Hosseinian Zahra, Lehan Ashley, Powers Jessica M, Melendez Adrian, Fisher Hannah M, Shelby Rebecca, Somers Tamara, Keefe Francis, Paice Judith, Kimmick Gretchen, Burns James, Flores Ann Marie, Fox Rina S, Kaiser Karen, Farrell David, Westbrook Kelly, Rini Christine
Department of Medical Social Sciences, Northwestern University Feinberg School of Medicine, Chicago, IL, United States of America.
Department of Psychiatry and Behavioral Sciences, Duke University, Durham, NC, United States of America.
Contemp Clin Trials. 2025 Feb;149:107780. doi: 10.1016/j.cct.2024.107780. Epub 2024 Dec 18.
Aromatase inhibitors (AIs) are a cornerstone of adjuvant systemic therapy for postmenopausal patients with hormone-receptor positive (HR+) breast cancer. Although AIs decrease cancer recurrence rates and improve survival rates, approximately 50 % of patients experience arthralgia-persistent pain related to worse patient outcomes and poor AI adherence. Current medical interventions for AI-associated arthralgia have limited efficacy and side effects that restrict their use among older patients.
The SKIP-Arthralgia trial will test the efficacy of Pain Coping Skills Training (PCST), a cognitive-behavioral therapy (CBT)-informed intervention, delivered via a web-based program called painTRAINER®. PCST and similar CBT-informed pain interventions are efficacious in non-cancer pain and commonly delivered via the Internet, although they have not been tested as a treatment for AI-associated arthralgia.
452 breast cancer survivors with AI-associated arthralgia will complete a baseline assessment before being randomized to either painTRAINER plus enhanced usual care (EUC; educational materials about AI therapy, arthralgia, and pain), or to EUC alone. Follow-up assessments will occur approximately 2 weeks after the 8- to 10-week intervention period (post-intervention) and at 3- and 6-months post-intervention. Primary outcomes are pain severity and interference at post-intervention. Secondary outcomes include emotional distress, AI adherence, and health-related quality of life.
This trial aims to fill a gap in evidence-based behavioral pain interventions for breast cancer survivors with AI-associated arthralgia by providing an effective, accessible intervention that could be implemented quickly, including in areas with limited PCST access. If successful, this study could enhance health outcomes for breast cancer survivors on AI therapy and improve adherence to this life-saving medication.
芳香化酶抑制剂(AIs)是激素受体阳性(HR+)绝经后乳腺癌患者辅助全身治疗的基石。尽管AIs可降低癌症复发率并提高生存率,但约50%的患者会出现关节痛——持续疼痛,这与更差的患者预后和对AI治疗的依从性差有关。目前针对AI相关关节痛的医学干预措施疗效有限,且副作用限制了其在老年患者中的使用。
SKIP-关节痛试验将测试疼痛应对技能训练(PCST)的疗效,这是一种基于认知行为疗法(CBT)的干预措施,通过名为painTRAINER®的网络程序提供。PCST和类似的基于CBT的疼痛干预措施在非癌性疼痛中有效,且通常通过互联网提供,尽管它们尚未作为AI相关关节痛的治疗方法进行测试。
452名患有AI相关关节痛的乳腺癌幸存者将在随机分组前完成基线评估,随机分为接受painTRAINER加强化常规护理(EUC;关于AI治疗、关节痛和疼痛的教育材料),或仅接受EUC。随访评估将在8至10周的干预期后约2周(干预后)以及干预后3个月和6个月进行。主要结局是干预后的疼痛严重程度和干扰程度。次要结局包括情绪困扰、AI依从性和健康相关生活质量。
本试验旨在通过提供一种有效、可及的干预措施来填补针对患有AI相关关节痛的乳腺癌幸存者的循证行为疼痛干预的空白,该干预措施可快速实施,包括在PCST获取有限的地区。如果成功,本研究可改善接受AI治疗的乳腺癌幸存者的健康结局,并提高对这种救命药物的依从性。