Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Jul;22(7):483-498.
doi: 10.1038/s41571-025-01025-x. Epub 2025 May 13.

Emerging advances and future opportunities in the molecular and therapeutic landscape of anal cancer

Affiliations
Review

Emerging advances and future opportunities in the molecular and therapeutic landscape of anal cancer

Franz Rödel et al. Nat Rev Clin Oncol. 2025 Jul.

Abstract

Anal squamous cell carcinoma (ASCC) is a rare malignancy with an increasing incidence. Primary chemoradiotherapy (CRT) is the standard-of-care treatment for patients with localized ASCC. In the metastatic setting, trials testing immune-checkpoint inhibitor monotherapy have demonstrated outcomes similar to those of patients receiving chemotherapy. Conversely, adding the anti-PD-1 antibody retifanlimab to chemotherapy in patients with recurrent or metastatic ASCC has been shown to significantly improve outcomes. Despite considerable efforts to develop personalized therapy, treatment guidance and prognosis remain reliant on baseline clinical characteristics. An improved understanding of the molecular characteristics of ASCC has provided insights into the mechanisms that mediate tumour progression and response to CRT. For example, human papillomavirus (HPV) infection is known to have an aetiological role in most ASCCs and can modulate cellular responses to CRT via several distinct mechanisms. In this Review, we summarize emerging advances in the molecular and therapeutic landscape of ASCC, including the implementation of biomarkers for treatment guidance and translation into new therapeutic approaches, with HPV infection constituting a global determinant of both tumour biology and clinical outcome. We also discuss the rationale for combining immune-checkpoint inhibitors with CRT in patients with HPV+ tumours.

PubMed Disclaimer

Conflict of interest statement

Competing interest: The authors declare no competing interests.

References

    1. Jemal, A. et al. Annual report to the nation on the status of cancer, 1975-2009, featuring the burden and trends in human papillomavirus (HPV)-associated cancers and HPV vaccination coverage levels. J. Natl Cancer Inst. 105, 175–201 (2013). - PubMed - PMC - DOI
    1. Gondal, T. A. et al. Anal cancer: the past, present and future. Curr. Oncol. 30, 3232–3250 (2023). - PubMed - PMC - DOI
    1. James, R. D. et al. Mitomycin or cisplatin chemoradiation with or without maintenance chemotherapy for treatment of squamous-cell carcinoma of the anus (ACT II): a randomised, phase 3, open-label, 2 x 2 factorial trial. Lancet Oncol. 14, 516–524 (2013). - PubMed - DOI
    1. Glynne-Jones, R. et al. Best time to assess complete clinical response after chemoradiotherapy in squamous cell carcinoma of the anus (ACT II): a post-hoc analysis of randomised controlled phase 3 trial. Lancet Oncol. 18, 347–356 (2017). - PubMed - PMC - DOI
    1. Deshmukh, A. A. et al. Incidence trends and burden of human papillomavirus-associated cancers among women in the United States, 2001-2017. J. Natl Cancer Inst. 113, 792–796 (2021). - PubMed - DOI

MeSH terms

Substances

LinkOut - more resources