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Published on: September 8, 2017
Extramammary Paget's disease treated with of anti-programmed cell death protein 1 therapy after docetaxel therapy
Midori Narasaki1, Junji Kato1, Sayuri Sato1
1Department of Dermatology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Abstract:
Extramammary Paget's disease (EMPD) is a rare skin cancer with no standard treatment for advanced-stage disease. Although docetaxel-based chemotherapy is common, no standard treatment exists. Pembrolizumab is approved for solid tumors with a high tumor mutation burden (TMB) and/or high microsatellite instability, and nivolumab was approved in Japan in February 2024 for unresectable advanced or recurrent epithelial skin malignancies. However, there is a lack of real-world data regarding the efficacy of anti-programmed cell death protein 1 (PD-1) therapy for EMPD. We present the case details of three EMPD patients treated with anti-PD-1 therapy after docetaxel treatment, with TMB values of 17.8, 14.3, and 5.0 mut/Mb, respectively, and we review similar reported cases. Even in the cases with a high TMB, the response to anti-PD-1 therapy was not sufficient. Most cases involve second-line or later treatments, so further research is needed to determine the precise effectiveness of anti-PD-1 therapy as a first-line treatment.
Insights
Extramammary Paget's disease (EMPD) lacks standard advanced treatments. Anti-programmed cell death protein 1 (PD-1) therapy shows insufficient efficacy in real-world EMPD cases, even with high tumor mutation burden.
Area of Science:
- Oncology
- Dermatology
- Immunotherapy
Background:
- Extramammary Paget's disease (EMPD) is a rare skin malignancy with limited treatment options for advanced stages.
- Docetaxel chemotherapy is a common treatment, but lacks standardization for advanced EMPD.
- Anti-programmed cell death protein 1 (PD-1) therapies are approved for certain cancers based on tumor mutation burden (TMB) or microsatellite instability.
Observation:
- This study presents three advanced EMPD cases treated with anti-PD-1 therapy post-docetaxel.
- Tumor mutation burden (TMB) values for these cases were 17.8, 14.3, and 5.0 mut/Mb.
- A review of similar reported cases was conducted to assess real-world efficacy.
Findings:
- Real-world data indicates insufficient response to anti-PD-1 therapy in EMPD patients, even those with high TMB.
- Most reported cases received anti-PD-1 therapy as second-line or later treatment.
- The efficacy of anti-PD-1 therapy in EMPD remains limited in current real-world evidence.
Implications:
- Further research is crucial to determine the precise effectiveness of anti-PD-1 therapy as a first-line treatment for EMPD.
- Investigating alternative treatment strategies or combinations may be necessary for advanced EMPD.
- The current findings highlight the need for novel therapeutic approaches for this rare skin cancer.
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