were compared by dividing the patients into two groups; patients who developed taxane induce peripheral neuropathy and patients who were not developed, these parameters were: patient age, body mass index , hormonal receptor status, human epidermal growth receptor 2 status, metastatic setting and duration and period of last cycle of taxane received. The clinical information, histological and immunohistochemistry laboratory results for each patient obtained from the Oncology Patients Archive Unit, then the statistical process was carried out on the collected information. RESULTS: Of 60 patients included in this study, 15 patients (25 %) developed taxane related peripheral neuropathy, of whom 13 (86.7%) developed mixed sensorimotor peripheral neuropathy and two (13.3%) patients developed sensory neuropathy. While the severity ranged from mild (one patient), mild to moderate (10 patients), moderate (4 patients) and there was neither sever nor life threatening peripheral neuropathy. The mean age of patients was 51.38 years and mean body mass index of patients was 26.24 Kg/m2. Peripheral neuropathy had statically significant association with age, body mass index and human epidermal growth receptor 2. Peripheral neuropathy was somewhat more in metastatic setting but statically insignificant. CONCLUSION: About one fourth of patients developed peripheral neuropathy after receiving taxane chemotherapy. Elderly, obese patients and patients who have human epidermal growth receptor 2 positive tumors are predictors for taxane induce peripheral neuropathy. |
REFERENCES:
- Siegel RL, Miller KD, Jemal A. Cancer statistics. CA Cancer J Clin. 2020;70:7–30.
- Denoix PF. Treatment plan adopted at the Gustave-Roussy Institute for malignant breast tumors. Ann Chir. 1997;51:544–46.
- Alwan NA. Breast cancer among Iraqi women :preliminary findings from a regional comparative Breast Cancer Research Project. Journal of global oncology. 2016 16;2:255-58.
- Tufia C. Haddad, MD, and Charles L. Loprinzi, MD, Breast cancer, ASCO-SEP MEDICAL ONCOLOGY SELF EVALUATION PROGRAM, Martee L. Hensley, 2016; 5th ed. 225-84.
- Kavallaris M. Microtubules and resistance to tubulin-binding agents. Nat Rev Cancer 2010;10.
- Nogales E. Structural insight into microtubule function. Annu Rev Biophys Biomol Struct 2001;30:397–420.
- Schiff PB, Fant J, Horwitz SB. Promotion of microtubule assembly in vitro by taxol. Nature. 1979; 277,665-67.
- Kudlowitz D, Muggia F. Defining risks of taxane neuropathy: insights from randomized clinical trials. Clin Cancer Res 2013;19.
- Gornstein E, Schwarz TL. The paradox of paclitaxel neurotoxicity: mechanisms and unanswered questions. Neuropharmacology 2014;76:175–83.
- Staff NP, Grisold A, Grisold W. Chemotherapy-induced peripheral neuropathy: A current review. Ann Neurol. 2017;81:772–81.
- Argyriou A.A., Bruna J., Marmiroli P., Cavaletti G. Chemotherapy-induced peripheral neurotoxicity (CIPN): An update. Crit. Rev. Oncol. Hematol. 2012; 82:51–77. doi: 10.1016/j.critrevonc.2011.04.012.
- SM, J. BH, W. BA, M. CC, E. DG, M. H, et al. NCCN task force report: Management of neuropathy in cancer. J Natl Compr Cancer Netw. 2009;7(suppl. 5).
- Pietrangeli A, Leandri M, Terzoli E, Jandolo B, Garufi C. Persistence of high- dose oxaliplatin-induced neuropathy at long-term follow-up. Eur Neurol. 2006; 56:13–16.
- Cornblath DR, Chaudhry V, Carter K, Lee D, Seysedadr M, Miernicki M, et al. Total neuropathy score: Validation and reliability study. Neurology. 1999;53:1660–60.
- Smith EML, Pang H, Cirrincione C, Fleishman S, Paskett ED, Ahles T, et al. Effect of duloxetine on pain, function, and quality of life among patients with chemotherapy-induced painful peripheral neuropathy: A randomized clinical trial. JAMA. 2013;309:1359.
- NCCN practice guidelines in oncology: breast cancer. (Ver. 5, 2020). Available from: https://www2.tri-kobe.org/nccn/guideline/breast/english/breast.pdf.
- Hausheer FH, Schilsky RL, Bain S, Berghorn EJ, Lieberman F. Diagnosis, management, and evaluation of chemotherapy-induced peripheral neuropathy. Semin Oncol. 2006;33:15–49.
- Swain SM, Arezzo JC. Neuropathy associated with microtubule inhibitors: diagnosis, incidence, and management. Clin Adv Hematol Oncol. 2008;6:455–67.
- Song SJ, Min J, Suh SY, Jung SH, Hahn HJ, Im S-A, et al. Incidence of taxane-induced peripheral neuropathy receiving treatment and prescription patterns in patients with breast cancer. Support Care Cancer. 2017;25:2241–48.
- Candelario N, Wongrakpanich S, Morginstin MS. Predictors of chemotherapy-induced peripheral neuropathy among breast cancer patients treated with taxanes. J Clin Oncol. 2015;33(28_suppl):90–90.
- Ghoreishi Z, Keshavarz S, Asghari Jafarabadi M, Fathifar Z, Goodman KA, Esfahani A. Risk factors for paclitaxel-induced peripheral neuropathy in patients with breast cancer. BMC Cancer [Internet]. 2018;18. Available from: http://dx.doi.org/10.1186/s12885-018-4869-5.
- Molassiotis A, Cheng HL, Leung KT, Li YC, Wong KH, Au JSK, et al. Risk factors for chemotherapy‐induced peripheral neuropathy in patients receiving taxane‐ and platinum‐based chemotherapy. Brain Behav [Internet]. 2019;9. Available from: http://dx.doi.org/10.1002/brb3.1312.
- Rivera E, Cianfrocca M. Overview of neuropathy associated with taxanes for the treatment of metastatic breast cancer. Cancer Chemother Pharmacol. 2015;75:659–70.
- Lichtman SM, Hurria A, Cirrincione CT, Seidman AD, Winer E, Hudis C, et al. Paclitaxel efficacy and toxicity in older women with metastatic breast cancer: combined analysis of CALGB 9342 and 9840. Ann Oncol. 2012;23:632–38.
- Carlson RH. HER2+ patients at higher risk for chemotherapy-induced peripheral neuropathy. Oncol times. 2015; 37:13–14.
- Seidman AD, Berry D, C C. Randomized phase III trial of weekly compared with every-3-weeks paclitaxel for metastatic breast cancer, with trastuzumab for all HER-2 overexpressors and random assignment to trastuzumab or not in HER-2 nonoverexpressors: final results of Cancer and Leukemia Group B protocol 9840. J Clin Oncol. 2008; 26:1642–49.
- Smith EML. Current methods for the assessment and management of taxane-related neuropathy. Clin J Oncol Nurs. 2013;17:22–34.
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