Molecular response and prognostic factors of patients with Philadelphia chromosome/BCR-ABL-positive acute lymphoblastic leukemia treated by imatinib with chemotherapy
OBJECTIVE: To evaluate the molecular response and prognostic factors of patients with Philadelphia chromosome/BCR-ABL-positive acute lymphoblastic leukaemia (Ph⁺ ALL) treated by imatinib with chemotherapy.
METHODS: From May 2006 to July 2012, 82 adult Ph⁺ ALL patients were enrolled in the study. Forty-eight patients combined imatinib in, and 34 patients after induction therapy. Forty-nine patients underwent allogeneic hematopoietic stem cell transplant (allo-HSCT) after 3 to 5 cycles of consolidation therapy. The molecular response of BCR-ABL mRNA was evaluated by real-time quantitative PCR in every chemotherapy course ending.
RESULTS: The complete remission (CR) rate after the first cycle of induction chemotherapy was 76.8% (63/82), with overall CR rate of 92.7% (76/82). The CR rate in the patients combined imatinib in was higher than of those combined imatinib after the first cycle of induction chemotherapy (93.8% vs 52.9%, P<0.001). 55.3% patients BCR-ABL decreased >1 log after induction therapy. Among 76 CR patients, cumulative incidence of relapse was 27.6%, the probabilities of disease-free survival (DFS) and overall survival (OS) at 3 years were 60.5% and 70.2%, respectively. allo-HSCT was an independent favorable factor for decrease of leukemia relapse (P<0.001). allo-HSCT, imatinib combined in the first cycle of induction therapy and female were independent favorable factors for DFS (P<0.01, 0.05 and 0.01, respectively), BCR-ABL mRNA reduction at least 1 log from baseline after the first induction therapy and allo-HSCT were independent favorable factors for OS (P=0.011 and 0.027, respectively).
CONCLUSION: Imatinib combined in the first cycle of induction therapy, BCR-ABL mRNA reduction at least 1 log from baseline after the first induction therapy and allo-HSCT improved outcomes of Ph⁺ ALL patients.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2014 |
---|---|
Erschienen: |
2014 |
Enthalten in: |
Zur Gesamtaufnahme - volume:35 |
---|---|
Enthalten in: |
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi - 35(2014), 2 vom: 20. Feb., Seite 120-5 |
Sprache: |
Chinesisch |
---|
Beteiligte Personen: |
Wang, Jing [VerfasserIn] |
---|
Links: |
---|
Themen: |
8A1O1M485B |
---|
Anmerkungen: |
Date Completed 19.02.2015 Date Revised 19.11.2015 published: Print Citation Status MEDLINE |
---|
doi: |
10.3760/cma.j.issn.0253-2727.2014.02.013 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM236193244 |
---|
LEADER | 01000naa a22002652 4500 | ||
---|---|---|---|
001 | NLM236193244 | ||
003 | DE-627 | ||
005 | 20231224105040.0 | ||
007 | cr uuu---uuuuu | ||
008 | 231224s2014 xx |||||o 00| ||chi c | ||
024 | 7 | |a 10.3760/cma.j.issn.0253-2727.2014.02.013 |2 doi | |
028 | 5 | 2 | |a pubmed24n0787.xml |
035 | |a (DE-627)NLM236193244 | ||
035 | |a (NLM)24606652 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a chi | ||
100 | 1 | |a Wang, Jing |e verfasserin |4 aut | |
245 | 1 | 0 | |a Molecular response and prognostic factors of patients with Philadelphia chromosome/BCR-ABL-positive acute lymphoblastic leukemia treated by imatinib with chemotherapy |
264 | 1 | |c 2014 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Completed 19.02.2015 | ||
500 | |a Date Revised 19.11.2015 | ||
500 | |a published: Print | ||
500 | |a Citation Status MEDLINE | ||
520 | |a OBJECTIVE: To evaluate the molecular response and prognostic factors of patients with Philadelphia chromosome/BCR-ABL-positive acute lymphoblastic leukaemia (Ph⁺ ALL) treated by imatinib with chemotherapy | ||
520 | |a METHODS: From May 2006 to July 2012, 82 adult Ph⁺ ALL patients were enrolled in the study. Forty-eight patients combined imatinib in, and 34 patients after induction therapy. Forty-nine patients underwent allogeneic hematopoietic stem cell transplant (allo-HSCT) after 3 to 5 cycles of consolidation therapy. The molecular response of BCR-ABL mRNA was evaluated by real-time quantitative PCR in every chemotherapy course ending | ||
520 | |a RESULTS: The complete remission (CR) rate after the first cycle of induction chemotherapy was 76.8% (63/82), with overall CR rate of 92.7% (76/82). The CR rate in the patients combined imatinib in was higher than of those combined imatinib after the first cycle of induction chemotherapy (93.8% vs 52.9%, P<0.001). 55.3% patients BCR-ABL decreased >1 log after induction therapy. Among 76 CR patients, cumulative incidence of relapse was 27.6%, the probabilities of disease-free survival (DFS) and overall survival (OS) at 3 years were 60.5% and 70.2%, respectively. allo-HSCT was an independent favorable factor for decrease of leukemia relapse (P<0.001). allo-HSCT, imatinib combined in the first cycle of induction therapy and female were independent favorable factors for DFS (P<0.01, 0.05 and 0.01, respectively), BCR-ABL mRNA reduction at least 1 log from baseline after the first induction therapy and allo-HSCT were independent favorable factors for OS (P=0.011 and 0.027, respectively) | ||
520 | |a CONCLUSION: Imatinib combined in the first cycle of induction therapy, BCR-ABL mRNA reduction at least 1 log from baseline after the first induction therapy and allo-HSCT improved outcomes of Ph⁺ ALL patients | ||
650 | 4 | |a English Abstract | |
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 7 | |a Benzamides |2 NLM | |
650 | 7 | |a Piperazines |2 NLM | |
650 | 7 | |a Protein Kinase Inhibitors |2 NLM | |
650 | 7 | |a Pyrimidines |2 NLM | |
650 | 7 | |a Imatinib Mesylate |2 NLM | |
650 | 7 | |a 8A1O1M485B |2 NLM | |
650 | 7 | |a Fusion Proteins, bcr-abl |2 NLM | |
650 | 7 | |a EC 2.7.10.2 |2 NLM | |
700 | 1 | |a Huang, Xiaojun |e verfasserin |4 aut | |
700 | 1 | |a Jiang, Bin |e verfasserin |4 aut | |
700 | 1 | |a Qin, Yazhen |e verfasserin |4 aut | |
700 | 1 | |a Bao, Li |e verfasserin |4 aut | |
700 | 1 | |a Jiang, Hao |e verfasserin |4 aut | |
700 | 1 | |a Chen, Huan |e verfasserin |4 aut | |
700 | 1 | |a Jia, Jinsong |e verfasserin |4 aut | |
700 | 1 | |a Yang, Shenmiao |e verfasserin |4 aut | |
700 | 1 | |a Jiang, Qian |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi |d 1993 |g 35(2014), 2 vom: 20. Feb., Seite 120-5 |w (DE-627)NLM081873417 |x 0253-2727 |7 nnns |
773 | 1 | 8 | |g volume:35 |g year:2014 |g number:2 |g day:20 |g month:02 |g pages:120-5 |
856 | 4 | 0 | |u http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2014.02.013 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 35 |j 2014 |e 2 |b 20 |c 02 |h 120-5 |