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DOI: 10.5935/2526-8732.20190012
Induction chemotherapy with cisplatin plus weekly paclitaxel followed by chemoradiotherapy for locally advanced squamous cell carcinoma of the head and neck
Quimioterapia de indução com cisplatina e paclitaxel semanal seguida de quimiorradioterapia para carcinoma de células escamosas de cabeça e pescoço localmente avançado
Financial support: none to declare.ABSTRACT
The paclitaxel-cisplatin is a non-infusional alternative for induction chemotherapy (IC) for LASCCHN based on phase-II trials. Here, we describe our institutional experience with this combination in Southern Brazil. Methods: Thirty-three consecutive patients with unresectable LASCCHN were selected between April/2012 and June/2014. They received weekly paclitaxel 80mg/m2 on days 1, 8, 15 and cisplatin 75mg/m2 on day 1 for three cycles followed by chemoradiotherapy (CRT) with cisplatin at standard dose. Overall response, toxicity, progression free survival (PFS) and overall survival (OS) were evaluated. Results: The median follow-up was 25.5 months. Median age was 58.6 years and 96% had PS 1. Most patients presented with bulky disease at stages IVA and IVB (60.6% and 21.2%, respectively). Concerning primary site of tumor, 33.3% were oropharingeal tumors, 27.3% larynx tumors and 33.3% oral cavity tumors. The majority of patients had both smoking and alcohol abuse records. Twenty-eight patients (84.8%) at the time of diagnosis had a BMI <25. Twenty-seven patients (81.8%) completed the planned treatment and three patients (9%) underwent exclusive radiotherapy after IC. All patients were evaluated for response; 75.7% presented complete response and 21.2% presented partial response. Severe toxicity (grades 3-5) for asthenia, neutropenia, anemia and thrombocytopenia were observed in 6.1%, 9.1%, 6.1% and 3% of patients, respectively. One treatment-related death was associated with febrile neutropenia. The 2- and 3-year PFS rates were 63.3% and 68.4%, respectively; 2- and 3-year OS rates were 62.3.5% and 50.6%. Conclusions: Our results corroborate previous observations that IC (paclitaxel-cisplatin) is a well-tolerated and highly active regimen for the treatment of patients with LASSHNC, being associated with acceptable toxicity, good locoregional control and survival rates. This may be a good treatment option for patients in developing countries.
RESUMO
O esquema paclitaxel-cisplatina é uma alternativa não-infusional como quimioterapia de indução (QI) para carcinomas escamosos de cabeça e pescoço localmente avançados, baseado em estudos de fase II. Descrevemos, aqui, nossa experiência institucional com esta modalidade de tratamento. Métodos: Trinta e três pacientes consecutivos diagnosticados com carcinoma escamoso de cabeça e pescoço localmente avançado, não-ressecável, foram selecionados entre abril/2012 e junho/2014. Receberam paclitaxel 80 mg/m2 nos dias 1, 8 e 15 + cisplatina 75 mg/m2 no D1 por três ciclos, seguidos por quimiorradioterapia com cisplatina em dose padrão. Foram avaliadas resposta global, toxicidade, sobrevida livre de progressão (SLP) e sobrevida global (SG). Resultados: A mediana de seguimento foi de 25,5 meses. A mediana de idade foi de 58,6 anos e 96% dos pacientes apresentaram PS 1. A maioria dos pacientes apresentou doença volumosa em estágios IVA e IVB (60,6% e 21,2%, respectivamente). Quanto ao sítio primário, 33,3% eram tumores orofaríngeos, 27,3% tumores de laringe e 33,3% tumores de cavidade oral. Vinte e oito pacientes (84,8%) apresentaram IMC <25 ao diagnóstico. Vinte e sete pacientes (81,8%) completaram o tratamento planejado e três pacientes (9%) foram submetidos à radioterapia exclusiva após QI. Todos os pacientes foram avaliados quanto à resposta; 75,7% apresentaram resposta completa e 21,2% apresentaram resposta parcial. Foi observada toxicidade grave (G3-5) para astenia, neutropenia, anemia e trombocitopenia em 6,1%, 9,1%, 6,1% e 3% dos pacientes, respectivamente. Um óbito relacionado ao tratamento foi atribuído à neutropenia febril. As taxas de SLP para 2 e 3 anos foram de 63,3% e 68,4%, respectivamente; as taxas de SG para 2 e 3 anos foram de 62,3,5% e 50,6%. Conclusões: Nossos resultados corroboram observações prévias de que QI (paclitaxel-cisplatina) é um regime bem tolerado e altamente ativo para o tratamento de pacientes com carcinomas escamosos de cabeça e pescoço localmente avançados, estando associado a toxicidade tolerável, controle locorregional e taxas de sobrevida satisfatórios. Esta pode ser uma opção de tratamento adequada a ser considerada para pacientes em países em desenvolvimento.
Keywords:
Head and Neck Cancer - Induction Chemotherapy - Chemoradiation Therapy - Squamous Cell Carcinoma.Descritores:
Câncer de Cabeça e Pescoço - Quimioterapia de Indução - Quimiorradioterapia - Carcinoma de Células Escamosas.Publication History
Received: 13 August 2018
Accepted: 28 May 2019
Article published online:
02 July 2019
© 2022. This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Thieme Revinter Publicações Ltda.
Rua do Matoso 170, Rio de Janeiro, RJ, CEP 20270-135, Brazil
Sargeele Silva, Rafael Grochot, Debora Cristina Weschenfelder, Cláudio Pescador, Catherine Gotardo, Diego Gnatta, André Reiriz, Janaina Brollo. Induction chemotherapy with cisplatin plus weekly paclitaxel followed by chemoradiotherapy for locally advanced squamous cell carcinoma of the head and neck. Brazilian Journal of Oncology 2019; 15: e-20190012.
DOI: 10.5935/2526-8732.20190012
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