Thomson Alastair, Gunn Lucinda, Victor Deborah, Adamson Ellis, Thakrar Kashyap
Oncology Department, Sunrise Centre, Royal Cornwall Hospital, Truro, Cornwall, UK.
Accord-UK Ltd, Barnstaple, Devon, UK.
Res Rep Urol. 2024 Oct 9;16:245-252. doi: 10.2147/RRU.S485238. eCollection 2024.
In the UK, relugolix, an oral gonadotropin-releasing hormone receptor antagonist, is indicated for advanced hormone-sensitive prostate cancer, and as neo-adjuvant and adjuvant treatment in combination with radiotherapy in patients with high-risk localised or locally advanced hormone-dependent prostate cancer. Experience with the combination of oral relugolix plus oral enzalutamide is limited.
A white British male (66 years old) with a history of myelodysplastic syndrome, chronic neutropenia and indeterminate colitis presented with metastatic adenocarcinoma of the prostate gland. The patient started subcutaneous leuprorelin acetate and oral enzalutamide. After 8 weeks, the oral enzalutamide dose was reduced because of fatigue. Following the second leuprorelin injection, the patient developed a subcutaneous abscess that required surgical incision and drainage. The patient switched to oral relugolix and continued with oral enzalutamide. Within 3 months of commencing leuprorelin and enzalutamide the prostate specific antigen (PSA) concentration fell from a peak of 269.00 ng/mL to 2.55 ng/mL. Following the switch to oral relugolix plus enzalutamide, the PSA remained stable until the most recent assessment 11 months later. Relugolix plus enzalutamide was well tolerated.
Relugolix plus enzalutamide produced a sustained reduction in PSA and the combination was well tolerated. Further research including real world data should assess relugolix in doublet and triplet combinations for prostate cancer.
在英国,口服促性腺激素释放激素受体拮抗剂瑞卢戈利适用于晚期激素敏感性前列腺癌,以及高危局限性或局部晚期激素依赖性前列腺癌患者与放疗联合的新辅助和辅助治疗。口服瑞卢戈利联合口服恩杂鲁胺的经验有限。
一名66岁的英国白人男性,有骨髓增生异常综合征、慢性中性粒细胞减少症和未确诊结肠炎病史,出现前列腺转移性腺癌。患者开始皮下注射醋酸亮丙瑞林和口服恩杂鲁胺。8周后,因疲劳减少了口服恩杂鲁胺的剂量。第二次注射亮丙瑞林后,患者出现皮下脓肿,需要手术切开引流。患者改用口服瑞卢戈利并继续口服恩杂鲁胺。在开始使用亮丙瑞林和恩杂鲁胺的3个月内,前列腺特异性抗原(PSA)浓度从峰值269.00 ng/mL降至2.55 ng/mL。改用口服瑞卢戈利加恩杂鲁胺后,PSA一直保持稳定,直到11个月后的最近一次评估。瑞卢戈利加恩杂鲁胺耐受性良好。
瑞卢戈利加恩杂鲁胺可使PSA持续降低,且该联合用药耐受性良好。包括真实世界数据在内的进一步研究应评估瑞卢戈利在前列腺癌双联和三联组合中的应用。