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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Retrospective study of the digestive tract mucositis derived from myeloablative and non-myeloablative/reduced-intensity conditionings with busulfan in hematopoietic cell transplantation patient

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Author(s):
Eduardo, Fernanda P. [1] ; Bezinelli, Leticia Mello [1] ; Gobbi, Marcella [1] ; Rosin, Flavia C. P. [1] ; Carvalho, Danielle L. C. [1, 2] ; Ferreira, Mariana Henriques [1, 2] ; da Silva, Cinthya Correa [1] ; Hamerschlak, Nelson [1] ; Correa, Luciana [2]
Total Authors: 9
Affiliation:
[1] HIAE, Hematol Oncol, Ave Albert Einstein 627-701, BR-05652900 Sao Paulo - Brazil
[2] Univ Sao Paulo, Sch Dent, Gen Pathol Dept, Ave Prof Lineu Prestes 2227, BR-05508000 Sao Paulo - Brazil
Total Affiliations: 2
Document type: Journal article
Source: SUPPORTIVE CARE IN CANCER; v. 27, n. 3, p. 839-848, MAR 2019.
Web of Science Citations: 0
Abstract

Busulfan is a major component of chemotherapy conditioning in hematopoietic cell transplantation (HCT). This alkylating agent is highly toxic at myeloablative doses, exposing HCT patients to risks of mortality. Non-myeloablative (NMA) and reduced-intensity conditioning (RIC) using busulfan have shown impaired toxicity. However, the toxicity of NMA/RIC in the digestive tract is poorly described. This study aimed to characterize the mucositis in the oral cavity (OM), oropharynx/esophagus, and gastrointestinal tract derived from conditionings with myeloablative and non-myeloablative doses of busulfan. We retrospectively retrieved clinical data of HCT patients (n=100) who underwent myeloablative conditioning (MAC) or NMA/RIC with busulfan. Frequency and time duration of mucositis in the oral cavity and oropharynx/esophagus, diarrhea, and prescription of total parenteral nutrition (TPN) and opioids were also collected. OM severity (p=0.009) and time duration of mucositis in oropharynx/esophagus (p=0.022) were frequently higher in MAC than NMA/RIC. A myeloablative dose of busulfan was a risk factor for OM grade 2 (OR=4.8, p=0.002) and for mucositis in oropharynx/esophagus 5days (OR=2.64, p=0.035). A longer duration of mucositis in the oropharynx/esophagus was also associated with an increase in the prescription of opioids (OR=7.10, p<0.001).Overall survival (OS) in MAC was significantly higher than that in NMA/RIC (p=0.017). No variables related to mucositis interfere significantly in OS. In conclusion, myelosuppression in busulfan-based regimens are predisposed to a high risk for severe OM and to prolonged mucositis in the oropharynx/esophagus. (AU)

FAPESP's process: 16/03650-4 - Salivary and serum concentrations of busulfan and their association with salivary alterations and mucositis in patients undergoing hematopoietic stem cell transplantation.
Grantee:Fernanda de Paula Eduardo Simões
Support Opportunities: Regular Research Grants