HPE CINV Pocket Guide 2018 | Page 37

do not want to waste the doctor’s time • do not know whether their symptoms are severe enough to warrant attention • believe symptoms will not last long • do not know treatment is available • see symptoms as proof that chemotherapy is having an effect • are afraid that if they ‘complain’ their chemotherapy dose will be reduced, delayed or stopped • do not want to seem weak • might have forgotten the severity by the time of their next assessment if symptoms develop after they have returned home. With the correct use of antiemetic drugs, CINV can be prevented in almost 70%, and even up to 80%, of patients. However, despite the availability of guidelines, there is emerging evidence that adherence to, and implementation of, treatment recommendations are less than optimal. 18 Only 11% of HEC, 29% of AC and 39% of MEC patients receive an antiemetic prophylaxis consistent with international antiemetic guidelines. 19 Adherence to treatment guidelines can improve outcomes. In a prospective observational study of almost 1000 chemotherapy-naïve patients receiving single-day HEC or MEC, 59.9% (172/287) of patients in the guideline consistent CINV prophylaxis group achieved a complete response (CR) compared with 50.7% (357/704) in the guideline-inconsistent CINV prophylaxis group (p=0.008). 1 Adherence to a single dose of NEPA and efficacy of NEPA was shown in those 1286 (88%) patients who participated in a Phase III trial with a multiple-cycle extension for a total of 5969 cycles. Out of these patients 76% completed ≥4 cycles. The proportion of patients with an overall CR was significantly greater for NEPA than oral palonosetron for cycles 1–4 (74.3 vs 66.6 %, 80.3 vs 66.7 %, 83.8 vs 70.3 %, and 83.8 vs 74.6 %, respectively; p≤0.001 each cycle). The cumulative percentage of patients with a sustained CR over all four cycles was also greater for NEPA (p<0.0001). 19 Choice and convenience Patient choice and patient preference might influence adherence to antiemesis regimens. For example, being offered an oral rather than an IV formulation hospitalpharmacyeurope.com | 2018 | 37