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Impact of COVID-19 After Autologous Hematopoietic Stem Cell Transplantation in Sweden

Impact of COVID-19 on Patients Treated With Autologous Hematopoietic Stem Cell Transplantation in Sweden - a Retrospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04760184
Acronym
AutoCOVID-19
Enrollment
20
Registered
2021-02-18
Start date
2021-04-01
Completion date
2021-12-31
Last updated
2022-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Covid19, Hematologic Neoplasms, Malignant Lymphoma, Myeloma Multiple, Stem Cell Transplant Complications

Keywords

Autologous stem cell transplantation, COVID-19

Brief summary

This retrospective observational cohort study aims to describe the impact of COVID-19 in patients treated with autologous stem cell transplantation (ASCT) for malignant disease in terms of risk factors, morbidity, need for supportive care and mortality. All patients treated with ASCT in Sweden from 1st January 2020 until 31st December 2020 are eligible for this study. Patients who also has tested positive for SARS-CoV-2 from start of conditioning or later will be identified through the national registry of the Public Health Agency of Sweden and a systematic analysis of their medical records will be performed.

Detailed description

Research question How does infection with SARS-CoV-2 affect patients with hematological malignancies who are treated with autologous hematopoietic stem cell transplantation? Study population All Swedish citizens treated with ASCT for malignant disease in Sweden from 1st January 2020 until 31st December 2020 are eligible for this study. There will be a minimum follow-up time of one month for all patients. Data collection and storage Patients will be identified using local ASCT registers at the seven university hospitals, as there is no national register for ASCT-patients in Sweden. These seven university hospitals are the only sights to perform ASCT in Sweden. The Public Health Agency of Sweden (Folkhälsomyndigheten - FHM) has the national responsibility to surveil and control communicable disease. The FHM uses several different surveillance systems to monitor the spread of COVID-19. Since COVID-19 is subject to mandatory reporting under the Communicable Diseases Act, physicians and laboratories continuously supply data to be analyzed daily by the FHM. The coverage of this database is estimated to be very high, close to 100%. For this study the investigators will link the patients identified through the ASCT-centers with the register of SARS-Cov-2 positive patients (SmiNet) held by the FHM. Patients who has tested positive for SARS-CoV-2 on the day of start of conditioning or at any given time thereafter will be included in the study. Inclusion of positive SARS-CoV-2 tests will start from 1st January 2020 until 31st March 2021 to allow for 3 months of follow-up after transplantation. For every ASCT-patient that has tested positive for COVID-19 after ASCT a systematic analysis of their medical records will be performed to describe the circumstances, impact and outcome of the COVID-19. All data collected will be stored in a deidentified data set on a secure server held by Dalarna Country Council where name and social security number have been erased and given a coded study number. Each patient will only be identified using a separately stored code key. All storage, correspondence and analysis with the code key and pseudonymized data set will adhere to current European General Data Protection Regulation (GDPR) guidelines. The code key will be destroyed as soon as data collection is completed, data quality is secured and the final report is published. The data set will be stored for 10 years and then be destroyed.

Interventions

OTHERAutologous stem cell transplantation

The study will describe the implications of COVID-19 infection following autologous stem cell transplantation

Sponsors

Karolinska University Hospital
CollaboratorOTHER
Sahlgrenska University Hospital
CollaboratorOTHER
Lund University Hospital
CollaboratorOTHER
University Hospital, Linkoeping
CollaboratorOTHER
University Hospital, Umeå
CollaboratorOTHER
Region Örebro County
CollaboratorOTHER
Uppsala University Hospital
CollaboratorOTHER
Uppsala University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of hematological cancer (C81-C96 according to the International Classification of Diseases 10th revision (ICD-10). * Autologous hematopoietic stem cell transplantation performed 1 January 2020 until 31st December 2020 at a Swedish transplantation center. * Positive RT-PCR test for SARS-CoV-2 performed in Sweden

Exclusion criteria

\- Age below 18 years and 0 months at the time of transplantation

Design outcomes

Primary

MeasureTime frameDescription
Overall survival30 daysOverall survival after infection with COVID-19
COVID-19 related mortalitywithin 6 months after infectionAs classified by the WHO; a death resulting from a clinically compatible illness in a confirmed COVID-19 case, unless there is a clear alternative cause of death that cannot be related to COVID disease (e.g., trauma). There should be no period of complete recovery between the illness and death

Secondary

MeasureTime frameDescription
HospitalizationUp to 15 monthsDuration of hospitalization
Oxygen treatmentUp to 15 monthsDuration of oxygen treatment
High-flow oxygen therapyUp to 15 monthsDuration of high-flow oxygen therapy
Non-invasive ventilationUp to 15 monthsDuration of non-invasive ventilation (NIV)
Intensive careUp to 15 monthsDuration of care in intensive care unit
Invasive mechanical ventilationUp to 15 monthsDuration of Invasive mechanical ventilation
ECMOUp to 15 monthsDuration of extracorporeal membrane oxygenation (ECMO)
Occurence of ARDSUp to 15 monthsDiagnosis of Acute respiratory distress syndrome (ARDS)
Occurence of arterial thrombosisUp to 15 monthsEvent of arterial thrombosis
Occurence of venous thrombosisUp to 15 monthsEvent of venous thrombosis
Occurence of arrhythmiasUp to 15 monthsEvent of recorded arrhythmias
Occurence of acute cardiac injuryUp to 15 monthsEvent of acute cardiac injury
Occurence of secondary infectionUp to 15 monthsEvent of any secondary infection
Occurence of cytokine release syndromeUp to 15 monthsEvent of cytokine release syndrome
Elevated liver enzymesAt autologous stem cell transplantation or up to 15 monthsEvent of elevated liver enzymes at diagnosis of COVID-19
Disease statusPrior to autologous stem cell transplantationDescription of disease status prior to autologous stem cell transplantation
Previous disease modifying treatmentPrior to autologous stem cell transplantationDescription of previous disease modifying treatment prior to autologous stem cell transplantation
Conditioning treatmentAt autologous stem cell transplantationDescription of conditioning treatment prior to autologous stem cell transplantation
Time of infectionAt autologous stem cell transplantation or up to 15 monthsTime of COVID-19 in relation to autologous stem cell transplantation
NeutropeniaAt autologous stem cell transplantation or up to 15 monthsEvent of neutropenia at diagnosis of COVID-19
Elevated CRPAt autologous stem cell transplantation or up to 15 monthsEvent of elevated C-reactive protein (CRP) at diagnosis of COVID-19
Elevated leukocyte countAt autologous stem cell transplantation or up to 15 monthsEvent of elevated leukocyte count at diagnosis of COVID-19
LymphocytopeniaAt autologous stem cell transplantation or up to 15 monthsEvent of lymphocytopenia at diagnosis of COVID-19
Elevated lactate dehydrogenaseAt autologous stem cell transplantation or up to 15 monthsEvent of elevated lactate dehydrogenase at diagnosis of COVID-19
Elevated ferritinAt autologous stem cell transplantation or up to 15 monthsEvent of elevated ferritin at diagnosis of COVID-19
Elevated d-dimerAt autologous stem cell transplantation or up to 15 monthsEvent of elevated d-dimer at diagnosis of COVID-19
Prolonged aPTTAt autologous stem cell transplantation or up to 15 monthsEvent of prolonged activated partial thromboplastin time (aPTT) at diagnosis of COVID-19
Elevated troponinAt autologous stem cell transplantation or up to 15 monthsEvent of elevated troponin at diagnosis of COVID-19
Elevated creatinineAt autologous stem cell transplantation or up to 15 monthsEvent of elevated creatinine at diagnosis of COVID-19
ComorbiditiesPrior to autologous stem cell transplantationDescription of comorbidities prior to autologous stem cell transplantation
Time of COVID-19 infectionUp to 15 monthsTime of SARS-CoV-2 infection in relation to autologous stem cell transplantation

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026