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
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7 DAYS
Rs. 3800
HISTOPATHOLOGY BIOPSY LARGE COMPLEX BIOPSY-I
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7 DAYS
Rs. 6500
HISTOPATHOLOGY BIOPSY LARGE SPECIMEN
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 7 DAYS
Rs. 5000
HISTOPATHOLOGY BIOPSY MEDIUM SPECIMEN
SAMPLE DAILY BY 7:00 PM, REPORT AFTER 5 DAYS
Rs. 3500
BRCA 1 & 2 GENE SEQUENCING (GERMLINE)
SAMPLE DAILY BY 4:00 PM REPORT AFTER 21 WORKING DAYS
Rs. 32000
BRCA 1 & 2 SOMATIC GENE SEQUENCING, FFPE TISSUE
SAMPLE DAILY BY 4:00 PM, REPORT AFTER 21 WORKING DAYS
Rs. 32000
HISTOPATHOLOGY BIOPSY SMALL SPECIMEN
SAMPLE DAILY BY 7:00 PM REPORT AFTER 5 DAYS
Rs. 2500
HISTOPATHOLOGY BIOPSY: SECOND OPINION
SAMPLE DAILY BY 8:00 PM, REPORT AFTER 7 DAYS
Rs. 2000
IMUNOHISTOCHEMISTRY: MICROSATELLITE INSTABILITY (MSI) PANEL OR MISMATCH REPAIR (MMR) PROTEIN IHC
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. |
