A Podcast on Practical Considerations in Patients with Advanced Urothelial Cancer Receiving First-Line Cisplatin- or Carboplatin-Based Chemotherapy Followed by Avelumab Maintenance in a Changing Therapeutic Landscape

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL Advances in Therapy Pub Date : 2024-07-18 DOI:10.1007/s12325-024-02922-w
Jun Gong, Melissa A. Reimers
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Abstract

Platinum-based chemotherapy has been the cornerstone of first-line treatment for advanced urothelial carcinoma for decades, based on its proven efficacy and well-characterized safety profile. Although enfortumab vedotin (EV) plus pembrolizumab showed superior efficacy versus platinum-based chemotherapy in the EV-302 phase 3 trial, common and potentially cumulative toxicities associated with EV plus pembrolizumab may make this combination less suitable for some patients, such as those with pre-existing neuropathy, hyperglycemia, or hepatic impairment, or patients likely to have favorable outcomes with platinum-based chemotherapy. The availability of EV plus pembrolizumab in various countries may also be limited by financial considerations. Thus, platinum-based chemotherapy is likely to remain a valuable option for advanced urothelial carcinoma. Eligibility for cisplatin- or carboplatin-based regimens can be determined by assessing renal function, performance status, and specific comorbidities. In cisplatin-eligible and -ineligible patients without disease progression following platinum-based chemotherapy, avelumab first-line maintenance is standard of care based on findings from the JAVELIN Bladder 100 phase 3 trial, which showed that avelumab first-line maintenance plus best supportive care prolonged overall survival and progression-free survival compared with best supportive care alone across clinically relevant subgroups. Adverse events associated with avelumab were generally consistent with those observed with other immune checkpoint inhibitors, and long-term follow-up showed no new safety concerns with prolonged treatment. Efficacy benefits and safety profiles were similar in patients who received avelumab first-line maintenance after cisplatin- or carboplatin-based chemotherapy. The effectiveness and safety of avelumab first-line maintenance have been confirmed in several real-world studies. Overall, these data support the use of avelumab first-line maintenance for all platinum-treated patients without disease progression. In this podcast, we discuss the evolving role of platinum-based chemotherapy in this disease setting in the context of EV-302 trial results and describe practical considerations in patients receiving first-line cisplatin- or carboplatin-based chemotherapy followed by avelumab maintenance therapy.

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播客:在不断变化的治疗环境中,晚期尿道癌患者接受一线顺铂或卡铂化疗后再接受阿维单抗维持治疗的实际考虑因素。
几十年来,铂类化疗一直是晚期尿路上皮癌一线治疗的基石,其疗效已得到证实,安全性也得到了很好的描述。尽管在 EV-302 3 期试验中,恩福单抗维多汀(EV)联合 pembrolizumab 的疗效优于铂类化疗,但与 EV 联合 pembrolizumab 相关的常见和潜在累积性毒性可能会使这种联合用药不太适合某些患者,如已有神经病变、高血糖或肝功能损害的患者,或铂类化疗可能取得良好疗效的患者。EV加pembrolizumab在不同国家的可用性也可能受到经济因素的限制。因此,铂类化疗可能仍然是晚期尿路上皮癌的重要选择。顺铂或卡铂方案的治疗资格可通过评估肾功能、表现状态和特定的合并症来确定。JAVELIN Bladder 100 3 期试验结果表明,在临床相关亚组中,阿维单抗一线维持治疗加最佳支持治疗与单纯最佳支持治疗相比,可延长总生存期和无进展生存期。与阿韦利单抗相关的不良事件与其他免疫检查点抑制剂观察到的不良事件基本一致,长期随访显示,长期治疗没有新的安全性问题。顺铂或卡铂化疗后接受阿维单抗一线维持治疗的患者的疗效和安全性相似。阿维单抗一线维持治疗的有效性和安全性已在多项真实世界研究中得到证实。总体而言,这些数据支持对所有未出现疾病进展的铂类药物治疗患者使用阿维单抗一线维持治疗。在本期播客中,我们将结合 EV-302 试验结果讨论铂类化疗在这种疾病中不断演变的作用,并介绍接受顺铂或卡铂一线化疗后再接受阿维单抗维持治疗的患者的实际注意事项。
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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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