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NCT04006405Completed

AURORAX-0087A: GAG Scores for Surveillance of Recurrence in Leibovich Points ≥5 Non-metastatic ccRCC

AURORAX-0087A: Glycosaminoglycan Scores for Surveillance of Recurrence in Leibovich Points ≥5 Non-metastatic Clear Cell Renal Cell Carcinoma

Source: ClinicalTrials.gov · Last updated 15 Jun 2025

Brief summary (registry, in English)

AUR87A is an observational prospective multicenter diagnostics test cohort study for detection of renal cell carcinoma recurrence as determined by the reference standard, which is imaging using computed tomography (CT) of the chest and abdomen at defined intervals after primary surgery.

Status (registry)
Completed
Study type
Observational
Enrollment
280 (actual)
First submitted
1 Jul 2019
Start date
10 Jan 2020
Primary completion date
7 May 2025
Lead sponsor
Elypta
NCT number
NCT04006405

What you commit to

  • Study type: Observational
  • Participants enrolled: 280
  • From 10 Jan 2020 to the primary completion date, 7 May 2025
  • 29 sites in 11 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Absence of preoperative chest imaging (chest CT) within 60 days prior to primary surgery
  • Previous history of curatively treated for other cancers, still not deemed fully cured and participant still under surveillance for said cancer
  • Participants offered active surveillance for RCC instead of curative intent surgery
  • Participants offered any type of thermal ablation treatment instead of surgery, i.e. LP cannot be assessed
    • Final screening exclusion criteria
  • Participants with AJCC cN0 status at preoperative imaging in whom a clinically suspicious regional lymph-node metastases (enlarged lymph node(s)) is noted during primary surgery, but who subsequently do not undergo any lymph node dissection. (Note: participants with cN0 status at pre-operative imaging and no clinical signs of regional lymph node metastases during primary surgery can still be included irrespective of lymph node dissection having been performed, i.e. being pN0 or pN1 if it is performed or pNx if it is not performed)
  • Elected for any adjuvant therapy (i.e. systemic therapy) outside or within any clinical study
  • Previous history of curatively treated for RCC with a suspected de novo RCC in the remaining kidney tissue
  • Prior or current use of instillation therapy with hyaluronic acid and/or chondroitin sulfate (HA-CS).
  • Use of heparin, including low molecular weight heparin (e.g. Enoxaparin, Dalteparin, Tinzaparin) for concurrent disease in need of blood dilution (e.g. ongoing deep vein thrombosis or lung emboli). Note: use of of heparin for thrombus prophylaxis in conjunction with primary surgery or postoperatively ≤4 weeks will be allowed.
  • Patients who were not radically operated during primary surgery with the exception of histological positive surgical margin in participants who have undergone partial nephrectomy.

Other illness

  • TNM-stage T(any) N(any) M1 according to AJCC, i.e. metastatic disease at diagnosis

Other

  • Pre-screening exclusion criteria
  • Participants with AJCC cN1 status at pre-operative imaging in which lymph node dissection is not performed (i.e. pNx).
  • Non-clear cell RCC histology or benign tumor (i.e. oncocytoma and angiomyolipoma, which are the most common benign types, but also any other rare types of benign renal tumors) after pathological analysis
  • Any hereditary form of RCC (e.g. Von Hippel-Lindau, Birt-Hogg-Dubé, Hereditary Papillary RCC)
  • RCC with pure sarcomatoid differentiation, also called sarcoma of the kidney

Who the study is looking for

  • Pre-screening inclusion criteria
  • Size of primary tumor \>4cm (\>cT1a) in greatest dimension on pre-operative abdominal CT-scan
  • Size of primary tumor ≤4cm is allowed if pre-operative abdominal CT-scan shows suspected RCCs with radiological sign of venous tumor thrombus (renal vein or caval).
  • Pre-operative CT-scan of chest and abdomen show no signs of metastatic disease
  • Localized and biopsy proven clear cell RCC (ccRCC) under active surveillance which at timepoint of study recruitment, opted for surgery because of growth rate of primary tumor to a size \> 4cm
  • Elected for curative intent surgery for RCC
    • Final screening inclusion criteria
  • Any gender being 18 years or older at timepoint of final inclusion
  • In postoperative pathology report shown to be ccRCC subtype according to 8th Edition of the American Joint Committee on Cancer (AJCC)
  • Leibovich points (LP) ≥5 according to Leibovich score system (2003)
  • If pathology report shows multiple subtypes in same tumor, as long as the majority of tumor is ccRCC (\>50%), participant can be included

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (29)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
UZ Leuven
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LeuvenBelgiumUnknown status
Prostate Cancer Centre
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CalgaryCanadaUnknown status
Aarhus University Hospital
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AarhusDenmarkUnknown status
Odense University Hospital
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OdenseDenmarkUnknown status
Zealand University Hospital
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RoskildeDenmarkUnknown status
Hospital Universitario Cabueñes
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GijónSpainUnknown status
University Hospital of Valencia
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ValenciaSpainUnknown status
Helsinki University Central Hospital
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HelsinkiFinlandUnknown status
Hopital Henri Mondor
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CréteilFranceUnknown status
Addenbrooke's Hospital
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CambridgeUnited KingdomUnknown status
Western General Hospital
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EdinburghUnited KingdomUnknown status
Frimley Park Hospital
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FrimleyUnited KingdomUnknown status
Guys & St Thomas Hospital
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LondonUnited KingdomUnknown status
Royal Free Hospital
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LondonUnited KingdomUnknown status
Norfolk & Norwich University Hospital
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NorwichUnited KingdomUnknown status
Royal Berkshire Hospital
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ReadingUnited KingdomUnknown status
Salford Royal NHS Foundation Trust
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SalfordUnited KingdomUnknown status
AOU San Orsola Malpighi
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BolognaItalyUnknown status
Careggi University Hospital
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FlorenceItalyUnknown status
San Raffaele Hospital
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MilanItalyUnknown status
Aou San Luigi Gonzaga
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OrbassanoItalyUnknown status
Istituto Nazionale Tumori "Regina Elena"
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RomaItalyUnknown status
AOU Integrata Verona
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VeronaItalyUnknown status
Hospital da Luz Coimbra
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CoimbraPortugalUnknown status
Sahlgrenska University Hospital
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GothenburgSwedenUnknown status
Norrlands University Hospital
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UmeåSwedenUnknown status
Emory University School of Medicine
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AtlantaUnited StatesUnknown status
MD Anderson Cancer Center
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HoustonUnited StatesUnknown status
Memorial Sloan-Kettering Cancer Center
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New YorkUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.