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Cancer Marker Profile - Ovarian

Also referred as
Ovarian Cancer Panel
+2
Ovarian Tumor Marker Panel
Ovarian Malignancy Panel
For women
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Contains
6 tests
Test price:
₹4299
₹4936
13% off
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The Cancer Marker Profile - Ovarian is a specialized ovarian cancer marker profile designed to support risk assessment, early detection, and disease monitoring. The panel includes CA 72.4, Carcino embryonic Antigen (CEA), Human Epididymis Protein 4 (HE4) with ROMA Index, and Lactate Dehydrogenase (LDH). It evaluates multiple tumor markers associated with ovarian malignancy, which may assist in the risk assessment of ovarian cancer, evaluation of disease burden, and monitoring of treatment response or disease progression, when interpreted in conjunction with clinical findings and imaging studies. 

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Understanding Cancer Marker Profile - Ovarian

The Cancer Marker Profile - Ovarian comprises a combination of tumor markers that play an important role in the assessment of suspected ovarian malignancy, especially when used alongside clinical examination and imaging studies. Tumor markers are substances produced either by cancer cells or by the body in response to cancer. 

The Cancer Marker Profile - Ovarian includes markers such as CA 72.4, CEA, HE4 with ROMA index, and Lactate Dehydrogenase (LDH). CA 72.4 is associated with certain ovarian tumors, particularly mucinous tumors, and may help in monitoring disease progression. However, its levels may also increase in other gastrointestinal cancers and some benign gastrointestinal conditions. Carcino embryonic Antigen (CEA) can be elevated in mucinous ovarian tumors and may help differentiate ovarian cancer subtypes. However, CEA is not specific to ovarian cancer and may also be elevated in smokers and benign gastrointestinal or inflammatory conditions. Human Epididymis Protein 4 (HE4), when combined with the Risk of Ovarian Malignancy Algorithm (ROMA) index, improves the accuracy of distinguishing benign ovarian masses from malignant ones, particularly in premenopausal and postmenopausal individuals with pelvic masses, by combining HE4 with CA 125. Lactate Dehydrogenase (LDH) may be elevated in ovarian malignancies, particularly germ cell tumors, and can reflect tumor burden or rapid cell turnover. However, it is a non-specific marker and may also increase in various non-malignant conditions such as tissue injury, hemolysis, or liver disease.

This panel is commonly recommended for individuals with ovarian masses, persistent abdominal bloating, pelvic pain, unexplained weight loss, or a family history of ovarian or related cancers. It is also useful for individuals with a known cancer diagnosis to monitor disease progression, assess treatment response, or detect recurrence after successful treatment. 

Provide a brief clinical history/doctor's prescription at the time of sample collection. Also, provide the date of the last menstrual period (LMP) or menopausal status. Inform your doctor about all your medications, as some can affect the test results, potentially requiring dosage adjustments or temporary discontinuation. Test result ranges are approximate and may vary between laboratories depending on the methodology and reference standards.

This package is intended for clinical support and disease monitoring only and is not meant for general population-based cancer screening or definitive diagnosis. Tumor markers may be influenced by benign conditions, physiological states, medications, or non-malignant diseases, and normal values do not exclude the presence of cancer. Results must always be interpreted by a qualified clinician in conjunction with medical history, physical examination, imaging studies, and, when indicated, histopathological confirmation. 

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What does Cancer Marker Profile - Ovarian measure?

Contains 6 tests

The Cancer Marker Profile - Ovarian measures levels of several tumor markers in the blood. HE4 with the ROMA index is a sensitive and clinically validated tool used to estimate the risk of ovarian malignancy in women with adnexal or pelvic masses, helping to guide referral and surgical planning, though it is less reliable in very early-stage disease and may be influenced by renal dysfunction or age. 

CA 72.4 supports the evaluation and follow-up of ovarian and other gynecological malignancies, particularly for monitoring treatment response and recurrence, but it lacks specificity and may be normal in early cancer or elevated in benign conditions. Carcino embryonic Antigen (CEA) acts as an adjunct marker useful in tracking disease progression or identifying mucinous tumors, yet it is non-specific and may be raised in smokers or gastrointestinal disorders. Serum LDH reflects tumor activity or tissue damage and is helpful in certain ovarian tumor subtypes and in monitoring disease burden, but it is highly non-specific and cannot distinguish malignant from benign causes. 

Together, these markers provide a broader and more informative assessment than any single test alone; however, none are suitable as standalone screening tools and results must always be interpreted in conjunction with clinical examination, imaging, and histopathology. When used appropriately, the Cancer Marker Profile - Ovarian supports informed clinical decision-making, timely intervention, and effective surveillance of ovarian health.

The HE4 With ROMA Index test measures key biomarkers to assess the risk of epithelial ovarian cancer. It includes Human Epididymis Protein 4 (HE4), CA 125, and the Risk of Ovarian Malignancy Algorithm (ROMA) index evaluation. In cases of ovarian cancer, the levels of HE4 and CA 125 are often elevated. The ROMA index combines HE4 levels with CA 125 along with other factors like the woman’s age and menopausal status for the calculation of a numerical score. This combination of biomarkers and clinical history enhances the accuracy of the HE4 With ROMA Index test in predicting the presence of epithelial ovarian cancer, particularly in its early stages. This test is instrumental in women with pelvic masses who have not yet undergone surgery.

What sets the HE4 With ROMA Index test apart is its ability to provide a nuanced assessment of epithelial ovarian cancer risk. While CA 125 alone can sometimes yield false positive results due to its elevation in other conditions like endometriosis, HE4 offers added specificity and precision. Moreover, the ROMA index considers factors like age and menopausal status, further refining the risk assessment. This comprehensive approach not only helps in the early detection of epithelial ovarian cancer but also helps differentiate between malignant (cancerous) and benign (non-cancerous) ovarian masses, guiding doctors in making informed decisions regarding further diagnostic workup and determining whether a woman with a pelvic mass is at high or low risk for ovarian cancer before surgery, which can guide treatment decisions and help in planning surgery. 

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This further contains

  • CA125 (Cancer Antigen 125)
  • HE4 - Human Epididymis Protein 4
  • ROMA Value

The Lactate Dehydrogenase, Serum test measures the level of the enzyme lactate dehydrogenase (LDH) in the blood. LDH is involved in energy production and is present in many types of cells, including those in the heart, liver, muscles, kidneys, brain, and blood cells. When these cells are damaged or destroyed, they release LDH into the bloodstream. Therefore, a minor amount of LDH is continuously released into the bloodstream as part of regular cell turnover and metabolic processes. However, elevated LDH is concerning because it usually signals underlying tissue damage, inflammation, or a wide range of diseases such as liver disease, heart disease, hemolytic anemia, and certain cancers. Its elevation necessitates further diagnostic evaluation to determine the specific cause and appropriate treatment.

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The CA 72.4 test measures the amount of cancer antigen 72.4 (CA 72.4) in the blood. CA 72.4 (or CA 72-4) is a tumor-associated glycoprotein that may be elevated in various cancers, particularly gastrointestinal cancers.

High levels of CA 72.4 may suggest active cancer or recurrence, while low levels may suggest effective treatment. However, the CA 72.4 is not a cancer-specific test and must be interpreted along with other clinical findings and diagnostic investigations.

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The Carcino Embryonic Antigen test measures the level of a specific tumor marker called CEA In the blood, often associated with colon and rectal cancer. This biomarker is produced by certain tissues in the body, specifically gastrointestinal tissues, during fetal development. CEA levels drop to low or nonexistent levels after birth. Elevated levels of CEA in the blood may indicate the presence of certain cancers, particularly colorectal cancer. However, it's important to note that high CEA levels can also be linked to non-cancerous conditions.

For a comprehensive evaluation, it is advised to consider other diagnostic tests in conjunction with Carcino Embryonic Antigen test and consult a doctor for a proper understanding of the test results.

Know more about Carcino Embryonic Antigen

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Cancer Marker Profile - Ovarian test price for other cities

Price inKolkataRs. 4299
Price inLucknowRs. 4299
Price inBangaloreRs. 4299
Price inNew DelhiRs. 4299
Price inHyderabadRs. 4299
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FAQs related to Cancer Marker Profile - Ovarian

The Cancer Marker Profile - Ovarian is designed to assess the risk of ovarian cancer, support diagnosis, and monitor treatment or recurrence.
Overnight fasting is not required for this test. You can eat and drink normally.
A blood sample is collected from a vein in the arm and analyzed in a laboratory.
The test is generally safe. Minor discomfort, bruising, or swelling may occur at the blood collection site.
It is recommended for individuals with ovarian masses, persistent abdominal or pelvic symptoms, or those undergoing evaluation or follow-up for ovarian cancer.
The ROMA (Risk of Ovarian Malignancy Algorithm) index combines HE4 levels, often with CA 125, and menopausal status to estimate the risk of ovarian cancer.
No. The panel only supports the risk assessment and monitoring but cannot confirm ovarian cancer on its own. Imaging and biopsy may be required.
Doctors may also recommend pelvic ultrasound, CT/MRI scans, or biopsy, depending on clinical findings.
Tata 1mg ensures accurate lab test results through certified laboratories that use advanced technology and adhere to stringent quality control measures. This commitment to high standards guarantees reliable results.
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