Presentation and Outcome of Patients with Multiple Myeloma (MM), Single Centre Experience from Windsor Essex Regional Cancer Centre.

IF 2.1 Q3 HEMATOLOGY Journal of Blood Medicine Pub Date : 2024-02-26 eCollection Date: 2024-01-01 DOI:10.2147/JBM.S434055
Dalia Kashash, Eric McArthur, Caroline Hamm, Rasna Gupta, Sindu Kanjeekal, Mohammad Jarrar, Lisa A Porter, John W Hudson, Adam Renaud, Indryas Woldie
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Abstract

Introduction: Outcomes for patients with multiple myeloma has significantly improved through the years. This is mainly related to the use of novel agents.

Methods: This is a retrospective study that reviewed presentation and outcome of 139 patients with multiple myeloma at the Windsor Essex Regional Cancer Centre from Jan. 1, 2015 to Dec. 31, 2019. Median age was 71 years and most patients had higher risk disease (65.5% either R ISS stage II or III). 30% had high risk FISH for myeloma including del.17P, t (4:14), t (14:16) and Gain (1q21). In terms of presentation, 38.8% had anemia (hemoglobin <100g/L), 18.7% had hypercalcemia, 74.1% had skeletal lytic lesions, 38.8% had pathologic fracture and 17.3% had plasmacytoma.

Results: Almost all (92%) of the patients were treated using at least one novel agent (proteasome inhibitor or immunomodulators [ImiDs]). Cyclophosphamide, bortezomib, and dexamethasone (CyBorD) was the most used treatment regimen (48.9%) followed by bortezomib, melphalan and prednisone (BMP) at 28.8% and lenalidomide, dexamethasone (LenDex) at 14.4%. With respect to response to therapy, 51.8% had at least Very good partial response (VGPR), while 9.4% had progressive disease. 33% had autologous stem cell transplant. After a median follow up of 2.4 years, median overall survival was 3.7 years. 2 years overall survival and relapse-free survival were 70% and 83%, respectively.

Discussion: Our study showed comparable outcome for patients with multiple myeloma despite older age and higher risk disease. Outcome is expected to improve with the introduction of more novel agents.

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温莎埃塞克斯地区癌症中心(Windsor Essex Regional Cancer Centre)的单中心经验:多发性骨髓瘤(MM)患者的表现和预后。
前言多年来,多发性骨髓瘤患者的治疗效果有了明显改善。这主要与新型药物的使用有关:这是一项回顾性研究,回顾了温莎埃塞克斯地区癌症中心自2015年1月1日至2019年12月31日期间139名多发性骨髓瘤患者的发病情况和治疗结果。中位年龄为71岁,大多数患者患有高风险疾病(65.5%为R ISS II期或III期)。30%的患者患有骨髓瘤高风险FISH,包括del.17P、t(4:14)、t(14:16)和Gain(1q21)。就表现而言,38.8%的患者有贫血(血红蛋白结果):几乎所有患者(92%)都接受了至少一种新型药物(蛋白酶体抑制剂或免疫调节剂[ImiDs])的治疗。环磷酰胺、硼替佐米和地塞米松(CyBorD)是最常用的治疗方案(48.9%),其次是硼替佐米、美法兰和泼尼松(BMP)(28.8%)和来那度胺、地塞米松(LenDex)(14.4%)。在治疗反应方面,51.8%的患者至少有非常好的部分反应(VGPR),9.4%的患者病情进展。33%的患者进行了自体干细胞移植。中位随访期为2.4年,中位总生存期为3.7年。2年总生存率和无复发生存率分别为70%和83%:我们的研究表明,尽管多发性骨髓瘤患者年龄较大、患病风险较高,但他们的治疗效果相当。随着更多新型药物的引入,预后有望得到改善。
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来源期刊
CiteScore
3.50
自引率
0.00%
发文量
94
审稿时长
16 weeks
期刊介绍: The Journal of Blood Medicine is an international, peer-reviewed, open access, online journal publishing laboratory, experimental and clinical aspects of all topics pertaining to blood based medicine including but not limited to: Transfusion Medicine (blood components, stem cell transplantation, apheresis, gene based therapeutics), Blood collection, Donor issues, Transmittable diseases, and Blood banking logistics, Immunohematology, Artificial and alternative blood based therapeutics, Hematology including disorders/pathology related to leukocytes/immunology, red cells, platelets and hemostasis, Biotechnology/nanotechnology of blood related medicine, Legal aspects of blood medicine, Historical perspectives. Original research, short reports, reviews, case reports and commentaries are invited.
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