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9.
JAMA Dermatol ; 158(12): 1394-1403, 2022 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-36129688

RESUMO

Importance: Psoriasis is an inflammatory condition associated with metabolic and cardiovascular disease. Apremilast, a phosphodiesterase 4 inhibitor, is commonly used for psoriasis and can cause weight loss. Objective: To determine the association between apremilast and aortic vascular inflammation as assessed by 18F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG-PET/CT), cardiometabolic markers (primary outcomes at week 16), and abdominal fat composition. Design, Setting, and Participants: A single-arm, open-label, interventional, nonrandomized clinical trial in which the imaging and laboratory outcomes were measured by an investigator who was blinded to time was conducted between April 11, 2017, and August 17, 2021, at 7 dermatology sites in the United States. A total of 101 patients with moderate to severe psoriasis were screened, 70 enrolled, 60 completed week 16, and 39 completed week 52. Intervention: Apremilast, 30 mg, twice daily. Main Outcomes and Measures: Aortic vascular inflammation (measured by FDG-PET/CT), 68 cardiometabolic biomarkers, and abdominal fat composition (measured by CT) at week 16 and week 52 compared with baseline. Results: The mean (SD) age of the 70 patients was 47.5 (14.6) years, 54 were male (77.1%), 4 were Black (5.7%), and 58 were White (82.9%). There was no change in aortic vascular inflammation at week 16 (target to background ratio, -0.02; 95% CI, -0.08 to 0.05; P = .61) or week 52 (target to background ratio, -0.07; 95% CI, -0.15 to 0.01; P = .09) compared with baseline. At week 16, potentially beneficial decreases in interleukin 1b, valine, leucine, isoleucine, fetuin A, and branched-chain amino acids were observed. At week 52 compared with baseline, potentially beneficial decreases in ferritin, ß-hydroxybutyrate, acetone, and ketone bodies, with an increase in apolipoprotein A-1, were observed, but there was a reduction in cholesterol efflux. There was an approximately 5% to 6% reduction in subcutaneous and visceral adiposity at week 16 that was maintained at week 52. Conclusions and Relevance: The findings of this nonrandomized clinical trial suggest that apremilast has a neutral association with aortic vascular inflammation, variable but generally beneficial associations with a subset of cardiometabolic biomarkers, and associations with reductions in visceral and subcutaneous fat, indicating that the drug may have an overall benefit for patients with cardiometabolic disease and psoriasis. Trial Registration: ClinicalTrials.gov Identifier: NCT03082729.


Assuntos
Doenças Cardiovasculares , Psoríase , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Doenças Cardiovasculares/etiologia , Fluordesoxiglucose F18 , Inflamação/tratamento farmacológico , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Psoríase/tratamento farmacológico , Psoríase/complicações , Índice de Gravidade de Doença , Resultado do Tratamento
10.
J Natl Compr Canc Netw ; 9 Suppl 4: S1-22, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-21976013

RESUMO

Biologics are essential to oncology care. As patents for older biologics begin to expire, the United States is developing an abbreviated regulatory process for the approval of similar biologics (biosimilars), which raises important considerations for the safe and appropriate incorporation of biosimilars into clinical practice for patients with cancer. The potential for biosimilars to reduce the cost of biologics, which are often high-cost components of oncology care, was the impetus behind the Biologics Price Competition and Innovation Act of 2009, a part of the 2010 Affordable Care Act. In March 2011, NCCN assembled a work group consisting of thought leaders from NCCN Member Institutions and other organizations, to provide guidance regarding the challenges health care providers and other key stakeholders face in incorporating biosimilars in health care practice. The work group identified challenges surrounding biosimilars, including health care provider knowledge, substitution practices, pharmacovigilance, naming and product tracking, coverage and reimbursement, use in off-label settings, and data requirements for approval.


Assuntos
Antineoplásicos/uso terapêutico , Medicamentos Biossimilares/uso terapêutico , Aprovação de Drogas/legislação & jurisprudência , Antineoplásicos/efeitos adversos , Antineoplásicos/economia , Medicamentos Biossimilares/efeitos adversos , Medicamentos Biossimilares/economia , Aprovação de Drogas/organização & administração , Medicamentos Genéricos/economia , Medicamentos Genéricos/uso terapêutico , Europa (Continente) , Humanos , Neoplasias/tratamento farmacológico , Estados Unidos , Organização Mundial da Saúde
11.
Mo Med ; 113(5): 407-408, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-30228509
12.
Mo Med ; 113(6): 444-445, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-30228523
13.
Health Aff (Millwood) ; 40(2): 235-242, 2021 02.
Artigo em Inglês | MEDLINE | ID: mdl-33476208

RESUMO

It is likely that 2021 will be a dynamic year for US health care policy. There is pressing need and opportunity for health reform that helps achieve better access, affordability, and equity. In this commentary, which is part of the National Academy of Medicine's Vital Directions for Health and Health Care: Priorities for 2021 initiative, we draw on our collective backgrounds in health financing, delivery, and innovation to offer consensus-based policy recommendations focused on health costs and financing. We organize our recommendations around five policy priorities: expanding insurance coverage, accelerating the transition to value-based care, advancing home-based care, improving the affordability of drugs and other therapeutics, and developing a high-value workforce. Within each priority we provide recommendations for key elected officials and political appointees that could be used as starting points for evidence-based policy making that supports a more effective, efficient, and equitable health system in the US.


Assuntos
Reforma dos Serviços de Saúde , Financiamento da Assistência à Saúde , Atenção à Saúde , Custos de Cuidados de Saúde , Humanos , Formulação de Políticas
14.
J Invest Dermatol ; 140(9): 1784-1793.e2, 2020 09.
Artigo em Inglês | MEDLINE | ID: mdl-32088207

RESUMO

Psoriasis, a chronic immune-mediated disease, is associated with an increased risk of cardiovascular events and mortality. Secukinumab selectively neutralizes IL-17A and has reported high efficacy with a favorable safety profile in various psoriatic disease manifestations. Subsequent to the 12-week randomized, placebo-controlled, double-blind treatment period, patients with moderate-to-severe psoriasis received secukinumab for 40 weeks. Vascular inflammation using 18F-2-fluorodeoxyglucose-positron emission tomography/computed tomography imaging and blood-based cardiometabolic was assessed at week 0, 12, and 52. The difference in change in aortic inflammation from baseline to week 12 for secukinumab (n = 46) versus placebo (n = 45) was -0.053 (95% confidence interval = -0.169 to 0.064; P= 0.37). Small increases in total cholesterol, low-density lipoprotein, and low-density lipoprotein particles, but no changes in markers of inflammation, adiposity, insulin resistance, or predictors of diabetes, were observed with secukinumab treatment compared with placebo. At week 52, reductions in TNF-α (P= 0.0063) and ferritin (P= 0.0354), and an increase in fetuin-A (P= 0.0024), were observed with secukinumab treatment compared with baseline. No significant changes in aortic inflammation or markers of advanced lipoprotein characterization, adiposity, or insulin resistance were observed with secukinumab treatment compared with baseline. Secukinumab exhibited a neutral impact on aortic vascular inflammation and biomarkers of cardiometabolic disease after 52 weeks of treatment.


Assuntos
Anticorpos Monoclonais Humanizados/administração & dosagem , Arterite/tratamento farmacológico , Síndrome Metabólica/diagnóstico , Psoríase/tratamento farmacológico , Adulto , Anticorpos Monoclonais Humanizados/efeitos adversos , Aorta/diagnóstico por imagem , Aorta/efeitos dos fármacos , Aorta/imunologia , Arterite/sangue , Arterite/diagnóstico , Arterite/imunologia , Biomarcadores/sangue , Método Duplo-Cego , Feminino , Fluordesoxiglucose F18 , Humanos , Interleucina-17/antagonistas & inibidores , Interleucina-17/imunologia , Masculino , Síndrome Metabólica/sangue , Síndrome Metabólica/imunologia , Síndrome Metabólica/prevenção & controle , Pessoa de Meia-Idade , Placebos/administração & dosagem , Placebos/efeitos adversos , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Psoríase/sangue , Psoríase/complicações , Psoríase/imunologia , Índice de Gravidade de Doença , Resultado do Tratamento
16.
JAMA Health Forum ; 5(7): e242691, 2024 Jul 05.
Artigo em Inglês | MEDLINE | ID: mdl-38990560

RESUMO

This JAMA Forum discusses pending legislation in the US House and Senate and the history of the "firm-based approach" the US Food and Drug Administration (FDA) could use when regulating artificial intelligence (AI) medical devices to augment patient care.


Assuntos
Inteligência Artificial , United States Food and Drug Administration , Estados Unidos , United States Food and Drug Administration/legislação & jurisprudência , Humanos , Inteligência Artificial/legislação & jurisprudência , Regulamentação Governamental
17.
JAMA Health Forum ; 5(4): e241233, 2024 Apr 05.
Artigo em Inglês | MEDLINE | ID: mdl-38602704

RESUMO

This JAMA Forum discusses the US Food and Drug Administration's efforts to implement the 2009 Family Smoking Prevention and Tobacco Control Act through approval of products that demonstrate evidence to help smokers quit and to reduce their risk of relapse.


Assuntos
Produtos do Tabaco , Produtos do Tabaco/efeitos adversos
18.
JAMA Health Forum ; 4(3): e230639, 2023 03 03.
Artigo em Inglês | MEDLINE | ID: mdl-36862406

RESUMO

This JAMA Forum discusses implementation of the Medicare drug pricing provision of the Inflation Reduction Act of 2022 and ways the new frameworks can be tweaked to achieve the desired public health goals.


Assuntos
Custos de Medicamentos , Medicare , Idoso , Estados Unidos , Humanos
19.
JAMA Health Forum ; 4(12): e235460, 2023 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-38153743

RESUMO

This JAMA Forum discusses 3 regulatory lessons from the US Food and Drug Administration that could be used for regulating new medical devices and technologies, such as those that include artificial intelligence.

20.
JAMA Health Forum ; 4(9): e233909, 2023 09 01.
Artigo em Inglês | MEDLINE | ID: mdl-37733359

RESUMO

This JAMA Forum discusses categories of artificial intelligence devices such as clinical decision support tools and large language models that are increasing being used in health care and the improvements needed to ensure the accuracy and rigor of these tools for patient use.


Assuntos
Atenção à Saúde , Instalações de Saúde
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