Potential of a Cetuximab‐based radioimmunotherapy combined with external irradiation manifests in a 3‐D cell assay. Issue 4 (11th February 2014)
- Record Type:
- Journal Article
- Title:
- Potential of a Cetuximab‐based radioimmunotherapy combined with external irradiation manifests in a 3‐D cell assay. Issue 4 (11th February 2014)
- Main Title:
- Potential of a Cetuximab‐based radioimmunotherapy combined with external irradiation manifests in a 3‐D cell assay
- Authors:
- Ingargiola, M.
Runge, R.
Heldt, J.‐M.
Freudenberg, R.
Steinbach, J.
Cordes, N.
Baumann, M.
Kotzerke, J.
Brockhoff, G.
Kunz‐Schughart, L.A. - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Targeting epidermal growth factor receptor (EGFR)‐overexpressing tumors with radiolabeled anti‐EGFR antibodies is a promising strategy for combination with external radiotherapy. In this study, we evaluated the potential of external plus internal irradiation by [<sup>90</sup>Y]Y‐CHX‐A″‐DTPA‐C225 (Y‐90‐C225) in a 3‐D environment using FaDu and SAS head and neck squamous cell carcinoma (HNSCC) spheroid models and clinically relevant endpoints such as spheroid control probability (SCP) and spheroid control dose 50% (SCD<sub>50</sub>, external irradiation dose inducing 50% loss of spheroid regrowth). Spheroids were cultured using a standardized platform. Therapy response after treatment with C225, CHX‐A″‐DTPA‐C225 (DTPA‐C225), [<sup>90</sup>Y]Y‐CHX‐A″‐DTPA (Y‐90‐DTPA) and Y‐90‐C225 alone or in combination with X‐ray was evaluated by long‐term monitoring (60 days) of spheroid integrity and volume growth. Penetration kinetics into spheroids and EGFR binding capacities on spheroid cells were identical for unconjugated C225 and Y‐90‐C225. Spheroid‐associated radioactivity upon exposure to the antibody‐free control conjugate Y‐90‐DTPA was negligible. Determination of the SCD<sub>50</sub> demonstrated higher intrinsic radiosensitivity of FaDu as compared with SAS spheroids. Treatment with unconjugated C225 alone did not affect spheroid growth and cell viability. Also, C225 treatment after external<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Targeting epidermal growth factor receptor (EGFR)‐overexpressing tumors with radiolabeled anti‐EGFR antibodies is a promising strategy for combination with external radiotherapy. In this study, we evaluated the potential of external plus internal irradiation by [<sup>90</sup>Y]Y‐CHX‐A″‐DTPA‐C225 (Y‐90‐C225) in a 3‐D environment using FaDu and SAS head and neck squamous cell carcinoma (HNSCC) spheroid models and clinically relevant endpoints such as spheroid control probability (SCP) and spheroid control dose 50% (SCD<sub>50</sub>, external irradiation dose inducing 50% loss of spheroid regrowth). Spheroids were cultured using a standardized platform. Therapy response after treatment with C225, CHX‐A″‐DTPA‐C225 (DTPA‐C225), [<sup>90</sup>Y]Y‐CHX‐A″‐DTPA (Y‐90‐DTPA) and Y‐90‐C225 alone or in combination with X‐ray was evaluated by long‐term monitoring (60 days) of spheroid integrity and volume growth. Penetration kinetics into spheroids and EGFR binding capacities on spheroid cells were identical for unconjugated C225 and Y‐90‐C225. Spheroid‐associated radioactivity upon exposure to the antibody‐free control conjugate Y‐90‐DTPA was negligible. Determination of the SCD<sub>50</sub> demonstrated higher intrinsic radiosensitivity of FaDu as compared with SAS spheroids. Treatment with unconjugated C225 alone did not affect spheroid growth and cell viability. Also, C225 treatment after external irradiation showed no additive effect. However, the combination of external irradiation with Y‐90‐C225 (1 µg/ml, 24 hr) resulted in a considerable benefit as reflected by a pronounced reduction of the SCD<sub>50</sub> from 16 Gy to 9 Gy for SAS spheroids and a complete loss of regrowth for FaDu spheroids due to the pronounced accumulation of internal dose caused by the continuous exposure to cell‐bound radionuclide upon Y‐90‐C225‐EGFR interaction.</p> </abstract> … (more)
- Is Part Of:
- International journal of cancer. Volume 135:Issue 4(2014:Aug. 15)
- Journal:
- International journal of cancer
- Issue:
- Volume 135:Issue 4(2014:Aug. 15)
- Issue Display:
- Volume 135, Issue 4 (2014)
- Year:
- 2014
- Volume:
- 135
- Issue:
- 4
- Issue Sort Value:
- 2014-0135-0004-0000
- Page Start:
- 968
- Page End:
- 980
- Publication Date:
- 2014-02-11
- Subjects:
- Cancer -- Periodicals
Cancer -- Prevention -- Periodicals
616.994 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0215 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ijc.28735 ↗
- Languages:
- English
- ISSNs:
- 0020-7136
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.156000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3869.xml