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1.
J Plast Reconstr Aesthet Surg ; 94: 50-53, 2024 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-38759511

RESUMEN

This study evaluated trends in Medicare reimbursement for commonly performed breast oncologic and reconstructive procedures. Average national relative value units (RVUs) for physician-based work, facilities, and malpractice were collected along with the corresponding conversion factors for each year. From 2010 to 2021, there was an overall average decrease of 15% in Medicare reimbursement for both breast oncology (-11%) and reconstructive procedures (-16%). Based on these findings, breast and reconstructive surgeons should advocate for reimbursement that better reflects the costs of their practice.


Asunto(s)
Neoplasias de la Mama , Mamoplastia , Medicare , Humanos , Estados Unidos , Neoplasias de la Mama/cirugía , Neoplasias de la Mama/economía , Medicare/economía , Femenino , Mamoplastia/economía , Mamoplastia/tendencias , Reembolso de Seguro de Salud/economía , Reembolso de Seguro de Salud/tendencias , Mecanismo de Reembolso
2.
Oncoimmunology ; 10(1): 1912892, 2021 04 21.
Artículo en Inglés | MEDLINE | ID: mdl-33996265

RESUMEN

Concurrent blockade of different checkpoint receptors, notably PD-1 and CTLA-4, elicits greater anti-tumor activity for some tumor types, and the combination of different checkpoint receptor inhibitors is an active area of clinical research. We have previously demonstrated that anti-tumor vaccination, by activating CD8 + T cells, increases the expression of PD-1, CTLA-4, LAG-3 and other inhibitory receptors, and the anti-tumor efficacy of vaccination can be increased with checkpoint blockade. In the current study, we sought to determine whether anti-tumor vaccination might be further improved with combined checkpoint blockade. Using an OVA-expressing mouse tumor model, we found that CD8 + T cells activated in the presence of professional antigen presenting cells (APC) expressed multiple checkpoint receptors; however, T cells activated without APCs expressed LAG-3 alone, suggesting that LAG-3 might be a preferred target in combination with vaccination. Using three different murine tumor models, and peptide or DNA vaccines targeting three tumor antigens, we assessed the effects of vaccines with blockade of PD-1 and/or LAG-3 on tumor growth. We report that, in each model, the anti-tumor efficacy of vaccination was increased with PD-1 and/or LAG-3 blockade. However, combined PD-1 and LAG-3 blockade elicited the greatest anti-tumor effect when combined with vaccination in a MycCaP prostate cancer model in which PD-1 blockade alone with vaccination targeting a "self" tumor antigen had less efficacy. These results suggest anti-tumor vaccination might best be combined with concurrent blockade of both PD-1 and LAG-3, and potentially other checkpoint receptors whose expression is increased on CD8 + T cells following vaccine-mediated activation.


Asunto(s)
Antígenos CD , Vacunas contra el Cáncer , Neoplasias , Receptor de Muerte Celular Programada 1 , Vacunas de ADN , Animales , Linfocitos T CD8-positivos , Masculino , Ratones , Neoplasias/tratamiento farmacológico , Proteína del Gen 3 de Activación de Linfocitos
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