Secondary clonal hematologic neoplasia following successful therapy for acute promyelocytic leukemia (APL): A report of two cases and review of the literature

Autor: Daria Gaut, Gary J. Schiller, Joshua P. Sasine
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Acute promyelocytic leukemia
Monosomy
medicine.medical_treatment
FISH
fluorescence in situ hybridization

ATRA
all-trans retinoic acid

Acute myelocytic leukemia (AML)
Bioinformatics
lcsh:RC254-282
Therapy-related myelodysplastic syndrome (t-MDS)
Article
03 medical and health sciences
0302 clinical medicine
Myelodysplastic syndrome (MDS)
Acute promyelocytic leukemia apl
immune system diseases
hemic and lymphatic diseases
ATO
arsenic trioxide

medicine
neoplasms
Complete response
Chromosome 7 (human)
Chemotherapy
PML-RARalpha
promyelocytic leukemia/Retinoic acid receptor alpha

business.industry
Clonal hematopoiesis
6-MP
6-mercaptopurine

Chromosome
Hematology
Secondary clone
CR
complete remission

lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
medicine.disease
Oncology
APL
acute promyelocytic leukemia

t-AML
therapy-related acute myelocytic leukemia

030220 oncology & carcinogenesis
t- MDS
therapy-related myelodysplastic syndrome

AML
acute myelocytic leukemia

ATG
antithymyocyte globulin

MDS
myelodysplastic syndrome

business
030215 immunology
Therapy-related acute myelocytic leukemia (t-AML)
Zdroj: Leukemia Research Reports
Leukemia Research Reports, Vol 9, Iss, Pp 65-71 (2018)
ISSN: 2213-0489
Popis: Although rare, secondary clonal hematologic neoplasia may occur after successful therapy for acute promyelocytic leukemia (APL). These secondary clonal events may be considered therapy-related, but may also be due to an underlying background of clonal hematopoiesis from which both malignancies may develop. In this manuscript, we describe two patients with secondary clones after APL therapy characterized in one patient by deletion of chromosome 11q23 and, in the other, by monosomy of chromosome 7, and also provide a review of all secondary clonal disorders described after APL therapy. We suggest that since most reports identify karyotypic abnormalities not typically associated with chemotherapy, there may be another mechanism underlying secondary clonal development after complete response to initial APL therapy. Keywords: Acute myelocytic leukemia (AML), Secondary clone, Myelodysplastic syndrome (MDS), Therapy-related acute myelocytic leukemia (t-AML), Therapy-related myelodysplastic syndrome (t-MDS)
Databáze: OpenAIRE