First-In-Human Study Demonstrating Tumor-Angiogenesis by PET/CT Imaging with 68 Ga-NODAGA-THERANOST,a High-Affinity Peptidomimetic for α v β 3 Integrin Receptor Targeting

Introduction

According to the World Health Organization, ∼24.6 million people are living with cancer worldwide, and the American Cancer Society has estimated approximately 1.6 million new cases in the United States in 2015. ¹ Medical imaging plays a key role in cancer diagnosis and clinical management of patients by highlighting noninvasively cancer presence, spread and metabolism, enabling staging, restaging and therapy monitoring, and contrasting differences between normal and malignant tissues. Positron emission tomography (PET), magnetic resonance imaging (MRI), computed tomography (CT), and fusion imaging (PET/CT or PET/MRI) represent important evolutions in technology. Clinicians are seeing dramatic improvements in cancer treatment moving toward individually tailored programs of personalized therapy. ² However, despite significant preclinical scientific progress, very few cancer imaging agents are currently available in the clinic.

The most frequently used PET tracer in this setting to date is 2-deoxy-2-(¹⁸F) fluoro-d-glucose (¹⁸F-FDG). However, several studies have demonstrated its limitations in distinguishing some malignant lesions. ³ A theranostic approach could allow targeted tumor detection, while potentially reducing the harmful collateral effects of chemotherapy or radiochemotherapy.

The cell adhesion motif α_vβ₃ arginine–glycine–aspartate (RGD) integrin receptor was discovered in fibronectin by Pytela, Pierschbacher, and Ruoslahti more than 20 years ago. ⁴ Shortly thereafter, Smith and Cheresh identified the vitronectin receptor as one of the adhesion molecules recognizing this sequence. ⁵ The α_vβ₃ integrin receptor is overexpressed on endothelial cells and on some tumor cells.

Integrins are amino acid-containing derivatives that are key regulators of tumor angiogenesis and metastasis and are heterodimeric transmembrane proteins involved in cell adhesion and cell signaling, and their expression is upregulated in cancers and inflammatory diseases. ⁶ Integrins play a vital role in angiogenesis, leukocyte function, and tumor growth and are potential targets for therapeutic agents, demonstrating an antiproliferative effect on tumor growth and the selective inhibition of endothelial α_vβ₃ integrin; also, they have been shown to increase the effectiveness of combination regimens such as chemotherapy and radiochemotherapy.

The α_vβ₃ integrin is significantly overexpressed in certain types of tumor cells and in almost all tumor vasculature. It is expressed on the luminal surface of neovasculature (but is not found on the endothelial surface of mature capillaries), has been shown to be upregulated in tumor blood vessels that undergo angiogenesis, and has been implicated in metastasis. ⁷ Increased levels of integrin α_vβ₃ are closely associated with increased cell invasion and metastases. Integrins are upregulated in many malignancies, mediate a variety of tumor integrin-targeting therapeutics, and have activity against many cancer subtypes. ^{8 –10}

Because α_vβ₃ is involved in neoangiogenesis in solid tumors and is also directly expressed in cancer cells (e.g., glioblastomas, melanomas, myelomas, ovarian, breast, and prostate cancers), these radiolabeled peptide ligands for α_vβ₃ targeting might become powerful new tools for molecular imaging and targeted radiotherapy of tumors undergoing angiogenesis. ^{7,10 –16}

Noninvasive imaging of α_vβ₃ expression could be of vital importance for patient selection and monitoring of anti-integrin treatment efficacy. The ability to image angiogenesis could potentially be used to identify patients who may benefit from antiangiogenic treatments, prognostication/risk stratification. ¹⁶ PET imaging with ¹⁸F-RGD peptides has been shown to visualize and quantify α_vβ₃ integrin expression in patients, but radiolabeling is complex and image contrast is limited in some tumor types. ¹⁷ Low tumor uptake, failure to differentiate inflammation, and high cost and difficulties in routine radiosynthesis have limited some clinical application of RGD agents. ¹⁸ Compared to the commercially available cyclic peptide RGDfv, this probe has at least 20 times better binding affinity for the α_vβ₃ receptor. ¹⁹

The PET tracer ¹⁸F-Galacto-RGD has been developed and while this agent shows favorable pharmacokinetics, tracer synthesis is labor intensive (duration 200 minutes), involving steps that cannot be automated. A promising alternative tracer that can be synthesized is ⁶⁸Ga-NODAGA-RGD, which has been used in animal studies and has the advantage of the availability of ⁶⁸Ga, convenient radiolabeling, high stability, and good imaging properties. ^{11 –13,18,20} Superior preclinical results were obtained in comparison with ¹⁸F-Galacto-RGD. Therefore, ⁶⁸Ga-NODAGA-cyclo-RGDyK may be a suitable replacement for ¹⁸F-Galacto-cyclo-RGDfK. ^12,13,18,21

Clinical data have been reported for the glycosylated peptide, cRGDfK, labeled with 2-¹⁸F-fluoropropionate to yield ¹⁸F-galacto-RGD (Fluciclatide) in patients with malignant melanoma. ¹⁶ According to clinicaltrials.gov, ²² the ¹⁸F-FPPRGD2 (2-fluoropropionyl)-labeled PEGylated dimeric RGD peptide [PEG3{c(RGDyk)}2]), based on the dimeric RGD peptide sequence targeting α_vβ₃ is in early-stage clinical trials. Lung cancer and cardiovascular imaging trials are underway using ⁶⁸Ga-BNOTA-PRGD2. Trials are also underway using ⁶⁸Ga-BNOTA-PRGD2 at the Peking Union Medical College Hospital 6).

While ¹⁸F- and ⁶⁴Cu-labeled RGD peptides have been used for quantification of α_vβ₃ expression by PET imaging, these are associated with problems, including limited image contrast and complex radiolabeling. ^12,13,23 Regardless, radiolabeled peptides have been the dominant molecular imaging strategy for imaging integrin expression that has been translated into the clinic. ²¹

A peptidomimetic is a small protein-like chain designed to mimic a peptide. They typically arise either from modification of an existing peptide or by designing similar systems that mimic peptides, such as peptoids and β-peptides. Irrespective of the approach, the altered chemical structure is designed to advantageously adjust the molecular properties, such as stability or biological activity. These modifications involve changes to the peptide that will not occur naturally such as altered backbones and the incorporation of unnatural amino acids.

Natural amino acids in peptides can be replaced with nonproteinogenic counterparts (proteinogenic means “protein building”). Proteinogenic amino acids can be condensed into a polypeptide (the subunit of a protein) through a process called translation. Proteinogenic amino acids are amino acids that are precursors to proteins, and are incorporated into proteins cotranslationally—that is, during translation to obtain drug-like targeting molecules that stimulate innovation leading to development of approaches that differ from conventional RGDs and can result in enhanced interactions. ²⁴

The α_vβ₃ integrin antagonist (IAC) peptidomimetic, 4-[2-(3,4,5,6-tetrahydropyrimidine-2-ylamino)ethyloxy]benzoyl-2-[N-(3-amino-neopenta-1-carbamyl)]-aminoethylsulfonyl-amino-β-alanine, THERANOST™, was developed to provide an alternate vector that selectively targets integrin α_vβ₃ receptor and clears rapidly from the whole body. Based on extensive lead optimization studies, this IAC demonstrated superior binding affinity to cells that express α_vβ₃. The compound accumulated in angiogenic blood vessels after systemic administration in the murine squamous cell carcinoma model. ^8,9,25 Thus, this novel integrin-targeting platform was expected to have potential applications for targeted delivery of drugs, and more directly, highly suitable for molecular imaging and possibly therapy applications. ²⁶

IAC has been labeled with ^99mTc and ¹¹¹In, ^9,25 conjugated with a dye, FITC, and evaluated as an optical imaging agent. ^19,26 Thus, in vivo studies were performed aimed at rapid targeting of integrin receptors to produce a high tumor-to-background ratio and as well in the cardiovascular setting as an optical imaging agent. ¹⁹

The ¹¹¹In-labeled compound was evaluated for in vitro receptor binding and carried forward through biodistribution and imaging studies in M21 human melanoma xenograft models demonstrating specific binding that could be blocked by an excess of unlabeled agent indicating receptor-mediated uptake. The radiolabeled agent was excreted primarily through the renal system resulting in high tumor-to-background ratios at 2 hours in imaging studies enabling visualization of receptor-positive tumors at 4 hours. Similarly, ^99mTc-labeled IAC resulted in equally positive results demonstrating good tumor-targeting properties with a rapid uptake, prolonged tumor retention, and fast whole-body clearance kinetics.

Overall, the tumor-targeting kinetics combined with the rapid accumulation and prolonged retention justified further studies of molecular imaging of tumor-induced angiogenic vessels and various malignant tumors expressing the receptor in humans.

During the course of the development of a positron-labeled peptidomimetic IAC targeting α_vβ₃, incorporation of ⁶⁸Ga as the radionuclide of choice was self-evident. Generator-derived radionuclides for PET/CT imaging are promising for optimizing targeted radiotherapy by an individual patient-based approach, applying pretherapeutic evaluation as well as dosimetric calculations and for measuring treatment response after radionuclide therapy. ²⁷

⁶⁸Ga is available from an in-house generator enabling ⁶⁸Ga radiopharmacy independent of an on-site cyclotron. ⁶⁸Ga has an ideal half-life (t _1/2=68 minutes) and decays by 89% through positron emission (β⁺ E _max=1.899 MeV) that provides PET images with high-quality resolution. The parent, ⁶⁸Ge, is accelerator produced and decays with a half-life of 270.8 days by electron capture. There are at least three commercial and several in-house generators available, positioning this radionuclide for further widespread clinical development. As such, ⁶⁸Ga was selected by this team as the optimal radionuclide for radiolabeling and clinical translation as a diagnostic agent for molecular imaging.

Appropriate chelation technology that complements the chemistry of Ga(III) and also meets the requirements for in vivo stability for retention of the ⁶⁸Ga prompted selection of a bifunctional NOTA derivative. Synthesis was performed in a straightforward aseptic procedure. All routine quality control requirements were met.

The stability of the Ga(III)-NOTA complex is well recognized. ²⁸ The NOTA derivative 1-(1-carboxy-3-carbo-tert-butoxypropyl)-4,7-(carbo-tert-butoxymethyl)-1,4,7-triazacyclononane [NODAGA(tBu)₃] is a bifunctional chelator, which conveniently lends itself to efficient active ester conjugation to the primary amine of IAC. Subsequent acidic deprotection provides an IAC-NODAGA (Fig. 1) suitable for labeling with ⁶⁸Ga. ²⁹ Having established both the conjugation chemistry for appending NODAGA to this novel peptidomimetic as well as radiolabeling with ¹¹¹In and ⁶⁷Ga, its efficient translation into the clinic became a logical forward step to follow in its development. Significant potential utility for noninvasive evaluation of angiogenic and metastatic activity in cancer as well as for monitoring tumor therapy using α_vβ₃ or other angiogenesis inhibitors appears possible, and as such, patient imaging studies were initiated.

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FIG. 1.

Structure of ⁶⁸Ga-NODAGA-THERANOST.

⁶⁸Ga-IAC-NODAGA, which was shown to exhibit high affinity for α_vβ₃ and high selectivity versus other integrin receptors, demonstrated high tumor uptake and produced excellent PET/CT images. Based on these promising results, investigations moved forward to evaluate NODAGA-IAC and DOTAGA-IAC conjugates for targeting tumor-associated angiogenesis and α_vβ₃ integrin-positive tumors so as to define their PET and SPECT imaging qualities as well as the potential for delivery of therapeutic radionuclides. Herein, the authors present the result of the first-in-human clinical results of PET/CT imaging using ⁶⁸Ga-NOTAGA-IAC, ⁶⁸Ga-NODAGA-THERANOST.

Materials and Methods

Results and Discussion

This is the first report on the ability of ⁶⁸Ga-NODAGA-THERANOST to detect solid tumors in humans, establish the absence of neovascularization, and predict the antitumor effect. The acronym ‘THERANOSTIC’ epitomizes the inseparability of diagnosis and therapy and takes into account personalized management of disease for a specific patient. Thus, what is hypothesized is that molecular imaging can be effectively followed by personalized treatment utilizing the same molecular vector.

Receptor PET/CT using ⁶⁸Ga enables imaging of metastases with high tumor-to-background ratio, diagnostic sensitivity, specificity and uptake, and desirable circulation half-life. This provides quantitative and reproducible data that can be used for selecting patients for therapy and, thereafter, evaluation of therapy response with probably low radiation burden (10–12 mSv) to the patient. ³²

Although assessment of tissue metabolism using ¹⁸F-FDG provides useful tumor imaging, it is not tumor specific and usually less useful for imaging tumors that have low growth rates as it actually is a metabolic marker or a guide for delivery of specific molecular therapy. The development of new tracers such as THERANOST that target specific molecular abnormalities is therefore essential for the development and utility of clinically relevant PET, which can be used to assess the efficacy of therapeutic drugs. The goals are to allow early detection and characterization of the disorder, to provide more timely and direct assessment of treatment, and to obtain a more fundamental understanding of the disease process. ³³

As opposed to benign tumors, malignant ones usually overexpress integrins on cancerous tumors. The purpose of this study was to assess the safety, biodistribution, and dosimetric properties and to establish ligand targeting of α_vβ₃ integrin receptors with ⁶⁸Ga-NODAGA-THERANOST, a potent α_vβ₃ peptidomimetic displaying a strong binding affinity for extracellular surface matrix proteins and epitopes, including α_vβ₃ and other integrins, fibronectin, vitronectin, fibrinogen, tenascin-C, osteopontin, gastrin-releasing peptide, and neuropilin-1. ^7,11,20,34

PET studies were evaluated and reported by 2 experienced nuclear physicians. Any disagreements were resolved by reaching a consensus.

Two patients were imaged using ⁶⁸Ga-NODAGA-THERANOST. The first patient was a 28-year-old female patient with extensive metastatic breast cancer (G3, HER2 3+) who presented with liver metastases 1 year after the initial diagnosis, indicating cancer with high malignancy potential. Reconstructed fused images of this patient demonstrated enhanced tumor-to-background ratios for ⁶⁸Ga-NODAGA-THERANOST and PET/CT images obtained 60 minutes postinjection of 472 MBq of ⁶⁸Ga-NODAGA-THERANOST revealed high uptake, sensitivity, and specificity in tumors at possible neoangiogenesis sites and enhanced detection of multiple skeletal metastases (Fig. 2).

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FIG. 2.

(A) PET/CT images using ⁶⁸Ga-NODAGA-THERANOST (left and right panels) as well as ¹⁸F-FDG (middle panel) of patient #1. Overall, 25 lesions were cRGD positive compared to 12 lesions detected by FDG (shown here are skeletal metastases on transverse slices in upper row: PET, middle row: CT, and lower row: fused PET/CT). Curved arrows (left panel) demonstrate cRGD positive vertebral pedicle lesions, which were negative on FDG. Straight arrows indicate FDG-avid lesion in left sacral ala (middle panel), which was cRGD negative (right panel). (B) The maximum intensity projection (A) and reconstructed fused images using ⁶⁸Ga-NODAGA-THERANOST revealed intense uptake (SUV_max=4.8) at neoangiogenesis sites in multiple skeletal metastases, for example, skull (B), vertebrae (C), and pelvis (D). The ¹⁸F-FDG-positive lung (E2) and lymph node (F2) metastases did not show any uptake of ⁶⁸Ga-NODAGA-THERANOST (E1 and F1, respectively), indicating the absence of neovascularization. CT, computed tomography; PET, positron emission tomography; ¹⁸F-FDG, 2-deoxy-2-(¹⁸F) fluoro-d-glucose; SUV, standardized uptake value; arrows pointing to the right indicate lung metastasis and to the left indicate lymph node metastasis.

The maximum intensity projection (Fig. 2A) and reconstructed fused images revealed intense uptake (SUV_max 4.8) at the sites of neoangiogenesis in multiple skeletal metastases, for example, the skull (Fig. 2B), vertebrae (Fig. 2C), and pelvis (Fig. 2D). Overall, 25 integrin α_νβ₃-positive lesions were detected by ⁶⁸Ga-NODAGA-THERANOST versus 12 by ¹⁸F-FDG PET/CT. The ¹⁸F-FDG-positive lung (Fig. 2E2) and lymph node (Fig. 2F2) metastases did not show any uptake of ⁶⁸Ga-NODAGA-THERANOST (Fig. 2E 1, F1, respectively), indicating the absence of neovascularization. ⁶⁸Ga-THERANOST accumulated more specifically than ¹⁸F-FDG in primary and metastatic tumors. ¹⁸F-FDG-positive lung and lymph node metastases did not show uptake, indicating the absence of neovascularization.

The second patient imaged using ⁶⁸Ga-NODAGA-THERANOST was a 61-year-old male with a neuroendocrine neoplasm of the right lower lobe of the lung (typical carcinoid), who had received two cycles of PRRT. PET/CT after injection of 496 MBq of ⁶⁸Ga-NODAGA-THERANOST demonstrated α_vβ₃ receptor expression and angiogenesis in the right pleural carcinomatosis (Fig. 3A). The SUV_max of the target lesion in the right dorsoapical pleura was 4.0 (tumor-to-liver ratio of SUV_max T/L was 1.43 and tumor-to-spleen ratio of SUV_max [T/S] was 1.48).

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FIG. 3.

PET/CT images using ⁶⁸Ga-NODAGA-THERANOST of patient #2. (A) Demonstrates integrin receptor expression and angiogenesis in the extensive right pleural carcinomatosis. SUV_max of target lesion in the right dorsoapical pleura was 4.0 (tumor-to-liver ratio of SUV_max, T/L was 1.43 and tumor-to-spleen ratio of SUV_max, T/S was 1.48). Pleural uptake was also noted on somatostatin receptor PET/CT with ⁶⁸Ga DOTATOC (B). SUV_max of the same lesion being 6.9, but with a lower target lesion-to-background ratio (T/L 0.78, T/S 0.17). MIP image on the left, coronal fused PET/CT in the middle, transverse CT on the right above, and transverse fused PT/CT on the right below. MIP images of ⁶⁸Ga-NODAGA-THERANOST PET/CT are shown in two different color scales.

Pleural uptake was also observed on somatostatin receptor PET/CT with ⁶⁸Ga-DOTATOC (Fig. 3B), SUV_max of the same lesion being 6.9, but with a lower target lesion-to-background ratio (T/L 0.78, T/S 0.17). This radiotracer was associated with rapid blood clearance and renal clearance. The minimum nonspecific activity accumulation in normal lung tissue and heart rendered high-quality tumor images, enabling clear demarcation of both the primary tumor at the upper lobe of the left lung as well as metastases in the mediastinum, contralateral lung, and diaphragm. Biodistribution, quantitative tissue uptake, and time–activity in tumor and normal organs appear acceptable. As a comparison, ¹⁸F-FDG scans were only able to identify the primary tumor, with the metastatic lesions masked by intense cardiac uptake.

The mean and standard deviation of the administered mass of ⁶⁸Ga-NODAGA-THERANOST was 37.5±12.5 μg (range, 25–50 μg). The mean administered activity was 333.5±162.5 MBq (range, 171–496 MBq). Mean standardized uptake values (SUVs) were calculated from each region of interest using the formula SUV=measured activity concentration (Bq/g)×body weight (g)/injected activity (Bq).

There were no adverse or clinically detectable pharmacological effects in any of the subjects. No significant changes in the vital signs or the results of laboratory studies or electrocardiograms were observed. With an injected dose of 370 MBq and a 1 hour voiding interval, a patient would be exposed to an effective radiation dose of 1.5 rem (15 mSv). Time–activity curves showed rapid clearance from the vasculature with most of the activity occurring in the plasma relative to cells.

Uptake was highest in the tumor, kidney, and urinary bladder. The compound appears safe and well tolerated in patients, exhibits rapid blood clearance, stability, good clearance kinetics and renal excretion, favorable biodistribution, pharmacokinetics, and pharmacodynamics to provide high-contrast PET images of integrin-expressing tumors, recorded 1 hour after injection.

Quantitatively, there were relevant differences in the biodistribution between ⁶⁸Ga-NODAGA-THERANOST and ¹⁸F-FDG resulting in a higher tumor lesion detection rate than ¹⁸F-FDG. Remarkably, this radioligand accumulated more specifically than ¹⁸F-FDG in both primary and metastatic tumor lesions enabling detection of more than twice the number of possible bone metastases in a breast cancer patient, accumulating more specifically in angiogenic tumors than ¹⁸F-FDG and accumulating in malignant tumors more specifically than ¹⁸F-FDG or ⁶⁸Ga-DOTATOC. The high tumor-to-lung contrast probably results from a lack of integrin expression in normal tissues and organs and minimal nonspecific cardiac accumulation. This makes ⁶⁸Ga-NODAGA-THERANOST an attractive alternative to more costly ¹⁸F-labeled compounds.

⁶⁸Ga-NODAGA-THERANOST, a nonpeptide α_vβ₃ targeting vector, demonstrated high diagnostic sensitivity, specificity, and binding to integrin-positive tumors. Imaging with ⁶⁸Ga-NODAGA-THERANOST dramatically improved image contrast, because this compound is only slowly cleared from α_vβ₃ integrin-expressing tumors, whereas clearance from normal tissues appears to be much faster.

Only 2 patients were included in this pilot study because the aim was to obtain clinical data on the potential usefulness of imaging integrin-positive tumors and differentiating angiogenic tumors and not to determine the sensitivity and specificity in a specific patient population. Regardless, even in this limited patient number study, a strong positive correlation of uptake and proliferation was detected as assessed by Ki-67 indexing.

Ki-67 is a nuclear protein that is associated with and may be necessary for cellular proliferation. It is an excellent marker to determine the growth fraction of a given cell population. The fraction of Ki-67-positive tumor cells (the Ki-67-labeling index) is often correlated with the clinical course of cancer. The best-studied examples in this context are carcinomas of the prostate, brain, lung, and breast. For these types of tumors, the prognostic value for survival and tumor recurrence has repeatedly been proven in uni- and multivariate analyses.

This study provides the first clinical evidence that ⁶⁸Ga-NODAGA-THERANOST is a useful positron-emitting radionuclide tracer for visualization of tumors and metastases demonstrating that PET imaging using ⁶⁸Ga-NODAGA-THERANOST is sensitive enough to detect α_vβ₃ integrin expression and may be a superior approach for imaging and therapy, as well as for selection of patients who could potentially benefit from therapy. Data, so far, justify further evaluation in larger cohorts, especially with regard to integration of ⁶⁸Ga-NODAGA-THERANOST for early response imaging and as a predictive or interim value tool in the clinical management of cancer patients.

Future aims would include studies to monitor, noninvasively, changes in vascularity after antiangiogenic therapies, and potentially to determine the clinical and pathological efficacy of neoadjuvant chemo-/immunotherapy or molecular targeted therapy with small molecules, for example, applying therapeutics that specifically inhibit angiogenesis in tumors.

THERANOST, carrying therapeutic cargoes, might also have potent activity with drugs of distinct chemotype, potentially including bevacizumab, sorafenib, paclitaxel, docetaxel, bortezomib, sunitinib, bosutinib, or dasatinib. Thus, coadministration of THERANOST in a drug delivery mode could potentially enhance the efficacy of anticancer drugs. Molecular targeted radionuclide therapy (TRNT) could have important applications for treating disseminated diseases with the cytotoxic radionuclide being specifically directed to the malignancy, sparing normal tissues. Radiolabeled with particle emitters such as ¹⁷⁷Lu, ⁹⁰Y, ²¹³Bi, or ²¹²Pb, the DOTAGA conjugate of THERANOST might be employed for TRNT or neoadjuvant peptidomimetic radiotherapy. ²⁹

On this basis, THERANOST might be a suitable drug for efficacious diagnosis, and further clinical trials and patient management evaluation before and after therapy may be warranted. In this groundbreaking investigation, the potential utility of this high-affinity tumor-penetrating ligand is suggested. In summary, PET/CT imaging provides clinicians with a noninvasive tool for assessment and response evaluation in the oncological setting. ⁶⁸Ga is an alternative generator-produced PET tracer, which has the potential to be more cost effective with fewer limitations compared to ¹⁸F-FDG.

Conclusions

Synthesis and clinical evaluation of ⁶⁸Ga-NODAGA-THERANOST for imaging of integrin receptors signal the potential clinical usefulness of this peptidomimetic to identify responders and nonresponders who may benefit at an early stage, an important factor in determining the most appropriate treatment for cancer patients. The ⁶⁸Ga-NODAGA-THERANOST probe was evaluated clinically and demonstrated selectively binding with high affinity and rapid accumulation in diseased tissue and tumor neovasculature, reporting biochemical and morphological characteristics. Initial evidence suggests that this radioligand has considerable potential for early tumor detection and noninvasive monitoring of tumor metastasis in a range of diseases.

Specific indications may include tumor staging, identifying patients who would benefit from antiangiogenesis therapy early and treatment regimen modification, and as a molecular marker of chemosensitivity. Noninvasive reproducible quantitative assessment (SUV_max) provides important information for planning and monitoring of antiangiogenic therapies, revealing involvement in tumor processes.

Molecular imaging using ⁶⁸Ga-NODAGA-THERANOST is a promising diagnostic tool for patient management, has the potential to localize metastatic lesions in vivo, adds qualitative information not available using conventional imaging techniques, and may allow the status to be determined for metastases not amenable to biopsy. These observations are clinically relevant, showing potential for determination of therapeutic response earlier than current methods that rely on changes in tumor size or less sensitive receptor agents. ⁶⁸Ga-NODAGA-THERANOST could potentially become a suitable substitute for ¹⁸F or ^99mTc molecular imaging agents and a preferred alternative to RGDfv, RGDyK, and other RGDs due to greater specific accumulation in integrin-expressing tumors. Larger trials with ⁶⁸Ga-NODAGA-THERANOST are needed to evaluate and support the value of this novel radioligand.