Targeted Oncology
Targeted Oncology
Targeted Oncology

Advances in Image-Guided Oncologic Treatment

Robert L. Bard, MD
Published Online: Sep 21,2016

Abstract



Three-dimensional sonography and power Doppler angiography are techniques that contribute new morphologic parameters and noninvasive functional tumoral angiogenic markers for evaluation and treatment follow up of hyperplastic diseases and prostate cancers. Accuracy in assessing bladder breast, skin/ melanoma, liver, endometrial, and thyroid malignancies have been documented. Diagnostic ultrasound is a viable means to assess these lesions and can be performed in the office setting accurately and rapidly due to the high resolution and low cost of today’s sonographic equipment. This diagnostic technology requires extensive experience and training in interpreting the images. However, advances in the computerization of the imaging, blood flow, and tumor measures of exact volume and vessel density are now less operator dependent. That provides for an accurate and repeatable diagnosis, and a means to follow the individual patient’s unique pattern of cancer development, progress, and response to treatment.
 

Introduction


Summer means more adults will seek reassurance about pigmented lesions and patients with a previous dermal or other malignancy will need a diagnosis on any palpable lesions that may be subdermal in location and, thus, invisible to the spatially restricted human eye. To assess the condition of these lesions, clinicians can look to biopsy or the use of gadolinium- based contrast agents—intravenous drugs to enhance the quality of magnetic resonance imaging (MRI) or magnetic resonance angiography. However, patients are concerned about possible side effects associated with these techniques.

Diagnostic ultrasound is a viable means to assess bladder1 breast2, skin/melanoma3, liver, endometrial4, prostate, and thyroid malignancies and can be performed in the office setting accurately and rapidly due to the high resolution and low cost of today’s sonographic equipment. This diagnostic technology requires extensive experience and training in interpreting the images. However, advances in the computerization of the imaging, blood ow, and tumor measures of exact volume and vessel density are now less operator dependent. That provides for an accurate and repeatable diagnosis, and a means to follow the individual patient’s unique pattern of cancer development, progress, and response to treatment. Recent technological advances also make these procedures available to much broader clinical application, without requiring years of unique training and experience, for example, with diagnoses of cystic versus solid lesions. These advances are applicable beyond prostate cancer, the example used here, because it has been shown to be reproducible over the last 20 years with pathologic confirmation of the findings of the various imaging modalities. For the clinician new to the use of these technologies, it must be emphasized that initial readings will be difficult to interpret and may contain many confusing artifacts. It is recommended that findings should be confirmed with all pertinent imaging modalities.
 

Prostate Cancer


One man in 6 will be diagnosed with this disease in his lifetime. It is, at the same time, the second biggest cancer killer in men, with an esti- mated 29,720 deaths in 2015 in the United States. Like other cancers in the past, our understanding of the science of prostate cancer has changed tremendously during the last 10 years. Pre-malignant conditions have been described leading to an extremely active search for genomic signatures of prostate cell transformation. Cohort studies are ongoing. The diagnosis of prostate cancer has become more sophisticated with the introduction of newer criteria, outside of the classi- cal Gleason classi cation, that could predict an individual’s tumor aggressiveness, with the hope of better and more personalized tailored therapeutic strategies.5 3D imaging may not detect regional and distant lymph nodes, so MRI remains the gold standard for nodal staging.

Among potential tailored treatments, active surveillance is more widely accepted and fewer patients are choosing to undergo an unnecessary prostatectomy, which has been on the rise in the last decade because of widely increased use of prostate-specific antigen (PSA) screening. This is a reason for some real concern, both in term of individual risk as well as for the economy of cancer. Because of the potential for overuse and overtreatment, the United States Preventive Services Task Force (USPSTF) recommended against routine PSA screening. Given the resulting shift towards fewer PSA tests and its low accuracy, we are seeing a rise in non-invasive screening with Doppler ultrasound and MRI.

 

Three-dimensional Doppler ultrasound with Dynamic Contrast Enhanced MRI are the gold standards by which cancers are initially diag- nosed and serially followed after treatment. The percentage of malignant vessels can be quantified and re-evaluated in the identical tumor volume as serial follow ups. Since vessel mapping is possible, embolic treatments may be used.

 

Three-dimensional sonography can demonstrate the prostate capsule more accurately than MRI because the resolution is 100 microns at 18MHz. The examination takes about 10 minutes and the probes are automated meaning that this is less operator dependent than other sonographic procedures. Vessel density index (VI) imaging is performed on the data set at an inde- pendent workstation and comparison made with prior examinations if available.

 

Three-dimensional power Doppler indices vary according to the tumor stage, the histologic grade, capsular disruption, and lymph node metastases. Histologic grade has been studied with this technology and the following approximation has proven useful: low- grade tumor (Gleason 3+2, 3+3) has VI <5%, medium-grade cancer (Gleason 3+4) has VI 5-9% and high-grade malignancies (Gleason 4+4, 4+5, 5+5) have VI >9%. This does not exactly correlate with histologic Gleason grading since this is a current functional measure while the microscopy is purely anatomical and may not represent current aggressive potential.
 

 

Skin Cancer

 

Major changes in the incidence, diagnosis, and treatment of skin cancer highlight a singular need for an up-to-date source of diagnosis and minimally invasive therapy of dermal tumors. The occurrence of melanoma is now at a median age of 28 years and the incidence is increasing rapidly. This means patients in their 30s are developing cancer that may be missed by current screening technologies of dermoscopy, confocal microscopy, and near infrared optical devices. Delays in treatment due to misdiagnosis have led to lawsuits. Earlier detection of tumors means smaller lesions are being discovered and focal nonsurgical treatment may be preferred to standard operative modalities with potential long-term postoperative side effects.

 

Medical imaging can map the arteries, veins, and nerves providing preoperative landmarks reducing postoperative bleeding and avoiding nerve damage. Tumors of low aggressive potential may be treated medically and followed by interval scans or locally reduced by radiation or laser ablation. Biopsies of certain abnormalities may be averted or postponed.

 

Dermal sonography has been used since 1980 and complements optical media such as dermoscopy, con-focal microscopy, optical coherence tomography (OCT), dermal CT, and MRI scanning. Collectively, these media help the clinician diagnose, stage, and grade cancer. Dermal sonography evaluates the extent of certain benign disorders such that biopsy may be limited or avoided. This is the case when part of a lesion is cancer and the adjacent areas of the clinical lesion are benign due to brosis, in ammation, hyperplasia, and immune-cell activity.

 

Clinical diagnosis of nonmelanoma skin cancer (NMSC) is accurate, however, the depth of a tumor is unknown. Imaging informs the surgeon whether the surgery will be limited or extensive and may require skin graft or cartilage replacement. Clinical diagnosis of malignant melanoma is 54% accurate by histology and 20% accurate by nonmicroscopic clinical modali- ties. Many benign pigmented lesions are removed pre- ventively. There is 1 melanoma found per 33,000 nevi. Ultrasound screening of pigmented lesions is highly accurate and well tolerated. MRI studies are currently sensitive but not speci c for screening. Dermoscopy and other optical technologies are complementary. Pa- thologists now preview clinical pictures of a suspect lesion before they nalize readings due to the inherent variability of interpretation. The finding of a subclinical metastatic focus near the lesion provided by the newer ultrasound and spectral technologies facilitates histologic interpretation.
 





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