493名接受现代疗法治疗的年轻骨髓瘤患者的疾病特征和疗效:加拿大骨髓瘤研究小组数据库研究》。

IF 2.9 2区 医学 Q2 ONCOLOGY
Cancer Medicine Pub Date : 2024-11-05 DOI:10.1002/cam4.70332
Mégane Tanguay, Jean Roy, Jiandong Su, Engin Gul, Donna Reece, Christopher P. Venner, Darrell White, Michael P. Chu, Victor H. Jimenez-Zepada, Kevin Song, Arleigh Mccurdy, Hira Mian, Michael Sebag, Debra Bergstrom, Julie Stakiw, Anthony Reiman, Rami Kotb, Muhammad Aslam, Rayan Kaedbey, Martha Louzada, Richard LeBlanc
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引用次数: 0

摘要

背景:50岁以下的多发性骨髓瘤(MM)年轻患者约占病例总数的10%,在文献中的代表性不足:方法:我们利用加拿大骨髓瘤研究组(CMRG)数据库研究了年轻MM患者的疾病特征、治疗方法和现代疗法的疗效。我们纳入了2010年1月1日至2022年7月1日期间确诊为MM或浆细胞白血病且未并发淀粉样变性或POEMS综合征的493名年龄小于50岁的患者:中位年龄为 46 岁(25.6-50 岁)。大多数患者属于 R-ISS II 类(72.7%),24.1%的患者具有高风险细胞遗传学。大多数患者(89.9%)接受了蛋白酶体抑制剂一线治疗,92.1%接受了干细胞移植,65.6%在自体干细胞移植(ASCT)后接受了维持治疗。从初始治疗到患者最后一次随访的中位随访时间为48.5个月(0-155个月)。中位无进展生存期(PFS)为45.0个月(95% CI:40.2-50.0)。ASCT后的维持治疗将中位无进展生存期提高到52.3个月(95% CI:43.1-68.2),而未进行维持治疗的中位无进展生存期为23.6个月(95% CI:20.0-34.8)[P 结论:ASCT后的维持治疗将中位无进展生存期提高到48.5个月(范围:0-155个月):尽管在这一年轻群体中尚未达到总生存期,但我们报告的中位 PFS 仅为 45 个月,这凸显了开发创新疗法以诱导更深入、更持久反应的迫切需要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Disease Characteristics and Outcomes of 493 Young Myeloma Patients Treated With Modern Therapies: A Canadian Myeloma Research Group Database Study

Disease Characteristics and Outcomes of 493 Young Myeloma Patients Treated With Modern Therapies: A Canadian Myeloma Research Group Database Study

Background

Young patients ≤ 50 years old with multiple myeloma (MM) account for about 10% of cases and are underrepresented in the literature.

Methods

We explored disease characteristics, treatments, and outcomes following modern therapies of young MM patients using the Canadian Myeloma Research Group (CMRG) database. We included 493 patients ≤ 50 years old diagnosed with MM or plasma cell leukemia without concurrent amyloidosis or POEMS syndrome from January 1, 2010, to July 1, 2022.

Results

The median age was 46 years old (range: 25.6–50). Most patients fell into the R-ISS II category (72.7%), and 24.1% had high-risk cytogenetics. The majority of patients (89.9%) received a proteasome inhibitor-based first-line treatment, 92.1% received a stem cell transplant, and 65.6% had maintenance therapy post–autologous stem cell transplant (ASCT). Median follow-up from initial treatment to patients' last follow-up was 48.5 (range: 0–155) months. Median progression-free survival (PFS) was 45.0 months (95% CI: 40.2–50.0). Maintenance therapy post-ASCT improved median PFS to 52.3 months (95% CI: 43.1–68.2), compared to 23.6 months (95% CI: 20.0–34.8) without maintenance [p < 0.001].

Conclusion

Although the overall survival has not yet been reached in this young population, our reported median PFS of only 45 months highlights the urgent need to develop innovative treatments to induce more profound and durable responses.

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来源期刊
Cancer Medicine
Cancer Medicine ONCOLOGY-
CiteScore
5.50
自引率
2.50%
发文量
907
审稿时长
19 weeks
期刊介绍: Cancer Medicine is a peer-reviewed, open access, interdisciplinary journal providing rapid publication of research from global biomedical researchers across the cancer sciences. The journal will consider submissions from all oncologic specialties, including, but not limited to, the following areas: Clinical Cancer Research Translational research ∙ clinical trials ∙ chemotherapy ∙ radiation therapy ∙ surgical therapy ∙ clinical observations ∙ clinical guidelines ∙ genetic consultation ∙ ethical considerations Cancer Biology: Molecular biology ∙ cellular biology ∙ molecular genetics ∙ genomics ∙ immunology ∙ epigenetics ∙ metabolic studies ∙ proteomics ∙ cytopathology ∙ carcinogenesis ∙ drug discovery and delivery. Cancer Prevention: Behavioral science ∙ psychosocial studies ∙ screening ∙ nutrition ∙ epidemiology and prevention ∙ community outreach. Bioinformatics: Gene expressions profiles ∙ gene regulation networks ∙ genome bioinformatics ∙ pathwayanalysis ∙ prognostic biomarkers. Cancer Medicine publishes original research articles, systematic reviews, meta-analyses, and research methods papers, along with invited editorials and commentaries. Original research papers must report well-conducted research with conclusions supported by the data presented in the paper.
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