To the editor, Encouraging seroconversion rates to SARS-CoV-2 vaccination in acute myeloid leukaemia (AML) and myelodysplastic syndrome (MDS) patients have been reported in large cohort studies [1][2][3][4] ; however, the majority of these patients were not receiving active systemic anti-cancer therapy (SACT) and its impact on vaccine responses remains to be fully elucidated. Mori et al. 5 report seroconversion rates of 94.7 and 100% respectively in Japanese patients with AML and MDS after two doses of mRNA SARS-CoV-2 vaccine, of which 39% received SACT. We report SARS-CoV-2 antibody responses following vaccination in a UK cohort of AML and HR-MDS patients all receiving, or having recently completed SACT, and stratified by prior SARS-CoV-2 infection. Demographics, SACT history and laboratory parameters were collected from the electronic health records of patients following two doses of SARS-CoV-2 vaccine (BNT162b2 or ChAdOx1nCoV-19) between December 2020 and July 2021. Serological testing was performed using Roche Elecsys anti-SARS-CoV-2 enzyme immunoassays. A total of 39 patients (85% AML, 15% HR-MDS, median age 63 ), underwent serological testing after receiving two doses of vaccine (Table 1). All were tested for anti-S antibodies after two doses (median 40 days post-dose) and 59% after the first dose (median 39 days). Thirty-three patients (85%) underwent testing for anti-N antibodies, and seven (21% of those tested) had previous SARS-CoV-2 infection. Eleven patients (28%) received intensive chemotherapy, 51% venetoclax-combination therapy (with azacitidine, low-dose cytarabine or gilteritinib) and 21% non-intensive azacitidine. Seropositivity rates and antibody titres increased with consecutive vaccine doses, from 74% in all patients (75% AML, 67% MDS) to 95% (94% AML, 100% MDS), with a median anti-S titre of 5.90 U/ml (IQR 0.58-56.7) after dose one, rising to 333 U/ml (IQR 86.8-1971) post dose two. Significantly higher titres were detected after dose two in AML patients, but not in MDS, though numbers are small (Figure 1B). We report similar seroconversion rates following two doses as seen by Mori et al. (Figure 1A, Table 1), despite all our patients receiving SACT compared to 39% of their cohort; however, we found no difference in anti-S titres between AML and HR-MDS patients receiving SACT after