Clinical and Serological Follow-Up of 216 Patients with Hematological Malignancies after Vaccination with Pfizer-BioNT162b2 mRNA COVID-19 in a Real-World Study
Jean-François Rossi,
Emmanuel Bonnet,
Christel Castelli,
Marion Velensek,
Emma Wisniewski,
Sophie Heraud,
Rania Boustany,
Céleste David,
Jérôme Dinet,
Roland Sicard,
Jean-Pierre Daures,
Marion Bonifacy,
Lysiane Mousset,
Emmanuel Goffart
Affiliations
Jean-François Rossi
Institut du Cancer Avignon-Provence, Sainte Catherine, 84000 Avignon, France
Emmanuel Bonnet
Recherche Clinique Clinique Beau Soleil—Nouvelles Technologies, 34070 Montpellier, France
Christel Castelli
Recherche Clinique Clinique Beau Soleil—Nouvelles Technologies, 34070 Montpellier, France
Marion Velensek
Institut du Cancer Avignon-Provence, Sainte Catherine, 84000 Avignon, France
Emma Wisniewski
Institut du Cancer Avignon-Provence, Sainte Catherine, 84000 Avignon, France
Sophie Heraud
Institut du Cancer Avignon-Provence, Sainte Catherine, 84000 Avignon, France
Rania Boustany
Institut du Cancer Avignon-Provence, Sainte Catherine, 84000 Avignon, France
Céleste David
Institut du Cancer Avignon-Provence, Sainte Catherine, 84000 Avignon, France
Jérôme Dinet
Thess Corporate Inc., 34070 Montpellier, France
Roland Sicard
Institut du Cancer Avignon-Provence, Sainte Catherine, 84000 Avignon, France
Jean-Pierre Daures
Recherche Clinique Clinique Beau Soleil—Nouvelles Technologies, 34070 Montpellier, France
Hematological malignancies (HMs) have heterogeneous serological responses after vaccination due to disease or treatment. The aim of this real-world study was to analyze it after Pfizer-BioNT162b2 mRNA vaccination in 216 patients followed up for 1 year. The first 43 patients had an initial follow-up by a telemedicine (TM) system with no major events reported. The anti-spike IgG antibodies were checked 3–4 weeks post-first vaccination and every 3–4 months, by two standard bioassays and a rapid serological test (RST). Vaccine boosts were given when the level was p p = 0.019). The median levels were 228 BAU/mL post-second dose if seroconverted post-first and second, or if seroconverted only post-second dose. A total of 68% of post-second dose negative patients were post-third dose positive. A total of 16% received TC, six with non-severe symptomatic COVID-19 within 15–40 days. Personalized serological follow-up should apply particularly to patients with HMs.