Molecular imaging for detection of sensitivity and resistance to EGFR tyrosine kinase inhibitors in non-small cell lung cancer
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Advancing knowledge of non-small cell lung cancer (NSCLC) has provided new treatment options based on the specific gene alterations found in individual tumors. The presence of activating mutations in the epidermal growth factor receptor (EGFR) in NSCLC is strongly associated with a high sensitivity to EGFR tyrosine kinase inhibitors (TKIs) and is also a criterion used to identify candidates for first-line therapy with these drugs among patients with advanced disease. However, acquired resistance to EGFR TKIs invariably emerges over time due in part to secondary mutations in EGFR or redundant lateral signaling. Molecular imaging, allowing the visualization of cellular processes and their modulation by both conventional anticancer drugs and molecularly targeted agents, may be effectively used in NSCLC patients during treatment with EGFR TKIs. In particular, positron emission tomography with 18F-FDG and 18F-FLT has been performed in both preclinical and clinical settings to distinguish treatment-sensitive from treatment-resistant NSCLCs. Here we provide a short overview of the mechanisms underlying sensitivity and resistance of NSCLCs to EGFR TKIs and then focus on the contribution that molecular imaging can make to the development of tailored therapy in NSCLC patients.
Keywords18F-FDG 18F-FLT EGFR Lung cancer
Non-small cell lung cancer (NSCLC) is the leading cause of cancer-related deaths in the world, showing only limited responsiveness to conventional anticancer agents. The development of molecularly targeted agents and, in particular, of small-molecule inhibitors of the epidermal growth factor receptor (EGFR) has provided alternative strategies for treating this disease. However, in initial clinical trials with first-generation EGFR tyrosine kinase inhibitors (TKIs) such as gefitinib and erlotinib, only 10 % of unselected patients with NSCLC were found to respond to treatment [1, 2, 3, 4]. In the context of efforts to understand the genetic alterations occurring in highly responsive tumors, subsequent molecular studies identified the presence of activating mutations in EGFR as a major determinant underlying effective tumor response of NSCLC to gefitinib and erlotinib [5, 6, 7]. These mutations cause enhanced kinase activity and transformation capability of EGFR, with the result that NSCLC cells become dependent on EGFR signaling for survival . Therefore, when mutant EGFR is blocked by gefitinib or erlotinib, tumor cells undergo apoptosis in addition to growth arrest. Clinical trials in patients with advanced EGFR-mutant NSCLC treated with gefitinib or erlotinib showed that approximately 75 % of patients achieved response and this rate was much higher than that found in unselected patients [9, 10, 11, 12, 13]. These clinical studies also showed that EGFR TKIs were superior to chemotherapy as an initial treatment for EGFR-mutant lung cancer, resulting in a three- to fourfold improvement of progression-free and overall survival rates. Furthermore, it should be noted that clinical benefit from treatment with EGFR TKIs is not limited to patients harboring EGFR mutations but may also be observed in patients with EGFR amplification  and in subgroups of patients with undetectable EGFR mutations .
Since approximately 25 % of patients with EGFR-mutant tumors do not respond to therapy with EGFR TKIs and not all patients with undetectable EGFR mutations are refractory to therapy, it is clinically relevant to distinguish between sensitive and resistant tumors early in the course of treatment. Furthermore, considering that almost 90 % of unselected patients are non-responders to EGFR TKIs and virtually all EGFR-mutant NSCLC patients who initially respond to therapy will subsequently develop resistance to EGFR inhibitors, early detection of resistance to EGFR TKIs may allow the timely adoption of alternative treatment strategies in refractory patients.
Although drug sensitivity and resistance are two sides of the same coin, they are governed by different mechanisms. We here provide a short overview of the mechanisms underlying sensitivity and resistance of NSCLC to EGFR TKIs and then focus on the contribution that molecular imaging can make to the non-invasive identification of responding and refractory NSCLC patients.
Sensitivity of NSCLC to EGFR TKIs
EGFR belongs to a family of receptor tyrosine kinases that also includes HER2, HER3 and HER4. EGFR exists as an inactive monomer composed of an extracellular ligand-binding domain, a transmembrane domain and an intracellular tyrosine kinase domain. Upon binding to ligands such as epidermal growth factor and transforming growth factor-α, the receptor undergoes conformational changes that allow homodimerization or heterodimerization with other members of the same family . Dimerization of EGFR is followed by autophosphorylation of key tyrosine residues in the tyrosine kinase domain, recruitment of several adapter proteins and initiation of the signaling cascade through several pathways including the Ras/Raf/MAPK, PI3K/AKT and signal transducers and activators of transcription (STAT) pathways. These signaling events ultimately control multiple cellular processes including proliferation and survival. EGFR TKIs compete with ATP for binding to the catalytic kinase domain of EGFR thus inhibiting ligand-stimulated receptor autophosphorylation.
The majority of activating mutations in EGFR occur within the tyrosine kinase domain . The most common of these are exon 19 deletions that eliminate four amino acids from the tyrosine kinase domain and an exon 21 missense mutation that substitutes arginine for leucine at position 858 (L858R). These mutations were found in 10 % of Caucasian and 30–40 % of Asian NSCLC patients and are associated with an increased sensitivity to EGFR TKIs. They are more frequent in patients with adenocarcinoma, never smokers, females and individuals of East Asian ethnicity, all clinical characteristics previously reported to be present in good responders to EGFR TKIs .
Exon 19 deletions and L858R substitutions are referred to as “activating mutations” because they cause a ligand-independent activation of EGFR tyrosine kinase activity, as a result of which the receptor continuously transduces signals inside the cell [18, 19]. As a consequence, downstream signaling pathways are persistently activated and drive oncogenesis and tumor progression. However, when EGFR-mutant NSCLCs are exposed to EGFR inhibitors, signaling through these pathways, being under the exclusive control of EGFR, is suppressed. This will result in growth arrest and in the activation of apoptosis through up-regulation of BIM, a pro-apoptotic member of the Bcl-2 family .
The presence of activating mutations in EGFR is currently a criterion used to identify, among NSCLC patients, candidates for first-line therapy with EGFR TKIs.
Primary resistance to EGFR TKIs
Small insertions or duplications in exon 20 are associated with primary resistance to EGFR TKIs and occur in about 5 % of NSCLC cases . Although rare, they are clinically relevant since most patients with tumors harboring exon 20 insertions show tumor progression despite treatment with EGFR TKIs.
Almost 5 % of NSCLCs harbor translocations in the anaplastic lymphoma kinase (ALK) gene which lead to transcription of the fusion protein EML4-ALK which comprises the amino-terminal half of echinoderm microtubule-associated protein-like 4 and the intracellular catalytic domain of ALK [22, 23]. The fusion transcript has transforming ability and ALK rearrangement is currently considered the second oncogenic driver in NSCLC after activating EGFR mutations . ALK translocations generally occur in tumors with wild-type EGFR and KRAS. ALK fusion-positive lung tumors are resistant to treatment with EGFR TKIs but sensitive to ALK inhibitors such as crizotinib . Despite the presence of activating mutations, primary resistance to EGFR TKIs can occur due to the presence of concurrent mutations causing gain or loss of function of downstream mediators such as PI3K or PTEN. Although rare, mutations of the catalytic subunit of PI3K and loss of PTEN are both correlated with decreased sensitivity to EGFR TKIs [26, 27].
Acquired resistance to EGFR TKIs
A second known mechanism of acquired resistance to EGFR TKIs is MET oncogene amplification, which is observed in up to 20 % of EGFR-mutant NSCLCs that become resistant to gefitinib or erlotinib . NSCLC cells with MET amplification are able to maintain activation of the PI3K/AKT pathway through HER3 phosphorylation despite the inhibition of EGFR by gefitinib or erlotinib. MET is a receptor tyrosine kinase also known as the hepatocyte growth factor (HGF)/scatter factor receptor whose aberrant activation and expression occurs in many types of cancer including NSCLC . Binding of HGF to MET causes receptor dimerization and autophosphorylation of tyrosine residues in the kinase domain, which leads to activation of downstream signaling cascades regulating multiple biological activities such as motility, proliferation, survival and morphogenesis. A major role of sustained MET activation in many types of cancer is to promote cell invasiveness and metastatic spread. MET amplification in NSCLC cells is reported to confer dependence on MET signaling and redundant activation of HER3 for growth and survival.
Reversal of resistance to EGFR TKIs
Overcoming primary resistance of NSCLC to EGFR TKIs is challenging since it is due to multiple and often rare genetic alterations. Molecular profiling of lung cancer specimens to assay multiple genetic lesions at the same time  may, therefore, be necessary to identify the primary cause of the resistance. Despite the fact that implementing these technically demanding procedures in routine clinical practice is difficult, ongoing clinical trials are investigating alternative treatment strategies in subgroups of NSCLC patients. For instance ALK-positive NSCLC patients have been enrolled in several clinical trials testing the activity of crizotinib, a potent ALK and MET inhibitor . Preliminary data showed that treatment with crizotinib results in high response rates and improved progression-free survival as compared to standard chemotherapy .
Considerable efforts are currently being made to overcome acquired resistance to EGFR TKIs. NSCLCs that become resistant to gefitinib or erlotinib due to secondary T790M mutation remain dependent on EGFR signaling for growth and survival. Therefore, the development of drugs capable of inhibiting EGFR T790M may constitute an alternative and effective therapeutic strategy in refractory patients. Second- and third-generation EGFR inhibitors were indeed developed in an attempt to overcome T790M-mediated resistance . These compounds, like gefitinib and erlotinib, compete with ATP for binding to the kinase domain of EGFR but unlike first-generation agents their binding to the receptor is covalent and irreversible. They were reported to inhibit autophosphorylation of EGFR in the presence of the T790M mutation and showed activity in gefitinib-resistant preclinical models of NSCLC bearing EGFR T790M [32, 33]. However, their clinical efficacy remains to be established in currently ongoing clinical trials. A major concern of early clinical studies has been toxicity, since these compounds can irreversibly block wild-type EGFR too. While most of the second-generation EGFR TKIs recognize receptors bearing activating mutations with a higher affinity than for the double-mutant EGFR, a third-generation EGFR TKI, namely WZ4002, selectively targets T790M-harboring receptors that can be effectively inhibited at doses that will not affect wild-type EGFR thus limiting potential toxicity .
In order to overcome MET-mediated resistance to EGFR TKIs, concomitant inhibition of both EGFR and MET is required. Multiple agents have been developed to target MET signaling and they are currently under clinical investigation in different types of solid tumors . Protein-based antagonists of HGF and MET disrupt the binding of HGF to MET and function outside the cells. Conversely, small kinase inhibitors function inside the cell and prevent receptor transactivation and downstream signaling. They constitute the largest class of MET inhibitors currently available and most of them compete with ATP for binding to the kinase domain of MET. Some MET inhibitors are selective for the receptor whereas others have multiple targets. Preclinical studies showed antitumor activity and antiangiogenic activity of MET TKIs in several models and many of these compounds are now in various stages of clinical development.
Molecular imaging with 18F-FDG and 18F-FLT
Molecular imaging, allowing the visualization of cellular processes and their modulation by both conventional anticancer drugs and molecularly targeted agents, may be effectively used in NSCLC patients during treatment with EGFR TKIs. In particular, positron emission tomography (PET) with 18F-FDG and 18F-FLT has been employed in both preclinical and clinical studies to test whether imaging studies performed with these tracers were able to distinguish sensitive from resistant NSCLCs.
The rationale for using 18F-FLT rests on the fact that all signaling pathways downstream of EGFR culminate in proliferation and when they are blocked by targeted therapy, proliferation is inhibited. Given that 18F-FLT uptake has been shown to be a sensitive and reliable marker of proliferation in different tumor types including NSCLC [35, 36, 37], changes in tracer uptake in response to EGFR TKI treatment may reflect modulation of proliferation.
The uptake of 18F-FDG has been reported to be a reliable predictor of clinical outcome in several types of solid and lymphoproliferative tumors [38, 39, 40, 41]. The rationale for using 18F-FDG to test inhibition of EGFR pathways is less direct than that supporting the use of 18F-FLT, but nevertheless robust. In fact, one of the major determinants of the glycolytic phenotype of cancer cells is the PI3K/AKT pathway which is persistently activated by aberrant EGFR signaling. Furthermore, downstream effector AKT phosphorylates key glycolytic enzymes such as hexokinase and phosphofructokinase 2 and increases the expression and membrane translocation of glucose transporters . Therefore, EGFR TKIs, by inhibiting pathways downstream of EGFR, including PI3K/AKT, promptly downregulate glycolysis and uptake of 18F-FDG. In addition, as a late effect, EGFR TKIs cause a reduction of cell viability and glucose uptake by inducing apoptosis in tumor cells.
In this section we will focus on the use of these tracers to identify sensitivity and resistance of NSCLC to EGFR TKIs through monitoring of treatment with these drugs.
In gefitinib-sensitive NSCLC cells, EGFR inhibition resulted in a rapid reduction in 18F-FDG uptake that correlated with AKT inhibition and preceded any measurable changes in S phase fraction, thymidine uptake, and annexin V binding . No significant change in 18F-FDG uptake was observed in gefitinib-resistant NSCLC cells, regardless of treatment time or dose. Similarly, 18F-FDG uptake decreased by at least 40 % in mice bearing sensitive tumors after only 2 days of treatment, at which time there was no measurable change in tumor size. By contrast no significant decrease in 18F-FDG uptake was observed in mice bearing resistant tumors.
Sunaga et al.  evaluated five patients with advanced NSCLC and known EGFR mutational status. They underwent 18F-FDG PET before, 2 days after and 4 weeks after gefitinib treatment and tumor response was evaluated using the Response Evaluation Criteria In Solid Tumors (RECIST) after 4 weeks. In patients with partial response or stable disease, 18F-FDG uptake decreased by 61 ± 18 and 59 ± 12 %, respectively, at 2 days and by 26 ± 6 and 43 ± 10 % at 4 weeks after the start of therapy. By contrast, increased 18F-FDG uptake was observed in a patient with progression both on the early (153 ± 21 %) and the late scan (232 ± 73 %).
In a multicenter study, previously untreated patients with operable NSCLC received neoadjuvant treatment with erlotinib and underwent 18F-FDG PET/CT at baseline and 7 days after the initiation of treatment . The European Organisation for Research and Treatment of Cancer (EORTC) criteria were used to assess metabolic tumor response: six patients showed a partial response, 16 patients had stable disease, and one patient had progressive disease. Pathologic response was determined in surgically resected tumors and the median percentage of necrosis was 70 % in patients showing more than 25 % reduction in 18F-FDG uptake after 1 week of treatment, whereas it was 40 % in the metabolic non-responders (stable disease and progression). Interestingly, of ten patients with unchanged or increased 18F-FDG uptake after 1 week of treatment, only one patient showed a pathologic response with more than 50 % necrosis in tumor specimen, indicating that persistently high 18F-FDG uptake after therapy is consistently associated with impaired tumor response.
Sohn et al.  evaluated 28 patients with recurrent adenocarcinoma of the lung before and 7 days after the start of gefitinib treatment with 18F-FLT PET; tumor response was subsequently evaluated by chest CT scan at 6 weeks of therapy. These authors found that percent changes in 18F-FLT uptake at 7 days were significantly different in responders (−36.0 ± 15.4 %) compared with non-responders (10.1 ± 19.5 %), whereas the pretreatment maximum standardized uptake value (SUVmax) of the tumors did not differ in the two groups of patients. Furthermore, the time to progression was significantly longer in 18F-FLT PET responders versus non-responders.
In a prospective trial, conducted with the aim of identifying predictors of non-progression following erlotinib treatment, 34 unselected patients with untreated advanced NSCLC underwent 18F-FDG PET and 18F-FLT PET . EGFR mutational status was determined in 28 of the 34 patients. Changes in 18F-FDG and 18F-FLT uptake after one and 6 weeks of erlotinib treatment were compared with non-progression measured by CT at 6 weeks. Four patients had a partial response (PR), seven stable disease (SD) and 23 progression, according to RECIST. A reduction of at least 30 % in 18F-FDG uptake after 1 week of therapy was observed in eight patients and found to predict non-progression (PR + SD) after 6 weeks of therapy (p = 0.02), whereas early 18F-FLT response (≥30 % reduction) was found in six patients and was not predictive of non-progression (p = 0.39). Furthermore, patients with early 18F-FDG response had significantly longer progression-free survival (p = 0.002) and overall survival (p = 0.04), whereas early 18F-FLT response predicted significantly longer progression-free survival (p = 0.04) but not overall survival. Activating EGFR mutations were found in four patients, three of whom had PR and one SD. These patients showed a significant reduction in early 18F-FDG uptake, whereas 18F-FLT uptake was reduced in three cases. Interestingly, almost half of the patients with an early 18F-FDG response did not have detectable EGFR mutations but nevertheless had prolonged progression-free survival, indicating that 18F-FDG PET can identify, also, a subgroup of patients that may benefit from erlotinib treatment independently of EGFR mutational status. Imaging data from the same trial were analyzed using different methods to define SUV and volume of interest . Patients with metabolic response on early 18F-FDG PET and 18F-FLT PET had a significantly prolonged progression-free interval regardless of the method used for SUV calculation. Furthermore, metabolically active volume measured either on early 18F-FLT scan or on late 18F-FDG scan was strongly associated with progression-free survival. In a retrospective analysis of data from the same study, absolute early and late residual 18F-FDG uptake, measured with different quantitative parameters, was also associated with non-progression at 6 weeks . By contrast, early and late residual 18F-FLT uptake was not associated with short-term outcome. Furthermore, low residual 18F-FDG and 18F-FLT uptake early or late in treatment was associated with improved progression-free survival.
In a multicenter trial 18F-FDG PET and 18F-FLT PET responses were evaluated in second/third line NSCLC patients treated with erlotinib . Baseline PET scans with both tracers were performed on separate days, and were repeated at day 14 and day 56 after the start of treatment in 51 patients. Tumor response was determined by CT performed at day 56 and four patients (8 %) showed partial response according to RECIST. PET partial metabolic response (PMR) was defined using EORTC criteria as a mean decrease in SUVmax (in ≤5 lesions/patient) of at least 15 %. At day 14 and day 56, PMR with 18F-FDG was found in 26 % and 16 % of patients, respectively, whereas PMR with 18F-FLT was found in 18 and 16 % of patients. Of the four patients with CT partial response, all showed PMR on both early and late 18F-FDG scans, whereas three showed PMR on early 18F-FLT scan and two on late 18F-FLT scan. The percentage of patients showing PMR on early 18F-FDG and 18F-FLT scans was higher than that found on late scanning with the two tracers. PMR at day 14 and at day 56, determined with 18F-FDG and 18F-FLT, was significantly associated with improved progression-free survival (p ≤ 0.02), whereas only 18F-FDG PMR at day 14 was significantly associated with improved overall survival (p = 0.03) even in the absence of subsequent RECIST response. Tumor tissues for mutational analysis were available in 35 patients and four had activating EGFR mutations, whereas seven had KRAS mutations. Three out of four EGFR-mutant tumors showed PMR on early 18F-FDG scan whereas EGFR wild-type tumors showed PMR only in six out of 31 patients. Early reduction of 18F-FDG uptake in EGFR-mutant tumors was higher (median 55 %) than that found in metabolic responding EGFR wild-type tumors (median 19.9 %). Tumors with KRAS mutations showed 18F-FDG PMR in one case at day 14 and in three patients at day 56.
The results of the 18F-FDG PET studies performed in this multicenter trial and in a second multicenter study were then grouped and analyzed to assess the predictive value of 18F-FDG PET, clinical parameters and EGFR mutational status for survival duration by fitting accelerated failure time models . Imaging data obtained at baseline and after 2 weeks of treatment with erlotinib were collected from a total of 125 NSCLC patients. The variables included in the model were performance status, sum of SUVmax of target lesions or total number of target lesions at baseline, percentage change in SUVmax at 2 weeks, appearance of new lesions at 2 weeks, and EGFR mutational status. New lesions on PET at 2 weeks, EGFR mutational status, performance status and baseline metabolic tumor burden were found to be independent and significant predictors of overall survival. Furthermore, a large (at least 35 %) reduction in SUVmax was strongly linked to EGFR mutational status and was predictive of survival only when EGFR mutational status was not considered.
In a prospective study 22 unselected patients with advanced NSCLC were evaluated by 18F-FDG PET/CT at baseline and after 2 weeks of therapy with erlotinib . On the basis of PERCIST, metabolic response was defined as complete, partial (≥30 % reduction in 18F-FDG uptake), progressive metabolic disease (≥30 % increase in 18F-FDG uptake in a measurable target lesion or new lesions) or stable disease (not complete or partial metabolic response, no progression). Patients with progressive metabolic disease on early follow-up PET showed a significantly shorter time to progression (47 vs. 119 days, p < 0.001) and overall survival (87 vs. 828 days, p = 0.01) than patients classified as having stable metabolic disease or partial or complete metabolic response.
In another study 20 patients with lung adenocarcinoma were evaluated with 18F-FDG PET/CT before and 2 days after the start of gefitinib treatment . Metabolic response was evaluated using the European Organization for Research and Treatment of Cancer (EORTC) criteria and compared with morphological response evaluated by CT scan at 1 month post-treatment. After 2 days of gefitinib treatment, ten patients showed partial metabolic response, eight had stable metabolic disease, and two patients had metabolic progression. The percentage change in SUVmax at 2 days was significantly correlated with morphovolumetric reduction of tumors on CT scan at 1 month. EGFR mutational status was evaluated in 15 patients and of 12 patients with activating mutations, eight showed a metabolic response at 2 days and six showed a morphovolumetric response at 1 month. No metabolic or morphological response was observed in three patients with wild-type EGFR.
In a recent study, Scheffler et al.  reported the case of a patient with EGFR-mutant NSCLC treated sequentially with erlotinib and with an irreversible EGFR TKI and monitored by serial 18F-FLT PET studies. After an initial response to erlotinib that was associated with a reduction in 18F-FLT uptake in tumor lesions and confirmed by CT, the patient showed clinical progression. 18F-FLT PET showed an increase in tracer uptake in tumor lesions, suggesting the development of resistance. The patient was then treated with afatinib and showed an improvement of clinical symptoms and a reduction in 18F-FLT uptake in targeted lesions. Unfortunately the response to afatinib was not durable and the treatment was discontinued.
Molecular imaging with other tracers
Besides 18F-FDG and 18F-FLT several radiolabeled agents have been developed for the non-invasive detection of EGFR expression, including antibodies, affibodies and small organic reversible and irreversible inhibitors . An extensive review of these tracers is beyond the scope of the present article and we here limit ourselves to mentioning a few studies with tracers that proved able to distinguish EGFR TKI-sensitive from EGFR TKI-resistant tumors. Yeh et al.  developed 18F-PEG6-IPQA, a radiotracer with increased selectivity and irreversible binding to the active mutant L858R EGFR kinase. PET studies in animal models showed that 18F-PEG6-IPQA is able to distinguish NSCLC xenografts bearing mutant L858R EGFR from those expressing wild-type EGFR. Furthermore, the expression of double-mutant L858R/T790M EGFR prevented the binding of 18F-PEG6-IPQA to the receptor both in vitro and in vivo.
The uptake and tumor kinetics of 11C-erlotinib were evaluated in ten patients with NSCLC, five with an EGFR exon 19 deletion and five without, using pharmacokinetic modeling and arterial blood sampling . Patients with activating EGFR mutations showed higher 11C-erlotinib uptake than those without mutant EGFR.
Twenty-one patients with advanced NSCLC were studied with 11C-PD153035 and PET/CT at baseline, at 1–2 weeks and at 6 weeks after the start of therapy with erlotinib . Uptake of 11C-PD153035 on the baseline scan significantly correlated with progression-free and overall survival. Patients with a higher SUVmax survived longer than those with a lower SUVmax. Uptake of 11C-PD153035 on follow-up scans was less predictive of outcome.
In conclusion, many studies indicate that 18F-FDG may identify, early in the course of treatment, NSCLC patients who may or may not benefit from treatment with EGFR TKIs. Although 18F-FLT has been shown to detect effective EGFR inhibition and reversal of EGFR TKI resistance in animal models, it was less efficient than 18F-FDG in predicting clinical outcome in NSCLC patients undergoing EGFR TKI treatment. There may be several reasons for this, including the lower tumor uptake of 18F-FLT, as compared to 18F-FDG and the use of metabolic tumor response criteria that were designed essentially for 18F-FDG studies. Furthermore, early reduction in 18F-FLT uptake in response to EGFR TKIs indicates growth arrest of tumor cells that is not necessarily associated with a concomitant induction of apoptosis. Conversely, the reduction in 18F-FDG uptake after treatment may reflect both inhibition of EGFR signaling and reduced cell viability. Therefore, 18F-FDG should be preferred to 18F-FLT for monitoring therapy with EGFR TKIs in NSCLC patients, even in those with unknown EGFR mutational status.
Due to the low rate of tumor response to EGFR TKIs in an unselected population of NSCLC patients and to the fact that EGFR-mutant NSCLC patients may also become refractory to treatment, the early detection of resistance is as important as the early identification of sensitivity. The existence of different therapeutic options and the availability of compounds that can be used to overcome acquired resistance to EGFR TKIs certainly open the way for designing rational strategies for the treatment of refractory patients. Although further clinical studies are needed, it is conceivable that 18F-FLT may be preferable to 18F-FDG for detecting reversal of EGFR TKI resistance because changes in 18F-FDG uptake in response to reversal agents may be uncoupled from changes in proliferation.
Although genetic profiling and mutational analysis are not fully integrated into daily oncology practice, it is to be hoped that newly diagnosed patients will be assigned to specific first-line therapy on the basis of molecular alterations found in tumor samples and then eventually monitored by functional imaging. NSCLC patients who initially respond to EGFR TKIs and then show disease progression may potentially benefit from treatment with irreversible EGFR TKIs or MET inhibitors. In such cases, the mechanism of resistance in each refractory patient should be identified. However, the biological detection of mechanisms of resistance in tumor samples is challenging for several reasons. Repeated biopsies are not usually performed in NSCLC patients whose tumors develop resistance. The methods currently available for the biological detection of T790M mutation and MET amplification are challenging and not sensitive enough. Furthermore, the two mechanisms of resistance are not mutually exclusive and may coexist in the same tumor or at different tumor sites. In this context, molecular imaging may provide tools for identifying refractory patients and for monitoring the effects of agents capable of overcoming EGFR TKI resistance in selected patients.
This work was partly supported by Ministry of University and Research, MERIT—MEdical Research in ITaly (project No. RBNE08YFN3_008) and AIRC, Associazione Italiana per la Ricerca sul Cancro (project no.11756).
Conflict of interest
F. Iommelli, V. De Rosa, R. Fonti, S. Del Vecchio declare no conflict of interest.
Human and animal studies
This article does not contain any new studies with human or animal subjects performed by any of the authors.
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