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评估Pluvicto在不适合化疗的九旬老人中的疗效和安全性:一项描述性病例系列研究。

Evaluating the Efficacy and Safety of Pluvicto in Chemotherapy-Ineligible Nonagenarians: A Descriptive Case Series.

作者信息

Charron Jacob, Maupin Kevin, Su Chrystal, Mancini Brandon, Kulkarni Harshad

机构信息

Theranostics, BAMF Health, Grand Rapids, USA.

Radiology, Michigan State University College of Human Medicine, East Lansing, USA.

出版信息

Cureus. 2025 Feb 16;17(2):e79119. doi: 10.7759/cureus.79119. eCollection 2025 Feb.

Abstract

Nonagenarians with metastatic castration-resistant prostate cancer (mCRPC) are often underrepresented in prostate cancer research due to their limited numbers among treated populations. For this group, traditional chemotherapy carries significant side effects that can severely impact quality of life. Targeted therapy designed to selectively bind to prostate cancer cells expressing the prostate-specific membrane antigen (PSMA) presents a promising alternative, particularly for those with widespread metastatic disease and contraindications to chemotherapy. This retrospective case series evaluated the response, side effects, and quality of life of three nonagenarian patients with mCRPC who received Pluvicto (177Lu-PSMA-617/177Lu-vipivotide tetraxetan) as standard care at BAMF Health in Grand Rapids, Michigan, USA. Prior to treatment, all patients underwent baseline PSMA PET/CT to confirm PSMA-expressing disease and assess eligibility. They then received standard cycles of 200 mCi Pluvicto every six to eight weeks, followed by a 24-hour single photon emission computed tomography (SPECT)/computed tomography (CT) scan to assess uptake and response. Blood work, including prostate-specific antigen (PSA) levels and a comprehensive review of hematology and chemistry parameters, was conducted before treatment and every two to three weeks. Total-body PSMA-positron emission tomography/CT with Illucix (Ga-68 PSMA-11/Ga-68 gozetotide) was performed for initial assessment and at restaging as needed. All patients showed substantial reductions in tumor burden, as measured by PSA levels and SPECT/CT. Two patients experienced a >70% reduction in PSMA-expressing tumor volume, with PSA nadirs ranging from an 84% to 98% reduction from baseline. Adverse events were mild, including low-grade xerostomia in two patients and a progression from grade 1 to grade 2 anemia in two patients. Only one patient did not complete all six cycles due to disease progression after the fourth cycle. Pluvicto appears to be a promising treatment option for medically fragile nonagenarians with mCRPC. In this case series, the therapy demonstrated strong clinical and radiographic responses, including significant PSA reductions, underscoring its potential efficacy in this population. Its favorable safety profile and minimal toxicities further support its use in these medically vulnerable patients. However, larger studies are needed to enable a more comprehensive analysis and establish the statistical significance of these findings.

摘要

患有转移性去势抵抗性前列腺癌(mCRPC)的九旬老人在前列腺癌研究中的代表性往往不足,因为他们在接受治疗的人群中数量有限。对于这一群体而言,传统化疗会带来严重的副作用,会严重影响生活质量。旨在选择性结合表达前列腺特异性膜抗原(PSMA)的前列腺癌细胞的靶向治疗是一种很有前景的替代方案,特别是对于那些患有广泛转移性疾病且有化疗禁忌症的患者。本回顾性病例系列评估了三名患有mCRPC的九旬老人在美国密歇根州大急流城的BAMF Health接受Pluvicto(177Lu-PSMA-617/177Lu-维普妥肽四钠)作为标准治疗的反应、副作用和生活质量。在治疗前,所有患者均接受基线PSMA PET/CT检查,以确认表达PSMA的疾病并评估是否符合条件。然后,他们每六至八周接受200毫居里Pluvicto的标准疗程,随后进行24小时单光子发射计算机断层扫描(SPECT)/计算机断层扫描(CT)以评估摄取和反应。在治疗前以及每两至三周进行血液检查,包括前列腺特异性抗原(PSA)水平以及对血液学和化学参数的全面检查。使用Illucix(Ga-68 PSMA-11/Ga-68戈泽肽)进行全身PSMA正电子发射断层扫描/CT检查以进行初始评估并根据需要进行再分期。所有患者的肿瘤负荷均大幅降低,这通过PSA水平和SPECT/CT测量得出。两名患者表达PSMA的肿瘤体积减少了70%以上,PSA最低点从基线降低了84%至98%。不良事件较轻,包括两名患者出现轻度口干,两名患者从1级贫血进展为2级贫血。只有一名患者由于第四个周期后疾病进展而未完成全部六个周期。对于身体状况脆弱的患有mCRPC的九旬老人来说,Pluvicto似乎是一种很有前景的治疗选择。在这个病例系列中,该疗法显示出强烈的临床和影像学反应,包括PSA显著降低,突出了其在该人群中的潜在疗效。其良好的安全性和最小的毒性进一步支持在这些身体状况脆弱的患者中使用。然而,需要进行更大规模的研究以进行更全面的分析并确定这些发现的统计学意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db5a/11920267/06b2ec64e084/cureus-0017-00000079119-i01.jpg

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