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. 2020 Jun 3;4(3):e380.
doi: 10.1097/HS9.0000000000000380. eCollection 2020 Jun.

Results of an Early Access Treatment Protocol of Daratumumab Monotherapy in Spanish Patients With Relapsed or Refractory Multiple Myeloma

Affiliations

Results of an Early Access Treatment Protocol of Daratumumab Monotherapy in Spanish Patients With Relapsed or Refractory Multiple Myeloma

Adrián Alegre et al. Hemasphere. .

Abstract

Daratumumab is a human CD38-targeted monoclonal antibody approved as monotherapy for heavily pretreated relapsed and refractory multiple myeloma. We report findings for the Spanish cohort of an open-label treatment protocol that provided early access to daratumumab monotherapy and collected safety and patient-reported outcomes data for patients with relapsed or refractory multiple myeloma. At 15 centers across Spain, intravenous daratumumab (16 mg/kg) was administered to 73 patients who had ≥3 prior lines of therapy, including a proteasome inhibitor and an immunomodulatory drug, or who were double refractory to both. The median duration of daratumumab treatment was 3.3 (range: 0.03-13.17) months, with a median number of 12 (range: 1-25) infusions. Grade 3/4 treatment-emergent adverse events were reported in 74% of patients and included lymphopenia (28.8%), thrombocytopenia (27.4%), neutropenia (21.9%), leukopenia (19.2%), and anemia (15.1%). Common (>5%) serious treatment-emergent adverse events included respiratory tract infection (9.6%), general physical health deterioration (6.8%), and back pain (5.5%). Infusion-related reactions occurred in 45% of patients. The median change from baseline in all domains of the EQ-5D-5L and EORTC QLQ-C30 was mostly 0. A total of 18 (24.7%) patients achieved a partial response or better, with 10 (13.7%) patients achieving a very good partial response or better. Median progression-free survival was 3.98 months. The results of this early access treatment protocol are consistent with previously reported trials of daratumumab monotherapy and confirm its safety and antitumoral efficacy in Spanish patients with heavily treated relapsed or refractory multiple myeloma. European Clinical Trials Database number: 2015-002993-19.

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Figures

Figure 1
Figure 1
Investigator-assessed objective disease response in Spanish RRMM patients. RRMM = relapsed and/or refractory multiple myeloma, ORR = objective response rate, CR = complete response, VGPR = very good partial response, PR = partial response, sCR = stringent complete response. Note: individual response rates may not sum to total response rates due to rounding.
Figure 2
Figure 2
Progression-free survival in Spanish patients with RRMM. RRMM = relapsed and/or refractory multiple myeloma.
Figure 3
Figure 3
Mean change from baseline (± standard deviation) for global health status (A), and pain and fatigue scores (B) of the European Organisation for Research and Treatment of Cancer (EORTC) Quality of Life (QLQ)-C30 Questionnaire. aThe number of patients shown are those who completed the assessment at both baseline and each respective time point.

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