Craig J. Gibson
Celgene
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Featured researches published by Craig J. Gibson.
Clinical Lymphoma, Myeloma & Leukemia | 2015
Katja Weisel; Meletios A. Dimopoulos; Kevin W. Song; Philippe Moreau; Antonio Palumbo; Andrew R. Belch; Stephen Schey; Pieter Sonneveld; Lars Sternas; Xin Yu; Ramesh Amatya; Craig J. Gibson; Mohamed H. Zaki; Christian Jacques; Jesús F. San Miguel
BACKGROUND Health-related quality of life (HRQoL) is an important element for consideration in treatment decisions in patients with relapsed/refractory multiple myeloma (RRMM). The pivotal MM-003 (A Phase 3, Multicenter, Randomized, Open-Label Study to Compare the Efficacy and Safety of Pomalidomide in Combination With Low-Dose Dexamethasone vs. High-Dose Dexamethasone in Patients With Refractory Multiple Myeloma or Relapsed and Refractory Multiple Myeloma and Companion Study [NIMBUS]) randomized, open-label, multicenter, phase III trial demonstrated improved progression-free survival (PFS) and prolonged overall survival (OS) with pomalidomide (POM) plus low-dose dexamethasone (POM + LoDEX) versus high-dose dexamethasone (HiDEX) in patients with RRMM in whom lenalidomide (LEN) and bortezomib (BORT) had failed. MM-003 also investigated HRQoL as a predefined secondary end point. PATIENTS AND METHODS Recruited patients (n = 455) were refractory to their last treatment and had failed LEN and BORT after ≥ 2 consecutive cycles of each (alone or in combination). Eight clinically relevant and validated HRQoL domains from the European Organisation for Research and Treatment of Cancer (EORTC) QLQ-C30, EORTC QLQ-MY20, and EQ-5D questionnaires were selected for analysis. Time to symptom worsening based on minimally important differences (MIDs) was calculated. RESULTS Clinically meaningful improvements in HRQoL as determined by MIDs, regression analyses, and best response analyses were observed more frequently in patients receiving POM + LoDEX than in those receiving HiDEX. POM + LoDEX significantly extended median time to clinically meaningful worsening in HRQoL versus HiDEX in 4 HRQoL domains and demonstrated a trend in an additional 3 domains. Patients in the HiDEX arm experienced earlier HRQoL deterioration compared with those in the POM + LoDEX arm in each domain analyzed. CONCLUSION POM + LoDEX offer good clinical outcomes that lead to improved and prolonged HRQoL compared with HiDEX in patients with RRMM and end-stage disease.
Current Medical Research and Opinion | 2015
Steven R. Arikian; Dejan Milentijevic; Gary Binder; Craig J. Gibson; X. Henry Hu; Yasir Nagarwala; Mohamad A. Hussein; Frank A. Corvino; Andy Surinach; Saad Z Usmani
Abstract Background: Few studies have addressed the cost patterns of patients with multiple myeloma (MM) before and after first relapse. This US claims analysis evaluated, from a US health plan perspective, patterns of total direct costs of care from treatment initiation to progression for patients with MM treated with novel agents, using time to next therapy (TTNT) as a proxy measure for progression. Methods: A retrospective study was conducted using a large US claims database, evaluating patients with claims for MM between 2006 and 2013. Patients with claims for stem cell transplant (SCT) were excluded. The analysis focused on patients receiving lenalidomide (LEN) or bortezomib (BORT) based treatment, for whom complete claim history was available through initiation of subsequent treatment. Average patient monthly direct costs were determined, including medical and pharmacy costs, and total cost patterns over quarterly time periods were calculated. Results: The study population comprised 2843 patients with newly diagnosed MM (NDMM) and 1361 with relapsed MM. Total monthly cost for patients with NDMM declined steadily, from
Journal of Medical Economics | 2016
S. Z. Usmani; J Cavenagh; Andrew R. Belch; C. Hulin; S. Basu; D. White; A. Nooka; Annette Ervin-Haynes; W. Yiu; Y. Nagarwala; A. Berger; C. G. Pelligra; S. Guo; Gary Binder; Craig J. Gibson; T. Facon
15,734 initially to
Leukemia & Lymphoma | 2016
Philippe Moreau; Katja Weisel; Kevin W. Song; Craig J. Gibson; Owain Saunders; Lars Sternas; Kevin Hong; Mohamed H. Zaki; Meletios A. Dimopoulos
5082 at 18+ months after therapy. Upon initiation of second-line therapy, total monthly costs rose to
Leukemia & Lymphoma | 2018
Dan T. Vogl; Michel Delforge; Kevin W. Song; Shien Guo; Craig J. Gibson; Annette Ervin-Haynes; Thierry Facon
13,876 and declined to
Annals of Hematology | 2018
Rafat Abonour; Lynne I. Wagner; Brian G. M. Durie; Sundar Jagannath; Mohit Narang; Howard R. Terebelo; Cristina Gasparetto; Kathleen Toomey; James W. Hardin; Amani Kitali; Craig J. Gibson; Shankar Srinivasan; Arlene S. Swern; Robert M. Rifkin
6446 18 months later. Although NDMM cost levels for individual ordinal months were similar between the LEN and BORT groups, TTNT was longer for LEN-based treatments (37 months). The BORT-treated cohort had higher average monthly total costs for NDMM and for the common time period through 37 months after initiation of therapy (
Blood | 2016
Rafat Abonour; Brian G. M. Durie; Sundar Jagannath; Jatin J. Shah; Mohit Narang; Howard R. Terebelo; Cristina Gasparetto; Kathleen Toomey; James W. Hardin; Amani Kitali; Craig J. Gibson; Shankar Srinivasan; Arlene S. Swern; Robert M. Rifkin
7534 vs
Oncology and Therapy | 2017
Steve Schey; Luis Felipe Casado Montero; Chloe Stengel-Tosetti; Craig J. Gibson; Sujith Dhanasiri
10,763 for LEN and BORT, respectively). Key limitations of this study, in addition to the lack of mortality and staging information available from claims data, include the definition of TTNT based on change in treatment or a defined gap in therapy prior to retreatment, which may differ from actual time of progression in some patients. Conclusions: For patients with NDMM receiving either LEN- or BORT-based treatment without SCT, followed until TTNT, total direct monthly costs (drug + medical) declined steadily over time. Monthly costs returned to near initial levels when patients began second-line therapy and then followed a similar pattern of decline. Due to the longer TTNT for patients initiated on LEN and the associated longer period of below-average costs, patients initiated with LEN-based treatments had mean monthly total costs >
Journal of Clinical Oncology | 2017
Philip L. McCarthy; Sarah A. Holstein; Sin-Ho Jung; Miranda Cooper; Craig J. Gibson; Edward A. Stadtmauer; Benjamin Winograd; Paul G. Richardson
3200 lower than total costs for patients initiated on BORT during the first 3 years after starting treatment, cumulating to nearly
American health & drug benefits | 2015
Safiya Abouzaid; Craig J. Gibson; Yasir Nagarwala
120,000 in lower costs for patients initiated on LEN.