Secondary Solid Cancers Among Patients with Philadelphia Chromosome-Negative Myeloproliferative Neoplasms: A Multicenter Study.

IF 1.5 4区 医学 Q3 HEMATOLOGY
Fehmi Hindilerden, Özge Nuran Akay, Elif Aksoy, Aynur Dağlar-Aday, Emine Gültürk, Meliha Nalçacı, İpek Yönal Hindilerden
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引用次数: 0

Abstract

Objective: We investigated the occurrence and characteristics of secondary solid cancers (SSC) in Philadelphia chromosome-negative myeloproliferative neoplasm (Ph- MPN) patients from Türkiye. We identified the potential risk factors for SSC development including the impact of cytoreductive therapies and assess the influence of SSC on patient survival.

Material and methods: 1013 Ph- MPN patients diagnosed between 1995 and 2022 was retrospectively analyzed. Data related to demographics, clinical and laboratory parameters, SSC development, cytoreductive therapy exposure and survival outcomes were collected. Statistical analyses were performed using SPSS 26.0 software.

Results: Of the Ph- MPN patients, 6.6% developed SSC, with carcinoma being the most common type. Older age at Ph- MPN diagnosis and male gender were associated with SSC occurrence. Ph- MPN patients diagnosed with SSC and patients with no diagnosis of SSC showed no significant difference for complete blood count, spleen size, Ph- MPN diagnostic groups and driver mutation frequencies. However, SSC patients showed a higher frequency of arterial thrombosis and tendency towards increased rate for total thrombosis (p=0.030, p=0.069; respectively). In multivariate analysis, arterial thrombosis was the sole independent risk factor and interferon (IFN)-based therapy the sole protective factor for SSC development. Median overall survival (OS) did not differ between patients with and without SSC except for polycythemia vera (PV) patients with SSC, who had shorter OS (175±15 and 321±26 months, respectively; p = 0.005).

Conclusion: Our study highlights the prevalence and characteristics of SSC in Turkish patients diagnosed with Ph- MPN. Arterial thrombosis was associated with increased SSC risk while IFN-based therapy offered potential protection from SSC. Screening for SSC in Ph- MPN patients with arterial thrombosis may be relevant. These findings emphasize the importance of malignancy screening in Ph- MPN patients, especially in high-risk subgroups and call for further research to elucidate the underlying mechanisms and optimize treatment strategies.

费城染色体阴性骨髓增殖性肿瘤患者的继发性实体癌:一项多中心研究。
目的:我们调查了土耳其费城染色体阴性骨髓增生性肿瘤(Ph- MPN)患者继发性实体瘤(SSC)的发生率和特征:我们调查了土耳其费城染色体阴性骨髓增殖性肿瘤(Ph- MPN)患者继发性实体瘤(SSC)的发生率和特征。我们确定了SSC发生的潜在风险因素,包括细胞再生疗法的影响,并评估了SSC对患者生存的影响。收集了与人口统计学、临床和实验室参数、SSC发展、细胞再生疗法暴露和生存结果相关的数据。统计分析使用SPSS 26.0软件进行:结果:在 Ph- MPN 患者中,6.6% 的患者出现了 SSC,其中癌是最常见的类型。诊断为 Ph- MPN 时年龄较大和男性与 SSC 的发生有关。确诊为间质性硬化的 Ph- MPN 患者与未确诊为间质性硬化的患者在全血细胞计数、脾脏大小、Ph- MPN 诊断组别和驱动基因突变频率方面无明显差异。然而,SSC 患者动脉血栓形成的频率较高,总血栓形成率也呈上升趋势(分别为 p=0.030 和 p=0.069)。在多变量分析中,动脉血栓形成是唯一的独立危险因素,而基于干扰素(IFN)的治疗是 SSC 发生的唯一保护因素。有SSC和无SSC患者的中位总生存期(OS)没有差异,但有SSC的红细胞增多症(PV)患者的OS较短(分别为175±15个月和321±26个月;P = 0.005):我们的研究强调了SSC在土耳其Ph-MPN患者中的发病率和特征。动脉血栓与SSC风险增加有关,而基于IFN的治疗则为SSC提供了潜在的保护。在有动脉血栓形成的 Ph- MPN 患者中筛查 SSC 可能是有意义的。这些研究结果强调了对Ph- MPN患者进行恶性肿瘤筛查的重要性,尤其是在高风险亚组中,并呼吁进一步研究以阐明其潜在机制并优化治疗策略。
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来源期刊
CiteScore
2.90
自引率
3.80%
发文量
45
审稿时长
1 months
期刊介绍: The Turkish Journal of Hematology is published quarterly (March, June, September, and December) by the Turkish Society of Hematology. It is an independent, non-profit peer-reviewed international English-language periodical encompassing subjects relevant to hematology. The Editorial Board of The Turkish Journal of Hematology adheres to the principles of the World Association of Medical Editors (WAME), International Council of Medical Journal Editors (ICMJE), Committee on Publication Ethics (COPE), Consolidated Standards of Reporting Trials (CONSORT) and Strengthening the Reporting of Observational Studies in Epidemiology (STROBE). The aim of The Turkish Journal of Hematology is to publish original hematological research of the highest scientific quality and clinical relevance. Additionally, educational material, reviews on basic developments, editorial short notes, images in hematology, and letters from hematology specialists and clinicians covering their experience and comments on hematology and related medical fields as well as social subjects are published. As of December 2015, The Turkish Journal of Hematology does not accept case reports. Important new findings or data about interesting hematological cases may be submitted as a brief report.
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