| Literature DB >> 31392600 |
Szilvia Lovas1, Gergely Varga2, Péter Farkas2, Tamás Masszi2, Nikolett Wohner2, Ágnes Bereczki3, Nóra Adamkovich3, Zita Borbényi3, Árpád Szomor4, Hussain Alizadeh4, Erika Szaleczky5, Krisztina Wolf5, Tamás Schneider5, Márk Plander6, Tamás Szendrei6, Ottó Csacsovszki7, Zoltán Csukly7, Péter Rajnics8, Miklós Egyed8, Zsolt Nagy9, László Rejtő10, Árpád Illés1, Gábor Mikala7, László Váróczy11.
Abstract
Daratumumab is a human anti-CD38 monoclonal antibody used in the treatment of refractory and relapsed multiple myeloma. We investigated the efficacy and safety of daratumumab therapy in a real-world setting. Ninety-nine Hungarian patients were included; 48 received monotherapy, while lenalidomide and bortezomib combinations were administered in 29 and 19 cases, respectively. Overall response rate was assessable in 88 patients, with 12 complete, 10 very good partial, 34 partial, and seven minor responses. At a median duration of follow-up of 18.6 months, median progression-free survival (PFS) among all patients was 17.0 months. These values were inferior in the bortezomib combination and monotherapy groups. Patients with early-stage disease (ISS1) had better survival results than those with stage 2 or 3 myeloma (p = 0.009). Heavily pretreated patients had inferior PFS compared to those with 1-3 therapies (p = 0.035). Patients with impaired renal function had PFS results comparable with those having no kidney involvement. There were 10 fatal infections, and the most frequent adverse events were mild infusion-associated reactions and hematologic toxicities. Our results confirm that daratumumab is an effective treatment option for relapsed/refractory MM with an acceptable safety profile in patients with normal and impaired renal function.Entities:
Keywords: Daratumumab; Multiple myeloma; Survival; Toxicity; Treatment response
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Year: 2019 PMID: 31392600 DOI: 10.1007/s12185-019-02715-w
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490