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1.
J Clin Oncol ; 39(32): 3623-3632, 2021 11 10.
Artigo em Inglês | MEDLINE | ID: mdl-34432481

RESUMO

PURPOSE: The Groningen International Study on Sentinel nodes in Vulvar cancer (GROINSS-V)-II investigated whether inguinofemoral radiotherapy is a safe alternative to inguinofemoral lymphadenectomy (IFL) in vulvar cancer patients with a metastatic sentinel node (SN). METHODS: GROINSS-V-II was a prospective multicenter phase-II single-arm treatment trial, including patients with early-stage vulvar cancer (diameter < 4 cm) without signs of lymph node involvement at imaging, who had primary surgical treatment (local excision with SN biopsy). Where the SN was involved (metastasis of any size), inguinofemoral radiotherapy was given (50 Gy). The primary end point was isolated groin recurrence rate at 24 months. Stopping rules were defined for the occurrence of groin recurrences. RESULTS: From December 2005 until October 2016, 1,535 eligible patients were registered. The SN showed metastasis in 322 (21.0%) patients. In June 2010, with 91 SN-positive patients included, the stopping rule was activated because the isolated groin recurrence rate in this group went above our predefined threshold. Among 10 patients with an isolated groin recurrence, nine had SN metastases > 2 mm and/or extracapsular spread. The protocol was amended so that those with SN macrometastases (> 2 mm) underwent standard of care (IFL), whereas patients with SN micrometastases (≤ 2 mm) continued to receive inguinofemoral radiotherapy. Among 160 patients with SN micrometastases, 126 received inguinofemoral radiotherapy, with an ipsilateral isolated groin recurrence rate at 2 years of 1.6%. Among 162 patients with SN macrometastases, the isolated groin recurrence rate at 2 years was 22% in those who underwent radiotherapy, and 6.9% in those who underwent IFL (P = .011). Treatment-related morbidity after radiotherapy was less frequent compared with IFL. CONCLUSION: Inguinofemoral radiotherapy is a safe alternative for IFL in patients with SN micrometastases, with minimal morbidity. For patients with SN macrometastasis, radiotherapy with a total dose of 50 Gy resulted in more isolated groin recurrences compared with IFL.


Assuntos
Excisão de Linfonodo , Doses de Radiação , Linfonodo Sentinela/efeitos da radiação , Linfonodo Sentinela/cirurgia , Neoplasias Vulvares/terapia , Idoso , Feminino , Humanos , Excisão de Linfonodo/efeitos adversos , Excisão de Linfonodo/mortalidade , Metástase Linfática , Pessoa de Meia-Idade , Micrometástase de Neoplasia , Estadiamento de Neoplasias , Estudos Prospectivos , Linfonodo Sentinela/patologia , Fatores de Tempo , Resultado do Tratamento , Neoplasias Vulvares/mortalidade , Neoplasias Vulvares/patologia
2.
Cancer Res ; 63(2): 400-3, 2003 Jan 15.
Artigo em Inglês | MEDLINE | ID: mdl-12543794

RESUMO

Polymorphisms in human leukocyte antigen (HLA) genes have been implicated in the risk for developing human papillomavirus (HPV)-associated cervical neoplasia. By comparison with local cadaver controls typed for HLA class I (n = 946) and II (n = 144) antigens, HPV-16-positive high grade vulval intraepithelial neoplasia patients (n = 42) showed significantly different frequencies of HLA-A2 [odds ratio (OR), 2.1; confidence interval (CI), 1.4-3.9], HLA-B7 (OR, 2.6; CI, 1.4-4.7), HLA-DRB1*01(01/02/04) (OR, 0.1; CI, 0.03-0.5), HLA-DRB1*11 (OR, 3.3; CI, 1.4-7.1), HLA-DRB1*13 (OR, 0), HLA-DQB1*05 (OR, 0.2; CI, 0.05-0.6), and HLA-DQB1*03032 (OR, 4.6; CI, 1.5-14.0). With the exception of HLA-B7 and HLA-DRB1*11, these significant differences were also seen comparative to local HPV-16-positive cervical carcinoma patients (n = 114), suggesting a specific immunogenetic contribution that is independent of HPV-16 infection in high-grade vulval intraepithelial neoplasia. Such factors are important to the development of HPV vaccines for treatment of cervical and vulval neoplasia.


Assuntos
Antígenos HLA-A/genética , Antígenos HLA-DR/genética , Papillomaviridae/classificação , Infecções por Papillomavirus/imunologia , Infecções Tumorais por Vírus/imunologia , Neoplasias Vulvares/imunologia , Neoplasias Vulvares/virologia , Biópsia , Feminino , Humanos , Infecções por Papillomavirus/genética , Infecções por Papillomavirus/patologia , Polimorfismo Genético , Infecções Tumorais por Vírus/genética , Infecções Tumorais por Vírus/patologia , Neoplasias Vulvares/genética , Neoplasias Vulvares/patologia
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