Safety and tolerability of lurbinectedin (PM01183) in patients with acute myeloid leukemia and myelodysplastic syndrome.
Christopher B BentonKelly Sharon ChienAyalew TefferiJose RodriguezFarhad RavandiNaval DaverElias JabbourNitin JainYesid AlvaradoMonica KwariSherry PierceAbhishek MaitiMarisa HornbakerMargarida A SantosSara MartinezMariano SigueroDarci ZblewskiAref Al-KaliWilliam J HoganHagop KantarjianAnimesh PardananiGuillermo Garcia-ManeroPublished in: Hematological oncology (2018)
Trabectedin is an FDA-approved DNA minor groove binder that has activity against translocation-associated sarcomas. Lurbinectedin is a next-generation minor groove binder with preclinical activity against myeloid leukemia cells. A dose-finding phase 1 clinical trial was performed in patients with acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) with further assessment of safety and tolerability. Forty-two patients with relapsed/refractory AML/MDS received lurbinectedin administered as a 1-hour intravenous infusion in a 3 + 3 study design. Two dosing schedules were used: 3.5, 5, 7, or 6 mg on days 1 and 8 or 2, 3, 1, or 1.5 mg for 3 consecutive days on days 1 to 3. Three patients experienced dose-limiting toxicities of rhabdomyolysis (grade 4), hyperbilirubinemia (grade 3), and oral herpes (grade 3) with the day 1 and 8 schedule. Otherwise, adverse events mainly consisted of gastrointestinal manifestations (n = 11), febrile neutropenia/infections (n = 4), pulmonary toxicity (n = 2), and renal failure (n = 2). The most common laboratory abnormalities observed were an increase in creatinine (93%) and anemia, neutropenia, and thrombocytopenia (100%). Overall, 33 of 42 patients (79%) had reduction in blasts in peripheral blood or bone marrow. One patient achieved a partial response and 2 patients a morphologic leukemia-free state. Most (n = 30, 71%) were discontinued due to progressive disease. Early deaths occurred from disease-related causes that were not attributable to lurbinectedin. Four patients with a chromosome 11q21-23 abnormality had significantly greater bone marrow blast reduction than those without such abnormality, with decrease of 31 ± 14% (n = 4) vs 8 ± 8% (n = 16), respectively (P = .04). Overall, lurbinectedin was safe and tolerated using the schedules and dose levels tested. While no sustained remissions were observed, single-agent lurbinectedin was transiently leukemia suppressive for some patients.
Keyphrases
- acute myeloid leukemia
- end stage renal disease
- bone marrow
- chronic kidney disease
- ejection fraction
- newly diagnosed
- clinical trial
- peritoneal dialysis
- peripheral blood
- air pollution
- high dose
- pulmonary hypertension
- gene expression
- allogeneic hematopoietic stem cell transplantation
- cell proliferation
- immune response
- blood pressure
- multiple sclerosis
- dendritic cells
- open label
- dna methylation
- diffuse large b cell lymphoma
- acute lymphoblastic leukemia
- patient reported
- genome wide
- high grade
- cell therapy
- heavy metals
- double blind
- induced apoptosis
- nucleic acid