Safety and utility of image-guided research biopsies in relapsed high-grade serous ovarian carcinoma-experience of the BriTROC consortium.
dc.contributor.author | Goranova, T | |
dc.contributor.author | Ennis, D | |
dc.contributor.author | Piskorz, AM | |
dc.contributor.author | Macintyre, Geoff | |
dc.contributor.author | Lewsley, LA | |
dc.contributor.author | Stobo, J | |
dc.contributor.author | Wilson, C | |
dc.contributor.author | Kay, D | |
dc.contributor.author | Glasspool, RM | |
dc.contributor.author | Lockley, M | |
dc.contributor.author | Brockbank, E | |
dc.contributor.author | Montes, A | |
dc.contributor.author | Walther, A | |
dc.contributor.author | Sundar, S | |
dc.contributor.author | Edmondson, R | |
dc.contributor.author | Hall, GD | |
dc.contributor.author | Clamp, A | |
dc.contributor.author | Gourley, C | |
dc.contributor.author | Hall, M | |
dc.contributor.author | Fotopoulou, C | |
dc.contributor.author | Gabra, H | |
dc.contributor.author | Freeman, S | |
dc.contributor.author | Moore, Luiza | |
dc.contributor.author | Jimenez-Linan, M | |
dc.contributor.author | Paul, J | |
dc.contributor.author | Brenton, James | |
dc.contributor.author | McNeish, IA | |
dc.date.accessioned | 2018-11-14T00:32:36Z | |
dc.date.available | 2018-11-14T00:32:36Z | |
dc.date.issued | 2017-05-09 | |
dc.identifier.issn | 0007-0920 | |
dc.identifier.uri | https://www.repository.cam.ac.uk/handle/1810/285091 | |
dc.description.abstract | BACKGROUND: Investigating tumour evolution and acquired chemotherapy resistance requires analysis of sequential tumour material. We describe the feasibility of obtaining research biopsies in women with relapsed ovarian high-grade serous carcinoma (HGSC). METHODS: Women with relapsed ovarian HGSC underwent either image-guided biopsy or intra-operative biopsy during secondary debulking, and samples were fixed in methanol-based fixative. Tagged-amplicon sequencing was performed on biopsy DNA. RESULTS: We screened 519 patients in order to enrol 220. Two hundred and two patients underwent successful biopsy, 118 of which were image-guided. There were 22 study-related adverse events (AE) in the image-guided biopsies, all grades 1 and 2; pain was the commonest AE. There were pre-specified significant AE in 3/118 biopsies (2.5%). 87% biopsies were fit-for-purpose for genomic analyses. Median DNA yield was 2.87 μg, and was higher in biopsies utilising 14 G or 16 G needles compared to 18 G. TP53 mutations were identified in 94.4% patients. CONCLUSIONS: Obtaining tumour biopsies for research in relapsed HGSC is safe and feasible. Adverse events are rare. The large majority of biopsies yield sufficient DNA for genomic analyses-we recommend use of larger gauge needles and methanol fixation for such biopsies, as DNA yields are higher but with no increase in AEs. | |
dc.format.medium | Print-Electronic | |
dc.language | eng | |
dc.publisher | Springer Science and Business Media LLC | |
dc.rights | Attribution-NonCommercial-ShareAlike 4.0 International | |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-sa/4.0/ | |
dc.subject | Peritoneum | |
dc.subject | Omentum | |
dc.subject | Liver | |
dc.subject | Lymph Nodes | |
dc.subject | Humans | |
dc.subject | Carcinoma | |
dc.subject | Peritoneal Neoplasms | |
dc.subject | Liver Neoplasms | |
dc.subject | Ovarian Neoplasms | |
dc.subject | Lymphatic Metastasis | |
dc.subject | Pain | |
dc.subject | Proto-Oncogene Proteins B-raf | |
dc.subject | DNA, Neoplasm | |
dc.subject | Feasibility Studies | |
dc.subject | DNA Mutational Analysis | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Aged, 80 and over | |
dc.subject | Middle Aged | |
dc.subject | Female | |
dc.subject | Tumor Suppressor Protein p53 | |
dc.subject | Proto-Oncogene Proteins p21(ras) | |
dc.subject | PTEN Phosphohydrolase | |
dc.subject | Phosphatidylinositol 3-Kinases | |
dc.subject | Class I Phosphatidylinositol 3-Kinases | |
dc.subject | Neoplasm Grading | |
dc.subject | Image-Guided Biopsy | |
dc.subject | ErbB Receptors | |
dc.title | Safety and utility of image-guided research biopsies in relapsed high-grade serous ovarian carcinoma-experience of the BriTROC consortium. | |
dc.type | Article | |
prism.endingPage | 1301 | |
prism.issueIdentifier | 10 | |
prism.publicationDate | 2017 | |
prism.publicationName | Br J Cancer | |
prism.startingPage | 1294 | |
prism.volume | 116 | |
dc.identifier.doi | 10.17863/CAM.32461 | |
dcterms.dateAccepted | 2017-03-03 | |
rioxxterms.versionofrecord | 10.1038/bjc.2017.86 | |
rioxxterms.licenseref.uri | http://www.rioxx.net/licenses/all-rights-reserved | |
rioxxterms.licenseref.startdate | 2017-05 | |
dc.contributor.orcid | Macintyre, Geoff [0000-0003-3906-467X] | |
dc.contributor.orcid | Moore, Luiza [0000-0001-5315-516X] | |
dc.contributor.orcid | Brenton, James [0000-0002-5738-6683] | |
dc.identifier.eissn | 1532-1827 | |
rioxxterms.type | Journal Article/Review | |
pubs.funder-project-id | Cancer Research UK (A15973) | |
pubs.funder-project-id | Cancer Research UK (A15601) | |
cam.issuedOnline | 2017-03-30 |
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