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[Clinical analysis of acute myeloid leukemia with t(8;21) (q22;q22) and loss of Y chromosome].
Zhu, Cheng-Ying; Yang, Hua; Niu, Jian-Hua; Zhang, Qi; Xie, Xu-Lei; Wang, Li-Jun; Zhu, Hai-Yan; Yao, Zi-Long; Yu, Li; Jing, Yu.
Afiliación
  • Zhu CY; Department of Hematology, Chinese PLA General Hospital Beijing 1000853.
  • Yang H; Department of Hematology, Chinese PLA General Hospital Beijing 1000853.
  • Niu JH; Department of Hematology, The Forth People's Hospital of Jinan, Jinan 250031, Shandong Province, China.
  • Zhang Q; Department of Hematology, People's Hospital of Gaochun, Nanjing 211300, Jiangsu Province, China.
  • Xie XL; Department of Hematology, The First People's Hospital of Baoding, Baoding 071000, Hebei Province, China.
  • Wang LJ; Department of Hematology, Chinese PLA 264 Hospital, Taiyuan 030001, Shaixi Province, China.
  • Zhu HY; Department of Hematology, Chinese PLA General Hospital Beijing 1000853.
  • Yao ZL; Department of Hematology, Chinese PLA General Hospital Beijing 1000853.
  • Yu L; Department of Hematology, Chinese PLA General Hospital Beijing 1000853.
  • Jing Y; Department of Hematology, Chinese PLA General Hospital Beijing 1000853. E-mail :jingyu301@126.com.
Zhongguo Shi Yan Xue Ye Xue Za Zhi ; 22(4): 950-6, 2014 Aug.
Article en Zh | MEDLINE | ID: mdl-25130809
ABSTRACT
This study was aimed to investigate the clinical characteristics of acute myeloid leukemia (AML) with t (8;21) (q22;q22) and loss of Y chromosomes. Clinical data of 267 cases of AML were collected from January 2010 to June 2013. Among 267 AML, there were 13 cases with t (8;21) (q22;q22) and loss of Y chromosomes. The clinical data including clinical indicators, treatment protocols, curative effect and prognosis were analyzed retrospectively. The results showed that after normalized chemotherapy, there were 4 patients with complete remission at the first cycle of treatment, 4 patients with complete remission at the second cycle, 4 patients with complete remission at the third cycle, but one patient without complete remission after 4 cycles. There were 6 patients who did not relapse during consolidation and intensive therapy. Among these 6 patients, 4 cases accepted chemotherapy combined with transplantation, other 2 cases accepted chemotherapy. In the remainder 6 patients, 4 cases relapsed once, one cases relapsed twice, 1 cases relapsed for three times. Moreover, 2 cases who accepted the chemotherapy and auto-hematopoietic stem cell trans-plantation, were diagnosed as relapse, after accepted allo-hematopoietic stem cell transplantation, currently are in disease-free status. In follow-up period, the relapse-free survival (RFS) time was 4.67 ± 3.45 months in chemotherapy group, the RFS time is 34.17 ± 21.37 months in chemotherapy and transplantation group. The chemotherapy combined with transplantation extended the RFS time (P < 0.05). It is concluded that the NCCN guide indicates that AML with t (8;21) ( q22;q22) showed a good prognosis. but the clinical course of treatment confirmed that the prognosis of AML patients with t (8;21) (q22;q22) and loss Y chromosomes is poor, including uneasy remission and easy relapse, for improving the prognosis of these patients, the hematopoietic stem cell transplantation should be recommended.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Translocación Genética / Leucemia Mieloide Aguda / Deleción Cromosómica Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Translocación Genética / Leucemia Mieloide Aguda / Deleción Cromosómica Tipo de estudio: Guideline / Observational_studies / Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: Zh Revista: Zhongguo Shi Yan Xue Ye Xue Za Zhi Asunto de la revista: HEMATOLOGIA Año: 2014 Tipo del documento: Article
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