PERFECT: PDL-1 Targeting in Resectable Oesophageal Cancer

Sponsor

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) (Other)

Overall Status

Completed

CT.gov ID

NCT03087864

Collaborator

UMC Utrecht (Other)

Enrollment

Location

Arm

24.1

Actual Duration (Months)

1.7

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Objectives The primary objective of this study is to assess the feasibility of preoperative treatment with atezolizumab combined with preoperative chemoradiation (carboplatin, paclitaxel and radiation) in terms of completion of treatment with atezolizumab.

Condition or Disease	Intervention/Treatment	Phase
Esophageal Cancer, Stage II Esophageal Cancer Stage III	Drug: Atezolizumab Drug: Carboplatin Drug: Paclitaxel Radiation: Radiotherapy 23 x 1.8 Gy	Phase 2

Detailed Description

Objectives The primary objective of the study of this study is to assess the feasibility of preoperative treatment with atezolizumab combined with preoperative chemoradiation (carboplatin, paclitaxel and radiation) in terms of completion of treatment with atezolizumab.

Secondary objectives are:

To assess toxicities of atezolizumab alone and in combination with chemoradiation.
To assess completion of chemotherapy and radiation treatment
To assess withdrawal rate from surgery
To assess post-operative complications.
To assess pathological response.
To assess R0 resection rate.
To assess the relation between gut microbiota composition and response.
To assess the relation between gut microbiota composition and toxicity.

Explorative objectives are:

To perform exploratory biomarker analyses from tumor tissue and blood-derived samples and correlate with safety and clinical outcome. Biomarker analyses include (but are not limited to):

Expression of PD-1, PD-L1 and FOXP3, presence of tumor infiltrating CD8+/CD4+ cytotoxic/helper T lymphocytes, IFNγ expression, presence of tumor macrophages, STAT3 and STAT6 expression, MHC classI, MHC class II, EBV and MSI status on tumor tissue.
RNA sequencing and whole exome sequencing to develop a predictive profile for response to treatment.
Analysis of ctDNA extracted from plasma of patients at four time points (baseline, directly after chemoradiation, at surgery and 3 months after surgery) and analyzed using Ion Torrent Next Generation sequence technology as a non-invasive marker for response to treatment.
Analysis of peripheral blood mononuclear cells (PBMCs) extracted from whole blood of patients at three time points ((baseline, directly after chemoradiation, at surgery) )
Duodenal biopsy and morning faeces sample analysis as predictor of response will be done by HIT Chip flora mapping, an established sensitive RT-qPCR method which is developed for exact and sensitive enumeration of bacterial population.

Study Design

Study Type:

Interventional

Actual Enrollment :

40 participants

Allocation:

N/A

Intervention Model:

Single Group Assignment

Masking:

None (Open Label)

Primary Purpose:

Treatment

Official Title:

PDL-1 Targeting in Resectable Oesophageal Cancer: a Phase II Feasibility Study of Atezolizumab and Chemoradiation.

Actual Study Start Date :

Jun 28, 2017

Actual Primary Completion Date :

Jul 1, 2019

Actual Study Completion Date :

Jul 1, 2019

Arms and Interventions

Arm	Intervention/Treatment
Experimental: Atezolizumab and Chemoradiation Atezolizumab 1200 mg i.v. day 1-22-43-64-85 Carboplatin AUC = 2 i.v day 1-8-15-22-29 Paclitaxel 50 mg/m2 i.v day 1-8-15-22-29 Radiotherapy 23 x 1.8 Gy	Drug: Atezolizumab Atezolizumab 1200 mg i.v. day 1-22-43-64-85 Drug: Carboplatin Chemotherapy Drug: Paclitaxel Chemotherapy Radiation: Radiotherapy 23 x 1.8 Gy Radiotherapy

Arm

Intervention/Treatment

Experimental: Atezolizumab and Chemoradiation

Atezolizumab 1200 mg i.v. day 1-22-43-64-85 Carboplatin AUC = 2 i.v day 1-8-15-22-29 Paclitaxel 50 mg/m2 i.v day 1-8-15-22-29 Radiotherapy 23 x 1.8 Gy

Drug: Atezolizumab

Atezolizumab 1200 mg i.v. day 1-22-43-64-85

Drug: Carboplatin

Chemotherapy

Drug: Paclitaxel

Chemotherapy

Radiation: Radiotherapy 23 x 1.8 Gy

Radiotherapy

Outcome Measures

Primary Outcome Measures

feasibility defined as percentage completion of treatment with atezolizumab. [up to 3 months]
The primary endpoint is feasibility defined as percentage completion of treatment with atezolizumab

Secondary Outcome Measures

Incidence and severity of toxicity [up to 3 months]
Incidence and severity of toxicity defined to CTCAE v4.03 and Radiation Oncology Group (RTOG) criteria.
Percentage completion of chemotherapy and radiation treatment [up to 3 months]
Percentage completion of chemotherapy and radiation treatment
Percentage withdrawal rate from surgery due to atezolizumab related complications [up to 3 months]
Percentage withdrawal rate from surgery due to atezolizumab related complications
Percentage delay of surgery due to atezolizumab related complications [up to 3 months]
Percentage delay of surgery due to atezolizumab related complications
Incidence and severity of post-operative complications to the Dindo classification [up to 3 months]
Incidence and severity of post-operative complications to the Dindo classification
Pathological response according to the Mandard criteria [up to 3 months]
Pathological response according to the Mandard criteria
R0 resection rate. [up to 3 months]
R0 resection rate.
Progression free survival [up to 3 months]
Progression free survival
Overall survival [up to 3 months]
Overall survival

Other Outcome Measures

Potential biomarker development based on assessment of tumour biopsies, blood- and faecal samples and the proposed mechanism of action of study drugs. [up to 3 months]
Potential biomarker development based on assessment of tumour biopsies, blood- and faecal samples and the proposed mechanism of action of study drugs.

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years and Older

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

Histologically proven adenocarcinoma of the esophagus or gastro esophageal junction.
Surgical resectable (<T4b, N0 or N+, M0), as determined by Endoscopic Ultra Sound (EUS) and CT scan of neck, thorax and abdomen. Tumors that cannot be passed with an endoscope for endoscopic ultrasound are eligible if all other criteria are fulfilled.
T1N+ tumors are eligible.
Tumor length longitudinal ≤ 10 cm; if larger than 10 cm, inclusion should be discussed with the principal investigator.
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 or 1 (cf. Appendix A).
Adequate hematological, renal and hepatic functions defined as:
neutrophiles ≥ 1.5 x 109/L
platelets ≥ 100 x 109/L
hemoglobin ≥ 5.6 mmol
total bilirubin ≤ 1.5 x upper normal limit
creatinine clearance (Cockroft) > 60 ml/min
Written, voluntary informed consent
Patients must be accessible to follow up and management in the treatment center

Exclusion Criteria:

Past or current history of malignancy other than entry diagnosis interfering with prognosis of esophageal cancer.
Invasion of the tracheobronchial tree or presence of tracheoesophageal fistula.
T1N0 tumors or in situ carcinoma.
Pregnancy (positive serum pregnancy test), planning to become pregnant, and lactation.
Patient (male or female) 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, radiotherapy, and/or treatment with checkpoint inhibitors.
Clinically significant cardiovascular disease (including myocardial infarction, unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia) precluding major surgery.
Pulmonary fibrosis and/or severely impaired lung function precluding major surgery.
Pre-existing motor or sensory neurotoxicity greater than WHO grade 1.
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.
Dementia or altered 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.
Has 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.
Has evidence of interstitial lung disease or active, non-infectious pneumonitis.
Has 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.
Patients with prior allogeneic stem cell or solid organ transplantation.