To the Editor:
We have read with great interest the paper of He et al. published in April 2020 about
haematological patients infected with SARS-COV-2 [1]. Although it was a small series
with 13 patients, it gave a good insight into the course and outcome of the infection
in this patient category. Interestingly, limited data about SARS-COV-2 in haematological
patients have become available since this report, with just two other cohorts published
[2, 3]. Because of the high mortality in this vulnerable group of patients, it is
important to have more information about the course and outcome of this disease in
larger patient series. We describe in this letter a cohort of 59 COVID-19 patients
with an underlying haematological disease from three European countries.
This retrospective case study was performed in four hospitals across Europe: Spain
(Hospital Ramón y Cajal, Madrid), Northern-Italy (ASST, Crema, and San Giovanni Bosco
General Hospital, Turin) and the Netherlands (University Medical Center Groningen).
Patients with COVID-19 infection and a concomitant haematological disease were identified
between 10 February 2020 and 15 May 2020. COVID-19 diagnosis was confirmed with a
positive RT-PCR assay. Clinical data were retrospectively retrieved from the medical
records, including clinical features, laboratory findings, imaging, treatment and
outcome.
We identified 59 patients with a haematological disease and concomitant COVID-19 infection.
Their mean age was 67 years (range 32–92) and 54% were male. Thirty-three patients
(56%) had a lymphoid malignancy and 20 patients (34%) suffered from a myeloid malignancy.
A relative high incidence of patients (10%) had an idiopathic thrombocytopenic purpura
(Table 1).
Table 1
Baseline demographic and clinical characteristics of patients infected by SARS-COV-2.
Demographics
Patients (N = 59)
Age, years (range)
67 (32–92)
Male sex, %
54
Patients’ hospital
Hospital Ramón y Cajal, Madrid, N
29
ASST, Crema, N
14
University Medical Center, Groningen, N
8
San Giovanni Bosco General Hospital, Turin, N
8
Haematological disease
Lymphoid malignancies,N (%)
33 (56)
Hodgkin lymphoma, N (%)
2 (3,4)
Multiple myeloma, N (%)
10 (16,9)
Chronic lymphatic leukaemia, N (%)
5 (8,5)
Non-Hodgkin lymphoma, N (%)
15 (25,5)
Acute lymphoblastic leukaemia, N (%)
1 (1,7)
Myeloid malignancies, N (%)
20 (34)
Acute myeloid leukaemia, N (%)
6 (10)
Myelodysplastic syndrome, N (%)
3 (5,1)
Myeloproliferative neoplasms, N (%)
11 (18,6)
Benign haematological disease, N (%)
6 (10)
Idiopathic thrombocytopenic purpura N (%)
6 (10)
Last haematological treatment
Haematopoietic cell transplantation, N (%)
2 (3,4)
Chemotherapy <30 days, N (%)
23 (39,0)
Immunotherapy <30 days, N (%)
29 (49,1)
Rituximab
9 (15,3)
Steroids
16 (27,1)
Daratumumab
1 (1,7)
Tyrosine kinase inhibitor
3 (5,1)
Thirty-nine (66%) patients were being treated for their underlying disease at the
time of COVID-19 diagnosis (Table 1). The mean duration of symptoms before the diagnosis
of COVID-19 was 5.8 days (range 0–34). Eighty-eight percent of patients had a community-acquired
infection and 54% had metabolic comorbidity (e.g. hypertension, diabetes, obesity
or cardiovascular events). The most common presenting symptoms were fever (93%), dyspnoea
(62%), dry cough (47%) and diarrhoea (29%). Almost all patients (94%) had CT imaging
abnormalities characteristic of COVID-19. The most common radiologic findings were
ground glass opacifications. Four patients (7%) had a neutropenia at presentation
and 23 (40%) a lymphopenia. The different treatments given for COVID-19 and their
outcome are shown in Table 2.
Table 2
Treatment and outcome of COVID-19-infected patients with a haematological disease.
Hospitalisation
Number of patients hospitalised, N (%)
54 (92)
Hospitalisation duration, days (range)
12 days (1–61)
Oxygen therapy
Oxygen support needed, N (%)
47 (79)
Mechanical ventilation needed, N (%)
14 (24)
Non-invasive ventilation/continuous positive airway pressure, N (%)
8 (14)
Mean duration between COVID-19 diagnosis and starting mechanical ventilation, days
(range)
5 (0–20)
Medicine treatment
Steroids, N (%)
29 (48)
(Hydroxy)chloroquine, N (%)
48 (80)
Tocilizumab, N (%)
7 (12)
Azithromycin, N (%)
28 (47)
Lopinavir/ritonavir, N (%)
26 (43)
Low-molecular-weight heparin, N (%)
20 (34)
Survival
Mortality rate, %
34
Mortality rate < 60 years, %
11
Mortality rate > 60 years, %
45
Seven patients with respiratory failure did not start mechanical ventilation due to
the underlying advanced haematological disease. Five patients (8.5%) developed a thrombotic
event during follow-up, mostly pulmonary embolisms.
At last follow-up 20 patients (34%) died due to COVID-19. The mortality rate for patients
above 60 years was 45%, and that for patients below 60 years was 11%. There was no
difference in survival between lymphoid and myeloid malignancies. In addition, we
did not observe any difference in survival between the different treatment strategies
of COVID-19 infection.
To the best of our knowledge this is the second European series of patients with COVID-19
and a haematological disease [3]. The estimated 1-month overall survival is 71%, which
conforms to the survival rate of haematological patients published by Lee et al. and
that of other series of patients with a malignancy [2–4]. It must be noted that like
other case series the average age of our series is above 60 years and more than 50%
of patients had metabolic comorbidities. In the series of Malard et al. there was
an overrepresentation of patients with a multiple myeloma [2]. This could not be confirmed
in our multinational cohort, although lymphoid malignancies seem to be more common.
In our series 92% of the patients needed to be hospitalised, so our data is biased
due to the fact that only patients with severe or critical illness were tested due
to the limited availability of test capacity. This is also represented in the presenting
symptoms: in the series by Lee et al. 61% had a fever, 47% a dry cough, 39% dyspnoea
and 6% diarrhoea; these symptoms were all more frequently present in our series at
presentation [3].
We did not observe any benefit of the given specific treatments for COVID-19. However,
for the role of possible interventions in this category of patients, trials with larger,
more uniform cohorts or randomised trials need to be conducted.
Overall, patients with a haematological disease seem to be more vulnerable to a more
severe course of COVID-19 compared to patients without a malignancy, as already shown
in the report by He et al. [1]. Pending a vaccine or treatment for COVID-19, precautions
should be taken. Haematology departments should remain a COVID-19-free zone, patients
and personnel should strictly comply with hygienic advices and social distancing,
and patients and personnel should be tested even upon the mildest symptoms. Because
of the expected long duration before normalisation of hospital care, treatment of
the underlying disease should be continued when possible.