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Pseudoprogression in a patient with metastatic melanoma treated with PD-1 and LAG-3 inhibition.
Wu, Lawrence W; Tao, Jacqueline J; McDonnell, Diana; Izar, Benjamin.
Afiliação
  • Wu LW; Division of Hematology and Oncology, Department of Medicine.
  • Tao JJ; Division of Hematology and Oncology, Department of Medicine.
  • McDonnell D; Division of Hematology and Oncology, Department of Medicine.
  • Izar B; Division of Hematology and Oncology, Department of Medicine, Columbia University Irving Medical Center, Vagelos College of Physicians & Surgeons, New York, New York, USA.
Melanoma Res ; 34(4): 382-385, 2024 08 01.
Article em En | MEDLINE | ID: mdl-38640504
ABSTRACT
Pseudoprogression encapsulates a process of temporary radiographic growth followed by subsequent regression of metastatic melanoma lesions in response to immune checkpoint blockade (ICB), such as the combination of anti-programmed cell death protein 1 (PD-1) and anticytotoxic T-lymphocyte-associated antigen 4 therapy. This occurs in approximately 5-10% of ICB-treated patients, but has not yet been described in the context of novel combination therapies. Here, we report a case of an 89-year-old patient with metastatic melanoma to the liver, lung and lymph nodes, who underwent treatment with Opdualag (combining anti-PD-1 nivolumab and anti-lymphocyte-activation gene 3 relatlimab ICBs), and developed pseudoprogression after two cycles of therapy. The patient experienced a radiographic increase in liver metastatic lesion size, but was found to have a subsequent reduction in these lesions. The patient has been on therapy for 18 months without evidence of disease progression and continues to be clinically well-appearing.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Receptor de Morte Celular Programada 1 / Melanoma Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Receptor de Morte Celular Programada 1 / Melanoma Idioma: En Ano de publicação: 2024 Tipo de documento: Article