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Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study

BACKGROUND: Selinexor is an oral, selective nuclear export inhibitor. STORM was a phase 2b, single-arm, open-label, multicenter trial of selinexor with low dose dexamethasone in patients with penta-exposed relapsed/refractory multiple myeloma (RRMM) that met its primary endpoint, with overall respon...

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Autores principales: Tremblay, Gabriel, Daniele, Patrick, Breeze, Janis, Li, Lingling, Shah, Jatin, Shacham, Sharon, Kauffman, Michael, Engelhardt, Monika, Chari, Ajaj, Nooka, Ajay, Vogl, Dan, Gavriatopoulou, Maria, Dimopoulos, Meletios-Athanasios, Richardson, Paul, Biran, Noa, Siegel, David, Vlummens, Philip, Doyen, Chantal, Facon, Thierry, Mohty, Mohamad, Meuleman, Nathalie, Levy, Moshe, Costa, Luciano, Hoffman, James E., Delforge, Michel, Kaminetzky, David, Weisel, Katja, Raab, Marc, Dingli, David, Tuchman, Sascha, Laurent, Frenzel, Vij, Ravi, Schiller, Gary, Moreau, Philippe, Richter, Joshua, Schreder, Martin, Podar, Klaus, Parker, Terri, Cornell, Robert Frank, Lionel, Karlin, Choquet, Sylvain, Sundar, Jagannath
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419947/
https://www.ncbi.nlm.nih.gov/pubmed/34488662
http://dx.doi.org/10.1186/s12885-021-08453-9
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author Tremblay, Gabriel
Daniele, Patrick
Breeze, Janis
Li, Lingling
Shah, Jatin
Shacham, Sharon
Kauffman, Michael
Engelhardt, Monika
Chari, Ajaj
Nooka, Ajay
Vogl, Dan
Gavriatopoulou, Maria
Dimopoulos, Meletios-Athanasios
Richardson, Paul
Biran, Noa
Siegel, David
Vlummens, Philip
Doyen, Chantal
Facon, Thierry
Mohty, Mohamad
Meuleman, Nathalie
Levy, Moshe
Costa, Luciano
Hoffman, James E.
Delforge, Michel
Kaminetzky, David
Weisel, Katja
Raab, Marc
Dingli, David
Tuchman, Sascha
Laurent, Frenzel
Vij, Ravi
Schiller, Gary
Moreau, Philippe
Richter, Joshua
Schreder, Martin
Podar, Klaus
Parker, Terri
Cornell, Robert Frank
Lionel, Karlin
Choquet, Sylvain
Sundar, Jagannath
author_facet Tremblay, Gabriel
Daniele, Patrick
Breeze, Janis
Li, Lingling
Shah, Jatin
Shacham, Sharon
Kauffman, Michael
Engelhardt, Monika
Chari, Ajaj
Nooka, Ajay
Vogl, Dan
Gavriatopoulou, Maria
Dimopoulos, Meletios-Athanasios
Richardson, Paul
Biran, Noa
Siegel, David
Vlummens, Philip
Doyen, Chantal
Facon, Thierry
Mohty, Mohamad
Meuleman, Nathalie
Levy, Moshe
Costa, Luciano
Hoffman, James E.
Delforge, Michel
Kaminetzky, David
Weisel, Katja
Raab, Marc
Dingli, David
Tuchman, Sascha
Laurent, Frenzel
Vij, Ravi
Schiller, Gary
Moreau, Philippe
Richter, Joshua
Schreder, Martin
Podar, Klaus
Parker, Terri
Cornell, Robert Frank
Lionel, Karlin
Choquet, Sylvain
Sundar, Jagannath
author_sort Tremblay, Gabriel
collection PubMed
description BACKGROUND: Selinexor is an oral, selective nuclear export inhibitor. STORM was a phase 2b, single-arm, open-label, multicenter trial of selinexor with low dose dexamethasone in patients with penta-exposed relapsed/refractory multiple myeloma (RRMM) that met its primary endpoint, with overall response of 26% (95% confidence interval [CI], 19 to 35%). Health-related quality of life (HRQoL) was a secondary endpoint measured using the Functional Assessment of Cancer Therapy – Multiple Myeloma (FACT-MM). This study examines impact of selinexor treatment on HRQoL of patients treated in STORM and reports two approaches to calculate minimal clinically important differences for the FACT-MM. METHODS: FACT-MM data were collected at baseline, on day 1 of each 4-week treatment cycle, and at end of treatment (EOT). Changes from baseline were analyzed for the FACT-MM total score, FACT-trial outcome index (TOI), FACT-General (FACT-G), and the MM-specific domain using mixed-effects regression models. Two approaches for evaluating minimal clinically important differences were explored: the first defined as 10% of the instrument range, and the second based on estimated mean baseline differences between Eastern Cooperative Oncology Group performance status (ECOG PS) scores. Post-hoc difference analysis compared change in scores from baseline to EOT for treatment responders and non-responders. RESULTS: Eighty patients were included in the analysis; the mean number of prior therapies was 7.9 (standard deviation [SD] 3.1), and mean duration of myeloma was 7.6 years (SD 3.4). Each exploratory minimal clinically important difference threshold yielded consistent results whereby most patients did not experience HRQoL decline during the first six cycles of treatment (range: 53.9 to 75.7% for the first approach; range: 52.6 to 72.9% for the second). Treatment responders experienced less decline in HRQoL from baseline to EOT than non-responders, which was significant for the FACT-G, but not for other scores. CONCLUSION: The majority of patients did not experience decline in HRQoL based on minimal clinically important differences during early cycles of treatment with selinexor and dexamethasone in the STORM trial. An anchor-based approach utilizing patient-level data (ECOG PS score) to define minimal clinically important differences for the FACT-MM gave consistent results with a distribution-based approach. TRIAL REGISTRATION: This trial was registered on ClinicalTrials.gov under the trial-ID NCT02336815 on January 8, 2015. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08453-9.
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spelling pubmed-84199472021-09-09 Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study Tremblay, Gabriel Daniele, Patrick Breeze, Janis Li, Lingling Shah, Jatin Shacham, Sharon Kauffman, Michael Engelhardt, Monika Chari, Ajaj Nooka, Ajay Vogl, Dan Gavriatopoulou, Maria Dimopoulos, Meletios-Athanasios Richardson, Paul Biran, Noa Siegel, David Vlummens, Philip Doyen, Chantal Facon, Thierry Mohty, Mohamad Meuleman, Nathalie Levy, Moshe Costa, Luciano Hoffman, James E. Delforge, Michel Kaminetzky, David Weisel, Katja Raab, Marc Dingli, David Tuchman, Sascha Laurent, Frenzel Vij, Ravi Schiller, Gary Moreau, Philippe Richter, Joshua Schreder, Martin Podar, Klaus Parker, Terri Cornell, Robert Frank Lionel, Karlin Choquet, Sylvain Sundar, Jagannath BMC Cancer Research Article BACKGROUND: Selinexor is an oral, selective nuclear export inhibitor. STORM was a phase 2b, single-arm, open-label, multicenter trial of selinexor with low dose dexamethasone in patients with penta-exposed relapsed/refractory multiple myeloma (RRMM) that met its primary endpoint, with overall response of 26% (95% confidence interval [CI], 19 to 35%). Health-related quality of life (HRQoL) was a secondary endpoint measured using the Functional Assessment of Cancer Therapy – Multiple Myeloma (FACT-MM). This study examines impact of selinexor treatment on HRQoL of patients treated in STORM and reports two approaches to calculate minimal clinically important differences for the FACT-MM. METHODS: FACT-MM data were collected at baseline, on day 1 of each 4-week treatment cycle, and at end of treatment (EOT). Changes from baseline were analyzed for the FACT-MM total score, FACT-trial outcome index (TOI), FACT-General (FACT-G), and the MM-specific domain using mixed-effects regression models. Two approaches for evaluating minimal clinically important differences were explored: the first defined as 10% of the instrument range, and the second based on estimated mean baseline differences between Eastern Cooperative Oncology Group performance status (ECOG PS) scores. Post-hoc difference analysis compared change in scores from baseline to EOT for treatment responders and non-responders. RESULTS: Eighty patients were included in the analysis; the mean number of prior therapies was 7.9 (standard deviation [SD] 3.1), and mean duration of myeloma was 7.6 years (SD 3.4). Each exploratory minimal clinically important difference threshold yielded consistent results whereby most patients did not experience HRQoL decline during the first six cycles of treatment (range: 53.9 to 75.7% for the first approach; range: 52.6 to 72.9% for the second). Treatment responders experienced less decline in HRQoL from baseline to EOT than non-responders, which was significant for the FACT-G, but not for other scores. CONCLUSION: The majority of patients did not experience decline in HRQoL based on minimal clinically important differences during early cycles of treatment with selinexor and dexamethasone in the STORM trial. An anchor-based approach utilizing patient-level data (ECOG PS score) to define minimal clinically important differences for the FACT-MM gave consistent results with a distribution-based approach. TRIAL REGISTRATION: This trial was registered on ClinicalTrials.gov under the trial-ID NCT02336815 on January 8, 2015. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12885-021-08453-9. BioMed Central 2021-09-06 /pmc/articles/PMC8419947/ /pubmed/34488662 http://dx.doi.org/10.1186/s12885-021-08453-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Tremblay, Gabriel
Daniele, Patrick
Breeze, Janis
Li, Lingling
Shah, Jatin
Shacham, Sharon
Kauffman, Michael
Engelhardt, Monika
Chari, Ajaj
Nooka, Ajay
Vogl, Dan
Gavriatopoulou, Maria
Dimopoulos, Meletios-Athanasios
Richardson, Paul
Biran, Noa
Siegel, David
Vlummens, Philip
Doyen, Chantal
Facon, Thierry
Mohty, Mohamad
Meuleman, Nathalie
Levy, Moshe
Costa, Luciano
Hoffman, James E.
Delforge, Michel
Kaminetzky, David
Weisel, Katja
Raab, Marc
Dingli, David
Tuchman, Sascha
Laurent, Frenzel
Vij, Ravi
Schiller, Gary
Moreau, Philippe
Richter, Joshua
Schreder, Martin
Podar, Klaus
Parker, Terri
Cornell, Robert Frank
Lionel, Karlin
Choquet, Sylvain
Sundar, Jagannath
Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study
title Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study
title_full Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study
title_fullStr Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study
title_full_unstemmed Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study
title_short Quality of life analyses in patients with multiple myeloma: results from the Selinexor (KPT-330) Treatment of Refractory Myeloma (STORM) phase 2b study
title_sort quality of life analyses in patients with multiple myeloma: results from the selinexor (kpt-330) treatment of refractory myeloma (storm) phase 2b study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8419947/
https://www.ncbi.nlm.nih.gov/pubmed/34488662
http://dx.doi.org/10.1186/s12885-021-08453-9
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