[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases]
Descripción del Articulo
Objectives: To determine the rate of optimal cytoreduction in patients with advanced ovarian cancer who received neoadjuvant chemotherapy with dose-dense carboplatin and paclitaxel followed by interval debulking surgery (IDS). Materials and methods: A retrospective study of a series of cases of Peru...
| Autores: | , , , , , , , , |
|---|---|
| Formato: | artículo |
| Fecha de Publicación: | 2018 |
| Institución: | Instituto Nacional de Enfermedades Neoplásicas |
| Repositorio: | INEN-Institucional |
| Lenguaje: | español |
| OAI Identifier: | oai:repositorio.inen.sld.pe:inen/138 |
| Enlace del recurso: | https://repositorio.inen.sld.pe/handle/inen/138 |
| Nivel de acceso: | acceso abierto |
| Materia: | https://purl.org/pe-repo/ocde/ford#3.02.21 |
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Alcarraz, CMuñiz, JMas, LOlivera, MMorante, ZAlvarez, MMantilla, RAraujo, JPinto, J2024-07-01T16:28:58Z2024-07-01T16:28:58Z2018Objectives: To determine the rate of optimal cytoreduction in patients with advanced ovarian cancer who received neoadjuvant chemotherapy with dose-dense carboplatin and paclitaxel followed by interval debulking surgery (IDS). Materials and methods: A retrospective study of a series of cases of Peruvian women treated with neoadjuvant chemotherapy with carboplatin (6 AUC mg/mL/min) and paclitaxel (80 mg/m2 weekly) followed by IDS, at the National Institute of Neoplastic Diseases during the 2010-2014 period. Results: The 41 patients who made it to the interval surgery had a median age of 59 years (range: 47-73 years). In 37 (90.2%) patients, high-grade serous adenocarcinoma histology was reported. Thirty-four (82.9%) achieved optimal cytoreduction and five (14.7%), a complete pathological response. Progression-free survival at one year and two years was 74.7% and 51.8%, respectively. Overall survival at one year and two years was 85.2% and 71.4%, respectively. The risk of progression and death was greater in patients without optimal cytoreduction and in patients with postsurgery levels of carcinoembryonic antigen 125 > 30 U/mL. Conclusions: Neoadjuvant therapy with dose-dense carboplatin and paclitaxel achieved an elevated frequency of optimal cytoreduction. The post-surgery levels of carcinoembryonic antigen 125 and optimal cytoreduction were independent factors of progression-free survival and overall survival.application/pdf10.17843/rpmesp.2018.351.3599https://repositorio.inen.sld.pe/handle/inen/138spaRev Peru Med Exp Salud PublicaPEInstituto Nacional de Saludinfo:eu-repo/semantics/openAccessdc.rights.uri: https//creativecomons.org/licenses/by/4.0/https://purl.org/pe-repo/ocde/ford#3.02.21[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases]info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionreponame:INEN-Institucionalinstname:Instituto Nacional de Enfermedades Neoplásicasinstacron:INENPublicationORIGINALAlcarraz, C 2018.pdfapplication/pdf298906https://repositorio.inen.sld.pe/bitstreams/2a547e8b-193d-439b-ad62-782636703c07/download3dec5977c31c83b9f09bb076b619657bMD51TEXTAlcarraz, C 2018.pdf.txtAlcarraz, C 2018.pdf.txtExtracted texttext/plain40507https://repositorio.inen.sld.pe/bitstreams/a82385a4-653b-415f-bf2f-b8bdd4e04690/downloadd464b2a5517dd38617062e2c5f02da93MD52THUMBNAILAlcarraz, C 2018.pdf.jpgAlcarraz, C 2018.pdf.jpgGenerated Thumbnailimage/jpeg5467https://repositorio.inen.sld.pe/bitstreams/a32b42f9-3221-495f-9a78-4f6ee8b89042/download3d3a8aaec68d6500b4bb36dc9c7fe438MD53inen/138oai:repositorio.inen.sld.pe:inen/1382024-10-23 18:04:06.74dc.rights.uri: https//creativecomons.org/licenses/by/4.0/info:eu-repo/semantics/openAccesshttps://repositorio.inen.sld.peRepositorio INENrepositorioinendspace@gmail.com |
| dc.title.none.fl_str_mv |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] |
| title |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] |
| spellingShingle |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] Alcarraz, C https://purl.org/pe-repo/ocde/ford#3.02.21 |
| title_short |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] |
| title_full |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] |
| title_fullStr |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] |
| title_full_unstemmed |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] |
| title_sort |
[Optimal cytoreduction in advanced ovarian cancer treated with dose-dense paclitaxel and carboplatin followed by interval surgery at the Peruvian National Institute of Neoplastic Diseases] |
| author |
Alcarraz, C |
| author_facet |
Alcarraz, C Muñiz, J Mas, L Olivera, M Morante, Z Alvarez, M Mantilla, R Araujo, J Pinto, J |
| author_role |
author |
| author2 |
Muñiz, J Mas, L Olivera, M Morante, Z Alvarez, M Mantilla, R Araujo, J Pinto, J |
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author author author author author author author author |
| dc.contributor.author.fl_str_mv |
Alcarraz, C Muñiz, J Mas, L Olivera, M Morante, Z Alvarez, M Mantilla, R Araujo, J Pinto, J |
| dc.subject.ocde.none.fl_str_mv |
https://purl.org/pe-repo/ocde/ford#3.02.21 |
| topic |
https://purl.org/pe-repo/ocde/ford#3.02.21 |
| description |
Objectives: To determine the rate of optimal cytoreduction in patients with advanced ovarian cancer who received neoadjuvant chemotherapy with dose-dense carboplatin and paclitaxel followed by interval debulking surgery (IDS). Materials and methods: A retrospective study of a series of cases of Peruvian women treated with neoadjuvant chemotherapy with carboplatin (6 AUC mg/mL/min) and paclitaxel (80 mg/m2 weekly) followed by IDS, at the National Institute of Neoplastic Diseases during the 2010-2014 period. Results: The 41 patients who made it to the interval surgery had a median age of 59 years (range: 47-73 years). In 37 (90.2%) patients, high-grade serous adenocarcinoma histology was reported. Thirty-four (82.9%) achieved optimal cytoreduction and five (14.7%), a complete pathological response. Progression-free survival at one year and two years was 74.7% and 51.8%, respectively. Overall survival at one year and two years was 85.2% and 71.4%, respectively. The risk of progression and death was greater in patients without optimal cytoreduction and in patients with postsurgery levels of carcinoembryonic antigen 125 > 30 U/mL. Conclusions: Neoadjuvant therapy with dose-dense carboplatin and paclitaxel achieved an elevated frequency of optimal cytoreduction. The post-surgery levels of carcinoembryonic antigen 125 and optimal cytoreduction were independent factors of progression-free survival and overall survival. |
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2018 |
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2018 |
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info:eu-repo/semantics/article |
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10.17843/rpmesp.2018.351.3599 |
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https://repositorio.inen.sld.pe/handle/inen/138 |
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spa |
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dc.rights.uri: https//creativecomons.org/licenses/by/4.0/ |
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Rev Peru Med Exp Salud Publica |
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).