To the editor.
Severe Acute Respiratory Syndrome CoronaVirus-2 (SARS-CoV-2) infection can result
in different clinical manifestations (COVID-19), from asymptomatic disease to life-threatening
respiratory insufficiency.1 Onco-hematologic patients are at higher risk of developing
severe COVID-19.2 In particular, patients affected by lymphoproliferative diseases,
given the impaired cell-mediated and antibody-mediated immunity and treatment toxicity,
more often develop a symptomatic and more serious COVID-19 disease.2–3 Various prophylactic
and therapeutic strategies are used against COVID-19, such as vaccines, antiviral
drugs, and S-protein monoclonal antibodies (anti-S MoAbs). The efficacy of antiviral
strategies often proved to be dependent on SARS-CoV-2 variants.4–6 Pre-exposure prophylaxis
with AZD442/Evusheld (tixagevimab-cilgavimab) may be a complementary strategy to decrease
the incidence or severity of COVID-19 for patients with hematologic malignancies.
Tixagevimab-cilgavimab is a combination of two monoclonal antibodies (T-C MoAb) that
bind SARS-CoV-2 spike protein and inhibit the attachment to the surface of cells,
preventing viral entry in the cell and COVID-19 development.7,8 In the PROVENT trial,
a phase 3 study, 5197 patients were randomized to receive T-C MoAB or placebo, reporting
a favorable incidence of only 0.2% of symptomatic COVID-19 in the T-C MoAb arm, even
if it included only 3.3% of cancer patients receiving T-C MoAb and was conducted before
the Omicron era.8 Based on these findings, T-C MoAB was approved by the Agenzia Italiana
del Farmaco (AIFA) as pre-exposure prophylaxis for patients at high risk of severe
COVID-19; therefore, it was regularly employed at our institution.9 However, recent
studies, mainly performed in vitro, suggested inferior efficacy against omicron variants.10–12
Our aim was to evaluate if this strategy’s upcoming reported clinical benefit and
safety to patients with hematologic malignancies were still in force in a real-life
setting of high-risk hematologic patients during the omicron-predominant COVID-19
wave in Italy.
Methods
We retrospectively collected data of patients affected by B-cell malignancies who
received T-C MoAb (300 mg: dose 150+150 mg, the authorized dose for pre-exposure prophylaxis
in our country) as pre-exposure prophylaxis at the Institute of Hematology, Sapienza
University of Rome, between February 2022 and February 2023. Outpatients were stratified
according to disease-specific clinical risk (Table 1). High risk patients received
T-C MoAb at different times (before chemoimmunotherapy started, before conditioning
regimen, before maintenance therapy) according to the treatment phase at the time
of T-C MoAb availability. This study respects the principles of the Declaration of
Helsinki and was approved by the internal review board. Diagnosis of SARS-CoV-2 infection
was performed with Reverse Transcription Polymerase Chain Reaction (RT-PCR) on nasal
swabs. Antigenic tests, as well as RT-PCR, were employed to determine the end of infection.
All patients received the standard of care in force at the time of infection. Infection
course and COVID-19 severity were monitored according to radiologically documented
pneumonia, hospitalization, and oxygen therapy requirement; major comorbidities were
registered.13 Statistical analysis was performed using IBM software SPSS statistics
v.25. Descriptive statistics are presented for normally distributed variables. Differences
between the groups were evaluated using univariate logistic regression to assess potential
risk factors associated with death or severe COVID-19 infection. The χ2 test was used
for categorical variables, and the Mann-Whitney U-test was used for continuous variables.
Results
A total of 106 patients received T-C MoAb prophylaxis. Median age at infusion was
64 years (range 30–83), the majority of patients were affected by non-odgkin lymphoma
(NHL) (65%, 69/106, 44% aggressive NHL, 21% indolent NHLs), followed by multiple myeloma
(MM) (21.7%), Hodgkin lymphoma (HL) (9.4%), chronic lymphocytic leukemia (CLL) (2.8%)
and hairy cell leukemia (1.5%) (Table 1). Nine-point four percent received T-C MoAb
before, 39.6% within 6 months, and 50.9% within 1 year of hematologic treatment (Table
1). Twelve-point-three percent (13/106) received maintenance treatment with anti-CD20
monoclonal antibodies. One-hundred and three patients (103/106 = 97.1%) received at
least 2 doses of BNT162b2 messenger RNA vaccine before infusion of T-C MoAb, 34% (36/106)
had a previously documented SARS-CoV-2 infection (Table 1). No serious adverse events
were related to T-C MoAb administration. Median follow-up was 124 days (25–380).
Of 106 patients, 18 developed COVID-19 (17%) after a median of 85 days (range 35–222)
from T-C MoAb infusion. Among them, 83.3% (15/18) developed symptoms and fever, 44.4%
(8/18) required hospitalization and 16.7% (3/18) required oxygen support. Antiviral
treatment was administered in 44.4% (8/18) of patients: 3 received remdesivir, 1 sotrovimab,
2 nilmatrelvir-ritonavir and 2 molnupinavir. Three out of 18 patients had previous
COVID-19, one was hospitalized and died. The median time of SARS-CoV-2 infection (since
positive nasal swab) was 17 days (range 6–52).
The baseline characteristics of patients receiving T-C MoAb were heterogeneous. Comparing
patients who developed breakthrough SARS-CoV-2 infection (n=18) to patients who did
not (n=88), we observed a significantly higher frequency of at least 1 comorbidity
among the former (77.8% vs 52.3%, p=0.047) (Table 1). Anti-spike antibodies were tested
before MoAb in 9 of 18 infected patients; 6 (66%) had a negative and 3 (33%) a positive
titer. SARS-CoV-2 breakthrough infection was not significantly related to any of the
following risk factors: active hematologic disease (20.9% vs. 14.9% infection rate,
p=0.41); age above 65 years (21.3% vs 14.5%, p=0.37); hematologic treatment regimen
including anti-CD20 MoAbs (21.4% vs. 9.4%, p=0.13), anti-CD38 MoAbs (6.7% vs. 19.5%,
p=0.22) and bendamustine (20.8% vs. 17.1%, p=0.67). Age above 65 years was related
to hospitalization (75% vs 25%, p=0.047).
Overall, the death rate was 6.8% (6/88) in patients without breakthrough infection
(due to hematologic disease progression in all cases) and 22.2% (4/18) in the group
with breakthrough infection (p=0.04); among the latter, 3 cases of COVID19 related
death (16.7%, 3/18) and 1 due to hematologic disease progression were observed. Patients
who experienced COVID-related death had positive nasal swabs after 34, 156, and 172
days after T-C MoAb administration, respectively; they received 1 nirmatrelvir-ritonavir,
1 remdesevir, and molnupinavir, respectively; two patients developed severe COVID-19
with subsequent admission to intensive care unit, 1 patient died from secondary bacterial
infection. Two of the 3 COVID-related deaths occurred after 5 months of T-C MoAb infusion.
Two COVID-related deaths had negative SARS-CoV-2 antispike titer and age above 65
years. For patients developing breakthrough COVID-19, hospitalization (3/4, p=0.02)
and oxygen therapy requirement (3/4, p=0.006) were the only significant death-related
risk factors.
Discussion
We present a real-life retrospective monocentric cohort of patients affected by high-risk
lymphoproliferative diseases who received the COVID-19 vaccine and prophylaxis with
T-C MoAb. We report a rate of breakthrough infection of 17%, hospitalization of 7.5%,
and COVID-related mortality of 2.8%. Our findings agree with those of the TACKLE randomized
trial that proved a significant reduction of 51% of severe infection or death among
immunocompromised outpatients who received T-C MoAb versus placebo and developed SARS-CoV-2
breakthrough infection.15
Real-life data are upcoming on the impact of pre-exposure prophylaxis in several hematological
malignancies (e.g., hematopoietic stem cell transplantation, CAR-T cell patients,
CLL), given the multiple factors involved in the clinical behavior of SARS-CoV-2,
as shown in table 2.10,12,14 A large recent Israelian retrospective experience highlighted
a significant reduction in infection rate (3.5%) and mortality (0%) among immunocompromised
patients receiving T-C MoAb versus no administration (Table 2).11 Our study’s breakthrough
infection rate agreed with the data reported by Davis et al. Patients with hematologic
malignancies receiving T-C MoAbs (150/150 mg or 300/300 mg) experienced a confirmed
COVID-19 breakthrough infection in 11% of cases (Table 2).16 This cohort received
B-cell-depleting therapy like our group, with 60.8% of patients receiving either rituximab,
obinutuzumab, or blinatumomab;16 no deaths were reported, and the hospitalization
rate was 15%. In the EPICOVIDEHA registry, a matched-control cases analysis was performed,
showing a 90% breakthrough infection rate, higher than in our study, with a comparable
death rate, but with the limit of a small cohort (n=47) (Table 2).12
In the present experience, no risk factors associated with severe COVID-19 or hospitalization,
or death were identified, in contrast with our previous experience, which focused
on the treatment of COVID-19 with MoAbs other than T-C, where the presence of comorbidity
was associated with the risk of developing COVID-19 infection, and hospitalization
and oxygen requirement were confirmed as prognostic factors for COVID-19 related death.5
Similarly, as recently reported by Laracy et al. in a large cohort of patients (n=892)
including different hematological malignancies, there were no risk factors that allowed
to foresee the infectious outcome in this setting except for the augmented schedule
of T-C MoAb (Table 2).17
The present study has several limitations given by the retrospective nature, the relatively
small sample size, and the lack of data about SARS-CoV-2 genomic variants. However,
it is possible to link the reported infections to the Omicron BA 1.1 and BA.4/5 variants,
according to the time of infection and the epidemiological waves in Italy. The impact
of genomic variants on in vivo T-C MoAb’s efficacy is controversial: a sub-analysis
of the PROVENT trial did not detect any variant predominance on the serum of patients
developing SARS-CoV-2 breakthrough infection among patients receiving T-C MoAb, nor
neutralizing test highlighted differences in SARS-CoV-2 Spike-based Lineages.18 Regarding
Omicron BA.1/2, a recent report from the US veteran registry showed a lower rate of
severe COVID-19 in immunocompromised patients receiving T-C MoAb (n=1878) compared
to untreated matched controls (n=7014) (Table II).19 Moreover, the activity of T-C
MoAb was demonstrated in neutralization test from serum samples (before T-C MoAbs
and after 3 weeks) of 75 solid organ recipients on sublineages BA.4/5, although 6
out of 75 of these patients still developed breakthrough infection from BA.4/5.20
On the one hand, the in vitro studies have reported some levels of evasion of T-C-induced
protection by different Omicron sub-variants, including those possibly responsible
for infections in the present cohort. Thus, excluding a sub-optimal degree of protection
in some of our cases is impossible. On the other hand, we add to the literature documenting
the clinical benefit of this prophylaxis in high-risk hematologic malignancies. Randomized
studies are ongoing, such as the ENDURE trial (https://classic.clinicaltrials.gov/ct2/show/NCT05375760),
on immunocompromised patients to optimize the benefit of this strategy with an augmented
dosage.
In conclusion, high-risk patients affected by lymphoproliferative B-cell malignancies
are at risk for SARS-CoV-2 breakthrough infections despite using COVID-19 vaccination
and pre-exposure prophylaxis with T-C MoAb. Nevertheless, the hospitalization rate
and COVID-related deaths were low. Our study’s results suggest maintaining a cautious
daily practice and full pre-exposure prophylaxis, including vaccination and anti-spike
monoclonal antibodies, that are mandatory to minimize the risk of developing a SARS-CoV-2
breakthrough infection.