Abstract

We retrospectively analyzed infectious complications during tandem high-dose chemotherapy and autologous stem cell transplantation (HDCT/auto-SCT) in children and adolescents with high-risk or recurrent solid tumors. A total of 324 patients underwent their first HDCT/auto-SCT between October 2004 and September 2014, and 283 of them proceeded to their second HDCT/auto-SCT (a total of 607 HDCT/auto-SCTs). During the early transplant period of 607 HDCT/auto-SCTs (from the beginning of HDCT to day 30 post-transplant), bacteremia, urinary tract infection (UTI), respiratory virus infection, and varicella zoster virus (VZV) reactivation occurred in 7.1%, 2.3%, 13.0%, and 2.5% of HDCT/auto-SCTs, respectively. The early transplant period of the second HDCT/auto-SCT had infectious complications similar to the first HDCT/auto-SCT. During the late transplant period of HDCT/auto-SCT (from day 31 to 1 year post-transplant), bacteremia, UTI, and VZV reactivation occurred in 7.5%, 2.5%, and 3.9% of patients, respectively. Most infectious complications in the late transplant period occurred during the first 6 months post-transplant. There were no invasive fungal infections during the study period. Six patients died from infectious complications (4 from bacterial sepsis and 2 from respiratory virus infection). Our study suggests that infectious complications are similar following second and first HDCT/auto-SCT in children.

Highlights

  • High-dose chemotherapy and autologous stem cell transplantation (HDCT/auto-SCT) has improved the outcomes of patients with high-risk solid tumors [1,2,3]

  • The second HDCT/auto-SCT could require a longer time for hematologic recovery than the first HDCT/auto-SCT, even when similar numbers of CD34+ cells are infused [17]. These findings suggest that infectious complications might be more frequent or severe in the second HDCT/ auto-SCT than in the first, but studies addressing infectious complications during tandem HDCT/auto-SCT have been limited

  • A total of 324 patients (196 males and 128 females) underwent their first HDCT/auto-SCT, and 283 of them proceeded to their second HDCT/auto-SCT; the remaining 41 patients could not proceed to the second HDCT/auto-SCT due to tumor progression (n = 14), off-treatment (n = 11), treatment-related mortality (n = 10), follow-up loss (n = 3), subsequent allogeneic transplantation (n = 2), or parental refusal (n = 1)

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Summary

Introduction

High-dose chemotherapy and autologous stem cell transplantation (HDCT/auto-SCT) has improved the outcomes of patients with high-risk solid tumors [1,2,3]. Infectious complications during HDCT/auto-SCT are a major cause associated with treatment-related morbidity and mortality [4,5]. Despite advances in infection prophylaxis and treatment during HDCT/autoSCT [6,7,8,9], many clinical problems including the emergence of multi-drug-resistant (MDR). Infectious Complications during Tandem HDCT/Auto-SCT and analysis, decision to publish, or preparation of the manuscript

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