TY - JOUR
T1 - Allogeneic hematopoietic stem cell transplantation in therapy-related myeloid neoplasms (t-MN) of the adult: Monocentric observational study and review of the literature
AU - Metafuni, Elisabetta
AU - Chiusolo, Patrizia
AU - Laurenti, Luca
AU - Sora', Federica
AU - Giammarco, Sabrina
AU - Bacigalupo, Andrea
AU - Leone, Giuseppe
AU - Sica, Simona
PY - 2018
Y1 - 2018
N2 - Background: Therapy related myeloid neoplasms (t-MN) occur due to direct mutational events of chemotherapeutic agents and radiotherapy. Disease latency, mutational events and prognosis vary with drugs categories. Methods: We describe a cohort of 30 patients, 18 females and 12 males, with median age of 52.5 years (range, 20 to 64), submitted to allogeneic stem cell transplantation (HSCT) in our department between September 1999 and March 2017. Patients had a history of solid tumour in 14 cases, haematological disease in 15 cases and both of them in one case. After a median of 36.5 months (range, 4 to 190) from first neoplasm, patients developed t-AML in 19 cases and t-MDS in 11 cases. Molecular abnormalities were detected in 5 patients, while karyotype aberrations were found in 17 patients. Patients received conventional chemotherapy in 14 cases, azacitidine in 10 cases and both of them in one case. Five patients were submitted to HSCT without previous treatment except for supportive therapy. Results: Seventeen patients obtained sustained CR after SCT, while 8 patients showed resistant or relapsed disease. The remaining five patients died early after SCT. At follow up time (May 2017) 13 patients were alive with a median OS of 48 months (range 3-195), while 17 patients died after a median of 4 months (range 1-27) by relapse mortality in 6 cases and non-relapse mortality in the other 11 patients. Conclusions: Global OS was 43%. After SCT, 72.2% of patients with t-MN maintained a sustained CR.
AB - Background: Therapy related myeloid neoplasms (t-MN) occur due to direct mutational events of chemotherapeutic agents and radiotherapy. Disease latency, mutational events and prognosis vary with drugs categories. Methods: We describe a cohort of 30 patients, 18 females and 12 males, with median age of 52.5 years (range, 20 to 64), submitted to allogeneic stem cell transplantation (HSCT) in our department between September 1999 and March 2017. Patients had a history of solid tumour in 14 cases, haematological disease in 15 cases and both of them in one case. After a median of 36.5 months (range, 4 to 190) from first neoplasm, patients developed t-AML in 19 cases and t-MDS in 11 cases. Molecular abnormalities were detected in 5 patients, while karyotype aberrations were found in 17 patients. Patients received conventional chemotherapy in 14 cases, azacitidine in 10 cases and both of them in one case. Five patients were submitted to HSCT without previous treatment except for supportive therapy. Results: Seventeen patients obtained sustained CR after SCT, while 8 patients showed resistant or relapsed disease. The remaining five patients died early after SCT. At follow up time (May 2017) 13 patients were alive with a median OS of 48 months (range 3-195), while 17 patients died after a median of 4 months (range 1-27) by relapse mortality in 6 cases and non-relapse mortality in the other 11 patients. Conclusions: Global OS was 43%. After SCT, 72.2% of patients with t-MN maintained a sustained CR.
KW - Hematology
KW - Hematopoietic stem cell transplantation
KW - Infectious Diseases
KW - Secondary leukemia
KW - Therapy-related myeloid neoplasm
KW - Hematology
KW - Hematopoietic stem cell transplantation
KW - Infectious Diseases
KW - Secondary leukemia
KW - Therapy-related myeloid neoplasm
UR - http://hdl.handle.net/10807/117518
UR - http://www.mjhid.org/index.php/mjhid/article/download/2018.005/pdf
U2 - 10.4084/MJHID.2018.005
DO - 10.4084/MJHID.2018.005
M3 - Article
SN - 2035-3006
VL - 10
SP - e2018005-007
JO - Mediterranean Journal of Hematology and Infectious Diseases
JF - Mediterranean Journal of Hematology and Infectious Diseases
ER -