Fosaprepitant Dimeglumine in Treating Patients With Nausea and Vomiting Caused By Chemotherapy

OBJECTIVES:

Primary

- To evaluate the efficacy and safety of fosaprepitant dimeglumine in patients with
breakthrough chemotherapy-induced nausea and vomiting (CINV) after failing prophylactic
antiemetic therapy.

Secondary

- To evaluate toxicity and serious adverse events associated with this regimen in these
patients.

- To evaluate the ability of patients to tolerate oral intake.

- To evaluate the health-related quality of life of patients treated with this regimen.

- To evaluate specific side effects associated with this regimen, including pain
sensation and/or soreness at the infusion site, headache, dizziness, and somnolence, in
these patients .

- To refine the study design for future phase II and III studies of rescue therapy for
breakthrough CINV using various secondary endpoints.

OUTLINE: Patients receive chemotherapy in combination with a pre-defined standard
5-Hydroxytryptamine-3 (5-HT3) antagonist or corticosteroid regimen with or without a
benzodiazepine on day 1. If breakthrough nausea or vomiting occurs, patients then receive
fosaprepitant dimeglumine IV once per standard administration guidelines. Patients with
treatment response may receive additional doses of oral aprepitant once on days 2 and 3.
Patients with persistent nausea/vomiting after 2 hours and who desire further treatment may
receive standard rescue therapy with prochlorperazine, metoclopramide, or haloperidol with
or without additional lorazepam until relief, at the discretion of the provider.

Patients complete a diary at baseline, and then at 2, 12, and 24 hours that includes a
Visual Analogue Scale (VAS) for nausea; VAS for sedation; and questions about emesis and
retching frequency, headache, dizziness, somnolence, and ability to take food and liquids
orally. Patients also complete the Functional Living Index-Emesis Quality of Life survey at
baseline and at 24 hours.

DISEASE CHARACTERISTICS:

- Diagnosis of cancer

- Scheduled to receive inpatient chemotherapy containing at least moderately emetogenic
agents

- May be given for adjuvant, neoadjuvant, curative, or palliative intent

- May be given orally, IV, or by continuous infusion on ≥ 1 day

- Scheduled to receive 5-HT3 receptor antagonist antiemetic (e.g., ondansetron,
granisetron, palonosetron, dolasetron mesylate, or dexamethasone with or without a
benzodiazepine) on the day of chemotherapy

- Self-report of at least mild nausea (for which the patient feels needs rescuing) or
moderate nausea (a score of ≥ 2 on a 4-point Likert scale) OR has had ≥ 1 episode of
emesis since receiving chemotherapy

- No history of chronic nausea and/or vomiting (without chemotherapy), anticipatory
nausea and/or vomiting, or emesis within 24 hours before chemotherapy

- No symptomatic brain metastases

PATIENT CHARACTERISTICS:

- Able to understand English

- Not pregnant or nursing

- Negative pregnancy test

- No clinical evidence of current or impending bowel obstruction (i.e., tumor pressing
on the bowel)

- No allergy or intolerance to study drugs

PRIOR CONCURRENT THERAPY:

- See Disease Characteristics

- Prior chemotherapy allowed

- No aprepitant as prophylaxis or rescue treatment during the current course of
chemotherapy (other than as a part of study therapy)

- Not scheduled to receive a dopamine antagonist after chemotherapy