Preview

Supportive Therapy in Oncology

Advanced search

Problems of oxaliplatin-induced neuropathy in patients with colorectal cancer

https://doi.org/10.17650/3034-2473-2024-1-1-21-30

Abstract

Aim. To investigate the methods of early diagnosis of oxaliplatin-induced peripheral neuropathy (PN).

Materials and methods. The study included 52 patients with diagnosis of metastatic colorectal cancer receiving 1st line polychemotherapy per the mFOLFOX6 scheme ± targeted therapy who prior to each cycle filled out the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Chemotherapy-Induced Peripheral Neuropathy (EORTC QLQ CIPN 20) and were subject to neurological examination using the Neuropathy Disability Scale (NDS).

Results. The analysis included 28 patients who completed polychemotherapy: 16 (57,2 %) men and 12 (42,8 %) women, mean age 60.0 ± 10.0 years. Fridman’s two-way analysis of variance by ranks showed significant changes in the scores (sensory, motor, autonomic) of the EORTC QLQ CIPN 20 questionnaire with the increase in the number of chemotherapy cycles (р = 0.001). Significant increase in the sensory and motor scores was observed after the 3rd cycle, in the autonomic – after the 6th cycle. Significant increase in NDS score was observed starting at the 3rd cycle, and vibration sensitivity on the medial ankle or at the base of the 1st toe significantly decreased after the 1stcycle. Median number of cycles at which oxaliplatin dose was reduced or the drug was discontinued due to clinically significant symptoms of PN irrespective of questionnaire results and neurological examination was 6.

Conclusion. According to the results of the study, the following conclusions were made: 1) sensory scale of the 3-part EORTC QLQ CIPN 20 questionnaire (9 questions of 20) or motor scale (7 questions of 20), vibration sensitivity can be considered as stand-alone informative tests; 2) in a large patient cohort, NDS score increase to 5, EORTC QLQ CIPN 20 sensory scale score increase to 12 and higher or decreased vibration sensitivity on the medial ankle or at the base of the 1st toe to 4.5 arbitrary units should be considered early manifestations of PN; 3) for a routine algorithm, it is acceptable to consider a combination of 9 questions of the sensory or 7 questions of the motor scales of the EORTC QLQ CIPN 20 questionnaire and evaluation of vibration sensitivity on the medial ankle or at the base of the 1st toe to decide on oxaliplatin dose reduction or measures for prevention of peripheral neuropathy symptom worsening. 

About the Authors

S. A. Natalenko
St. Petersburg City Clinical Oncological Dispensary; St. Petersburg University
Russian Federation

3/5 2nd Berezovaya Alley, St. Petersburg 197022;  7/9, Universitetskaya Emb., St. Petersburg 199034



R. V. Orlova
St. Petersburg City Clinical Oncological Dispensary; St. Petersburg University
Russian Federation

3/5 2nd Berezovaya Alley, St. Petersburg 197022;  7/9, Universitetskaya Emb., St. Petersburg 199034



S. I. Kutukova
St. Petersburg City Clinical Oncological Dispensary; I.P. Pavlov First Saint Petersburg State Medical University
Russian Federation

3/5 2nd Berezovaya Alley, St. Petersburg 197022;  6–8 L’va Tolstogo St., St. Petersburg 197022



N. P. Belyak
St. Petersburg City Clinical Oncological Dispensary; St. Petersburg University
Russian Federation

3/5 2nd Berezovaya Alley, St. Petersburg 197022;  7/9, Universitetskaya Emb., St. Petersburg 199034



S. M. Malyshev
V.L. Polenov Russian Research Neurosurgical Institute – branch of the Almazov National Medical Research Center, Ministry of Health of Russia
Russian Federation

2 Mayakovskogo St., St. Petersburg 191014



References

1. Cancer today. International Agency for Research on Cancer. WHO. Available at: https://gco.iarc.fr/en

2. The state of cancer care for the Russian population in 2022. Ed. by A.D. Kaprin, V.V. Starinsky, A.O. Shakhzadova. Moscow: MNIOI im. P.A. Gertsena – filial FGBU “NMITS radiologii” Minzdrava Rossii, 2022. 239 p. (In Russ.).

3. Fedyanin M.Yu., Gladkov O.A., Gordeev S.S. et al. Practical recommendations for the drug treatment of cancer of the colon, recto-sigmoid junction and rectum. Practical recommendations of the Russian Society of Clinical Oncology. Part 1. Zlokachestvenniye opukholi = Malignant Tumors 2023;13(3s2):425–82. (In Russ.).

4. Malignant neoplasms of the colon and rectosigmoid region. Clinical recommendations of the Ministry of Health of Russia. 2018. Available at: https://oncology.ru/association/clinicalguidelines/2018/rak_obodochnoy_kishki_pr2018.pdf (In Russ.).

5. Tournigand C., André T., Achille E. et al. FOLFIRI followed by FOLFOX6 or the reverse sequence in advanced colorectal cancer: a randomized GERCOR study. J Clin Oncol 2004;22(2):229–37. DOI: 10.1200/JCO.2004.05.113

6. Thibault V., Leguelinel-Blache G., Obled S. et al. [Chemotherapy for colorectal cancer: pragmatic assessment of prescription changes and relative dose intensity (In French)]. Bull Cancer 2017;104(9):714–20. DOI: 10.1016/j.bulcan.2017.04.006

7. Wang R.Y., Lin X.L., Xiang S.T. et al. Risk factors for oxaliplatininduced peripheral neuropathy: a systematic review and metaanalysis. Eur Rev Med Pharmacol Sci 2022;26(11):4028–43. DOI: 10.26355/eurrev_202206_28973

8. Sánchez-Barroso L., Apellaniz-Ruiz M., Gutiérrez-Gutiérrez G. et al. Concomitant medications and risk of chemotherapy-induced peripheral neuropathy. Oncologist 2019;24(8):e784–92. DOI: 10.1634/theoncologist.2018-0418

9. Schmitt L.I., Leo M., Kleinschnitz C., Hagenacker T. Oxaliplatin modulates the characteristics of voltage-gated calcium channels and action potentials in small dorsal root ganglion neurons of rats. Mol Neurobiol 2018;55(12):8842–55. DOI: 10.1007/s12035-018-1029-5

10. Mou J., Paillard F., Turnbull B. et al. Qutenza (capsaicin) 8 % patch onset and duration of response and effects of multiple treatments in neuropathic pain patients. Clin J Pain 2014;30(4):286–94. DOI: 10.1097/AJP.0b013e31829a4ced

11. Latipova D.H., Andreev V.V., Maslova D.A. et al. Neurolo-gical complications of antitumor drug therapy Practical recommendations of the Russian Society of Clinical Oncology. Part 1. Zlokachestvenniye opukholi = Malignant Tumors 2023;13(3s2):300–9. (In Russ.).

12. Avan A., Postma T.J., Ceresa C. et al. Platinum-induced neurotoxicity and preventive strategies: past, present, and future. Oncologist 2015;20(4):411–32. DOI: 10.1634/theoncologist.2014-0044

13. Ali N.T., Mohamed A.A., Yousef B.A. The incidence of oxaliplatininduced peripheral neurotoxicity at Khartoum Oncology Hospital: a cross-sectional survey. Asia Pac J Oncol Nurs 2020;7(3):266–72. DOI: 10.4103/apjon.apjon_12_20

14. Denduluri N., Lyman G.H., Wang Y. et al. Chemotherapy dose intensity and overall survival among patients with advanced breast or ovarian cancer. Clin Breast Cancer 2018;18(5):380–6. DOI: 10.1016/j.clbc.2018.02.003

15. Sprowl J.A., Ciarimboli G., Lancaster C.S. et al. Oxaliplatin-induced neurotoxicity is dependent on the organic cation transporter OCT2. Proc Natl Acad Sci U S A 2013;110(27):11199–204. DOI: 10.1073/pnas.1305321110

16. Yang Y., Zhao B., Gao X. et al. Targeting strategies for oxaliplatininduced peripheral neuropathy: clinical syndrome, molecular basis, and drug development. J Exp Clin Cancer Res 2021;40(1):331. DOI: 10.1186/s13046-021-02141-z

17. Illias A.M., Gist A.C., Zhang H. et al. Chemokine CCL2 and its receptor CCR2 in the dorsal root ganglion contribute to oxaliplatininduced mechanical hypersensitivity. Pain 2018;159(7):1308–16. DOI: 10.1097/.pain.0000000000001212

18. Maruta T., Nemoto T., Hidaka K. et al. Upregulation of ERK phosphorylation in rat dorsal root ganglion neurons contributes to oxaliplatin-induced chronic neuropathic pain. PLoS One 2019;14(11):e0225586. DOI: 10.1371/journal.pone.0225586

19. Common Terminology Criteria for Adverse Events (CTCAE), version 5.0. U.S. Department of Health and Human Services, 2017.

20. Fallon M.T., Storey D.J., Krishan A. et al. Cancer treatment-related neuropathic pain: proof of concept study with menthol – a TRPM8 agonist. Support Care Cancer 2015;23(9):2769–77. DOI: 10.1007/s00520-015-2642-8

21. Maihöfner C.G., Heskamp M.L. Treatment of peripheral neuropathic pain by topical capsaicin: impact of pre-existing pain in the QUEPPstudy. Eur J Pain 2014;18(5):671–9.

22. Maihöfner C., Diel I., Tesch H. et al. Chemotherapy-induced peripheral neuropathy (CIPN): current therapies and topical treatment option with high-concentration capsaicin. Support Care Cancer 2021;29(8):4223–38. DOI: 10.1007/s00520-021-06042-x

23. Burgess J., Ferdousi M., Gosal D. et al. Chemotherapy-induced peripheral neuropathy: epidemiology, pathomechanisms and treatment. Oncol Ther 2021;9(2):385–450. DOI: 10.1007/s40487-021-00168-y

24. Ling B., Authier N., Balayssac D. et al. Behavioral and pharmacological description of oxaliplatin-induced painful neuropathy in rat. Pain 2007;128(3):225–34. DOI: 10.1016/j.pain.2006.09.016

25. Smith E.M.L., Pang H., Cirrincione C. 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(13):1359–67. DOI: 10.1001/jama.2013.2813

26. Hirayama Y., Ishitani K., Sato Y. et al. Effect of duloxetine in Japanese patients with chemotherapy-induced peripheral neuropathy: a pilot randomized trial. Int J Clin Oncol 2015;20(5):866–71. DOI: 10.1007/s10147-015-0810-y

27. Chow R., Novosel M., So O.W. et al. Duloxetine for prevention and treatment of chemotherapy-induced peripheral neuropathy (CIPN): systematic review and meta-analysis. BMJ Support Palliat Care 2023;13(1):27–34.

28. Zimmerman C., Atherton P.J., Pachman D. et al. MC11C4: a pilot randomized, placebo-controlled, double-blind study of venlafaxine to prevent oxaliplatin-induced neuropathy. Support Care Cancer 2016;24(3):1071–8. DOI: 10.1007/s00520-015-2876-5

29. Franck H., Potter J., Caballero J. Venlafaxine and duloxetine: a comparison of efficacy and tolerability for the treatment of depression in elderly patients. Mental Health Clinician 2013;3(5):258–65. DOI: 10.9740/mhc.n178920

30. De Andrade D.C., Jacobsen Teixeira M., Galhardoni R. et al. Pregabalin for the prevention of oxaliplatin-induced painful neuropathy: a randomized, double-blind trial. Oncologist 2017;22(10): 1154–e105. DOI: 10.1634/theoncologist.2017-0235

31. Zhao M., Nakamura S., Miyake T. et al. Pharmacological characterization of standard analgesics on oxaliplatin-induced acute cold hypersensitivity in mice. J Pharmacol Sci 2014;124(4):514–7. DOI: 10.1254/jphs.13249sc

32. Klafke N., Bossert J., Kröger B. et al. Prevention and treatment of chemotherapy-induced peripheral neuropathy (CIPN) with nonpharmacological interventions: clinical recommendations from a systematic scoping review and an expert consensus process. Med Sci (Basel) 2023;11(1):15. DOI: 10.3390/medsci11010015

33. Boulton A.J., Gries F.A., Jervell J.A. Guidelines for the diagnosis and outpatient management of diabetic peripheral neuropathy. Diabet Med 1998;15(6):508–14. DOI: 10.1002/(SICI)1096- 9136(199806)15:63.0.CO;2-L


Review

For citations:


Natalenko S.A., Orlova R.V., Kutukova S.I., Belyak N.P., Malyshev S.M. Problems of oxaliplatin-induced neuropathy in patients with colorectal cancer. Supportive Therapy in Oncology. 2024;1(1):21-30. (In Russ.) https://doi.org/10.17650/3034-2473-2024-1-1-21-30

Views: 244


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 3034-2473 (Print)
ISSN 3034-3178 (Online)