TUMOUR PANEL (FEMALE)
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TUMOUR PANEL (FEMALE)

Comprehensive Cancer Marker Screening for Women.

The Ibn Sina Trust
Praava Health
Dr Lal PathLabs
Omnicare Diagnostic Limited
Thyrocare Bangladesh Ltd
Brac Healthcare
Popular Diagnostic Centre Ltd
JG Healthcare
Sample Type
blood
Fasting Required
No
Description

A Tumour Panel (Female) is a diagnostic test designed to identify and measure specific markers related to various cancers affecting women. This panel typically includes markers for breast cancer, ovarian cancer, cervical cancer, and other female-specific cancers. It helps detect the presence of cancerous cells, assess the extent of the disease, and monitor treatment efficacy.

Covid Safety

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How our test process works!

Step 1

Sample Collection

Vaccinated Phlebotomists collects from syringe in the barcoded vials

Step 2

Sample Storage

Only vaccinated phelbos are assigned orders

Step 3

High Tech Facility

Lab ingests the sample into processing machines which are 100% automated

Step 4

Accurate Digital Reports

The reports are generated by the processing machines and clinically correlated by doctors

Overview

Overview

  • Purpose: It helps assess a woman's genetic predisposition to certain cancers and can guide personalized treatment or preventive care options.
  • Genes Tested: The panel typically tests for several key genes, such as BRCA1, BRCA2 (associated with breast and ovarian cancer), TP53, and others related to various cancers.
  • Cancer Risk: Identifies genetic mutations that may increase the risk of developing cancers such as breast, ovarian, uterine, and others. This test can provide an assessment of inherited cancer risk.
Risk Assessment

Risk Assessment

  • Genetic Mutations: Some mutations, such as BRCA1/2 mutations, significantly increase the risk of breast and ovarian cancers. These mutations are inherited and can be passed down through generations.
  • Personalized Recommendations: Based on the results, healthcare providers may recommend increased monitoring, preventive surgeries (like mastectomy or oophorectomy), or targeted therapies if a woman is found to be at a higher risk.
  • Family History: A family history of certain cancers may increase the likelihood of a woman carrying genetic mutations related to those cancers.

 

Normal Range

Normal Range

  • Normal Range: For genetic testing, "normal" usually means no significant mutations or alterations in the genes being tested. Variations outside of the normal sequence might suggest a genetic predisposition, but not all variants are necessarily harmful.

 

Interpretation

Interpretation

  • Positive Results: If a mutation is detected, it may indicate an increased risk of certain cancers. In some cases, it might suggest the need for further testing, increased screening, or prophylactic measures.
  • Negative Results: A negative result means no significant genetic mutations were found. However, this does not mean the individual is free of cancer risk, as many factors (including lifestyle, environmental exposures) can also contribute to cancer development.
  • Variants of Unknown Significance (VUS): Sometimes, the test might identify genetic changes whose significance is not fully understood. These results may require follow-up with genetic counseling or additional testing.

 

Sample Type

Sample Type

  • Sample Type: Blood, saliva, or cheek swab are common sample types for tumor panels. The most common method is a blood sample, which provides DNA that is analyzed in the lab.

Frequently Asked Question