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多发性骨髓瘤:来自阿曼的关于临床表现和治疗结果的真实世界数据。

Multiple Myeloma: Real-world Data on the Clinical Presentation and Outcomes From Oman.

作者信息

Al Nabhani Ibrahim, Al Lawati Jaber, Al Mahrooqi Nooh, Al Rawahi Adnan, Kumar Vinodh, Al Riyami Nafila, Al Waili Khalid, Jabeen Zeba, Al-Riyami Arwa Z, Khan Hammad, Al Huneini Mohammed, Al Busaidi Thuraya, Al Kindi Salam, Al Khabori Murtadha, Al Abri Mahmood, Fawaz Najla, Al Farsi Khalil

机构信息

Department of Hematology Sultan Qaboos University Hospital Muscat Oman.

Department of Medicine Royal Hospital Muscat Oman.

出版信息

EJHaem. 2025 Jul 21;6(4):e70096. doi: 10.1002/jha2.70096. eCollection 2025 Aug.

Abstract

OBJECTIVE

There is a paucity of data on multiple myeloma (MM) from Oman and the region. This study reports the clinical presentation and survival outcomes in Omani patients with MM at Sultan Qaboos University Hospital (SQUH), a tertiary care academic center.

METHODS

This retrospective included all patients diagnosed, treated, and followed up for MM at SQUH between June 2008 and December 2018. Patient demographics, disease characteristics, clinical presentation, prognostic parameters, and survival data were obtained from the patients' electronic medical records. The Kaplan-Meier method was used to estimate the progression-free survival (PFS) and overall survival (OS), and the log-rank test was used to compare survival according to the international staging system (ISS) stage.

RESULTS

Ninety-eight patients were analyzed, 49 (50%) of whom were males. The median age was 61 years (range: 30-88). Immunoglobulin G (IgG) was the most common subtype of myeloma (59.6%), followed by IgA (24.2%) and IgD (4%). Twelve patients (12%) had light chain myeloma. The most common manifestation of myeloma at the time of initial diagnosis was anemia (50%), followed by lytic lesions (41.5%), renal insufficiency (24.2%), and hypercalcemia (23.2%). Forty-three patients (44%) had ISS stage III disease at presentation. Over the study period, patients received different types of induction therapy. Ninety patients received therapy at SQUH and had complete data on first-line treatment. Thirty-six patients (41%) received proteasome inhibitor (PI) based regimens, 23 patients (25%) had immunomodulatory-based (IMID-based) therapy, and 23 patients (25%) had combination PI and IMiD-based induction therapy. For patients with complete data on treatment, responses and outcome ( = 90), after a median follow-up of 76 months (95% confidence interval [CI]: 54-97 m), median PFS was 59 months (95% CI: 20.1-78), with an estimated five year PFS of 41%. Median OS was 109 months (95% CI: 65-173) with a 5-year OS of 61%. ISS stage predicted OS (ISS stage I and stage II: 133 m, 95% CI: 94-173 m, stage III: 36 m, 95% CI: 25-47 m; log-rank < 0.001) but not PFS.

CONCLUSION

The median age of our patients is younger than what is published in the literature. Most of our patients presented with advanced-stage disease, which was predictive of survival in our cohort. The lack of uniformity of treatment and the small number of patients precluded concluding the effect of treatment on survival. Collaboration with other centers in Oman and the region to collect retrospective and prospective data on a larger cohort of patients is recommended.

CLINICAL TRIAL REGISTRATION

The authors have confirmed that clinical trial registration is not needed for this submission.

摘要

目的

阿曼及该地区关于多发性骨髓瘤(MM)的数据匮乏。本研究报告了在三级医疗学术中心苏丹卡布斯大学医院(SQUH)的阿曼MM患者的临床表现和生存结果。

方法

这项回顾性研究纳入了2008年6月至2018年12月期间在SQUH诊断、治疗和随访的所有MM患者。从患者的电子病历中获取患者人口统计学、疾病特征、临床表现、预后参数和生存数据。采用Kaplan-Meier方法估计无进展生存期(PFS)和总生存期(OS),并使用对数秩检验根据国际分期系统(ISS)分期比较生存情况。

结果

分析了98例患者,其中49例(50%)为男性。中位年龄为61岁(范围:30 - 88岁)。免疫球蛋白G(IgG)是骨髓瘤最常见的亚型(59.6%),其次是IgA(24.2%)和IgD(4%)。12例患者(12%)患有轻链骨髓瘤。初次诊断时骨髓瘤最常见的表现是贫血(50%),其次是溶骨性病变(41.5%)、肾功能不全(24.2%)和高钙血症(23.2%)。43例患者(44%)在就诊时处于ISS III期疾病。在研究期间,患者接受了不同类型的诱导治疗。90例患者在SQUH接受治疗并拥有一线治疗的完整数据。36例患者(41%)接受了基于蛋白酶体抑制剂(PI)的方案,23例患者(25%)接受了基于免疫调节剂(IMiD)的治疗,23例患者(25%)接受了PI与IMiD联合诱导治疗。对于有完整治疗数据的患者,在中位随访76个月(95%置信区间[CI]:54 - 97个月)后,反应和结局(n = 90),中位PFS为59个月(95% CI:20.1 - 78),估计五年PFS为41%。中位OS为109个月(95% CI:65 - 173),五年OS为61%。ISS分期可预测OS(ISS I期和II期:133个月,95% CI:94 - 173个月,III期:36个月,95% CI:25 - 47个月;对数秩P < 0.001),但不能预测PFS。

结论

我们患者的中位年龄比文献报道的要年轻。我们的大多数患者表现为晚期疾病,这可预测我们队列中的生存情况。治疗缺乏一致性以及患者数量较少使得无法得出治疗对生存的影响。建议与阿曼及该地区的其他中心合作,收集更大患者队列的回顾性和前瞻性数据。

临床试验注册

作者已确认本提交不需要临床试验注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bae1/12277647/edcdac227aae/JHA2-6-e70096-g002.jpg

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