DCEP as a bridge to ongoing therapies for advanced relapsed and/or refractory multiple myeloma.
Hiu Lam Agnes YuenMichael Sze Yuan LowPasquale FedeleAnna KalffPatricia WalkerKrystal BerginJohn CoutsouvelisGeorge GrigoriadisAndrew SpencerPublished in: Leukemia & lymphoma (2018)
There is limited data describing dexamethasone, cyclophosphamide, etoposide, and cisplatin (DCEP) in relapsed refractory multiple myeloma (RRMM). We reviewed 65 patients with RRMM receiving DCEP between 2005 and 2017 in two Melbourne Hospitals. Patients had received a mean of three prior treatment lines (range, 1-11). The mean number of cycles of DCEP was two (range, 1-4). Overall response rate (ORR) was 55% whilst 19% achieved MR and SD. Median overall survival (OS) was 9.6 months. Those bridged to autologous stem cell transplant (ASCT) had significantly improved OS compared to those who were not (median 32.8 vs. 10.7 months, p=.0004). Significant treatment-related mortality (TRM) was observed (9.7%), mostly attributable to grade 3-4 neutropenia and febrile neutropenia. Mandatory use of G-CSF is, therefore, warranted to prevent septic complications. In heavily pretreated RRMM, DCEP is an effective bridge to definitive therapy but in the absence of the latter, its value is questionable.
Keyphrases
- multiple myeloma
- stem cells
- acute myeloid leukemia
- acute lymphoblastic leukemia
- end stage renal disease
- healthcare
- high dose
- diffuse large b cell lymphoma
- chronic kidney disease
- newly diagnosed
- hodgkin lymphoma
- cardiovascular disease
- prognostic factors
- coronary artery disease
- chemotherapy induced
- magnetic resonance imaging
- bone marrow
- locally advanced
- replacement therapy
- peritoneal dialysis
- urinary tract infection
- contrast enhanced
- cerebrospinal fluid
- data analysis