Perioperative Treatment of Combined Radiotherapy With SOX, Apatinib and Camrelizumab for Oesophagogastric Cancer

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorRuijin Hospital

About this trial

The study is being conducted to evaluate the efficacy, safety and tolerability of radiotherapy and chemotherapy, apatinib with camrelizumab in the neoadjuvant (prior to surgery) and adjuvant (after surgery) treatment of previously untreated adults with gastric and gastroesophageal junction (GEJ) adenocarcinoma.

Eligibility criteria

Qualifiers

Has previously untreated localized gastric or GEJ adenocarcinoma as defined by T3-4N+M0;

Plans to proceed to surgery following pre-operative chemotherapy. Has an Eastern Cooperative Oncology Group (ECOG) performance status score of 0 to 1.

Has adequate organ function.

Male participants of childbearing potential must agree to use an adequate method of contraception for the course of the study through 120 days after the last dose of therapy.

Disqualifiers

Uncontrolled hypertension ( systolic ≥140 mmHg or diastolic ≥90 mmHg despite antihypertensive therapy)

Known hypersensitivity to any of the study drugs or excipients.

Known hereditary or acquired bleeding and thrombotic tendencies (e.g. hemophiliacs, coagulation disorders, thrombocytopenia, etc.);

Congenital or acquired immune deficiency (e.g. HIV infected)

Trial design

Treatments tested in this trial

  • Apatinib+Camrelizumab+SOX
  • Preoperative Radiotherapy

Treatment groups

30 Participants
are divided into 1 treatment group

Sponsors and collaborators