Checkpoint inhibitor-based salvage regimens prior to autologous stem cell transplant improve event-free survival in relapsed/refractory classic Hodgkin lymphoma

被引:12
|
作者
Desai, Sanjal H. [1 ,2 ]
Spinner, Michael A. [3 ]
David, Kevin [4 ]
Bachanova, Veronika [2 ,5 ]
Goyal, Gaurav [6 ]
Kahl, Brad [7 ]
Dorritie, Kathleen [8 ]
Azzi, Jacques [9 ]
Kenkre, Vaishalee P. [10 ]
Arai, Sally [3 ]
Chang, Cheryl [3 ]
Fusco, Brendon [4 ]
Sumransub, Nuttavut [2 ,5 ]
Hatic, Haris [6 ]
Saba, Raya [7 ]
Ibrahim, Uroosa [9 ]
Harris, Elyse, I [10 ]
Shah, Harsh [11 ]
Murphy, Jacob [12 ]
Ansell, Stephen [1 ]
Jagadish, Deepa [13 ]
Orellana-noia, Victor [14 ]
Diefenbach, Catherine [15 ]
Iyenger, Siddharth [11 ]
Rappazzo, K. C. [12 ]
Mishra, Rahul [13 ]
Choi, Yun [15 ]
Nowakowski, Grzegorz S. [1 ]
Advani, Ranjana H. [3 ]
Micallef, Ivana N. [1 ]
机构
[1] Mayo Clin, Div Hematol, Rochester, MN USA
[2] Univ Minnesota, Div Hematol Oncol & Transplantat, Minneapolis, MN USA
[3] Stanford Univ, Med Ctr, Dept Med, Div Oncol, Stanford, CA 94305 USA
[4] Rutgers Canc Inst New Jersey, Dept Hematol & Med Oncol, New Brunswick, NJ USA
[5] Univ Minnesota, Dept Med, Div Hematol Oncol & Transplantat, Box 736 UMHC, Minneapolis, MN 55455 USA
[6] Univ Alabama Birmingham, ONeal Comprehens Canc Ctr, Birmingham, AL USA
[7] Washington Univ, Sch Med, Div Hematol & Oncol, St Louis, MO 63110 USA
[8] UPMC Hillman Canc Ctr, Div Hematol Oncol, Pittsburgh, PA USA
[9] Icahn Sch Med Mt Sinai, Div Hematol & Med Oncol, New York, NY 10029 USA
[10] Univ Wisconsin, Dept Hematol, Madison, WI USA
[11] Univ Utah, Huntsman Canc Inst, Div Hematol, Salt Lake City, UT USA
[12] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Dept Oncol, Baltimore, MD USA
[13] Cleveland Clin Fdn, 9500 Euclid Ave, Cleveland, OH 44195 USA
[14] Emory Univ, Winship Canc Inst, Div Hematol & Med Oncol, Atlanta, GA 30322 USA
[15] NYU Grossman Med Sch, Perlmutter Canc Ctr, New York, NY USA
关键词
BRENTUXIMAB VEDOTIN; FOLLOW-UP; THERAPY; CHEMOTHERAPY; DISEASE; RISK;
D O I
10.1002/ajh.26827
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Clinical trials of novel salvage therapies have encouraging outcomes for relapsed/refractory transplant-eligible classic Hodgkin lymphoma (R/R cHL) but comparison with conventional chemotherapy is lacking. Herein, we report the final analysis of a multicenter retrospective cohort of R/R cHL assessing outcomes by type of salvage therapy before autologous stem cell transplant (ASCT). R/R cHL patients who underwent ASCT at 14 institutions across the United States were included. Outcomes were compared among patients receiving conventional chemotherapy, brentuximab vedotin (BV) + chemotherapy, BV alone, and a checkpoint inhibitor (CPI)-based regimens before ASCT. Study endpoints included event-free survival (EFS), progression-free survival (PFS), and overall survival (OS). All endpoints are defined from relapse. Of 936 patients, 728 received conventional chemotherapy, 73 received BV + chemotherapy, 70 received BV alone, and 65 received CPI-based regimens prior to ASCT. When adjusted for time to relapse, pre-ASCT response and use of BV maintenance, patients receiving CPI-based regimens had superior 2-year EFS compared to conventional chemotherapy, BV + chemotherapy, and BV alone (79.7, 49.6, 62.3, and 36.9%, respectively, p < .0001). Among 649 patients transplanted after 1 line of salvage therapy, CPI-based regimens were associated with superior 2-year PFS compared to conventional chemotherapy (98% vs. 68.8%, hazard ratio: 0.1, 95% confidence interval: 0.03-0.5, p < .0001). OS did not differ by pre-ASCT salvage regimen. In this large multicenter retrospective study, CPI-based regimens improved EFS and PFS compared to other salvage regimens independent of pre-ASCT response. These data support earlier sequencing of CPI-based regimens in R/R cHL in the pre-ASCT setting.
引用
收藏
页码:464 / 471
页数:8
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