Viewing Study NCT06288802



Ignite Creation Date: 2024-05-06 @ 8:11 PM
Last Modification Date: 2024-10-26 @ 3:22 PM
Study NCT ID: NCT06288802
Status: RECRUITING
Last Update Posted: 2024-03-01
First Post: 2024-02-24

Brief Title: Study of Wilms Tumors Among Patients of Shefa Al-Orman Children Cancer Hospital
Sponsor: South Egypt Cancer Institute
Organization: South Egypt Cancer Institute

Study Overview

Official Title: Study of Wilms Tumors Among Patients of Shefa Al-Orman Children Cancer Hospital
Status: RECRUITING
Status Verified Date: 2024-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this cross sectional observational study is to determine the percentage of Wilms tumors among pediatric cancers at Shefa Al-Orman Children Cancer Hospital from june 2020 to june 2024to study the outcome of patients with Wilms tumor treated according to SIOP Umbrella protocol during the study period and to study the treatment related complications during therapy according to common terminology criteria of adverse events version 50 CTCAE Version 50
Detailed Description: Research Design and Methods

Study design cross sectional study Study setting Shefa Al-Orman Children Cancer hospital Study period from June 2020 to June 2024

Study Objectives

1 To determine the percentage of Wilms tumors among pediatric cancers
2 To study the outcome of patients with Wilms tumor treated according to SIOP Umbrella protocol 1
3 To study the treatment related complications during therapy according to common terminology criteria of adverse events version 50 CTCAE Version 50 2

Data collection Each patient is subjected to all the following according to the centre policy

I History and physical examination at presentation

1 Demographic data as Age sex residence and date of diagnosis
2 Clinical history and Physical examination including

Initial signs and symptoms of pediatric renal tumors including palpable abdominal mass abdominal pain hypertension hematuria weight loss constipation diarrhea urinary tract infection previous traumaetc
Associated congenital anomalies including Aniridia genitourinary anomalies hemihypertrophy
Family history of cancer

II Laboratory studies done for diagnosis of renal tumors at presentation

- Complete blood count presenceabsence of polycythemia anemia thrombocytopenia

Serum chemistries blood urea nitrogen creatinine uric acid Alanin transaminases aspartate aminotransferase serum bilirubin
Assessment of coagulation factors prothrombin time partial thromboplastin time

III Imaging Studies

1 Abdominal ultrasound
2 Abdominal CT scan or MRI with special attention to

Presence and function of the opposite kidney

Evidence of bilateral lesions

Evidence of involvement of renal vein or inferior vena cava with tumor

Lymph node involvement

Liver metastasis
3 Chest computed tomography scan
4 Echocardiography To

Assess myocardial contractility before starting cardiotoxic chemotherapy
Detect the presence of tumor in the inferior vena cava or right atrium

IV Pathology

1 Ultrasound or CT guided True cut needle biopsy is indicated in the following conditions

A- Unusual clinical presentations

- Age 5-6 years or less than 6 months

B- Unusual findings by imaging

- Calcification

- Voluminous adenopathies

- Renal parenchyma not visible

- Almost totally extrarenal process

C- Contraindications for the use of Needle Biopsy
Suspicion of rupture or hemorrhage
Needle biopsy is unlikely to be of benefit in pure cystic structures with no solid component Immediate surgery to establish the diagnosis is recommended in such cases

V Reporting of treament related complications include

Chemotherapy toxicity will be determined according to WHO Common Terminology Criteria for Adverse Events CTCAE Version 50 2017 2

VI Treatment Patients are treated according to SIOP Umbrella protocol 1

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None