Cervical cancer
ICD-10 C53 · ICD-11 2C77

Treatment of Cervical Cancer in Small-Cell Neuroendocrine Carcinoma

Clinical scenario

This protocol addresses cervical small-cell neuroendocrine carcinoma (SCNEC), a rare and distinctly aggressive histological subtype of cervical cancer. SCNEC accounts for only up to 2% of all invasive cervical cancers, yet carries a particular propensity for distant spread — a behaviour analogous to small-cell carcinoma of the lung.

Why this subtype is managed differently

The aggressive biology and tendency for early metastasis in cervical SCNEC mean that management strategy is determined by extent of disease at presentation — from potentially resectable limited-stage disease through to locoregionally advanced and metastatic settings — rather than following standard cervical carcinoma protocols.

Treatment approach — overview

For limited-stage, potentially resectable disease, a combined-modality approach is favoured. The strategy shifts for locoregionally advanced or metastatic presentations. Chemotherapy regimens draw from experience in a related small-cell malignancy outside the cervix.

Full stage-by-stage regimen and options available via the structured protocol →
Instant Access to Structured Evidence-Based Regimens

References

Cervical small-cell neuroendocrine carcinoma is a rare disease, accounting for only up to 2% of all invasive cervical cancers but has a particular propensity to spread distantly, which is similar to small-cell carcinoma of the lung.

Most clinicians favour: the use of combined modality therapy (surgery followed by chemotherapy or combined CRT) for limited-stage potentially resectable disease; definitive CRT for locoregionally advanced unresectable but non-metastatic disease; and palliative chemotherapy alone for those with metastatic disease, using chemotherapy regimens that are typically used for small-cell lung cancer.

DOI: 10.1093/annonc/mdx220

View source ↗