Literature DB >> 15916682

Long-term outcomes of previously untreated myeloma patients: responses to induction chemotherapy and high-dose melphalan incorporated within a risk stratification model can help to direct the use of novel treatments.

Caroline L Alvares1, Faith E Davies, Clive Horton, Gita Patel, Ray Powles, Bhawna Sirohi, Roslin Zuha, Alex Gatt, Radovan Saso, Jennifer G Treleaven, Claire E Dearden, Michael N Potter, Mark E Ethell, Gareth J Morgan.   

Abstract

Induction chemotherapy followed by high-dose melphalan (HDM) is the standard treatment for fitter patients with myeloma. The place of bortezomib and the thalidomide analogues within this treatment paradigm is yet to be established. We sought to identify patients who may benefit from the introduction of novel agents during their initial management. An intention-to-treat analysis was performed on 383 patients with newly diagnosed myeloma eligible for HDM to determine whether the extent of response to induction therapy and HDM correlated with long-term survival. Early response [complete response (CR) and partial response (PR)] to induction therapy was predictive of overall survival (OS) [median OS, 7.47 years for responders (CR and PR) versus 4.89 years for non-responders; P = 0.035]. The attainment of CR at 3 months post-HDM correlated with a prolonged progression-free survival (PFS) (median PFS, 7.4 years in CR group versus 5.3 years in non-CR group; P = 0.023). This data suggests that, at every stage of treatment, the aim should be to achieve CR. Patients with suboptimal responses could be offered alternative therapy. We propose a multiparametric risk-adapted model that includes response to induction chemotherapy and HDM, for identifying patients who may benefit from novel approaches to treatment.

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Year:  2005        PMID: 15916682     DOI: 10.1111/j.1365-2141.2005.05514.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  6 in total

1.  Impact of informative censoring on the Kaplan-Meier estimate of progression-free survival in phase II clinical trials.

Authors:  Federico Campigotto; Edie Weller
Journal:  J Clin Oncol       Date:  2014-09-20       Impact factor: 44.544

2.  Phase III trial of bortezomib, cyclophosphamide and dexamethasone (VCD) versus bortezomib, doxorubicin and dexamethasone (PAd) in newly diagnosed myeloma.

Authors:  E K Mai; U Bertsch; J Dürig; C Kunz; M Haenel; I W Blau; M Munder; A Jauch; B Schurich; T Hielscher; M Merz; B Huegle-Doerr; A Seckinger; D Hose; J Hillengass; M S Raab; K Neben; H-W Lindemann; M Zeis; C Gerecke; I G H Schmidt-Wolf; K Weisel; C Scheid; H Salwender; H Goldschmidt
Journal:  Leukemia       Date:  2015-03-19       Impact factor: 11.528

3.  Outcomes with early response to first-line treatment in patients with newly diagnosed multiple myeloma.

Authors:  Nidhi Tandon; Surbhi Sidana; S Vincent Rajkumar; Morie A Gertz; Francis K Buadi; Martha Q Lacy; Prashant Kapoor; Wilson I Gonsalves; Angela Dispenzieri; Taxiarchis V Kourelis; Rahma Warsame; David Dingli; Amie L Fonder; Suzanne R Hayman; Miriam A Hobbs; Yi Lisa Hwa; Robert A Kyle; Nelson Leung; Ronald S Go; John A Lust; Stephen J Russell; Shaji K Kumar
Journal:  Blood Adv       Date:  2019-03-12

Review 4.  Controversies in the assessment of minimal residual disease in multiple myeloma: clinical significance of minimal residual disease negativity using highly sensitive techniques.

Authors:  Noa Biran; Scott Ely; Ajai Chari
Journal:  Curr Hematol Malig Rep       Date:  2014-12       Impact factor: 3.952

5.  Bortezomib (Velcadetrade mark) in the Treatment of Multiple Myeloma.

Authors:  Antonia Field-Smith; Gareth J Morgan; Faith E Davies
Journal:  Ther Clin Risk Manag       Date:  2006-09       Impact factor: 2.423

6.  Salvage bortezomib-dexamethasone and high-dose melphalan (HDM) and autologous stem cell support (ASCT) in myeloma patients at first relapse after HDM with ASCT. A phase-2 trial.

Authors:  P Gimsing; Ø Hjertner; N Abildgaard; N F Andersen; T G Dahl; H Gregersen; T W Klausen; U-H Mellqvist; O Linder; R Lindås; N Tøffner Clausen; S Lenhoff
Journal:  Bone Marrow Transplant       Date:  2015-06-29       Impact factor: 5.483

  6 in total

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