TY - JOUR KW - Acute hemolytic anemia KW - Dapsone KW - Dapsone hypersensitivity syndrome KW - G6PD deficiency KW - HLA-B13:01 KW - Indonesia KW - Leprosy KW - Low- and middle-income countries KW - Morbus Hansen KW - Multidrug therapy KW - Pharmacogenetics AU - Krismawati H AU - Harianja M AU - Oktavian A AU - Bøgh C AU - Ataupah MR AU - Laiskodat RD AU - Pongtiku A AU - Geluk A AU - Baird JK AU - Hamers RL AU - Soebono H AU - Walker SL AU - Grijsen ML AB -

Leprosy is effectively treated with multi-drug therapy (MDT), a regimen containing three antibiotic drugs, including dapsone - a sulfone drug associated with potentially life-threatening adverse drug reactions. Specifically, dapsone hypersensitivity syndrome (DHS), linked to HLA-B∗13:01 polymorphism, and hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency (G6PDd).

Both of these pharmacogenetic polymorphisms can be prevented through diagnostic screening before MDT initiation averting potential complications. However, in leprosy-endemic areas like Indonesia, access to these tests often remains inaccessible due to high costs and limited laboratory capacity. Additionally, alternative dapsone-sparing treatment regimens are usually unavailable or unaffordable, restraining individuals onto suboptimal dual-therapy with rifampicin and clofazimine, which has uncertain efficacy. We raise concerns regarding the safety of dapsone-containing MDT without routine pharmacogenetic screening and the unavailability of alternative regimens. We call for action to address persisting global health inequities in care delivery, ensuring all individuals receive the safest and most effective leprosy treatment options.

BT - The Lancet Regional Health - Southeast Asia DO - 10.1016/j.lansea.2025.100555 LA - ENG M3 - Article N2 -

Leprosy is effectively treated with multi-drug therapy (MDT), a regimen containing three antibiotic drugs, including dapsone - a sulfone drug associated with potentially life-threatening adverse drug reactions. Specifically, dapsone hypersensitivity syndrome (DHS), linked to HLA-B∗13:01 polymorphism, and hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency (G6PDd).

Both of these pharmacogenetic polymorphisms can be prevented through diagnostic screening before MDT initiation averting potential complications. However, in leprosy-endemic areas like Indonesia, access to these tests often remains inaccessible due to high costs and limited laboratory capacity. Additionally, alternative dapsone-sparing treatment regimens are usually unavailable or unaffordable, restraining individuals onto suboptimal dual-therapy with rifampicin and clofazimine, which has uncertain efficacy. We raise concerns regarding the safety of dapsone-containing MDT without routine pharmacogenetic screening and the unavailability of alternative regimens. We call for action to address persisting global health inequities in care delivery, ensuring all individuals receive the safest and most effective leprosy treatment options.

PB - Elsevier BV PY - 2025 EP - 5 T2 - The Lancet Regional Health - Southeast Asia TI - Challenges associated with dapsone for leprosy treatment in Indonesia - urgent need for access to alternative antimicrobial drugs UR - https://www.thelancet.com/action/showPdf?pii=S2772-3682%2825%2900026-5 VL - 34 SN - 2772-3682 ER -