通过免疫疗法和积极的再放射治疗长期控制转移至脊椎的基底细胞癌:罕见骨转移的病例报告和文献综述

Andrew R. Cunningham , Amanda Goetz , Hayley Behm , Andrew W. Ju , Matthew S. Peach
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引用次数: 0

摘要

背景皮肤基底细胞癌(BCC)是一种常见的恶性肿瘤,发病率呈上升趋势,但很少发生转移,发病率为 0.0028-0.5%。血行转移性 BCC(mBCC)尤为罕见,中位生存期为 8-14 个月。本病例报告详细介绍了一名 59 岁男性的病例,他左肩的原发性 BCC 转移至肺部和脊柱。尽管接受了积极的多模式治疗,包括手术、放疗和使用刺猬抑制剂(维斯莫德吉布、索尼德吉布)进行全身治疗,但病情仍在发展。确诊后 55 个月,由于肿瘤突变负荷较高(TMB-H),患者开始使用 pembrolizumab,结果治疗反应显著,生存期延长。该患者接受了广泛的随访,包括脊柱转移灶的再次放射治疗和免疫治疗,在超过 101 个月的时间里病情保持稳定。结果/文献综述系统性文献综述仅发现 26 例骨性 mBCC,主要采用手术和放射治疗,生存结果各不相同。该病例的突出之处在于其延长的生存期和对pembrolizumab的新颖使用,凸显了免疫疗法在TMB-H mBCC中的潜在作用。该患者的 TMB-H 状态很可能是对免疫疗法产生良好反应的原因之一。研究结果表明,高突变负荷的 mBCC 患者可能会从 pembrolizumab 中获益,为这种罕见的骨转移瘤提供了新的治疗途径。
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Long-term control with immunotherapy and aggressive re-irradiation for basal cell carcinoma metastatic to the vertebra: A case report and literature review of rare osseous metastasis

Background

Cutaneous basal cell carcinoma (BCC) is a prevalent malignancy with a rising incidence, though it rarely metastasizes, with an incidence of 0.0028–0.5 %. Hematogenous metastatic BCC (mBCC) is particularly rare and associated with a median survival of 8–14 months.

Case details

This case report details a 59-year-old male with a primary BCC on his left shoulder metastasizing to the lungs and spine. Despite aggressive multimodal treatment, including surgery, radiation, and systemic therapy with hedgehog inhibitors (vismodegib, sonidegib), the disease progressed. At 55 months post-diagnosis, pembrolizumab was introduced due to the high tumor mutation burden (TMB-H), resulting in a notable therapeutic response and prolonged survival. The patient underwent extensive follow-up, including re-irradiation of spinal metastases and immunotherapy, maintaining stable disease for over 101 months.

Results/literature review

A systematic literature review identified only 26 cases of osseous mBCC, primarily treated with surgery and radiation, with variable survival outcomes. This case stands out due to its prolonged survival and novel use of pembrolizumab, highlighting the potential role of immunotherapy in TMB-H mBCC. The patient’s TMB-H status likely contributed to the favorable response to immunotherapy.

Conclusion

This report underscores the importance of genetic profiling in mBCC to identify candidates for emerging immunotherapy treatments. The findings suggest that patients with high mutational burden mBCC may benefit from pembrolizumab, offering a new therapeutic avenue for this rare osseous metastasis.
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