2021 AAPM Virtual 63rd Annual Meeting
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Session Title: HyTEC SBRT Dose Constraints
Question 1: The landmaark work relating NTCP to dose distributions in the image based treatment planning era (3DCRT era) that historically preceded current efforts such as HyTEC was published in:
Reference:Emami B, et al, Tolerance of normal tissue to therapeutic irradiation, IJROBP 1991;21:109-12 Grimm J, Marks LB, Jackson A et al, High Dose per Fraction, Hypofractionated Treatment Effects in the Clinic (HyTEC): An Overview, IJROBP 2021; 110: 1-10.
Choice A:1940
Choice B:1963
Choice C:1991
Choice D:1998
Choice E:2010
Question 2: The HyTEC project Red Journal issue provides:
Reference:Reference: Grimm J, Marks LB, Jackson A et al, High Dose per Fraction, Hypofractionated Treatment Effects in the Clinic (HyTEC): An Overview, IJROBP 2021; 110: 1-10; especially Tables 2 and 3
Choice A:Only NTCP guidelines for hypofractionated radiation therapy based on analyses of published, peer reviewed clinical studies.
Choice B:Only NTCP guidelines for conventionally fractionated radiation therapy based on national randomized clinical trials.
Choice C:Both NTCP and TCP guidelines for hypofractionated radiation therapy based on analysis of published, peer reviewed clinical studies.
Choice D:NTCP and TCP guidelines for hypofractionated radiation therapy based on the experiences of the members of the WGSBRT.
Choice E:Both NTCP and TCP guidelines for brachytherapy based on analysis of published, peer reviewed clinical studies.
Question 3: The dose axis in most of the HyTEC paper mathematical models is most often:
Reference:Reference: See the 16 TCP and NTCP site-specific articles in the HyTEC issue: International Journal of Radiation Oncology Biology Physics Vol 110 (1), May 2021
Choice A:Fractionation-corrected (modified to account for the total dose and number of fractions); several radiobiological models are used in different papers
Choice B:Purely physical dose
Choice C:Given in terms of RBE
Choice D:Fractionation corrected only with the universal survival curve.
Choice E:Always given by mean organ or tumor dose.
Question 4: SBRT is a desirable form of radiation therapy for pancreatic cancer because:
Reference:Reference: Mahadevan A, Moningi S, Grimm J, et al. , Maximizing tumor control and limiting complications with stereotactic body radiation therapy for pancreatic cancer, IJROBP 2021; 110 : 206-216.
Choice A:A short treatment schedule interferes minimally with chemotherapy.
Choice B:A short treatment schedule interferes minimally with surgery.
Choice C:Short treatment schedules are more compatible with respiratory motion management.
Choice D:Short treatment schedules are more compatible with constant risk-organ positions.
Choice E:The SBRT total doses are low.
Question 5: All the following features of published studies made it difficult to synthesize their data into coherent sbrt outcomes models except:
Reference:International Journal of Radiation Oncology Biology Physics 2021; 110: all organ-specific papers Jackson A, Marks LB, Bentzen SM, et al , The Lessons of QUANTEC: Recommendations for reporting and gathering data on dose-volume dependencies of treatment outcome, IJROBP 2010; 76 (3S), S155-S160.
Choice A:Lack of individual patient dose-volume histograms associated with a particular outcome
Choice B:Lack of community-wide agreement on how a given risk organ should be segmented for treatment planning and dose evaluation.
Choice C:Lack of community-wide agreement regarding complication and tumor control endpoints.
Choice D:Adherence to standards for reporting
Question 6: Clinicians can best view the HyTEC guidelines expressed in the TCP and NTCP papers as:
Reference:Reference: Grimm J, Marks LB, Jackson A et al, High Dose per Fraction, Hypofractionated Treatment Effects in the Clinic (HyTEC): An Overview, IJROBP 2021; 110: 1-10.
Choice A:Ground truth as of 2021
Choice B:Works in progress based on analysis of literature selected by the authors of the HyTEC paper after search of available peer-reviewed publications.
Choice C:Dose-response models based on mechanistic descriptions of the organ or tumor.
Choice D:The best results of modern randomized controlled national trials.
Choice E:The result of comparing Kaplan-Meier and competing risks models for each endpoint.
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