Introduction
The prognosis of allogeneic stem cell transplant recipients admitted to the intensive care unit (ICU) has improved over the last decades [
1,
2]. A large retrospective study analyzed the outcome of 330 patients who had undergone allogeneic stem cell transplantation (aSCT) between 2000 and 2013 and had been admitted to the ICU at least once thereafter. The ICU and hospital survival rates improved from 44 and 26%, respectively, for patients treated on the ICU between 2000 and 2006 to 60% and 43%, respectively, for patients who had treatment on the ICU between 2007 and 2013. However, several factors remain associated with a poor prognosis for critically ill allogeneic stem cell transplant recipients. Those include mechanical ventilation (MV), renal replacement therapy (RRT), the use of vasopressors, liver impairment, and graft-versus-host disease (GvHD) [
1,
3‐
5].
Reports focusing on patients admitted to the ICU during the peri-transplant period are scarce [
6,
7]. To shed more light on characteristics and course of this patient group, we conducted an analysis including allogeneic stem cell transplant recipients who required treatment in the ICU between the initiation of conditioning therapy and day 30 after transplantation.
Patients and methods
Patients aged ≥ 18 years who had aSCT at the University Hospital Cologne between January 1, 2014, and December 31, 2020, and were admitted to the ICU during the peri-transplant period (defined as the time between the initiation of conditioning therapy and day 30 after transplantation) were included in the present analysis. Patient characteristics, laboratory parameters, the Hematopoietic Cell Transplantation-specific Comorbidity Index (HCT-CI) score (a score consisting of comorbidities and predicting non-relapse mortality and survival in patients undergoing aSCT) at initiation of conditioning therapy, aSCT-related information, causes for ICU admission, the Sequential Organ Failure Assessment (SOFA) score (a score describing organ function and extent of organ failure in critically ill patients) at ICU admission, and procedures performed during the stay on the ICU were extracted from the patient charts [
8,
9].
Numbers and proportions were indicated for categorical variables. Medians and ranges were calculated for continuous variables. Survival curves were obtained using the Kaplan–Meier method. Overall survival (OS) was defined as the time from admission to the ICU until death and was censored at the time of last information for surviving patients. The influence of variables on OS was investigated using the log-rank test (Mantel-Cox). Statistical significance was set to p < 0.05 (two-sided). The statistical analyses were performed using Microsoft Excel (version 16.45), SPSS (IBM, version 27.0.1.0), and R-project/RStudio software (version 3.6.2 /1.4.1103) for Mac as well as GraphPad Prism (version 8.0.1) for Windows.
Discussion
Data on characteristics and course of allogeneic stem cell transplant recipients admitted to the ICU during the peri-transplant period are scarce. We therefore performed a single-center retrospective analysis comprising 70 patients treated on the ICU between the initiation of conditioning therapy and day 30 after transplantation. The major findings were as follows: 1) 11.0% of allogeneic stem cell transplant recipients required treatment on the ICU during the peri-transplant period; 2) Despite an ICU survival rate close to 50%, the 1-year OS of patients treated on the ICU during the peri-transplant period was only 16.2%; 3) Only 2/44 patients (4.5%) requiring MV and/or RRT, 2/45 patients (4.4%) necessitating vasopressors, and no patient undergoing CPR were alive at 1 year.
In the present analysis, 11.0% of allogeneic stem cell transplant recipients were admitted to the ICU between the initiation of conditioning therapy and day 30 after transplantation. Patients had a median age of 59 years. Males and females accounted for 50% of cases each. Hence, the ICU admission rate was comparable to previous studies from Germany and the US (ICU admission rates: 14.9% and 13.0%, respectively) including patients that had been hospitalized for aSCT. The median age and the proportion of females in the present analysis were slightly higher than in the previous reports (median age: 54.4 years and 52 years, respectively; proportion of females: 42.3% and 42%, respectively) [
6,
7].
The most common cause for ICU admission in the present analysis was sepsis (34/70 patients; 48.6%). The median SOFA score at the time of ICU admission was 9.5 and thus lower than in the already mentioned German study that had reported a median SOFA score of 14 [
7]. However, the lower median SOFA score did not result in improved ICU and 1-year survival rates. This is in contrast to earlier studies [
10,
11]. For instance, a retrospective Swedish analysis evaluating the course of critically ill allogeneic stem cell transplant recipients was able to discriminate 3 risk groups according to the SOFA score at ICU admission (risk group 1: SOFA score < 8; risk group 2: SOFA score 8–11; risk group 3: SOFA score > 11) [
10].
The present analysis indicated a dismal prognosis for the 16 patients who presented with progression of the underlying malignancy at the initiation of conditioning therapy. None of these patients was alive at 1 year. This finding is consistent with studies evaluating the impact of the remission status on the outcome of allogeneic stem cell transplant recipients. A recent analysis comprising 392 patients who had reduced-intensity or non-myeloablative aSCT for acute myeloid leukemia revealed inferior event-free survival and overall survival rates for patients with active disease prior to aSCT (
n = 130) as compared with patients who had measurable residual disease (MRD) but no increased blast count (
n = 115) and individuals with no MRD (
n = 147), respectively [
12].
Overall, 39/70 patients (55.7%) taken into account for the present analysis required MV and 19/70 patients (27.1%) had RRT. Thus, the proportion of individuals who had MV and/or RRT was similar to previous studies including patients hospitalized for aSCT [
6,
7]. In the present analysis, only 2 patients necessitating MV and 1 patient requiring RRT were alive at 1 year. This is also in agreement with previous publications consistently reporting poor outcomes for critically ill allogeneic stem cell transplant recipients undergoing MV and/or RRT [
6,
7,
13,
14]. Death rates for patients who had RRT were up to 100% [
7,
15].
The ICU, hospital, 90-day, and 1-year survival rates for the 70 patients included in the present analysis were 48.6%, 38.6%, 35.7%, and 16.2%, respectively. A previous analysis evaluating characteristics and outcomes of 78 patients admitted to the ICU during hospitalization for aSCT indicated similar results (ICU survival: 56.4%; 100-day survival: 42.3%) [
7]. In contrast, analyses investigating critically ill allogeneic stem cell transplant recipients irrespective of the time interval between aSCT and ICU admission reported better survival outcomes. According to two recent studies, almost 50% of patients survived 90 days and roughly 30% were alive at 1 year [
1,
2].
Besides its retrospective single-center design, the present analysis has some limitations. Those include the inability to calculate the Prognostic Index For Intensive Care After Allogeneic Stem Cell Transplantation (PICAT) due to insufficient information regarding some parameters contained in this score that allows the allocation of critically ill allogeneic stem cell transplant recipients into three distinct risk groups with hospital mortality rates ranging between 34 and 91% [
16].
Taken together, the present study confirms that patients admitted to the ICU during the peri-transplant period have unfavorable outcomes. Admission to the ICU is nonetheless justified given the long-term survival of a significant minority of patients. However, in line with previous reports, the importance of advance care planning in allogeneic stem cell transplant recipients is underscored given the high mortality especially in individuals developing multi-organ failure [
17‐
19]. A time-limited trial of intensive care treatment for 3 to 5 days can represent an option in this patient group. If the patient´s condition improves during the determined time interval, intensive care treatment is being continued whereas treatment goals are shifted towards palliation and reduction of the symptom burden alone if the condition deteriorates [
20].
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