SARS-CoV-2 vaccine response and rate of breakthrough infection in patients with hematological disorders.

Allogeneic stem cell transplantation Autologous stem cell transplantation Breakthrough SARS-CoV-2 infection COVID-19 Correlates of protection Hematological malignancies Immunocompromised patients Moderna mRNA-1273 Pfizer-BioNTech BNT162b2 SARS-CoV-2 vaccines Vaccine

Journal

Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937

Informations de publication

Date de publication:
07 05 2022
Historique:
received: 04 03 2022
accepted: 25 04 2022
entrez: 7 5 2022
pubmed: 8 5 2022
medline: 11 5 2022
Statut: epublish

Résumé

The clinical efficacy of SARS-CoV-2 vaccines according to antibody response in immunosuppressed patients such as hematological patients has not yet been established. A prospective multicenter registry-based cohort study conducted from December 2020 to December 2021 by the Spanish transplant and cell therapy group was used to analyze the relationship of antibody response at 3-6 weeks after full vaccination (2 doses) with breakthrough SARS-CoV-2 infection in 1394 patients with hematological disorders. At a median follow-up of 165 days after complete immunization, 37 out of 1394 (2.6%) developed breakthrough SARS-CoV-2 infection at median of 77 days (range 7-195) after full vaccination. The incidence rate was 6.39 per 100 persons-year. Most patients were asymptomatic (19/37, 51.4%), whereas only 19% developed pneumonia. The mortality rate was 8%. Lack of detectable antibodies at 3-6 weeks after full vaccination was the only variable associated with breakthrough infection in multivariate logistic regression analysis (Odds Ratio 2.35, 95% confidence interval 1.2-4.6, p = 0.012). Median antibody titers were lower in cases than in non-cases [1.83 binding antibody units (BAU)/mL (range 0-4854.93) vs 730.81 BAU/mL (range 0-56,800), respectively (p = 0.007)]. We identified 250 BAU/mL as a cutoff above which incidence and severity of the infection were significantly lower. Our study highlights the benefit of developing an antibody response in these highly immunosuppressed patients. Level of antibody titers at 3 to 6 weeks after 2-dose vaccination links with protection against both breakthrough infection and severe disease for non-Omicron SARS-CoV-2 variants.

Sections du résumé

BACKGROUND
The clinical efficacy of SARS-CoV-2 vaccines according to antibody response in immunosuppressed patients such as hematological patients has not yet been established.
PATIENTS AND METHODS
A prospective multicenter registry-based cohort study conducted from December 2020 to December 2021 by the Spanish transplant and cell therapy group was used to analyze the relationship of antibody response at 3-6 weeks after full vaccination (2 doses) with breakthrough SARS-CoV-2 infection in 1394 patients with hematological disorders.
RESULTS
At a median follow-up of 165 days after complete immunization, 37 out of 1394 (2.6%) developed breakthrough SARS-CoV-2 infection at median of 77 days (range 7-195) after full vaccination. The incidence rate was 6.39 per 100 persons-year. Most patients were asymptomatic (19/37, 51.4%), whereas only 19% developed pneumonia. The mortality rate was 8%. Lack of detectable antibodies at 3-6 weeks after full vaccination was the only variable associated with breakthrough infection in multivariate logistic regression analysis (Odds Ratio 2.35, 95% confidence interval 1.2-4.6, p = 0.012). Median antibody titers were lower in cases than in non-cases [1.83 binding antibody units (BAU)/mL (range 0-4854.93) vs 730.81 BAU/mL (range 0-56,800), respectively (p = 0.007)]. We identified 250 BAU/mL as a cutoff above which incidence and severity of the infection were significantly lower.
CONCLUSIONS
Our study highlights the benefit of developing an antibody response in these highly immunosuppressed patients. Level of antibody titers at 3 to 6 weeks after 2-dose vaccination links with protection against both breakthrough infection and severe disease for non-Omicron SARS-CoV-2 variants.

Identifiants

pubmed: 35526045
doi: 10.1186/s13045-022-01275-7
pii: 10.1186/s13045-022-01275-7
pmc: PMC9077637
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
BNT162 Vaccine N38TVC63NU

Types de publication

Journal Article Multicenter Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

54

Informations de copyright

© 2022. The Author(s).

Références

Clin Lymphoma Myeloma Leuk. 2021 Oct;21(10):e801-e809
pubmed: 34376375
Lancet. 2020 Aug 15;396(10249):467-478
pubmed: 32702298
Transplant Cell Ther. 2021 Sep;27(9):788-794
pubmed: 34214738
Clin Infect Dis. 2019 May 17;68(11):1894-1903
pubmed: 30239624
Science. 2022 Jan 07;375(6576):43-50
pubmed: 34812653
Bone Marrow Transplant. 2021 Sep;56(9):2212-2220
pubmed: 33947980
Am J Hematol. 2022 Jan 1;97(1):30-42
pubmed: 34695229
Lancet. 2021 May 15;397(10287):1819-1829
pubmed: 33964222
Lancet Infect Dis. 2019 Jun;19(6):e200-e212
pubmed: 30744963
J Hematol Oncol. 2021 Oct 14;14(1):168
pubmed: 34649563
Nat Med. 2021 Nov;27(11):2032-2040
pubmed: 34588689
MMWR Morb Mortal Wkly Rep. 2021 May 07;70(18):674-679
pubmed: 33956782
Br J Haematol. 2021 Oct;195(2):186-193
pubmed: 34196388
Blood. 2021 Oct 7;138(14):1278-1281
pubmed: 34339501
Leuk Lymphoma. 2022 Mar;63(3):538-550
pubmed: 34668835
N Engl J Med. 2021 Apr 15;384(15):1412-1423
pubmed: 33626250
Lancet Infect Dis. 2019 Jun;19(6):e188-e199
pubmed: 30744964
J Clin Oncol. 2022 May 1;40(13):1414-1427
pubmed: 35286152
Exp Hematol Oncol. 2020 Aug 25;9:21
pubmed: 32864192
Blood Adv. 2022 Jan 8;6(3):848-853
pubmed: 34905620
Leukemia. 2021 Oct;35(10):2885-2894
pubmed: 34079042
Transplant Cell Ther. 2021 Nov;27(11):938.e1-938.e6
pubmed: 34274492
Lancet Haematol. 2021 Mar;8(3):e185-e193
pubmed: 33482113
Blood Adv. 2022 Mar 8;6(5):1537-1546
pubmed: 35114690
Am J Hematol. 2021 Oct 1;96(10):1195-1203
pubmed: 34185336
Lancet. 2021 Jul 24;398(10297):298-299
pubmed: 34270933
Cancer Cell. 2021 Aug 9;39(8):1031-1033
pubmed: 34331856
Lancet Haematol. 2021 Aug;8(8):e583-e592
pubmed: 34224668
BMJ. 2021 May 13;373:n1088
pubmed: 33985964
Blood. 2021 Jun 10;137(23):3165-3173
pubmed: 33861303
N Engl J Med. 2021 Oct 14;385(16):1474-1484
pubmed: 34320281
J Hematol Oncol. 2020 Oct 8;13(1):133
pubmed: 33032660
Lancet. 2021 Apr 10;397(10282):1351-1362
pubmed: 33798499

Auteurs

José Luis Piñana (JL)

Division of Clinical Hematology, Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain. jlpinana@gmail.com.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain. jlpinana@gmail.com.

Lucia López-Corral (L)

Hematology Division, Hospital Universitario de Salamanca, Salamanca, Spain.

Rodrigo Martino (R)

Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Lourdes Vazquez (L)

Hematology Division, Hospital Universitario de Salamanca, Salamanca, Spain.

Ariadna Pérez (A)

Division of Clinical Hematology, Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.

Gabriel Martin-Martin (G)

Hematology Division, Hospital Universitario de Salamanca, Salamanca, Spain.

Beatriz Gago (B)

Hematology Division, Hospital Regional Universitario Carlos Haya, Malaga, Spain.

Gabriela Sanz-Linares (G)

Hematology Division, Institut Català Oncologia-Hospital Duran i Reynals, IDIBELL, Universitat de Barcelona, Barcelona, Spain.

Andrés Sanchez-Salinas (A)

Hematology Division, Hospital Clínico Universitario Virgen de la Arrixaca, Murcia, Spain.

Lucia Villalon (L)

Hematology Division, Hospital Universitario Fundación Alcorcón, Madrid, Spain.

Venancio Conesa-Garcia (V)

Hematology Division, Hospital General Universitario de Elche, Elche, Spain.

María T Olave (MT)

Hematology Division, Hospital Clínico Universitario Lozano Blesa, IIS Aragon, Saragossa, Spain.

Magdalena Corona (M)

Hematology Division, Hospital Ramon y Cajal, Madrid, Spain.

Sara Marcos-Corrales (S)

Hematology Division, Hospital Universitario de Salamanca, Salamanca, Spain.

Mar Tormo (M)

Division of Clinical Hematology, Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.

José Ángel Hernández-Rivas (JÁ)

Hematology Division, Hospital Universitario Infanta Leonor, Madrid, Spain.

Juan Montoro (J)

Hematology Division, Hospital universitario y politécnico La Fe, Valencia, Spain.

Alicia Rodriguez-Fernandez (A)

Hematology Division, Hospital Universitario Virgen Macarena, Seville, Spain.

Irene Risco-Gálvez (I)

Hematology Division, Hospital Arnau de Vilanova, Valencia, Spain.

Pablo Rodríguez-Belenguer (P)

Research Program on Biomedical Informatics (GRIB), Department of Experimental and Health Sciences, Hospital del Mar Medical Research Institute (IMIM), Universitat Pompeu Fabra, Barcelona, Spain.

Juan Carlos Hernandez-Boluda (JC)

Division of Clinical Hematology, Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.

Irene García-Cadenas (I)

Hematology Division, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Montserrat Ruiz-García (M)

Hospital General Universitari d'Elx, Elche, Spain.

Juan Luis Muñoz-Bellido (JL)

Hospital Universitario de Salamanca, Salamanca, Spain.

Carlos Solano (C)

Division of Clinical Hematology, Hematology Department, Hospital Clínico Universitario de Valencia, Avda Blasco Ibañez, 17, 46010, Valencia, Spain.
Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
Department of Medicine, School of Medicine, University of Valencia, Valencia, Spain.

Ángel Cedillo (Á)

Hematopoietic Stem Cell Transplantation and Cell Therapy Group (GETH) Office, Madrid, Spain.

Anna Sureda (A)

Hematology Division, Institut Català Oncologia-Hospital Duran i Reynals, IDIBELL, Universitat de Barcelona, Barcelona, Spain.

David Navarro (D)

Fundación INCLIVA, Instituto de Investigación Sanitaria Hospital Clínico Universitario de Valencia, Valencia, Spain.
Hospital Clinico Universitario de Valencia, Valencia, Spain.

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