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One third of individuals aged >60 years will be diagnosed with at least one renal cyst following abdominal imaging. These cystic lesions are categorized according to the Bosniak classification which categorizes cysts according to their degree of complexity and risk of malignancy. Growing evidence suggests that a significant proportion of Bosniak III and IV cysts are benign and that the malignant ones present low metastatic potential. Since renal surgery carries substantial morbidity (20%) and potential mortality (0.5%), active surveillance has gained attention as a potential tradeoff to surgery to overcome overtreatment. Therefore, prospective studies of long-term follow-up are needed to confirm the oncologic safety of this strategy for patients with Bosniak III/IV cysts.
This is an multicenter prospective observational longitudinal study. The main objective is to compare the 5-year follow-up cancer-specific survival between the active surveillance and the surgical groups.
Background: One in three patients over 60 years old will be diagnosed with a renal cyst following abdominal imaging. Traditionally, experts have recommended that complex cystic lesions (also known as Bosniak III - IV cysts) should be surgically removed, but recent evidences suggest that many are benign or have low metastatic potential. Thus, active surveillance which involves close follow-up of a patient's condition, was proposed as a tradeoff option to surgery.
Design: Multicenter observational longitudinal prospective cohort study
Objectives: The goal of this multicenter project is to conduct a prospective study with a 5-year follow-up to confirm the oncologic outcomes of active surveillance in the management of complex cysts. The main objectives are: 1) to compare the 5-year cancer specific survival between cysts managed by surgery and active surveillance; 2) to evaluate disease progression; 3) to evaluate patient's well-being according to each management strategy; and 4) to compare the 5-year healthcare cost of both management approaches.
Study population: Patients incidentally diagnosed with a Bosniak III and/or IV cysts, who are deemed to have at least 5 years of life, and who opted to be managed by either surgery or active surveillance. (N=330)
Follow-up: Patients will DECIDE if they want to have a surgery or to be followed by active surveillance. All patients will be followed as per standard of care with either semi-annual and annual visits. Research visits will serve to assess vital status and quality of life scores (through validated questionnaires). Patients on active surveillance will also be assessed for cyst progression and might be offered invasive or systemic therapy if progression is observed.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| active surveillance | 220 participants will be included in the active surveillance group. Active surveillance is close monitoring (every 6 months the first 3 years following diagnosis and annually the following years), done per standard of care Close monitoring include: abdominal imaging (ultrasound, CT or MRI), chest X-ray or CT scan and blood tests |
| |
| surgery | 110 participants will be included in the surgery group. Surgery is done per standard of care. The type of surgery is at the discretion of the treating physician and may include: partial resection, total resection, thermoablation. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Active surveillance | Procedure | Per standard of care: Imaging and blood tests every 6 months (3 first years) and annually (following years) |
|
| Measure | Description | Time Frame |
|---|---|---|
| 5-year cancer-specific survival | Defined as kidney cancer survival 5 years after the enrollment | from the date of enrollment (defined by signed consent) to the end of follow-up (up to 5 years) |
| Measure | Description | Time Frame |
|---|---|---|
| 5-year overall survival | Defined as survival 5 years after enrollment | from the date of enrollment (defined by signed consent) to the end of follow-up (up to 5 years) |
| 2-year overall survival | Defined as survival 2 years after enrollment |
| Measure | Description | Time Frame |
|---|---|---|
| Radiomic | Predictive ability of radiomics (comparison between imaging and clinical/research data) | On diagnostic imaging, up to 12 months prior consent form |
Inclusion Criteria:
Exclusion Criteria:
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Patients incidentally diagnosed with a Bosniak III or IV cysts and who opted to be managed by either surgery or active surveillance
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Amelie Tetu | Contact | 819-346-1110 | 15571 | amelie.tetu.ciussse-chus@ssss.gouv.qc.ca |
| Name | Affiliation | Role |
|---|---|---|
| Patrick O Richard, MD,MSc,FRCSC | Université de Sherbrooke | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Prostate Cancer Center | Recruiting | Calgary | Alberta | T2V 1P9 | Canada |
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| ID | Term |
|---|---|
| D057832 | Watchful Waiting |
| D013514 | Surgical Procedures, Operative |
| ID | Term |
|---|---|
| D017063 | Outcome Assessment, Health Care |
| D010043 | Outcome and Process Assessment, Health Care |
| D011787 | Quality of Health Care |
| D006298 | Health Services Administration |
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| Surgery | Procedure | Per standard of care: partial or full resection of the kidney, imaging annually |
|
| from the date of enrollment (defined by signed consent) up to 2 years of follow-up |
| 2-year cancer-specific survival | Defined as kidney cancer survival 2 years after the enrollment | from the date of enrollment (defined by signed consent) up to 2 years of follow-up |
| Treatment-free survival | Defined as survival without treatment (in active surveillance group) | from the date of enrollment (defined by signed consent) up to 2 and 5 years of follow-up |
| Discontinuation rate | Defined as the number of people who discontinued active surveillance at the end of the study (over the total) | from the date of enrollment (defined by signed consent) to the end of follow-up (up to 5 years) |
| Tumor growth rate | Defined by change in volume (cm3 ) and change in maximal diameter measured over time (years). Volume will be calculated using the formula for ellipsoid volume: 0.5326 x length x width x height. | if there is a progression, at the time of imaging (undefined, between 6 months and 5 years post-enrollment) |
| Tumor progression rate | Defined as the percentage of patients with tumors that have met our pre-specified progression endpoints | if there is a progression, at the time of imaging (undefined, between 3 months and 5 years post-enrollment) |
| Time to tumor progression (Progression-free survival) | Defined as the time from the date of enrollment to the date where an individual experienced tumor progression or censoring due to lost to follow-up or the end of follow-up period | range of time from enrollment to progression (undefined, between 3 months and 5 years post-enrollment) or end of follow-up (5 years post-enrollment) |
| Patient and tumor characteristics in correlation with cancer-specific death | Defined as demographic (i.e. age, sex, comorbidities, medical history, etc) and tumor characteristics (i.e. tumor size, tumor complexity, etc) associated with kidney cancer deaths | at the baseline visit (no more than 30 days after signed consent) |
| Patient and tumor characteristics in correlation with disease progression | Defined as demographic (i.e. age, sex, comorbidities, medical history, etc) and tumor characteristics (i.e. tumor size, tumor complexity, etc) associated with disease progression. | at the baseline visit (no more than 30 days after signed consent) |
| Perceived health change over time | Defined as the change in EQ5D-5L scores over time (enrollment to censoring due to lost of follow-up or the end of follow-up period). | range of time from enrollment to end of follow-up (maximum 5 years post-enrollment) |
| Quality of life change over time | Defined as the change in short form health survey (SF-12) scores over time (enrollment to censoring due to lost of follow-up or the end of follow-up period). | range of time from enrollment to end of follow-up (maximum 5 years post-enrollment) |
| Anxiety change over time | Defined as the change in Hospital Anxiety and Depression Scale (HADS) scores over time (enrollment to censoring due to lost of follow-up or the end of follow-up period). | range of time from enrollment to end of follow-up (maximum 5 years post-enrollment) |
| Health cost | Defined as the total direct (patients) and indirect (healthcare system) cost associated with the management of a complex cyst according to each treatment strategy (active surveillance and surgery). | range of time from enrollment to end of follow-up (maximum 5 years post-enrollment) |
| Northern Alberta Urology Center | Recruiting | Edmonton | Alberta | T6G 1Z1 | Canada |
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| Vancouver Prostate Centre | Recruiting | Vancouver | British Columbia | Canada |
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| Mens Health Clinic | Recruiting | Winnipeg | Manitoba | Canada |
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| Nova Scotia Health Authority | Recruiting | Halifax | Nova Scotia | Canada |
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| St-Joseph's Hospital | Recruiting | Hamilton | Ontario | Canada |
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| The Ottawa Hospital | Recruiting | Ottawa | Ontario | Canada |
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| Thunder Bay Health Sciences Center | Recruiting | Thunder Bay | Ontario | Canada |
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| Princess Margaret Hospital | Recruiting | Toronto | Ontario | Canada |
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| Woodstock hospital | Recruiting | Woodstock | Ontario | Canada |
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| Centre intégré de santé et de services sociaux de Chaudière-Appalaches - Hôtel-Dieu de Lévis | Recruiting | Lévis | Quebec | G6V 3Z1 | Canada |
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| CHUM | Recruiting | Montreal | Quebec | Canada |
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| Hôpital Maisonneuve-Rosemont (CISSS-EIMtl) | Recruiting | Montreal | Quebec | Canada |
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| McGill University Health Centre | Recruiting | Montreal | Quebec | Canada |
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| CHU de Québec - Université Laval | Recruiting | Québec | Quebec | Canada |
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| Centre de recherche du Centre hospitalier Universitaire de Sherbrooke | Recruiting | Sherbrooke | Quebec | J1H 5N4 | Canada |
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| CIUSSS Mauricie-Centre-du-Québec | Recruiting | Trois-Rivières | Quebec | Canada |
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| CHU Bordeaux (URO-CCR) | Recruiting | Bordeaux | France |
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