Tumor Motion Management in Radiotherapy Using 4D-MRI
Evaluation of Tumor Motion Management Strategies in Radiotherapy Using 4D-MRI
The main goal of this research is to characterize patient-specific respiration-induced tumor and surrogate motion to evaluate the accuracy and effectiveness of the surrogate-based motion management strategies currently used in clinics. Specifically, the investigators hypothesize that dynamic MRI (Magnetic Resonance Imaging) obtained over a temporal duration consistent with radiotherapy treatments will provide spatio-temporal information of both the tumor and surrogate, and therefore can serve as a means to assess the quality of the tumor motion tracking with the surrogate. To test this hypothesis, the investigators specifically propose to 1) track and characterize the tumor and surrogate motion with 4D (4 dimensional)-MRI and 2) evaluate surrogate-based motion tracking in a cohort of patients with thoracic tumors.
External and internal surrogate-based strategies commonly used in clinics have not been appropriately validated. With the increasing adaptation of these surrogate methods for motion management, the proposed research addresses these urgent issues in clinical radiotherapy while providing a means to achieve patient-specific motion management.
調査の概要
状態
状態
条件
条件
詳細な説明
Respiration-induced patient motion has become a major obstacle for achieving high-precision radiotherapy of cancers especially in the thorax and upper abdomen. As the target is continuously moving, an additional margin has to be added to the clinical target volume to compensate for the uncertainty in the tumor and organ motion, causing toxicity to the normal tissue and limiting the dose delivered to the target. To account for the tumor motion, surrogate tracking methods are commonly used in clinics during radiotherapy. However, the relationship between the surrogate and tumor motion is hard to generalize as it depends on individual patients, tumor location, treatment fractions, and sometimes shows complex patterns or transient, unpredictable changes. Hence, there is an urgent need to better scrutinize the current surrogate-based motion management strategies. Moreover, the most robust motion management strategy for the given patient should be determined in the pre-treatment setting but the investigators currently lack a sufficient tool to provide this information.
4D-CT is typically used to characterize the tumor motion over the course of the radiotherapy. However, 4D-CT is an oversimplified snapshot representation of a single-breathing cycle with low soft tissue contrast while imparting a considerable amount of radiation dose to the patient. Consequently, the limitations of 4D-CT prevent applicability in acquiring information over timescales that represent a treatment session. MRI is highly advantageous as it is non-ionizing and provides excellent soft tissue contrast. Although real-time 3D dynamic MRI is limited by low image quality and temporal resolution, 2D dynamic MRI techniques have high fidelity and spatio-temporal resolution requisite for real-time tracking of the moving target. Furthermore, a respiration-correlated 4D-MRI can be reconstructed from multi-slice 2D dynamic MR images, enabling volumetric image processing and analysis. Therefore, 4D-MRI is an attractive solution to address breathing motion and tumor tracking obstacles in radiotherapy.
The main goal of this research is to characterize patient-specific respiration-induced tumor and surrogate motion to evaluate the accuracy and effectiveness of the surrogate-based motion management strategies currently used in clinics. Specifically, the investigators hypothesize that dynamic MRI obtained over a temporal duration consistent with radiotherapy treatments will provide spatio-temporal information of both the tumor and surrogate, and therefore can serve as a means to assess the quality of the tumor motion tracking with the surrogate. To test their hypothesis, the investigators specifically propose to 1) track and characterize the tumor and surrogate motion with 4D-MRI and 2) evaluate surrogate-based motion tracking in a cohort of patients with thoracic tumors.
External and internal surrogate-based strategies commonly used in clinics have not been appropriately validated. With the increasing adaptation of these surrogate methods for motion management, the proposed research addresses these urgent issues in clinical radiotherapy while providing a means to achieve patient-specific motion management.
研究の種類
研究の種類
入学 (実際)
入学
連絡先と場所
研究場所
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Maryland
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Baltimore、Maryland、アメリカ、21287
- The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
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参加基準
適格基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:
- Histologically-confirmed primary lung cancer (non-small cell OR small cell)
- Plan to undergo external radiation treatment of lung cancer
Exclusion Criteria:
- Patients who cannot undergo MRIs.
- Patients who have a cardiac device or other electronic or metal implant
研究計画
研究はどのように設計されていますか?
デザインの詳細
この研究は何を測定していますか?
主要な結果の測定
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Tumor motion characterization during radiation therapy
時間枠:1 year
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To characterize patient-specific respiration-induced tumor and surrogate motion to evaluate the accuracy and effectiveness of the surrogate-based motion management strategies currently used in radiotherapy.
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1 year
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二次結果の測定
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
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Correlation of tumor and surrogate motion
時間枠:1 year
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Tumor and surrogate motion will be quantified by measuring the displacements from their end-exhale positions.
Since the tumor may deform during motion, we will not only consider the trajectories of the center of mass but also the tumor borders.
The tumor position as a function of the surrogate position will be analyzed along each moving direction.
Pearson correlation coefficients and the sum of squared residual errors based on a regression analysis will be computed to provide a quantitative measure of the correlation between the surrogate and tumor positions.
To measure the tumor deformation, correlations of the motion between the SI borders, AP borders, LR borders will also be computed.
Although lung tumor likely does not significantly deform, this analysis will be useful for tumors that may deform significantly during motion.
The motion under the different breathing patterns will be analyzed separately, and compared to each other.
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1 year
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Sensitivity and specificity of gating
時間枠:1 year
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Respiratory gating is one predominant technique for managing respiratory motion.
Gating attempts to minimize normal tissue dose by delivering radiation during a portion of the respiratory cycle where the respiratory state is typically determined from an external surrogate as an optical signal.
We will use different gating boundaries, e.g.
10%, 20% of the surrogate motion range (from mean exhale to mean inhale) on each axes as commonly used in clinical practice.
Sensitivity and specificity of the gating will be computed by comparing the portion of time the surrogate is below/above the gating boundary and that the tumor is below/above the gating boundary.
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1 year
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Pre- and intra-treatment motion variability
時間枠:1 year
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MRI scans of the patient will be acquired pre- and intra-treatment.
Tumor motion variability will be computed between these two scans.
We will evaluate the correlation of the target location captured at different time points by computing target volume overlap and systematic volume shift.
We will also analyze the tumor position as a function of the surrogate position for both pre- and intra-treatment scans, and will investigate how well these two distributions match.
To quantitatively measure the differences, we will compute various statistical similarity measures such as correlation coefficient and mutual information.
We will also calculate pre-treatment margins to account for the tumor motion using the pre-treatment retrospective 4D-MRI reconstruction, and calculate the portion of treatment time the tumor moves within or outside the specified margins during the successive scans.
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1 year
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協力者と研究者
スポンサー
スポンサー
捜査官
捜査官
- 主任研究者:Russell Hales, M.D.、Johns Hopkins University
研究記録日
主要日程の研究
研究開始
研究開始
一次修了 (実際)
一次修了
研究の完了 (実際)
研究の完了
試験登録日
最初に提出
最初に提出
QC基準を満たした最初の提出物
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
最初の投稿
学習記録の更新
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投稿された最後の更新
QC基準を満たした最後の更新が送信されました
QC基準を満たした最後の更新が送信されました
最終確認日
最終確認日
詳しくは
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