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Survival of non-transplant patients with multiple myeloma in routine care differs from that in clinical trials—data from the prospective German Tumour Registry Lymphatic Neoplasms

机译:非移植性多发性骨髓瘤患者在常规治疗中的存活率与临床试验中的存活率不同-来自前瞻性德国肿瘤登记处淋巴肿瘤的数据

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摘要

Despite increasing treatment options, multiple myeloma (MM) remains incurable for most patients. Data on improvement of outcomes are derived from selected patient populations enrolled in clinical trials and might not be conferrable to all patients. Therefore, we assessed the trial eligibility, sequential treatment, and survival of non-transplant patients with MM treated in German routine care. The prospective clinical cohort study TLN (Tumour Registry Lymphatic Neoplasms) recruited 285 non-transplant patients with symptomatic MM at start of first-line treatment in 84 centres from 2009 to 2011. Demographic and clinical data were collected until August 2016. Trial-ineligibility was determined by presence of at least one of the common exclusion criteria: heart/renal failure, liver/renal diseases, polyneuropathy, HIV positivity. All other patients were considered potentially trial-eligible. Thirty percent of the patients in our study were classified as trial-ineligible. Median first-line progression-free survival (PFS) and overall survival (OS) of trial-ineligible patients were inferior to that of potentially trial-eligible patients: PFS 16.2 months (95% CI (confidence interval) 11.1–20.4) vs. 27.3 months (95% CI 23.3–33.0); OS 34.2 months (95% CI 21.6–48.1) vs. 58.6 months (95% CI 48.6–64.4). A high percentage of non-transplant patients with MM in German routine care would be ineligible for participation in clinical trials. Despite similar treatment algorithms, their first-line PFS and OS were shorter than those of potentially trial-eligible patients; the survival data of the latter were similar to results from clinical trials. Physicians should be aware of the fact that results from clinical trials may not mirror “real world” patient outcomes when discussing outcome expectations with patients. Trial registration: identifier: .
机译:尽管增加了治疗选择,但大多数患者仍无法治愈多发性骨髓瘤(MM)。关于改善结局的数据来自于参加临床试验的特定患者人群,可能并不适用于所有患者。因此,我们评估了在德国常规护理中接受治疗的非移植性MM患者的试验资格,顺序治疗和生存期。这项前瞻性临床队列研究TLN(肿瘤登记淋巴瘤)于2009年至2011年在84个中心的一线治疗开始时招募了285例有症状MM的非移植患者。收集的人口统计学和临床​​数据至2016年8月。由以下至少一项常见排除标准确定:心/肾衰竭,肝/肾疾病,多发性神经病,HIV阳性。所有其他患者均被认为可能具有试验资格。在我们的研究中,有30%的患者被归为不符合试验条件的患者。不符合试验条件的患者的中位一线无进展生存期(PFS)和总生存期(OS)低于可能符合试验条件的患者:PFS 16.2个月(95%CI(置信区间)11.2–20.4)vs。 27.3个月(95%CI 23.3–33.0); OS 34.2个月(95%CI 21.6–48.1)与58.6个月(95%CI 48.6-64.4)。接受德国常规护理的非移植性MM病患者中,有很大比例不符合参加临床试验的条件。尽管有类似的治疗算法,但他们的一线PFS和OS均比那些有可能接受试验的患者要短。后者的生存数据与临床试验结果相似。医生应与患者讨论预期结果时,应意识到临床试验的结果可能无法反映“现实世界”中患者的结果。试用注册:标识符:。

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