# Anal Canal Squamous Cell Carcinoma Following Low-Dose-Rate Prostate Brachytherapy: A Report of Two Cases and Literature Review

**Authors:** Naoto Shibuya, Takashi Fukagai, Yoshiki Tsunokawa, Kazuhiko Oshinomi, Masakazu Nagata, Masashi Morita, Masako Kato, Madoka Morota, Yoshinori Ito, Toshiko Yamochi

PMC · DOI: 10.7759/cureus.92602 · Cureus · 2025-09-18

## TL;DR

Two men developed rare anal cancer years after prostate cancer treatment with low-dose radiation, suggesting a possible link to the therapy.

## Contribution

Reports two rare cases of anal cancer following prostate brachytherapy, highlighting potential long-term risks.

## Key findings

- Anal canal SCC developed 8-10 years after low-dose-rate prostate brachytherapy in two patients.
- Radiation-induced secondary cancer is a possible explanation for these rare cases.
- Long-term surveillance is crucial for patients undergoing prostate brachytherapy.

## Abstract

We report two cases of anal canal squamous cell carcinoma (SCC) that developed following low-dose-rate (LDR) brachytherapy for prostate cancer.

Case 1 involved a 73-year-old man who had undergone LDR brachytherapy (145 Gy) for prostate cancer (prostate-specific antigen (PSA) 8.3 ng/mL, Gleason score 3+3=6, T2N0M0) in December 2009. He remained disease-free for eight years and four months, but later presented with anal pain and an anal mass. Biopsy confirmed SCC. Based on CT findings demonstrating perineal invasion, the clinical stage was determined as cT4N1bM0, with right obturator lymph node metastasis.

Due to poor general condition, only diverting colostomy and external beam radiation therapy (EBRT, 70 Gy in 30 fractions) were performed. The patient died of aspiration pneumonia and sepsis on hospital day 94, in July 2018, eight years and seven months after the initial LDR treatment.

Case 2 was a 61-year-old man with prostate cancer (PSA 6.1 ng/mL, Gleason score 3+5=8, T1N0M0) treated with LDR brachytherapy (110 Gy) combined with EBRT (45 Gy in 25 fractions) in July 2006. He remained disease-free for eight years and seven months, after which he developed anal pain in February 2015. Endoscopic biopsy confirmed anal canal SCC (T1N1M0). Laparoscopic abdominoperineal resection (Miles’ operation) was performed, but local recurrence occurred one year later. Despite subsequent chemoradiation (5-fluorouracil plus mitomycin C) and systemic chemotherapy with XELOX (capecitabine plus oxaliplatin), the disease progressed, and he died in October 2016, 10 years and three months after the initial LDR treatment.

Anal canal SCC is a rare malignancy, and its development following prostate cancer radiotherapy is extremely uncommon. These two cases may represent radiation-induced secondary cancers, underscoring the importance of long-term surveillance for secondary malignancies in patients undergoing prostate brachytherapy.

## Linked entities

- **Chemicals:** 5-fluorouracil (PubChem CID 3385), mitomycin C (PubChem CID 5746), capecitabine (PubChem CID 60953), oxaliplatin (PubChem CID 9887053)
- **Diseases:** prostate cancer (MONDO:0005159), anal canal squamous cell carcinoma (MONDO:0004132), aspiration pneumonia (MONDO:0000265)

## Full-text entities

- **Genes:** KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}
- **Diseases:** anal pain (MESH:D010146), anal (MESH:D001005), prostate cancer (MESH:D011471), cancers (MESH:D009369), lymph node metastasis (MESH:D008207), sepsis (MESH:D018805), aspiration pneumonia (MESH:D011015), Anal Canal Squamous Cell Carcinoma (MESH:D002294)
- **Chemicals:** mitomycin C (MESH:D016685), oxaliplatin (MESH:D000077150), XELOX (MESH:C519688), capecitabine (MESH:D000069287), 5-fluorouracil (MESH:D005472)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12534856/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12534856/full.md

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Source: https://tomesphere.com/paper/PMC12534856