Radiotherapy Plus Durvalumab in Elderly Esophageal Squamous Cell Carcinoma
Primary Purpose
Esophageal Squamous Cell Carcinoma
Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Radiotherapy
Durvalumab
Sponsored by
About this trial
This is an interventional treatment trial for Esophageal Squamous Cell Carcinoma
Eligibility Criteria
Inclusion Criteria:
- Age 70-85 years old, both men and women
- Histologically confirmed esophageal squamous cell carcinoma located in thoracic segment, treatment naive
- Stage cT2-4aNanyM0 (AJCC 8 TNM classification)
- Unresectable, unable to tolerate or refuse surgery and concurrent chemoradiotherapy
- ECOG PS 0-2
- Measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST) 1.1
- No severe abnormalities of the Hematologic system, heart, lung, liver, kidney, and immunodeficiency
Adequate bone marrow and organ function as defined below (excluding the use of any blood components and cell growth factors within 7 days):
- Absolute neutrophil count≥1,500/mm3
- Platelets ≥ 100,000/mm3
- Hemoglobin ≥ 5.6 mmol/L (9g/dL)
- Serum creatinine ≤ 1.5 x ULN or Creatinine clearance ≥50 mL/min by Cockcroft-Gault estimation
- Total bilirubin ≤ 1.5 x ULN
- ALT and AST ≤ 2.5 x ULN
- Proteinuria < 2+, for subjects with urine protein ≥ 2 + at baseline, urine samples should be collected within 24 hours and urine protein in 24 hours should be ≤ 1g
- INR or PT or aPTT ≤ 1.5 x ULN
- Life expectancy more than 6 months
- Ability to understand and willingness to sign an IRB approved written informed consent document, and capable of proper therapeutic compliance, and accessible to correct follow-up
Exclusion Criteria:
- Complete esophageal obstruction that unable to eat fluid and cannot provide necessary nutrition through nasal feeding
- Patients with obvious ulcer or esophageal perforation or hematemesis
- Placement of esophagotracheal stents
- Has a history or current evidence of pulmonary fibrosis, interstitial pneumonia, pneumonoconiosis, drug-associated pneumonia, severe impairment of pulmonary function
- Has had major surgery within 28 days prior to the start of the treatment
- Immunosuppressive drugs used within 4 weeks prior to the initial study treatment, excluding local glucocorticoids, or systemic glucocorticoids at physiological doses (i.e., no more than 10 mg/ day of prednisone or equivalent doses of other glucocorticoids);
- The patient has any active autoimmune disease or a history of autoimmune disease (such as the following, but not limited to: interstitial pneumonia, uveitis, enteritis, hepatitis, hypophysitis, vasculitis, glomerulonephritis, thyroiditis (patients with vitiligo or asthma has been completely relieved in childhood, and do not need any intervention during adulthood can be included; patients with type I diabetes with good insulin control can also be included; hypothyroidism caused by autoimmune thyroiditis requiring hormone replacement therapy can also be included)
- Has had congenital or acquired immunodeficiency, such as human immunodeficiency virus (HIV) infection, active hepatitis B (HBV-DNA ≥ 104 copies/ml) or hepatitis C (HCV-RNA ≥ 103 copies/ml; For chronic hepatitis B virus carriers, HBV viral load must be < 2000 IU/ml (< 104 copies / ml), and must receive antiviral therapy at the same time before they can be enrolled
- Known allogeneic organ transplantation (except corneal transplantation) or allogeneic hematopoietic stem cell transplantation
- Uncontrolled clinically significant disease, including active infection, uncontrolled hypertension, unstable angina pectoris, angina within the past 3 months, heart failure > NYHA II, myocardial infarction within the past 6 months, severe arrhythmias requirement for treatment or intervention, liver/kidney or metabolic disease
- System infections that require treatment
- Received a live vaccine within 4 weeks of the first dose of study medication
- Synchronous or metachronous second primary malignancy. Participants with basal cell carcinoma of the skin, or cervical cancer in situ that have undergone potentially curative therapy are not excluded from the study
- Patients who have participated in other clinical trials within 30 days
- Drug addiction, chronic alcoholism and AIDS
- Patients with uncontrollable seizures or loss of self-control due to mental illness
- Those with a history of severe allergy or specific physique
- The investigators judge not suitable for inclusion
Sites / Locations
- National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Exprimental Arm
Arm Description
IMRT plus Durvalumab
Outcomes
Primary Outcome Measures
Progression-free survival (PFS)
PFS was assessed by Response Evaluation Criteria in Solid Tumors (RECIST)1.1. Progression-free survival defined as the time from enrollment to the first documented disease progression of local recurrence or distant metastasis or death due to any cause.
Secondary Outcome Measures
Overall survival (OS)
Overall survival defined as the time from enrollment to death due to any cause.
Progression-free survival (PFS)
PFS was assessed by Response Evaluation Criteria in Solid Tumors (RECIST)1.1. Progression-free survival defined as the time from enrollment to the first documented disease progression of local recurrence or distant metastasis or death due to any cause.
Objective Response Rate (ORR)
ORR was Assessed by Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1).
Disease Control Rate (DCR)
DCR was Assessed by Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1).
Number of participants with an adverse event
Evaluanted by CTCAE 5.0
Quality of Life (QOL): questionnaire EORTC QLQ-C30 (version 3)
Evaluate the quality of life via questionnaire EORTC QLQ-C30 (version 3), minimum value 30, maximum value 126, higher scores mean a worse outcome.
Full Information
NCT ID
NCT04851132
First Posted
April 5, 2021
Last Updated
June 20, 2021
Sponsor
Chinese Academy of Medical Sciences
1. Study Identification
Unique Protocol Identification Number
NCT04851132
Brief Title
Radiotherapy Plus Durvalumab in Elderly Esophageal Squamous Cell Carcinoma
Official Title
Radiotherapy Plus Durvalumab in Elderly Esophageal Squamous Cell Carcinoma: A Prospective Phase II Clinical Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
March 11, 2021 (Actual)
Primary Completion Date
March 2023 (Anticipated)
Study Completion Date
June 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese Academy of Medical Sciences
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
The incidence and mortality of esophageal cancer are at the forefront in China, among which the elderly patients account for a large proportion. Concurrent chemoradiotherapy is the standard treatment for inoperable locally advanced esophageal cancer. Most elderly patients with esophageal cancer cannot tolerate concurrent chemotherapy because of complications and other reasons. Immunotherapy has definite efficacy and low toxicity in advanced esophageal squamous cell carcinoma, and the results combined with radiotherapy have also been preliminarily reported. Therefore, it is necessary to further explore the efficacy and safety of radiotherapy combined with immunotherapy in elderly patients with esophageal cancer.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Squamous Cell Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
RT + Durvalumab
Masking
None (Open Label)
Allocation
N/A
Enrollment
33 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Exprimental Arm
Arm Type
Experimental
Arm Description
IMRT plus Durvalumab
Intervention Type
Radiation
Intervention Name(s)
Radiotherapy
Intervention Description
IMRT (Intensity Modulated RT) or 3D-CRT (three-dimensional conformal radiotherapy); 95% PGTV 59.92Gy/2.14Gy/28f; 95% GTVnd 59.92Gy/2.14Gy/28f; 95% PTV 50.40Gy/1.80Gy/28f; 5 days a week; 6 weeks.
Intervention Type
Drug
Intervention Name(s)
Durvalumab
Intervention Description
Durvalumab 1000 mg, intravenously (IV), on Day 1 of radiotherapy, every 3 weeks for up to 18 administrations.
Primary Outcome Measure Information:
Title
Progression-free survival (PFS)
Description
PFS was assessed by Response Evaluation Criteria in Solid Tumors (RECIST)1.1. Progression-free survival defined as the time from enrollment to the first documented disease progression of local recurrence or distant metastasis or death due to any cause.
Time Frame
1-year
Secondary Outcome Measure Information:
Title
Overall survival (OS)
Description
Overall survival defined as the time from enrollment to death due to any cause.
Time Frame
1-, 2- and 3-year
Title
Progression-free survival (PFS)
Description
PFS was assessed by Response Evaluation Criteria in Solid Tumors (RECIST)1.1. Progression-free survival defined as the time from enrollment to the first documented disease progression of local recurrence or distant metastasis or death due to any cause.
Time Frame
2- and 3-year
Title
Objective Response Rate (ORR)
Description
ORR was Assessed by Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1).
Time Frame
during the intervention up to 60 weeks
Title
Disease Control Rate (DCR)
Description
DCR was Assessed by Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1).
Time Frame
during the intervention up to 60 weeks
Title
Number of participants with an adverse event
Description
Evaluanted by CTCAE 5.0
Time Frame
Up to 60 weeks
Title
Quality of Life (QOL): questionnaire EORTC QLQ-C30 (version 3)
Description
Evaluate the quality of life via questionnaire EORTC QLQ-C30 (version 3), minimum value 30, maximum value 126, higher scores mean a worse outcome.
Time Frame
up to 60 weeks
Other Pre-specified Outcome Measures:
Title
Quality of Life (QOL): questionnaire EORTC QLQ-OES18
Description
Evaluate the quality of life via questionnaire EORTC QLQ-OES18, minimum value 18, maximum value 72, higher scores mean a better outcome.
Time Frame
up to 60 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age 70-85 years old, both men and women
Histologically confirmed esophageal squamous cell carcinoma located in thoracic segment, treatment naive
Stage cT2-4aNanyM0 (AJCC 8 TNM classification)
Unresectable, unable to tolerate or refuse surgery and concurrent chemoradiotherapy
ECOG PS 0-2
Measurable disease based on Response Evaluation Criteria In Solid Tumors (RECIST) 1.1
No severe abnormalities of the Hematologic system, heart, lung, liver, kidney, and immunodeficiency
Adequate bone marrow and organ function as defined below (excluding the use of any blood components and cell growth factors within 7 days):
Absolute neutrophil count≥1,500/mm3
Platelets ≥ 100,000/mm3
Hemoglobin ≥ 5.6 mmol/L (9g/dL)
Serum creatinine ≤ 1.5 x ULN or Creatinine clearance ≥50 mL/min by Cockcroft-Gault estimation
Total bilirubin ≤ 1.5 x ULN
ALT and AST ≤ 2.5 x ULN
Proteinuria < 2+, for subjects with urine protein ≥ 2 + at baseline, urine samples should be collected within 24 hours and urine protein in 24 hours should be ≤ 1g
INR or PT or aPTT ≤ 1.5 x ULN
Life expectancy more than 6 months
Ability to understand and willingness to sign an IRB approved written informed consent document, and capable of proper therapeutic compliance, and accessible to correct follow-up
Exclusion Criteria:
Complete esophageal obstruction that unable to eat fluid and cannot provide necessary nutrition through nasal feeding
Patients with obvious ulcer or esophageal perforation or hematemesis
Placement of esophagotracheal stents
Has a history or current evidence of pulmonary fibrosis, interstitial pneumonia, pneumonoconiosis, drug-associated pneumonia, severe impairment of pulmonary function
Has had major surgery within 28 days prior to the start of the treatment
Immunosuppressive drugs used within 4 weeks prior to the initial study treatment, excluding local glucocorticoids, or systemic glucocorticoids at physiological doses (i.e., no more than 10 mg/ day of prednisone or equivalent doses of other glucocorticoids);
The patient has any active autoimmune disease or a history of autoimmune disease (such as the following, but not limited to: interstitial pneumonia, uveitis, enteritis, hepatitis, hypophysitis, vasculitis, glomerulonephritis, thyroiditis (patients with vitiligo or asthma has been completely relieved in childhood, and do not need any intervention during adulthood can be included; patients with type I diabetes with good insulin control can also be included; hypothyroidism caused by autoimmune thyroiditis requiring hormone replacement therapy can also be included)
Has had congenital or acquired immunodeficiency, such as human immunodeficiency virus (HIV) infection, active hepatitis B (HBV-DNA ≥ 104 copies/ml) or hepatitis C (HCV-RNA ≥ 103 copies/ml; For chronic hepatitis B virus carriers, HBV viral load must be < 2000 IU/ml (< 104 copies / ml), and must receive antiviral therapy at the same time before they can be enrolled
Known allogeneic organ transplantation (except corneal transplantation) or allogeneic hematopoietic stem cell transplantation
Uncontrolled clinically significant disease, including active infection, uncontrolled hypertension, unstable angina pectoris, angina within the past 3 months, heart failure > NYHA II, myocardial infarction within the past 6 months, severe arrhythmias requirement for treatment or intervention, liver/kidney or metabolic disease
System infections that require treatment
Received a live vaccine within 4 weeks of the first dose of study medication
Synchronous or metachronous second primary malignancy. Participants with basal cell carcinoma of the skin, or cervical cancer in situ that have undergone potentially curative therapy are not excluded from the study
Patients who have participated in other clinical trials within 30 days
Drug addiction, chronic alcoholism and AIDS
Patients with uncontrollable seizures or loss of self-control due to mental illness
Those with a history of severe allergy or specific physique
The investigators judge not suitable for inclusion
Facility Information:
Facility Name
National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College
City
Beijing
ZIP/Postal Code
100021
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhouguang Hui, M.D.
Phone
8610-87787230
Email
drhuizg@163.com
First Name & Middle Initial & Last Name & Degree
Zhouguang Hui, M.D.
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Radiotherapy Plus Durvalumab in Elderly Esophageal Squamous Cell Carcinoma
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