Department of Medical Oncology, Imperial College Healthcare National Health Service Trust, Charing Cross Hospital, Fulham Palace Road, London, W6 8RF, UK.
BMC Cancer. 2019 Aug 5;19(1):770. doi: 10.1186/s12885-019-5968-7.
Etoposide (E) at 100 mg/m combined with Cisplatin (P) at 20 mg/m represents an induction 2-day regimen embedded in our clinical practice for patients with advanced GCT or TN at high risk of early death. We evaluated 24/7 Em-EP administration to a combined GCT-TN cohort at our Emergency Cancer Treatment Centre (ECTC) to determine its efficacy within the acute setting.
Patients who received Em-EP during a five-year interval were identified from electronic databases at Imperial College Healthcare NHS Trust. Data collected included demographics, treatment details and clinical outcome.
Em-EP was administered in the emergency setting to 104 patients, predominantly young adults (median age 35, range 17-71). Half the cases were GCT (n = 52): 22 male (6 seminomas, 13 non-seminomas); 30 female (2 dysgerminomas, 28 non-dysgerminomas). The other 50% were treated for TN (n = 52): 45 gestational (GTN) and 7 non-gestational. Most patients received Em-EP for a new cancer diagnosis (n = 100, 96%), within 24 h (n = 93, 89%) and out-of-hours (n = 74, 70%). Indications for Em-EP included symptomatic disease (n = 66, 63%), high-burden disease, (n = 51, 49%) and organ failure requiring Intensive Care Unit support (n = 9, 9%). Neutropenic sepsis was observed in 5%. Four-week overall survival after Em-EP administration was 98%.
Despite the potentially fatal complications encountered in the acute setting, early mortality with Em-EP is low at our ECTC. Specialist units that treat unwell patients with advanced GCT or TN should consider making Em-EP available 24/7 for emergency administration. Its efficacy within a prospective cohort and in other platinum-sensitive malignancies requires evaluation.
依托泊苷(E)100mg/m 联合顺铂(P)20mg/m 代表了我们临床实践中用于高危早期死亡的晚期 GCT 或 TN 患者的 2 天诱导方案。我们在我们的急症癌症治疗中心(ECTC)评估了联合 GCT-TN 队列的 24/7 Em-EP 给药,以确定其在急性环境中的疗效。
从帝国理工大学医疗保健国民保健服务信托的电子数据库中确定了在五年期间接受 Em-EP 治疗的患者。收集的数据包括人口统计学资料、治疗细节和临床结果。
Em-EP 在急症环境中用于 104 名患者,主要是年轻人(中位年龄 35 岁,范围 17-71 岁)。一半的病例为 GCT(n=52):22 例男性(6 例精原细胞瘤,13 例非精原细胞瘤);30 例女性(2 例卵黄囊瘤,28 例非卵黄囊瘤)。另一半为 TN 治疗(n=52):45 例妊娠性(GTN)和 7 例非妊娠性。大多数患者接受 Em-EP 治疗新诊断的癌症(n=100,96%),在 24 小时内(n=93,89%)和非工作时间(n=74,70%)。Em-EP 的适应症包括有症状的疾病(n=66,63%)、高负担疾病(n=51,49%)和需要重症监护室支持的器官衰竭(n=9,9%)。观察到中性粒细胞减少性败血症 5%。Em-EP 给药后四周的总生存率为 98%。
尽管在急症环境中存在潜在的致命并发症,但我们的 ECTC 中 Em-EP 的早期死亡率较低。治疗晚期 GCT 或 TN 患者的专科单位应考虑 24/7 提供 Em-EP 以便紧急给药。其在前瞻性队列中的疗效和其他铂类敏感恶性肿瘤的疗效需要评估。