PMID- 31242231 OWN - NLM STAT- MEDLINE DCOM- 20200224 LR - 20200309 IS - 1932-6203 (Electronic) IS - 1932-6203 (Linking) VI - 14 IP - 6 DP - 2019 TI - Comparative study on liposomal amphotericin B and other therapies in the treatment of mucosal leishmaniasis: A 15-year retrospective cohort study. PG - e0218786 LID - 10.1371/journal.pone.0218786 [doi] LID - e0218786 AB - BACKGROUND: Liposomal amphotericin B (L-AMB) has been used for mucosal leishmaniasis (ML), but comparative studies on L-AMB and other drugs used for the treatment of ML have not been conducted. The present study aimed to evaluate the outcome of patients with ML who were treated with L-AMB. METHODS: This is a 15-year retrospective study of Brazilian patients with a confirmed diagnosis of ML. The therapeutic options for the treatment of ML consisted of L-AMB, amphotericin B lipid complex (ABLC), deoxycholate amphotericin B (d-AMB), itraconazole, antimonial pentavalent, or pentamidine. Healing, cure rate and adverse effects (AEs) associated with the drugs used to treat this condition were analyzed. RESULTS: In 71 patients, a total of 105 treatments were evaluated. The outcome of the treatment with each drug was compared, and results showed that L-AMB was superior to other therapeutic regimens (P = 0.001; odds ratio [OR] = 4.84; 95% confidence interval [CI] = 1.78-13.17). d-AMB had worse AEs than other treatment regimens (P = 0.001, OR = 0.09; 95% CI = 0.09-0.43). Approximately 66% of the patients presented with AEs during ML treatment. Although L-AMB was less nephrotoxic than d-AMB, it was associated with acute kidney injury compared with other drugs (P <0.05). CONCLUSION: L-AMB was more effective than other therapies for the treatment of ML. However, a high incidence of toxicity was associated with its use. Therapeutic choices should be reassessed, and the development of new drugs is necessary for the treatment of ML. FAU - Santos, Carolina Rocio AU - Santos CR AD - Departamento de Molestias Infecciosas e Parasitarias, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Sao Paulo, Brasil. FAU - Tuon, Felipe Francisco AU - Tuon FF AD - School of Medicine, Pontificia Universidade Catolica do Parana, Curitiba, Parana, Brasil. FAU - Cieslinski, Juliette AU - Cieslinski J AD - School of Medicine, Pontificia Universidade Catolica do Parana, Curitiba, Parana, Brasil. FAU - de Souza, Regina Maia AU - de Souza RM AD - Laboratorio de Parasitologia LIM-46, Instituto de Medicina Tropical, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Sao Paulo, Brasil. FAU - Imamura, Rui AU - Imamura R AD - Departamento de Otorrinolaringologia, Hospital das Clinicas HCFMUSP, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Sao Paulo, Brasil. FAU - Amato, Valdir Sabbaga AU - Amato VS AUID- ORCID: 0000-0003-1245-9348 AD - Departamento de Molestias Infecciosas e Parasitarias, Faculdade de Medicina, Universidade de Sao Paulo, Sao Paulo, Sao Paulo, Brasil. LA - eng PT - Comparative Study PT - Journal Article DEP - 20190626 PL - United States TA - PLoS One JT - PloS one JID - 101285081 RN - 0 (Antiprotozoal Agents) RN - 0 (Drug Combinations) RN - 0 (Liposomes) RN - 0 (liposomal amphotericin B) RN - 005990WHZZ (Deoxycholic Acid) RN - 304NUG5GF4 (Itraconazole) RN - 673LC5J4LQ (Pentamidine) RN - 7XU7A7DROE (Amphotericin B) RN - 87687-70-5 (amphotericin B, deoxycholate drug combination) RN - 9IT35J3UV3 (Antimony) SB - IM MH - Acute Kidney Injury/chemically induced MH - Adult MH - Aged MH - Aged, 80 and over MH - Amphotericin B/adverse effects/*therapeutic use MH - Antimony/adverse effects/therapeutic use MH - Antiprotozoal Agents/adverse effects/*therapeutic use MH - Brazil MH - Cohort Studies MH - Deoxycholic Acid/adverse effects/therapeutic use MH - Drug Combinations MH - Female MH - Humans MH - Itraconazole/adverse effects/therapeutic use MH - *Leishmania braziliensis MH - Leishmaniasis, Mucocutaneous/*drug therapy MH - Liposomes MH - Male MH - Middle Aged MH - Pentamidine/adverse effects/therapeutic use MH - Retrospective Studies MH - Treatment Outcome PMC - PMC6594680 COIS- The authors have declared that no competing interests exist. EDAT- 2019/06/27 06:00 MHDA- 2020/02/25 06:00 PMCR- 2019/06/26 CRDT- 2019/06/27 06:00 PHST- 2019/03/09 00:00 [received] PHST- 2019/06/11 00:00 [accepted] PHST- 2019/06/27 06:00 [entrez] PHST- 2019/06/27 06:00 [pubmed] PHST- 2020/02/25 06:00 [medline] PHST- 2019/06/26 00:00 [pmc-release] AID - PONE-D-19-06939 [pii] AID - 10.1371/journal.pone.0218786 [doi] PST - epublish SO - PLoS One. 2019 Jun 26;14(6):e0218786. doi: 10.1371/journal.pone.0218786. eCollection 2019.