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Peer-reviewedCC BY-NC-ND 4.0Communications Medicine

Clinical characteristics and diagnostic performance of vaginal squamous cell carcinoma after hysterectomy

  1. 1Medical Center for Lower Genital Tract & Anal Diseases and Shanghai Jiai Genetic & IVF Institute, Obstetrics and Gynecology Hospital of Fudan University, Shanghai Key Lab of Reproduction and Development, Shanghai Key Lab of Female Reproductive Endocrine Related Diseases, Shanghai, China

Abstract

Background: Vaginal squamous cell carcinoma (SCC) is a rare gynecological malignancy. Current guidelines do not recommend routine cancer screening after hysterectomy for non-cervical conditions based on the assumption of negligible risk. However, clinical characteristics of vaginal SCC in post-hysterectomy women remain inadequately defined, particularly for those with non-cervical indications.

Methods: We conducted a retrospective cohort study of 227 patients with vaginal SCC diagnosed at a Chinese tertiary center between 2017 and 2025. Clinical characteristics, high-risk human papillomavirus (HPV) status, diagnostic yields of cytology, colposcopy, ultrasound and MRI, and latency from hysterectomy to cancer diagnosis were analyzed.

Results: We found that 66.5% (151/227) of vaginal SCC cases occurred in women with prior hysterectomy; 86.1% had surgery for cervical lesions and 13.9% for non-cervical indications. The overall high-risk HPV positivity rate was 94.7%, with HPV16 predominating (74.9%). Regular post-hysterectomy surveillance was associated with earlier stage at diagnosis: 90.6% of surveilled patients presented with stage I disease versus 65.8% of non-surveilled patients. Latency to diagnosis was significantly shorter for women with prior cervical lesions (median 46.5 versus 120 months). Cytology and colposcopy demonstrated diagnostic yields exceeding 90%, while imaging showed lower detection rates.

Conclusions: Vaginal SCC after hysterectomy is predominantly HPV-driven, including in women with non-cervical indications. Regular post-hysterectomy surveillance is strongly associated with earlier stage at diagnosis. While universal screening is not warranted due to disease rarity, these findings support individualized HPV-informed risk counseling for sexually active women after hysterectomy and reinforce current surveillance recommendations for those with prior cervical lesions.

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BibTeX
@article{xiao2026clinical,
  title = {{Clinical characteristics and diagnostic performance of vaginal squamous cell carcinoma after hysterectomy}},
  author = {Fengyi Xiao and Min Xiao and Tingting Su and Long Sui},
  journal = {Communications Medicine},
  year = {2026},
  month = jul,
  doi = {10.1038/s43856-026-01803-3},
  url = {https://doi.org/10.1038/s43856-026-01803-3},
  note = {CC BY-NC-ND 4.0},
}
RIS
TY  - JOUR
TI  - Clinical characteristics and diagnostic performance of vaginal squamous cell carcinoma after hysterectomy
AU  - Fengyi Xiao
AU  - Min Xiao
AU  - Tingting Su
AU  - Long Sui
PY  - 2026
DA  - 2026/07/18
JO  - Communications Medicine
DO  - 10.1038/s43856-026-01803-3
UR  - https://doi.org/10.1038/s43856-026-01803-3
AB  - Background: Vaginal squamous cell carcinoma (SCC) is a rare gynecological malignancy. Current guidelines do not recommend routine cancer screening after hysterectomy for non-cervical conditions based on the assumption of negligible risk. However, clinical characteristics of vaginal SCC in post-hysterectomy women remain inadequately defined, particularly for those with non-cervical indications.  Methods: We conducted a retrospective cohort study of 227 patients with vaginal SCC diagnosed at a Chinese tertiary center between 2017 and 2025. Clinical characteristics, high-risk human papillomavirus (HPV) status, diagnostic yields of cytology, colposcopy, ultrasound and MRI, and latency from hysterectomy to cancer diagnosis were analyzed.  Results: We found that 66.5% (151/227) of vaginal SCC cases occurred in women with prior hysterectomy; 86.1% had surgery for cervical lesions and 13.9% for non-cervical indications. The overall high-risk HPV positivity rate was 94.7%, with HPV16 predominating (74.9%). Regular post-hysterectomy surveillance was associated with earlier stage at diagnosis: 90.6% of surveilled patients presented with stage I disease versus 65.8% of non-surveilled patients. Latency to diagnosis was significantly shorter for women with prior cervical lesions (median 46.5 versus 120 months). Cytology and colposcopy demonstrated diagnostic yields exceeding 90%, while imaging showed lower detection rates.  Conclusions: Vaginal SCC after hysterectomy is predominantly HPV-driven, including in women with non-cervical indications. Regular post-hysterectomy surveillance is strongly associated with earlier stage at diagnosis. While universal screening is not warranted due to disease rarity, these findings support individualized HPV-informed risk counseling for sexually active women after hysterectomy and reinforce current surveillance recommendations for those with prior cervical lesions.
SN  - 2730-664X
ER  -