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Nurse-Led Screening-Triggered Early Specialized Palliative Care Program for Patients With Advanced Lung Cancer: A Multicenter Randomized Controlled Trial

  • Yoshihisa Matsumoto
  • , Shigeki Umemura
  • , Ayumi Okizaki
  • , Daisuke Fujisawa
  • , Takuhiro Yamaguchi
  • , Shunsuke Oyamada
  • , Tempei Miyaji
  • , Tomoe Mashiko
  • , Naoko Kobayashi
  • , Eriko Satomi
  • , Daisuke Kiuchi
  • , Tatsuya Morita
  • , Yosuke Uchitomi
  • , Koichi Goto
  • , Yuichiro Ohe

研究成果: Article査読

抄録

Background: We aimed to examine the effectiveness of a nurse-led, screening-triggered early specialized palliative care intervention program for patients with advanced lung cancer. Methods: Patients with advanced lung cancer who underwent initial chemotherapy were randomized to intervention and usual care groups between January 2017 and September 2019. The intervention comprised comprehensive needs assessments, counseling, and service coordination by advanced-level nurses. Patients in the usual care group received the usual oncological care. The primary end point was a change in the trial outcome index (TOI) scores from baseline to 12 weeks. The secondary end-points were TOI scores at week 20, depression, anxiety, and survival. Results: In total, 102 patients were assigned to each group. Compared with the usual care group, no significant improvement in TOI scores was observed at 12 weeks in the intervention group (mean group difference: 2.13; 90% confidence interval: −0.70, 4.95; p = 0.107, one-sided), whereas significant improvement was observed at 20 weeks (3.58; 90% confidence interval: 0.15, 7.00; p = 0.043). There were no significant differences in the change from baseline depression and anxiety between the groups from baseline at week 12 and 20 weeks (depression: p = 0.60 and 0.10, anxiety: p = 0.78 and 0.067). Survival did not significantly differ between the groups (median survival time: 12.1 vs. 11.1 months; p = 0.302). Conclusions: Nurse-led, screening-triggered, early specialized palliative care did not show significant superiority over usual care during the 12-week study period. However, it may have yielded delayed clinical benefits, such as improved quality of life and this feasible model can be acceptable in clinical practice. Trial Registration: The University Hospital Medical Information Network Clinical Trials Registry: UMIN000025491.

本文言語English
論文番号e70325
ジャーナルCancer medicine
13
22
DOI
出版ステータスPublished - 2024 11月

UN SDG

この成果は、次の持続可能な開発目標に貢献しています

  1. SDG 3 - すべての人に健康と福祉を
    SDG 3 すべての人に健康と福祉を

ASJC Scopus subject areas

  • 放射線学、核医学およびイメージング
  • 腫瘍学
  • 癌研究

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