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Cited by 265

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

Persistent Overall Survival Benefit and No Increased Risk of Second Malignancies With Bortezomib-Melphalan-Prednisone Versus Melphalan-Prednisone in Patients With Previously Untreated Multiple Myeloma

Open access
San Miguel, Jesús F., Schlag, Rudolf, Khuageva, Nuriet K., Dimopoulos, Meletios A., Shpilberg, Ofer, Kropff, Martin, Spicka, Ivan, Petrucci, Maria Teresa, Palumbo, Antonio, Samoilova, Olga S., Dmoszynska, Anna, Abdulkadyrov, Kudrat M., Delforge, Michel, Jiang, Bin, Mateos, Maria-Victoria, Anderson, Kenneth C., Esseltine, Dixie-Lee, Liu, Kevin, Deraedt, William, Cakana, Andrew, van de Velde, Helgi, Richardson, Paul G.·2013·Journal of Clinical Oncology

Abstract

Purpose: This final analysis of the phase III VISTA trial (Velcade As Initial Standard Therapy in Multiple Myeloma: Assessment With Melphalan and Prednisone) was conducted to determine whether the overall survival (OS) benefit with bortezomib-melphalan-prednisone (VMP) versus melphalan-prednisone (MP) in patients with myeloma who were ineligible for transplantation was maintained after 5 years of follow-up and to explore the risk of second primary malignancies. Patients and Methods: In all, 682 patients received up to nine 6-week cycles of VMP or MP and were then observed every 12 weeks or less. Data on second primary malignancies were collected by individual patient inquiries at all sites from 655 patients. Results: After median follow-up of 60.1 months (range, 0 to 74 months), there was a 31% reduced risk of death with VMP versus MP (hazard ratio [HR], 0.695; P < .001; median OS 56.4 v 43.1 months). OS benefit with VMP was seen across prespecified patient subgroups (age ≥ 75 years, stage III myeloma, creatinine clearance < 60 mL/min). Sixty-three percent of VMP patients and 73% of MP patients had received subsequent therapy. Time to next therapy (median, 30.7 v 20.5 months; HR, 0.557; P < .001) was longer with VMP than with MP. Among patients who received subsequent therapies, survival from start of subsequent therapy was similar following VMP (median, 28.1 months) or MP (median, 26.8 months; HR, 0.914). Following VMP/MP, incidence proportions of hematologic malignancies (1%/1%) and solid tumors (5%/3%) and exposure-adjusted incidence rates (0.017/0.013 per patient-year) were similar and were consistent with background rates. Conclusion: VMP resulted in a significant reduction in risk of death versus MP that was maintained after 5 years' follow-up and despite substantial use of novel-agent-based salvage therapies. There is no emerging safety signal for second primary malignancies following VMP.

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Metadata

Authors
San Miguel, J. F., Schlag, R., Khuageva, N. K., Dimopoulos, M. A., Shpilberg, O., Kropff, M., Spicka, I., Petrucci, M. T., Palumbo, A., Samoilova, O. S., Dmoszynska, A., Abdulkadyrov, K. M., Delforge, M., Jiang, B., Mateos, M.-V., Anderson, K. C., Esseltine, D.-L., Liu, K., Deraedt, W., Cakana, A., van de Velde, H., & Richardson, P. G.
Venue
Journal of Clinical Oncology
Published
2013-02-01
Volume
31
Issue
4
Pages
448-455
ISSN
  • 0732-183X (ISSN-L)
  • 1527-7755
OpenAlex
W2158106888
Cited by
265
References
40
FWCI
18.44
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Persistent Overall Survival Benefit and No Increased Risk of Second Malignancies With Bortezomib-Melphalan-Prednisone Versus Melphalan-Prednisone in Patients With Previously Untreated Multiple Myeloma. https://app.cochat.ai/papers/10.1200/jco.2012.41.6180
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San Miguel, J. F., Schlag, R., Khuageva, N. K., Dimopoulos, M. A., Shpilberg, O., Kropff, M., Spicka, I., Petrucci, M. T., Palumbo, A., Samoilova, O. S., Dmoszynska, A., Abdulkadyrov, K. M., Delforge, M., Jiang, B., Mateos, M.-V., Anderson, K. C., Esseltine, D.-L., Liu, K., Deraedt, W., . . . Richardson, P. G. (2013). Persistent Overall Survival Benefit and No Increased Risk of Second Malignancies With Bortezomib-Melphalan-Prednisone Versus Melphalan-Prednisone in Patients With Previously Untreated Multiple Myeloma. Journal of Clinical Oncology. https://doi.org/10.1200/jco.2012.41.6180

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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