Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Stepping Stones Pediatric Palliative Care, C.S. Mott Children's Hospital, Ann Arbor, Michigan, USA.
Pediatr Blood Cancer. 2023 Mar;70(3):e30115. doi: 10.1002/pbc.30115. Epub 2022 Dec 2.
Palliative care (PC) provides numerous benefits for children with cancer. Pediatric patients with high-grade glioma (HGG) are particularly well suited for early PC involvement given their high symptom burden and poor prognosis. However, studies continue to reveal that children with cancer, including HGG, have delayed PC involvement. We hypothesized that clinical trial enrollment may lead to a lack of or delay in PC involvement in this population.
For each patient in our cohort of 43 pediatric patients with HGG, demographic, diagnostic, therapeutic, clinical trial enrollment, and PC information were collected. Statistical analysis was performed comparing PC characteristics between patients who did and did not enroll in a clinical trial.
Seventy-two percent of patients had at least one visit with a PC provider. Fifty-six percent of patients enrolled in a clinical trial with HGG-directed therapy. Seventy-one percent of patients who enrolled in a clinical trial received specialty PC compared to 74% of non-trial participants (p = 1.000). Patients who enrolled in clinical trials received PC earlier in their disease course measured in days before death (mean = 177 days) compared to those who did not enroll (mean = 113 days, p = .180), though not statistically significant.
The prevalence of clinical trial enrollment is high in patients with HGG and will likely increase as the genomic/epigenomic landscape of these tumors is better understood. As such, our data reassuringly suggest that trial participation does not interfere with the receipt of specialty PC in this population.
姑息治疗(PC)为癌症患儿带来诸多益处。鉴于高级别胶质瘤(HGG)患儿症状负担重、预后差,他们非常适合早期接受 PC 治疗。然而,研究表明,癌症患儿,包括 HGG 患儿,接受 PC 治疗的时间较晚。我们假设临床试验的参与可能导致这一人群中 PC 治疗的缺乏或延迟。
对我们队列中的 43 名 HGG 儿科患者的每位患者,收集人口统计学、诊断、治疗、临床试验参与和 PC 信息。对参加和未参加临床试验的患者的 PC 特征进行比较,进行统计学分析。
72%的患者至少接受过一次 PC 提供者的就诊。56%的 HGG 定向治疗患者参加了临床试验。与非试验参与者(74%)相比,71%参加临床试验的患者接受了专业 PC(p=1.000)。接受临床试验的患者在死亡前的疾病进程中接受 PC 的时间更早(平均 177 天),而未参加临床试验的患者(平均 113 天,p=0.180),虽然没有统计学意义。
在 HGG 患者中,临床试验的参与率很高,随着这些肿瘤的基因组/表观基因组图谱得到更好的理解,这一比例可能会增加。因此,我们的数据令人安心地表明,试验参与并不影响这一人群接受专业 PC 治疗。