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TGF‐β And PDL‐1 inhibition with Bintrafusp alfa in Esophageal Squamous Cell carcinoma combined with chemoradiation TheRapY (TAPESTRY)
EU CTIS ID: 2023-503312-32-00
What this study is testing
The primary objective of the study is to assess the feasibility of bintrafusp alfa combined with definitive chemoradiation (carboplatin, paclitaxel and radiation) in terms of completion of treatment with bintrafusp alfa of patients with squamous cell carcinoma of the esophagus or gastroesophageal junction.
- Therapeutic exploratory (Phase II)
A plain-language read of the study's public EU CTIS listing. The study team confirms the details.
Who can take part
You may be able to join if
- Histologically proven squamous cell carcinoma of the esophagus or gastro esophageal junction
- Adequate hematological, renal and hepatic functions
- Tumors that cannot be passed with an endoscope for endoscopic ultrasound are eligible if all other criteria are fulfilled.
- Written, voluntary informed consent
- Patients must be accessible to management and follow-up in the treatment center
- Surgically irresectable (T1-T4a, N0 or N+, M0), as determined by Endoscopic Ultra Sound (EUS), PET scan and diagnostic CT scan of neck, thorax and abdomen. Patients with M1 disease solely on the basis of supraclavicular metastasis are eligible. Patients with resectable tumors refusing radical surgery or inoperable patients due to comorbidity are eligible
You likely can't join if
- Past or current history of malignancy other than entry diagnosis interfering with prognosis of esophageal cancer
- Presence of an esophageal stent
- History of bleeding diathesis or major bleeding event (grade ≥ 2) in the month prior to first dose of trial treatment
- Current use of direct oral anticoagulants or coumarins
- Clinically significant cardiovascular disease precluding safe treatment with chemoradiation
- Evidence of pulmonary fibrosis and/or clinically significant impairment of lung function precluding safe treatment with chemoradiation. In case of doubt about pulmonary function, a lung function test should be performed and, in case of abnormalities, discussed with the principle investigator
See the full eligibility criteria
Who can join
- Histologically proven squamous cell carcinoma of the esophagus or gastro esophageal junction
- Adequate hematological, renal and hepatic functions
- Tumors that cannot be passed with an endoscope for endoscopic ultrasound are eligible if all other criteria are fulfilled.
- Written, voluntary informed consent
- Patients must be accessible to management and follow-up in the treatment center
- Surgically irresectable (T1-T4a, N0 or N+, M0), as determined by Endoscopic Ultra Sound (EUS), PET scan and diagnostic CT scan of neck, thorax and abdomen. Patients with M1 disease solely on the basis of supraclavicular metastasis are eligible. Patients with resectable tumors refusing radical surgery or inoperable patients due to comorbidity are eligible
- Locoregional recurrences without distant metastasis after surgery alone or endoscopical resection
- Locoregional recurrences without distant metastasis after neoadjuvant chemoradiation + resection or definitive chemoradiation outside the previously irradiated area, provided that full dose of radiation can safely be delivered
- If the tumor extends below the gastroesophageal (GE) junction into the proximal stomach, the bulk of the tumor must involve the esophagus or GE junction
- Age ≥ 18
- ECOG performance status 0-2
What rules you out
- Past or current history of malignancy other than entry diagnosis interfering with prognosis of esophageal cancer
- Presence of an esophageal stent
- History of bleeding diathesis or major bleeding event (grade ≥ 2) in the month prior to first dose of trial treatment
- Current use of direct oral anticoagulants or coumarins
- Clinically significant cardiovascular disease precluding safe treatment with chemoradiation
- Evidence of pulmonary fibrosis and/or clinically significant impairment of lung function precluding safe treatment with chemoradiation. In case of doubt about pulmonary function, a lung function test should be performed and, in case of abnormalities, discussed with the principle investigator
- Serious underlying medical condition which would impair the ability of the patient to receive the planned treatment, including prior allergic reactions to drugs containing cremophor, such as teniposide or cyclosporine
- Mental status that would prohibit the understanding and giving of informed consent
- Inadequate caloric- and/or fluid intake despite consultation of a dietician and/or tube feeding
- Has an active autoimmune disease that has required systemic treatment in past 2 years (i.e. with use of disease modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapy (e.g., thyroxine for patients with a history of autoimmune-related hypothyroidism, insulin for patients with type 1 diabetes mellitus, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment. Patients with vitiligo with dermatological manifestations only are eligible to enter the study
- Diagnosis of HIV unless stable on antiretroviral therapy for at least 4 weeks, no evidence of multi-drug resistance, viral load of < 400 copies/ml and CD4+ T-cells ≥ 350 cells/μl
- Patient with tracheo-esophageal fistula or extension into the mucosal layer of the trachea, highly at risk to develop fistula. Thus, tumor extension to the trachea is allowed, but not through the trachea
- Active HBV/HCV. Participants on a stable dose of antiviral therapy with HBV/HCV viral load below the limit of quantification are eligible
- A diagnosis of immunodeficiency or is receiving systemic steroid therapy (>10 mg/day prednisone or equivalent) or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatment
- Evidence of interstitial lung disease or active, non-infectious pneumonitis
- An active infection requiring systemic therapy, which has not resolved 3 days (simple infection such as cystitis) to 7 days (severe infection such as pyelonephritis) prior to the first dose of trial treatment
- Administration of a live vaccine within 30 days prior to the first dose of trial treatment. Seasonal flu vaccines that do not contain a live virus are permitted. Locally approved COVID vaccines are permitted
- Patients with prior allogeneic stem cell or solid organ transplantation
- Patient with aortal involvement with high risk of bleeding or developing a fistula
- Patients with pathological lymph nodes at both supraclavicular and truncus coeliacus level
- Pregnancy (positive serum pregnancy test), planning to become pregnant, and lactation
- Patient (male or female) in the reproductive age is not willing to use highly effective methods of contraception (per institutional standard) during treatment and for 6 months (male or female) after the end of treatment
- Previous chemotherapy, radiation and/or treatment with checkpoint inhibitors for the currently present esophageal tumor
- Previous chemotherapy and/or treatment with targeted agents and/or checkpoint inhibitors for other forms of cancer within the last six months
- Previous radiation to the mediastinum precluding full dose radiation of the currently present esophageal tumor
The study team makes the final eligibility decision.
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 65+ years, 18-64 years. The study team makes the final eligibility decision.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from EU CTIS; the study team decides eligibility.