Better transplant outcome with pre-transplant marrow response after hypomethylating treatment in higher-risk MDS with excess blasts

被引:37
作者
Yahng, Seung-Ah [1 ]
Kim, Myungshin [2 ,3 ]
Kim, Tae-Min [4 ]
Jeon, Young-Woo [5 ]
Yoon, Jae-Ho [5 ]
Shin, Seung-Hwan [6 ]
Lee, Sung-Eun [5 ]
Eom, Ki-Seong [3 ,5 ]
Lee, Seok [3 ,5 ]
Min, Chang-Ki [3 ,5 ]
Kim, Hee-Je [3 ,5 ]
Kim, Dong-Wook [3 ,5 ]
Lee, Jong-Wook [5 ]
Min, Woo-Sung [5 ]
Kim, Yoo-Jin [3 ,5 ]
机构
[1] Catholic Univ Korea, Coll Med, Incheon St Marys Hosp, Incheon, South Korea
[2] Catholic Univ Korea, Coll Med, Seoul St Marys Hosp, Dept Lab Med, Seoul, South Korea
[3] Catholic Univ Korea, Coll Med, Leukemia Res Inst, Seoul, South Korea
[4] Catholic Univ Korea, Coll Med, Dept Med Informat, Seoul, South Korea
[5] Catholic Univ Korea, Coll Med, Seoul St Marys Hosp, Catholic Blood & Marrow Transplantat Ctr, Seoul, South Korea
[6] Catholic Univ Korea, Coll Med, Yeoido St Marys Hosp, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
higher-risk myelodysplastic syndrome; marrow response; hypomethylating treatment; allogeneic hematopoietic stem cell transplantation; STEM-CELL TRANSPLANTATION; ACUTE MYELOID-LEUKEMIA; MYELODYSPLASTIC SYNDROME PATIENTS; INDUCTION CHEMOTHERAPY; INTENSIVE CHEMOTHERAPY; THERAPIE-CELLULAIRE; SOCIETE FRANCAISE; TREATMENT FAILURE; UNRELATED DONORS; DISEASE BURDEN;
D O I
10.18632/oncotarget.12511
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hypomethylating treatment (HMT) has been suggested as a feasible bridge to hematopoietic stem cell transplantation (HSCT), but controversies exist around influences of HMT response on transplant outcomes. To assess the safety and influences of pre-transplant HMT focusing on debulking effects and transplant outcomes, we retrospectively analyzed consecutive HSCT-eligible patients who received HMT for higher-risk MDS with excess blasts. Of all 98 patients, 11 patients failed to proceed to HSCT and HMT-related mortality occurred in 8 patients. When excluding 9 patients who refused HSCT, 87% of scheduled HSCT (77 of 89) was performed after a median of 3 cycles (range, 1-8) of HMT. The 4-year overall survival after HMT (n = 98) and HSCT (n = 77) was 44.0% and 53.6%, respectively. Transplant outcomes were significantly different by the final response at HSCT; marrow response group (complete remission, marrow complete remission with or without hematologic improvement) showed significantly better 4-year disease-free survival compared to no marrow response group (n = 36, 87.3% vs. n = 41, 10.7%, P < 0.001). This difference between the groups was also evident in overall survival (90.9% vs. 8.6%, P < 0.001) and cumulative incidences of relapse (6.5% vs. 45.4%, P < 0.001) and treatment-related mortality (6.2% vs. 43.9%, P < 0.001). These observations indicate that pre-transplant HMT is a feasible bridging treatment in patients with excess blasts regarding high success rate of proceeding to transplantation and good survival rate. Marrow response at HSCT regardless of concomitant hematological improvement is an independent predictor of better survival, suggesting that immediate HSCT rather than continuing HMT should be performed once marrow response is achieved.
引用
收藏
页码:12342 / 12354
页数:13
相关论文
共 51 条
[1]  
[Anonymous], 2017, NCCN clinical practice guidelines in oncology: Survivorship
[2]   TET2 mutations predict response to hypomethylating agents in myelodysplastic syndrome patients [J].
Bejar, Rafael ;
Lord, Allegra ;
Stevenson, Kristen ;
Bar-Natan, Michal ;
Perez-Ladaga, Albert ;
Zaneveld, Jacques ;
Wang, Hui ;
Caughey, Bennett ;
Stojanov, Petar ;
Getz, Gad ;
Garcia-Manero, Guillermo ;
Kantarjian, Hagop ;
Chen, Rui ;
Stone, Richard M. ;
Neuberg, Donna ;
Steensma, David P. ;
Ebert, Benjamin L. .
BLOOD, 2014, 124 (17) :2705-2712
[3]   Somatic Mutations Predict Poor Outcome in Patients With Myelodysplastic Syndrome After Hematopoietic Stem-Cell Transplantation [J].
Bejar, Rafael ;
Stevenson, Kristen E. ;
Caughey, Bennett ;
Lindsley, R. Coleman ;
Mar, Brenton G. ;
Stojanov, Petar ;
Getz, Gad ;
Steensma, David P. ;
Ritz, Jerome ;
Soiffer, Robert ;
Antin, Joseph H. ;
Alyea, Edwin ;
Armand, Philippe ;
Ho, Vincent ;
Koreth, John ;
Neuberg, Donna ;
Cutler, Corey S. ;
Ebert, Benjamin L. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (25) :2691-+
[4]   Chemotherapeutic Drug-Induced ABCG2 Promoter Demethylation as a Novel Mechanism of Acquired Multidrug Resistance [J].
Bram, Eran E. ;
Stark, Michal ;
Raz, Shachar ;
Assaraf, Yehuda G. .
NEOPLASIA, 2009, 11 (12) :1359-U133
[5]   Clinical application and proposal for modification of the International Working Group (IWG) response criteria in myelodysplasia [J].
Cheson, Bruce D. ;
Greenberg, Peter L. ;
Bennett, John M. ;
Lowenberg, Bob ;
Wijermans, Pierre W. ;
Nimer, Stephen D. ;
Pinto, Antonio ;
Beran, Miloslav ;
de Witte, Theo M. ;
Stone, Richard M. ;
Mittelman, Moshe ;
Sanz, Guillermo F. ;
Gore, Steven D. ;
Schiffer, Charles A. ;
Kantarjian, Hagop .
BLOOD, 2006, 108 (02) :419-425
[6]   Upfront Allogeneic Stem Cell Transplantation after Reduced-Intensity/Nonmyeloablative Conditioning for Patients with Myelodysplastic Syndrome: A Study by the Societe Francaise de Greffe de Moelle et de Therapie Cellulaire [J].
Damaj, Gandhi ;
Mohty, Mohammad ;
Robin, Marie ;
Michallet, Mauricette ;
Chevallier, Patrice ;
Beguin, Yves ;
Nguyen, Stephanie ;
Bodes, Pierre ;
Blaise, Didier ;
Maillard, Natacha ;
Rubio, Marie Therese ;
Fegueux, Nathalie ;
Cornillon, Jerome ;
Clavert, Aline ;
Huynh, Anne ;
Ades, Lionel ;
Thiebaut-Bertrand, Anne ;
Hermine, Olivier ;
Vigouroux, Stephane ;
Fenaux, Pierre ;
Duhamel, Alain ;
Yakoub-Agha, Ibrahim .
BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2014, 20 (09) :1349-1355
[7]   Impact of Azacitidine Before Allogeneic Stem-Cell Transplantation for Myelodysplastic Syndromes: A Study by the Societe Francaise de Greffe de Moelle et de Therapie-Cellulaire and the Groupe-Francophone des Myelodysplasies [J].
Damaj, Gandhi ;
Duhamel, Alain ;
Robin, Marie ;
Beguin, Yves ;
Michallet, Mauricette ;
Mohty, Mohamad ;
Vigouroux, Stephane ;
Bories, Pierre ;
Garnier, Alice ;
El Cheikh, Jean ;
Bulabois, Claude-Eric ;
Huynh, Anne ;
Bay, Jacques-Olivier ;
Legrand, Faeyzeh ;
Deconinck, Eric ;
Fegueux, Nathalie ;
Clement, Laurence ;
Dauriac, Charles ;
Maillard, Natacha ;
Cornillon, Jerome ;
Ades, Lionel ;
Guillerm, Gaelle ;
Schmidt-Tanguy, Aline ;
Marjanovic, Zora ;
Park, Sophie ;
Rubio, Marie-Therese ;
Marolleau, Jean-Pierre ;
Garnier, Federico ;
Fenaux, Pierre ;
Yakoub-Agha, Ibrahim .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (36) :4533-4540
[8]   Intensive chemotherapy followed by allogeneic or autologous stem cell transplantation for patients with myelodysplastic syndromes (MDSs) and acute myeloid leukemia following MDS [J].
de Witte, T ;
Suciu, S ;
Verhoef, G ;
Labar, B ;
Archimbaud, E ;
Aul, C ;
Selleslag, D ;
Ferrant, A ;
Wijermans, P ;
Mandelli, F ;
Amadori, S ;
Jehn, U ;
Muus, P ;
Boogaerts, M ;
Zittoun, R ;
Gratwohl, A ;
Zwierzina, H ;
Hagemeijer, A ;
Willemze, R .
BLOOD, 2001, 98 (08) :2326-2331
[9]   Value of allogeneic versus autologous stem cell transplantation and chemotherapy in patients with myelodysplastic syndromes and secondary acute myeloid leukemia. Final results of a prospective randomized European Intergroup Trial [J].
de Witte, Theo ;
Hagemeijer, Anne ;
Suciu, Stefan ;
Belhabri, Amin ;
Delforge, Michel ;
Kobbe, Guido ;
Selleslag, Dominik ;
Schouten, Harry C. ;
Ferrant, Augustin ;
Biersack, Harald ;
Amadori, Sergio ;
Muus, Petra ;
Jansen, Joop H. ;
Hellstrom-Lindberg, Eva ;
Kovacsovics, Tibor ;
Wijermans, Pierre ;
Ossenkoppele, Gert ;
Gratwohl, Alois ;
Marie, Jean-Pierre ;
Willemze, Roel .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2010, 95 (10) :1754-1761
[10]   Conditioning with targeted busulfan and cyclophosphamide for hemopoietic stem cell transplantation from related and unrelated donors in patients with myelodysplastic syndrome [J].
Deeg, HJ ;
Storer, B ;
Slattery, JT ;
Anasetti, C ;
Doney, KC ;
Hansen, JA ;
Kiem, HP ;
Martin, PJ ;
Petersdorf, E ;
Radich, JP ;
Sanders, JE ;
Shulman, HM ;
Warren, EH ;
Witherspoon, RP ;
Bryant, EM ;
Chauncey, TR ;
Getzendaner, L ;
Storb, R ;
Appelbaum, FR .
BLOOD, 2002, 100 (04) :1201-1207