National Path Lab
Cancer & Molecular Diagnostics

Ovarian & Endometrial Cancer

Gynecological cancers may require a combination of pathology, immunohistochemistry, and molecular investigations for accurate classification. Ovarian and endometrial cancers, while both arising in the female reproductive tract, have distinct diagnostic and molecular evaluation pathways.

For ovarian cancer, BRCA1/BRCA2 and related homologous recombination testing can inform both hereditary risk and treatment options. For endometrial cancer, modern classification increasingly incorporates molecular and immunohistochemical characteristics (MMR, p53, and POLE status) alongside traditional histopathology.

At National Path Lab (NPL), comprehensive diagnostic and molecular testing is available for both ovarian and endometrial cancers.

Tests available
9
Tests available
Health packages
2
Health packages

Tests Available at NPL

IMMUNOHISTOCHEMISTRY, P53

Turn Around Time
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7 DAYS

Rs. 3800

HISTOPATHOLOGY BIOPSY LARGE COMPLEX BIOPSY-I

Turn Around Time
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7 DAYS

Rs. 6500

HISTOPATHOLOGY BIOPSY LARGE SPECIMEN

Turn Around Time
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7 DAYS

Rs. 5000

HISTOPATHOLOGY BIOPSY MEDIUM SPECIMEN

Turn Around Time
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 5 DAYS

Rs. 3500

BRCA 1 & 2 GENE SEQUENCING (GERMLINE)

Turn Around Time
SAMPLE DAILY BY 4:00 PM REPORT AFTER 21 WORKING DAYS

Rs. 32000

BRCA 1 & 2 SOMATIC GENE SEQUENCING, FFPE TISSUE

Turn Around Time
SAMPLE DAILY BY 4:00 PM, REPORT AFTER 21 WORKING DAYS

Rs. 32000

HISTOPATHOLOGY BIOPSY SMALL SPECIMEN

Turn Around Time
SAMPLE DAILY BY 7:00 PM REPORT AFTER 5 DAYS

Rs. 2500

HISTOPATHOLOGY BIOPSY: SECOND OPINION

Turn Around Time
SAMPLE DAILY BY 8:00 PM, REPORT AFTER 7 DAYS

Rs. 2000

IMUNOHISTOCHEMISTRY: MICROSATELLITE INSTABILITY (MSI) PANEL OR MISMATCH REPAIR (MMR) PROTEIN IHC

Turn Around Time
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7 DAYS

Rs. 16000

About Ovarian & Endometrial Cancer

Causes & Risk Factors

Risk factors differ somewhat between ovarian and endometrial cancer, though both share some hereditary and hormonal influences:

•  Family history and inherited variants — a family history of ovarian, breast, or colorectal cancer, or a known BRCA1/BRCA2 or Lynch syndrome variant, increases risk of both cancers.

•  Hormonal and reproductive factors — nulliparity (never having given birth) and endometriosis are associated with increased ovarian cancer risk.

•  Unopposed estrogen exposure — obesity, certain hormone therapies, and tamoxifen use are associated with increased endometrial cancer risk.

•  Age — both cancers are more common with increasing age, particularly after menopause.

•  Lynch syndrome — associated with increased risk of both endometrial and ovarian cancer, alongside colorectal cancer risk.

Symptoms & When to Test

Both ovarian and endometrial cancer can present with subtle or nonspecific symptoms, which is part of why they can be identified at a later stage than some other cancers.

•  Ovarian cancer — persistent bloating, pelvic or abdominal pain, early satiety (feeling full quickly), and urinary urgency or frequency, particularly if new and persistent

•  Endometrial cancer — abnormal vaginal bleeding, including postmenopausal bleeding or irregular bleeding between periods, which is the most common and important warning symptom

•  Unexplained pelvic pain or pressure

•  Unexplained weight loss

When Should You Consider Testing?

Persistent bloating, pelvic pain, or early satiety lasting more than a few weeks warrants evaluation for possible ovarian cancer. Any postmenopausal bleeding, or abnormal bleeding between periods, should be evaluated promptly, as this is the key warning symptom for endometrial cancer.

Why Tests Are Combined

For ovarian cancer, histopathology establishes the diagnosis and tumor type, while BRCA1/BRCA2 and homologous recombination-related testing serve two purposes — identifying hereditary risk relevant to the patient and family, and determining eligibility for PARP inhibitor therapy, a targeted treatment option specifically effective in tumors with these genetic features.

For endometrial cancer, modern classification combines MMR IHC (relevant to Lynch syndrome and immunotherapy eligibility), p53 IHC (associated with more aggressive tumor behavior when abnormal), and POLE testing (associated with a favorable prognosis) — together these provide a molecular classification that refines the prognostic and treatment information beyond histopathology alone.

This molecular classification approach for endometrial cancer, in particular, reflects an important shift in how gynecological cancers are now understood — where molecular subtype often carries as much or more clinical significance than traditional histological grading alone.

Tests Available at NPL

Test Code

Test

Clinical Relevance

 

Histopathology Biopsy

Establishes the diagnosis, tumor type, and pathological grading.

 

Molecular NGS – Based Testing; Core HRR Genes (BRCA1, BRCA2, PALB2) + DNA Damage Response Genes (ATM, BARD1, BRIP1, CHEK1, CHEK2, CDK12) + Fanconi Pathway Genes (FANCA, FANCD2, FANCL) + RAD51 Pathway Genes (RAD51B, RAD51C, RAD51D, RAD54L) + MRN Complex Genes (MRE11, NBN) + Genomic Instability Markers (TP53, PPP2R2A) + Co-Alterations (AKT1, PIK3CA, PTEN, CCNE1, ESR1, FGFR1, FGFR2, FGFR3, POLE)

 

T0077

MMR IHC (Endometrial)

Assesses mismatch-repair status, relevant to prognosis, immunotherapy eligibility, and Lynch syndrome screening.

T0023

p53 IHC (Endometrial)

Provides molecular classification information; abnormal p53 is associated with more aggressive tumor behavior.

 

POLE Gene (Endometrial)

Identifies a molecular subtype associated with a generally favorable prognosis, where clinically indicated.

NG011

BRCA 1 & 2 GENE SEQUENCING (GERMLINE)

 

NG012

BRCA 1 & 2 SOMATIC GENE SEQUENCING, FFPE

TISSUE

 

Most tumor molecular tests, histopathology, IHC, and genetic tests do not require fasting. However, some blood-based investigations ordered alongside cancer testing may have specific preparation requirements. Please follow the instructions provided by your doctor or NPL.

Home Sample Collection

Ovarian and endometrial cancer diagnosis requires a tissue biopsy or surgical specimen, obtained by a specialist gynecologic oncologist or surgeon — this is not a home sample collection service.

Once your tissue sample is obtained, NPL arranges secure transport to our accredited laboratory for histopathology and molecular testing.

Germline BRCA1/BRCA2 testing (assessing inherited risk, as opposed to tumor-based testing) can, in some cases, be arranged via a standard blood draw — ask your care team whether NPL's home collection service applies to your specific germline testing request.

Reports are delivered securely to your treating gynecologic oncologist, and to you, within the timeframe specified for the tests ordered.

When to See a Doctor

•  Persistent bloating, pelvic pain, or early satiety lasting more than a few weeks

•  Any postmenopausal bleeding

•  Abnormal bleeding between periods

•  Unexplained pelvic pain or pressure

•  Family history of ovarian, endometrial, breast, or colorectal cancer, or known BRCA/Lynch syndrome variant in the family

Medical Disclaimer

Laboratory and molecular tests support gynecological cancer diagnosis and treatment planning but must be interpreted by a qualified gynecologic oncologist or pathologist together with clinical and imaging findings. This content is for general information only and is not a substitute for medical advice, diagnosis, or treatment.

Related Packages

MULTIPLE MYELOMA SCREENING PANEL

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7 Tests

Rs. 16000

MULTIPLE MYELOMA MONITORING PANEL ADVANCED

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13 Tests

Rs. 17000

Frequently Asked Questions

It may indicate eligibility for PARP inhibitor therapy, a targeted treatment option, in addition to informing hereditary risk for the patient and family members. Your oncologist will interpret this alongside your full clinical picture.
Postmenopausal bleeding is the most common presenting symptom of endometrial cancer and should always be evaluated promptly, even though most cases of postmenopausal bleeding are not due to cancer.
POLE testing identifies a specific molecular subtype of endometrial cancer that is generally associated with a favorable prognosis, which can meaningfully affect treatment planning.
No, tissue-based molecular testing does not require fasting. Germline blood-based BRCA testing also does not require fasting.
A positive germline BRCA result has implications for blood relatives, who may wish to consider genetic counselling and testing themselves. This is best discussed with a genetic counsellor.