Adverse drug reaction profile of cisplatin-based chemotherapy regimen in a tertiary care hospital in India

Authors

  • M. B. Sasmi Department of Pharmacology, Government Medical College, Thiruvananthapuram, Kerala, India

DOI:

https://doi.org/10.18203/2319-2003.ijbcp20151361

Keywords:

Causality, Chemotherapy, Cisplatin, Pharmacovigilance

Abstract

Background: This study was undertaken to analyze the pattern of occurrence of adverse drug reaction (ADR) to cisplatin-based chemotherapy regimen in an oncology ward of a tertiary care hospital.

Methods: Cancer patients who received cisplatin-based chemotherapy were monitored for ADRs. The collected reports were analyzed for demographic and drug details; causality, preventability, and severity of ADRs. Causality assessed by the WHO Causality Assessment Scale and Naranjo’s Algorithm. Preventability and severity assessed by Schumock–Thornton scale and modified Hartwig–Siegel scale, respectively.

Results: Among 138 patients, 125 developed adverse reactions to cisplatin-based chemotherapy. The results observed were alopecia, nausea, vomiting, renal toxicity, peripheral neuropathy, electrolyte imbalance, etc. The WHO Assessment Scale showed 95% possible and 5% probable reactions. Whereas Naranjo’s Algorithm showed 83% probable and 17% possible reactions. Most of the reactions belonged to the category of “not preventable.” Reactions such as nausea and vomiting belonged to the category of “definitively preventable.” Modified Hartwig–Siegel scale showed most of the reactions were of mild Level 1 category.

Conclusions: Cisplatin-based regimen has high potential to cause adverse effects. Most of the reactions were mild in nature, but not preventable. The common adverse effects, such as nausea and vomiting, were preventable.

References

Lazarou J, Pomeranz BH, Corey PN. Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies. JAMA. 1998;279(15):1200-5.

Adithan C. National Pharmacovigilance Programme. Indian J Pharmacol. 2005;37:347.

World Health Organisation. Uppsala Monitoring Center. Causality Assessment of Suspected Adverse Reactions. Available at http://www.who-umc.org/DynPage.aspx. Accessed 24 August 2011.

Jose J, Rao PG. Pattern of adverse drug reactions notified by spontaneous reporting in an Indian tertiary care teaching hospital. Pharmacol Res. 2006;54(3):226-33.

Mallik S, Palaian S, Ojha P, Mishra P. Pattern of adverse drug reactions due to cancer chemotherapy in a tertiary care teaching hospital in Nepal. Pak J Pharm Sci. 2007;20(3):214-8.

Chu E, Sartorelli AC. Cancer chemotherapy. In: Katzung BG, editor. Basic and Clinical Pharmacology. 11th Edition. New York: McGraw Hill; 2009: 943-4.

Surendiran A, Balamurugan N, Gunaseelan K, Akhtar S, Reddy KS, Adithan C. Adverse drug reaction profile of cisplatin-based chemotherapy regimen in a tertiary care hospital in India: an evaluative study. Indian J Pharmacol. 2010;42(1):40-3.

World Health Organisation. Uppsala Monitoring Center. Causality Assessment of Suspected Adverse Reactions. Available at http://www.who-umc.org/DynPage. Cited 31 December 2008.

Naranjo CA, Busto U, Sellers EM, Sandor P, Ruiz I, Roberts EA, et al. A method for estimating the probability of adverse drug reactions. Clin Pharmacol Ther. 1981;30(2):239-45.

Schumock GT, Thornton JP. Focusing on the preventability of adverse drug reactions. Hosp Pharm. 1992;27(6):538.

Hartwig SC, Siegel J, Schneider PJ. Preventability and severity assessment in reporting adverse drug reactions. Am J Hosp Pharm. 1992;49(9):2229-32.

Bahl A, Sharma DN, Julka PK, Rath GK. Chemotherapy related toxicity in locally advanced non-small cell lung cancer. J Cancer Res Ther. 2006;2(1):14-6.

Chen SC, Lin MC, Chang JW, Wang SW, Lee CH, Tsao TC. Phase II study of regimen of gemcitabine and cisplatin in advanced non-small cell lung cancer. Jpn J Clin Oncol. 2000;30(11):494-8.

Lee SM, James LE, Qian W, Spiro S, Eisen T, Gower NH, et al. Comparison of gemcitabine and carboplatin versus cisplatin and etoposide for patients with poor-prognosis small cell lung cancer. Thorax. 2009;64(1):75-80.

Chadha V, Shenoi SD. Hair loss in cancer chemotherapeutic patients. Indian J Dermatol Venereol Leprol. 2003;69(2):131-2.

Botchkarev VA. Molecular mechanisms of chemotherapy-induced hair loss. J Investig Dermatol Symp Proc. 2003;8(1):72-5.

Zucali PA, Soto Parra HJ, Cavina R, Campagnoli E, Latteri F, De Vincenzo F, et al. Short schedule of cisplatin and vinorelbine: a dose-finding study in non-small-cell lung cancer. Oncology. 2006;71(3-4):229-36.

Georgoulias V, Ardavanis A, Tsiafaki X, Agelidou A, Mixalopoulou P, Anagnostopoulou O, et al. Vinorelbine plus cisplatin versus docetaxel plus gemcitabine in advanced non-small-cell lung cancer: a phase III randomized trial. J Clin Oncol. 2005;23(13):2937-45.

Reichman B, Markman M, Hakes T, Hoskins W, Rubin S, Jones W, et al. Intraperitoneal cisplatin and etoposide in the treatment of refractory/recurrent ovarian carcinoma. J Clin Oncol. 1989;7(9):1327-32.

Sharma M, Gupta SK, Gupta VB, Chatterjee A. A comparative study of causality assessment scales used in the analysis of spontaneously reported events: WHO-UMC criteria vs naranjo probability scale. Indian J Pharm. 2008;40(2):64.

Downloads

Published

2017-01-16

How to Cite

Sasmi, M. B. (2017). Adverse drug reaction profile of cisplatin-based chemotherapy regimen in a tertiary care hospital in India. International Journal of Basic & Clinical Pharmacology, 4(6), 1214–1219. https://doi.org/10.18203/2319-2003.ijbcp20151361

Issue

Section

Original Research Articles