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Efficacy and safety of the BNT162b2 mRNA COVID-19 vaccine in participants with a history of cancer: subgroup analysis of a global phase 3 randomized clinical trial.
Thomas, Stephen J; Perez, John L; Lockhart, Stephen P; Hariharan, Subramanian; Kitchin, Nicholas; Bailey, Ruth; Liau, Katherine; Lagkadinou, Eleni; Türeci, Özlem; Sahin, Ugur; Xu, Xia; Koury, Kenneth; Dychter, Samuel S; Lu, Claire; Gentile, Teresa C; Gruber, William C.
  • Thomas SJ; State University of New York, Upstate Medical University, 750 East Adams Street, Syracuse, NY 13210, USA. Electronic address: ThomStep@upstate.edu.
  • Perez JL; Pfizer Inc., 500 Arcola Rd., Collegeville, PA 19426, USA. Electronic address: John.Perez@pfizer.com.
  • Lockhart SP; Pfizer Inc., Horizon Honey Lane, Maidenhead SL6 6RJ, UK. Electronic address: Stephen.P.Lockhart@pfizer.com.
  • Hariharan S; Pfizer Inc., 235 East 42nd Street, New York, NY 10017, USA. Electronic address: s.hariharan@pfizer.com.
  • Kitchin N; Pfizer Inc., Horizon Honey Lane, Maidenhead SL6 6RJ, UK. Electronic address: Nicholas.Kitchin@pfizer.com.
  • Bailey R; Pfizer Inc., Horizon Honey Lane, Maidenhead SL6 6RJ, UK. Electronic address: Ruth.Bailey@pfizer.com.
  • Liau K; Pfizer Inc., 10555 Science Center Drive, San Diego, CA 92121, USA. Electronic address: Katherine.F.Liau@pfizer.com.
  • Lagkadinou E; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany. Electronic address: Eleni.Lagkadinou@biontech.de.
  • Türeci Ö; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany. Electronic address: Oezlem.Tuereci@biontech.de.
  • Sahin U; BioNTech SE, An der Goldgrube 12, 55131 Mainz, Germany. Electronic address: sahin@uni-mainz.de.
  • Xu X; Pfizer Inc., 500 Arcola Rd., Collegeville, PA 19426, USA. Electronic address: Xia.Xu3@pfizer.com.
  • Koury K; Pfizer Inc., 401 N. Middletown Rd, Pearl River, NY 10965, USA. Electronic address: Kenneth.Koury@pfizer.com.
  • Dychter SS; Pfizer Inc., 10555 Science Center Drive, San Diego, CA 92121, USA. Electronic address: Samuel.Dychter@pfizer.com.
  • Lu C; Pfizer Inc., 401 N. Middletown Rd, Pearl River, NY 10965, USA. Electronic address: Claire.Lu@pfizer.com.
  • Gentile TC; State University of New York, Upstate Medical University, 750 East Adams Street, Syracuse, NY 13210, USA. Electronic address: GentileT@upstate.edu.
  • Gruber WC; Pfizer Inc., 401 N. Middletown Rd, Pearl River, NY 10965, USA. Electronic address: Bill.Gruber@pfizer.com.
Vaccine ; 40(10): 1483-1492, 2022 03 01.
Article in English | MEDLINE | ID: covidwho-1586269
ABSTRACT

INTRODUCTION:

Individuals with an underlying malignancy have high risk of poor COVID-19 outcomes. In clinical trials, COVID-19 vaccines were safe and efficacious against infection, hospitalization, and death, but most trials excluded participants with cancer. We report results from participants with a history of past or active neoplasm (malignant or benign/unknown) and up to 6 months' follow-up post-dose 2 from the placebo-controlled, observer-blinded trial of the 2-dose BNT162b2 mRNA COVID-19 vaccine. PATIENTS AND

METHODS:

Between July 2020-January 2021, 46,429 participants aged ≥ 12 years were randomized at 152 sites in 6 countries. Healthy participants with pre-existing stable neoplasm could participate; those receiving immunosuppressive therapy were excluded. Data are reported for participants, aged ≥ 16 years for safety and ≥ 12 years for efficacy, who had any history of neoplasm at baseline (data cut-off March 13, 2021). Adverse-event (AE) data are controlled for follow-up time before unblinding and reported as incidence rates (IRs) per 100 person-years follow-up.

RESULTS:

At baseline, 3813 participants had a history of neoplasm; most common malignancies were breast (n = 460), prostate (n = 362), and melanoma (n = 223). Four BNT162b2 and 71 placebo recipients developed COVID-19 from 7 days post-dose 2; vaccine efficacy was 94.4% (95% CI 85.2, 98.5) after up to 6 months' follow-up post-dose 2. This compares favorably with vaccine efficacy of 91.1% in the overall trial population after the same follow-up. AEs were reported at IRs of 95.4(BNT162b2) and 48.3 (placebo) per 100 person-years. Most common AEs were reactogenicity events (injection-site pain, fatigue, pyrexia). Three BNT162b2 and 1 placebo recipients withdrew because of vaccine-related AEs. No vaccine-related deaths were reported.

CONCLUSION:

In participants with past or active neoplasms, BNT162b2 vaccine has a similar efficacy and safety profile as in the overall trial population. These results can inform BNT162b2 use during the COVID-19 pandemic and future trials in participants with cancer. Clinical trial number NCT04368728.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Neoplasms Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adolescent / Child / Humans / Male Language: English Journal: Vaccine Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Neoplasms Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study / Randomized controlled trials Topics: Vaccines Limits: Adolescent / Child / Humans / Male Language: English Journal: Vaccine Year: 2022 Document Type: Article