ABSTRACT
BACKGROUND: Currently, pediatric-inspired regimens are commonly applied to adults with acute lymphoblastic leukemia (ALL) after the recent recognition that these protocols improve survival. While asparaginase in whatever available formulation is a key component of modern treatment of ALL, many adult oncologists and hematologists struggle to deal with its particular toxicities in clinical practice. We reviewed toxicity outcomes of pegylated asparaginase (PEG-ASP) in adults with ALL treated in 3 reference centers in Brazil. PATIENTS AND METHODS: This was a cross-sectional retrospective chart-review study encompassing patients aged 15 years and older diagnosed with ALL or ambiguous-lineage leukemia who received at least one dose of PEG-ASP, regardless of the adopted regimen. RESULTS: A total of 57 patients were included (age range, 15-57 years). Most patients (70%) received 2000 IU/m2 as the initial dose, by intravenous route (72%). The incidence of thromboembolic events was 17.5%, and the main site was cerebral venous sinus (4/10). Thrombosis was more frequent in patients receiving second-line treatment. In obese patients, grade 3 hepatotoxicity and hyperbilirubinemia were more common. Clinical pancreatitis (grade 3 or higher) was found in 2 of 57 cases. PEG-ASP had to be discontinued in 19.3% of exposed patients (11/57). CONCLUSION: By reviewing the medical charts of adult patients with ALL from 3 reference centers, we found that our incidence of thrombotic and hepatic adverse events is similar to those reported in other trials involving PEG-ASP. Usually these effects should not preclude further use of the drug because most events are manageable in routine clinical practice.
Subject(s)
Antineoplastic Agents/therapeutic use , Asparaginase/adverse effects , Asparaginase/therapeutic use , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Adolescent , Adult , Antineoplastic Agents/pharmacology , Asparaginase/pharmacology , Cross-Sectional Studies , Female , Humans , Male , Middle Aged , Retrospective Studies , Young AdultABSTRACT
Os pacientes com neoplasias hematológicas são submetidos a tratamento quimioterápico que induz uma intensa alteração na integridade da mucosa intestinal, favorecendo um aumento da sua morbi-mortalidade. O presente trabalho foi desenvolvido na Unidade de Transplante de Medula Óssea do Centro de Pesquisas Oncológicas em Florianópolis - SC e teve como objetivo estudar a ação do prebiótico na resposta de proteína da fase aguda de pacientes com neoplasias hematológicas submetidos à quimioterapia. Foi realizado um estudo clínico randomizado duplo cego envolvendo 25 pacientes divididos em dois grupos que receberam por 15 dias: 12g de FOS (n=14) ou placebo (maltodextrina) (n=11). Todas as variáveis foram determinadas antes e após a suplementação. Foram avaliados os níveis séricos das proteínas de fase aguda negativas (albumina e pré-albumina) e a proteína de fase aguda positiva, proteína C reativa (PCR). Verificaram-se a presença de diarréia e de constipação, bem como a quantidade de bifidobactérias e valores de pH fecal. A redução dos níveis séricos de proteínas de fase aguda negativas (albumina e pré-albumina) comprovam o intenso catabolismo protéico, priorizando a síntese de proteína de fase aguda positiva (PCR). O grupo suplementado apresentou um aumento significante na quantidade de bifidobactérias e o pH fecal não foi alterado em ambos os grupos. Os níveis séricos de PCR foram estatisticamente superiores no grupo controle, indicando a ocorrência de processos inflamatórios e maior demanda metabólica, sugerindo que a quantidade de bifidobactérias pode ter favorecido a redução deste quadro no grupo suplementado, confirmado pela correlação negativa entre estas variáveis.
Patients with hematologic neoplasias are submitted to chemotherapeutic treatment that induces intense alterations in the integrity of the intestinal mucous membrane, favoring an increase in the morbimortality rate. The current work was developed in the Bone Marrow Transplantation Unit of the Oncology Research Center in Florianopolis and was aimed at studying the action of prebiotic agents on protein response in the acute phase of hematologic neoplastic patients submitted to chemotherapy. A double-blind randomized clinical trial was performed involving 25 patients divided into two groups. Patients received 12 g FOS (n=14) or placebo (maltdextrine) (n=11) over 15 days. All the variables were determined before and after supplementation. The serum levels of negative acute phase proteins, albumin and pre-albumin, and positive acute phase proteins, C-reactive protein, were evaluated. The presence of diarrhea and constipation are reported, as are the quantity of bifidobacteria and fecal pH measurements. Reductions in the serum levels of negative acute phase proteins (albumin and pre-albumin) show intense proteic catabolism thereby, favoring the synthesis of protein in the positive acute phase. The supplemented group presented with a significant increase in the quantity of bifidobacteria. The fecal pH levels were affected in both groups. The serum levels of positive acute phase proteins were statistically higher in the control group indicating the occurrence of inflammatory processes and a higher metabolic demand suggesting that the quantity of bifidobacteria may favor a reduction of these adverse conditions in the supplemented group as was confirmed by the negative correlation between variables.
