Authors’ response to: Relationship between leukopenia and mortality among patients with haematological malignancies

IF 9.3 1区 医学 Q1 CRITICAL CARE MEDICINE Critical Care Pub Date : 2025-02-09 DOI:10.1186/s13054-025-05272-3
Aleece MacPhail, Michael Bailey, David Pilcher, Zoe McQuilten
{"title":"Authors’ response to: Relationship between leukopenia and mortality among patients with haematological malignancies","authors":"Aleece MacPhail, Michael Bailey, David Pilcher, Zoe McQuilten","doi":"10.1186/s13054-025-05272-3","DOIUrl":null,"url":null,"abstract":"<p>To the editor,</p><p>We thank Caibao et al. [1] for taking the time to comment on our study “Sepsis mortality among patients with haematological malignancy admitted to Intensive Care 2000–2022: a binational cohort study\" [2], recently published in <i>Critical Care</i>.</p><p>We agree that the relationship between leukopenia (a surrogate for neutropenia) and sepsis mortality in patients with haematological malignancies is complex. In our retrospective cohort study of patients with sepsis and haematological malignancies, we fitted a single mixed effects multivariable logistic regression model to identify risk factors for mortality. In this model we included an interaction term between leukopenia and haematological malignancy (leukopenia x HM status), each coded as a binary variable, with leukopenia defined as total white cell count &lt; 1.0 × 10<sup>9</sup> cells/L. In our model output we report the marginal effect of neutropenia in the presence or absence of haematological malignancy. This choice was made for interpretability and clinical relevance. For clinicians, the impact of neutropenia on mortality risk for septic patients with haematological malignancy is important to guide prognostication, escalation of treatment, and recognition of non-neutropenic patients in local guidelines for management of sepsis.</p><p>As noted by Caibao and colleagues, we further observed that leukopenia was associated with mortality in a univariable model, both in the presence and absence of haematological malignancy, but not in a multivariable model. Formal assessment of collinearity was performed using variance inflation factor (VIF) and all included variables had VIF &lt; 10. This indicates that while crude mortality was higher in the neutropenic group, after adjustment for confounders including age, illness severity and year of admission, this was non-significant. Our findings are in keeping with previous studies reporting that neutropenia alone is not necessarily predictive of mortality after confounders including illness severity are accounted for [3, 4].</p><p>The complex relationship between leukopenia and mortality in septic patients with haematological malignancies warrants further study. Based on existing data, neutropenic patients should not be assumed to have a poorer prognosis, and sepsis in non-neutropenic patients should not be under-estimated.</p><p>No datasets were generated or analysed during the current study.</p><ol data-track-component=\"outbound reference\" data-track-context=\"references section\"><li data-counter=\"1.\"><p>Hu C, Li Q, Ding X. Relationship between leukopenia and mortality among patients with hematological malignancies. Crit Care. 2025;28:402.</p><p>Article Google Scholar </p></li><li data-counter=\"2.\"><p>MacPhail A, Dendle C, Slavin M, Weinkove R, Bailey M, Pilcher D, et al. Sepsis mortality among patients with haematological malignancy admitted to intensive care 2000–2022: a binational cohort study. Crit Care. 2024;28(1):148.</p><p>Article PubMed PubMed Central Google Scholar </p></li><li data-counter=\"3.\"><p>Kim S-M, Kim Y-J, Kim Y-J, Kim W-Y. Prognostic impact of neutropenia in cancer patients with septic shock: a 2009–2017 nationwide cohort study. Cancers. 2022;14(15):3601.</p><p>Article PubMed PubMed Central Google Scholar </p></li><li data-counter=\"4.\"><p>Geerse DA, Span LF, Pinto-Sietsma S-J, van Mook WN. Prognosis of patients with haematological malignancies admitted to the intensive care unit: Sequential Organ Failure Assessment (SOFA) trend is a powerful predictor of mortality. Eur J Internal Med. 2011;22(1):57–61.</p><p>Article Google Scholar </p></li></ol><p>Download references<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><p>No funding was sought for this study. AM is supported by an Australian National Health and Medical Research Council (NHMRC) Postgraduate scholarship (GNT2022415) and ZM is supported by an NHMRC Emerging Leader Fellowship (GNT1194811).</p><h3>Authors and Affiliations</h3><ol><li><p>School of Public Health and Preventive Medicine, Faculty of Medicine, Nursing and Health Sciences, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia</p><p>Aleece MacPhail, Michael Bailey &amp; Zoe McQuilten</p></li><li><p>Department of Infectious Diseases, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia</p><p>Aleece MacPhail</p></li><li><p>Department of Intensive Care, Alfred Health, 55 Commercial Road, Prahran, VIC, 3004, Australia</p><p>David Pilcher</p></li><li><p>Australian and New Zealand Intensive Care Society Centre for Outcome and Resource Evaluation (ANZICS-CORE), 101 High St, Prahran, VIC, 3001, Australia</p><p>David Pilcher</p></li><li><p>The Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventative Medicine, Monash University, 553 St Kilda Rd, Prahran, VIC, 3004, Australia</p><p>David Pilcher</p></li><li><p>Department of Haematology, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia</p><p>Zoe McQuilten</p></li></ol><span>Authors</span><ol><li><span>Aleece MacPhail</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Michael Bailey</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>David Pilcher</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Zoe McQuilten</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li></ol><h3>Contributions</h3><p>AM MB DP and ZM contributed to writing and review of the manuscript.</p><h3>Corresponding author</h3><p>Correspondence to Zoe McQuilten.</p><h3>Ethical approval and consent to participate</h3>\n<p>The study was approved by the Alfred Hospital human research ethics committee, Melbourne, Australia, with a waiver of informed consent (Project number 292/20).</p>\n<h3>Consent for publication</h3>\n<p>Not applicable.</p>\n<h3>Competing interests</h3>\n<p>The authors declare no competing interests.</p><h3>Publisher's Note</h3><p>Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.</p><p><b>Open Access</b> This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.</p>\n<p>Reprints and permissions</p><img alt=\"Check for updates. 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response to: Relationship between leukopenia and mortality among patients with haematological malignancies. <i>Crit Care</i> <b>29</b>, 70 (2025). https://doi.org/10.1186/s13054-025-05272-3</p><p>Download citation<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><ul data-test=\"publication-history\"><li><p>Received<span>: </span><span><time datetime=\"2025-01-05\">05 January 2025</time></span></p></li><li><p>Accepted<span>: </span><span><time datetime=\"2025-01-11\">11 January 2025</time></span></p></li><li><p>Published<span>: </span><span><time datetime=\"2025-02-09\">09 February 2025</time></span></p></li><li><p>DOI</abbr><span>: </span><span>https://doi.org/10.1186/s13054-025-05272-3</span></p></li></ul><h3>Share this article</h3><p>Anyone you share the following link with will be able to read this content:</p><button data-track=\"click\" 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Abstract

To the editor,

We thank Caibao et al. [1] for taking the time to comment on our study “Sepsis mortality among patients with haematological malignancy admitted to Intensive Care 2000–2022: a binational cohort study" [2], recently published in Critical Care.

We agree that the relationship between leukopenia (a surrogate for neutropenia) and sepsis mortality in patients with haematological malignancies is complex. In our retrospective cohort study of patients with sepsis and haematological malignancies, we fitted a single mixed effects multivariable logistic regression model to identify risk factors for mortality. In this model we included an interaction term between leukopenia and haematological malignancy (leukopenia x HM status), each coded as a binary variable, with leukopenia defined as total white cell count < 1.0 × 109 cells/L. In our model output we report the marginal effect of neutropenia in the presence or absence of haematological malignancy. This choice was made for interpretability and clinical relevance. For clinicians, the impact of neutropenia on mortality risk for septic patients with haematological malignancy is important to guide prognostication, escalation of treatment, and recognition of non-neutropenic patients in local guidelines for management of sepsis.

As noted by Caibao and colleagues, we further observed that leukopenia was associated with mortality in a univariable model, both in the presence and absence of haematological malignancy, but not in a multivariable model. Formal assessment of collinearity was performed using variance inflation factor (VIF) and all included variables had VIF < 10. This indicates that while crude mortality was higher in the neutropenic group, after adjustment for confounders including age, illness severity and year of admission, this was non-significant. Our findings are in keeping with previous studies reporting that neutropenia alone is not necessarily predictive of mortality after confounders including illness severity are accounted for [3, 4].

The complex relationship between leukopenia and mortality in septic patients with haematological malignancies warrants further study. Based on existing data, neutropenic patients should not be assumed to have a poorer prognosis, and sepsis in non-neutropenic patients should not be under-estimated.

No datasets were generated or analysed during the current study.

  1. Hu C, Li Q, Ding X. Relationship between leukopenia and mortality among patients with hematological malignancies. Crit Care. 2025;28:402.

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  2. MacPhail A, Dendle C, Slavin M, Weinkove R, Bailey M, Pilcher D, et al. Sepsis mortality among patients with haematological malignancy admitted to intensive care 2000–2022: a binational cohort study. Crit Care. 2024;28(1):148.

    Article PubMed PubMed Central Google Scholar

  3. Kim S-M, Kim Y-J, Kim Y-J, Kim W-Y. Prognostic impact of neutropenia in cancer patients with septic shock: a 2009–2017 nationwide cohort study. Cancers. 2022;14(15):3601.

    Article PubMed PubMed Central Google Scholar

  4. Geerse DA, Span LF, Pinto-Sietsma S-J, van Mook WN. Prognosis of patients with haematological malignancies admitted to the intensive care unit: Sequential Organ Failure Assessment (SOFA) trend is a powerful predictor of mortality. Eur J Internal Med. 2011;22(1):57–61.

    Article Google Scholar

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No funding was sought for this study. AM is supported by an Australian National Health and Medical Research Council (NHMRC) Postgraduate scholarship (GNT2022415) and ZM is supported by an NHMRC Emerging Leader Fellowship (GNT1194811).

Authors and Affiliations

  1. School of Public Health and Preventive Medicine, Faculty of Medicine, Nursing and Health Sciences, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia

    Aleece MacPhail, Michael Bailey & Zoe McQuilten

  2. Department of Infectious Diseases, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia

    Aleece MacPhail

  3. Department of Intensive Care, Alfred Health, 55 Commercial Road, Prahran, VIC, 3004, Australia

    David Pilcher

  4. Australian and New Zealand Intensive Care Society Centre for Outcome and Resource Evaluation (ANZICS-CORE), 101 High St, Prahran, VIC, 3001, Australia

    David Pilcher

  5. The Australian and New Zealand Intensive Care Research Centre (ANZIC-RC), School of Public Health and Preventative Medicine, Monash University, 553 St Kilda Rd, Prahran, VIC, 3004, Australia

    David Pilcher

  6. Department of Haematology, Monash Health, 246 Clayton Road, Clayton, VIC, 3168, Australia

    Zoe McQuilten

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  1. Aleece MacPhailView author publications

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AM MB DP and ZM contributed to writing and review of the manuscript.

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Correspondence to Zoe McQuilten.

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The study was approved by the Alfred Hospital human research ethics committee, Melbourne, Australia, with a waiver of informed consent (Project number 292/20).

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MacPhail, A., Bailey, M., Pilcher, D. et al. Authors’ response to: Relationship between leukopenia and mortality among patients with haematological malignancies. Crit Care 29, 70 (2025). https://doi.org/10.1186/s13054-025-05272-3

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作者对血液学恶性肿瘤患者白细胞减少与死亡率的关系的回应
我们感谢Caibao等人[1]抽出时间评论我们的研究“2000-2022年入住重症监护的血液恶性肿瘤患者败血症死亡率:一项两国队列研究”[1],该研究最近发表在《重症监护》杂志上。我们同意白细胞减少症(中性粒细胞减少症的替代品)和血液学恶性肿瘤患者败血症死亡率之间的关系是复杂的。在我们对脓毒症和血液恶性肿瘤患者的回顾性队列研究中,我们拟合了一个单一混合效应多变量logistic回归模型来确定死亡率的危险因素。在这个模型中,我们纳入了白细胞减少和血液恶性肿瘤(白细胞减少x HM状态)之间的相互作用项,每个项都编码为二进制变量,白细胞减少定义为白细胞总数&lt; 1.0 × 109细胞/L。在我们的模型输出中,我们报告了在存在或不存在血液恶性肿瘤时中性粒细胞减少的边际效应。这个选择是为了可解释性和临床相关性。对于临床医生来说,中性粒细胞减少对脓毒症合并血液学恶性肿瘤患者死亡风险的影响,对于指导脓毒症管理指南中的预后、治疗升级和对非中性粒细胞减少患者的识别具有重要意义。正如Caibao及其同事所指出的,我们进一步观察到白细胞减少与死亡率在单变量模型中相关,无论是存在还是不存在血液恶性肿瘤,但在多变量模型中没有。使用方差膨胀因子(VIF)对共线性进行正式评估,所有纳入的变量都具有VIF &lt; 10。这表明,虽然中性粒细胞减少组的粗死亡率更高,但在调整混杂因素(包括年龄、疾病严重程度和入院年份)后,这是不显著的。我们的研究结果与先前的研究一致,即在考虑了包括疾病严重程度在内的混杂因素后,嗜中性粒细胞减少并不一定能预测死亡率[3,4]。脓毒症合并恶性血液病患者白细胞减少与死亡率之间的复杂关系值得进一步研究。根据现有数据,不能认为中性粒细胞减少患者预后较差,也不应低估非中性粒细胞减少患者的脓毒症。在本研究中没有生成或分析数据集。胡晨,李强,丁霞。恶性血液病患者白细胞减少与死亡率的关系。危重护理。2025;28:402。[8]学者MacPhail A, Dendle C, Slavin M, Weinkove R, Bailey M, Pilcher D,等。2000-2022年住院重症监护的血液恶性肿瘤患者败血症死亡率:一项两国队列研究危重症护理,2024;28(1):148。文章PubMed PubMed Central谷歌学者金世民,金玉君,金玉君,金伟勇。中性粒细胞减少对感染性休克癌症患者预后的影响:2009-2017年全国队列研究癌症。2022;14(15):3601。文章来源:PubMed PubMed Central bbb学者Geerse DA, Span LF, Pinto-Sietsma S-J, van Mook WN。重症监护病房血液恶性肿瘤患者的预后:序贯器官衰竭评估(SOFA)趋势是死亡率的有力预测指标。中华内科杂志。2011;22(1):57-61。本研究未寻求资助。AM由澳大利亚国家卫生和医学研究委员会(NHMRC)研究生奖学金(GNT2022415)支持,ZM由NHMRC新兴领袖奖学金(GNT1194811)支持。莫纳什大学医学院、护理与健康科学学院公共卫生与预防医学学院,澳大利亚维多利亚州墨尔本圣基尔达路553号,维多利亚州,3004澳大利亚和新西兰重症监护协会结果和资源评估中心(ANZICS-CORE),维多利亚州普拉兰高街101号,维多利亚州普拉兰,3001,澳大利亚和新西兰重症监护研究中心(ANZIC-RC),澳大利亚和新西兰重症监护研究中心(ANZIC-RC),澳大利亚和新西兰重症监护研究中心(ANZIC-RC),澳大利亚维多利亚州克莱顿克莱顿克莱顿路246号,澳大利亚维多利亚州克莱顿,3168,澳大利亚;莫纳什大学公共卫生与预防医学学院,澳大利亚维多利亚州普拉兰市圣基尔达路553号,维多利亚州克莱顿市克莱顿路246号,维多利亚州克莱顿,3168;AustraliaZoe McQuiltenAuthorsAleece MacPhailView作者出版物您也可以在PubMed b谷歌ScholarMichael BaileyView作者出版物中搜索该作者您也可以在PubMed谷歌ScholarDavid PilcherView作者出版物中搜索该作者您也可以在PubMed谷歌ScholarZoe McQuiltenView作者出版物中搜索该作者您还可以在PubMed谷歌ScholarContributionsAM MB DP和ZM中搜索该作者手稿。 通讯作者:Zoe McQuilten受试者的伦理批准和同意本研究由澳大利亚墨尔本阿尔弗雷德医院人类研究伦理委员会批准,并放弃知情同意(项目编号292/20)。发表同意不适用。利益竞争作者声明没有利益竞争。出版商声明:对于已出版的地图和机构关系中的管辖权要求,普林格·自然保持中立。开放获取本文遵循知识共享署名-非商业-非衍生品4.0国际许可协议,该协议允许以任何媒介或格式进行非商业用途、共享、分发和复制,只要您适当注明原作者和来源,提供知识共享许可协议的链接,并注明您是否修改了许可材料。根据本许可协议,您无权分享源自本文或其部分内容的改编材料。本文中的图像或其他第三方材料包含在文章的知识共享许可协议中,除非在材料的署名中另有说明。如果材料未包含在文章的知识共享许可中,并且您的预期用途不被法律法规允许或超过允许的用途,您将需要直接获得版权所有者的许可。要查看本许可证的副本,请访问http://creativecommons.org/licenses/by-nc-nd/4.0/.Reprints和permissionsCite这篇文章macphail, a ., Bailey, M., Pilcher, D.等人。作者对血液学恶性肿瘤患者白细胞减少与死亡率的关系的回应。重症护理29,70(2025)。https://doi.org/10.1186/s13054-025-05272-3Download citation:收稿日期:2025年1月5日接受日期:2025年1月11日发布日期:2025年2月9日doi: https://doi.org/10.1186/s13054-025-05272-3Share本文任何人与您分享以下链接将能够阅读此内容:获取可共享链接对不起,本文目前没有可共享链接。复制到剪贴板由施普林格自然共享内容倡议提供
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来源期刊
Critical Care
Critical Care 医学-危重病医学
CiteScore
20.60
自引率
3.30%
发文量
348
审稿时长
1.5 months
期刊介绍: Critical Care is an esteemed international medical journal that undergoes a rigorous peer-review process to maintain its high quality standards. Its primary objective is to enhance the healthcare services offered to critically ill patients. To achieve this, the journal focuses on gathering, exchanging, disseminating, and endorsing evidence-based information that is highly relevant to intensivists. By doing so, Critical Care seeks to provide a thorough and inclusive examination of the intensive care field.
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