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• H1A: The first research hypothesis (H1) is that phase gating will increase liver motion by
0.5 cm superiorly and inferiorly compared to EEBH Commented [NL2]: so do we mean greater than/equal to
o You want to state this as what you want to prove. I just want to double check here 0.5 cm?
– this is what you think will happen, correct? Seems like this is opposite of H2
below where you are saying EEBH will spare more healthy liver.
• H10: The first Null hypothesis (H10) is that phase gating will not increase liver motion by
0.5 cm superiorly and inferiorly compared to EEBH
• H2A: The second research hypothesis (H2) is that utilizing EEBH will lead to 5% fewer
cubic centimeters of healthy liver volume receiving 15 Gy compared to phase gating Commented [NL3]: @Jacob Wudtke OK - so using EEBH
o Isn’t this the same as EEBH will deliver ≥ 5% liver sparing compared to phase will decrease healthy liver dose by < 5% compared to phase
gating??? Meaning you plan to decrease dose delivered to
gating ??? (more scholarly language) the healthy liver by 5%?
• H20: The second research hypothesis (H20) is that utilizing EEBH will not lead to 5%
Commented [JW4R3]: @Nishele Lenards Correct! We
fewer cubic centimeters of healthy liver volume receiving 15 Gy compared to phase use the first hypothesis to establish the overall liver volume
gating difference. It is mainly just a measurable that shows that
there is a difference between the two respiratory
Literature Review Summary techniques. For the actual volumetric data, we will be using
the liver constraint that specifies how many CC's of healthy
Stereotactic body radiation therapy (SBRT) is utilized in radiation oncology to treat small tissue are receiving 15 Gy or more per the RTOG Liver SBRT
Guidelines. So, hypothesis 2 is stating that the amount (in
CC) of healthy liver tissue encompassed within the 15Gy
lesions to a high dose with small margins.1 This results in a greater amount of spared healthy
isodose line with EEBH will be 5% less than with phase
gating. So instead of thinking of it as a decrease in healthy
tissue. Since SBRT delivers a large dose of radiation, up to around 74Gy,1 it is important for the liver dose, we are using the volumetric CC as our
quantitative value to compare the two. Would you like me
treatment to be reproducible. Without reproducibility, the high dose of radiation could be to add the 15 Gy portion to the second hypothesis? I did not
want to get super specific but I could add that for clarity
deposited into healthy tissue instead of the lesion. Hepatocellular carcinoma (HCC) is a Commented [NL5R3]: @Jacob Wudtke you want it to be
as specific as the dose constraint is that you are measuring.
It has to be clear but not wordy.
malignancy that is commonly treated using SBRT. Since these lesions are in the liver and
therefore in the abdominal cavity, respiratory motion greatly affects the treatment. The liver Commented [JW6R3]: @Nishele Lenards I adjusted H2 to
reflect both the metric of cubic centimeters and 15 Gy.
moves with the patient’s respiration cycle since it is located near the diaphragm. Previously, the
attending physician would create a larger internal treatment volume (ITV)2 to account for the
lesion’s respiratory motion. However, treating a greater amount of tissue comes with more side
effects for the patient.2 Radiation Therapy Oncology Group (RTOG) 11123 studied the effects of
radiation therapy on the liver. This created the knowledge base of which organs are at risk
(OAR) of being damaged by SBRT to the liver, including the small bowel, large bowel, stomach,
esophagus, healthy liver, and more.3 When these OARs are damaged, the patient experiences
side effects such as liver cirrhosis and diarrhea.3 These side effects can be reduced by managing
respiratory motion during SBRT with reduced ITV volumes, amount of tissue treated, and
Respiratory management is a tactic used during radiation therapy that restricts internal
motion caused by breathing. Popularly, deep inspiration breath hold (DIBH) and end expiration
breath hold (EEBH) and utilized.2,4,5 Both DIBH and EEBH require the patient to hold their
breath, either at the top of their breath cycle or the bottom, respectively.4 Patients may have
trouble with this, because certain comorbidities such as Chronic Obstructive Pulmonary Disease
(COPD) can make it difficult to hold your breath for a long time. Otherwise, those who are
naturally short of breath may also have difficulty with the breath hold. Patients who have
difficulty holding their breath often struggle through these treatments, but respiratory
management is required to achieve optimal treatment outcomes. Not only is this uncomfortable
for patients, but inadequate breath holding can cause variances in treatment position from day to
day. Another option for respiratory management is to choose a respiratory phased gating window
for treatment.6 When this tactic is used, the patient will breathe naturally, but the treatment
system will only treat while the patient is in a specific window of their breathing cycle, most
commonly between 30% and 60% of their full inspiration.6 All of these methods allow patients to
receive the highest quality of radiation treatment with the least amount of side effects.
Many liver cancers are treated with radiation therapy, which produces great results.
However, the problem is that sparing healthy liver tissue is difficult due to respiratory motion. Commented [MK7]: Problem Statement
Respiratory motion management must be used, but patients continually struggle to properly
perform EEBH. Phased gating is much easier for the patient, but there is a large lapse in
literature comparing the effectiveness of EEBH and phased gating windows. The purpose of this
study is to determine whether the use of phase gating or EEBH is better for sparing healthy liver
tissue by limiting respiratory motion. Researchers tested that using EEBH and respiratory gating Commented [MK8]: Purpose Statement
will comparably reduce respiratory motion, and that using these methods of respiratory Commented [MK9]: H1/H2
management will reduce radiation dose to healthy liver tissue. Commented [MK10]: H3
References
1. Su, TS., Liu, QH., Zhu, XF. et al. Optimal stereotactic body radiotherapy dosage for
hepatocellular carcinoma: a multicenter study. Radiat Oncol 16, 79 (2021).
https://doi.org/10.1186/s13014-021-01778-6
2. Gargett M, Haddad C, Kneebone A, Booth JT, Hardcastle N. Clinical impact of removing
respiratory motion during liver SABR. Radiat Oncol. 2019;14(1):93. Published 2019 Jun 3.
doi:10.1186/s13014-019-1300-6.
3. Dawson LA, Winter KA, Knox JJ, Zhu A, Krishnan S, Guha C, Kachnic LA, Gillin MT,
Hong TS, Craig TD, Hosni A, Chen E, Noonan A, Koay EJ, Sinha R, Lock MI, Ohri N,
Dorth JA, Moughan J, Crane CH. NRG/RTOG 1112: randomized phase III study of
sorafenib vs. stereotactic body radiation therapy followed by sorafenib in hepatocellular
carcinoma (HCC) (NCT01730937). ASTRO (American Society for Radiation Oncology).
10/23/2022. 52345
4. Oh SA, Yea JW, Kim SK, Park JW. Optimal Gating Window for Respiratory-Gated
Radiotherapy with Real-Time Position Management and Respiration Guiding System for
Liver Cancer Treatment. Sci Rep. 2019;9(1):4384. Published 2019 Mar 13.
doi:10.1038/s41598-019-40858-2
5. Motoharu Sasaki, Hitoshi Ikushima, Kanako Sakuragawa, Michihiro Yokoishi, Akira
Tsuzuki, Wataru Sugimoto, Determination of reproducibility of end-exhaled breath-holding
in stereotactic body radiation therapy, Journal of Radiation Research, Volume 61, Issue 6,
November 2020, Pages 977–984, https://doi.org/10.1093/jrr/rraa079
6. Zeng C, Li X, Lu W, et al. Accuracy and efficiency of respiratory gating comparable to deep
inspiration breath hold for pancreatic cancer treatment. J Appl Clin Med Phys.
2021;22(1):218-225. doi:10.1002/acm2.13137