Héctor Carlos García-Díaz , María Larrosa-Garcia , Javier Gómez-Alonso , Mara Cruellas , Enriqueta Felip , Teresa Macarulla , Anna Farriols , Maria J. Carreras
{"title":"奥拉帕尼在同源重组基因受损患者罕见肿瘤部位的超说明书使用。","authors":"Héctor Carlos García-Díaz , María Larrosa-Garcia , Javier Gómez-Alonso , Mara Cruellas , Enriqueta Felip , Teresa Macarulla , Anna Farriols , Maria J. Carreras","doi":"10.1016/j.farma.2025.04.005","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>To describe the effectiveness and safety of olaparib off-label indications in patients with impaired homologous recombination genes and solid tumors different than those authorized.</div></div><div><h3>Methods</h3><div>A single-center, observational and retrospective study including patients treated with olaparib for off-label use. The main variables were patient characteristics, prior therapies, response to therapy, progression-free survival, overall survival and adverse events.</div></div><div><h3>Results</h3><div>A total of 6 patients were included. All patients had metastases and received 3 or more lines of prior treatment. The primary tumor locations and mutations were partner and localizer of <em>BRCA2</em> (<em>PALB2)</em> intrahepatic cholangiocarcinoma, ataxia telangiectasia mutated (<em>ATM)</em> non-small cell lung adenocarcinoma, somatic breast cancer gene (<em>sBRCA2)</em> colorectal cancer, germinal breast cancer gene 2 (<em>gBRCA2)</em> breast neuroendocrine tumor, <em>gBRCA2</em> ampullary cancer and <em>gBRCA2</em> pancreatic neuroendocrine tumor. At the end of the study, one patient was still receiving olaparib showing more than 25 months of sustained stable disease response. No novel toxicities were observed besides those included in the product information.</div></div><div><h3>Conclusions</h3><div>There is limited published evidence on the use of olaparib in patients harboring pathogenic variants other than breast cancer genes<em>,</em> like <em>PALB2</em> and <em>ATM</em> and conditions different than those authorized such as digestive tract, neuroendocrine and lung tumors. Further research is to assess the efficacy of olaparib in these patients.</div></div>","PeriodicalId":45860,"journal":{"name":"FARMACIA HOSPITALARIA","volume":"49 5","pages":"Pages T286-T290"},"PeriodicalIF":1.3000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Artículo traducido] Uso fuera de indicación de olaparib en localizaciones tumorales poco frecuentes en pacientes con genes alterados de la recombinación homóloga\",\"authors\":\"Héctor Carlos García-Díaz , María Larrosa-Garcia , Javier Gómez-Alonso , Mara Cruellas , Enriqueta Felip , Teresa Macarulla , Anna Farriols , Maria J. Carreras\",\"doi\":\"10.1016/j.farma.2025.04.005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Objective</h3><div>To describe the effectiveness and safety of olaparib off-label indications in patients with impaired homologous recombination genes and solid tumors different than those authorized.</div></div><div><h3>Methods</h3><div>A single-center, observational and retrospective study including patients treated with olaparib for off-label use. The main variables were patient characteristics, prior therapies, response to therapy, progression-free survival, overall survival and adverse events.</div></div><div><h3>Results</h3><div>A total of 6 patients were included. All patients had metastases and received 3 or more lines of prior treatment. The primary tumor locations and mutations were partner and localizer of <em>BRCA2</em> (<em>PALB2)</em> intrahepatic cholangiocarcinoma, ataxia telangiectasia mutated (<em>ATM)</em> non-small cell lung adenocarcinoma, somatic breast cancer gene (<em>sBRCA2)</em> colorectal cancer, germinal breast cancer gene 2 (<em>gBRCA2)</em> breast neuroendocrine tumor, <em>gBRCA2</em> ampullary cancer and <em>gBRCA2</em> pancreatic neuroendocrine tumor. At the end of the study, one patient was still receiving olaparib showing more than 25 months of sustained stable disease response. No novel toxicities were observed besides those included in the product information.</div></div><div><h3>Conclusions</h3><div>There is limited published evidence on the use of olaparib in patients harboring pathogenic variants other than breast cancer genes<em>,</em> like <em>PALB2</em> and <em>ATM</em> and conditions different than those authorized such as digestive tract, neuroendocrine and lung tumors. Further research is to assess the efficacy of olaparib in these patients.</div></div>\",\"PeriodicalId\":45860,\"journal\":{\"name\":\"FARMACIA HOSPITALARIA\",\"volume\":\"49 5\",\"pages\":\"Pages T286-T290\"},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"FARMACIA HOSPITALARIA\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1130634325000625\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"FARMACIA HOSPITALARIA","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1130634325000625","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
[Artículo traducido] Uso fuera de indicación de olaparib en localizaciones tumorales poco frecuentes en pacientes con genes alterados de la recombinación homóloga
Objective
To describe the effectiveness and safety of olaparib off-label indications in patients with impaired homologous recombination genes and solid tumors different than those authorized.
Methods
A single-center, observational and retrospective study including patients treated with olaparib for off-label use. The main variables were patient characteristics, prior therapies, response to therapy, progression-free survival, overall survival and adverse events.
Results
A total of 6 patients were included. All patients had metastases and received 3 or more lines of prior treatment. The primary tumor locations and mutations were partner and localizer of BRCA2 (PALB2) intrahepatic cholangiocarcinoma, ataxia telangiectasia mutated (ATM) non-small cell lung adenocarcinoma, somatic breast cancer gene (sBRCA2) colorectal cancer, germinal breast cancer gene 2 (gBRCA2) breast neuroendocrine tumor, gBRCA2 ampullary cancer and gBRCA2 pancreatic neuroendocrine tumor. At the end of the study, one patient was still receiving olaparib showing more than 25 months of sustained stable disease response. No novel toxicities were observed besides those included in the product information.
Conclusions
There is limited published evidence on the use of olaparib in patients harboring pathogenic variants other than breast cancer genes, like PALB2 and ATM and conditions different than those authorized such as digestive tract, neuroendocrine and lung tumors. Further research is to assess the efficacy of olaparib in these patients.
期刊介绍:
Una gran revista para acceder a los mejores artículos originales y revisiones de la farmacoterapia actual. Además, es Órgano de expresión científica de la Sociedad Española de Farmacia Hospitalaria, y está indexada en Index Medicus/Medline, EMBASE/Excerpta Médica, Alert, Internacional Pharmaceutical Abstracts y SCOPUS.