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Published on: May 27, 2011
Use of remdesivir for COVID-19 in patients with hematologic cancer
Alexandra Martin-Onraët1, Corazón Barrientos-Flores2, Diana Vilar-Compte2
1Infectious Diseases Department, Instituto Nacional de Cancerología, Avenida San Fernando 22, Col Sección 16 Belisario Dominguez, 14080, Tlalpan CDMX, Mexico. alexitemaon@gmail.com.
Insights
Patients with hematologic malignancies (HM) face high COVID-19 risks. Remdesivir showed no benefit in hospitalized HM patients, but ambulatory use prevented progression, suggesting potential for early intervention in this vulnerable group.
Area of Science:
- Hematology
- Infectious Diseases
- Oncology
Background:
- Patients with hematologic malignancies (HM) are at increased risk for severe COVID-19 outcomes.
- The Omicron variant presented unique challenges for managing COVID-19 in immunocompromised populations.
Purpose of the Study:
- To evaluate the impact of remdesivir on COVID-19 progression in patients with hematologic malignancies (HM) during the Omicron wave in Mexico City.
- To identify factors associated with COVID-19 progression in this high-risk patient group.
Main Methods:
- A retrospective study included 115 patients with HM and COVID-19 from December 2021 to March 2022.
- Data collected included socio-demographic information, clinical status, vaccination history, and remdesivir treatment details.
- The primary outcome was progression to severe or critical COVID-19, with logistic regression used for variable analysis.
Main Results:
- Of 115 patients, 24% received remdesivir. Overall, 19% progressed to severe/critical COVID-19, and 8% died.
- Remdesivir did not reduce progression risk in hospitalized patients.
- Notably, none of the nine patients receiving ambulatory remdesivir progressed to severe COVID-19 or died.
Conclusions:
- Patients with HM remain at high risk for severe COVID-19 complications.
- Early administration of remdesivir in an ambulatory setting may prevent severe outcomes in HM patients.
- Further prospective studies are essential to determine optimal antiviral strategies and treatment durations for this population.
Purposes:
Patients with hematologic malignancies (HM) are among the individuals with highest risk of COVID-19 complications. We report the impact of remdesivir in patients with hematologic malignancies (HM) during Omicron in Mexico City.
Methods:
All patients with HM and COVID-19 during December 2021-March 2022 were included. Socio-demographic and clinical data were collected. The primary outcome was COVID-19 progression. Variables associated with progression were analyzed.
Results:
115 patients were included. Median age was 50 years (IQR 35-63); 36% (N = 41) had at least one comorbidity. Fifty-two percent had non-Hodgkin lymphoma. Fifty patients (44%) had at least two doses of SARS-CoV-2 vaccine. COVID-19 was classified as mild (52.6%), moderate (9.7%), and severe/critical (28%). Twenty-eight patients (24%) received remdesivir. Nine patients received remdesivir at the ambulatory clinic (33%), the rest during hospital admission. Overall, 22(19%) patients progressed to severe/critical COVID-19; nine died due to COVID-19(8%). Hospital admission for non-COVID-19 causes was associated with higher odds of progression. Remdesivir did not reduce the risk of progression in hospitalized patients; none of the patients who received remdesivir in the ambulatory clinic progressed to severe COVID-19 or died.
Conclusions:
Patients with HM and COVID-19 continue to present with high risk of complications. More prospective studies are needed to define the impact of antivirals in this high-risk group, including the best duration of treatment. Also, better vaccine coverage and access to treatment are mandatory.
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