Results of an early access treatment protocol of daratumumab in United States patients with relapsed or refractory multiple myeloma

被引:27
作者
Chari, Ajai [1 ]
Lonial, Sagar [2 ]
Mark, Tomer M. [3 ,11 ]
Krishnan, Amrita Y. [4 ,5 ]
Stockerl-Goldstein, Keith E. [6 ]
Usmani, Saad Z. [7 ]
Londhe, Anil [8 ]
Etheredge, Delores [8 ]
Fleming, Sarah [8 ]
Liu, Baolian [9 ]
Ukropec, Jon [10 ]
Lin, Thomas S. [10 ]
Jagannath, Sundar [1 ]
Nooka, Ajay K. [2 ]
机构
[1] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
[2] Emory Univ, Winship Canc Inst, Dept Hematol & Oncol, Atlanta, GA 30322 USA
[3] Weill Cornell Med Coll, New York, NY USA
[4] City Hope Natl Med Ctr, Dept Hematol & Hematopoiet Cell Transplantat, 1500 E Duarte Rd, Duarte, CA 91010 USA
[5] City Hope Natl Med Ctr, Judy & Bernard Briskin Ctr Multiple Myeloma, 1500 E Duarte Rd, Duarte, CA 91010 USA
[6] Washington Univ, Div Med Oncol, Bone Marrow Transplantat & Leukemia Sect, St Louis, MO USA
[7] Levine Canc Inst, Charlotte, NC USA
[8] Janssen Res & Dev LLC, Titusville, NJ USA
[9] Janssen Res & Dev LLC, Spring House, PA USA
[10] Janssen Sci Affairs LLC, Horsham, PA USA
[11] Univ Colorado, Anschutz Med Ctr, Aurora, CO USA
关键词
CD38; daratumumab; montelukast; monoclonal antibodies; multiple myeloma; MONOTHERAPY; DESENSITIZATION; DEXAMETHASONE; BORTEZOMIB; ANTIBODY; CD38;
D O I
10.1002/cncr.31706
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Daratumumab is a human CD38-directed monoclonal antibody indicated for the treatment of relapsed and refractory multiple myeloma (MM). Methods A multicenter, open-label treatment protocol provided early access to daratumumab for patients who had progressive MM after they received >= 3 prior lines of therapy that included a proteasome inhibitor and an immunomodulatory agent or if they were refractory to both a proteasome inhibitor and an immunomodulatory agent. Patients received daratumumab 16 mg/kg weekly for 8 weeks, every other week for 16 weeks, and monthly until they developed disease progression, unacceptable toxicity, or 60 days after the drug gained US approval. Treatment-emergent grade >= 3 adverse events (AEs), serious AEs, and AEs of special interest were collected. Results Three hundred forty-eight patients were enrolled at 39 US sites between June and December 2015. Patients received study therapy for a median of 1.9 months (range, 0.03-6.0 months). Fifty-two percent of patients transitioned to commercially-available daratumumab and 37% discontinued because of progressive disease. Grade >= 3 AEs occurred in 50% of patients, including thrombocytopenia (15%) and anemia (14%). Serious AEs occurred in 35% of patients (12% were drug-related), including infections (11%). Infusion reactions occurred in 56%, 2%, and 2% of patients during the first, second, and all subsequent infusions, respectively; respiratory symptoms (cough, dyspnea, throat irritation, nasal congestion) were common. The infusion reaction rate for the first infusion was 38% in 50 patients at 2 sites who received montelukast as premedication for their first infusion and 59% in patients who did not receive montelukast. Conclusions The current findings are consistent with previously reported trials and confirm the safety profile of daratumumab in heavily pretreated US patients who have relapsed or refractory MM. Cancer 2018;124:000-000. (c) 2018 The Authors. Cancer published by Wiley Periodicals, Inc. on behalf of American Cancer Society.
引用
收藏
页码:4342 / 4349
页数:8
相关论文
共 19 条
[1]  
[Anonymous], 2016, DARZ PRESCR INF
[2]   Brentuximab vedotin desensitization in a patient with refractory Hodgkin's lymphoma [J].
Arora, Anubha ;
Bhatt, Vijaya Raj ;
Liewer, Susanne ;
Armitage, James O. ;
Bociek, R. Gregory .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2015, 95 (04) :361-364
[3]   Daratumumab, a Novel Therapeutic Human CD38 Monoclonal Antibody, Induces Killing of Multiple Myeloma and Other Hematological Tumors [J].
de Weers, Michel ;
Tai, Yu-Tzu ;
van der Veer, Michael S. ;
Bakker, Joost M. ;
Vink, Tom ;
Jacobs, Danielle C. H. ;
Oomen, Lukas A. ;
Peipp, Matthias ;
Valerius, Thomas ;
Slootstra, Jerry W. ;
Mutis, Tuna ;
Bleeker, Wim K. ;
Anderson, Kenneth C. ;
Lokhorst, Henk M. ;
van de Winkel, Jan G. J. ;
Parren, Paul W. H. I. .
JOURNAL OF IMMUNOLOGY, 2011, 186 (03) :1840-1848
[4]   Daratumumab, Lenalidomide, and Dexamethasone for Multiple Myeloma [J].
Dimopoulos, M. A. ;
Oriol, A. ;
Nahi, H. ;
San-Miguel, J. ;
Bahlis, N. J. ;
Usmani, S. Z. ;
Rabin, N. ;
Orlowski, R. Z. ;
Komarnicki, M. ;
Suzuki, K. ;
Plesner, T. ;
Yoon, S. -S. ;
Ben Yehuda, D. ;
Richardson, P. G. ;
Goldschmidt, H. ;
Reece, D. ;
Lisby, S. ;
Khokhar, N. Z. ;
O'Rourke, L. ;
Chiu, C. ;
Qin, X. ;
Guckert, M. ;
Ahmadi, T. ;
Moreau, P. .
NEW ENGLAND JOURNAL OF MEDICINE, 2016, 375 (14) :1319-1331
[5]   Improved survival in multiple myeloma and the impact of novel therapies [J].
Kumar, Shaji K. ;
Rajkumar, S. Vincent ;
Dispenzieri, Angela ;
Lacy, Martha Q. ;
Hayman, Suzanne R. ;
Buadi, Francis K. ;
Zeldenrust, Steven R. ;
Dingli, David ;
Russell, Stephen J. ;
Lust, John A. ;
Greipp, Philip R. ;
Kyle, Robert A. ;
Gertz, Morie A. .
BLOOD, 2008, 111 (05) :2516-2520
[6]   Daratumumab granted breakthrough drug status [J].
Laubach, Jacob P. ;
Tai, Yu-Tzu ;
Richardson, Paul G. ;
Anderson, Kenneth C. .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2014, 23 (04) :445-452
[7]   Hypersensitivity reactions to rituximab: 53 successful desensitizations in 7 patients with severe, near-fatal reactions [J].
Lebel, Eyal ;
Ben-Yehuda, Dina ;
Bohbot, Emilie ;
Dranitzki, Zvi ;
Shalit, Meir ;
Tal, Yuval .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY-IN PRACTICE, 2016, 4 (05) :1000-1002
[8]   Targeting CD38 with Daratumumab Monotherapy in Multiple Myeloma [J].
Lokhorst, H. M. ;
Plesner, T. ;
Laubach, J. P. ;
Nahi, H. ;
Gimsing, P. ;
Hansson, M. ;
Minnema, M. C. ;
Lassen, U. ;
Krejcik, J. ;
Palumbo, A. ;
van de Donk, N. W. C. J. ;
Ahmadi, T. ;
Khan, I. ;
Uhlar, C. M. ;
Wang, J. ;
Sasser, A. K. ;
Losic, N. ;
Lisby, S. ;
Basse, L. ;
Brun, N. ;
Richardson, P. G. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (13) :1207-1219
[9]   Daratumumab monotherapy in patients with treatment-refractory multiple myeloma (SIRIUS): an open-label, randomised, phase 2 trial [J].
Lonial, Sagar ;
Weiss, Brendan M. ;
Usmani, Saad Z. ;
Singhal, Seema ;
Chari, Ajai ;
Bahlis, Nizar J. ;
Belch, Andrew ;
Krishnan, Amrita ;
Vescio, Robert A. ;
Victoria Mateos, Maria ;
Mazumder, Amitabha ;
Orlowski, Robert Z. ;
Sutherland, Heather J. ;
Blade, Joan ;
Scott, Emma C. ;
Oriol, Albert ;
Berdeja, Jesus ;
Gharibo, Mecide ;
Stevens, Don A. ;
LeBlanc, Richard ;
Sebag, Michael ;
Callander, Natalie ;
Jakubowiak, Andrzej ;
White, Darrell ;
de la Rubia, Javier ;
Richardson, Paul G. ;
Lisby, Steen ;
Feng, Huaibao ;
Uhlar, Clarissa M. ;
Khan, Imran ;
Ahmadi, Tahamtan ;
Voorhees, Peter M. .
LANCET, 2016, 387 (10027) :1551-1560
[10]   Daratumumab plus Bortezomib, Melphalan, and Prednisone for Untreated Myeloma [J].
Mateos, M. -V. ;
Dimopoulos, M. A. ;
Cavo, M. ;
Suzuki, K. ;
Jakubowiak, A. ;
Knop, S. ;
Doyen, C. ;
Lucio, P. ;
Nagy, Z. ;
Kaplan, P. ;
Pour, L. ;
Cook, M. ;
Grosicki, S. ;
Crepaldi, A. ;
Liberati, A. M. ;
Campbell, P. ;
Shelekhova, T. ;
Yoon, S. -S. ;
Iosava, G. ;
Fujisaki, T. ;
Garg, M. ;
Chiu, C. ;
Wang, J. ;
Carson, R. ;
Crist, W. ;
Deraedt, W. ;
Nguyen, H. ;
Qi, M. ;
San-Miguel, J. .
NEW ENGLAND JOURNAL OF MEDICINE, 2018, 378 (06) :518-528