A Clinical Study Of Camrelizumab With Or Without Radiotherapy In The Treatment Of Esophageal Cancer

Esophageal Cancer Clinical Trial

Official title:

A Multi-Center, Randomized Controlled, Phase II Clinical Study Of Camrelizumab With Or Without Radiotherapy For The Treatment Of Recurrent Or Metastatic Esophageal Cancer That Has Progressed After Chemotherapy

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04512417
• Other study ID #: IRB-2020-176
• Status: Recruiting
• Phase: Phase 2
• Start date: August 31, 2020
• Est. completion date: August 31, 2022

Study information

• Verified date: August 2020
• Source: Zhejiang Cancer Hospital
• Contact: Chen Ming, MD
• Phone: 0571-88122199
• Email: chenming[@]zjcc.org.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to observe and evaluate the efficacy and safety of Camrelizumab combined with or without radiotherapy for the treatment of recurrent or metastatic esophageal cancer that has progressed after chemotherapy

Description:

In China, the incidence of esophageal cancer has declined in recent years, but the mortality rate has been ranked fourth. Morbidity and mortality were ranked sixth and fourth in all malignancies, respectively. Therefore, esophageal cancer has always been a major malignant tumor that threatens the health of our residents. We designed a multi-center, randomized controlled, phase II clinical study of camrelizumab with or without radiotherapy for the treatment of recurrent or metastatic esophageal cancer that has progressed after chemotherapy. The purpose of this study is to observe and evaluate the efficacy and safety of camrelizumab with or without radiotherapy for advanced esophageal cancer.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 63
• Est. completion date: August 31, 2022
• Est. primary completion date: August 31, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• 1. Volunteer to participate in clinical research: fully understand and know the research and sign the Informed Consent Form (ICF); willing to follow and have the ability to complete all trial procedures;

• 2. Recurrent or metastatic esophageal cancer confirmed by histology or cytology, patients with =4 metastatic lesions;

• 3. Progress after first-line chemotherapy;

• 4. There are lesions measurable according to RECIST standards

• 5. Age =18 years old and =75 years old, regardless of gender

• 6. ECOG physical strength status score is 0~2;

• 7. Have not received immunotherapy or biological therapy before;

• 8. Hemoglobin =90g/L, platelets =10×109/L, absolute neutrophil count =1.5×109/L;

• 9. Serum creatinine =1.25 times UNL or creatinine clearance =60 mL/min;

• 10. Serum bilirubin=1.5×UNL, AST (SGOT) and ALT (SGPT)=2.5×UNL, alkaline phosphatase=5×UNL;

• 11. No history of interstitial pneumonia or previous interstitial pneumonia;

Exclusion Criteria:

• 1. Previously received anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137 or anti-CTLA-4 antibody treatment, or any other antibodies targeting T cell costimulation or checkpoint pathways as specific targets or drug;

• 2. Have received radiotherapy in the past, and the tumor in the irradiation field has progressed;

• 3. Metastasis of meninges, pleura or pericardium;

• 4. Esophageal perforation and active esophageal bleeding, with invasion of trachea and large blood vessels in the thoracic cavity;

• 5. Patients with severe cardiovascular or pulmonary diseases, interstitial pneumonia or previous history of interstitial pneumonia:

• 6. Patients who cannot understand the test requirements or may not comply with the test requirements;

• 7. Autoimmune diseases (such as: systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, autoimmune thyroid disease), but allow the following diseases to enter the next step of screening: type I diabetes, skin that does not require systemic treatment Diseases (such as vitiligo, psoriasis);

• 8. Active hepatitis B or C that requires treatment;

• 9. Suffered from an active infection requiring systemic treatment 14 days before the first administration;

• 10. Patients with other malignant lesions, except for curable skin cancer (non-melanoma), cervical carcinoma in situ or malignant disease cured =5 years;

• 11. The researcher believes that some obvious diseases should be excluded from this research;

• 12. The dose limit of radiotherapy cannot meet the limit requirement set by this study.

Related Conditions & MeSH terms

• Esophageal Cancer
• Esophageal Neoplasms

Intervention

Drug:
• Camrelizumab+Radiotherapy
The combined treatment group received radiotherapy for recurring or metastatic lesions: at least one or more lesions were irradiated, stereotactic body radiotherapy (SBRT, 8Gy/time, 3-5 times) or conventional radiotherapy (parts not suitable for SBRT, total Dose 30Gy or more); start immunotherapy within 8 weeks after radiotherapy.Until PD or toxicity is intolerable or up to 24 months.
• Camrelizumab
Camrelizumab,200mg,Q3W,Until PD or toxicity is intolerable or up to 24 months.

Locations

Country	Name	City	State
China	Zhejiang Province Cancer Hospital	Hanzhou	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
Zhejiang Cancer Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression-free Survival (PFS) per RECIST 1.1	PFS is defined as the time from randomization to the first documented disease progression per RECIST 1.1 based on blinded independent central review or death due to any cause, whichever occurs first.	Up to 24 months
Secondary	Objective Response Rate (ORR) per Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1	ORR is defined as the percentage of participants in the analysis population who have a Complete Response (CR: Disappearance of all target lesions) or a Partial Response (PR: =30% decrease in the sum of diameters of target lesions) per RECIST 1.1.	Up to approximately 6 months.
Secondary	Overall Survival (OS)	defined as the time from randomization to death from any cause during the course of the study.	Up to 24 months
Secondary	Number of Subjects with treatment-related adverse events (AEs)	Incidence, nature, and severity of adverse events graded according to the NCI CTCAE v5.0.	Up to 24 months
Secondary	Failure mode	Observe and collect the reasons for the treatment failure of the subjects during the study	Up to 24 months