Skip to content

Nordic Cystectomy Study I - Neutrophil-lymphocyte Ratio (NLR)

Nordic Cystectomy Study I - Prospective Validation of Neutrophil/Lymphocyte Ratio as Predictor of Bladder Cancer Survival Risk After Radical Cystectomy for Bladder Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04523025
Acronym
NorCys-NLR
Enrollment
230
Registered
2020-08-21
Start date
2020-08-30
Completion date
2025-08-30
Last updated
2020-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder Cancer, Invasive Bladder Cancer

Brief summary

Around 7200 cases of Muscle Invasive Bladder Cancer are diagnosed annually in the Nordic countries combined. Muscle Invasive Bladder Cancer is an aggressive disease and it is linked with high mortality rates. The golden standard of treatment is radical cystectomy (RC) (the surgical removal of the bladder) and radical removal of lymph nodes in the pelvis. In addition to surgical treatment, and especially in cases where the tumour invades tissues surrounding the bladder or lymph nodes, chemotherapy is recommended. Chemotherapy can be administered before or after surgery, in a neoadjuvant (NAC) or adjuvant setting (AC). Although most patients recover well from surgery, there are significant risks regarding radical cystectomy. The greatest challenges in planning the treatment are making individual risk assessments and prognosis for the treated patients. Neoadjuvant chemotherapy is also insufficiently used and it is hard to predict how the tumour responds to chemotherapy. The purpose of this study is to collect prospective clinical data on radical cystectomy -patients in co-operation with other Nordic countries: Sweden, Denmark, Iceland and Norway. The collected data is used to validate existing prediction tools and discover novel tools for prediction of morbidity related to RC and prediction of oncological outcome after RC. The study is divided into three sub-studies. The second sub-study is on the preoperative neutrophil-lymphocyte ratio (NLR). Some studies suggest that NLR might be a predictor of oncological outcome of BC after RC. In addition, NLR has been suggested to correlate with NAC response and outcome after NAC and RC. The used cut-off value for NLR has varied between 2.26-3.0. Patients will be allocated into two groups: low NLR ratio (NLR\<3), and high NLR ratio (NLR≥3). The lab test will be retrieved before RC at the time of routine clinical laboratory testing for all patients and also before the initiation of NAC for patients planned to have chemotherapy. The primary end-point is bladder-cancer specific survival and, and secondary endpoints include progression-free, and overall survival.

Interventions

DIAGNOSTIC_TESTNLR-ratio

The ratio of neutrophils and lymphocytes in patients blood sample prior to surgical operation

Sponsors

Nordic Urothelial Cancer Group
CollaboratorOTHER
Turku University Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Histologically confirmed urinary BC planned to be treated with RC with or without neoadjuvant chemotherapy. 2. Histologically confirmed urinary BC planned to be treated with palliative cystectomy 2) Signed informed consent 3) Patient age \>18 years

Exclusion criteria

1. RC for other reasons than BC 2. Other forms of surgical treatment of BC than RC (e.g. bladder resection). 3. Patient unwillingness to participate in the study for any reason (i.e. lack of signed consent).

Design outcomes

Primary

MeasureTime frame
Bladder-cancer specific survival24 months

Secondary

MeasureTime frame
Progression-free survival24 months
overall survival24 months

Countries

Finland

Contacts

Primary ContactOtto Ettala, MD, PhD
otto.ettala@tyks.fi23130280
Backup ContactIlkka Nikulainen, MD
ilkka.nikulainen@tyks.fi23137928

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 27, 2026