Salvage autologous hematopoietic stem cell transplantation for multiple myeloma performed with stem cells procured after previous high dose therapy - a multicenter report by the Polish Myeloma Study Group.
Joanna Drozd-SokołowskaAnna Waszczuk-GajdaPrzemysław BiecekKatarzyna KobylińskaJoanna MańkoIwona HusAnna Szmigielska-KapłonMateusz NowickiJoanna Romejko-JarosińskaMagdalena KoziołMariola SędzimirskaWojciech SachsKrzysztof MądryPiotr BoguradzkiMałgorzata KrólMarek HusGrzegorz Władysław BasakJadwiga Dwilewicz-TrojaczekPublished in: Leukemia & lymphoma (2021)
Salvage autologous hematopoietic stem cell transplantation (auto-HSCT) constitutes a therapeutic option for a group of well-selected patients with relapsed multiple myeloma (MM). However, if an insufficient number of stem cells were harvested and stored before the first auto-HSCT, stem cells need to be remobilized. Patients diagnosed with MM who following relapse after auto-HSCT, had remobilization and afterward, auto-HSCT with remobilized cells were included in this retrospective analysis. Thirty-three patients, 61% males, the median age 61 years, were included. With a median follow-up of 1.8 years, 2-year progression-free survival was 56.2%, non-relapse mortality 4.8%. The 2-year cumulative incidence of t-MDS was 4.9%. Factors important for the outcome were: the quality of response, previous radiotherapy, the time between the first and salvage auto-HSCT. To conclude, salvage auto-HSCT performed with cells procured after the previous auto-HSCT can be efficacious in relapsed MM, especially if a sufficiently long response had been obtained to the first auto-HSCT(s).
Keyphrases
- stem cells
- multiple myeloma
- hematopoietic stem cell
- free survival
- end stage renal disease
- newly diagnosed
- acute myeloid leukemia
- ejection fraction
- high dose
- cell therapy
- induced apoptosis
- chronic kidney disease
- acute lymphoblastic leukemia
- prognostic factors
- type diabetes
- cell cycle arrest
- clinical trial
- diffuse large b cell lymphoma
- radiation therapy
- bone marrow
- squamous cell carcinoma
- cardiovascular disease
- low dose
- rectal cancer
- cardiovascular events
- platelet rich plasma
- cross sectional
- locally advanced