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1.
J Thorac Dis ; 15(8): 4367-4378, 2023 Aug 31.
Artigo em Inglês | MEDLINE | ID: mdl-37691657

RESUMO

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.
Artigo em Inglês | MEDLINE | ID: mdl-35121033

RESUMO

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.


Assuntos
Neoplasias Encefálicas , Melanoma , Neoplasias Encefálicas/tratamento farmacológico , Humanos , Melanoma/patologia , Mutação , Inibidores de Proteínas Quinases/uso terapêutico , Proteínas Proto-Oncogênicas B-raf/genética , Proteínas Proto-Oncogênicas B-raf/uso terapêutico , Inquéritos e Questionários
3.
Med J Aust ; 201(1): 58-60, 2014 Jul 07.
Artigo em Inglês | MEDLINE | ID: mdl-24999901

Assuntos
Carcinoma de Células Renais/genética , Carcinoma de Células Renais/terapia , Sistemas de Liberação de Medicamentos , Exantema/genética , Indóis/uso terapêutico , Neoplasias Renais/genética , Neoplasias Renais/terapia , Leiomiomatose/genética , Leiomiomatose/terapia , Neoplasias Primárias Múltiplas/genética , Neoplasias Primárias Múltiplas/terapia , Medicina de Precisão , Pirróis/uso terapêutico , Neoplasias Cutâneas/genética , Neoplasias Cutâneas/terapia , II Guerra Mundial , Adulto , Alelos , Carcinoma de Células Renais/diagnóstico , Carcinoma de Células Renais/patologia , Deleção Cromossômica , Terapia Combinada , Fumarato Hidratase/genética , Aconselhamento Genético , Humanos , Medula Renal/patologia , Neoplasias Renais/diagnóstico , Neoplasias Renais/patologia , Leiomiomatose/diagnóstico , Leiomiomatose/patologia , Neoplasias Hepáticas/diagnóstico , Neoplasias Hepáticas/genética , Neoplasias Hepáticas/patologia , Neoplasias Hepáticas/secundário , Excisão de Linfonodo , Metástase Linfática/patologia , Masculino , Técnicas Analíticas Microfluídicas , Reação em Cadeia da Polimerase Multiplex , Invasividade Neoplásica , Estadiamento de Neoplasias , Neoplasias Primárias Múltiplas/diagnóstico , Neoplasias Primárias Múltiplas/patologia , Nefrectomia , New South Wales , Análise de Sequência com Séries de Oligonucleotídeos , Opsinas de Bastonetes/genética , Pele/patologia , Neoplasias Cutâneas/diagnóstico , Neoplasias Cutâneas/patologia , Sunitinibe
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