Do Changes in ctDNA Predict Response for Patients With Oesophageal Cancer Receiving Durvalumab

NCT ID: NCT03653052

Last Updated: 2025-04-24

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 18 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-10-30
• Study Completion Date: 2026-06-30

Brief Summary

Patients with cancer are increasingly being treated with drugs designed to modulate the response of their immune system, broadly to boost their body's defences against cancer. However, there is an unmet need to identify which patients are unlikely to benefit. Deciding on benefit from therapy uses standard imaging methods (e.g. CT scans), which can take time (months) whereas DNA in the bloodstream could be measured more rapidly.

The main aim of this study is to assess whether changes in the level of circulating tumour DNA (ctDNA) can quickly determine a patients response. This would enable patients to change therapies more quickly if they are not responding and reduce exposure to unnecessary side effects.

Detailed Description

Measuring circulating (plasma) tumour DNA has been described as a 'liquid biopsy' able to study a tumour without invasive biopsy. By measuring ctDNA at different time points the investigators can detect tumour changes that indicate if the patient is responding to treatment or not.

This trial has been designed as a prospective, open label, non-randomised trial where patient with advanced oesophageal cancer will be treated with MEDI4736 (durvalumab), a drug designed to alter the immune system response. Samples will be taken to regularly to measure ctDNA levels and compared to patients response at 6 months when undergoing standard CT scans.

The study will run at a single centre (Addenbrookes Hospital, Cambridge). Nineteen, evaluable, patients will receive durvalumab until progression while detailed studies will assess their tumour and immune response.

Conditions

Oesophageal Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Durvalumab

Patients with advanced oesophageal cancer will be administered with 1500mg of durvalumab once every 4 weeks for up to 6 months.

Group Type: EXPERIMENTAL

Durvalumab

Intervention Type: DRUG

Durvalumab will be administered via an infusion in the arm, over a duration of up to 1 hour.

Interventions

Durvalumab

Durvalumab will be administered via an infusion in the arm, over a duration of up to 1 hour.

Intervention Type: DRUG

Other Intervention Names

MEDI4736

Eligibility Criteria

Inclusion Criteria

• Provide written, informed consent to participate
• Aged ≥ 18 years at time of consent
• Confirmed advanced oesophageal cancer for which the patient must have received at least one prior line of standard of care treatment
• Predicted life expectancy ≥ 3 months
• Eastern Cooperative Oncology Group (ECOG) PS 0 or 1
• Measurable disease, as defined by RECIST v1.1.
• In the investigator's opinion, have an accessible and biopsiable tumour lesion for additional research biopsy, to which the patient will have to consent at screening.
• Adequate hematologic and organ function, defined by:

• ANC ≥ 1500 cells/μL (no GCSF support 2 weeks prior to trial entry)
• Platelet count ≥ 100,000/μL
• Haemoglobin ≥ 9.0 g/dL
• AST or ALT ≤ 2.5 times the upper limit of normal (ULN), (except patients with documented liver metastases where AST and/or ALT can be ≤ 5×ULN)
• Serum bilirubin ≤1.5 × ULN. (Except patients with confirmed Gilbert's syndrome)
• INR and APTT ≤ 1.5×ULN.
• Calculated creatinine clearance (CrCl) ≥ 40 mL/min (Cockcroft-Gault formula)
• Negative pregnancy test in women of child-bearing potential or evidence of postmenopausal status

Exclusion Criteria

• Weight of ≤30kg
• Any concurrent chemotherapy, immunotherapy, biologic or hormonal therapy for cancer treatment.
• Participation in other clinical trials involving active treatment for the malignant disease.
• Received radiotherapy treatment on a wide body field, or an equivalent to more than 30% of the bone marrow, within the last 4 weeks.
• Any unresolved symptom NCI CTCAE Grade ≥2 from previous anticancer therapy (with the exception of alopecia and vitiligo).
• Active or prior documented autoimmune or inflammatory disease (except vitiligo) within the last 3 years, for example:

• Intestinal: Inflammatory Bowel Disease (Colitis, Crohn's Disease), Diverticulitis (with the exception of Diverticulosis), Coeliac Disease, Irritable Bowel Disease
• Vascular: any type of Vasculitic disorder, i.e.: Wegner syndrome.
• Endocrine: any endocrine alteration related to an auto-immune process i.e.: Hashimoto syndrome. NOTE: patients with hypothyroidism (eg, following Hashimoto syndrome) stable on hormone replacement treatment may be included at the discretion of the CI.
• Respiratory: Active Pneumonitis (of any origin: inflammatory or infectious), Sarcoidosis.
• Dermatological: Psoriasis, Lupus/SLE.
• Other: Rheumatoid Arthritis, Hypophysitis, Uveitis.
• History of organ transplant that requires use of immunosuppressive medications or any medical condition in which immunosuppressive agents were administered, including but, not limited to:

• Systemic corticosteroids.
• Methotrexate, azathioprine
• Tumour necrosis factor alpha (TNF-α) blockers
• History of active primary immunodeficiency.
• Receipt of live, attenuated vaccine within the last 30 days.
• Other invasive malignancy within the last 3 years. Patients with previous history of malignancies with a negligible risk of metastasis or death and treated with expected curative intent are eligible at the investigator's discretion, for example:

• Carcinoma in situ of the cervix
• Basal or squamous cell skin cancer
• Localized low to intermediate risk prostate cancer treated with curative intent and absence of prostate-specific antigen (PSA) relapse; or prostate cancer (Stage T1/T2a, Gleason ≤ 6 and PSA < 10 ng/mL) undergoing active surveillance and treatment naive
• Women who are pregnant or lactating/ breast feeding.
• Male or female patients with reproductive potential who are not willing to employ effective birth control from screening to 90 days after the last dose of durvalumab.
• Uncontrolled intercurrent illness, including but not limited to, on-going or active infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, cardiac arrhythmia, interstitial lung disease, serious chronic gastrointestinal conditions associated with diarrhea or psychiatric illness/social situations that would limit compliance with study requirement, substantially increase risk of incurring AEs or compromise the ability of the patient to give written informed consent.
• Brain metastases unless asymptomatic, treated and stable and not requiring steroids in the last 4 weeks. Patients with known or suspected brain metastases at screening should have a CT/ MRI of the brain prior to trial entry.
• History of leptomeningeal carcinomatosis.
• Active infection or use of antibiotics (ATB) 14 days prior to Cycle 1 Day 1 of treatment. Patients receiving prophylactic treatment are eligible.
• Active infection including tuberculosis (clinical history, physical examination and radiographic findings, and TB testing in line with local practice), hepatitis B (known positive HBV surface antigen (HBsAg) result), hepatitis C, or known human immunodeficiency virus (positive HIV1/2 antibodies).

• Subjects with a past or resolved HBV infection (defined as: presence of hepatitis B core antibody -anti-HBc- and absence of hepatitis B surface antigen -HbsAg-) are eligible.
• Subjects positive for hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative for HCV RNA.
• Major surgical procedure (investigator defined) within 4 weeks prior to first dose or anticipation of the need for a major surgical procedure during the course of the trial other than for diagnosis.
• History of severe allergic, anaphylactic, or other hypersensitivity reactions to durvalumab or any of its excipients, chimeric or humanized antibodies or fusion proteins.
• Patients previously treated with immune (checkpoint inhibition) therapy
• Any medical condition that would, in the investigator's judgment, prevent the patient's participation in the clinical trial due to safety concerns, compliance with clinical trial procedures or interpretation of trial results.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

AstraZeneca

INDUSTRY

Sponsor Role: collaborator

Simon C Pacey, MD

OTHER

Sponsor Role: lead

Responsible Party

Simon C Pacey, MD

Chief Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Simon Pacey

Role: PRINCIPAL_INVESTIGATOR

Cambridge University Hospitals

Locations

Cambridge University Hospitals NHS Foundation Trust

Cambridge, , United Kingdom

Countries

United Kingdom

Other Identifiers

CALIBRATION

Identifier Type: -

Identifier Source: org_study_id