Impact of critical illness on continuation of anticancer treatment and prognosis of patients with aggressive hematological malignancies

IF 5.7 1区 医学 Q1 CRITICAL CARE MEDICINE
Swann Bredin, Justine Decroocq, Clément Devautour, Julien Charpentier, Clara Vigneron, Frédéric Pène
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引用次数: 0

Abstract

Background

Maintaining the dose-intensity of cancer treatment is an important prognostic factor of aggressive hematological malignancies. The objective of this study was to assess the long-term outcomes of intensive care unit (ICU) survivors with acute myeloid leukemia (AML) or aggressive B-cell non-Hodgkin lymphoma (B-NHL) with emphasis on the resumption of the intended optimal regimen of cancer treatment.

Patients and methods

We conducted a retrospective (2013–2021) single-center observational study where we included patients with AML and B-NHL discharged alive from the ICU after an unplanned admission. The primary endpoint was the change in the intended optimal cancer treatment following ICU discharge. Secondary endpoints were 1-year progression-free survival and overall survival rates. Determinants associated with modifications in cancer treatment were assessed through multivariate logistic regression.

Results

Over the study period, 366 patients with AML or B-NHL were admitted to the ICU, of whom 170 survivors with AML (n = 92) and B-NHL (n = 78) formed the cohort of interest. The hematological malignancy was recently diagnosed in 68% of patients. The admission Sequential Organ Failure Assessment (SOFA) score was 5 (interquartile range 4–8). During the ICU stay, 30 patients (17.6%) required invasive mechanical ventilation, 29 (17.0%) vasopressor support, and 16 (9.4%) renal replacement therapy. The one-year survival rate following ICU discharge was 59.5%. Further modifications in hematologic treatment regimens were required in 72 patients (42%). In multivariate analysis, age > 65 years (odds ratio (OR) 3.54 [95%-confidence interval 1.67–7.50], p < 0.001), ICU-discharge hyperbilirubinemia > 20 µmol/L (OR 3.01 [1.10–8.15], p = 0.031), and therapeutic limitations (OR 16.5 [1.83–149.7], p = 0.012) were independently associated with modifications in cancer treatment. Post-ICU modifications of cancer treatment had significant impact on in-hospital, 1-year overall survival and progression-free survival.

Conclusion

The intended cancer treatment could be resumed in 58% of ICU survivors with aggressive hematological malignancies. At the time of ICU discharge, advanced age, persistent liver dysfunction and decisions to limit further life-support therapies were independent determinants of cancer treatment modifications. These modifications were associated with worsened one-year outcomes.

Abstract Image

危重病对继续抗癌治疗和侵袭性血液恶性肿瘤患者预后的影响
背景保持癌症治疗的剂量强度是侵袭性血液恶性肿瘤的一个重要预后因素。本研究的目的是评估重症监护病房(ICU)中急性髓性白血病(AML)或侵袭性 B 细胞非霍奇金淋巴瘤(B-NHL)幸存者的长期预后,重点是癌症治疗最佳方案的恢复情况。患者和方法我们开展了一项回顾性(2013-2021 年)单中心观察研究,研究对象包括意外入院后从重症监护病房存活出院的 AML 和 B-NHL 患者。主要终点是ICU出院后癌症最佳治疗方案的变化。次要终点为1年无进展生存率和总生存率。结果在研究期间,有366名急性髓细胞白血病或B-NHL患者入住重症监护室,其中170名急性髓细胞白血病(92人)和B-NHL(78人)幸存者组成了研究队列。68%的患者最近才确诊血液恶性肿瘤。入院时的序贯器官衰竭评估(SOFA)评分为 5 分(四分位间范围为 4-8 分)。在重症监护室住院期间,30 名患者(17.6%)需要有创机械通气,29 名患者(17.0%)需要血管加压支持,16 名患者(9.4%)需要肾脏替代治疗。重症监护室出院后的一年存活率为 59.5%。72名患者(42%)需要进一步修改血液学治疗方案。在多变量分析中,年龄超过 65 岁(比值比 (OR) 3.54 [95% 置信区间 1.67-7.50],P = 0.001)、ICU 出院时高胆红素血症超过 20 µmol/L(比值比 3.01 [1.10-8.15],P = 0.031)和治疗限制(比值比 16.5 [1.83-149.7],P = 0.012)与癌症治疗方案的调整密切相关。结论 58% 的侵袭性血液恶性肿瘤 ICU 存活者可以恢复原定的癌症治疗。重症监护室出院时,高龄、持续肝功能障碍和限制进一步生命支持疗法的决定是癌症治疗改变的独立决定因素。这些改变与一年期预后的恶化有关。
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来源期刊
Annals of Intensive Care
Annals of Intensive Care CRITICAL CARE MEDICINE-
CiteScore
14.20
自引率
3.70%
发文量
107
审稿时长
13 weeks
期刊介绍: Annals of Intensive Care is an online peer-reviewed journal that publishes high-quality review articles and original research papers in the field of intensive care medicine. It targets critical care providers including attending physicians, fellows, residents, nurses, and physiotherapists, who aim to enhance their knowledge and provide optimal care for their patients. The journal's articles are included in various prestigious databases such as CAS, Current contents, DOAJ, Embase, Journal Citation Reports/Science Edition, OCLC, PubMed, PubMed Central, Science Citation Index Expanded, SCOPUS, and Summon by Serial Solutions.
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