Delivery of Radiation at the Lowest Dose Rate by a Modern Linear Accelerator is Most Effective in Inhibiting Prostate Cancer Growth

Author:

Tazat Keren1,Reshetnyak Oleg1,Shtraus Natan23,Sayag Ifat1,Mabjeesh Nicola J.14,Amir Sharon1ORCID

Affiliation:

1. Prostate Cancer Research Laboratory, Tel Aviv University, Tel Aviv, Israel

2. Institute of Radiotherapy, Tel Aviv Medical Center, Tel Aviv, Israel

3. Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel

4. Department of Urology, Soroka University Medical Center and Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel

Abstract

Purpose: External beam radiotherapy is one of the treatment options for organ-confined prostate cancer. A total dose of 70 to 81 Gray (Gy) is given daily (1.8-2.5 Gy/d), with a dose rate of 3 to 6 Gy/min over 28 to 45 treatments during 8 to 9 weeks. We applied the latest technological development in linear accelerators for enabling a wide range of dose rates (from 0.2-21 Gy/min) to test the effect of different delivery dose rates on prostate tumor growth in an animal xenograft model. Materials and Methods: A prostate cancer xenograft model was established in CD1/nude mice by means of PC-3 and CL-1 cells. The animals were radiated by a TrueBeam linear accelerator that delivered 4 dose rates ranging from 0.6 to 14 Gy/min, and reaching a total dose of 20 Gy. The mice were weighed and monitored for tumor development twice weekly. A 2-way analysis of variance was used to compare statistical differences between the groups. Results: Tumor growth was inhibited by radiation at all 4 dose rates in the 20 study mice compared to no radiation (n = 5, controls). The most significant reduction in tumor volumes was observed when the same dose of radiation was delivered at a rate of 0.6 Gy/min ( P < .01). The animals’ weights were not affected by any dose rate. Conclusions: Delivery of radiation with a TrueBeam linear accelerator at the lowest possible rate was most effective in prostate cancer growth inhibition and might be considered a preferential treatment mode for localized prostate cancer.

Funder

Dr. Miriam and Sheldon G. Adelson Medical Research Foundation

Publisher

SAGE Publications

Subject

Cancer Research,Oncology

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