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Squamous cell carcinoma of the head and neck (HNSCC) is the seventh most common cancer in the United States. Angiogenesis, the process by which new blood vessels are formed, is an essential element at the basis of both tumor growth and metastases. This review discusses pertinent aspects of the role of imaging modalities in assessing angiogenesis and anti-angiogenic therapy in advanced HNSCC.
In 2009, it was estimated that 48,010 new cases of head and neck (HN) cancer would be diagnosed in the United States and 11,260 deaths would occur due to the disease . HN cancers generally stem from the mucosal epithelia of the oral cavity, pharynx, and larynx and have been etiologically associated with tobacco smoking and alcohol consumption . Due to the wide variation in tissues of origin, HN cancer is a heterogeneous disease, representing a variety of histologies and differentiation patterns. The most common histology is squamous cell carcinoma (SCC), which accounts for greater than 90% of HN cancers. Early HN cancers are treated with radiation or surgery and have encouraging locoregional control [3, 4]. After standard therapy (induction or concurrent chemotherapy administered with radiation or prior to surgery) for advanced HN disease, only 60% of patients survive 5 years . Even with aggressive intervention, HN cancers often metastasize to the cervical lymph nodes before invading distant organs including the lungs. Despite advances in surgical techniques and oncologic treatment, the survival rate has remained the same over the past decade . The two main reasons for poor outcome in advance HN cancer are a delayed diagnosis leading to locoregional failure and a late intervention with salvage treatment when disease recurs [5, 6]. Therefore, even if the initial carcinoma is successfully removed, the risk of a patient with HN cancer dying from this or a second malignancy remains high. This review will focus on advanced HNSCC.
Angiogenesis is a critical element of tumor growth and metastasis. It is a complex process, consisting of multiple steps concerning endothelial cell cessation, proliferation and migration of endothelial cells, and formation of new blood vessels . During angiogenesis, vessels form to provide the expanding tumor with cells of endothelial origin, which divide much faster than normal endothelial cells. Once tumors grow beyond a diameter of a few millimeters, passive diffusion cannot sustain the viability of malignant cells anymore, and hence the formation of a new vascular network is necessary . Tumors that grow beyond this stage, therefore, are capable of activating the “angiogenic switch.” Induction of this angiogenic switch depends on how heavily the balance tips in favor of angiogenesis. The induction can occur at different stages of tumor formation, depending on factors such as tumor type and the microenvironment. Blood vessel formation will persist as long as the tumor is growing and is aimed at feeding essential nutrients and oxygen to hypoxic and necrotic areas of the tumor. Angiogenesis plays an important role in head and neck squamous cell carcinoma (HNSCC) as in any other solid tumor . The ability of the tumor to start angiogenesis is a prerequisite for metastatic spread. Traditionally, microvessel density (MVD) has been the parameter most often used for assessing angiogenesis . Another approach involves the assessment of circulating angiogenic serum markers (e.g., vascular endothelial growth factor (VEGF)) .
Several studies [10–12] have shown that monitoring tumor angiogenesis has prognostic value. Angiogenesis is linked to an increased risk of local regional recurrence, distant metastases, and reduced survival in patients with cancers at various organs, including breast, lung, and ovary. Hence, angiogenesis is an interesting area of oncologic research. However, accurate means are needed for detecting tumor angiogenesis and monitoring treatment-induced changes in angiogenesis that precede changes in tumor size . Promising developments in HNSCC angiogenesis research have engendered a need for a reliable pre-clinical platform to develop new therapies and validate surrogate markers of their efficacy in vivo .
The “gold-standard” MVD measure of angiogenesis is the histological estimate of the average number of micro-vessels within a selected region. Several studies have found that intratumoral MVD is predictive of outcome in a number of HNSCC disease sites and could aid the identification of patients who may need aggressive or adjuvant therapy [13–15]. However, the histological MVD assessment is inherently invasive and cannot clarify whether there are functional vessels with blood flow and whether vessels are of a hyperpermeable nature. Also, the assessment of serum marker VEGF lacks sufficient sensitivity and specificity .
Tumors are heterogeneous. Angiogenesis usually peaks in the tumor rim, and therefore MVD measures will fluctuate at different locations where the biopsy is obtained and may under- or over-estimate the degree of angiogenesis. Hence, the MVD parameter is more similar to a static “snap-shot” that does not lend itself to either dynamic in situ assessment of the tumor vasculature or of the molecular factors that regulate its growth . Intratumoral MVD determination requires an invasive process with associated risks of hemorrhage and infection. Development of alternative, non-invasive methods for the evaluation of angiogenesis could spare patients from the aforementioned dangers .
Imaging has many advantages as a means for improving the evaluation of angiogenesis, as it offers the ability to non-invasively sample the entire tumor, can be performed repetitively, and can be used to monitor changes in large numbers of patients at regular intervals . The ability to accurately monitor angiogenesis response to therapy would allow drug efficacy to be established at a very early stage of treatment, long before traditional criteria, such as size changes, can be assessed; likewise, it would allow early identification of patients that do not response to treatment, so their treatment management plan can be altered. The modalities that have mainly been used for imaging angiogenesis include magnetic resonance imaging (MRI), computed tomography (CT), positron emission tomography (PET), and ultrasound (US).
Angiogenesis is typically heterogeneous within tumors: Some vessels are mature, whereas other vessels demonstrate incomplete layers with high permeability and fragility . Angiogenic vessels have large gaps between the endothelial cells and the endothelium, making the vessels hyperpermeable to many macromolecules . These properties can be exploited by imaging techniques that are aimed at assessing the leakiness of the tumor. The two most common modalities used for this purpose are CT perfusion (CTP) and dynamic contrast-enhanced MRI (DCE-MRI); both are well-established imaging techniques that can help assess physiologic parameters .
CTP provides the ability to quantify the microvascular blood flow of tissue by looking at dynamic scan series during injection enhancement of an iodine-based contrast agent . As a clinical tool, CTP has been used mainly in evaluating intracranial vascular disorders such as stroke and vasospasm and to characterize intracranial masses and pathologic processes . In oncology, it has been shown that the CTP parameters of blood flow (BF), blood volume (BV), mean transit time (MTT), and capillary permeability (CP) can be helpful in assessing tumors . In HNSCC, BF, BV, and CP values have been reported to be elevated, and MTT values reduced relative to the values of these parameters in normal adjacent structures . Additionally, Hermans et al.  demonstrated that perfusion assessed on CTP in HNSCC is an independent predictor of outcome after definitive radiation therapy with or without chemotherapy. Specifically, they reported that a lower pre-treatment (radiation) perfusion rate had a significantly higher local failure rate. Interestingly, Gandhi et al.  and Zima et al.  demonstrated that CT-determined BV before treatment or after induction chemotherapy correlated significantly with response in advanced HNSCC. High pre-treatment (induction chemotherapy) BV was linked to beneficial outcome; and a reduced BV post-treatment was linked to good response. Finally, Ash et al.  demonstrated that in HNSCC, the CTP-derived parameters BF and BV correlated positively with MVD as determined through histology, indicating the potential of CTP for assessing angiogenesis in vivo (Fig. 1).
In DCE-MRI, injection of the contrast agent gadopentetate dimeglumine (Gd-DTPA) intravenously is followed by the agent passing from the intravascular space to the interstitial space at a rate that depends on perfusion, vascularity, and tissue permeability . In addition to above factors, the signal enhancement is also influenced by the leakage (interstitial) space. The contrast agent decreases the T1 (longitudinal relaxation time) value of blood and hence enhances the signal intensity on T1-weighted imaging. The blood signal can be sampled by rapid serial T1-weighted imaging covering the tissue or organ of interest using intervals in the seconds range, for periods of up to several minutes after injection.
Using compartmental modeling, DCE-MR images can be converted into parameters reflecting tumor biology. The signal enhancement on T1-weighted images can be modeled using semi-quantitative or quantitative methods. Semi-quantitative methods can provide parameters like peak enhancement, maximum slope, and washout slope. Quantitative methods yield parameters such as Ktrans (volume transfer constant in min−1), ve (volume fraction of the extravascular extracellular space which is dimensionless), and kep (rate constant in min−1) . Figure 2 displays a typical temporal resolution obtained in the pre-treatment DCE-MRI exam of a patient with HNSCC. This patient died of disease after initial treatment with surgery. The VEGF immunohistochemistry assay was performed on the surgical specimen (neck node metastases). More than 50% positive immunostaining for VEGF expression was observed in the nodal tissue.
So far, few studies have described the characteristic DCE-MRI enhancement patterns of tumors in the HN region. Konouchi et al.  have studied 30 patients with primary oral cavity and oropharyngeal SCC with DCE-MRI and correlated the findings with PCNA (proliferating cell nuclear antigen). The PCNA labeling index showed a significant correlation with maximum contrast index (CI) and maximum CI gain. Hoskin et al.  found in 13 patients with advanced HN cancer that tumors with diminished perfusion at the end of radiotherapy were those most sensitive to treatment and that tumors which showed greater enhancement after accelerated radiotherapy were likely to fail locally. Cao et al.  performed quantification of blood volume (BV) and blood flow (BF) from DCE-MRI data pre-therapy and 2 weeks after initiation of chemoradiation in 14 HNSCC patients with advanced disease; they showed that an increase in available primary tumor blood (i.e., BV) for oxygen extraction during RT was associated with increased local control. Finally, in a cohort of 33 patients with HNSCC with neck nodal metastases, Kim et al.  have shown that the average pre-treatment DCE-MRI parameter Ktrans value was predictive of response to chemoradiation with a 6-month follow-up. Specifically, high pre-treatment perfusion (as measured by Ktrans) was indicative of better treatment outcome.
Most HNSCC perfusion (CTP and DCE-MRI) studies so far report that high pre-treatment perfusion is linked to favorable treatment outcome [23–25, 32] and that a large reduction in perfusion after treatment is also linked to better response [24, 30]. Conflicting results, where an increase in BV after treatment is linked to favorable outcome, as reported by Cao et al. , have been tentatively been attributed to differences in treatment modalities, endpoints for local control, and data analyses methods . Perfusion studies done with either CTP or DCE-MRI have shown their potential for monitoring treatment response in HNSCC. However, larger prospective trials are needed to confirm these findings.
Diffusion-weighted Imaging (DWI) is a technique that allows the non-invasive measurement of water diffusivity. It probes the structure and integrity of biological tissue at a microscopic level and may be used for in vivo tumor characterization . Since freedom of translational motion of water molecules is hindered by interactions with other molecules and cellular barriers, such as membranes or different organelles, DWI abnormalities exhibit changes of tissue organization at the cellular level. These microstructural changes affect the (hindered) motion of water molecules and consequently alter the water diffusion properties and therefore the MRI signal. The signal loss in DWI can be quantified using the apparent diffusion coefficient (ADC), which can be interpreted as a measure of the average molecular motion that is affected by cellular organization.
In most DWI studies in patients with HN cancer, a combination of 2 or 3 b-factors was typically acquired, and the ADC values were calculated using the assumption that the signal intensity decay is of monoexponential origin [34–40]. Jansen et al.  recently showed the feasibility of non-Gaussian fitting by using the kurtosis model of the signal intensity decay curves obtained from performing DWI with an extended range of b-values in patients with HNSCC; the method they proposed yielded a significantly better fit of the data than did monoexponential modeling. The method also provided an additional parameter, Kapp, which may provide added value. (Fig. 3).
The link between DWI findings and angiogenesis is not direct, but it has been hypothesized previously that tumors with a higher pre-treatment ADC are more susceptible to the effects of therapy with vascular disrupting or anti-angiogenesis agents . In particular, Koh et al.  suggested, based on results of DWI in 15 patients with solid tumors (mostly colorectal and ovarian), that immature tumor vessels which predominate at the edge of necrotic regions (with high ADC values) are more susceptible to the anti-angiogenic agent bevacizumab. Another tentative link between angiogenesis and ADC was given by Liu et al.  in a preliminary report, who performed ADC, MVD, and VEGF measurements in 38 patients with prostate cancer. They observed a negative correlation between ADC values and MVD (and VEGF). This can be interpreted as higher cell density will result in restricted water motion (diffusion). However, these results need to be validated.
In HN cancers, mean ADC values have been mainly used to monitor treatment response, differentiate between benign and cancerous tissue, and to assess residual or recurrent tumors [34–40]. Wang et al.  studied 97 patients with HN at 1.5T and reported mean ADC values for lesions with different underlying pathologies. They showed that ADC values helped in characterizing HN lesions. Vandecaveye et al.  reported a study on four patients in which the mean ADC values of the lesions could be used to differentiate between persistent or recurrent tumor after radiotherapy for laryngeal squamous cell carcinoma and radiotherapy-induced tissue alterations. Recently, Dirix et al.  found that assessment of mean ADC values of regions of interest could yield important information about salivary gland function before and after therapy and holds promise for investigating radiation-induced xerostomia. In HNSCC, there is some evidence that DWI is useful for predicting and detecting early response to treatment. Kim et al.  have reported on the use of DWI for the prediction and detection of early response to chemoradiation treatment in 33 patients with HNSCC. It was shown that low pre-treatment ADC values correspond to better outcome and that an increase of ADC’s after treatment was also favorable for response. Additionally, Galban et al.  showed that DWI could provide both prognostic and spatial information during non-surgical organ preservation therapy in HNSCC. The results reported in this study were in agreement with Kim et al. that increase in ADC values after treatment (chemoradiation) was linked to favorable outcome.
Magnetic resonance spectroscopy (MRS) is a technique which allows quantification of in vivo metabolite concentrations of tissue, thus offering a window onto cell metabolism . MRS has been performed in HN cancers for both primary tumors and neck nodal metastases . The metabolites most commonly studied with in vivo 1H-MRS are total choline (tCho, a product of phospholipid metabolism that is composed mainly of free choline, phosphocholine, phosphatidylcholine, and glycerophosphocholine) and lactate (a product of glycolysis). There is not a direct one-to-one link between angiogenesis and metabolism seen on MRS. However, elevated levels of lactate may be observed during the process of aggressive tumor development accompanied by angiogenesis (the evolution of the microenvironment) . Also, the rate of tumor cell proliferation has been linked to choline and metabolites seen with phosphorus (31P) MRS [50, 51].
Numerous investigators have found elevated total choline in tumors and it has been suggested that the elevated tCho peak reflects an increased cell proliferation rate . The accumulation of lactate in tumors may be caused by both aerobic glycolysis (a common process in tumors) and by anaerobic glycolysis due to hypoxic conditions. Detection of lactate (a potential biomarker) in tumor tissues using non-invasive MR is difficult because of the presence of lipids, which typically have high co-resonating peaks. Hence, data acquisitions need to be tailored to observe this peak in vivo. In HN cancer, spectral editing techniques have been used to observe the lactate peak [53, 54]. 31P MRS can show a number of metabolites that may offer critical information about the tumor: nucleoside triphosphates (NTPs); phosphocreatine (PCr) (energy metabolism); inorganic phosphate (Pi, intracellular pHi); phosphocholine and phosphoethanolamine, jointly denoted as phosphomonoesters (PMEs, phospholipid precursors); and glycerol esters of phosphocholine and phosphoethanolamine (glycerophosphocholine and glycerophosphoethanolamine), collectively referred to as phosphodiesters (PDEs) (phospholipid catabolites). PME and PDE metabolites are elevated in tumors with high cell membrane turnover and are therefore markers of proliferation. In HN cancers, 1H-MRS has been used mainly to differentiate between normal and primary tumors via the choline peak, while 31P-MRS has been used to predict response via the PME/NTP ratio . MRS is a tool to study cell membrane metabolism, pH, and tumor energy status that may find applications in monitoring anti-angiogenic therapies.
Positron emission tomography (PET) is a highly sensitive non-invasive technology that is well suited for the visualization of changes in metabolism in cancer. Before PET imaging, radiolabeled tracers are injected in non-pharmacological tracer doses. Three-dimensional PET data can then be obtained and reconstructed to show the concentrations and locations of the radionuclide . PET imaging, like MRS, offers a window into the tumor metabolism and microenvironment. 18F-fluorodeoxyglucose (18F-FDG) is the radiotracer most commonly used to image HN cancer . 18F-FDG uptake is proportional to tissue glucose consumption. Most tumors have an elevated glucose consumption which can be quantified by 18F-FDG PET imaging. This tracer has applications ranging from staging to prediction of outcome in HN cancers .
Many other PET tracers have been used to better understand the tumor microenvironment, especially angiogenesis, and related processes such as hypoxia and proliferation. The radiotracer 18F-Galacto RGD has been developed for PET imaging of αvβ3 expression of a receptor involved in angiogenesis and metastases . Beer et al.  tested the feasibility of using this tracer in eleven patients with HNSCC. They performed immunohistochemistry (IHC) using an αvβ3-specific antibody and expression of the antibody was seen in all cases. 18F-Galacto RGD PET identified 10 of the 12 tumors correctly, and two tumors of size <0.5 mm were missed. They established the feasibility of using this tracer to open up new possibilities for studying angiogenesis with PET. An important application of this new radiotracer would be in monitoring treatment response of anti-angiogenic therapy.
18F-fluoromisonidazole (FMISO) PET has been used to study hypoxia [58, 59]. Hypoxia is a pathological condition in which tissue is deprived of adequate oxygen supply. Numerous investigators have stated that tumor oxygenation (using invasive Eppendorf pO2 measurements) in HN cancers is linked to poor outcome [60, 61]. Nordsmark et al.  assessed the pre-treatment tumor oxygen tension in a multicentric trial with 397 patients with HN cancer and concluded that tumor hypoxia is associated with a poor outcome. 18F-FMISO PET is only susceptible to hypoxia in viable cells; it can cover large regions of interest and is well tolerated by patients. Jansen et al.  showed that 18F-FMISO PET hypoxia data correlated with DCE-MRI perfusion data in patients with HNSCC. They found that in metastatic neck lymph nodes, hypoxic nodes were poorly perfused relative to those that were non-hypoxic (Fig. 4).
Another tracer that has been used in HN cancer is 18F-fluorothymidine (18F-FLT), the uptake of which reflects proliferation . Cellular proliferation, or cell growth, is a major feature of cancer, in which cells exhibit uncontrolled growth and division at a larger rate than normal. This tracer is captured in proliferating tissues through the activity of thymidine kinase. 18F-FLT uptake has been shown to be a marker of thymidine kinase-1 (TK1) activity, which is an enzyme that is overexpressed during the DNA synthesis phase of the cell cycle. Accumulation of 18F-FLT inside the cell is, therefore, interpreted as a putative marker of proliferation. Few studies have used this tracer in primary HN cancers. Cobben et al.  showed in a prospective 18F-FLT and 18F-FDG PET study performed on 21 patients with suspected recurrent and primary laryngeal cancer that both techniques detected histologically proven laryngeal cancer correctly in 15 of 17 patients. Linecker et al.  took a step further and correlated 18F-FLT data with the proliferative molecular marker Ki-67 assessed by IHC assay. They studied 20 untreated patients with HNCC by both 18F-FLT and 18F-FDG PET and compared the PET results with histological and IHC results. They found a significant inverse correlation between both 18F-FLT uptake and survival but no correlation between Ki-67 expression level and 18F-FLT PET data (which could be attributed to the small patient population). As seen by these studies, it is clear that PET tracers are being continuously tested for various applications in HN cancers and their role in better understanding the tumor microenvironment is still evolving. Mostly they have been used for detection and staging of the disease . Going forward, roles for these tracers in monitoring anti-angiogenic therapy are expected to unfold.
Ultrasound offers an inexpensive and readily accessible means to evaluate cervical adenopathy, and it is the standard tool used for this purpose in the clinic . Typically, clinical examinations are performed with a high-frequency, linear transducer, usually with Doppler capability. Substitution of neoplastic tissue for normal lymph node tissue makes lymph nodes unusually clear on ultrasonic examination. The complex, multi-step process of angiogenesis is critically associated with blood flow and blood flow regulation. It has been hypothesized that laser Doppler ultrasound could provide a non-invasive and reliable method of quantifying blood flow within tumors . Jacob et al.  showed that laser Doppler ultrasound is a potentially useful tool for studying blood flow in the HN region.
Molecular imaging (MI) has been defined as the in vivo visual representation, characterization, and quantification of biologic processes and molecular pathways at a cellular and molecular level . As long as a suitable target, probe, and detection method are available, the MI concept can be applied to various imaging modalities, including MR, CT, PET, US, and optical imaging. MI is rapidly gaining acceptance in oncology, as it detects differences in molecular properties in vivo between cancer and normal tissue that arise as a result of malignant transformation . The above mentioned 18F-Galacto RGD PET approach using the αvβ3-specific antibody is an excellent example of MI use in angiogenesis . Receptors play a key role in signal transduction and proliferation of cancer cells . Another example of such a receptor is the transferrin receptor (TfR), which is a cell membrane-internalizing receptor that is responsible for iron sequestration in mammalian cells . Expression of TfR is elevated in malignant cells due to a need for iron as a cofactor for the ribonucleotide reductase enzyme . TfR is overexpressed in the majority of cases of HNSCC but minimally expressed in normal oral squamous epithelium and benign lesions . A high expression level of TfR indicates a high grade of tumor malignancy and a poor prognosis. TfR expression can be targeted in vivo by conjugating a transferrin (Tf) probe to a nanoparticle suited for MI, as shown elegantly by Shan et al.  in an animal model of HNSCC.
In addition to the two aforementioned MI approaches in HNSCC (TfR and αvβ3), many other angiogenesis-related receptors can be targeted using MI. As new molecular therapies are by definition directed at specific targets, MI directed at the same targets can be useful in predicting the response to anti-angiogenic drug treatment. Such a targeted approach depends on the binding of labeled molecules to highly expressed markers. Interestingly, nanoparticles used for MI of angiogenesis may be designed such to have both diagnostic and anti-tumor features. This allow investigators to precisely monitor drug delivery and efficacy in tumors (theranostics) . Molecules that are possible targets for imaging include VEGF and its receptors, integrins, and matrix metalloproteinases (MMPs) . The application of MI of angiogenesis in HNSCC has been very limited so far, therefore we would like to refer to articles by Turkbey et al.  and Cai et al.  who provide excellent, more extensive reviews of potential targets for MI of angiogenesis.
Current HNSCC treatment protocols for advanced disease include aggressive induction chemotherapy and concurrent chemoradiation, with an increasing role for novel, rationally designed, molecularly targeted agents . There is a growing need for additional clinical diagnostic tests to help select treatments with maximal efficacy and minimal toxicity . Unlike cytotoxic chemotherapy, which interrupts normal mitotic activity in dividing cells, targeted therapies are designed to interact primarily with cancer-specific attributes and signaling pathways . One of these pathways is angiogenesis, a characteristic of all advanced cancers.
Pre-clinical and early clinical trials provide evidence of the promise of anti-angiogenic therapy for HNSCC . Seiwert et al.  recently provided an overview of the currently available data and future directions for treatment, including ongoing pivotal clinical trials. Contrary to earlier fears that anti-angiogenic therapies could augment hypoxia and thereby might make treatment failure more likely, anti-angiogenic therapies in pre-clinical HNSCC models so far do not appear to have a propensity for resistance and go well with traditional therapies (such as radiation).
Clinical use of anti-angiogenic agents for HNSCC often focus on inhibitors of tyrosine kinase receptors, including bevacizumab, sorafenib, sunitinib, semaxanib, and others. Their use is currently limited to clinical trials, and therefore, literature on the use of imaging to monitor angiogenesis in HNSCC patients treated with anti-angiogenic drugs is scarce. It is pertinent to point out that most of the aforementioned studies of the use of imaging techniques to monitor treatment in HNSCC did not pertain to anti-angiogenic drugs, but to radiation or cytotoxic chemotherapy . In a recent Phase II study by Machiels et al. , 38 patients with HNSCC were treated with sunitinib and a small subset of patients underwent DCE-MRI monitoring pre- and post-treatment. The DCE-MRI results showed that in all but one of the patients studied, a significant decrease was observed in Ktrans after treatment, suggesting that sunitinib indeed decreased the amount of angiogenesis. In another Phase II study, Fury et al.  used power Doppler ultrasound and serum VEGF levels to monitor anti-angiogenic activity of semaxanib in 35 patients with HNSCC. They found that tumor vascularity decreased during semaxanib treatment even in patient with progression of disease. They concluded that semaxanib achieved suboptimal inhibition of angiogenesis and that changes observed with ultrasound were probably not related to anti-tumor activity of semaxanib. These Phase II feasibility studies indicate the need for reliable imaging techniques to monitor angiogenesis (or angiogenesis-related processes) in HNSCC trials of anti-angiogenic agents.
The ability to detect diverse aspects of angiogenesis and angiogenesis-related processes makes in vivo imaging attractive for following the entire time course of drugs’ anti-angiogenic activity in HNSCC. Anti-angiogenic agents target tumor vasculature and reduce vessel permeability by ‘normalizing’ the vessel morphology, which restores vascular integrity . Clinically, imaging can be applied before, during, and after anti-angiogenic treatment to monitor response. A comprehensive overview of the presented imaging techniques and their relation to angiogenesis is provided in Fig. 5 and Table 1.
As indicated above, most imaging modalities, with the exception of 18F-Galacto RGD PET, do not provide direct information about angiogenesis itself, but merely about a related process. Therefore, the exact relevance of the changes observed in tissue contrast (as measured using one of the imaging modalities) to angiogenesis remains speculative in nature. However, sufficient evidence is available showing that techniques as CTP , DCE-MRI , and US  closely correlate with MVD measurements, which can be regarded as a gold-standard. Unfortunately, for other techniques, a similar validation with MVD is not conclusive (DWI , FDG PET , and FMISO PET ) or lacks completely (MRS and FLT PET). Another relevant issue for all techniques used for imaging angiogenesis or angiogenesis-related processes is the proper analysis (e.g. modeling) of the data and the reproducibility of the imaging measurements. These are prerequisites in order to objectively infer whether measured changes in imaging parameters truly reflect the biological process.
Considering the diversity and demonstrated potential of available imaging methods, the importance of imaging in assessing angiogenesis in HNSCC is expected to grow.
We thank Ms. Ada Muellner (B.A.) for editing the manuscript and Dr Diane Carlson (Dept of Pathology) for molecular pathology data on surgical specimens. The work from MSKCC reported in this review was supported by the National Cancer Institute/National Institutes of Health (grant number 1 R01 CA115895).