The Efficacy and Safety of Fosrolapitant and Palonosetron Hydrochloride for Injection in Preventing Nausea and Vomiting Caused by Multi-cycle Immunotherapy and Chemotherapy in Patients With Esophageal Cancer and Lung Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorSecond Affiliated Hospital, School of Medicine, Zhejiang University

About this trial

This study was a randomized, parallel, cohort study to evaluate the efficacy and safety of Fosrolapitant and Palonosetron Hydrochloride for Injection in preventing nausea and vomiting caused by multi-cycle immunotherapy and chemotherapy in patients with esophageal cancer and lung cancer. A total of 120 subjects are planned to be enrolled, with 60 in each cohort. 40% of the subjects will undergo an interim analysis upon completion of the study.

The trial consists of a screening period, a treatment period and a safety follow-up period. Drug treatment was administered in accordance with the trial protocol, and then the corresponding follow-up and examination were completed in accordance with the trial process table. During the research period, if the researcher assesses that the subjects indeed need to use remedial antiemetic drugs, remedial treatment can be carried out based on clinical practice. The specific types, usage, dosage and frequency of the drugs are determined by the researcher.

Eligibility criteria

Qualifiers

Age ≥18 years old, gender not limited;

Histologically or cytologically confirmed untreated locally advanced/metastatic esophageal cancer and lung cancer;

Has not received any chemotherapy drugs in the past (anti-tumor drugs are not used for cancer treatment);

Plan to receive at least 4 cycles of chemotherapy combined with immunotherapy based on cisplatin and carboplatin;

Disqualifiers

Abdominal (including the diaphragmatic plane and below) or pelvic radiotherapy was received within 7 days prior to randomization, or is planned to be received within 1 to 8 days of treatment;

It is planned to administer chemotherapy drugs with a high risk of vomiting within 2 to 8 days after platinum infusion.

Plan to receive chemotherapy regimens including common paclitaxel (using castor oil as the solvent);

Take drugs with potential antiemetic effects within 2 days before randomization: The first-generation 5-HT3 receptor antagonists (such as ondansetron), phenthiazide drugs (such as prochlorazine), butanylbenzene drugs (such as haloperidol), benzamides (such as metoclopramide), domperidone, cannabinoids, traditional Chinese medicines with potential antiemetic effects, scopolamine, cyclezine, etc.

Trial design

Treatments tested in this trial

  • Fosrolapitant and Palonosetron Hydrochloride for Injection combined with dexamethasone acetate
  • For injection, fosapirtan dimeglumine combined with palonosetron hydrochloride and dexamethasone acetate

Treatment groups

120 Participants
are divided into 2 treatment groups