Resumen
The effects of romiplostim on bone marrow morphology were evaluated in adults with immune thrombocytopenia (ITP). Patients with platelet counts <50 × 109/L, ≥1 prior ITP therapies, and no collagen at baseline received weekly subcutaneous romiplostim starting at 1 μg/kg, adjusted to maintain platelet counts between 50 and 200 × 109/L. Biopsies were scheduled after 1, 2, or 3 years of romiplostim (cohorts 1, 2, and 3, respectively). Irrespective of scheduled time, biopsies were performed earlier if patients discontinued or failed to achieve/maintain a response to romiplostim. Reticulin (silver stain) and collagen (trichrome stain) were graded by two hematopathologists using the modified Bauermeister scale (0–4). Of 169 patients, 131 had evaluable biopsies; 9/131 (6.9 %) had increases of ≥2 grades on the modified Bauermeister scale (cohort 1: 0/34; cohort 2: 2/39; cohort 3: 7/58), including two with collagen. Three of the nine patients had follow-up biopsies, including one patient with collagen; changes were reversible after romiplostim discontinuation. Of the nine patients, one had neutropenia detected by laboratory test and two had adverse events of anemia, both non-serious and not treatment-related. By actual exposure (as some biopsies did not occur as scheduled), the number of patients with grade increases ≥2 were year 1: 3/41, year 2: 1/38, year 3: 5/52. Twenty-four patients sustained platelet counts ≥50 × 109/L for ≥6 months with no ITP medications after discontinuing romiplostim, i.e., they entered clinical remission of their ITP. In conclusion, in patients with ITP receiving romiplostim, bone marrow changes were observed in a small proportion of patients. ClinicalTrials.gov identifier: NCT#00907478
Idioma original | English |
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Páginas (desde-hasta) | 1077-1087 |
Número de páginas | 11 |
Publicación | Annals of Hematology |
Volumen | 95 |
N.º | 7 |
DOI | |
Estado | Published - jun. 1 2016 |
Nota bibliográfica
Funding Information:All authors had full access to all data, contributed to critically interpreting the data, and participated in writing the manuscript. They did not receive remuneration for authorship. AJ is on the speakers’ bureau/advisory boards for Amgen Inc., GSK, Roche, and Mundipharma. FR has research grants from GSK and Amgen Inc. and is on speakers’ bureau/advisory boards for GSK and Amgen Inc. DA and ZB have no disclosures. BC received research grants from GSK and Amgen Inc. and is on their speakers’ bureau. IP has research grants from CSL Behring and honoraria from CSL Behring, Amgen Inc., Boehringer Ingelheim, Bayer, Baxter, and Pfizer and is on speakers’ bureau/advisory boards for CSL Behring, Amgen Inc., Boehringer Ingelheim, Bayer, Baxter, and Pfizer. LC is a consultant for Amgen Inc., GSK, and Alexion. DT was a consultant for Amgen Inc. XW and JF are employees of and stockholders in Amgen Inc.
Publisher Copyright:
© 2016, The Author(s).
ASJC Scopus Subject Areas
- Hematology