Lymphoma represents a heterogeneous hematological malignancy (HM), which is characterized by severe immunosuppression. Patients diagnosed of coronavirus disease 2019 (COVID-19) during the course of HM have been described to have poor outcome, with only few reports specifically addressing lymphoma patients. Here, we investigated the clinical behavior and clinical parameters of a large multicenter cohort of adult patients with different lymphoma subtypes, with the aim of identifying predictors of death. The study included 856 patients, of whom 619 were enrolled prospectively in a 1-year frame and were followed-up for a median of 66 days (range 1-395). Patients were managed as outpatient (not-admitted cohort, n = 388) or required hospitalization (n = 468), and median age was 63 years (range 19-94). Overall, the 30-and 100-days mortality was 13% (95% confi-dence interval (CI), 11% to 15%) and 23% (95% CI, 20% to 27%), respectively. Antilymphoma treatment, including anti-CD20 containing regimens, did not impact survival. Patients with Hodgkin's lymphoma had the more favorable survival, but this was partly related to signifi-cantly younger age. The time interval between lymphoma diagnosis and COVID-19 was inversely related to mortality. Multivariable analysis recognized 4 easy-to-use factors (age, gender, lymphocyte, and platelet count) that were associated with risk of death, both in the admitted and in the not-admitted cohort (HR 3.79 and 8.85 for the intermediate-and high risk group, respectively). Overall, our study shows that patients should not be deprived of the best available treatment of their underlying disease and indicates which patients are at higher risk of death. This study was registered with ClinicalTrials.gov, NCT04352556.

A prognostic model for patients with lymphoma and COVID-19: a multicentre cohort study / Visco, C.; Marcheselli, L.; Mina, R.; Sassone, M.; Guidetti, A.; Penna, D.; Cattaneo, C.; Bonuomo, V.; Busca, A.; Ferreri, A. J. M.; Bruna, R.; Petrucci, L.; Cairoli, R.; Salvini, M.; Bertu, L.; Ladetto, M.; Pilerci, S.; Pinto, A.; Ramadan, S.; Marchesi, F.; Cavo, M.; Arcaini, L.; Coviello, E.; Romano, A.; Musto, P.; Massaia, M.; Fracchiolla, N.; Marchetti, M.; Scattolin, A.; Tisi, M. C.; Cuneo, A.; Porta, M. D.; Trentin, L.; Turrini, M.; Gherlinzoni, F.; Tafuri, A.; Galimberti, S.; Bocchia, M.; Cardinali, V.; Cilloni, D.; Corso, A.; Armiento, D.; Rigacci, L.; La Barbera, E. O.; Gambacorti-Passerini, C.; Visani, G.; Vallisa, D.; Venditti, A.; Selleri, C.; Conconi, A.; Tosi, P.; Lanza, F.; Candoni, A.; Krampera, M.; Corradini, P.; Passamonti, F.; Merli, F.. - In: BLOOD ADVANCES. - ISSN 2473-9537. - 6:1(2022), pp. 327-338. [10.1182/bloodadvances.2021005691]

A prognostic model for patients with lymphoma and COVID-19: a multicentre cohort study

Candoni A.;
2022

Abstract

Lymphoma represents a heterogeneous hematological malignancy (HM), which is characterized by severe immunosuppression. Patients diagnosed of coronavirus disease 2019 (COVID-19) during the course of HM have been described to have poor outcome, with only few reports specifically addressing lymphoma patients. Here, we investigated the clinical behavior and clinical parameters of a large multicenter cohort of adult patients with different lymphoma subtypes, with the aim of identifying predictors of death. The study included 856 patients, of whom 619 were enrolled prospectively in a 1-year frame and were followed-up for a median of 66 days (range 1-395). Patients were managed as outpatient (not-admitted cohort, n = 388) or required hospitalization (n = 468), and median age was 63 years (range 19-94). Overall, the 30-and 100-days mortality was 13% (95% confi-dence interval (CI), 11% to 15%) and 23% (95% CI, 20% to 27%), respectively. Antilymphoma treatment, including anti-CD20 containing regimens, did not impact survival. Patients with Hodgkin's lymphoma had the more favorable survival, but this was partly related to signifi-cantly younger age. The time interval between lymphoma diagnosis and COVID-19 was inversely related to mortality. Multivariable analysis recognized 4 easy-to-use factors (age, gender, lymphocyte, and platelet count) that were associated with risk of death, both in the admitted and in the not-admitted cohort (HR 3.79 and 8.85 for the intermediate-and high risk group, respectively). Overall, our study shows that patients should not be deprived of the best available treatment of their underlying disease and indicates which patients are at higher risk of death. This study was registered with ClinicalTrials.gov, NCT04352556.
2022
6
1
327
338
A prognostic model for patients with lymphoma and COVID-19: a multicentre cohort study / Visco, C.; Marcheselli, L.; Mina, R.; Sassone, M.; Guidetti, A.; Penna, D.; Cattaneo, C.; Bonuomo, V.; Busca, A.; Ferreri, A. J. M.; Bruna, R.; Petrucci, L.; Cairoli, R.; Salvini, M.; Bertu, L.; Ladetto, M.; Pilerci, S.; Pinto, A.; Ramadan, S.; Marchesi, F.; Cavo, M.; Arcaini, L.; Coviello, E.; Romano, A.; Musto, P.; Massaia, M.; Fracchiolla, N.; Marchetti, M.; Scattolin, A.; Tisi, M. C.; Cuneo, A.; Porta, M. D.; Trentin, L.; Turrini, M.; Gherlinzoni, F.; Tafuri, A.; Galimberti, S.; Bocchia, M.; Cardinali, V.; Cilloni, D.; Corso, A.; Armiento, D.; Rigacci, L.; La Barbera, E. O.; Gambacorti-Passerini, C.; Visani, G.; Vallisa, D.; Venditti, A.; Selleri, C.; Conconi, A.; Tosi, P.; Lanza, F.; Candoni, A.; Krampera, M.; Corradini, P.; Passamonti, F.; Merli, F.. - In: BLOOD ADVANCES. - ISSN 2473-9537. - 6:1(2022), pp. 327-338. [10.1182/bloodadvances.2021005691]
Visco, C.; Marcheselli, L.; Mina, R.; Sassone, M.; Guidetti, A.; Penna, D.; Cattaneo, C.; Bonuomo, V.; Busca, A.; Ferreri, A. J. M.; Bruna, R.; Petruc...espandi
File in questo prodotto:
File Dimensione Formato  
advancesadv2021005691.pdf

Open access

Tipologia: Versione pubblicata dall'editore
Dimensione 1.29 MB
Formato Adobe PDF
1.29 MB Adobe PDF Visualizza/Apri
Pubblicazioni consigliate

Licenza Creative Commons
I metadati presenti in IRIS UNIMORE sono rilasciati con licenza Creative Commons CC0 1.0 Universal, mentre i file delle pubblicazioni sono rilasciati con licenza Attribuzione 4.0 Internazionale (CC BY 4.0), salvo diversa indicazione.
In caso di violazione di copyright, contattare Supporto Iris

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/1293924
Citazioni
  • ???jsp.display-item.citation.pmc??? 16
  • Scopus 38
  • ???jsp.display-item.citation.isi??? 35
social impact