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新型药物时代日本浆细胞肿瘤患者前瞻性队列研究的初步分析(2016-2021 年)。

Primary analysis of a prospective cohort study of Japanese patients with plasma cell neoplasms in the novel drug era (2016-2021).

机构信息

Department of Hematology, NHO Osaka National Hospital, 2-1-14 Hoenzaka Chuo-ku, Osaka City, Osaka, 540-0006, Japan.

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, Suita, Japan.

出版信息

Int J Hematol. 2024 Jun;119(6):707-721. doi: 10.1007/s12185-024-03754-8. Epub 2024 Mar 29.


DOI:10.1007/s12185-024-03754-8
PMID:38548963
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11136844/
Abstract

The emergence of novel drugs has significantly improved outcomes of patients with plasma cell neoplasms (PCN). The Japanese Society of Hematology conducted a prospective observational study in newly diagnosed PCN patients between 2016 and 2021. The analysis focused on 1385 patients diagnosed with symptomatic PCN between 2016 and 2018. The primary endpoint was the 3-year overall survival (OS) rate among patients requiring treatment (n = 1284), which was 70.0% (95%CI 67.4-72.6%). Approximately 94% of these patients received novel drugs as frontline therapy. The 3-year OS rate was 90.3% (95%CI 86.6-93.1%) in the 25% of patients who received upfront autologous stem cell transplantation (ASCT), versus just 61.4% (95%CI 58.0-64.6%) in those who did not receive upfront ASCT. The only unfavorable prognostic factor that affected OS in ASCT recipients was an age of 65 or higher. For patients who did not receive ASCT, independent unfavorable prognostic factors included frontline treatment with conventional chemotherapies, international staging system score of 2/3, extramedullary tumors, and Freiberg comorbidity index of 2/3. This study unequivocally demonstrates that use of novel drugs improved OS in Japanese myeloma patients, and underscores the continued importance of upfront ASCT as the standard of care in the era of novel drugs.

摘要

新型药物的出现显著改善了浆细胞肿瘤(PCN)患者的预后。日本血液学会在 2016 年至 2021 年间对新诊断的 PCN 患者进行了一项前瞻性观察性研究。该分析重点关注了 2016 年至 2018 年间诊断为有症状 PCN 的 1385 名患者。主要终点是需要治疗的患者(n=1284)的 3 年总生存率(OS),为 70.0%(95%CI 67.4-72.6%)。大约 94%的患者接受了新型药物作为一线治疗。25%接受 upfront 自体干细胞移植(ASCT)的患者的 3 年 OS 率为 90.3%(95%CI 86.6-93.1%),而未接受 upfront ASCT 的患者仅为 61.4%(95%CI 58.0-64.6%)。唯一影响 ASCT 受者 OS 的不利预后因素是年龄在 65 岁或以上。对于未接受 ASCT 的患者,独立的不良预后因素包括一线使用传统化疗、国际分期系统评分 2/3、髓外肿瘤和 Freiberg 合并症指数 2/3。这项研究明确表明,新型药物的使用改善了日本骨髓瘤患者的 OS,并强调了 upfront ASCT 在新型药物时代作为标准治疗的持续重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/cc46b57ee0c1/12185_2024_3754_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/57f09c849e21/12185_2024_3754_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/40c1b58c0d90/12185_2024_3754_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/49910f1e6173/12185_2024_3754_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/348c0249740c/12185_2024_3754_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/cc46b57ee0c1/12185_2024_3754_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/57f09c849e21/12185_2024_3754_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/40c1b58c0d90/12185_2024_3754_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/49910f1e6173/12185_2024_3754_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/348c0249740c/12185_2024_3754_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8e/11136844/cc46b57ee0c1/12185_2024_3754_Fig5_HTML.jpg

相似文献

[1]
Primary analysis of a prospective cohort study of Japanese patients with plasma cell neoplasms in the novel drug era (2016-2021).

Int J Hematol. 2024-6

[2]
Improved survival of multiple myeloma patients treated with autologous transplantation in the modern era of new medicine.

Cancer Sci. 2021-12

[3]
Changing trends in prognostic factors for patients with multiple myeloma after autologous stem cell transplantation during the immunomodulator drug/proteasome inhibitor era.

Cancer Sci. 2015-2

[4]
[A Propensity Score Matching Study of Autologous Hematopoietic Stem Cell Transplantation and New Drug Chemotherapy for Newly Diagnosed Multiple Myeloma].

Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2022-2

[5]
Risk factors of early disease progression and decreased survival for multiple myeloma patients after upfront autologous stem cell transplantation.

Ann Hematol. 2024-8

[6]
Complete remission status before autologous stem cell transplantation is an important prognostic factor in patients with multiple myeloma undergoing upfront single autologous transplantation.

Biol Blood Marrow Transplant. 2009-4

[7]
Efficacy of Autologous Stem Cell Transplantation for Myeloma Patients with Suboptimal Response: A Multicenter Retrospective Analysis.

Transplant Cell Ther. 2023-11

[8]
Treatment benefit of upfront autologous stem cell transplantation for newly diagnosed multiple myeloma: a systematic review and meta-analysis.

BMC Cancer. 2023-5-16

[9]
Favorable Long-Term Outcomes with Autologous Stem Cell Transplantation for High-Risk Multiple Myeloma Patients with a Positive Result On F-FDG PET/CT at Baseline.

Clin Lymphoma Myeloma Leuk. 2022-2

[10]
Autologous Transplantation for Newly Diagnosed Multiple Myeloma in the Era of Novel Agent Induction: A Systematic Review and Meta-analysis.

JAMA Oncol. 2018-3-1

引用本文的文献

[1]
Real-World Treatment Outcomes of Different Sequencing Options with Daratumumab, Lenalidomide, and Dexamethasone in Patients with Transplant-Ineligible Multiple Myeloma in Japan.

Cancers (Basel). 2025-4-22

[2]
Treatment pathways and clinical outcomes in newly diagnosed multiple myeloma outside Europe and North America: The INTEGRATE study.

Int J Hematol. 2025-4-15

本文引用的文献

[1]
Antibodies and bispecifics for multiple myeloma: effective effector therapy.

Hematology Am Soc Hematol Educ Program. 2022-12-9

[2]
Cellular therapy for multiple myeloma: what's now and what's next.

Hematology Am Soc Hematol Educ Program. 2022-12-9

[3]
Triplet Therapy, Transplantation, and Maintenance until Progression in Myeloma.

N Engl J Med. 2022-7-14

[4]
Daratumumab, lenalidomide, and dexamethasone in Japanese patients with transplant-ineligible newly diagnosed multiple myeloma: a phase 1b study.

Int J Hematol. 2020-1-30

[5]
Daratumumab plus bortezomib, melphalan, and prednisone in East Asian patients with non-transplant multiple myeloma: subanalysis of the randomized phase 3 ALCYONE trial.

Ann Hematol. 2019-10-16

[6]
Daratumumab plus Lenalidomide and Dexamethasone for Untreated Myeloma.

N Engl J Med. 2019-5-30

[7]
Daratumumab plus Bortezomib, Melphalan, and Prednisone for Untreated Myeloma.

N Engl J Med. 2017-12-12

[8]
Trends of survival in patients with multiple myeloma in Japan: a multicenter retrospective collaborative study of the Japanese Society of Myeloma.

Blood Cancer J. 2015-9-18

[9]
Revised International Staging System for Multiple Myeloma: A Report From International Myeloma Working Group.

J Clin Oncol. 2015-9-10

[10]
International Myeloma Working Group updated criteria for the diagnosis of multiple myeloma.

Lancet Oncol. 2014-10-26

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