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1.
J Thorac Dis ; 15(8): 4367-4378, 2023 Aug 31.
Artículo en Inglés | MEDLINE | ID: mdl-37691657

RESUMEN

Background: The role for radiotherapy or surgery in the upfront management of brain metastases (BrM) in epidermal growth factor receptor mutant (EGFRm) or anaplastic lymphoma kinase translocation positive (ALK+) non-small cell lung cancer (NSCLC) is uncertain because of a lack of prospective evidence supporting tyrosine kinase inhibitor (TKI) monotherapy. Further understanding of practice heterogeneity is necessary to guide collaborative efforts in establishing guideline recommendations. Methods: We conducted an international survey among medical (MO), clinical (CO), and radiation oncologists (RO), as well as neurosurgeons (NS), of treatment recommendations for asymptomatic BrM (in non-eloquent regions) EGFRm or ALK+ NSCLC patients according to specific clinical scenarios. We grouped and compared treatment recommendations according to specialty. Responses were summarized using counts and percentages and analyzed using the Fisher exact test. Results: A total of 449 surveys were included in the final analysis: 48 CO, 85 MO, 60 NS, and 256 RO. MO and CO were significantly more likely than RO and NS to recommend first-line TKI monotherapy, regardless of the number and/or size of asymptomatic BrM (in non-eloquent regions). Radiotherapy in addition to TKI as first-line management was preferred by all specialties for patients with ≥4 BrM. NS recommended surgical resection more often than other specialties for BrM measuring >2 cm. Conclusions: Recommendations for the management of BrM from EGFRm or ALK+ NSCLC vary significantly according to oncology sub-specialties. Development of multidisciplinary guidelines and further research on establishing optimal treatment strategies is warranted.

2.
Radiother Oncol ; 168: 89-94, 2022 03.
Artículo en Inglés | MEDLINE | ID: mdl-35121033

RESUMEN

BACKGROUND: Radiotherapy (RT) and surgery (Sx) are effective in treating brain metastases. However, immune checkpoint inhibitors (ICI) have shown activity against asymptomatic melanoma brain metastases (MBM). BRAF/MEK inhibitors can be used to treat BRAF V600 mutation positive (BRAF+) MBM. METHOD: We conducted an international survey among experts from medical oncology (MO), clinical oncology (CO), radiation oncology (RO), and neurosurgery (NS) about treatment recommendations for patients with asymptomatic BRAF+ or BRAF mutation negative (BRAF-) MBM. Eighteen specific clinical scenarios were presented and a total of 267 responses were collected. Answers were grouped and compared using Fisher's exact test. RESULTS: In most MBM scenarios, survey respondents, regardless of specialty, favored RT in addition to systemic therapy. However, for patients with BRAF+ MBM, MO and CO were significantly more likely than RO and NS to recommend BRAF/MEK inhibitors alone, without the addition of RT, including the majority of MO (51%) for patients with 1-3 MBM, all <2 cm. Likewise, for BRAF- MBM, MO and CO more commonly recommended single or dual agent ICI only and dual agent ICI therapy alone was the most common recommendation from MO or CO for MBM <2 cm. When at least 1 of 3 MBM (BRAF+ or BRAF-) was >2 cm, upfront Sx was recommended by all groups with the exception that MO and RO recommended RT for BRAF- MBM. CONCLUSIONS: In most clinical settings involving asymptomatic MBM, experts recommended RT in addition to systemic therapy. However, recommendations varied significantly according to specialty, with MO and CO more commonly recommending dual systemic therapy alone for up to 9 BRAF- MBM <2 cm.


Asunto(s)
Neoplasias Encefálicas , Melanoma , Neoplasias Encefálicas/tratamiento farmacológico , Humanos , Melanoma/patología , Mutación , Inhibidores de Proteínas Quinasas/uso terapéutico , Proteínas Proto-Oncogénicas B-raf/genética , Proteínas Proto-Oncogénicas B-raf/uso terapéutico , Encuestas y Cuestionarios
3.
Med J Aust ; 201(1): 58-60, 2014 Jul 07.
Artículo en Inglés | MEDLINE | ID: mdl-24999901

Asunto(s)
Carcinoma de Células Renales/genética , Carcinoma de Células Renales/terapia , Sistemas de Liberación de Medicamentos , Exantema/genética , Indoles/uso terapéutico , Neoplasias Renales/genética , Neoplasias Renales/terapia , Leiomiomatosis/genética , Leiomiomatosis/terapia , Neoplasias Primarias Múltiples/genética , Neoplasias Primarias Múltiples/terapia , Medicina de Precisión , Pirroles/uso terapéutico , Neoplasias Cutáneas/genética , Neoplasias Cutáneas/terapia , Segunda Guerra Mundial , Adulto , Alelos , Carcinoma de Células Renales/diagnóstico , Carcinoma de Células Renales/patología , Deleción Cromosómica , Terapia Combinada , Fumarato Hidratasa/genética , Asesoramiento Genético , Humanos , Médula Renal/patología , Neoplasias Renales/diagnóstico , Neoplasias Renales/patología , Leiomiomatosis/diagnóstico , Leiomiomatosis/patología , Neoplasias Hepáticas/diagnóstico , Neoplasias Hepáticas/genética , Neoplasias Hepáticas/patología , Neoplasias Hepáticas/secundario , Escisión del Ganglio Linfático , Metástasis Linfática/patología , Masculino , Técnicas Analíticas Microfluídicas , Reacción en Cadena de la Polimerasa Multiplex , Invasividad Neoplásica , Estadificación de Neoplasias , Neoplasias Primarias Múltiples/diagnóstico , Neoplasias Primarias Múltiples/patología , Nefrectomía , Nueva Gales del Sur , Análisis de Secuencia por Matrices de Oligonucleótidos , Opsinas de Bastones/genética , Piel/patología , Neoplasias Cutáneas/diagnóstico , Neoplasias Cutáneas/patología , Sunitinib
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