Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

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

15. mai 2026 oppdatert av: RenJi Hospital

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

Studieoversikt

Status

Har ikke rekruttert ennå

Intervensjon / Behandling

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Antatt)

33

Fase

  • Fase 2

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Neoadjuvant TQB2450 + Anlotinib
Neoadjuvant TQB2450 + Anlotinib 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
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

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Rate of Successful Nephron-Sparing Surgery
Tidsramme: At the time of surgery
Defined as the proportion of patients who undergo partial nephrectomy
At the time of surgery

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
MDT-Defined Conversion to Nephron-Sparing Surgery
Tidsramme: 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
Pre-surgery
Objective Response Rate (ORR)
Tidsramme: Pre-surgery
Assessed by RECIST v1.1
Pre-surgery
Pathologic Complete Response (pCR)
Tidsramme: 1 month after surgery
Pathologic Complete Response (pCR) after surgery
1 month after surgery
Renal Function Preservation
Tidsramme: 3 month after surgery
Proportion of patients with ≤20% decline in eGFR at 3 months postoperatively
3 month after surgery
Safety and Tolerability
Tidsramme: enrollment to 90 days after surgery
Incidence of Grade ≥3 treatment-related adverse events (CTCAE v5.0)
enrollment to 90 days after surgery

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
ctDNA methylation-based MRD dynamics across 4 time points
Tidsramme: enrollment to 90 days after surgery
ctDNA methylation-based MRD dynamics across 4 time points
enrollment to 90 days after surgery
Tumor RNA expression and DNA methylation profiling
Tidsramme: enrollment to 90 days after surgery
Tumor RNA expression and DNA methylation profiling
enrollment to 90 days after surgery

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

31. mai 2026

Primær fullføring (Antatt)

31. desember 2027

Studiet fullført (Antatt)

31. desember 2028

Datoer for studieregistrering

Først innsendt

7. mai 2026

Først innsendt som oppfylte QC-kriteriene

15. mai 2026

Først lagt ut (Faktiske)

22. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

22. mai 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

15. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere