Search citation statements
Paper Sections
Citation Types
Year Published
Publication Types
Relationship
Authors
Journals
Cerebellar toxicity in the form of ataxia and slurring of speech: case reportA 19-year-old man developed cerebellar toxicity in the form of ataxia and slurring of speech during treatment with cytarabine for acute myeloid leukaemia (AML).The man, who was diagnosed with AML, started receiving unspecified antibacterials [antibiotics] and empirical amphotericin-Bliposomal [liposomal amphotericin]. He started receiving nasal oxygen and admitted in the ICU. He was shifted to HEPA filter room following day on nasal oxygen. He received hydroxycarbamide [hydroxyurea]. Further, investigation suggested possible infective endocarditis. Then, amphotericin-B-liposomal was continued and polymyxin B was started empirically. He was noted to have hyperbilirubinaemia. One week following admission, he continued to be hypoxic on supplemental oxygen requirement. Further, he received azacitidine, anidulafungin and venetoclax. Although, he continued to have fever, tachycardia, tachypnoea and worsening liver function tests. Based on findings, hemophagocytic lymphohistiocytosis was suspected. Later, he was treated with hydrocortisone, immune globulin and methylprednisolone. Eventually, his condition improved. Further, methylprednisolone was changed to dexamethasone. The dual antifungal treatment with amphotericin-B-liposomal and anidulafungin completed for 14 days. Based on his continuous improvement, he was discharged. He was found to have presence of mutation in WT1 and PTPN11 genes. Then, he received first cycle consolidation with cytarabine [route and dosage not stated]; however, he developed cerebellar toxicity in the form of ataxia and slurring of speech 24 hours following the last dose of cytarabine.The man was received conservative treatment and a complete recovery with mild slurring of speech was noted. He underwent successful matched sibling allogeneic stem cell transplantation.
Cerebellar toxicity in the form of ataxia and slurring of speech: case reportA 19-year-old man developed cerebellar toxicity in the form of ataxia and slurring of speech during treatment with cytarabine for acute myeloid leukaemia (AML).The man, who was diagnosed with AML, started receiving unspecified antibacterials [antibiotics] and empirical amphotericin-Bliposomal [liposomal amphotericin]. He started receiving nasal oxygen and admitted in the ICU. He was shifted to HEPA filter room following day on nasal oxygen. He received hydroxycarbamide [hydroxyurea]. Further, investigation suggested possible infective endocarditis. Then, amphotericin-B-liposomal was continued and polymyxin B was started empirically. He was noted to have hyperbilirubinaemia. One week following admission, he continued to be hypoxic on supplemental oxygen requirement. Further, he received azacitidine, anidulafungin and venetoclax. Although, he continued to have fever, tachycardia, tachypnoea and worsening liver function tests. Based on findings, hemophagocytic lymphohistiocytosis was suspected. Later, he was treated with hydrocortisone, immune globulin and methylprednisolone. Eventually, his condition improved. Further, methylprednisolone was changed to dexamethasone. The dual antifungal treatment with amphotericin-B-liposomal and anidulafungin completed for 14 days. Based on his continuous improvement, he was discharged. He was found to have presence of mutation in WT1 and PTPN11 genes. Then, he received first cycle consolidation with cytarabine [route and dosage not stated]; however, he developed cerebellar toxicity in the form of ataxia and slurring of speech 24 hours following the last dose of cytarabine.The man was received conservative treatment and a complete recovery with mild slurring of speech was noted. He underwent successful matched sibling allogeneic stem cell transplantation.
SummaryVenetoclax (VEN) combined with hypomethylating agents (HMA) decitabine or azacitidine is used for adult acute myeloid leukaemia (AML), but its application in paediatric, adolescent and young adult (AYA) AML lacks prospective studies. We performed a retrospective chart review of paediatric and AYA AML patients treated with HMA + VEN at Cincinnati Children's Hospital Medical Centre. Twenty‐seven patients received 30 HMA + VEN treatment courses for relapsed/refractory (R/R, n = 21) or newly diagnosed (n = 9) AML due to ineligibility for intensive chemotherapy. The R/R cohort had high‐risk cytomolecular genetic alterations and prior extensive treatments, with 50% (n = 9) of relapse patients (n = 18) having undergone haematopoietic stem cell transplantation (HSCT). Venetoclax treatment using the 400 mg adult exposure‐equivelant dosing (AED) had a median duration of 21 days (range 7–30 days). Grade 3–4 toxicities included neutropenia (90%), anaemia (64%), thrombocytopenia (64%) and febrile neutropenia (44%). The overall complete remission (CR)/CR with incomplete blood count recovery (CRi) rate was 73% (77% minimal residual disease [MRD] negativity <0.1%), with 60% undergoing HSCT. Among newly diagnosed patients (n = 9), 89% achieved CR/CRi (78% MRD negativity) and 78% proceeded to HSCT. The R/R cohort (n = 21) showed a 67% CR/CRi rate (71% MRD negativity), with 52% undergoing HSCT. These findings support the safety and efficacy of HMA + VEN in paediatric/AYA AML, indicating it as a viable option for patients unfit for intensive chemotherapy. Further studies are necessary to determine optimal venetoclax dosing, chemotherapy combinations and pharmacokinetics in this population.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
customersupport@researchsolutions.com
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
This site is protected by reCAPTCHA and the Google Privacy Policy and Terms of Service apply.
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.