Image-guided tumour biopsies in a prospective molecular triage study (MOSCATO-01): What are the real risks?. (November 2018)
- Record Type:
- Journal Article
- Title:
- Image-guided tumour biopsies in a prospective molecular triage study (MOSCATO-01): What are the real risks?. (November 2018)
- Main Title:
- Image-guided tumour biopsies in a prospective molecular triage study (MOSCATO-01): What are the real risks?
- Authors:
- Prud'homme, Clara
Deschamps, Fréderic
Allorant, Adrien
Massard, Christophe
Hollebecque, Antoine
Yevich, Steve
Ngo-Camus, Maud
Gravel, Guillaume
Nicotra, Claudio
Michiels, Stefan
Scoazec, Jean-Yves
Lacroix, Ludovic
Solary, Eric
Soria, Jean-Charles
De Baere, Thierry
Tselikas, Lambros - Abstract:
- Abstract: Purpose: To evaluate efficacy, complications and preprocedural risk factors for percutaneous image-guided core needle biopsy of malignant tumours for genomic tumour analysis. Materials and methods: Procedural data for core biopsies performed at a single centre for the MOSCATO-01 clinical trial were prospectively recorded between December 2011 and March 2016. Data assessed included patient demographics, tumour characteristics, procedural outcomes and complications. Results: A total of 877 biopsies were performed under computed tomography (38.4%) or ultrasound guidance (61.6%) for tumours in the liver (n = 363), lungs (n = 229), lymph nodes (n = 138), bones (n = 15) and other miscellaneous sites (n = 124). Each biopsy harvested a mean 4.4 samples [1–15], with adequate tumour yield for genomic analysis in 95.3% of cases. Procedural complications occurred in 89 cases (10.1%), with minor grade I complications in 59 (66.3%); grade II in 16 (18%) and grade III in 14 (15.7%). No grade IV complications and no procedure-related death occurred. The most common complications were pneumothorax (51/89, 57.3%), haemorrhage (24/89, 27%) and pain (8/89, 8.9%). Predictive factors for complications by univariate analysis included biopsied organ (lung vs other), sample number, prone position, lesion size, lesion depth and biopsy approach. By multivariate analysis, only pulmonary biopsy was a significant risk factor (odds ratio = 27.23 [4.93–242.76], p < 0.01). Conclusion: PercutaneousAbstract: Purpose: To evaluate efficacy, complications and preprocedural risk factors for percutaneous image-guided core needle biopsy of malignant tumours for genomic tumour analysis. Materials and methods: Procedural data for core biopsies performed at a single centre for the MOSCATO-01 clinical trial were prospectively recorded between December 2011 and March 2016. Data assessed included patient demographics, tumour characteristics, procedural outcomes and complications. Results: A total of 877 biopsies were performed under computed tomography (38.4%) or ultrasound guidance (61.6%) for tumours in the liver (n = 363), lungs (n = 229), lymph nodes (n = 138), bones (n = 15) and other miscellaneous sites (n = 124). Each biopsy harvested a mean 4.4 samples [1–15], with adequate tumour yield for genomic analysis in 95.3% of cases. Procedural complications occurred in 89 cases (10.1%), with minor grade I complications in 59 (66.3%); grade II in 16 (18%) and grade III in 14 (15.7%). No grade IV complications and no procedure-related death occurred. The most common complications were pneumothorax (51/89, 57.3%), haemorrhage (24/89, 27%) and pain (8/89, 8.9%). Predictive factors for complications by univariate analysis included biopsied organ (lung vs other), sample number, prone position, lesion size, lesion depth and biopsy approach. By multivariate analysis, only pulmonary biopsy was a significant risk factor (odds ratio = 27.23 [4.93–242.76], p < 0.01). Conclusion: Percutaneous image-guided core needle biopsy in cancer patients provides an effective method to obtain molecular screening samples, with an overall low complication rate. Lung mass biopsies present a higher risk of complication, although complications are manageable by minimally invasive techniques without prolonged sequelae. Highlights: Percutaneous biopsy allows effective molecular screening to better tailor patient treatment with a low risk of complication. The number of samples does not increase the complication rate. No biopsy-related death was reported in this large series. Other sites than lung should be favoured whenever possible for percutaneous biopsies. … (more)
- Is Part Of:
- European journal of cancer. Volume 103(2018)
- Journal:
- European journal of cancer
- Issue:
- Volume 103(2018)
- Issue Display:
- Volume 103, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 103
- Issue:
- 2018
- Issue Sort Value:
- 2018-0103-2018-0000
- Page Start:
- 108
- Page End:
- 119
- Publication Date:
- 2018-11
- Subjects:
- Image guided -- Biopsies -- Percutaneous -- Complications -- Pneumothorax -- Haemorrhagic -- Risk factors
Cancer -- Periodicals
Neoplasms -- Periodicals
Cancer -- Périodiques
Cancer
Tumors
Electronic journals
Periodicals
Electronic journals
616.994 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09598049 ↗
http://rzblx1.uni-regensburg.de/ezeit/warpto.phtml?colors=7&jour_id=2879 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/09598049 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/09598049 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.ejca.2018.08.003 ↗
- Languages:
- English
- ISSNs:
- 0959-8049
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 3829.725100
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