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NCT Number: NCT07602101

Neoadjuvant PD-L1 Inhibitor Plus Anlotinib for Kidney Preservation in Complex Renal Cell Carcinoma

This is a prospective, multicenter, single-arm phase II study evaluating the efficacy and safety of neoadjuvant PD-L1 inhibitor TQB2450 in combination with anlotinib in patients with locally advanced, high-complexity (RENAL score ≥10) clear cell renal cell carcinoma (ccRCC).

The primary objective is to determine whether neoadjuvant therapy can increase the rate of successful nephron-sparing surgery.

In addition, this study incorporates a pre-specified translational research platform including circulating tumor DNA (ctDNA) methylation-based minimal residual disease (MRD) monitoring, tumor multi-omics profiling, and radiomics analysis. Artificial intelligence-based models will be developed to predict treatment response and surgical conversion, enabling precision neoadjuvant strategies.

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Key information

About this study

Patients with anatomically high-complexity locally advanced ccRCC (RENAL score ≥10) often require radical nephrectomy or technically challenging partial nephrectomy, resulting in increased perioperative risks and long-term renal function impairment. Evidence supporting neoadjuvant strategies in this specific high-complexity population remains limited.

This study evaluates a novel neoadjuvant approach combining PD-L1 blockade (TQB2450) with the multi-target tyrosine kinase inhibitor anlotinib. PD-L1 inhibition restores anti-tumor immunity, while antiangiogenic therapy promotes vascular normalization and enhances immune cell infiltration. This dual mechanism may improve tumor shrinkage and facilitate surgical conversion, particularly in central or hilar tumors.

Patients will receive 2-4 cycles of neoadjuvant therapy, followed by imaging assessment and multidisciplinary team (MDT) evaluation. Surgery will be performed within a predefined window after treatment completion.

A key translational component includes longitudinal ctDNA methylation-based MRD monitoring at four time points (baseline, after 2 cycles, pre-surgery, and post-surgery), combined with tumor tissue RNA expression and DNA methylation profiling, as well as radiomics feature extraction. These data will be integrated using machine learning algorithms to construct predictive models for treatment response and nephron-sparing surgery feasibility.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • • Age ≥18 years
  • ECOG performance status 0-2
  • Histologically confirmed clear cell renal cell carcinoma
  • Clinical stage cT2-T3aN0M0 (AJCC 8th edition)
  • RENAL nephrometry score ≥10
  • Tumor assessed as requiring radical nephrectomy or complex partial nephrectomy
  • Adequate organ function
  • Signed informed consent

Exclusion criteria

  • • Prior systemic therapy for RCC (including ICIs or TKIs)
  • Non-clear cell histology or sarcomatoid/rhabdoid differentiation >20%
  • Active autoimmune disease requiring systemic therapy
  • Active uncontrolled infection (HBV/HCV/HIV)
  • Prior organ transplantation
  • Uncontrolled cardiovascular or pulmonary disease
  • Pregnancy or breastfeeding

Treatment and study plan

TQB2450 + Anlotinib

Drug

Drug: TQB2450 (PD-L1 inhibitor) 1200 mg intravenously every 3 weeks Drug: Anlotinib 12 mg orally once daily (2 weeks on, 1 week off) Treatment duration: 2-4 cycles prior to surgery

Primary outcomes

  1. Rate of Successful Nephron-Sparing Surgery

    Time frame: At the time of surgery

    Defined as the proportion of patients who undergo partial nephrectomy

Secondary outcomes

  1. MDT-Defined Conversion to Nephron-Sparing Surgery

    Time frame: Pre-surgery

    o Defined as conversion from pre-treatment planned radical nephrectomy or complex partial nephrectomy to post-treatment feasibility of standard or simplified partial nephrectomy;o Determined by a centrally reviewed multidisciplinary team based on imaging

  2. Objective Response Rate (ORR)

    Time frame: Pre-surgery

    Assessed by RECIST v1.1

  3. Pathologic Complete Response (pCR)

    Time frame: 1 month after surgery

    Pathologic Complete Response (pCR) after surgery

  4. Renal Function Preservation

    Time frame: 3 month after surgery

    Proportion of patients with ≤20% decline in eGFR at 3 months postoperatively

  5. Safety and Tolerability

    Time frame: enrollment to 90 days after surgery

    Incidence of Grade ≥3 treatment-related adverse events (CTCAE v5.0)

Other outcomes

  1. ctDNA methylation-based MRD dynamics across 4 time points

    Time frame: enrollment to 90 days after surgery

    ctDNA methylation-based MRD dynamics across 4 time points

  2. Tumor RNA expression and DNA methylation profiling

    Time frame: enrollment to 90 days after surgery

    Tumor RNA expression and DNA methylation profiling

Study contacts

Contact information is provided by the study sponsor or research team.

jiwei huang

CONTACT

[email protected]

86-13651682825

Sponsors and collaborators

Lead sponsor

RenJi Hospital

Other

Collaborators

  • Chinese PLA General Hospital
  • Huadong Hospital

Registry information

Official study title

Neoadjuvant PD-L1 Blockade Combined With Anlotinib to Enable Nephron-Sparing Surgery in Patients With High-Complexity Locally Advanced Clear Cell Renal Cell Carcinoma

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
May 22, 2026
Registry last updated
May 22, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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