A Study of Toripalimab in Adjuvant Therapy After Resection of High-risk Renal Cancer Tumors

Last updated: September 2, 2024
Sponsor: Tianjin Medical University Second Hospital
Overall Status: Active - Recruiting

Phase

2

Condition

Urologic Cancer

Urothelial Tract Cancer

Urothelial Cancer

Treatment

Tremelimumab

Clinical Study ID

NCT06584435
TUOAD-RCC
  • Ages > 18
  • All Genders

Study Summary

This is a phase II study to investigate the effect of treprolizumab on tumor control and survival in high-risk renal cancer after radical nephrectomy. Patients will be treated with treprolizumab, which will be administered every 3 weeks until tumor recurrence or intolerable toxicities

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Willing and able to provide written informed consent

  • Age ≥ 18 years

  • Subjects with pathologically and radiologically confirmed renal cell carcinoma:Stage III/IV

  • There are no suspected brain metastases

  • There are lesions that can be measured by imaging

  • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0-1

  • Organ function level must meet the following requirements:

Hematological indexes: neutrophil count >= 1.5x10^9/L, platelet count >= 100x10^9/L, hemoglobin >= 9.0 g/dl (can be maintained by blood transfusion); Liver function: total bilirubin <=1.5 ULN, alanine aminotransferase and aspartate aminotransferase <=1.5 ULN

  • Women were required to use an effective contraceptive method for three months afterthe end of the study, and men were required to consent to use an effectivecontraceptive method with their spouse during and for three months after the end ofthe study

  • The subjects volunteered to join the study, signed informed consent, and had goodcompliance with follow-up

Exclusion

Exclusion Criteria:

  • Prior treatment with radiation, chemotherapy, long-term or high-dose hormonetherapy, or immune checkpoint inhibitors

  • Previous or concurrent other malignancy

  • Previous PD-L1 or PD-L1 treatment, or allergy to PD-L1

  • History of primary immunodeficiency

  • Active, known or suspected autoimmune diseases

  • Known history of allogeneic organ transplantation and allogeneic hematopoietic stemcell transplantation

  • Pregnant or lactating female patients;

  • Untreated acute or chronic active hepatitis B or hepatitis C infection. Under thecondition of monitoring the virus copy number of patients receiving antiviraltreatment, doctors can judge whether they are in line with the patients' individualconditions;

  • Have a clear history of active tuberculosis;

  • Participating in other clinical researchers;

  • Men with reproductive capacity or women who are likely to become pregnant do nottake reliable contraceptive measures;

  • Uncontrolled concurrent diseases, including but not limited to:

HIV infected (HIV antibody positive); Severe infection in active stage or poorly controlled; Evidence of serious or uncontrollable systemic diseases (such as severe mental, neurological, epilepsy or dementia, unstable or uncompensated respiratory, cardiovascular, liver or kidney diseases, uncontrolled hypertension [i.e. hypertension greater than or equal to CTCAE grade 2 after drug treatment]); Patients with active bleeding or new thrombotic disease

Study Design

Total Participants: 40
Treatment Group(s): 1
Primary Treatment: Tremelimumab
Phase: 2
Study Start date:
October 01, 2022
Estimated Completion Date:
March 03, 2025

Study Description

This is a phase II study to investigate the effect of treprolizumab on tumor control and survival in high-risk renal cancer after radical nephrectomy. Patients will be treated with treprolizumab, which will be administered every 3 weeks until tumor recurrence or intolerable toxicities. The primary outcome measure was PFS and OS.

Connect with a study center

  • Changyi Quan

    Tianjin, Tianjin 300211
    China

    Site Not Available

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