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Monoclonal Antibodies
Durvalumab + FLOT for Gastric Cancer
Phase 3
Waitlist Available
Research Sponsored by AstraZeneca
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Patients must undergo radical surgery.
World Health Organization (WHO)/ECOG performance status of 0 or 1 at enrollment.
Must not have
Patients with adenosquamous cell carcinoma, squamous cell carcinoma, or GI stromal tumor.
History of allogeneic organ transplantation.
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 5 years
Awards & highlights
Pivotal Trial
Summary
This trial is testing whether adding durvalumab to a standard chemotherapy mix around the time of surgery can help patients with stomach or gastroesophageal cancer. Durvalumab helps the immune system fight cancer, while the chemotherapy drugs kill cancer cells.
Who is the study for?
This trial is for patients with resectable gastric or gastroesophageal junction adenocarcinoma, who haven't had cancer treatment before. They must be in good physical condition (WHO/ECOG status 0 or 1), have a life expectancy of at least 24 weeks, and adequate organ function. Those on recent immunosuppressants, with certain contraindications, metastasis, non-adenocarcinoma cancers, or an organ transplant history can't join.
What is being tested?
The study tests Durvalumab (an immunotherapy drug) combined with FLOT chemotherapy against a placebo plus FLOT chemotherapy in patients undergoing surgery for their cancer. It's designed to see if adding Durvalumab before and after surgery can improve outcomes.
What are the potential side effects?
Durvalumab may cause immune-related side effects like inflammation in various organs, infusion reactions similar to allergic responses, fatigue and infections. FLOT chemotherapy could lead to nausea, hair loss, low blood cell counts increasing infection risk and bleeding problems.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I will have a major surgery to remove my cancer.
Select...
I am fully active or restricted in physically strenuous activity but can do light work.
Select...
My stomach cancer is operable and at least stage II.
Select...
I have not received any treatment for my current cancer.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
My cancer is either adenosquamous, squamous cell, or a GI stromal tumor.
Select...
I have received an organ transplant from another person.
Select...
My cancer has spread to the lining of my abdomen or other distant parts.
Select...
I am not allergic or intolerant to the drugs used in this study.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 5 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 5 years
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Event-free survival (EFS)
Secondary study objectives
To compare Arm A relative to Arm B on overall survival (OS)
To compare Arm A relative to Arm B on pathological complete response (pCR) rate
Side effects data
From 2022 Phase 3 trial • 867 Patients • NCT0308447126%
Asthenia
20%
Anaemia
20%
Constipation
17%
Decreased appetite
16%
Diarrhoea
15%
Nausea
13%
Pruritus
10%
Urinary tract infection
10%
Cough
10%
Fatigue
9%
Vomiting
9%
Dyspnoea
9%
Back pain
9%
Oedema peripheral
9%
Pyrexia
7%
Arthralgia
7%
Hypothyroidism
7%
Haematuria
7%
Abdominal pain
6%
Blood creatinine increased
5%
Weight decreased
2%
Sepsis
1%
Tumour hyperprogression
1%
General physical health deterioration
1%
Pneumonia
1%
Death
1%
Acute kidney injury
1%
Pyelonephritis
1%
Device related infection
1%
Urosepsis
1%
Pulmonary embolism
100%
80%
60%
40%
20%
0%
Study treatment Arm
Durvalumab
Awards & Highlights
Pivotal Trial
The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Arm AExperimental Treatment2 Interventions
Durvalumab and FLOT chemotherapy
Group II: Arm BPlacebo Group1 Intervention
placebo product and FLOT chemotherapy
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Durvalumab
2017
Completed Phase 2
~3750
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for gastrointestinal tumors include immune checkpoint inhibitors like Durvalumab, which block the PD-L1 pathway, allowing the immune system to better recognize and attack cancer cells. HER2 inhibitors, such as trastuzumab, target the HER2 protein overexpressed in some tumors, inhibiting cell proliferation.
VEGF inhibitors like ramucirumab block the vascular endothelial growth factor, reducing tumor blood supply and growth. These targeted therapies are crucial for gastrointestinal tumor patients as they offer more personalized and effective treatment options, potentially leading to better clinical outcomes.
Recurrent glioma clinical trial, CheckMate-143: the game is not over yet.Neoadjuvant treatment of locally advanced esophageal and junctional cancer: the evidence-base, current key questions and clinical trials.
Recurrent glioma clinical trial, CheckMate-143: the game is not over yet.Neoadjuvant treatment of locally advanced esophageal and junctional cancer: the evidence-base, current key questions and clinical trials.
Find a Location
Who is running the clinical trial?
AstraZenecaLead Sponsor
4,388 Previous Clinical Trials
289,108,816 Total Patients Enrolled
1 Trials studying Gastrointestinal Tumors
96 Patients Enrolled for Gastrointestinal Tumors
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You are expected to live for at least 24 weeks.My organs and bone marrow are working well.I will have a major surgery to remove my cancer.My cancer is either adenosquamous, squamous cell, or a GI stromal tumor.I am fully active or restricted in physically strenuous activity but can do light work.My stomach cancer is operable and at least stage II.I have not received any treatment for my current cancer.I haven't taken immunosuppressive drugs in the last 14 days.I have received an organ transplant from another person.My cancer has spread to the lining of my abdomen or other distant parts.I am not allergic or intolerant to the drugs used in this study.
Research Study Groups:
This trial has the following groups:- Group 1: Arm B
- Group 2: Arm A
Awards:
This trial has 1 awards, including:- Pivotal Trial - The final step before approval, pivotal trials feature drugs that have already shown basic safety & efficacy.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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