Determinants of lenalidomide response with or without erythropoiesis-stimulating agents in myelodysplastic syndromes: the HOVON89 trial.
Arjan A van de LoosdrechtE M P CremersC AlhanC DuetzF E M In 't HoutH A Visser-WisselaarD A ChituA VerbruggeS M CunhaG J OssenkoppeleJ J W M JanssenSaskia K KleinE VellengaG A HulsP MuusS M C LangemeijerG E de GreefP A W Te BoekhorstM H G RaaijmakersM van Marwijk KooyM C LegdeurJ J WegmanW DeenikO de WeerdtT M van Maanen-LammeP JobseR J W van KampenA BeekerP W WijermansB J BiemondB C TanisJ W J van EsserC G SchaarH S Noordzij-NooteboomE M G JacobsA O de GraafM Jongen-LavrencicM J P L Stevens-KroefT M WestersJ H JansenPublished in: Leukemia (2024)
A randomized phase-II study was performed in low/int-1 risk MDS (IPSS) to study efficacy and safety of lenalidomide without (arm A) or with (arm B) ESA/G-CSF. In arm B, patients without erythroid response (HI-E) after 4 cycles received ESA; G-CSF was added if no HI-E was obtained by cycle 9. HI-E served as primary endpoint. Flow cytometry and next-generation sequencing were performed to identify predictors of response. The final evaluation comprised 184 patients; 84% non-del(5q), 16% isolated del(5q); median follow-up: 70.7 months. In arm A and B, 39 and 41% of patients achieved HI-E; median time-to-HI-E: 3.2 months for both arms, median duration of-HI-E: 9.8 months. HI-E was significantly lower in non-del(5q) vs. del(5q): 32% vs. 80%. The same accounted for transfusion independency-at-week 24 (16% vs. 67%), but similar in both arms. Apart from presence of del(5q), high percentages of bone marrow lymphocytes and progenitor B-cells, a low number of mutations, absence of ring sideroblasts, and SF3B1 mutations predicted HI-E. In conclusion, lenalidomide induced HI-E in patients with non-del(5q) and del(5q) MDS without additional effect of ESA/G-CSF. The identified predictors of response may guide application of lenalidomide in lower-risk MDS in the era of precision medicine. (EudraCT 2008-002195-10).
Keyphrases
- newly diagnosed
- end stage renal disease
- bone marrow
- chronic kidney disease
- ejection fraction
- peritoneal dialysis
- multiple myeloma
- flow cytometry
- clinical trial
- gene expression
- squamous cell carcinoma
- low dose
- radiation therapy
- oxidative stress
- cardiac surgery
- peripheral blood
- high dose
- dna methylation
- high glucose
- phase iii
- endothelial cells
- locally advanced
- drug induced
- diabetic rats
- double blind