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Published Online, 3 February 2009, www.theannals.com, DOI 10.1345/aph.1L437.
The Annals of Pharmacotherapy: Vol. 43, No. 3, pp. 444-452. DOI 10.1345/aph.1L437
© 2009 Harvey Whitney Books Company.
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ONCOLOGY

Clinical Predictors of Chemotherapy-Induced Nausea and Vomiting in Breast Cancer Patients Receiving Adjuvant Doxorubicin and Cyclophosphamide

Vivianne Shih, BSc (Pharm)Hons BCOP BCPS

Senior Pharmacist, National Cancer Centre Singapore, Singapore

Hee Siew Wan, MSc

Biostatistician, Division of Clinical Trials & Epidemiological Sciences, National Cancer Centre Singapore

Alexandre Chan, PharmD BCPS BCOP

Assistant Professor, Department of Pharmacy, Faculty of Science, National University of Singapore, Singapore; Clinical Pharmacist, Department of Pharmacy, National Cancer Centre Singapore

Reprints: Dr. Chan, Department of Pharmacy, Faculty of Science, National University of Singapore, 18 Science Dr. 4, Block S4, Singapore 117543, fax 65 6779-1554, phaac{at}nus.edu.sg

BACKGROUND: Patients with breast cancer often receive emetogenic anthracycline–based chemotherapy as part of their treatment. Chemotherapy-induced nausea and vomiting (CINV) has been commonly reported as one of the distressing adverse effects among patients with cancer. Despite the advent of newer antiemetics and better understanding of the CINV pathophysiology, total eradication of CINV has yet to be achieved.

OBJECTIVE: To assess the incidence of nausea and vomiting in patients who have breast cancer and are receiving adjuvant doxorubicin and cyclophosphamide (AC) bolus chemotherapy, ascertain patients' risk factors affecting CINV response, and study patient adherence to delayed antiemetics.

METHODS: This was a single-institution, prospective, observational study conducted at an outpatient cancer center in Singapore from December 2006 to December 2007. Clinical events such as CINV were collated using a standardized diary. Use of rescue antiemetics and unscheduled clinic visits due to CINV were documented.

RESULTS: Of a total of 108 participants, 16 patients were lost to follow-up and 1 provided incomplete information; thus, 91 patients were included in the analysis. Delayed antiemetics were given according to the institution's guideline and only 9 (9.9%) patients received aprepitant. Neither acute nor delayed vomiting was reported by a majority of patients and only 4 (4.4%) experienced grade 3 vomiting. The incidence of severe nausea was highest on day 3 of chemotherapy and affected 14.3% of patients. Anxiety and history of chemotherapy-induced nausea were associated with both acute and delayed nausea, and history of motion sickness was associated with delayed vomiting. Approximately 65% of patients were adherent to their prescribed delayed antiemetics.

CONCLUSIONS: Most of our patients adhered to their antiemetics and tolerated AC chemotherapy reasonably well, without vomiting; yet nausea persisted. To improve CINV control, clinicians must actively communicate with patients to facilitate accurate assessment of risk factors and CINV response and to encourage adherence to delayed antiemetics.

Key Words: breast cancer, chemotherapy, nausea, vomiting

Published Online, February 3, 2009. www.theannals.com, DOI 10.1345/aph.1L437





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