Figure 6 Double opposed-field irradiation of an idealized geometry

Slides:



Advertisements
Similar presentations
Some remaining questions in particle therapy radiation biology Bleddyn Jones University of Oxford 1. Gray Institute for Radiation Oncology & Biology 2.
Advertisements

Tumour Therapy with Particle Beams Claus Grupen University of Siegen, Germany [physics/ ] Phy 224B Chapter 20: Applications of Nuclear Physics 24.
Study of the fragmentation of Carbon ions for medical applications Protons (hadrons in general) especially suitable for deep-sited tumors (brain, neck.
BIOLOGICAL EFFICIENCY OF A THERAPEUTIC PROTON BEAM: A STUDY OF HUMAN MELANOMA CELL LINE I. Petrović 1, A. Ristić-Fira 1, D. Todorović 1, L. Korićanac 1,
Heavy Ion Tumor Therapy
The Increased Biological Effectiveness of Heavy Charged Particle Radiation: From Cell Culture Experiments to Biophysical Modelling Michael Scholz GSI Darmstadt.
Mathematical Modelling within Radiotherapy: The 5 R’s of Radiotherapy and the LQ model. Helen McAneney 1 and SFC O’Rourke 1,2 1 School Mathematics and.
Karolina Kokurewicz Supervisors: Dino Jaroszynski, Giuseppe Schettino
Experimental Cave at Trento CPT: status update Francesco Tommasino RDH/IRPT Meeting – Roma, 1 Feb 2016.
RBE: open issues and next challenges Francesco Tommasino Workshop: la radiobiologia in INFN Trento, Maggio 2016.
Particle Therapy at GSI
Linear Energy Transfer and Relative Biological Effectiveness
Figure 1 Food, nutrition, obesity, physical activity, and the cellular processes linked to cancer Figure 1 | Food, nutrition, obesity, physical activity,
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 2 Underreporting by physicians of specific treatment-associated symptoms by physicians in the TORCH trial Figure 2 | Underreporting by physicians.
Figure 2 Response after initial increase in total tumour burden
Figure 5 Mutational heterogeneity in oesophageal and gastric cancer
Figure 1 Concept of the therapeutic index
Figure 4 Example of PK/PD simulation to optimize a vinorelbine treatment regimen Figure 4 | Example of PK/PD simulation to optimize a vinorelbine treatment.
Figure 2 Multiscale modelling in oncology
Figure 3 Risk-adapted and response-adapted
Figure 5 Schematic illustration of different clinical trial designs
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 3 Monitoring clonal evolution using liquid biopsies
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 2 Copy-number variations in multiple myeloma
Figure 5 Identification of mucinous carcinoma
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 1 Underreporting of treatment-related toxicities by physicians, relative to patients with either advanced-stage lung cancer, or early-stage breast.
Figure 2 Therapeutic targeting of the PI3K/AKT/mTOR pathway
Figure 1 Proposed treatment algorithm for advanced gastroesophageal cancer based on publish recommendations Figure 1 | Proposed treatment algorithm for.
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 1 CAR-T-cell design
Figure 2 Examples of histopathological validation
Figure 4 Effects of delaying cardioprotective medications after anthracycline administration Figure 4 | Effects of delaying cardioprotective medications.
Figure 1 Cost of one month of treatment with
Figure 2 The association between CD8+ T‑cell density of the tumour
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 5 The biological effects of charged particles
Figure 3 Drug cycling with collateral sensitivity
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 2 Differences between MC and AC
Figure 3 Possible modalities for reconciliation of patient's and physician's report of symptomatic treatment-associated toxicities Figure 3 | Possible.
Figure 3 Algorithm for the determination of the clinical
chemotherapy for patients with MC versus those with AC
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 1 NIR fluorescence is more suitable for
Figure 2 Nonmalignant tissue can be spared from radiation
Figure 4 Treatment plans using stereotactic body radiotherapy (SBRT)
Figure 3 Summary of overall survival by Kaplan–Meier
Figure 3 Clinical trial design in charged-particle therapy (CPT)
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 3 The yin and yang of tumour-associated
Figure 2 Median monthly launch price of a new anticancer drug,
Figure 1 Translocations involved in multiple myeloma
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 2 Host immune responses, not the radiosensitivity
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Overcoming resistance of cancer stem cells
Figure 2 Frequency and overlap of alterations
Figure 2 Variations between planned and delivered doses of radiation
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 5 Schematic overview of a clinical decision-support
Nat. Rev. Clin. Oncol. doi: /nrclinonc
Figure 4 Radiogenomics analysis can reveal relationships
Figure 1 Overview of the imaging biomarker roadmap
Figure 3 Determination of the primary site
Presentation transcript:

Figure 6 Double opposed-field irradiation of an idealized geometry simulating a typical head and neck tumour using ionization from 1H, 4He, 12C, or 16O Figure 6 | Double opposed-field irradiation of an idealized geometry simulating a typical head and neck tumour using ionization from 1H, 4He, 12C, or 16O. The simulated tumour is a cube with 25 mm sides, centred in an irradiation volume with a 16 cm length. The relative biological effectiveness (RBE)-weighted dose optimizations for a radioresistant or for a radiosensitive tumour were performed using TRiP98 software (GSI Helmholtz Center for Heavy Ion Research; Darmstadt, Germany), used in treatment planning with carbon ions in Europe and China. The performance of helium, evaluated as the ratio of peak to plateau dose, was good in both sensitive and resistant tumours. As expected, heavy oxygen ions result in a higher dose irradiation of nonmalignant tissue in patients with tumours with a high α/β ratio, corresponding to high radiosensitivity (right panel), compared with tumours with a low α/β ratio (radioresistant). For the latter, the use of heavy oxygen ions can be beneficial. N, nonmalignant tissue; T, tumour. Figure adapted from Tommasino, F., Scifoni, E. & Durante, M. New ions for therapy. Int. J. Part. Ther. 2, 428–438 (2015), under a Creative Commons CC-BY licence, https://creativecommons.org/licenses/by/3.0/us/. Figure adapted from Tommasino, F., Scifoni, E. & Durante, M. New ions for therapy. Int. J. Part. Ther. 2, 428–438 (2015), under a Creative Commons CC-BY licence, https://creativecommons.org/licenses/by/3.0/us/. Durante, M. et al. (2017) Charged-particle therapy in cancer: clinical uses and future perspectives Nat. Rev. Clin. Oncol. doi:10.1038/nrclinonc.2017.30