GLORIA

GEOMAR Library Ocean Research Information Access

Ihre E-Mail wurde erfolgreich gesendet. Bitte prüfen Sie Ihren Maileingang.

Leider ist ein Fehler beim E-Mail-Versand aufgetreten. Bitte versuchen Sie es erneut.

Vorgang fortführen?

Exportieren
  • 1
    In: JBMTCT, Journal of Bone Marrow Transplantation and Cellular Therapy, Vol. 2, No. 1 ( 2021-03-11), p. 138-146
    Kurzfassung: THE BRAZILIAN SOCIETY FOR BLOOD AND MARROW TRANSPLANTATION (SBTMO) PRESENTS THE BRAZILIAN GUIDELINES ON HEMATOPOIETIC STEM CELL TRANSPLANTATION
    Materialart: Online-Ressource
    ISSN: 2675-374X
    URL: Issue
    Sprache: Unbekannt
    Verlag: Journal of Bone Marrow Transplantation and Cellular Therapy
    Publikationsdatum: 2021
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 2
    In: Archives of Medical Research, Elsevier BV, Vol. 47, No. 8 ( 2016-11), p. 656-667
    Materialart: Online-Ressource
    ISSN: 0188-4409
    Sprache: Englisch
    Verlag: Elsevier BV
    Publikationsdatum: 2016
    ZDB Id: 2010312-8
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 3
    Online-Ressource
    Online-Ressource
    Journal of Bone Marrow Transplantation and Cellular Therapy ; 2021
    In:  JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY Vol. 2, No. 4 ( 2021-12-01), p. 152-
    In: JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY, Journal of Bone Marrow Transplantation and Cellular Therapy, Vol. 2, No. 4 ( 2021-12-01), p. 152-
    Kurzfassung: Langerhans cell histiocytosis (LCH) is a rare disease, with an estimated incidence of 0.5 per 100,000 children in the United States of America1. HCL occurs due to differentiation of myeloid precursors into CD1a+ / CD207+ cells and is characterized by constitutional activation of the MAPK2 signaling pathway, leading to a spectrum of organ involvement and dysfunction. Treatment of HCL is risk-adjusted: single lesions may respond to local treatment whereas multisystem disease requires systemic therapy. Although survival for patients without organ dysfunction is excellent3, mortality in those with compromised organs at risk (hematopoietic system, liver, and/or spleen) reaches 20%2,4. Despite the progress made in the treatment of HCL, disease reactivation rates remain above 30% and the best second-line treatment has not yet been established. Treatment failure is associated with increased morbidity and mortality, including an association with neurodegeneration2. As it is a rare disease and generally has a good prognosis, few scientific studies are evaluating the role of allogeneic hematopoietic stem cell transplantation (HSCT) in the treatment of this disease. In 2015 Veys et al5 published retrospective results of 87 high-risk patients transplanted between 1990 and 2013. Myeloablative conditioning regimens (MAC) based on total body irradiation or busulfan6 were the most used until the 2000s, and reduced-intensity conditioning regimens (RIC) – predominantly a combination of Melphalan and Fludarabine – were most used between 2000 and 2013. Transplant-associated mortality rates in 3 years were similar between RIC and MAC conditioning regimens (21% versus 15%, respectively). Recurrence was higher in the RIC group compared to the MAC group (28% versus 8%, respectively), however, the 3-year overall survival (OS) was similar (77% versus 71%, respectively), since the patients who relapsed after RIC transplantation could be rescued with chemotherapy. More recently, Kudo et al7 published a retrospective study with 30 patients with refractory LCH who underwent HSCT between 1996 and 2014. Eleven patients received myeloablative conditioning regimen based on total body radiotherapy (RCT) with a dose equal to or greater than 8 Gy or busulfan, and 19 of reduced intensity based on Fludarabine and Melphalan, associated or not with low dose of RCT. There was no significant difference between the conditioning regimen modalities, with OS of 56.8% for the RIC group and 63.6% for the MAC group. Disease status was the main prognostic factor, with a 5-year OS of 100% for patients who arrived at HSCT with disease in remission or with partial remission, versus 54.5% for those who had active disease at the time of the procedure. Regarding the type of donor used and the source of stem cells, there is great variation, with greater frequency for unrelated and extensive use of bone marrow and umbilical cord, and apparently, there is no impact on survival rates.5, 6 There are few case reports and extremely restricted performance of autologous HSCT in HCL.
    Materialart: Online-Ressource
    ISSN: 2675-374X
    URL: Issue
    Sprache: Unbekannt
    Verlag: Journal of Bone Marrow Transplantation and Cellular Therapy
    Publikationsdatum: 2021
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 4
    In: Pediatric and Developmental Pathology, SAGE Publications, Vol. 16, No. 5 ( 2013-09), p. 387-390
    Kurzfassung: Although children with osteosarcoma have a higher incidence of a 2nd malignancy than the general population, its development in the lung is rare. The few reported cases belong to examples of carcinomas. Here we present the case of a 13-year-old boy with a primary pulmonary adenocarcinoma diagnosed 3 years after the osteosarcoma diagnosis and present a review of the literature.
    Materialart: Online-Ressource
    ISSN: 1093-5266 , 1615-5742
    Sprache: Englisch
    Verlag: SAGE Publications
    Publikationsdatum: 2013
    ZDB Id: 1480654-X
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 5
    In: Blood, American Society of Hematology, Vol. 136, No. Supplement 1 ( 2020-11-5), p. 3-4
    Kurzfassung: Introduction: Children with newly diagnosed acute myeloid leukemia (AML) may have a high early mortality when resources are limited by infrastructure or by a widespread worldwide crisis, as being faced with the SARS-Cov-2 pandemic. Many elective treatments were postponed, but newly diagnosed AML is a life-threatening disease that needs prompt therapy. With acute shortage of infra-structure as intensive care unit beds, blood supply, medication, healthcare personnel, an optimal therapy must balance anti-neoplastic efficacy and the chance of treatment-related mortality. The induction chemotherapy of pediatric patients with AML living in low- and middle-income countries has been thoroughly discussed because early mortality remains 10%-20%, much higher than in developed counties. Mild treatment schemas have been used in Japan, China and Latin America with impressive results, comparable to other intensive induction regimens. Our objective is to describe the results of this mild induction regimen used in Brazil to treat children simultaneously diagnosed with AML and Covid-19 infections. Methods: This is a retrospective multicentric trial including Brazilian children diagnosed with AML, also found to have a positive nasal and oropharyngeal PCR for SARS-Cov-2 and uniformly treated with mild induction protocol ("MAG") that included Mitoxantrone at 5 mg/m2, by i.v. infusion over 4 to 6 hours once a day on days 1, 3, and 5 (three doses in total), Cytarabine at 10 mg/m2, subcutaneous (s.c.), q 12 h for 10 days (20 doses in total) and G-CSF 5 𝜇 g/kg, s.c., once a day for 10 days (10 doses in total) [Bansal D, et al. Pediatr Blood Cancer. 2019 Nov 27:e28087]. Results: From March 15 to July 1, 2020, nine children from four different institutions were diagnosed with AML (Table 1). Their median age was 9 years (range, 5 to 18), 6 female gender, all but one diagnosed with Covid-19 by nasal PCR; one had typical chest CT and positive IgM. The institutions had previously agreed on following the same induction when treating AML children infected by the SARS-Cov-2. Five of the nine had severe illness, three of them needed mechanical ventilation and one did not need supplementary oxygen despite radiologically diagnosed pneumonia. Two children had mild symptoms and two were completely asymptomatic. All children tolerated MAG chemotherapy. Neutropenia lasted for a median of 29 days (17-33) and none of them had neither thrombotic complications nor acute renal failure. All children recovered from the Covid-19 infection and 8 of 9 already evaluable children achieved complete remission of the leukemia with MRD 0-1% after the two planned cycles. All patients are alive, on therapy. Table 1: Patients characteristics Pt#AgeGenderAML-FABMolecular BiologyCytogeneticsCNS diseaseSeverelly IllDuration of Neutropenia (days)Response to 1st InductionResponse to 2nd InductionCOVID SymptomsOxygen TherapyCOVID TreatmentStatus19MM0NegativeComplex karyotype with del11NoNo330% blastsMRD 0,12%NoneNoAAlive28FM2Negativet(10,11)NoYes261% blastsToo earlyInflamatory syndromeMechanical VentilationA,C,IVIGAlive317FNOSNegativeNormalNoYes227% blastsMRD 1%PneumoniaMechanical VentilationA,I,O,C,HAlive45MM4EoInv16Inv. 16NoYes222% blastsMRD negativeMildNo-Alive58MM2Amltot(8;21)YesYes190%MRD negativeNoneNoAAlive68FNOSNot doneNot doneNoNo254% blastsMRD negativePneumoniaNoA,O,CAlive710FNOSNot doneTrisomy 22NoYes17Too earlyToo earlyPneumonia, Respiratory DistressMechanical VentilationA,O,C, IVIGAlive810FM5ASXL1NormalNoNo310%Too earlyNoneNoA,I,CiproAlive918FM2NegativeNot doneNoNo270%MRD negativeMildNoAAlive A - Azythromycin; I - Ivermectin; C - Corticosteroids, O - Oseltamivir; IVIG - Immunoglobulin; H- Heparin; Cipro- Coprofloxacin Conclusions: Against all odds, MAG was well tolerated in children and adolescents newly diagnosed with AML and active Covid-19, with no treatment-related mortality. All evaluable patients achieved remission and are currently proceeding therapy. The high prevalence of Covid-19 in our country may have to be taken into account in all oncological treatment strategies. With a shorter duration of neutropenia, the absence of mucositis or invasive fungal infections, MAG may be implemented in low- and middle-income countries as an optimal strategy to overcome induction mortality and improve outcome of children and adolescents with AML. Disclosures No relevant conflicts of interest to declare.
    Materialart: Online-Ressource
    ISSN: 0006-4971 , 1528-0020
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: American Society of Hematology
    Publikationsdatum: 2020
    ZDB Id: 1468538-3
    ZDB Id: 80069-7
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 6
    Online-Ressource
    Online-Ressource
    Journal of Bone Marrow Transplantation and Cellular Therapy ; 2021
    In:  JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY Vol. 2, No. 4 ( 2021-11-30), p. 128-
    In: JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY, Journal of Bone Marrow Transplantation and Cellular Therapy, Vol. 2, No. 4 ( 2021-11-30), p. 128-
    Kurzfassung: Juvenile Myelomonocytic Leukemia (JMML) is a clonal hematopoietic disorder that usually occurs in early childhood, characterized by hyperactivation of the RAS signaling pathway. About 90% of patients have mutations in 1 of 5 genes (PTPN11, NRAS, KRAS, NF1, CBL) that define genetically and clinically distinct subtypes of the disease, with a highly variable clinical course. Allogeneic hematopoietic stem cell transplantation (HSCT) remains the therapy of choice for most patients with JMML, although children with CBL mutations and few of those with N-RAS mutations may have spontaneous resolution of hematologic abnormalities. The results of HSCT in patients with JMML have progressively improved over time, but relapse is still an important cause of treatment failure.
    Materialart: Online-Ressource
    ISSN: 2675-374X
    URL: Issue
    Sprache: Unbekannt
    Verlag: Journal of Bone Marrow Transplantation and Cellular Therapy
    Publikationsdatum: 2021
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 7
    Online-Ressource
    Online-Ressource
    Journal of Bone Marrow Transplantation and Cellular Therapy ; 2021
    In:  JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY Vol. 2, No. 4 ( 2021-11-30), p. 127-
    In: JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY, Journal of Bone Marrow Transplantation and Cellular Therapy, Vol. 2, No. 4 ( 2021-11-30), p. 127-
    Kurzfassung: MDS in children is a rare group of hematopoietic stem cell clonal disorder. Allogeneic HSCT is the only curative treatment. HLA typing and the search for a compatible donor must be carried out upon diagnosis, for all patients.  However, patients with refractory cytopenia of childhood without an unfavorable karyotype can keep the disease stable for a long time. Thus, in the absence of transfusion dependence or severe neutropenia, a careful observation strategy without treatment is recommended. The treatment of children diagnosed with MDS with excess blasts remains a major challenge. Allogeneic HSCT is the only curative treatment, although the data published in the literature generally include a small number of patients, heterogeneously transplanted. For children with MDS secondary to therapy, despite HSCT, the evolution is generally unfavorable.
    Materialart: Online-Ressource
    ISSN: 2675-374X
    URL: Issue
    Sprache: Unbekannt
    Verlag: Journal of Bone Marrow Transplantation and Cellular Therapy
    Publikationsdatum: 2021
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
  • 8
    Online-Ressource
    Online-Ressource
    Journal of Bone Marrow Transplantation and Cellular Therapy ; 2021
    In:  JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY Vol. 2, No. 4 ( 2021-11-30), p. 129-
    In: JOURNAL OF BONE MARROW TRANSPLANTATION AND CELLULAR THERAPY, Journal of Bone Marrow Transplantation and Cellular Therapy, Vol. 2, No. 4 ( 2021-11-30), p. 129-
    Kurzfassung:   In addition to the chronic myeloid leukemia (CML) BCR-ABL1+, classic myeloproliferative neoplasms include polycythemia vera, essential thrombocythemia and primary myelofibrosis. These have a very low incidence in the pediatric age group and there is no consensus on treatment in children.
    Materialart: Online-Ressource
    ISSN: 2675-374X
    URL: Issue
    Sprache: Unbekannt
    Verlag: Journal of Bone Marrow Transplantation and Cellular Therapy
    Publikationsdatum: 2021
    Standort Signatur Einschränkungen Verfügbarkeit
    BibTip Andere fanden auch interessant ...
Schließen ⊗
Diese Webseite nutzt Cookies und das Analyse-Tool Matomo. Weitere Informationen finden Sie hier...