Results 191 to 200 of about 26,607 (237)
Some of the next articles are maybe not open access.

Acute Promyelocytic Leukemia

New England Journal of Medicine, 1993
Perhaps the most important advance in this field is not the specific actions of all-trans-retinoic acid in acute promyelocytic leukemia, but rather the conclusive documentation of differentiation as a practical and consistently effective method of treating human cancer. As a drug, all-trans-retinoic acid has certain undesirable pharmacologic properties
R P, Warrell   +3 more
openaire   +2 more sources

Thrombosis in acute promyelocytic leukemia

Thrombosis Research, 2013
Compared to bleeding, major thromboses are a less commonly encountered problem in acute promyelocytic leukemia (APL), and our knowledge about the epidemiology of major thromboses in APL stems mainly from individual case reports. The purpose of this study was to provide a better understanding of the epidemiology of APL-related thrombosis as a first step
Armin, Rashidi   +3 more
openaire   +2 more sources

Retinoic Acid and Arsenic Trioxide for Acute Promyelocytic Leukemia

open access: yesNew England Journal of Medicine, 2013
All-trans retinoic acid (ATRA) with chemotherapy is the standard of care for acute promyelocytic leukemia (APL), resulting in cure rates exceeding 80%.
Giuseppe Avvisati   +2 more
exaly   +2 more sources

Management of acute promyelocytic leukemia

Current Oncology Reports, 2002
Acute promyelocytic leukemia (APL) has become the most potentially curable subtype of acute myeloid leukemia (AML) in adults. With current treatment strategies that incorporate all-trans retinoic acid (ATRA), long-term disease-free survival and potential cure rates of 70% to 80% can be expected.
Martin S, Tallman, Chadi, Nabhan
openaire   +2 more sources

Acute Promyelocytic Leukemia: A Perspective

Clinical Lymphoma Myeloma and Leukemia, 2017
Treatment of patients with acute promyelocytic leukemia has significantly improved with the introduction of target specific agents all-trans retinoic acid (ATRA) and arsenic trioxide (ATO) with long term survival a reality for the majority of patients.
Farhad Ravandi, Richard Stone
openaire   +2 more sources

The biology of acute promyelocytic leukemia

Current Oncology Reports, 2001
Acute promyelocytic leukemia (APL) is a disease associated with fusion oncoproteins invariably involving the retinoic acid receptor (Raralpha). Retinoic acid induces differentiation in APL cells and is successfully used in conjunction with chemotherapy to treat and cure a significant percentage of patients with APL.
K K, Mann, W, Shao, W H, Miller
openaire   +2 more sources

Coagulopathy of Acute Promyelocytic Leukemia

Acta Haematologica, 2001
Life-threatening bleeding is frequent in acute leukemias, particularly in acute promyelocytic leukemia (APL), a distinct subtype of acute myelogenous leukemia, characterized by the balanced reciprocal translocation between chromosomes 15 and 17.
A, Falanga, T, Barbui
openaire   +2 more sources

Acute promyelocytic leukemia in childhood

Current Oncology Reports, 2009
Acute promyelocytic leukemia (APL) is a relatively rare form of acute myelogenous leukemia (AML). In the United States, APL in children constitutes only 5% to 10% of AML. Molecularly, the disease is characterized by a fusion protein, promyelocytic leukemia (PML)-retinoic acid receptor (RAR)-alpha that results from a balanced reciprocal translocation ...
John, Gregory, James, Feusner
openaire   +2 more sources

Acute promyelocytic leukemia

Current Treatment Options in Oncology, 2000
The treatment of acute promyelocytic leukemia (APL) is different from other subtypes of acute myelocytic leukemia (AML). All trans-retinoic acid (ATRA) is an essential component of the standard remission induction for all newly diagnosed APL patients. Remission induction with ATRA and chemotherapy given concurrently appears to be associated with fewer ...
openaire   +2 more sources

Acute promyelocytic leukemia in children

Medical and Pediatric Oncology, 1981
AbstractSixteen children (ages 2–17) with acute promyelocytic leukemia (APL) were studied retrospectively. Diagnosis was based on clinical features and morphological criteria of the FAB classification. Bleeding diathesis was the predominant presenting symptom (>85%), associated with laboratory findings of disseminated intravascular coagulation (DIC).
K W, Chan, P G, Steinherz, D R, Miller
openaire   +2 more sources

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