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Case Reports
. 2024 May 27:2024:7525757.
doi: 10.1155/2024/7525757. eCollection 2024.

Bladder Cancer Invading the Prostate and Penis and Multiple Bone Metastases Showing Significant Improvement after a Short-Term Pembrolizumab Therapy following Radiation and Gemcitabine and Cisplatin Therapy Leading to a Pathologically Complete Remission

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Case Reports

Bladder Cancer Invading the Prostate and Penis and Multiple Bone Metastases Showing Significant Improvement after a Short-Term Pembrolizumab Therapy following Radiation and Gemcitabine and Cisplatin Therapy Leading to a Pathologically Complete Remission

Kyohei Ishida et al. Case Rep Urol. .

Abstract

A 65-year-old man was diagnosed with bladder cancer invading the prostate and penis and multiple bone metastases. He underwent palliative radiation (30 Gy/10 fr) through vertebral bones (Th3 and Th12-L5) and pelvic bones for pain control. The patient received pembrolizumab therapy after three courses of gemcitabine and cisplatin therapy. CT four weeks after starting pembrolizumab therapy showed that both the primary and metastatic lesions had notably reduced in size, and no new lesion was detected. He subsequently fell, resulting in a femoral neck pathological fracture, and underwent hemiarthroplasty. Pathological examination of the pathological fracture site revealed no residual tumor tissue.

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Conflict of interest statement

No conflict of interest exists.

Figures

Figure 1
Figure 1
CT findings before treatments showed an invasive bladder tumor with (a) bilateral hydroureters (arrows) and (b) osteolytic metastasis (arrow). Pathological findings of needle biopsy of bladder and prostate lesions revealed luminal-type urothelial carcinoma ((c) hematoxylin and eosin), (d) androgen receptor-negative, (e) GATA3-positive, (f) CK20-positive, and (g) PD-L1 negative. There were almost no tumor-infiltrating lymphocytes within the tumor tissue ((g) circles). Internal control histiocytes are PD-L1 positive ((g) arrow).
Figure 2
Figure 2
CT findings four weeks after starting pembrolizumab therapy revealed a significant reduction in the size of the primary lesion (a), as well as a decrease in osteolytic lesions at the bone metastatic sites with a shift towards osteoblastic change (b, arrow).
Figure 3
Figure 3
Pathological findings of fracture lesion revealed no residual cancer tissue with osteoblastic change.

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References

    1. Patel V. G., Oh W. K., Galsky M. D. Treatment of muscle-invasive and advanced bladder cancer in 2020. CA: A Cancer Journal for Clinicians . 2020;70(5):404–423. doi: 10.3322/caac.21631. - DOI - PubMed
    1. Bellmunt J., de Wit R., Vaughn D. J., et al. Pembrolizumab as second-line therapy for advanced urothelial carcinoma. The New England Journal of Medicine . 2017;376(11):1015–1026. doi: 10.1056/NEJMoa1613683. - DOI - PMC - PubMed
    1. Tsuda Y., Nakagawa T., Shinoda Y., et al. Skeletal-related events and prognosis in urothelial cancer patients with bone metastasis. International Journal of Clinical Oncology . 2017;22(3):548–553. doi: 10.1007/s10147-016-1075-9. - DOI - PubMed
    1. Sjödahl G., Eriksson P., Holmsten K., et al. Metastasis and recurrence patterns in the molecular subtypes of urothelial bladder cancer. International Journal of Cancer . 2024;154(1):180–190. doi: 10.1002/ijc.34715. - DOI - PubMed
    1. Powles T., Rosenberg J. E., Sonpavde G. P., et al. Enfortumab vedotin in previously treated advanced urothelial carcinoma. The New England Journal of Medicine . 2021;384(12):1125–1135. doi: 10.1056/NEJMoa2035807. - DOI - PMC - PubMed

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