Department of Medicine, University of Washington, Seattle, Washington; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Department of Medicine, University of Washington, Seattle, Washington; Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
Transplant Cell Ther. 2021 Aug;27(8):684.e1-684.e9. doi: 10.1016/j.jtct.2021.04.021. Epub 2021 May 5.
Patients with hematologic malignancy or bone marrow failure are typically required to achieve radiographic improvement or stabilization of invasive fungal infection (IFI) before hematopoietic cell transplantation (HCT) owing to a concern for progression before engraftment. Refractory IFI with a mixture of improvement and progression on serial imaging (ie, mixed response) poses a clinical dilemma, because a delay in HCT may allow for a hematologic relapse or other complications. Furthermore, HCT itself may yield the immune reconstitution necessary for clearance of infection. We sought to describe the characteristics and outcomes of patients who underwent HCT with mixed response IFI. We performed a chart review of all patients who underwent HCT between 2014 and 2020 in whom imaging within 6 weeks before HCT indicated a mixed response to treatment of a diagnosed IFI. Fourteen patients had evidence of a mixed response in low-to-moderate burden of diagnosed IFI by imaging before HCT, including 9 with pulmonary aspergillosis, 2 with hepatosplenic candidiasis (1 also with aspergillosis), and 4 with pulmonary nodules of presumed fungal etiology. Five had refractory severe neutropenia at evaluation for HCT (median, 95 days). All 14 patients showed radiographic stability or improvement in imaging following engraftment; no IFI-related surgeries were required, and no IFI-related deaths occurred. For patients without relapse who underwent HCT more than 1 year earlier, 7 of 8 (88%) were alive at 1 year. Our findings suggest that low-to-moderate burden IFI with mixed response is unlikely to progress on appropriate therapy before engraftment during allogeneic HCT.
患有血液系统恶性肿瘤或骨髓衰竭的患者通常需要在造血细胞移植(HCT)前实现影像学上的侵袭性真菌感染(IFI)改善或稳定,因为在植入前存在进展的担忧。连续影像学检查显示改善和进展混合的难治性 IFI(即混合反应)会带来临床困境,因为 HCT 的延迟可能会导致血液学复发或其他并发症。此外,HCT 本身可能会产生清除感染所需的免疫重建。我们旨在描述混合反应 IFI 患者接受 HCT 的特征和结局。我们对所有在 2014 年至 2020 年期间接受 HCT 的患者进行了图表回顾,这些患者在 HCT 前 6 周内的影像学检查表明对诊断为 IFI 的治疗有混合反应。14 名患者在 HCT 前影像学检查中有中低负荷的诊断性 IFI 表现出混合反应,包括 9 例肺曲霉病、2 例肝脾念珠菌病(1 例也有曲霉病)和 4 例肺部结节疑似真菌感染。5 名患者在评估 HCT 时患有难治性严重中性粒细胞减少症(中位数为 95 天)。所有 14 名患者在植入后影像学显示稳定或改善;不需要与 IFI 相关的手术,也没有与 IFI 相关的死亡。对于在 HCT 前 1 年以上未复发且接受 HCT 的患者,8 例中的 7 例(88%)在 1 年内存活。我们的研究结果表明,在异基因 HCT 期间,低至中负荷 IFI 伴混合反应不太可能在植入前的适当治疗下进展。