© 2003 AlphaMed Press Signal Events: Cell Signal Transduction and Its Inhibition in CancerInstitute for Drug Development, Cancer Therapy and Research Center, San Antonio, Texas, USA Correspondence: Eric K. Rowinsky, M.D., Institute for Drug Development, Cancer Therapy and Research Center, 7979 Wurzbach Road, 4th Floor Zeller Building, San Antonio, Texas 78229, USA. Telephone: 210-616-5945; Fax: 210-616-5865; e-mail: erowinsk{at}saci.org
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Signal transduction refers to communication processes used by regulatory molecules to mediate the essential cell processes of growth, differentiation, and survival. Signal transduction elements interact through complex biochemically related networks. Aberrations in signal transduction elements can lead to increased proliferative potential, sustained angiogenesis, tissue invasion and metastasis, and apoptosis inhibition. Most human neoplasms have aberrant signal transduction elements. Several compounds that target aberrant signal transduction elements, such as those in the ErbB family of tyrosine kinase receptors and mammalian target of rapamycin, are in development. To date, commercially available signal-transduction-targeting compounds include trastuzumab, a monoclonal antibody against the ErbB-2 receptor for the treatment of metastatic breast cancer overexpressing the ErbB-2 (HER-2) receptor, and gefitinib, an inhibitor of the ErbB-1 receptor tyrosine kinase that recently received regulatory approval for the treatment of patients with non-small cell lung cancer. In contrast to traditional cytotoxic treatments, although signal transduction inhibitors are capable of inducing tumor regression, particularly in malignancies that are principally driven by specific target aberrations, preclinical and early clinical investigations suggest that their predominant beneficial effects are growth inhibitory in nature; therefore, new clinical trial designs and evaluation end points may be required to ultimately assess their value. Prospective profiling of patients and tumors to determine treatment response is also essential to the success of these clinical trials. However, responsiveness to these novel therapies is dependent on a multitude of factors that ultimately determine the robustness and quality of the downstream response. Key Words. Signal transduction • Targeted cancer therapy • mTOR • ErbB family • Rapamycin
A plethora of recently acquired information about specific molecular abnormalities that "drive" the malignant phenotype, together with profound advances in biotechnology, has resulted in the beginning of an era of abundant novel therapeutic options to treat patients with a variety of malignant diseases. It has also brought about many unique challenges for clinical investigators. As anticancer therapeutics with distinct targeting capabilities against malignant cells are developed, prioritization of these therapies for efficient allotment of clinical trial resources, identification of patients whose malignancies most likely express the molecular constituents resembling the true target, and derivation of relevant end points for both screening and assessment of clinical relevance will be critical to their successful development and optimization. The predominant biologic effects of these agents in preclinical studies (i.e., tumor growth delay) and their much more disparate effects on malignant and normal tissues compared with nonspecific cytotoxic agents suggest that clinical evaluation and regulatory end points that are generally considered secondary for nonspecific cytotoxic agents, such as improvements in disease-related symptoms and quality of life, may evolve into primary end points similar to the situations typically encountered in the assessment of therapeutic benefit in other medical disciplines. The cellular processes that are specifically being targeted for therapeutic development are those that are principally responsible for the proliferative advantage inherent in the malignant phenotype, including: aberrant signal transduction (ST); cell cycle dysregulation; evasion of apoptosis; sustained angiogenesis; tissue invasion and metastasis; and immune tolerance [14]. The development of novel therapeutic agents that are highly selective between host and tumor should enable the achievement of high therapeutic indices with low toxicity in the treatment of cancer [5].
The term "signal transduction" refers to the means by which regulatory molecules that govern the fundamental processes of cell growth, differentiation, and survival (e.g., extracellular hormones, growth factors, cytokines, and specialized proteins) communicate within the cell, resulting in the tight coordination of proliferative and other essential processes among various tissues. Cellular signaling processes are essential to the life cycle and biologic function of all cells and are critically important in governing processes such as proliferation and differentiation. ST elements interact through biochemical cascades in interrelated networks within cells and among tissues [2, 6]. The robustness and diversity of these signals are enhanced by many redundant routes within the various pathways and elaborate interconnections among the networks [7]. Most malignancies have aberrant ST elements of variable magnitudes, so they are logical targets for therapeutic development [8]. Highly aberrant ST elements often give rise to constitutive activation of the cell growth process. The autonomy of cell growth is the dominant feature of the malignant phenotype [1, 2, 4]. Aberrant or overexpressed ST elements or growth factor receptors may result in an increased proliferative rate and potential for invasion, metastasis, and angiogenesisand shift the equilibrium between survival and cell death (apoptosis) control toward survival [1]. Resistance to traditional cytotoxic chemotherapy and radiation therapy may be due, at least in part, to the development of aberrant ST elements; therefore, therapeutics targeting these aberrations may be useful adjuncts to these standard therapies [8].
ST Systems
Cells are constantly exposed to a variety of external stimuli, ranging from soluble endocrine and paracrine factors to signaling molecules on neighboring cells. Thus, it is extremely important that the cell correctly interprets these extracellular signals to create an appropriate developmental or proliferative response. The most common stimuli use secondary messenger networks that rely upon a relay system for signal amplification and diversity. Examples of relay systems are the seven-transmembrane receptor group [9] and enzyme-linked receptors [6, 10]. These systems process signals by different methods. For the seven-transmembrane receptor group, which includes hormones and neurotransmitters, conformational changes upon ligand binding lead to dissociation of heterotrimeric G-proteins [9]. Enzyme-linked receptors will, upon ligand binding, increase enzymatic activity in the receptor, causing activation. Examples include systems activated by receptor tyrosine kinases (RTKs), transforming growth factor beta, and cytokines. Receptors of the tyrosine kinase family play principal roles in these processes because they are able to integrate a wide range of external stimuli with specific internal signals and responses, ultimately allowing the cell to respond correctly to its environment. Other relay systems use methods such as ligand gate ion channels that open or close in response to ligand binding (e.g., postsynaptic receptors) or ST via intermembrane cleavage of the receptor. In the latter case, ligand binding leads to regulated proteolytic cleavage of a transmembrane receptor that releases an intercellular fragment of the receptor into the cytoplasm. The receptor fragment is then translocated to the nucleus, where it regulates a response. Examples of this system include the ErbB family of receptors, CD44, and amyloid precursor protein [7]. Another type of signaling process is by ligand passage through the membrane. This is the process by which thyroid hormones, retinoids, vitamin D receptors, and androgens are transduced. Passage of the ligand across the membrane induces a conformational change in the cytoplasmic or nuclear receptor, which then becomes activated. In these well-regulated systems, the receptor is often associated with an inhibitor that prevents ligand-independent activation of signaling. Finally, there is a somewhat controversial proposal that transmembrane receptors may directly signal to the nucleus. This theory was based upon the discovery in the nucleus of transmembrane receptors with and without their ligands. Whether these intranuclear receptors can directly mediate transcriptional responses is unknown.
ST Pathways as Targets for Therapeutics Development
ErbB Receptor Family ErbB receptor function begins upon ligand binding and is followed by receptor dimerization. The dimerization process can occur between two receptors of the same family (heterodimerization, e.g., ErbB-1 and ErbB-3) or between two of the same receptors (homodimerization, e.g., ErbB-1 and ErbB-1) [15]. Stimulation by a specific ligand confers a specific dimerization profile that is tissue specific or tumor specific [15]. The process of dimerization activates the tyrosine kinase domain of the receptor and is followed by the phosphorylation of multiple tyrosine residues, which in turn activates downstream receptor proteins that ultimately lead to physiologic responses [15, 18]. Upon ligand binding, the ErbB receptor becomes activated and downregulated through a series of steps [7, 1113, 15, 16, 18]. Ligand binding leads to receptor aggregation, which in turn facilitates the formation of both ErbB homodimers and heterodimers. ErbB homodimers and heterodimers are able to activate intrinsic tyrosine kinases of receptors via intermolecular phosphorylation within their cytoplasmic domains. The resulting phosphorylated tyrosine residues modulate the readiness of, or serve as docking sites for, downstream signaling molecules and cytoplasmic messenger proteins, which then initiate a cascade of signals that emanates from the cytoplasm to the nucleus. Key tyrosine phosphorylation sites responsible for the recruitment of downstream receptor targets are located in the juxtamembrane region and C-terminal tail of the receptor, which flank the tyrosine kinase domain. Signaling through ErbB-1 and other family members triggers a powerful network of downstream cellular pathways, ending in responses that range from cell division to cell death, and from motility to adhesion, and include invasiveness and angiogenesis. Ultimately, effects on gene expression determine the biologic response to receptor activation. Because the network is often dysregulated in human cancers, a molecular comprehension of these processes may lead to the development of new therapeutics with clinical ramifications.
It has been suggested and supported by experimental data that aberrant activation of the kinase activity of ErbB receptors plays a primary role in the development and/or progression of human cancer. The ErbB receptors are associated with a number of tumor types, one example being the well-known HER-2 receptor, which is identified in 20%-30% of invasive breast cancer cases and is associated with a poor prognosis. A variety of different mechanisms leads to increased ErbB receptor activation and, ultimately, increased cellular proliferation (Fig. 2
Aberrant ErbB subfamilies are associated with the development of a variety of human tumor types, many of which lack effective therapeutic agents [20]. For instance, ErbB subfamilies are overexpressed in breast and colorectal cancers, gastric carcinoma, gliomas, and tumors that arise in mesodermal tissue [15, 16, 18]. In breast cancer, approximately 25% of patients have amplification of HER-2/neu genes, leading to overexpression of ErbB-2 [15, 20].
Factors Affecting ErbB Signals
The nature of the ligand determines the nature of the dimer formed upon binding; this very complex process involves the possibility of multiple ligands and subsequent dimer profiles that each confer a particular mitogenic response to the cell [7]. Therefore, the magnitude and type of mitogenic response downstream is a contextual summation of the individual effects of multiple ligands and receptor dimerization profiles. Consequently, targeting one specific ErbB subfamily may be insufficient to impart a significant therapeutic benefit [15, 21].
The magnitude of signals transduced differs among dimer profiles, for example, between homodimers and heterodimers. The homodimer ErbB-3 does not confer any signaling, while both ErbB-1 and ErbB-4 are weak signaling homodimers [20]. Conversely, ErbB-2 is a preferred heterodimer partner that conveys a potent signal [20]. The specific features of ErbB-2 heterodimers that allow for potent signaling include slow ligand dissociation, relaxed ligand specificity, rapid recycling of the ligand, and prolonged firing of the ligand [10, 20]. Taken together, the ErbB-2 heterodimer features lead to dramatic increases in cell proliferation and cell migration, as well as resistance to apoptosis [7, 10, 16] (Fig. 4
In addition to the dimer profile, the conformation of the phosphotyrosine groups on the activated ErbB receptor determines which downstream adaptor protein will react with it. For example, the ErbB-1-ErbB-3 heterodimer preferentially provides docking sites for the phosphoinositide-3 kinase (PI3K) adaptor proteins, while the ErbB-2-ErbB-1 heterodimer leads to preferential activation of the PI3K pathway, resulting in the phosphorylation of a variety of survival proteins and increased translation of cell cycle proteins [10]. Another determinant of the quality and magnitude of the downstream signal is the rate of dimer degradation, which is an endocytotic process [10, 22]. Dimer degradation is initiated by ligand binding, which then induces receptors to cluster in clathrin-coated membrane pits. This process is followed by endocytosis and eventual lysosomal degradation of the dimer. The rate of endocytosis determines the amplification or attenuation of the signal [6, 7]. Dimer degradation is also dependent on the nature of the dimer and its tyrosine kinase activity. For example, kinase-negative mutants recycle to the cell surface for reutilization and are, therefore, not preferentially degraded [11]. The receptor degradation process effectively "turns off" the ErbB response; consequently, it is a valuable target for rational therapy. One such therapeutic target is the signaling protein Cbl, which is important in receptor processing. The Cbl protein attracts ubiquitin-loaded molecules that tag the receptor with ubiquitin for recognition and sorting, eventually leading to proteosomal digestion [6]. Currently, rational therapeutics to target dimer degradation are in development. For example, the irreversible, pan-ErbB tyrosine kinase inhibitor CI-1033 (Pfizer Inc.; Groton, CT) is a strong inducer of poly-ubiquitylation and ErbB-2 degradation [23]. Finally, the integration of heterologous signals outside the ErbB signaling system, that is, crosstalk with pathways outside its system, also can affect the quality and magnitude of ErbB signals [7]. For example, lysophosphatidic acid, endothelin, and thrombin can activate G-protein-coupled receptors (GPCRs) that, in turn, untether membrane-bound ErbB ligands, such as heparin-bound epidermal growth factor (HB-EGF), subsequently freeing them to bind to ErbBs. Activation of GPCRs may then activate Src kinases, leading to phosphorylation of tyrosine residues on the intracellular ErbB domains. These actions set in motion downstream ErbB-1 events that may contribute to the mitogenic potential of heterologous agonists [24].
ErbB-Targeted Therapeutics in Development
The first ErbB receptor inhibitor to be approved by the U.S. Food and Drug Administration (FDA) was the monoclonal antibody trastuzumab (Herceptin®; Genentech, Inc.; South San Francisco, CA). This agent is indicated for the treatment of patients with metastatic breast cancer whose tumors overexpress the ErbB-2 (HER-2/neu) receptor [7, 25, 26]. Currently, many other ErbB receptor-targeted therapies are in development, including monoclonal antibodies and small molecules that target the tyrosine kinase domain of the receptors [10, 17, 2730]. Other compounds are being developed to target only the external domain of ErbB-1, such as cetuximab (Erbitux®, IMC C-225; ImClone Systems, Inc.; New York, NY), EMD 72000 (Merck Kga; Darmstadt, Germany), ABX-EGF (Abgenix, Inc.; Fremont, CA), and MDX-447 (Medarex Inc.; Princeton, NJ). Another approach is to target the tyrosine kinase domain of ErbB-1, as exhibited by gefitinib (Iressa®; AstraZeneca Pharmaceuticals; Wilmington, DE), which recently received regulatory approval in the U.S. for the treatment of patients with non-small cell lung cancer (NSCLC) resistant to platinum agents and docetaxel, and by erlotinib (TarcevaTM; OSI Pharmaceuticals; Melville, NY) [27, 31]. Yet other agents target multiple ErbB receptor subfamilies. The compound GW572016 (GlaxoSmithKline; Middlesex, UK) is an example, as it targets the RTKs of both ErbB-1 and ErbB-2 [10]. CI-1033 and EKB-569 (Wyeth-Ayerst; Philadelphia, PA) bind irreversibly to the ATP-binding site and inhibit the tyrosine kinase activity of multiple ErbB subfamily members [32, 33]. Table 1
Therapeutic Development Considerations The magnitude and quality of the downstream response to targeted therapies may be determined by a variety of factors that need to be identified in tumors. Thus, another important consideration in the development of targeted therapeutic agents is tumor markers; that is, the subcellular determinants of the ErbB inhibitory response, such as phosphorylated (p)-ErbB-1, p-Erk, and p-Akt. Following treatment with a particular compound, immunohistochemical staining of receptors, phosphorylated aspects of receptors, and ST elements has permitted seimiquantitation of these determinants [35]. Clearly, there are many different approaches to developing targeted therapies, and the relative merits of each of these approaches have yet to be determined. Prospective profiling of tumor types in large studies would help researchers to understand the complexities of the systems involved and to determine the links between tumor profiles and responses to treatment. However, this is a considerable enterprise that has yet to be undertaken extensively.
Tumor Growth Inhibition and Regression
Another area of research is the development of inhibitors of mTOR, a downstream ST element in the PI3K pathway and a member of the recently identified family of protein kinases termed PI3K-related kinases. These kinases are involved in a number of critical regulatory cellular functions concerning cell cycle progression and cell cycle checkpoints that govern cellular responses to DNA damage, repair, and recombination [39]. mTOR regulates essential ST pathways and is involved in the coupling of growth stimuli with cell cycle progression. PI3K/protein kinase B (Akt) appears to be the key modulatory factor in the upstream pathway by which growth factor-growth factor receptor interactions affect the phosphorylation state of mTOR [40, 41]. PI3K plays a central role in cellular proliferation, cell adhesion, catabolism, and apoptosis, and is upregulated in cancer cells [42]. Activation of the PI3K pathway leads to the production of secondary messengers downstream that activate proliferative elements, for example, Akt and p70s6k [8, 27, 43]. In turn, these elements initiate a variety of local responses, including polymerization of actin, assembly of signaling complexes, and priming of protein kinase cascades [43]. In particular, phosphorylation of Akt stimulates its catalytic activity, leading to the phosphorylation of a number of other proteins that affect cell growth, cell cycle entry, and cell survival. Thus, inhibition of mTOR could eliminate the transduction of proliferative signals and thereby inhibit tumor growth where aberrant signals or mutations occur. mTOR lies at a critical branching junction in the pathway between the PI3K/Akt/PTEN signaling pathway and downstream proliferative elements [27], and serves to regulate growth stimuli and subsequent cell cycle progression. Experimental data demonstrate that mTOR functions downstream of the PI3K/Akt pathway and is phosphorylated in response to stimuli that activate the PI3K/Akt pathway [40, 41, 44]. Upon stimulation, mTOR phosphorylates a variety of downstream proteins that augment or activate the translation of proteins that are important in the G1-to-S phase traverse and ribosome biogenesis [8, 45]. There are other signaling pathways that are activated downstream of PI3K, but the Akt pathway is of primary interest because of its role in inhibiting apoptosis and promoting cell proliferation by affecting the phosphorylation status of cell-survival and apoptosis-induction proteins such as BAD [46]. Upstream abnormalities can also activate mTOR and lead to proliferation.
Rapamycin, an mTOR Inhibitor Some cell abnormalities and mutations have a hypersensitivity to rapamycin and its analogs [48]. In particular, aberrations in the PTEN tumor suppressor oncogene, prostate cancer xenograft, and hyperactivated Akt are hypersensitive to the rapamycin analog CCI-779 (Wyeth-Ayerst; Collegeville, PA), which is currently in broad clinical evaluations [8]. The PTEN tumor suppressor gene can be inactivated by deletions, mutations, and hypermethylation. Aberrations in PTEN are found in a wide variety of sporadic and inherited neoplasms [48]. Solid tumors with high frequencies of PTEN mutations or deletions include glioblastomas (27%-44%), prostate tumors (43%-50%), and endometrial tumors (up to 50%). However, the frequency of PTEN mutations is comparatively lower in endometrial, breast, bladder, and lung cancers, and in melanomas and lymphomas [4850].
mTOR Inhibitors in Development In tissue culture studies, several cancer cell lines, including human prostate, breast, small cell lung carcinoma, glioblastoma, melanoma, and T-cell leukemia, have shown a high sensitivity to CCI-779. Human tumor xenografts treated with CCI-779 also showed significant growth inhibition, although the predominance of tumor growth inhibition, rather than overt tumor regression, advocates that subsequent disease-directed trials should be specifically designed to detect this potential outcome (i.e., randomized trials with well-designed control arms) [8]. Further, several intermittent CCI-779 dosing regimens were shown to be effective in human tumor xenograft studies, which is important in that extended immunosuppression may result from both rapamycin and CCI-779 administered using a continuous-dose schedule and because the immunosuppressive effects of rapamycin analogs have been shown to resolve within 24 hours following treatment [51]. CCI-779 has been evaluated in two phase I studies, in which the agent was administered as a 30-minute i.v. infusion weekly and as a 30-minute i.v. infusion daily for 5 days every 2 weeks [52, 53]. Those studies were designed to determine the maximum-tolerated dose based on classically defined dose-limiting toxicities. In those studies, the primary toxicities included dermatologic toxicity, myelosuppression, reversible increases in liver function tests, and asymptomatic hypocalcemia. However, the majority of these toxicities were mild to moderate in severity and the maximum-tolerated dose had not yet been determined for CCI-779 administered weekly. In addition, tumor regression of a variety of tumors was observed, including partial responses in patients with previously treated renal cell carcinoma and non-small cell lung carcinoma, and minor responses in previously treated patients with soft tissue sarcoma, serous papillary carcinoma of the endometrium, breast carcinoma, squamous cell carcinoma of the skin, and non-Hodgkins lymphoma [8]. In early phase II studies, tumor regression has been consistently observed in patients with breast and renal carcinoma, and a phase III study is under way in patients with renal cell carcinoma [54]. The fact that CCI-779 produced tumor regression at relatively nontoxic doses in these trials suggests that the optimal therapeutic dose of this agent may be lower than the maximum-tolerated dose [53].
Numerous challenges are evident in the clinical development process of ST inhibitors, all of which may make the clinical trial process more difficult both to plan and to execute. These challenges include defining the optimal doses and administration schedules associated with maximal antitumor activities and minimal toxicities, determining long-term toxicity, and incorporating optimal and sound end points into clinical evaluations based on expectations determined in preclinical studies. Finding solutions to these obstacles may affect the time required to make appropriate go/no go decisions, and to obtain regulatory approval for these agents.
Phase I and Feasibility Studies In addition to dosage, determining optimal administration routes and schedules for ST inhibitors is of primary importance. Current data suggest that continuous long-term treatment may be highly effective in achieving maximal and sustained efficacy. However, extended treatment durations may lead to acquired drug resistance, as well as potentially exposing patients to unique toxic effects. Both of these concerns must be addressed when defining optimal dosing schedules for these agents. Notably, any long-term toxicities associated with continuous long-term treatment with ST inhibitors may not be identified using standard preclinical toxicology studies, which primarily focus on highly proliferative tissues. For ST inhibitors, as well as any other rationally designed, target-based therapeutic agents, organs in which the target is highly expressed or tissues that play a role in the function(s) of those organs will require careful monitoring.
Disease-Directed Screening Evaluations
Clinical End Points Delayed tumor growth can exhibit in at least three discrete circumstances. In the first, treatment does not completely stop tumor growth but decreases growth rate. In this setting, the degree of antiproliferative effect may not be evident to the clinician who cannot objectively measure drug-induced effects on the rate of tumor growth when obvious regression has not been demonstrated. Instead, the clinician may interpret any tumor growth as disease progression or treatment failure, although the decrease in tumor growth rate may result in increased time to tumor progression or overall survival, in addition to a global improvement in quality of life for the patient. In the second circumstance, a more significant antiproliferative effect occurs when the rates of tumor cell proliferation and cell death are equivalent, often interpreted as stable disease. In this setting, the clinician is likely to continue treatment as long as the patient does not demonstrate intolerable adverse effects. Although the results of preclinical studies suggest that these first two circumstances are likely to be the most common following treatment with ST inhibitors, the beneficial effects may not be obvious or unequivocally attributed to the agent in nonrandomized phase II screening studies. In the third, less common circumstance, the ST inhibitor significantly inhibits tumor cell proliferation and/or enhances tumor cell death, resulting in net tumor regression. This is most likely to occur when the target is a major driver of tumor proliferation. Thus, designing phase II and III disease-directed studies to assess the relevant antitumor activities of ST inhibitors is a daunting task. Although many of these agents may be able to induce tumor regression in animals, tumor growth inhibition may not be the principal therapeutic effect in human cancers where the tumor is not driven by a single primary anomaly but by multiple causative anomalies of the specific target. Therefore, clinical situations that are sufficiently sensitive to detect a relevant magnitude of tumor growth inhibition will need to be incorporated into disease-directed clinical evaluations. Understanding the biology of the target is paramount with regard to selecting tumors that are most apt to be driven by the target in early screening studies. Tumor growth delay as the primary benefit of ST inhibitors offers a new challenge for the selection of appropriate end points for phase II and III studies, specifically because only randomized clinical trials can unequivocally demonstrate such effects on tumor growth. In reality, however, some type of "lead" or indication that the ST inhibitor possesses relevant clinical activity, with the ability to modify the natural history of disease progression, ultimately will need to be observed before resource-intensive, large, randomized, phase III trials are initiated. One way of obtaining such a lead is to compare the relative time to tumor progression in patients receiving single-agent treatment with an ST inhibitor against that resulting from treatment with a relevant standard therapy or supportive care, measured just prior to administration of the experimental agent [60]. Using experience with agents that were later shown to have relevant clinical activity in randomized trials, a 30% prolongation in the time to progression may be a reasonable threshold to use before proceeding to phase III trials. As an alternative, "exploratory" single-arm or randomized phase II trials designed with sufficient power to detect and quantify tumor growth inhibition may provide meaningful leads regarding activity prior to phase III randomized studies. For example, in advanced pancreatic cancer, the percentage of patients surviving at least 1 year in exploratory nonrandomized studies may be considered a reasonable end point to gauge whether to proceed with randomized phase III trials. The randomized discontinuation trial has been proposed as a potentially highly efficient method to detect drug effects on time to progression, survival, and symptoms. In this design, all patients receive the study drug but only patients who do not demonstrate tumor progression are randomized to treatment with or without the study drug. On a similar note, the proportion of patients with progressive disease as their best response appears to inversely correlate with the ultimate utility of any specific agent in a given clinical setting, and a maximum acceptable threshold of patients with progressive disease as their best response may be a valuable predictor of the potential usefulness of the agent [61]. Such benchmarks, once validated, may be effective in screening ST inhibitors prior to initiating large, randomized, phase III trials. Finally, for agents that are capable of inducing a low level of tumor regression in preclinical evaluations, large phase II studies may be necessary to detect this low level of activity with sufficient confidence intervals. Additional surrogate end points that may be considered for efficacy in phase II trials include assessment of target inhibition, relevant changes on positron emission scanning (PET) that reflect decreased cell proliferation, and decrements in tumor markers. While all these potential end points remain intriguing for future trials, only changes on PET scanning have been associated with tumor regression (or progression) in a randomized clinical trial evaluating the efficacy of imatinib for the treatment of GISTs [55], and none of these surrogate end points have been validated in a wide range of tumor types or in a large population of patients. Thus, the challenge is to successfully integrate these proposed end points as new paradigms for evaluating these novel agents. The primary end points for phase III trials will continue to be based on those reflecting survival. However, the relatively low toxicity of ST inhibitors may allow for more emphasis on other end points related to clinical benefit, such as time to progression, performance status, disease-related symptoms, and quality of life. Further, preclinical data and early clinical results indicate that major tumor regression is unlikely to be the primary effect of ST inhibitors. Because clinical trials are often conducted in patients with advanced disease who require cytoreduction for clinical benefit, reasonable developmental strategies will likely involve evaluations of ST-targeted agents in combination with other therapeutic modalities, particularly because a number of these therapeutic agents have shown synergistic, additive, and supra-additive activities when combined with radiation and a variety of chemotherapeutic agents.
Within only a few years, anticancer therapeutic development has moved from almost a standstill, with a paucity of new agents showing potential for major effect, to the rapid development of agents targeted against the inherent basis of cancer. This transition is based largely on the exponential rate of information acquisition regarding the cancer cell, particularly in terms of aberrant growth ST and the microenvironment of the cell. Because the ultimate goal of any signaling pathway is to regulate cell growth and division, much of the investigation into novel anticancer agents has focused on the development of ST inhibitors. Examples of some key signaling pathway elements currently being targeted with specific therapeutics include the ErbB receptor family and mTOR. Therapeutic agents targeting these signaling pathways should provide greater specificity, less toxicity, and higher therapeutic indices. However, adequately designed clinical trials are necessary to ensure that the usefulness of ST inhibitors is correctly evaluated and that potentially useful agents are not rejected solely on the basis of poor performance in an inadequately designed trial with an inappropriate clinical or biologic end point. The full potential of these new agents may only be realized with the implementation of radically different therapeutic development, evaluation, and treatment paradigms.
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