Phase 1 study of the PI3Kδ inhibitor INCB040093 ± JAK1 inhibitor itacitinib in relapsed/refractory B-cell lymphoma

被引:48
|
作者
Phillips, Tycel J. [1 ]
Forero-Torres, Andres [2 ]
Sher, Taimur [3 ]
Diefenbach, Catherine S. [4 ]
Johnston, Patrick [5 ]
Talpaz, Moshe [1 ]
Pulini, Jennifer [6 ]
Zhou, Li [6 ]
Scherle, Peggy [6 ]
Chen, Xuejun [6 ]
Barr, Paul M. [7 ]
机构
[1] Univ Michigan, Div Hematol & Oncol, 1500 E Med Ctr Dr, Ann Arbor, MI 48109 USA
[2] Univ Alabama Birmingham, Div Hematol & Oncol, Birmingham, AL USA
[3] Mayo Clin, Jacksonville, FL 32224 USA
[4] NYU, Sch Med, Perlmutter Canc Ctr, New York, NY USA
[5] Mayo Clin, Rochester, MN USA
[6] Incyte Corp, Wilmington, DE USA
[7] Univ Rochester, Wilmot Canc Inst, Rochester, NY USA
关键词
SELECTIVE INHIBITOR; SIGNALING PATHWAY; IL-10; LEVELS; IDELALISIB; INCB039110; BLOCKADE; SUBTYPES; PI3K;
D O I
10.1182/blood-2017-10-812701
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Because both phosphatidylinositol 3-kinase delta (PI3K delta) and Janus kinase (JAK)-signal transducer and activator of transcription pathways contribute to tumor cell proliferation and survival in B-cell malignancies, their simultaneous inhibition may provide synergistic treatment efficacy. This phase 1 dose-escalation/expansion study assessed the safety, efficacy, pharmacokinetics, and pharmacodynamics of INCB040093, a selective PI3K delta inhibitor, as monotherapy or combined with itacitinib (formerly INCB039110), a selective JAK1 inhibitor, in adult patients with relapsed or refractory (R/R) B-cell lymphomas. Final results are reported. Overall, 114 patients were treated (monotherapy, n = 49; combination therapy, n = 72 [7 patients crossed over from monotherapy to combination]). INCB040093 100 mg twice daily (monotherapy) and INCB040093 100 mg twice daily 1 itacitinib 300 mg once daily (combination) were the recommended phase 2 doses. One dose-limiting toxicity (gastrointestinal bleed secondary to gastric diffuse large B-cell lymphoma [DLBCL] regression) occurred with monotherapy. The most common serious adverse events with monotherapy were pneumonia (n = 5) and pyrexia (n = 4), and with combination Pneumocystis jiroveci pneumonia (n = 5), pneumonia (unrelated to P jiroveci; n = 5), and pyrexia (n = 4). Grade 3 or higher transaminase elevations were less common with combination. INCB040093 was active across the B-cell lymphomas; 63% of patients (5/8) with follicular lymphoma responded to monotherapy. Adding itacitinib provided promising activity in select subtypes, with responses of 67% (14/21) in classic Hodgkin lymphoma (vs 29% [5/17] with monotherapy) and 31% (4/13) in nongerminal center B-cell-like DLBCL. INCB040093 with/without itacitinib was tolerated and active in this study, and is a promising treatment strategy for patients with select R/R B-cell lymphomas. This trial was registered at www.clinicaltrials.gov as #NCT01905813.
引用
收藏
页码:293 / 306
页数:14
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