Toripalimab or Placebo With Paclitaxel and Cisplatin in Esophageal Squamous Cell Carcinoma

NCT ID: NCT03829969

Last Updated: 2025-07-23

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 514 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2019-01-31
• Study Completion Date: 2023-09-30

Brief Summary

This is one randomized, double-blind, multi-center, placebo-controlled phase III study. The objective of this study is to compare the effectiveness and safety of JS001 combined with paclitaxel and cisplatin(TP regimen )with placebo combined with TP regimen in patients with advanced or metastatic Esophageal Squamous Cell Carcinoma(ESCC )who have not received systemic chemotherapy previously.

Conditions

Advanced or Metastatic Esophageal Squamous Cell Cancer Without Previous Systemic Chemotherapy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: SEQUENTIAL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Toripalimab

Toripalimab combine with paclitaxel and cisplatin

Group Type: EXPERIMENTAL

Toripalimab

Intervention Type: BIOLOGICAL

TORIPALIMAB INJECTION(JS001 ) combine with chemotherapy or placebo combine with chemotherapy

placebo

Placebo combine with paclitaxel and cisplatin

Group Type: PLACEBO_COMPARATOR

Toripalimab

Intervention Type: BIOLOGICAL

TORIPALIMAB INJECTION(JS001 ) combine with chemotherapy or placebo combine with chemotherapy

Interventions

Toripalimab

TORIPALIMAB INJECTION(JS001 ) combine with chemotherapy or placebo combine with chemotherapy

Intervention Type: BIOLOGICAL

Other Intervention Names

JS001, TAB001

Eligibility Criteria

Inclusion Criteria

General requirements for inclusion:

Signed informed consent; Male or female aged 18 to 70 years ECOG score 0 or 1; Expected survival longer than 3 months; Agreement upon providing previously reserved tumor tissue specimen or biopsied tumor lesion tissue for biomarker analysis.

At least one measurable lesion in accordance with RECIST 1.1 (only when clear progression of disease occurs after radiotherapy for the previously irradiated lesion, the lesion can be used as measurable lesion).

Good organ function level:

Hematology: neutrophil ≥1.5×10^9/L, hemoglobin ≥9 g/dL and platelet ≥100×10^9/L.

Hepatic function: bilirubin ≤1.5 time of upper limit of normal (ULN) (patients who are known to have Gilbert disease and serum bilirubin level ≤3 times of ULN can be enrolled), AST and ALT ≤2.5 times of ULN (in case of hepatic metastasis, AST /ALT≤5 times of ULN), and alkaline phosphatase≤3 times of ULN (in case of hepatic or bone metastasis, ALP≤5 times of ULN); albumin ≥3g / dL; International normalized ratio (INR) or prothrombin time (PT) or activated partial thromboplastin time (aPTT) ≤1.5 x ULN.

Renal function: serum creatinine ≤1.5 × ULN or estimated glomerular filtration rate in accordance with Cockcroft-Gault formula: creatinine clearance ≥60 mL/min ((140 - age)x(weight，kg)x(0.85，for women))/(72 x(serum creatinine，mg/dL))

Or:

((140 - age)x(weight，kg)x(0.85，for women))/(0.818 x(serum creatinine，μmol/L))

Women who meet the following criteria are eligible to be included and participate in the study:

No childbearing potential (e.g., physiologically infertile), women meeting any one of the following conditions:

Having undergone uterectomy, Having undergone bilateral oophorectomy (oophorectomy), Having undergone ligation of bilateral fallopian tubes, or Postmenopause (total duration of menopause ≥1 year).

Having childbearing potential, serum pregnancy test negative at screening (within 7 days prior to the first dose of study drug), and adequate contraceptive measures taken prior to entry in the study and throughout the study, until 60 days after the last dose of the study drug. The adequate contraceptive measure taken continuously in accordance with the instruction on the contraceptive product and physician's guidance is defined as below:

Any intrauterine device confirmed to have a failure rate for contraception less than 1% per year Dual barrier contraception is defined as the condom with spermicidal gel, foam, suppository or film; or diaphragma with spermicide; or male condom and diaphragma.

Exclusion Criteria

Active or untreated CNS metastasis determined through CT or magnetic resonance imaging (MRI) evaluation in screening period and previous radiological evaluation (e.g., brain or leptomeningeal metastasis). Patients who have received previous treatment of brain or meningeal metastases, who have been stabilized for at least 2 months and discontinued systemic hormone therapy (> 10 mg/d of prednisone or equivalent) for > 4 weeks prior to randomization; Uncontrolled tumor related pain; Uncontrolled pleural effusion, pericardial effusion, or ascites requiring repeated drainage (once per month or more frequent); indewlling catheter (e.g. PleurX®) is allowed; Uncontrollable or symptomatic hypercalcemia (ionized calcium>1.5 mmol/L or calcium >12 mg/dL or corrected serum calcium >ULN); History of malignant tumors except esophageal cancer within 5 years prior to randomization, but except the malignant tumors that risk of metastasis or death can be neglected [e.g., expected 5-year survival rate> 90%], and are expected to be cured after treatment, for example, appropriately treated carcinoma in situ of cervix, basal or squamous cell skin cancer, local prostate cancer treated with radical operation, and ductal carcinoma in situ treated with radical operation; Palliative Radiotherapy within 4 weeks prior to enrollment, or radiopharmaceutical therapy within 8 weeks, however, except locally palliative radiotherapy for bone metastatic lesions; in case of symptomatic lesion suitable for palliative chemotherapy, the therapy should be given prior to enrollment. The effect of previous radiotherapy has been recovered. The shortest recovery period is not required; Subjects with bone metastases of multiple vertebra are prone to fractures and may cause risk of paraplegia, except for Subjects who are assessed as stable and do not need to be treated for the time being evaluated by a specialist.

Subjects with advanced tumors spreading to vital organs and being in risk of developing life-threatening complications in the short term ( eg. metastatic disease burden of liver ≥ 50% of total liver volume).

Subjects with known complete obstruction under endoscopy requiring interventions or surgery to remove obstruction and who have undergone tracheal or esophageal stenting; Subjects whose BMI are less than 17.5, or body weight decrease >10% within 2 months prior to first dose of study treatment (considering changes of massive pleural effusion and ascites) or with severe malnutrition as indicated by other indicators.

Women who are pregnant or lactating, or plan to be pregnant during the study; History of serious allergic reaction, anaphylactoid or other hypersensitive reactions to chimeric or humanized antibody or fusion protein; Known allergy or hypersensitivity to the biological products manufactured from Chinese hamster ovary cells or any component of JS001 preparation; History of autoimmune disease, including but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, antiphospholipid syndrome-related vascular thrombosis, Wegener's granulomatosis, Sjogren's syndrome, Guillain-Barre syndrome, multiple sclerosis, vasculitis, glomerulonephritis; Patients with hypothyroidism who receive stable-dose thyroid hormone replacement therapy can be enrolled in this study (the replacement therapy for hypothyroidism is seen in Appendix 6); Patients with type I diabetes whose blood glucose can be controlled through stable-dose insulin can be enrolled in this study;

Patients with eczema, psoriasis, chronic lichen simplex or only the dermatological manifestations of vitiligo (e.g., patients with psoriatic arthritis will be excluded from the study) are allowed to be enrolled in this study if they meet the following conditions:

The coverage area of rashes must be lower than 10% of body surface area (BSA); The disease has been sufficiently controlled at baseline and only low-potency topical steroid therapy is needed; No acute exacerbation of underlying diseases in the past 12 months [no need of PUVA (Psoralen plus ultraviolet A radiation), methotrexate, retinol, biological preparation, oral calcineurin inhibitor, high-potency or oral steroid therapy].

History of idiopathic pulmonary fibrosis, organized pneumonia (e.g., obliterative bronchiolitis), drug induced pneumonia, idiopathic pneumonia interstitial pneumonia or evidence of active pneumonia found during chest CT scanning for screening; Patients with positive result of human immunodeficiency virus (HIV) test

Patients with hepatitis B (known positive HBV surface antigen HBsAg and HBV DNA ≥1000 cps/ml or 200 IU/ml or higher than upper limit of normal at each study site) or hepatitis C:

Subjects with previous hepatitis B virus (HBV) infection can be included in this study. Such subjects must undergo HBV deoxyribonucleic acid (DNA) testing prior to randomization, and can participate in this study only when HBV DNA is negative (HBV DNA ˂1000 cps/mL or 200 IU/mL or below the upper limit of its normal value); In patients with positive hepatitis C virus (HCV) antibody, only the patients with negative polymerase chain reaction (PCR) HCV ribonucleic acid (RNA) can participate in this study.

Patients with active pulmonary tuberculosis (clinical diagnosis includes clinical history, physical examination and radiological findings, as well as the TB test performed in accordance with local medical routines); Serious infection within 4 weeks prior to randomization, including but not limited to the infection complications, bacteremia and severe pneumonia requiring hospitalization; Oral or intravenous antibiotics within two weeks prior to randomization; patients receiving preventive antibiotic therapy (e.g., for prevention of urinary tract infection or prevention of exacerbation of chronic obstructive pulmonary disease) can be enrolled.

Important cardiovascular diseases, e.g., heart disease defined by New York Heart Association (Grade II or above), myocardial infarction within three months prior to randomization, unstable arrhythmia, unstable angina pectoris, cerebrovascular accident or transient cerebral ischemic attack; patients with known coronary artery disease, congestive heart failure not meeting the above criteria or left ventricular ejection fraction < 50% must receive the regimen that is considered by the attending physician as the optimal for stabilizing therapy, and can consult a cardiologist when necessary; Major surgery (except for diagnostic operation) within 28 weeks prior to randomization or expected major surgery during the study; Previous allogeneic bone marrow transplantation or solid organ transplantation. Use of attenuated live vaccine within 4 weeks prior to randomization, or plan to use such attenuated live vaccine during the study Any other disease, metabolic disorder, physical examination finding or abnormal laboratory examination, with the reason to suspect that it can lead to contraindicated use of the investigational product, or affect reliability of the study results, or place the patient at high risk;

Patients who have previously received any approved Chinese patent medicine as anti-tumor indication within 2 weeks before first dose of study drug; Subjects treated with other investigational product or participation in the clinical study for other therapeutic objectives within 28 days prior to randomization (including signature of ICF for other trials, and failure of screening); Previous use of immune checkpoint blocking therapy, for example, anti-programmed death receptor -1 (anti-PD-1) and anti-PD-L1 antibody and other therapeutic antibody; Use of systemic immunostimulator therapy [including but not limited to interferon (IFN) or interleukin-2] within 2 weeks or 5 half-lives (t1/2) prior to randomization, whichever comes later; vaccination of cancer vaccine is allowed in previous treatment; Use of systemic immunosuppressive drugs (>10 mg/d Prednisone or equivalent drug) within two weeks prior to randomization, including but not limited to Prednisone, Cyclophosphamide, azathioprine, methotrexate, thalidomide and tumor necrosis factor (TNF); Patients who have received short-term, low-dose, systemic immunosuppressant (e.g., one single dose of Dexamethasone for nausea) can participate in this study after discussion by investigators and medical monitor and approval by medical monitor; Patients who use inhaled corticosteroids for treatment of chronic obstructive pulmonary disease, mineralocorticoids (e.g., fludrocortisone) for treatment of orthostatic hypotension and low-dose glucocorticoid (≤10mg /d Prednisone or equivalent drug) supplement for treatment of hypoadrenocorticism can be enrolled.

Patients who have previously received the hematopoietic growth factors (e.g. granulocyte colony-stimulating factor (G-CSF) and erythropoietin) or blood transfusion within 2 week before randomization.

History of allergy to cisplatin, carboplatin or other platinum-based compounds; Grade 2 or above peripheral neuropathy in accordance with common terminology criteria for adverse event (CTCAE) v5.0.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 75 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shanghai Junshi Bioscience Co., Ltd.

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Ruihua Xu, Prof

Role: PRINCIPAL_INVESTIGATOR

Sun Yat-sen University

Locations

Sun Yat-Sen University Cancer Center

Guangzhou, Guangdong, China

Countries

China

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

JS001-021-III-ESCC

Identifier Type: -

Identifier Source: org_study_id