Adverse reactions to docetaxel: an active survey

Author:

Pereira Leandro Cabral1,Nogueira Thaísa Amorim2,Barbosa Leandro Augusto de Oliveira3,Calil-Elias Sabrina4,Castilho Selma Rodrigues de4

Affiliation:

1. Instituto Nacional do Câncer, Brazil

2. Universidade Federal do Rio de Janeiro, Brazil

3. Universidade Federal de São João del-Rei, Brazil

4. Federal Fluminense University, Brazil

Abstract

The rates of breast cancer mortality remain high in Brazil. Docetaxel is a semi-synthetic taxane used to treat various tumors, particularly tumors of the breast, lung and prostate. In this study ADR that occurred in 45 docetaxel users with breast cancer were surveyed. They were identified by type, causality (Naranjo algorithm and World Health Organization categories) and, if considered probable or defined, rated for severity according to SOBRAFO proposal (2007). A total of 325 ADR were observed: 165 in the first, 137 in the second and 23 in the third cycle. Fifty seven ADR were immediate and the others, late. Fatigue and exhaustion for more than five days, classified as Grade 3 by SOBRAFO (2007), were reported as the primary late RAM. There was no significant difference in the occurrence of immediate and late ADR between cycles (p=1 and p=0.3577, respectively). The presence of a pharmacist gave the patients a better understanding of the occurrence of RAM, especially those that occur outside the hospital, between chemotherapy cycles and are often not reported to the healthcare team, creating institutional demands and reaching the goal to track, observe and correlate the RAM for each user.

Publisher

FapUNIFESP (SciELO)

Subject

General Pharmacology, Toxicology and Pharmaceutics

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