Actualización de resultados demográficos y terapéuticos de pacientes con Leucemia Mieloide Aguda no promielocítica en el Hospital Clínico de la Pontificia Universidad Católica de Chile / Acute myeloid leukemia. Analysis of 114 patients

BACKGROUND: Acute myeloid leukemia (AML) is the most common leukemia in adults. Aim: To Describe our population of patients with AML and report the outcomes of our treatments. MATERIAL AND METHODS: Review of electronic clinical records of 114 patients with AML with a median age of 57 years (59% men). Results: Seventeen percent of patients were classified as low risk, 38% as intermediate risk and 33% as high risk. Seventy-six percent of patients were treated with intensive chemotherapy. Five years overall survival according to cytogenetic risk was 59, 41, and 12% in low, intermediate, and high-risk patients, respectively. The outcomes were better in patients under 60 years. The median survival of patients treated with intensive chemotherapy aged less than 60 years and 60 years and above was 3.4 and 1 year, respectively. CONCLUSIONS: Our results are comparable to those reported in developed countries. Improving the survival of patients 60 years and older is our main challenge.

Resultados a largo plazo de una cohorte chilena: la edad del paciente no incide en el resultado del trasplante alogénico de precursores hematopoyéticos para leucemia mieloide aguda

Background: In our country, transplantation centers differ in the age limit for allogeneic hematopoietic transplantation (ALOHT). In our program, transplants with age- adjusted conditioning are performed in patients until 70 years old. Currently more than 60% of ALOHT reported to the Center for International Bone Marrow Transplantation Research (CIBMTR) are performed in patients older than 40 years. Aim: To report our experience with ALOHT in acute myelogenous leukemia (AML), analyzing patient age at transplantation in different periods and transplant results in different age groups. Material and Methods: A retrospective analysis of the database of adult hematopoietic transplants in AML patients was performed. Demographic data, disease characteristics, transplant data, survival and relapse times, and mortality were collected. Results: In our program, 1030 transplants were performed in adults and 119 ALOHT were performed in AML patients, between 1990 and 2020. The median age of patients in all periods was 41 years, (range 16-69). The median age was 33 and 45 years, in the periods 1990-2000 and 2000-2020 respectively (p < 0.01). Seventy-eight patients received myeloablative conditioning (median age 44 years) and 41 reduced intensity conditioning (median age 53 years). Five-year overall survival was 44.6% (confidence intervals (CI) 41-48). Non relapse mortality of all periods was 19% (CI 17 - 40%) and relapse rate was 17 % (CI 16-22). No difference in five years overall survival among patients younger than 40, 41 to 50 and over 51 years was observed. Conclusions: Overall Survival, non-relapse mortality and relapse rate were similar in younger and older patients in our program and similar to those previously reported in other centers.

Asociación entre enfermedad de von Willebrand y angiodisplasia: ¿casualidad o causalidad? / Association between von Willebrand disease and angiodysplasia

Von Willebrand factor (vWf) is a fundamental multimeric plasma glycoprotein in the coagulation process. Its function is to mediate platelet adhesion and to stabilize circulating factor VIII. A functional or quantitative alteration of vWf gives rise to von Willebrand disease (vWD). The association between vWD and angiodysplasia was described in 1967, but it was only until 2011 that Starke et al demonstrated the in vitro and in vivo role of vWf in angiogenesis. Congenital or acquired vWf deficiency, especially of high molecular weight multimeters, not only favors bleeding, but also contributes to increased angiogenesis in these patients. The treatment should be focused both on the control of the acute episode of gastrointestinal bleeding, with vWf replacement therapy and local endoscopic treatment, as well as on the prevention of the progression of angiodysplasia and future bleeding. There are different published therapeutic approaches using vWf replacement that are not effective in all patients. Recently, angiogenesis inhibitor medications have been used.

Erradicación de Helicobacter pylori para la trombocitopenia inmune: protocolo de una revisión sistemática / Eradication of Helicobacter pylori for immune thrombocytopenia: protocol of a systematic review

Introducción: La trombocitopenia inmune es una enfermedad caracterizada por destrucción plaquetaria mediada por anticuerpos. Se ha planteado que Helicobacter pylori podría actuar como gatillante y modulador de dicha enfermedad, por lo que el objetivo de esta revisión es evaluar si la erradicación de este agente podría constituir un tratamiento efectivo para la trombocitopenia inmune. Métodos: El protocolo fue diseñado, y será reportado, en línea con Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P). Se realizará una búsqueda de estudios controlados aleatorizados, que incluyan pacientes con trombocitopenia inmune y que hayan recibido terapia de erradicación para Helicobacter pylori. Los desenlaces a evaluar serán el sangrado, la mortalidad, la necesidad de esplenectomía, el incremento en el recuento plaquetario, entre otros. Realizaremos búsquedas sensibles en MEDLINE, CENTRAL y EMBASE, sin restricción por lenguaje o publicación, las cuales serán complementadas con búsquedas en otras fuentes. Al menos dos investigadores realizarán de manera independiente la selección de los estudios y la extracción de los datos. Se evaluará el riesgo de sesgo utilizando la herramienta recomendada por la colaboración Cochrane. Se realizará metanálisis y se presentarán los datos mediante el método GRADE. Fortalezas y debilidades: Esta revisión sistemática entregará una síntesis rigurosa y actualizada de los efectos de la erradicación de Helicobacter pylori en la trombocitopenia inmune. La principal limitación podría provenir de la baja revisión sistemática (PROSPERO): CRD42015022161.(AU)

Background: Immune Thrombocytopenia is a condition characterized by antibody-mediated platelet destruction. Helicobacter pylori has been postulated as a potential trigger or modulator in this disease, so Helicobacter pylori eradication has been proposed as a reported in line with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses Protocols (PRISMA-P). We will conduct a search of randomized controlled trials, including patients with immune thrombocytopenia that received eradication therapy for Helicobacter pylori. The evaluated outcomes will be bleeding, mortality, need of splenectomy, platelet count, among others. We will develop sensitive search strategies for MEDLINE, EMBASE and CENTRAL, with no language or publication restriction. We will complement electronic searches with other sources. At least two reviewers will independently select trials and extract data. We will use Cochrane tool for risk of bias assessment to assess included studies. We will conduct meta-analysis and data will be presented using the GRADE approach. Strengths and limitations: This systematic review will provide a rigorous and updated summary of the effects of Helicobacter pylori eradication on immune thrombocytopenia. The main limitation might arise from the low quantity or quality of trials identified for this topic. Systematic review register number (PROSPERO): CRD42015022161(AU)