Cargando…

Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report

RATIONALE: Pancreatic acinar cell carcinoma (PACC) is a relatively rare malignancy of the exocrine pancreas. BRCA2, a cancer susceptibility gene, has been widely studied in breast and ovarian carcinomas as mutation carriers for this gene are at a high risk for cancer development. Olaparib, an oral p...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Mao, Mou, Yu, Hou, Shengzhong, Cao, Dan, Li, Ang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250555/
https://www.ncbi.nlm.nih.gov/pubmed/30407325
http://dx.doi.org/10.1097/MD.0000000000013113
_version_ 1783372939080499200
author Li, Mao
Mou, Yu
Hou, Shengzhong
Cao, Dan
Li, Ang
author_facet Li, Mao
Mou, Yu
Hou, Shengzhong
Cao, Dan
Li, Ang
author_sort Li, Mao
collection PubMed
description RATIONALE: Pancreatic acinar cell carcinoma (PACC) is a relatively rare malignancy of the exocrine pancreas. BRCA2, a cancer susceptibility gene, has been widely studied in breast and ovarian carcinomas as mutation carriers for this gene are at a high risk for cancer development. Olaparib, an oral poly(adenosine diphosphate-ribose) polymerase (PARP) inhibitor, has been approved for the treatment of ovarian cancer with any BRCA 1/2 mutations. Herein, we report the first case of a germline BRCA2-mutated unresectable advanced PACC patient who responded well to olaparib treatment. PATIENT CONCERNS: A 59-year-old male with a family history of cancer presented with a persistent epigastric dull pain for 3 months. DIAGNOSIS: The patient was diagnosed with advanced PACC based on computed tomography (CT) scan, laparotomy, and pathology. INTERVENTIONS: Exploratory laparotomy, intratumoral brachytherapy by radioiodine-125 seeds, modified FOLFIRINOX chemotherapy, and targeted therapy with olaparib were administered. OUTCOMES: The patient responded well to olaparib until the occurrence of severe adverse drug reactions, he died as a result of multiple organ failure with an overall survival period of 12 months. LESSONS: As a PARP inhibitor, olaparib has remarkable curative effect not only on breast and ovarian cancers, but also on other malignancies with BRCA mutations. Patients with advanced cancer could benefit from active targeted therapy with improvement in overall survival and quality of life.
format Online
Article
Text
id pubmed-6250555
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Wolters Kluwer Health
record_format MEDLINE/PubMed
spelling pubmed-62505552018-12-10 Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report Li, Mao Mou, Yu Hou, Shengzhong Cao, Dan Li, Ang Medicine (Baltimore) Research Article RATIONALE: Pancreatic acinar cell carcinoma (PACC) is a relatively rare malignancy of the exocrine pancreas. BRCA2, a cancer susceptibility gene, has been widely studied in breast and ovarian carcinomas as mutation carriers for this gene are at a high risk for cancer development. Olaparib, an oral poly(adenosine diphosphate-ribose) polymerase (PARP) inhibitor, has been approved for the treatment of ovarian cancer with any BRCA 1/2 mutations. Herein, we report the first case of a germline BRCA2-mutated unresectable advanced PACC patient who responded well to olaparib treatment. PATIENT CONCERNS: A 59-year-old male with a family history of cancer presented with a persistent epigastric dull pain for 3 months. DIAGNOSIS: The patient was diagnosed with advanced PACC based on computed tomography (CT) scan, laparotomy, and pathology. INTERVENTIONS: Exploratory laparotomy, intratumoral brachytherapy by radioiodine-125 seeds, modified FOLFIRINOX chemotherapy, and targeted therapy with olaparib were administered. OUTCOMES: The patient responded well to olaparib until the occurrence of severe adverse drug reactions, he died as a result of multiple organ failure with an overall survival period of 12 months. LESSONS: As a PARP inhibitor, olaparib has remarkable curative effect not only on breast and ovarian cancers, but also on other malignancies with BRCA mutations. Patients with advanced cancer could benefit from active targeted therapy with improvement in overall survival and quality of life. Wolters Kluwer Health 2018-11-09 /pmc/articles/PMC6250555/ /pubmed/30407325 http://dx.doi.org/10.1097/MD.0000000000013113 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Li, Mao
Mou, Yu
Hou, Shengzhong
Cao, Dan
Li, Ang
Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report
title Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report
title_full Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report
title_fullStr Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report
title_full_unstemmed Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report
title_short Response of germline BRCA2-mutated advanced pancreatic acinar cell carcinoma to olaparib: A case report
title_sort response of germline brca2-mutated advanced pancreatic acinar cell carcinoma to olaparib: a case report
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6250555/
https://www.ncbi.nlm.nih.gov/pubmed/30407325
http://dx.doi.org/10.1097/MD.0000000000013113
work_keys_str_mv AT limao responseofgermlinebrca2mutatedadvancedpancreaticacinarcellcarcinomatoolaparibacasereport
AT mouyu responseofgermlinebrca2mutatedadvancedpancreaticacinarcellcarcinomatoolaparibacasereport
AT houshengzhong responseofgermlinebrca2mutatedadvancedpancreaticacinarcellcarcinomatoolaparibacasereport
AT caodan responseofgermlinebrca2mutatedadvancedpancreaticacinarcellcarcinomatoolaparibacasereport
AT liang responseofgermlinebrca2mutatedadvancedpancreaticacinarcellcarcinomatoolaparibacasereport