Sequential Preoperative Penpulimab Combined With Chemoradiotherapy(CRT) for Locally Advanced Esophageal Squamous Cell Cancer (SPEED)
Primary Purpose
Esophageal Squamous Cell Carcinoma
Status
Not yet recruiting
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Penpulimab Combined With CRT
Sponsored by
About this trial
This is an interventional treatment trial for Esophageal Squamous Cell Carcinoma
Eligibility Criteria
Inclusion Criteria:
- Resectable t2,3,4an0-1-2m0 esophageal squamous cell carcinoma initially diagnosed by histology or cytology;
- Without any systematic anti-tumor treatment;
- ECOG 0-1;
- ANC≥ 1.5×109/L;
- PLT≥ 75×109/L;
- HB≥ 8.0 g/dL;
- TBIL ≤ 1.5´ ULN;
- ALT and AST ≤ 2.5´ULN;
- Cr ≤ 1.5´ULN or CCr ≥ 60ml/min;
- Urine protein < +, if urine protein + then the total protein in 24 hours must be <500mg;
- Blood glucose is within the normal range and / or patients with diabetes are in treatment, but blood glucose is controlled in a stable state;
- FEV1 ≥ 2L; If the baseline FEV1 is less than 2L, it is estimated that the FEV1 after surgery is greater than 800ml;
- No myocardial infarction within 1 year; No unstable angina pectoris; No symptomatic severe arrhythmia; No cardiac insufficiency;
- There are no serious complications or other major diseases that have not been cured;
- Thoracic surgeons judge those who can tolerate the operation;
- Female subjects with fertility and male subjects with partners of childbearing age need to use a medically approved contraceptive measure during the study treatment and at least 6 months after the last chemotherapy;
- The subjects voluntarily joined the study and signed the informed consent form
Exclusion Criteria:
- Received any kind of systematic anti-tumor treatment before the first use of the study drug;
- At the same time, another clinical study will be included, unless it is an observational (non intervention) clinical study;
- Subjects who need to be given corticosteroids (more than 10mg prednisone equivalent dose per day) or other immunosuppressants for systematic treatment within 2 weeks before the first use of the study drug;
- Have been vaccinated with tumor vaccine or have been vaccinated with live vaccine within 4 weeks before administration;
- Have a history of active autoimmune diseases and autoimmune diseases; Except for patients who have recovered from childhood asthma / allergy and do not need any intervention after adulthood; Autoimmune mediated hypothyroidism treated with a stable dose of thyroid hormone replacement; Use a stable dose of insulin for type I diabetes;
- Serious interference occurred within 4 weeks before the first use of the study drug (CTC AE>2); Baseline chest imaging examination showed active pulmonary inflammation, symptoms and signs of infection within 2 weeks before the first use of the study drug, or the need for oral or intravenous antibiotics;
- Have a history of interstitial lung disease;
- The subjects had active hepatitis B (HBV DNA ≥ 2000 IU/ml or 104copies/ml), hepatitis C (hepatitis C antibody positive and HCV-RNA higher than the lower limit of the analysis method);
- Pregnant or lactating women;
- There are serious complications or other major diseases that have not been cured;
- Patients judged by thoracic surgeons to be intolerant of surgery
Sites / Locations
- Zhongshan Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Penpulimab Combined With Chemoradiotherapy(CRT)
Arm Description
Outcomes
Primary Outcome Measures
pathological complete remission(pCR)rate
Proportion of subjects who achieved pathological complete remission (PCR),PCR was defined as the microscopic absence of tumor cells in the pathological evaluation of excised esophageal cancer lesions and regional lymph node samples after surgery.
safety(AE or SAE)
Incidence of adverse events or serious adverse events
Secondary Outcome Measures
Tumor regression grade(TRG)
Evaluation of the focus of primary tumor after radiotherapy and chemotherapy
R0 resection rate
Proportion of subjects reaching R0 resection. resection was defined as no tumor cells remained within 1mm of the two cutting edges of the esophageal cancer lesions removed during the operation.
Event free survival(EFS)
Date of first administration to date of first recording of relevant events
Overall survival(OS)
Date of first administration to date of death due to any cause
Disease free survival(DFS)
Date from the operation to the first recording of relevant events
Full Information
NCT ID
NCT05561699
First Posted
September 28, 2022
Last Updated
September 28, 2022
Sponsor
Shanghai Zhongshan Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05561699
Brief Title
Sequential Preoperative Penpulimab Combined With Chemoradiotherapy(CRT) for Locally Advanced Esophageal Squamous Cell Cancer
Acronym
SPEED
Official Title
Sequential Preoperative Penpulimab Combined With Chemoradiotherapy(CRT) for Locally Advanced Esophageal Squamous Cell Cancer: A Prospective, Single Arm, Single Center,Exploratory Study
Study Type
Interventional
2. Study Status
Record Verification Date
August 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 28, 2022 (Anticipated)
Primary Completion Date
September 30, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Zhongshan Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
This study used an open single center study design to observe the efficacy and safety of Penpulimab combined with Chemoradiotherapy(CRT) in preoperative T2,3,4aN0-1-2M0 esophageal squamous cell carcinoma (ESCC).
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
Masking
None (Open Label)
Allocation
N/A
Enrollment
66 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Penpulimab Combined With Chemoradiotherapy(CRT)
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Penpulimab Combined With CRT
Intervention Description
Penpulimab: 200mg, intravenous infusion, once every two weeks. After completing two courses of CRT, continue to send Penpulimab 200mg every two weeks on the first and 14th days after the completion of CRT, two courses of treatment, a total of four courses.
Radiotherapy 40gy/20fx, once a day from Monday to Friday, completed in 4 weeks;
PC regimen: Paclitaxel 50mg/m2, intravenous drip, carboplatin AUC=2mg/ml/min, intravenous drip, once a week during radiotherapy, a total of 4 courses, the specific time is D1, 8, 15, 22 days after the beginning of radiotherapy.
Gastrointestinal reactions such as nausea and vomiting should be routinely prevented before chemotherapy. Dexamethasone 10mg should be used 30 ~ 60 minutes before paclitaxel, and intramuscular injection should be stopped immediately in case of drug or infusion reactions.
Primary Outcome Measure Information:
Title
pathological complete remission(pCR)rate
Description
Proportion of subjects who achieved pathological complete remission (PCR),PCR was defined as the microscopic absence of tumor cells in the pathological evaluation of excised esophageal cancer lesions and regional lymph node samples after surgery.
Time Frame
3 to 4 months
Title
safety(AE or SAE)
Description
Incidence of adverse events or serious adverse events
Time Frame
2 to 3 years from baseline
Secondary Outcome Measure Information:
Title
Tumor regression grade(TRG)
Description
Evaluation of the focus of primary tumor after radiotherapy and chemotherapy
Time Frame
3 to 4 months
Title
R0 resection rate
Description
Proportion of subjects reaching R0 resection. resection was defined as no tumor cells remained within 1mm of the two cutting edges of the esophageal cancer lesions removed during the operation.
Time Frame
3 to 4 months
Title
Event free survival(EFS)
Description
Date of first administration to date of first recording of relevant events
Time Frame
2 to 3 years from baseline
Title
Overall survival(OS)
Description
Date of first administration to date of death due to any cause
Time Frame
2 to 3 years from baseline
Title
Disease free survival(DFS)
Description
Date from the operation to the first recording of relevant events
Time Frame
2 to 3 years from baseline
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Resectable t2,3,4an0-1-2m0 esophageal squamous cell carcinoma initially diagnosed by histology or cytology;
Without any systematic anti-tumor treatment;
ECOG 0-1;
ANC≥ 1.5×109/L;
PLT≥ 75×109/L;
HB≥ 8.0 g/dL;
TBIL ≤ 1.5´ ULN;
ALT and AST ≤ 2.5´ULN;
Cr ≤ 1.5´ULN or CCr ≥ 60ml/min;
Urine protein < +, if urine protein + then the total protein in 24 hours must be <500mg;
Blood glucose is within the normal range and / or patients with diabetes are in treatment, but blood glucose is controlled in a stable state;
FEV1 ≥ 2L; If the baseline FEV1 is less than 2L, it is estimated that the FEV1 after surgery is greater than 800ml;
No myocardial infarction within 1 year; No unstable angina pectoris; No symptomatic severe arrhythmia; No cardiac insufficiency;
There are no serious complications or other major diseases that have not been cured;
Thoracic surgeons judge those who can tolerate the operation;
Female subjects with fertility and male subjects with partners of childbearing age need to use a medically approved contraceptive measure during the study treatment and at least 6 months after the last chemotherapy;
The subjects voluntarily joined the study and signed the informed consent form
Exclusion Criteria:
Received any kind of systematic anti-tumor treatment before the first use of the study drug;
At the same time, another clinical study will be included, unless it is an observational (non intervention) clinical study;
Subjects who need to be given corticosteroids (more than 10mg prednisone equivalent dose per day) or other immunosuppressants for systematic treatment within 2 weeks before the first use of the study drug;
Have been vaccinated with tumor vaccine or have been vaccinated with live vaccine within 4 weeks before administration;
Have a history of active autoimmune diseases and autoimmune diseases; Except for patients who have recovered from childhood asthma / allergy and do not need any intervention after adulthood; Autoimmune mediated hypothyroidism treated with a stable dose of thyroid hormone replacement; Use a stable dose of insulin for type I diabetes;
Serious interference occurred within 4 weeks before the first use of the study drug (CTC AE>2); Baseline chest imaging examination showed active pulmonary inflammation, symptoms and signs of infection within 2 weeks before the first use of the study drug, or the need for oral or intravenous antibiotics;
Have a history of interstitial lung disease;
The subjects had active hepatitis B (HBV DNA ≥ 2000 IU/ml or 104copies/ml), hepatitis C (hepatitis C antibody positive and HCV-RNA higher than the lower limit of the analysis method);
Pregnant or lactating women;
There are serious complications or other major diseases that have not been cured;
Patients judged by thoracic surgeons to be intolerant of surgery
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yang Qian, MD
Phone
0086-13817929371
Email
qy19792006@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jian Wang, MD
Organizational Affiliation
Fudan University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Zhongshan Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200000
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jian Wang, MD
Phone
0086-13816101686
Email
wang.jian3@zs-hospital.sh.cn
12. IPD Sharing Statement
Learn more about this trial
Sequential Preoperative Penpulimab Combined With Chemoradiotherapy(CRT) for Locally Advanced Esophageal Squamous Cell Cancer
We'll reach out to this number within 24 hrs