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Departments of Otolaryngology (S.M.T., M.J.O., M.L.F., J.R.G.), Pharmaceutical Sciences (S.S., D.R.W., W.C.Z.), Biostatistics (W.E.G.), Pharmacology (J.R.G.), and Medicine (W.C.Z.), University of Pittsburgh and the University of Pittsburgh Cancer Institute, Pittsburgh, Pennsylvania
Received September 6, 2007; accepted November 19, 2007
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Abstract |
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). The epidermal growth factor receptor (EGFR) is overexpressed in 90% of SCCHN tumors. Activated EGFR triggers increased cell proliferation, angiogenesis, and metastasis, contributing to tumor progression and decreased survival and indicating that EGFR may serve as a therapeutic target for SCCHN. Various strategies targeting EGFR have demonstrated antitumor efficacy in preclinical models. Recently the Food and Drug Administration approved the use of the anti-EGFR antibody cetuximab as a monotherapy or in combination with radiotherapy for SCCHN patients. In addition to blocking EGFR activation, down-modulating EGFR protein levels via an antisense DNA approach has been reported to be an effective way of inhibiting EGFR-mediated growth. A direct comparison between EGFR antisense gene targeting and an EGFR tyrosine kinase-specific inhibitor or EGFR monoclonal antibodies demonstrated increased growth inhibition with antisense gene treatment compared with either of the other EGFR-targeting modalities (Grandis et al., 1997). Intratumoral injections of lipid formulations with antisense EGFR gene therapy and antisense EGFR oligonucleotides reduced SCCHN tumor growth in vivo without evidence of toxicity (He et al., 1998; Niwa et al., 2003). However, given the obstacles associated with intratumoral administration, the concerns regarding gene therapy raised by the death of the patient at the University of Pennsylvania in 1999, and the potential toxicity of liposomes, we initiated studies to examine therapeutic targeting of EGFR using systemically administered phosphorothioated antisense oligonucleotides. Phosphorothioate modifications improve the stability of oligonucleotides in the plasma by increasing their resistance to nuclease degradation. Preclinical studies with antisense phosphorothioate-modified oligonucleotides demonstrated successful down-regulation of the antiapoptotic proteins, X-linked inhibitor of apoptosis and Bcl-2, via systemic delivery in mice (Hu et al., 2003). However, emerging evidence suggests that no single treatment regimen results in sustained antitumor efficacy. In the last decade, the field of oncology has witnessed the development of combined chemotherapeutic agents, with therapies targeting signal transduction molecules in cancer cells (Wang et al., 2001).
In this study, we tested the antitumor efficacy of systemically administered EGFR antisense oligonucleotides alone and combined with a low dose of the chemotherapeutic agent docetaxel. Docetaxel is a taxane analog that is active both as monotherapy and in combination with molecular targeting agents, including bevacizumab in patients with solid tumors (Dreyfuss et al., 1996; Schöffski et al., 1999; Herbst et al., 2007). Combining EGFR inhibitors with chemotherapy has been reported to result in added tumor growth inhibition in several cancer cell lines, including ovary, breast, and colon (Ciardiello et al., 2000). The plasma, tumor, and tissue disposition of taxane analogs has been previously evaluated in preclinical models (Bissery et al., 1995; Sparreboom et al., 1998; Strychor et al., 2005). However, the plasma and tumor disposition of docetaxel has not been evaluated in combination with agents that target EGFR. Here, we report the feasibility and explore the antitumor mechanisms of a novel therapeutic strategy combining low-dose docetaxel with systemically delivered EGFR antisense oligonucleotides for the treatment of SCCHN.
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Materials and Methods |
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; Heo et al., 1989). Cells were maintained at 37°C in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum in presence of 5% CO2. Docetaxel (Taxotere) was obtained from sanofi-aventis (Bridgewater, NJ) as a solution of 10 mg/ml in 13% ethanol (Clarke and Rivory, 1999). Docetaxel was further diluted to a concentration of 0.5 mg/ml in saline. Phosphorothioate-modified antisense and sense oligonucleotides targeting EGFR mRNA were obtained from the University of Pittsburgh DNA Synthesis Facility (Pittsburgh, PA) as described previously (Niwa et al., 2003). The oligonucleotides were dissolved in water and further diluted in saline. Antibodies used for immunoblotting and immunohistochemistry included anti-EGFR monoclonal antibody (BD Transduction Laboratories, Lexington, KY); β-actin monoclonal mouse IgM (Calbiochem, San Diego, CA); phospho-AKT (Ser473; Cell Signaling Technology Inc., Danvers, MA); phospho-Stat3 (Tyr705; Cell Signaling Technology Inc.), and Ki67 (Dako Denmark A/S, Glostrup, Denmark). Apoptosis was measured by TUNEL (Roche Applied Science, Mannheim, Germany). In Vivo Studies. Animal use and care was in strict compliance with institutional guidelines established by the University of Pittsburgh, Institutional Animal Care and Use Committee. Female athymic nude mice (Harlan, Indianapolis, IN) between the age of 5 and 6 weeks were injected with 1 x 106 1483 cells in 100 µl of Hanks' balanced salt solution subcutaneously on the left flank. Treatment was initiated 8 days after inoculation when tumors reached an average volume of 15 mm3. Tumor volumes were calculated using the formula: length x (width)2/2, where length is the largest diameter and width is the smallest diameter perpendicular to the length. Mice were randomized into treatment groups based on the tumor volumes. Five mice were randomly assigned to vehicle control (saline), EGFR sense oligonucleotide alone, EGFR antisense oligonucleotide alone, or docetaxel alone. Ten mice were assigned to the docetaxel plus EGFR sense oligonucleotide and docetaxel plus EGFR antisense oligonucleotide groups. EGFR antisense and sense oligonucleotides were administered at 5 mg/kg i.p. once daily for 30 days alone or in combination with docetaxel administered i.p. at 2.5 mg/kg once a week alone. Tumors were measured twice a week in two dimensions, with a vernier caliper. At the end of the study, tumors were excised, and they were divided into three sections. One section was snap frozen for molecular analyses by immunoblotting. The second section was fixed in 10% buffered formalin for immunohistochemical analyses. Blood was collected from anesthetized mice via cardiac puncture using heparinized syringes. Part of the blood was analyzed for hematological and serum chemistry parameters by Antech Diagnostics (Farmingdale, NY).
Pharmacokinetic studies were carried out on docetaxel concentrations in plasma and tumors of mice administered a single dose of docetaxel (2.5 mg/kg i.p.) alone or in combination with EGFR antisense oligonucleotides (5 mg/kg i.p.). Plasma and tumor tissue were harvested at 0.25, 1, 3, 6, and 24 h after administration of docetaxel alone or docetaxel injected 30 min after EGFR antisense oligonucleotide administration. In a separate study, the concentration of docetaxel in the tumor was assessed in mice administered multiple doses of both agents over 30 days. Specifically mice (n = 5 per treatment arm) were treated for 30 days (720 h) with EGFR antisense or sense oligonucleotides administered at 5 mg/kg i.p. once daily for 30 days alone or in combination with docetaxel administered i.p. at 2.5 mg/kg once a week. At the end of the study mice were anesthetized with isofluorane, and approximately 0.8 to 1 ml of blood was collected, by cardiac puncture using heparinized syringes. Blood was transferred to microcentrifuge tubes, and the tubes were immediately placed on ice. Plasma was harvested from the blood samples after centrifugation at 12,000g for 4 min at 4°C, and it was snap frozen in a dry ice-ethanol bath. Mice were euthanized by cervical dislocation, and the tumor tissue was harvested, weighed, and snap frozen in a dry ice-ethanol bath. Plasma samples were processed using solid phase extraction, whereas tumor samples were processed using acetonitrile precipitation followed by solid phase extraction (Strychor et al., 2005). Docetaxel concentrations in plasma and tumors were determined by a liquid chromatography/mass spectrometry assay as described previously (Parise et al., 2003).
Immunoblotting. Xenograft tumors were minced on dry ice and suspended in 500 µl of lysis buffer (10 mM Tris HCl, pH 7.6, 50 mM Na4P2O7, 50 mM NaF, 1 mM NaV3O4, 1% Triton X-100, and 1x protease inhibitor cocktail tablet that included a broad-spectrum potent inhibitor of protein tyrosine phosphatases (Roche Applied Science). The lysates were sonicated, and the supernatant was collected after centrifugation at 13,000 rpm for 5 min. Forty micrograms of protein was fractionated through 8% SDS polyacrylamide gels, and it was analyzed via immunoblotting for biomarker modulation. Autoradiograms were scanned, and the bands were quantified using the DigiDoc 1000 digital imaging system (Alpha Innotech, San Leandro, CA). Values obtained were normalized to β-actin levels and positive control lysates run on every gel. Cell lysates obtained from a well characterized HNSCC cell line, PCI-15b, were used as the positive controls. Relative intensities were averaged across tumors from the same group, and the cumulative results were graphed using Prism version 6 (GraphPad Software Inc., San Diego, CA).
Immunohistochemistry. Four-micrometer-thick sections of paraffin-fixed tumor samples from the EGFR antisense oligonucleotide alone and EGFR sense oligonucleotide alone treatment groups were removed, and they were adhered to slides by heating overnight at 57°C in a dry slide incubator. The specimens were deparaffinized, rehydrated, and placed in a 1:10 diluted mixture of methanol/H2O2 for 15 min at room temperature, and then they were rinsed two times with distilled water. Slides were placed in boiling citrate buffer for 10 min to enable antigen retrieval, and then they were examined for Ki67 expression. Sections from paraffin-embedded tissues were also examined for apoptosis by TUNEL (Roche Applied Science) according to the manufacturer's instructions. The average number of positive cells was determined from five separate fields under 400x magnification. Cumulative findings from blinded assessments of sections by two independent investigators were graphed using Graph-Pad Prism version 6.
Pharmacokinetic Analysis. The compartmental pharmacokinetic analysis of docetaxel in plasma and tumors was performed using maximum likelihood estimation in the ADAPT II modeling program as described previously (Zamboni et al., 1999). The estimation procedure and variance model used in the compartmental pharmacokinetic analysis was maximum likelihood estimation and linear models for the variance of the additive errors, respectively. Various pharmacokinetic model structures were considered to characterize the disposition of docetaxel. Akaike's Information Criteria, estimated error of the model parameters, and residual analysis were use to select the model structure that maximized the fit accuracy and simultaneously minimized the number of model parameters. The final model structure used for the pharmacokinetic analysis produced identifiable parameters.
Statistical Analysis. Tumor volumes were (natural) log transformed before analysis. Adequacy of random assignment of animals to treatment groups was checked by one-way analysis of variance. Day 30 differences were compared in an omnibus test with a one-way analysis of variance. Contrasts of specific interest were tested with a t test using the pooled estimate of standard error. P values were adjusted with the multivariate t distribution to simulate the data under the complete null hypothesis (Edwards and Berry, 1987). P values were also adjusted using the Bonferroni correction. Serum chemistries were compared among the six animal treatment groups with the Kruskal-Wallis test. P values were adjusted by the Sidak method and by permutation testing.
The tumor concentrations of docetaxel obtained after the end of the 4-week treatment regimen on day 30 after administration of docetaxel alone or docetaxel in combination with EGFR antisense or sense oligonucleotides was evaluated using the exact two-tailed Kruskal-Wallis test for equality of the three groups and the exact two-tailed Wilcoxon test to compare each group. The exact two-tailed Wilcoxon test was used to compare the tumor concentrations of docetaxel at 24 h after administration of docetaxel alone and docetaxel in combination with EGFR antisense oligonucleotides. The numbers of Ki67 or TUNEL-positive cells from the docetaxel and EGFR antisense oligonucleotide group was compared with the docetaxel and EGFR sense oligonucleotide-treated group using the exact two-tailed Kruskal-Wallis test. Exact nonparametric tests were performed using StatXact with Cytel Studio version 6.1 software (Cytel Inc., Cambridge MA). P values less than 0.05 was considered statistically significant.
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Results |
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). However, intratumoral administration of EGFR antisense oligonucleotides likely reaches a limited number of tumor cells at the site of injection, and it may be impractical in the clinical setting. In a preliminary study, we compared the antitumor efficacy of i.p.- versus i.v.-administered EGFR antisense oligonucleotides in SCCHN tumor-bearing mice, and we found no difference in the post-treatment tumor volumes using the two routes of delivery (data not shown). The i.p. route was chosen due to greater ease of administration. To examine the antitumor efficacy of EGFR antisense oligonucleotides, tumor-bearing mice were treated systemically with either EGFR antisense or sense oligonucleotides at 5 mg/kg i.p. daily for 4 weeks. Tumors in EGFR antisense oligonucleotide-treated group had significantly smaller tumor volumes compared with EGFR sense oligonucleotide-treated mice (P < 0.05) (Fig. 1A). Furthermore, tumor volumes of mice treated with EGFR antisense oligonucleotides plus docetaxel were significantly lower than the EGFR sense oligonucleotides plus docetaxel group after the Bonferroni correction (P < 0.01). The Bonferroni correction was applied since three-paired comparisons were made among three treatment groups. In two of the 10 mice administered systemic EGFR antisense oligonucleotides plus docetaxel, the tumors regressed completely by day 30. Differences among the tumor volumes between the various groups on day 30 are represented in Fig. 1B. Mice treated with EGFR antisense oligonucleotides in combination with docetaxel had the smallest tumors among all the groups.
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). To examine the effects of EGFR antisense oligonucleotides with or without docetaxel on proliferation of SCCHN tumor cells, tumors were examined by immunohistochemical analysis for Ki67 expression. The dark nuclei were counted, and the cumulative findings from two independent blinded assessments of all the tumors in each group were represented in the graph. The error bars represent the ± S.E.M. EGFR antisense oligonucleotide-treated tumors demonstrated fewer proliferating cells compared with EGFR sense oligonucleotide-treated tumors (Fig. 3A). Docetaxel administration further reduced the number of proliferating SCCHN cells in mice treated with EGFR antisense oligonucleotides compared with that in tumors treated with EGFR sense oligonucleotides and docetaxel (P < 0.01). We also examined the xenografts for apoptosis using TUNEL staining for DNA fragmentation. Apoptotic cell nuclei stained brown were counted, and the cumulative findings from two independent blinded assessments of all the tumors in each group were represented in the graph. The combination of EGFR antisense oligonucleotides and docetaxel induced greater apoptotic cell death in tumors as measured by the increased nuclear staining of fragmented DNA compared with the combination of EGFR sense oligonucleotides and docetaxel (P < 0.001) (Fig. 3B).
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Pharmacokinetic Analysis Demonstrated Increased Docetaxel Exposure in the Tumors after Multiple Treatments with EGFR Antisense Oligonucleotides. To determine the mechanisms whereby the tumors demonstrated an increased sensitivity to chemotherapeutic agent docetaxel in the presence of EGFR inhibition, we examined the levels of docetaxel in the plasma and tumors of mice treated with both agents. A four-compartment model with administration of docetaxel into the intraperitoneal cavity was fit to the plasma concentration versus time data as reported previously (Strychor et al., 2005). The model parameters consisted of the rate constant for absorption (ka) from the intraperitoneal cavity to the central plasma compartment, rate constant representing first pass clearance via the liver (kfp), the volume of the central compartment (Vc), intercompartment rate constants (k12, k21, k13, and k31), and the elimination rate constant from the central compartment (k10) (Fig. 4). Due to the limited concentration versus time data, especially during the elimination phase, and to get an accurate estimate of the ka, the parameters presenting the plasma disposition were fixed to values from our prior study of docetaxel administered i.v. at 10 mg/kg (Strychor et al., 2005). The Vc, k12, k21, k13, k31, and k10 were fixed at 1.22 l/m2, 2.06 h-1, 2.02 h-1, 0.66 h-1, 0.17 h-1, and 3.78 h-1, respectively (Strychor et al., 2005). The corresponding half-life and clearance in all studies were fixed at 0.2 h and 4.6 l/h/m2 (Zamboni et al., 1999). The systemic disposition of docetaxel was similar in both studies, and fixing the k10 and Vc values allowed us to accurately determined the rate constant describing the absorption of docetaxel from the i.p. cavity. The area under the concentration versus time curves (AUC) of docetaxel in plasma (AUCPlasma) and tumor (AUCTumor) from 0 to 24 h were estimated using the log trapezoidal method by simulating the concentration versus time data based upon model-specific parameters.
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A fifth compartment describing the tumor disposition was added to the four-compartment model described above for the plasma disposition after i.p. administration. The model structure was based on our prior model of tumor disposition (Zamboni et al., 1999). The model parameters describing the tumor disposition were the rate constants from the plasma to the tumor (k14) and from the tumor to the plasma (k41) and the volume of the tumor compartment (Vt). The Vt was fixed to 0.17 l/m2 based on our previous study (Zamboni et al., 1999). The docetaxel tumor AUC from 0 to 720 h after administration of docetaxel in combination with EGFR antisense oligonucleotides and docetaxel alone was 23,280 and 12,070 ng/ml · h, respectively (Table 1). The pharmacokinetic model parameters suggest that the increase in docetaxel tumor exposure in combination with EGFR antisense oligonucleotides is due to tumor-related factors (i.e., k14) induced by EGFR antisense oligonucleotides and not associated with altered absorption of docetaxel from the i.p. cavity or systemic clearance.
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Administrations of antisense oligonucleotides against cAMP-dependent protein kinase has been reported to increase the tissue and tumor uptake of chemotherapeutic agent irinotecan in athymic nude mice (Wang et al., 2002). To evaluate the effect of a single dose of EGFR antisense oligonucleotides on the plasma and tumor uptake of docetaxel, pharmacokinetic studies in plasma and tumor were performed from 0 to 24 h after administration of docetaxel alone or in combination with EGFR antisense oligonucleotides. The concentration versus time profiles of docetaxel in plasma and tumor from 0 to 24 h after a single dose of docetaxel alone or 30 min after administration of EGFR antisense oligonucleotides were similar (Fig. 5). Overall, the plasma and tumor concentrations of docetaxel were near the lower limit of quantitation (1 nM). The tumor concentrations of docetaxel at 24 h after administration of docetaxel alone and in combination with EGFR antisense oligonucleotides were 24.2 ± 4.6 and 23.8 ± 4.3 ng/ml, respectively (P > 0.05). The pharmacokinetic parameters of docetaxel after administration of docetaxel alone and in combination with EGFR antisense oligonucleotides are summarized in Table 1. The parameters describing the intratumoral and systemic disposition of docetaxel were found to be similar after administration of docetaxel alone and in combination with the EGFR antisense oligonucleotides. These results suggest that although there is an accumulation of docetaxel in tumors relative to plasma over 24 h, a single dose of the EGFR antisense oligonucleotide does not alter the plasma or tumor levels of docetaxel.
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Systemic Administration of EGFR Antisense Oligonucleotides and Docetaxel Was Well Tolerated in Vivo. Mice in this study were examined for evidence of toxicity resulting from due to systemic administration of EGFR antisense oligonucleotides with or without docetaxel. Blood from mice treated with EGFR antisense or sense oligonucleotides alone and in combination with docetaxel was evaluated for hemoglobin, hematocrit, albumin, red blood cells, and white blood cells and for liver enzymes serum glutamic-oxalocetic transaminase and serum glutamic-pyruvic transaminase (Table 2). There were no differences in hematological and liver enzyme values among the treatment groups (Table 3). Thus, the combination of EGFR antisense and docetaxel produced no observed toxicity.
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Discussion |
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TopAbstractMaterials and MethodsResultsDiscussionReferences |
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). A direct comparison between EGFR tyrosine kinase inhibitors and EGFR antisense oligonucleotides demonstrated that down-modulating protein expression may have more antitumor efficacy than inhibiting receptor activation (Rubin Grandis et al., 1997). We have previously demonstrated that down-modulation of EGFR protein expression with liposome-mediated antisense gene therapy is an effective strategy for the treatment of SCCHN tumors (He et al., 1998). However, given the potential toxicity of liposomes, difficulty with formulating liposomal products, and the concerns regarding systemic delivery of gene therapy vectors, we elected to target EGFR with an antisense approach.
We previously demonstrated that intratumoral injections of EGFR antisense oligonucleotides have antitumor efficacy against SCCHN xenografts (Niwa et al., 2003). Although oral cavity tumors are relatively accessible for intratumoral injections, therapies that rely on intratumoral delivery are unlikely to reach all tumor cells in all locations. Hence, we have elected to pursue therapeutic targeting of EGFR using systemic administration of antisense EGFR oligonucleotides. DNA with a phosphodiester backbone is susceptible to enzymatic degradation with half-lives of approximately 5 min in plasma (Eder et al., 1991). The phosphorothioate modification of the backbone serves to protect the oligonucleotides from endogenous nuclease degradation, increasing the plasma half-life, and they persist in the plasma up to 6 h (Yuen et al., 1999; Chen et al., 2000). Phosphorothioated antisense oligonucleotides have been administered systemically in cancer patients with minimal toxicity and efficient modulation of target genes (Waters et al., 2000). Previous reports demonstrate that phosphorothioate oligonucleotides have similar pharmacokinetic profiles when administered via intravenous, intraperitoneal, or subcutaneous routes (Agrawal, 1996).
Daily i.p. injections of EGFR antisense oligonucleotides reduced SCCHN tumor volume. Administration of EGFR antisense oligonucleotides alone and in combination with docetaxel was well tolerated. Oligonucleotides are negatively charged polyanions that could potentially result in poor cellular uptake. However, phosphorothioate oligonucleotides can enter the cytoplasm via several mechanisms, including pinocytosis (Gao et al., 1993; Beltinger et al., 1995). Our studies demonstrate that systemic administration of phosphorothioate-modified oligonucleotides is well tolerated in mice. Systemic administration of EGFR antisense oligonucleotides also reduced target gene expression. To maximize the antitumor efficacy of EGFR down-modulation we examined the effect of combining systemic delivery of EGFR antisense oligonucleotides with a chemotherapeutic agent. Combining EGFR targeting strategies with chemotherapy or radiation has been reported to enhance the antitumor efficacy compared with administration of the agents alone (Mendelsohn, 2001). In a recent report, combining radiation with the EGFR inhibitor cetuximab increased patient survival rates compared with patients administered radiation alone (Bonner et al., 2006).
We have previously demonstrated that targeting EGFR with intratumoral administration of EGFR antisense oligonucleotides results in down-modulation of EGFR and it attenuates the activation of downstream signaling molecules, including Akt (Niwa et al., 2003). Here, we demonstrate for the first time that systemically administered EGFR antisense oligonucleotides effectively down-modulate EGFR levels in SCCHN xenografts. Furthermore, we observed an attenuation of Akt phosphorylation on EGFR antisense oligonucleotide treatment. In addition to examining effects on biomarkers, we examined the effects of EGFR down-modulation on tumor cell proliferation and apoptosis. We have previously demonstrated that EGFR activation triggers downstream signaling pathways that result in increased HNSCC proliferation and survival (Grandis et al., 1998; Zhang et al., 2004). Combining EGFR inhibitors with chemotherapy has been reported to demonstrate enhanced antitumor effects in lung and pancreatic cells (Ng et al., 2002; Higgins et al., 2004). However, few studies have examined the mechanisms behind the increased sensitivity. To examine the effects of EGFR antisense oligonucleotide administration on the pharmacokinetics of docetaxel in vivo, we evaluated the plasma and tumor disposition of an anticancer agent after single and repeated administration of an EGFR antisense oligonucleotide.
The plasma and tumor disposition of docetaxel from 0 to 24 h after administration of a single dose of docetaxel alone or in combination with EGFR antisense oligonucleotides was similar, suggesting no acute effects of the EGFR antisense oligonucleotides on the i.p. absorption, systemic clearance, or tumor distribution of docetaxel. The model simulations suggest there is a higher and prolonged docetaxel tumor exposure from 24 h to 30 days (720 h) after administration of docetaxel in combination with EGFR antisense oligonucleotides compared with docetaxel alone. However, additional plasma and tumor samples of docetaxel during this interval are required to confirm these results. The levels of docetaxel in the tumor on day 30 after administration of docetaxel in combination with EGFR antisense oligonucleotide was significantly greater compared with docetaxel alone or in combination with EGFR sense oligonucleotides. A potential mechanism associated with the increased tumor delivery of chemotherapeutic agents in combination with antiangiogenesis agents is known as pruning (Jain, 2001). Unlike normal blood vessels, tumor vessels are structurally and functionally abnormal, which can increase the resistance to blood flow, increase interstitial hypertension, and ultimately inhibit the delivery of anticancer agents to tumors (Jain, 1998). Antiangiogenic agents prune the immature and inefficient blood vessels by eliminating the excess endothelial cells, which results in normalization of vasculature (McDonald and Baluk, 2002). Normalization of the tumor vasculature improves the penetration of molecules in tumors (Tong et al., 2004). The normalization of tumor vasculature during tumor regression has been reported for imatinib, cetuximab, and trastuzumab (Jain, 2001; Uehara et al., 2001; Viloria-Petit et al., 2001). However, the optimal sequence and timing to combine antiangiogenic agents with chemotherapy to improve the delivery of anticancer agents to tumors and deprive the tumor of its blood supply are currently unknown (Jain, 2001). Based on the results of our study, it seems that these effects only occur after repeated dosing of the antiangiogenic therapy and that the effects are tumor-specific.
Thus, systemic administration of EGFR antisense oligonucleotides is feasible for down-modulating EGFR levels in SCCHN tumors without any apparent systemic toxicity. Combination therapy with EGFR antisense oligonucleotides and low doses of docetaxel results in an increase in intratumoral concentrations of docetaxel, thereby enhancing the antitumor effects of the single agents, and it may be a feasible therapeutic approach for HNSCC.
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Footnotes |
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ABBREVIATIONS: SCCHN, squamous cell carcinoma of the head and neck; EGFR, epidermal growth factor receptor; TUNEL, terminal deoxynucleotidyl transferase dUTP nick-end labeling; STAT, signal transducer and activator of transcription.
Address correspondence to: Dr. Sufi Mary Thomas, University of Pittsburgh, 200 Lothrop St., W915 BST, Pittsburgh, PA 15213. E-mail: smt30{at}pitt.edu
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) i.p. once weekly, EGFR antisense (x), and sense oligonucleotides (
) i.p. daily at 5 mg/kg body weight. Ten mice per group were treated with EGFR antisense (
) or sense (
) oligonucleotides i.p. daily at 5 mg/kg body weight in combination with one weekly injection of docetaxel (2.5 mg/kg). The graph depicts the median tumor volume by day and treatment group. Mice treated with EGFR antisense oligonucleotides demonstrated reduced tumor growth compared with mice treated with EGFR sense oligonucleotides (P < 0.05). A significant reduction in tumor growth rate in the EGFR antisense oligonucleotide plus docetaxel-treated tumors was observed compared with the EGFR sense plus docetaxel-treated tumors (P < 0.01). B, graph depicts tumor volumes of mice in all treatment groups on day 30 of the experiment. The actual tumor volume for each mouse is shown as an open circle. The group means after log transformation are plotted as squares, and the estimated standard deviation for each group are depicted as error bars. Standard errors were derived from the residual mean squared error of the one-way analysis of variance of log-transformed tumor volumes.
,—) and tumor (
,—- -) docetaxel concentration versus time profiles after administration of docetaxel alone are presented. Individual data and best fit line for plasma (
, - -) and tumor (
) is presented.