Dr. Bharat Kwatra Comp. Precision Oncology
Gynaecologic

Cervical Cancer

Cervical cancer is overwhelmingly associated with persistent high-risk human papillomavirus infection, which places it among the most preventable cancers through vaccination and screening.

Disease categories

Major disease categories

  • Squamous cell carcinoma
  • Adenocarcinoma
  • Adenosquamous carcinoma
  • Neuroendocrine carcinoma of the cervix

Molecular

Molecular considerations

HPV integration is central. PIK3CA alterations are frequently described. PD-L1 expression and mismatch repair status are assessed in advanced disease.

Fig. 1 · Biomarker panel 5 markers

Markers commonly discussed in cervical cancer

  • HPV status
  • PD-L1
  • PIK3CA
  • MMR / MSI
  • TMB

Not exhaustive, and not every marker is assessed in every patient. Which of these is relevant depends on the individual case and should be discussed with the treating team.

Testing

Genomic testing considerations

Profiling is discussed in recurrent and metastatic disease.

Germline

Germline considerations

Not routinely indicated, but considered where the clinical picture is unusual.

Cancer genetics and hereditary risk

Molecular monitoring

ctDNA and liquid biopsy considerations

HPV circulating DNA is an area of research interest for monitoring.

More on ctDNA

Single-cell & computation

Single-cell and algorithmic approaches

Single-cell analysis in gynaecological cancer is applied to clonal structure at relapse, where the question is whether resistant disease was present from the outset or emerged under treatment. Single-cell DNA sequencing can identify reversion events in a subpopulation before they are detectable in bulk. Algorithmic work includes homologous recombination deficiency scoring from sequencing data, mutational signature analysis, and molecular classification pipelines.

scDNA-seqscRNA-seqClonal reconstructionAlgorithm developmentPipeline engineering

Technical expertise

Decisions

Treatment decision questions

Questions worth raising with a treating team when a decision is being made:

  • Is the histological subtype documented, including neuroendocrine features if present?
  • Has PD-L1 been assessed in advanced disease?

Resistance

Resistance and recurrence questions

  • Has the disease been re-characterised at recurrence?

Trials

Clinical trial considerations

Biomarker status and prior therapy affect eligibility.

Clinical trial matching

When a precision oncology review may help

A review is most useful where the standard pathway has been exhausted or where the picture is more complicated than a protocol accounts for — rare presentations, treatment resistance, complex or apparently contradictory molecular findings, or a decision between several defensible options.

The output is a structured analysis and a set of questions for the treating team. It is not treatment, and it does not replace the treating oncologist.

Educational information. Medical information on this page is educational. It is not a treatment guideline and should be discussed with your treating medical team.
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Talk it through before you decide

Monday to Saturday, 12:00 – 18:00 · by appointment at KPCIRC, Paschim Vihar. Remote review available for patients and clinicians elsewhere.

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