New targeted molecular therapies for cancer: radiological response in intrathoracic malignancies and cardiopulmonary toxicity: what the radiologist needs to know
© Souza et al.; licensee BioMed Central Ltd. 2014
Received: 13 March 2014
Accepted: 13 March 2014
Published: 23 July 2014
The emergence of new novel therapeutic agents which directly target molecules that are uniquely or abnormally expressed in cancer cells (molecular targeted therapy, MTT) has changed dramatically the treatment of cancer in recent years. The clinical benefit associated with these agents is typically limited to a subset of treated patients, who in many cases are defined by a specific genomic mutations and expression lesion within their tumor cells. All these new therapy modalities represent new challenges to radiologists as their mechanism of action and side effect profiles differ from conventional chemotherapy agents. In this article we will discuss radiological patterns of response to molecular targeted therapies MTT in lung cancer, typical and atypical radiological responses of targeted molecular therapy for other intra thoracic malignancies, cardiopulmonary toxicity and other side effects of molecular targeted therapy MTT in the thorax.
KeywordsMolecular targeted therapies Tumor response Computed tomography
The emergence of novel therapeutic agents that directly target molecules that are uniquely or abnormally expressed in cancer cells (molecular targeted therapy, MTT) has changed dramatically the treatment of cancer in recent years. The clinical benefit associated with these agents is typically limited to a subset of treated patients, who in many cases are defined by specific genomic mutations and expression within their tumor cells. All these new therapy modalities represent new challenges to radiologists as their mechanism of action and side effect profiles differ from conventional chemotherapy agents. In this article we will discuss radiological patterns of response to MTT in lung cancer, typical and atypical radiological responses of targeted molecular therapy for other intrathoracic malignancies, cardiopulmonary toxicity and other side effects of MTT in the thorax.
New concepts in molecular targeted therapy
The role of MTT is to reduce or inhibit proliferative activity in cancer cells and block intracellular signaling pathways, blocking specific enzymes responsible for cancer growth and proliferation. Among these important MTT agents approved by the US Food and Drug Administration (FDA) are imatinib mesylate (Gleevec®), approved to treat gastrointestinal stromal tumor, trastuzumab (Herceptin®), approved to treat certain types of breast cancer as well as some types of gastric or gastroesophageal junction adenocarcinomas, and everolimus (Afinitor®), approved to treat patients with advanced kidney cancer whose disease has progressed after treatment with other therapies. In the highly vascular metastatic tumors hepatocellular carcinoma (HCC) and renal cell carcinoma (RCC), successful response to anti-angiogenic therapy has been associated with the use of sunitinib (Sutent®) and sorafenib (Nexavar®), respectively. The response is assessed by decreased tumor size, decreased tumor attenuation, and tumor necrosis on the post-therapy contrast-enhanced computed tomography (CT) studies.
Molecular targeted therapy for lung cancer
First-line chemotherapy for lung cancer often includes a platinum-based drug (cisplatin or carboplatin) in combination with another FDA-approved chemotherapy drug (paclitaxel, docetaxel, etoposide, gemcitabine, pemetrexed). However, in a subset of patients with non-small-cell-lung cancer (NSCLC), there is overexpression of epidermal growth factor receptor (EGFR). Stimulation of the EGFR pathway leads to a series of intracellular events culminating in increased mitotic and growth potential, increased ability to metastasize, and increased angiogenesis (new blood vessel formation) in the cancer cells.
Many factors that correlate with favorable response occur in patients with particular clinical characteristics, such as a higher frequency of EGFR mutations (which themselves appear to be closely associated with higher likelihood of response to EGFR inhibitors) among Asians vs. non-Asians, women vs. men, never-smokers vs. current or prior smokers, and/or patients with adenocarcinomas vs. squamous histology tumors. New developments in the management of NSCLC include more aggressive surgical techniques, the use of neoadjuvant chemoradiation prior to surgery and use of molecular targeted therapeutic agents[4–7]. The MTT agents currently FDA approved for lung cancer are gefitinib and erlotinib. These MTT agents have shown efficacy in first and second-line treatment regimens as monotherapy or in combination with conventional chemotherapy agents.
Radiological assessment of response to treatment in cancer
Radiological assessment of response to treatment in lung cancer can be further divided into typical and atypical patterns of response. Typical patterns of response include: A) decrease in tumor size, B) decrease in vascularity (e.g. anti-angiogenic agent effect), C) presence of cavitary changes within the mass, and D) decrease in metabolism when F18fluorodeoxyglucose (FDG)- positron emission tomography (PET)/CT is used to evaluate treatment response. Atypical patterns of response include: A) increase in the size of a mass with decreased tracer uptake, B) presence of intralesional and/or perilesional hemorrhage with stable or increased size of the mass.
Typical response patterns
Tumor response criteria — WHO, RECIST 1.0 and RECIST 1.1 and classification of tumor assessment
No particular number of lesions specified
Requires 10 targets per five organs when measuring the tumor burden
Requires only five targets (two per organ).
Bi dimensionally measurable lesion; no stipulation of minimal size of the lesion
Measures the long axis of lymph nodes as for other lesions
Measures the short axis of lymph nodes and long axis for other lesions
50% decrease in target lesions, without a 25% increase in any one target lesion; confirmed at 4 wk
Defines progression as a 20% increase in sum
A 20% increase and at least 5 mm absolute increase.
States that disease progression for non-measurable disease “must be unequivocal”
Expands that definition to convey an impact on the overall burden of disease.
States that confirmation is required but in new version only if response is primary endpoint
Includes a new section that incorporates a comment on FDG PET interpretation
Decrease in tumor size
Histopathology is often used as the reference standard for assessing the response to primary chemotherapy in lung cancer. However, there is no single definition of a histopathologic response, and response criteria vary among studies. Most commonly, a pathologic complete response is defined by the absence of residual invasive tumor[8, 9]. Other response classifications include changes in tumor cellularity and the presence of regressive changes in residual tumor tissue (Figures 1 and2).
In radiology, is generally accepted that a decrease in tumor size correlates with treatment effect; as a result, imaging was adopted for lesion measurement in the World Health Organization (WHO) criteria in 1979. However, because of some limitations of the WHO criteria, the Response Evaluation Criteria in Solid Tumors (RECIST) was introduced in 2000. Subsequently in October 2008 at the 20th EORTC-NCI-AACR Symposium on Molecular Targets and Cancer Therapeutics (Geneva, October 2008) a New Response Evaluation Criteria in Solid Tumors: Revised RECIST Guidelines (version 1.1) was adopted [Table 1].
Both WHO and RECIST make use of anatomic imaging, predominantly CT, to obtain measurements of reference tumor lesions before and after treatment for response assessment and follow-up. However, functional imaging such as dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI), perfusion CT and PET imaging have been found to be more useful than morphological changes in the assessment of tumor response. Goudarzi et al. in their retrospective analysis of 630 patients with biopsy proven lung cancer demonstrated that patients with pure bronchoalveolar carcinoma (BAC) exhibit a lower FDG uptake and lower tumor attenuation compared with those with adenocarcinoma.
Decrease in tumor vascularity
Tumor vascularity can be assessed by measuring blood flow kinetics using dynamic contrast enhancement either with dual energy CT or perfusional MRI. Subjective evaluation using changes in tumor attenuation and tumor vascularization, in addition to changes in tumor size, is considered a good way to evaluate response by computed tomography (Figure 3). Measuring Hounsfield units can serve as a surrogate of tumor vascularity as tumors decrease in density due to necrosis as they respond to therapy. Early clinical trials have indicated, however, that conventional imaging strategies that use tumor size or other structural criteria may not be suitable for monitoring the effects of anti-angiogenesis drugs. An effective imaging strategy for assessing tumor vascularity would also be of value to monitor “anti-angiogenesis” drugs that aim to halt cancer progression by suppressing the tumor blood supply. Perfusion CT is potentially well suited to monitoring tumor response to anti-angiogenesis agents. Dynamic enhanced CT techniques using quantitative enhancement parameters may provide a tool to evaluate the heterogeneity of tumor vascularity and angiogenesis and CT measurements of perfusion have been shown to be reproducible and have been validated against a range of reference methods[15–25].
Cavitation has been commonly associated with squamous subtypes and can be seen occasionally in adenocarcinoma. Bevacizumab (Avastin) is a humanized monoclonal antibody against vascular endothelial growth factor (VEGF) that has been associated with cavitation in primary and metastatic lung cancer. Trials of VEGF inhibitors have shown that responding lesions frequently exhibit marked central cavitation. It has been postulated that cavitation occurs through central necrosis of lesions after inhibition of angiogenesis. Marom et al described a retrospective single-institution experience of 124 patients treated with various angiogenesis inhibitors in which 14% of patients developed cavitation. A potential link between clinically relevant pulmonary hemorrhage and cavitation has been raised by studies of bevacizumab warrants further investigation, however (Figures 4 and5).
Frequently, there is a discrepancy between the anatomic appearance and the metabolic activity of the tumor during evaluation of response to anti-angiogenic drugs. Changes in tumor size do not necessarily correlate with changes in tumor viability and outcome. Therefore, it might be more appropriate to assess tumor response by metabolic activity, which can be measured by FDG uptake on PET or [18 F] FDG PET/CT. Decrease in FDG uptake after treatment may prove to be a better indicator of a favorable response rather than change in tumor size (Figure 6).
Hicks et al evaluated aggregated data on the use of 18 F-FDG PET and PET/CT in therapeutic response assessment in NSCLC and the data strongly indicated that a reduction in tissue 18 F-FDG uptake, measured at whatever time after treatment, is more likely to be associated with both a pathologic response and improved survival than when there was no evidence of decreased uptake by the tissue.
Atypical response patterns
Increase in the size of a mass with decreased metabolism
The overall increase in size and decrease in tracer uptake in a mass is a phenomenon that has been extensively described in gastrointestinal stromal tumor treated with imatinib mesylate (Gleevec), reflecting therapy response. In our series we also observed similar findings in patients with lung cancer. Once the patient is treated, the tumor usually decreases in size upon response. In some responding tumors, the tumor size increases as a result of intratumoral and perilesional hemorrhage, necrosis, or myxoid degeneration. The attenuation of the tumor decreases significantly, as the tumor becomes homogeneous.
Presence of intralesional and/or perilesional hemorrhage with stable or increased size of the mass.
Challenges and future directions
The discovery of the correlation of EGFR mutations and response to EGFR TKI therapy has demonstrated that molecular typing of tumors to guide therapy selection for lung cancer is possible. Prospective trials will need to validate the feasibility and efficacy of selecting therapy based on tumor molecular profiles. Also, numerous molecularly targeted agents are in clinical development, and future studies will need to identify molecular and clinical tools to guide the use of these agents, particularly in combination with current therapies such as surgery, radiation, cytotoxic chemotherapy, and other targeted therapies.
The role of computed tomography-guided core-needle biopsy in demonstrating epidermal growth factor receptor mutations in patients with non-small-cell lung cancer
The use of surgical specimens to identify EGFR mutations obtained is invasive, expensive, and increases morbidity and mortality. Alternatively, prior reports on EGFR mutation analysis in nonsurgical materials such as biopsy specimens, pleural effusions, and serum have noted problems of contamination by non-target normal cells within the samples[29–32]. CT-guided coaxial core-needle biopsy of the lung has been proven to have high diagnostic accuracy, sensitivity, specificity, and negative predictive values in advanced NSCLC and enables the acquisition of sufficient tissue for EGFR gene mutation analysis.
Pulmonary toxicity from novel antineoplastic agents
Antineoplastic agent-induced pulmonary toxicity is complex and a diagnosis of exclusion. Similarly, the pathogenesis of antineoplastic agent-induced lung injury is poorly understood and several mechanisms have been suggested, including direct injury to pneumocytes (chemical alveolitis) or the alveolar capillary endothelium and the subsequent release of cytokines and recruitment of inflammatory cells[35–37].
Other causes of respiratory failure, including pneumonia, cardiogenic pulmonary edema, and diffuse alveolar hemorrhage, should be excluded. These conditions are not easily differentiated based on clinical presentation and radiographic findings. Furthermore, as patients usually receive multiple antineoplastic agents, it is usually difficult to identify the culprit agent.
The clinical and radiologic manifestations of these drugs generally reflect the underlying histopathologic processes and include diffuse alveolar damage (DAD), interstitial pneumonitis, cryptogenic organizing pneumonia (COP), eosinophilic pneumonia, obliterative bronchiolitis, pulmonary hemorrhage, edema, hypertension, or veno-occlusive disease. Intra-thoracic and extra pulmonary side effects of these drugs include skin thickening, pleural effusions and thromboembolism.
Diffuse alveolar damage
DAD is a common manifestation of drug-induced lung injury that results from necrosis of type II pneumocytes and alveolar endothelial cells. DAD is divided into an acute exudative phase and a late reparative or proliferative phase.
Interstitial pneumonitis is characterized by areas of scattered expansion of the interstitium by inflammatory cells, mild interstitial fibrosis, and reactive hyperplastic type II pneumocytes. New targeted molecular therapies for lung cancer that can cause interstitial pneumonitis include: erlotinib, trastuzumab, temsirolimus, everolimus and gefitinib.
Erlotinib (Tarceva) is indicated for the treatment of patients with locally advanced or metastatic NSCLC. Vahid and Esmaili described two cases of erlotinib-induced pneumonitis that resulted in respiratory failure. The patients presented 4 to 6 days after the initiation of erlotinib therapy with fever, cough, and hypoxemia.
Trastuzumab is a humanized monoclonal antibody that selectively binds to the human EGFR (HER)-2 protein, indicated for the treatment of metastatic breast cancers with over expression of HER-2 protein. The incidence of trastuzumab-induced pneumonitis is 0.4 to 0.6%. Trastuzumab-induced pneumonitis may present with rapidly progressive pulmonary infiltrates and respiratory failure. Infusion-related symptoms, including hypotension, angioedema, bronchospasm, dyspnea, fever, chills, and urticaria, have been reported to occur in about 15% of patients. Severe episodes of hypotension, bronchospasm, and hypoxemia were also observed[45–49].
Temsirolimus is a rapamycin analog that is active against renal cell carcinoma, endometrial carcinoma, breast cancer, glioblastoma multiforme, and gastrointestinal neuroendocrine tumors. Interstitial pneumonitis is a non–dose-dependent complication of temsirolimus. Interstitial pneumonitis has been reported in 1 to 36% of patients and the onset of pneumonitis usually takes place within 16 weeks (range 2 to 16 weeks) after temsirolimus treatment[50, 51].
Everolimus is an mTOR inhibitor that has been used as an investigational antineoplastic agent (e.g. for the treatment of sarcoma or renal cell cancer). Although clinical data in patients with malignancy are sparse, there have been previous reports of interstitial pneumonitis with everolimus in heart transplant recipients.
Rituximab was first approved for the treatment of low-grade follicular lymphoma, and is now also approved for high-grade lymphomas, while it has also been used in other hematological diseases. The mechanism of action targets CD20+ B lymphocytes. Although rituximab-induced lung injury is rare, it has been well documented[53–56].
Interstitial pneumonitis has been reported with rituximab monotherapy, thus proving the potential of this agent for lung injury. In all cases lung toxicity resolved after steroid treatment, with no late sequelae. Nevertheless, it should be mentioned that concomitant administration of steroids may not prevent the occurrence of pneumonitis.
Cryptogenic organizing pneumonia
COP is a nonspecific histopathologic pattern of lung injury characterized by the proliferation of immature fibroblastic plugs within the respiratory bronchioles, alveolar ducts, and adjacent alveolar spaces. Affected patients present with progressive dyspnea, dry cough, and fever.
Trastuzumab treatment has been reported to be a causative agent of COP. Infusion-related symptoms, including hypotension, angioedema, bronchospasm, dyspnea, fever, chills, and urticaria, have been reported to occur in about 15% of patients.
Pulmonary edema and fluid retention
The pathogenesis of antineoplastic agent-induced pulmonary edema is poorly understood and has been suggested to be due to direct injury to pneumocytes (chemical alveolitis) or the alveolar capillary endothelium and the subsequent release of cytokines, which induce pulmonary edema due to leaky capillaries. Drugs that may lead to increased permeability and subsequent edema include imatinib, dasatinib and rituximab.
Imatinib is a potent tyrosine kinase inhibitor, which is mainly used in the treatment of chronic myelogenous leukemia (CML) and is also effective in patients with gastrointestinal stromal tumor (GIST). Although most cases of imatinib-induced pulmonary adverse events have been reported in patients with CML, there have been cases of dyspnea during imatinib therapy, most often related to fluid retention and pulmonary edema.
Pulmonary complications are uncommon and are usually associated with a fluid retention syndrome. The manifestations from the lungs are pleural effusions and pulmonary edema[67, 68] seen in patients treated with imatinib and dasatinib. It seems that these drugs are associated with rare but well documented lung toxicity and this should be taken into consideration in the differential diagnosis of otherwise unexplained pleural effusions.
VEGF antagonism could cause decreased matrix deposition in the supporting layers of vessels; therefore, the final picture of anti-VEGF therapy might consist of increased frequency of thrombotic events, as a result of tissue factor activation secondary to the exposure of the subendothelial collagen.
More recently, two small molecules blocking the VEGF receptor (VEGFR) have shown promising results in the treatment of renal cell carcinoma and gastrointestinal stromal tumors (GISTs): sorafenib (Nexavar; Bayer Pharmaceuticals Corporation, West Haven, CT), approved by the FDA in 2005 as a second-line treatment for advanced renal cell carcinoma after cytokine failure, and sunitinib (Sutent; Pfizer, Inc., New York), approved in 2006 for patients with GIST previously treated with imatinib and for advanced renal cell carcinoma as a first-line treatment. Both of these agents have been strongly associated with thromboembolic events.
New imaging modalities are available to assess treatment response. PET have the ability to assess tissue viability more precisely than CT and detect metastatic lesions that would have been missed on conventional imaging. Other functional imaging techniques, such as dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) and perfusion CT imaging, have been found to be more useful than morphological changes in the assessment of tumor response, although not frequently used in most institutions.
With the discovery and introduction of new MTT agents, the treatment for a wide variety of cancers has been revolutionized. As these treatments become increasingly recognized as therapeutic options, physicians who interpret imaging studies should be aware of different patterns of response and possible side effects of these new MTT agents.
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