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Off-label prescribing of immune checkpoint inhibitor therapy at a single pediatric cancer center.
Gikandi, Ajami; Chi, Susan N; Yeo, Kee Kiat; O'Neill, Allison F; Shulman, David S; DuBois, Steven G; Collins, Natalie B.
Afiliação
  • Gikandi A; Harvard Medical School, Boston, Massachusetts, USA.
  • Chi SN; Harvard Medical School, Boston, Massachusetts, USA.
  • Yeo KK; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.
  • O'Neill AF; Harvard Medical School, Boston, Massachusetts, USA.
  • Shulman DS; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.
  • DuBois SG; Harvard Medical School, Boston, Massachusetts, USA.
  • Collins NB; Dana-Farber/Boston Children's Cancer and Blood Disorders Center, Harvard Medical School, Boston, Massachusetts, USA.
Cancer Med ; 13(8): e7154, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38629258
ABSTRACT

BACKGROUND:

Immune checkpoint inhibitors (ICI) have improved outcomes in a variety of adult cancers and are prescribed with increasing frequency across oncology. However, patterns of off-label use of ICI in pediatrics remain unclear.

METHODS:

This is a single-institution, retrospective cohort study evaluating off-label ICI use in pediatric and young adult patients with cancer treated at our institution from 2014 to 2022. Response was based on clinician assessment derived from clinical records. Immune-related adverse events (iRAEs) were classified according to CTCAE v5.0.

RESULTS:

We identified 50 unique patients treated with off-label ICI (28 with solid tumors, 20 with central nervous system (CNS) tumors, 2 with hematologic malignancies). At time of ICI initiation, only five patients (10%) had localized disease, and all but one patient was treated in the relapsed/refractory setting. All patients were treated with the FDA-approved weight-based dosing recommendations. Overall, there was disease control in 21 patients (42%), with best response including one complete response (melanoma), two partial responses (high-grade glioma, CNS nongerminomatous germ cell tumor), and 18 patients with stable disease. Forty-four patients (88%) eventually experienced disease progression. Among 22 patients (44%) experiencing iRAEs, 10 (20%) had a grade ≥3 irAE, 12 (24%) required corticosteroids, and 14 (28%) required ICI discontinuation. irAE occurrence was associated with significantly improved progression-free survival (HR 0.35; 95% CI 0.18 to 0.68; p = 0.002) and overall survival (HR 0.33; 95% CI 0.17 to 0.66; p = 0.002).

CONCLUSIONS:

At our institution, ICI was most commonly prescribed in the relapsed/refractory setting to patients with metastatic disease. The treatment was generally well-tolerated in the pediatric population. The overall response rate was low, and the majority of patients eventually experienced disease progression. A few patients, however, had durable treatment responses. Further studies are needed to identify which pediatric patients are most likely to benefit from ICI.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores de Checkpoint Imunológico / Glioma Limite: Adult / Child / Humans Idioma: En Revista: Cancer Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Inibidores de Checkpoint Imunológico / Glioma Limite: Adult / Child / Humans Idioma: En Revista: Cancer Med Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos