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Oncological Disease » Articles » Advances in Radiation Therapy
Tuesday, 08 July, 2008



Advances in Radiation Therapy

Daniel Low Professor, Department of Radiation Oncology and Director, Division of Medical Physics, Washington University School of Medicine

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Radiation therapy has made significant advances over the past two decades. The beginning of the 1980s saw radiation therapy as a prescriptive medicine.Treatments using megavoltage X-rays were planned using the crude imaging tools available in the day. Radiation portals were typically defined using radiographic planar imaging, where only bony anatomy and large air cavities were visualized. The radiation oncologist used previous experience based on the tumor type, location, and extent (determined using planar imaging and palpation), to define the portals. Significant customization of the radiation portals based on a quantitative understanding of the patient’s tumor geometry was not possible due to the poor access to three-dimensional (3-D) imaging modalities.

The advent of broader access to computed tomography (CT) and computing technology led to the first technological revolution in the 1980s. 3-D radiotherapy treatment planning (3DRTP), where the tumor is defined in 3-D using CT scans and the radiation portals are designed based on the 3-D tumor and normal organ shapes, was introduced and made rapid inroads into radiation therapy practice. The use of 3-D imaging allowed the radiation oncologist to customize the radiation dose distribution to the patient’s specific tumor and normal organ geometry. Studies showed that in many cases, the earlier (called the 2-D approach) often underestimated the required beam portal size, causing underdosing of the tumor.

3DRTP also allowed a quantitative understanding of the radiation dose to critical structures. Physicians were provided with feedback on the radiation dose throughout the normal organs, and dose summary tools were invented that enabled the physicians to efficiently determine if the doses were within clinically acceptable limits.

3DRTP also allowed a quantitative understanding of the radiation dose to critical structures. Physicians were provided with feedback on the radiation dose throughout the normal organs, and dose summary tools were invented that enabled the physicians to efficiently determine if the doses were within clinically acceptable limits.

As an example, the position of the prostate depends greatly on the fill status of the bladder and rectum.A CT acquired with a full rectum will show the prostate in a more anterior position than when the rectum is empty. Consequently, the treatment plan will be designed with the dose more anterior than the average tumor position and a ‘geometric miss’ could occur. Other similar tumorpositioning errors included patient positioning reproducibility and gradual tumor shrinking or tissue swelling that modified the size, shape, and position of the tumor. In order to combat these limitations, the concept of a tumor margin was defined. A margin was a 3-D expansion of the imaged tumor (gross tumor volume (GTV)) that was sufficiently large that the tumor would be positioned within the margin surface on a daily basis. The radiation dose was designed to encompass the margin volume (planning target volume (PTV)) rather than the imaged tumor volume. While this presumably guaranteed full irradiation of the tumor, it also led to treatment portals that irradiated more normal tissues than necessary given the tumor size and shape.

Secondly, the CT image could not show the entire extent of the tumor. Tumors typically invade with microscopic extensions, often infiltrating many centimeters from the bulky disease. The microscopic extensions cannot be visualized using CT imaging, so a method for identifying the suspected occult disease volume was developed, termed the clinical target volume (CTV). By definition, the CTV encompassed suspected tumor cells and its design was therefore less quantitative and required more clinical judgment to define than the GTV. Because the tumor burden was less in the CTV than the GTV, the dose required to sterilize the tumor in the CTV was assumed to be less than in the GTV. CTV doses were therefore often smaller than the GTV doses. The PTV margin concept was also applied to the CTV.

The second technological revolution occurred from treatment planning simulation studies conducted in the late 1980s. During that time, scientists identified the fact that the radiation dose distributions could be made significantly more conformal if the radiation fluence (intensity) from each beam could be optimized using software-based algorithms. Luckily, the linear accelerators of the day were capable of delivering these optimized fluence patterns.This technology was labeled intensity modulated radiation therapy (IMRT), and it allowed the design of very conformal dose distributions. IMRT provided for the capability of irradiating tumors while sparing nearly surrounding normal organs.





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Author(s) Biography
Daniel Low, PhD, is a Professor in the Department of Radiation Oncology and is the Director of the Division of Medical Physics at Washington University School of Medicine. He joined the faculty of Washington University in 1991. Dr Low is an author of more than 80 peer-reviewed manuscripts and is a fellow of the American Association of Physicists in Medicine. He earned his PhD in intermediate energy nuclear physics from Indiana University in 1988 and then joined M.D. Anderson Cancer Center as a postdoctoral fellow in medical physics.

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