alexa Induction Therapy with Bortezomib, Thalidomide and Dexamethasone (VTD) in Caucasian Patients with Multiple Myeloma: A Single Center Experience | Open Access Journals
ISSN: 2155-9864
Journal of Blood Disorders & Transfusion
Like us on:
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Induction Therapy with Bortezomib, Thalidomide and Dexamethasone (VTD) in Caucasian Patients with Multiple Myeloma: A Single Center Experience

Normann Steiner, Stephanie Riehl, David Nachbaur, Wolfgang Willenbacher, Gunther Gastl and Eberhard Gunsilius*

Department of Internal Medicine V (Hematology and Medical Oncology), Innsbruck Medical University, Anichstr. 35, A-6020 Innsbruck, Austria

*Corresponding Author:
Eberhard Gunsilius
Professor, Department of Internal Medicine V
Innsbruck Medical University, Anichstr. 35
A-6020 Innsbruck, Austria
Tel: +43 5125040
Fax: +43 512504 25615
E-mail: [email protected]

Received date: June 10, 2015 Accepted date: August 14, 2015 Published date: August 18, 2015

Citation: Steiner N, Riehl S, Nachbaur D, Willenbacher W, Gastl G, et al. (2015) Induction Therapy with Bortezomib, Thalidomide and Dexamethasone (VTD) in Caucasian Patients with Multiple Myeloma: A Single Center Experience. J Blood Disord Transfus 6:296. doi:10.4172/2155-9864.1000296

Copyright: © 2015 Steiner N, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Visit for more related articles at Journal of Blood Disorders & Transfusion


Objective: In clinical trials, the combination of bortezomib, thalidomide, and dexamethasone (VTD) has shown excellent results as induction treatment in patients with multiple myeloma. However, “real-life” data in unselected Caucasian patients are lacking.

Methods: We retrospectively analyzed 41 patients treated with VTD between 2005 and 2014. 

Results: Post induction, the overall response rate was 78%, with ≥very good partial response (≥VGPR) in 54% and near complete/complete responses (nCR/CR) in 17% of the patients  respectively. For patients proceeding to autologous stem cell transplantation (ASCT), post-transplant rates were 96% ≥VGPR and 48% nCR/CR. Median progression free survival (PFS) was 24 months and the estimated 1-year and 2-year overall survival (OS) rates were 95% and 76%, respectively. Subgroup analyses revealed significantly longer OS and PFS in patients with a ≥VGPR as first response status compared to those with a <VGPR [OS 44 vs. 25 months (p=0.036); PFS 29.5 vs. 16 months (p=0.011)], as well as in patients who underwent ASCT compared to not transplanted patients [OS 41 vs. 23.5 months (p=0.002); PFS 28 vs. 23 months (p=0.003)]. In 6 patients (15%) therapy was switched to another regimen due to lack of response (<PR, n=4), cardiac decompensation (n=1) or prolonged neutropenia (n=1). Non-hematological grade III/IV toxicities were peripheral neuropathy (2%), infections (7%), herpes zoster (5%), and thromboembolic events (2%). Dose reductions of thalidomide and/or bortezomib were necessary in 24% of the patients because of peripheral neuropathy.

Conclusion: The VTD regimen was found to be a highly effective and well tolerated induction regimen for multiple myeloma patients outside clinical trials.


VTD; ASCT; Multiple myeloma; Induction therapy; Toxicity


The implementation of novel drugs, such as bortezomib, thalidomide, and lenalidomide into induction regimens before high-dose melphalan treatment (HDT) and autologous hematopoietic stem cell transplantation (ASCT) has improved the survival of patients with multiple myeloma (MM) [1,2]. The three drug combination of bortezomib, thalidomide and dexamethasone (VTD) has shown particularly high response rates, as well as the potential to even achieve deep molecular remissions, and does not impair the mobilization and collection of hematopoietic stem cells [3,4]. The aim of this retrospective single center study was to evaluate the efficacy and toxicity of VTD as an induction therapy for MM outside a clinical trial in Caucasian patients.

Patients and Methods

Between October 2005 and June 2014, 41 adult patients aged between 35 and 77 years, identified by a search in the local database fraction of the Austrian Myeloma Registry, with symptomatic MM requiring treatment according to the International Myeloma Working Group (IMWG) criteria [5], received induction therapy with VTD, consisting of bortezomib 1.3 mg/m² intravenously on days 1, 4, 8, and 11, oral dexamethasone 40 mg on days 1, 2, 4, 5, 8, 9, 11 and 12, and oral thalidomide 100 mg daily in the evening.

All patients received low-molecular weight heparin and oral antiviral prophylaxis. After three to four cycles of VTD, peripheral blood progenitor cells (PBPC) were harvested after priming with G-CSF 2 x 10 µg/kg over five days in patients scheduled for high-dose therapy (mean of collected stem cells 7.22 x 106/kg bodyweight) without additional chemotherapy. Thalidomide was omitted in the last cycle before PBPC mobilization to optimize stem cell yield [6]. For these patients consolidation treatment consisted of 200 mg/m2 melphalan followed by reinfusion of PBPC. Routinely, no further anti-myeloma treatment was given. Transplant ineligible patients received VTD if a rapid response was required, e.g. due to renal insufficiency.

Sampling and evaluation of patients’ data was approved by the local institutional ethics committee (vote number: UN3252) in accordance with the principles of the Declaration of Helsinki.

The first response assessment was performed after three cycles of VTD according to International Uniform Response Criteria for MM [7] with the additional response category of nCR, defined as complete disappearance of monoclonal protein on electrophoresis but positive immunofixation [8]. Toxicities were graded according to the “Common Terminology Criteria of Adverse Events” (CTCAE v4.03) [9].

Patients were allocated to high-risk or standard-risk groups according to IMWG criteria [10]. High-risk cytogenetics were defined as t(4;14), t(14;16) and/or del17p, all by fluorescence in-situ hybridization (FISH) analysis of myeloma cells.

Statistical evaluation was performed using GraphPad PrismTM software for Windows. All tests of statistical significance were two-sided. Unpaired t-test and survival analysis (Log rank-test) were used to identify differences between two groups.


Patient characteristics

41 patients were treated with VTD. Table 1 summarizes the relevant clinical data and disease characteristics. Data on cytogenetic aberrations, detected by FISH on bone marrow plasma cells, were available and informative in 71%; 9 patients (22%) had high-risk cytogenetics with t(4;14), t(14;16) and/or del17p.

    N = 41 %
Age at diagnosis Median age 58  
Range 35-77  
Sex Male 29 71
Female 12 29
ISS I 16 39
II 12 29
III 13 32
Immunoglobulin isotype IgG 24 59
IgA 5 12
IgM 3 7
LC 9 22
Karyotype Normal 8 20
Aberrant 28 68
Not reported 5 12
Cytogenetic risk group (by FISH) High risk* 9 22
Standard risk 27 66

Table 1: Clinical data and disease characteristics of the patients.

High response to VTD-induction therapy and comparison before and after ASCT

Table 2a shows the results of VTD-induction therapy. The median number of VTD-cycles applied was 3 (1-6 cycles). A ≥VGPR was achieved in 54% (n=22) of the patients and 24% (n=10) reached a partial response (PR). A minor response (MR) was achieved in 1 patient and a stable disease (SD) in 3 patients (7%), respectively, whereas in 5 patients the disease progressed. Table 2b shows the response rates of patients after VTD-induction therapy compared to the results of other VTD-trials [11-15].

  N = 41 %
No. of VTD-cycles (mean) 3  
ORR 32 78
CR 6 15
nCR 1 2
VGPR 15 37
PR 10 24
MR 1 2
Stable disease 3 7
PD 5 12

Table 2a: Response rate after VTD-induction therapy according to the International Myeloma Working Group response criteria [7].

References Patients (n) ORR (%) ≥nCR (%) ≥VGPR (%) PR (%) MR/SD (%)
Our pts. 41 78 17 54 24 10
Cavo et al. [11] 236 93 31 62 31 7
Rosinol et al. [12]* 130 85 35 60 25 6
Moreau et al. [13]** 100 88 31 49 39 NR
Kaufman et al.[14]*** 44 91 20 57 34 5
Buda et al. [15]** 43 91 30 51 40 7

Table 2b: Response rate after VTD-induction therapy compared with the results of other VTD-trials.

In 28 patients (68%) PBPC were collected. The mean number of collected CD34+ cells was 7.22 x 106/kg bodyweight (range 2.13 x 106–26 x 106/kg). 25 patients received HDT and ASCT. The median of VTD-cycles before ASCT was 4. 16 patients (39%) did not proceed to ASCT due to age (n=4; 10%), comorbidity (n=5; 12%), mycobacterial infection (n=1; 2%) or insufficient response (<PR, n=6; 15%). Post-induction, 64% of the transplant eligible 25 patients reached a ≥VGPR, thereof 12% a CR (n=3), and 36% reached a PR (n=9). Three months after ASCT the ORR was 100% with a ≥VGPR in 96% of the patients 48% CR/nCR (n=12), 48% VGPR (n=12) and 1 PR.

35 patients were evaluable for OS and PFS. 6 patients (15%) discontinued VTD-induction due to lack of response (<PR, n=4), cardiac decompensation (n=1) or prolonged neutropenia (n=1). At data cut-off (May 31, 2014), the median follow-up was 32 months (range 7-88). The median PFS was 24 months. The median OS has not been reached, the estimated 1-year and 2-year OS rates were 95% and 76%, respectively. An analysis of PFS and OS according to the first response status revealed significant differences between patients with a ≥VGPR (n=20; 57%) and patients with <VGPR (n=15; 43%) [OS 44 vs. 25 months (p=0.036); PFS 29.5 vs. 16 months (p=0.011)]. Significant differences in OS and PFS were also evident in patients who underwent ASCT (n=25; 71%) and patients who did not undergo ASCT (n=10; 29%) [OS 41 vs. 23.5 months (p=0.002); PFS 28 vs. 23 months (p=0.003)]. Overall, there was no significant difference regarding OS and PFS between cytogenetic high-risk (n=7; 20%) and standard-risk patients (n=24; 69%). Median OS was 29 months in the high-risk group vs. 40 month in the standard-risk group (p=0.27), median PFS was 21 months (high-risk) vs. 28 months (standard-risk; p=0.17). Results are shown in Figure 1A-1C.


Figure 1: Survival - results of subgroups of patients (patients). A) Comparison of OS and PFS between patients with a ≥VGPR and patients with a <VGPR; 35 patients. Both OS and PFS were significantly longer in patients with a ≥VGPR (p values <0.05). B) Comparison of OS and PFS between patients who underwent ASCT (ASCT yes) or not (ASCT no); 35 patients. Both OS and PFS were significantly longer in patients who underwent ASCT (p values <0.05). C) Comparison of OS and PFS based on cytogenetic risk groups (high-risk vs. standard-risk); 31 patients P values <0.05 indicate statistical significance (log rank). OS and PFS are time-toevents data. N=number of events/number of patients HR=Hazard ratio.

Toxicities and adverse events associated with therapy

Toxicities are shown in Table 3a. Peripheral neuropathy (PN) was the most common adverse event. Severe infections as defined by CTCAE v4.03 occurred in 3 patients (Mycobacterial infection n=1, febrile neutropenia n=2). Two patients developed a herpes zoster reactivation despite adequate prophylaxis. Hematological toxicities grade III/IV were thrombocytopenia (n=3) and neutropenia (n=2). 2 patients had a thromboembolic event, of which one were grade III/IV (catheter-associated thrombosis of the vena subclavian n=1, ischemic stroke n=1). Table 3b shows the side effects of the patients compared to the results of other VTD-trials [11-14].

  All grades Grade III/IV
N = 41 % N = 41 %
Herpes zoster 2 5 2 5
Infections (bacterial) 8 20 3 7
Peripheral neuropathy 18 44 1 2
Neutropenia 8 20 2 5
Thrombocytopenia 6 15 3 7
Thromboembolic events 2 5 1 2
Nausea 1 2 0 0

Table 3a: Adverse events associated with VTD therapy.

References Infections (%) Peripheral neuropathy (%) Neutropenia (%) Thrombo-cytopenia (%) Thrombo-embolic events (%)
Our pts. 7 2 5 7 2
Cavo et al. [11] 3 10 NR NR 3
Rosinol et al. [12] 21 14 10 8 12
Moreau et al. [13] 10 3 0 3 2
Kaufman et al. [14] 0 9 0 2 4

Table 3b: Grade III/IV toxicities associated with VTD-induction therapy - Comparison to the results of other VTD-trials.

Dose reductions of thalidomide and/or bortezomib were necessary in 10 patients (24%) because of PN.


Various combinations of doublet, triplet and quadruplet regimes including proteasome inhibitors, antracyclines, corticosteroids, immune-modulatory drugs and alkylators, have been used for the initial therapy of patients with MM before ASCT. Still, the optimal choice of a regimen for initial therapy is yet not clear, but regimens combining the most active class of drugs (proteasome inhibitors and immunomodulatory drugs) seem to be most logical therapeutic backbones.

The aim of this retrospective study was to evaluate the response, side effects, and the outcome of patients with MM using the VTD-protocol as induction therapy in unselected Caucasian patients outside a clinical trial, thereby reflecting “real life” myeloma treatment. Comparing our results to published data from clinical trials and retrospective studies in which VTD was given as induction regimen [11-15] (Table 2b), our data confirm that the VTD protocol is a very effective induction regimen outside clinical trials. The observed ORR in our cohort was 78%, with 17% of the patients reaching a CR/nCR, and 37% of the patients reaching VGPR (54% ≥VGPR). These are impressive results in an unselected patient cohort, due to excellent disease control in a short period of time, which is in accordance with published data on VTD-induction therapy [14].

For patients proceeding to ASCT, 12% of the patients reached a CR and 64% a ≥VGPR. After ASCT, all but one patient (96%) reached ≥VGPR, thereof 48% a CR/nCR. Optimal response is considered a prerequisite for long-term disease control [16]. Our post-transplant results are similar to that of the large, randomized phase 3 GIMEMA trial, which compared VTD and TD as a pre-transplant induction therapy followed by double ASCT and further consolidation in patients with newly diagnosed MM [11]. In this trial, 31% of the patients who received induction therapy with VTD reached a CR/nCR, and 62% achieved ≥VGPR. After ASCT-consolidation, rates of CR/nCR and ≥VGPR were 52% and 79%, respectively. As the GIMEMA trial used further post-transplantation VTD consolidation only long-term results will proof the potential additional benefit of this therapeutic element. Furthermore, Ladetto [17] and co-workers reported persistent molecular remission with this approach arguing for minimal residual disease (MRD) triggered allocation of therapies in future clinical trials. Comparing VTD with TD and VBMCP/VBAD/B, also the PETHEMA/GEM study showed similar results in the VTD arm as we observed in our patients after ASCT [12]. The rate of CR increased from 35% after VTD-induction therapy to 46% after ASCT. Of note, our study represents data of an unselected patient cohort.

In our patients the median PFS was 24 months. The median OS from initiation of VTD induction had not been reached after a median follow-up of 32 months, and the estimated 1-year and 2-year OS rates were 95% and 76%, respectively. These data are comparable to the retrospective data of Kaufman et al. (median follow-up 25 months; PFS 27.5 months; 1-year OS rate 95%, 2-year OS rate 82%) [14]. Several studies suggest that the quality of response after induction therapy is a predictor for survival time [18-21]. Consistently, our data show significant differences in OS and PFS between patients with initial response ≥VGPR and <VGPR (Figure 1B).

In general, the VTD-regime is well tolerated [11]. The most common non-hematological toxicity we observed was PN in 44% of the patients (all grades n=18, grade III n=1), which is in accordance to published toxicity data. However, only one patient (2%) developed a PN grade III and no grade IV PN was observed. In the GIMEMA trial 10% of the patients had PN grade III/IV [11]. Kaufman et al. reported similar results regarding the overall incidence of PN as we observed (55%) [14]. In Table 3a, additional grade III/IV toxicities associated with VTD-induction therapy are shown. A dose reduction was necessary in 24% of the patients due to development of PN. The Intergroupe Francophone du Myelome (IFM) conducted a phase 3 trial comparing a reduced dose of bortezomib (1 mg/m² i.v. on days 1, 4, 8 and 11 of a 3 week cycle) and thalidomide (100 mg/day) plus dexamethasone (vtD) with the standard VD-regimen [13]. They could show that in spite of adding thalidomide to the vD-group, there were less cases of PN noticed as in the VD-regime group [13]. Another strategy to improve tolerability of bortezomib was published first in the MMY-3021 Phase III trial [22], where subcutaneous administration of bortezomib in patients with relapsed MM showed a non-inferior efficacy (ORR after induction in both groups 42%) and low rates of PN compared to the intravenous administration of bortezomib (PN all grades: s.c. 38% vs i.v. 53%). These results are confirmed by a number of other prospective and retrospective studies with subcutaneous bortezomib in diverse settings (Cavallo et al. [23]).

In summary, our data confirm VTD as an effective and well tolerated induction therapy in unselected Caucasian patients with MM outside clinical trials. Both tolerance (bortezomib s.c.) as well as applicability of the regimen in elderly patients (bortezomib s.c./weekly) might be further optimized to achieve even better treatment results in more myeloma patients.


This work was supported by an educational grant from Janssen Austria for data analysis and the diploma thesis of Stephanie Riehl. Patients were identified by Mag. Roman Weger from the Austrian Myeloma Registry. Author’s contributions to this work: Steiner and Riehl performed the data analysis & interpretation. Gunsilius, Gastl, Nachbaur, Willenbacher and Steiner wrote the paper.

Conflict of Interest

The authors declare no financial conflict of interest.


Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Relevant Topics

Recommended Conferences

Article Usage

  • Total views: 11684
  • [From(publication date):
    August-2015 - Oct 21, 2017]
  • Breakdown by view type
  • HTML page views : 7920
  • PDF downloads :3764

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2017-18
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri, Food, Aqua and Veterinary Science Journals

Dr. Krish

[email protected]

1-702-714-7001 Extn: 9040

Clinical and Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals


[email protected]

1-702-714-7001Extn: 9042

Chemical Engineering and Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001 Extn: 9040

Earth & Environmental Sciences

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

General Science and Health care Journals

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics and Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001 Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Informatics Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Material Sciences Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Mathematics and Physics Journals

Jim Willison

[email protected]

1-702-714-7001 Extn: 9042

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001 Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

John Behannon

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001 Extn: 9042

© 2008-2017 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version