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Squamous Cell Carcinoma Antigen as a surrogate tumour marker in carcinoma cervix

Role of Serum Squamous Cell Carcinoma Antigen as a Prognostic and Predictive Marker in Patients of Carcinoma Cervix treated with Definitive Chemoradiation - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/091155
Enrollment
20
Registered
2025-07-18
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: C538- Malignant neoplasm of overlappingsites of cervix uteri

Interventions

Intervention1: Nil: Nil

Sponsors

Saarthak Miglani
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with histopathologically confirmed squamous cell carcinoma of cervix with FIGO stage IB3 to IVA 2. Eastern Co-operative Oncology Group (ECOG) performance score of less than or equal to 2

Exclusion criteria

Exclusion criteria: 1. Adenocarcinoma or other non-squamous histology of cervical cancer 2. Histopathologically proven squamous cell carcinoma of any site other than cervix 3. Synchronous malignancy 4. History of any previous malignancy or cancer directed treatment 5. Distant metastases 6. Haemoglobin less than 10 gm/dl 7. Liver function tests more than 3 times from the baseline 8. Chronic Kidney Disease Stage 3 9. Left Ventricular Ejection Fraction less than 45% 10. Pregnancy

Design outcomes

Primary

MeasureTime frame
Association of serum squamous cell carcinoma antigen levels with treatment response (as per WHO criteria) in cervical cancer patients staged FIGO IB3 to IVATimepoint: Baseline, at treatment completion, at 6 weeks post treatment completion and at 12 weeks post treatment completion

Secondary

MeasureTime frame
Association of serum squamous cell carcinoma antigen levels with FIGO stage, tumour size, lymph node status, parametrical invasion (unilateral vs bilateral), grade & histology (keratinising vs non-keratinising)Timepoint: At baseline, at treatment completion, at 6 weeks post treatment completion & 12 weeks post treatment completion

Countries

India

Contacts

Public ContactSavita Arora

Maulana Azad Medical College

savita.arora.onco@gmail.com9999354955

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026