Single arm phase II trial designed to assess the efficacy of durvalumab treatment in terms of 6-month progression-free survival. We will include 22 patients who will receive 1500 mg durvalumab (MEDI4736) via IV infusion Q4W <<for up to a maximum of 12 months (up to 13 doses/cycles) with the last administration on week 48>> or <<until confirmed disease progression>> unless there is unacceptable toxicity, withdrawal of consent, or another discontinuation criterion is met. If a patient's weight falls to 30 kg or below for 1 week or longer ( ≥ 7 days) durvalumab will be permanently discontinued.

A) Study Title: Durvalumab (MEDI4736) as maintenance treatment following chemoradiation for locally advanced unresectable esophageal squamous cell carcinoma (DESC)

B) Protocol Number: ESR-17-12757

C) Clinical Phase: 2

D) Study Duration: 36 months

E) Investigational Product(s) and Reference Therapy: Durvalumab (MEDI4736)

F) Research Hypothesis: Is Durvalumab efficient in delay progression in patients with persistent disease after chemoradiation for locally advanced esophageal squamous cell carcinoma?

G) Objectives:

G1) Primary Objectives:

To assess the efficacy of durvalumab treatment in terms of 6-month progression-free survival.

G2) Secondary Objective(s):

To assess the incidence of grade 3 or higher toxicities; To further assess the efficacy of durvalumab in terms of overall survival, incidence of locoregional progression and incidence of distant progression.>>

G3) Exploratory Objective(s):

To investigate the relationship between immune biomarkers within the tumor microenvironment (immunohistochemistry) with efficacy outcomes with durvalumab

H) Study Design: Single arm phase II trial

I) Number of Centers: 1

J) Number of Patients:22

K) Study Population:

Patients with locally advanced unresectable or inoperable esophageal squamous cell carcinoma who had a persistent disease after completing definitive chemoradiotherapy, with no progressive disease.

L) Inclusion Criteria:

• Body weight >30kg and body mass index ≥ 16 kg / m2;
• Patients who are aphagic or able to ingest only liquids should also receive enteral nutritional support before inclusion in the study;
• Patients with histologically and/or cytologically confirmed esophageal or esophagogastric junction (Siewert I or II) squamous cell carcinoma, irrespective of PD-1/PD-L1 or any other biomarker expression;
• Patients who had a persistent disease 6-8 weeks after completing chemoradiotherapy with at least 50 Gy and platinum-based chemo and without clinical complete response or progressive disease;
• CT scans within 4 weeks revealing persistent disease;
• Must be included <12 weeks after completing chemoradiotherapy to ensure durvalumab begins no later than 16 weeks after completion of chemoradiotherapy;
• Patients unsuitable to salvage esophagectomy;
• All the tumor volume should have been treated with CRT (included in the radiation field); ECOG 0 - 1;
• Age 18 years or older;
• Life expectancy of higher than 3 months;
• Laboratory values must meet the following criteria: Absolute neutrophil count (ANC) > 1.5 (>1500 per mm3); Platelet count ≥ 100 x109/L. Hemoglobin >9.0 g/dL. Creatinine < 1.5 times institutional ULN or CrCl > 40 mL/min. AST (SGOT)/ALT (SGPT) ≤2.5 x institutional upper limit of normal. Serum bilirubin ≤ 1.5 times institutional ULN (This will not apply to patients with confirmed Gilbert's syndrome - persistent or recurrent hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis or hepatic pathology, who will be allowed only in consultation with their physician)
• All toxicities attributed to prior chemoradiotherapy other than alopecia, fatigue, or peripheral neuropathy must have resolved to grade 2 or less.

M) Exclusion Criteria:

• Presence of any site of metastatic disease, including lymph node which has not been included in radiation field;
• Are currently receiving or have had prior use of immunosuppressive medication within 28 days before the first dose of study drug (10 milligrams/day of prednisone or an equivalent corticosteroid is allowed);
• Received any immunotherapy for esophageal cancer;
• Has known active hepatitis B, hepatitis C or human immunodeficiency virus (HIV1/2 antibodies);
• Has known active or prior autoimmune disease, except for:
• skin diseases (vitiligo, psoriasis, alopecia)
• diabetes mellitus type 1, with hormone replacement
• hypothyroidism, with hormone replacement
• Receipt of live attenuated vaccination within 30 days prior to study entry.
• Grade 3 or higher pulmonary toxicity of dyspnea, hypoxia, or pneumonitis experienced during chemoradiation;
• Presence of tracheoesophageal fistula that has not been treated with endoprosthesis>>

N) Investigational Product(s), Dose and Mode of Administration:

Patients in the durvalumab (MEDI4736) monotherapy treatment group will receive 1500 mg durvalumab (MEDI4736) via IV infusion Q4W <\

Inclusion Criteria:

1. Body weight >30kg and body mass index ≥ 16 kg / m2;

2. Patients aphagic or able to ingest only liquids should also receive enteral nutritional sup-port before being included in the study;

3. Patients must have histologically confirmed esophageal or esophagogastric junction (Siewert I or II) squamous cell carcinoma, irrespective of PD-1/PD-L1 or other biomarkers expression;

4. Patients must have had a persistent disease 6-8 weeks after completing chemoradiotherapy with at least 50 Gy and platinum-based chemo and without complete response or progressive disease, based on upper endoscopy and/or CT scans;

5. Patients must have realized CT scans within 6-8 weeks after completion of chemoradiotherapy, revealing persistent disease;

6. Patients must be included <12 weeks after completing chemoradiotherapy;

7. Patients must be unsuitable to salvage esophagectomy, according multidisciplinary local board;

8. All the tumor volume should have been treated with CRT (included in the radiation field);

9. Eastern Cooperative Oncology Group (ECOG)>><<World Health Organisation (WHO) performance status of 0 or 1;

10. Male or female aged 18 years or older at time of study entry;

11. Life expectancy of > 12 weeks;

12. Adequate normal organ and marrow function as defined below:

    • Haemoglobin ≥9.0 g/dL
    • Absolute neutrophil count (ANC) 1.5 x (> 1500 per mm3)
    • Platelet count ≥100 x 109/L
    • Serum bilirubin ≤1.5 x institutional upper limit of normal (ULN). <<This will not apply to patients with confirmed Gilbert's syndrome (persistent or recurrent hyperbilirubinemia that is predominantly unconjugated in the absence of hemolysis or hepatic pathology), who will be allowed only in consultation with their physician.
    • AST (SGOT)/ALT (SGPT) ≤2.5 x institutional upper limit of normal unless liver metastases are present, in which case it must be ≤5x ULN
    • Measured creatinine clearance (CL) >40 mL/min or Calculated creatinine CL>40 mL/min by the Cockcroft-Gault formula (Cockcroft and Gault 1976) or by 24-hour urine collection for determination of creatinine clearance: CrCl, mL/min = (140 - age) × (weight, kg) × (0.85 if female) / (72 × Cr)

13. All toxicities attributed to prior chemoradiotherapy other than alopecia, fatigue, or peripheral neuropathy must have resolved to grade 2 or less;

Exclusion Criteria:

1. Patients with metastases including lymph node not included in the radiation field;

2. Patients currently receiving or have had prior use of immunosuppressive medication within 28 days before the first dose of study drug (10 milligrams/day of prednisone or an equivalent corticosteroid is allowed);

3. Received any immunotherapy for esophageal cancer;

4. Patients with active hepatitis B, hepatitis C or human immunodeficiency virus (HIV1/2 antibodies);

5. Has known active or prior autoimmune disease, except for:

   • skin diseases (vitiligo, psoriasis, alopecia)
   • diabetes mellitus type 1, with hormone replacement
   • hypothyroidism, with hormone replacement

6. Receipt of live attenuated vaccine within 30 days prior to the first dose of IP.

7. Grade 3 or higher pulmonary toxicity of dyspnea, hypoxia, or pneumonitis experienced during chemoradiation;

8. Presence of fistula between esophagus and trachea unless treated with endoscopic prosthesis.