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Regular Articles

Phase I and Pharmacokinetic Study of ABI-007, a Cremophor-free, Protein-stabilized, Nanoparticle Formulation of Paclitaxel

Nuhad K. Ibrahim, Neil Desai, Sewa Legha, Patrick Soon-Shiong, Richard L. Theriault, Edgardo Rivera, Bita Esmaeli, Sigrid E. Ring, Agop Bedikian, Gabriel N. Hortobagyi and Julie A. Ellerhorst
Nuhad K. Ibrahim
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Neil Desai
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Sewa Legha
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Patrick Soon-Shiong
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Richard L. Theriault
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Edgardo Rivera
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Bita Esmaeli
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Sigrid E. Ring
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Agop Bedikian
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Gabriel N. Hortobagyi
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Julie A. Ellerhorst
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DOI:  Published May 2002
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Abstract

Purpose: ABI-007 is a novel Cremophor-free, protein-stabilized, nanoparticle formulation of paclitaxel. The absence of Cremophor EL may permit ABI-007 to be administered without the premedications used routinely for the prevention of hypersensitivity reactions. Furthermore, this novel formulation permits a higher paclitaxel concentration in solution and, thus, a decreased infusion volume and time. This Phase I study examines the toxicity profile, maximum tolerated dose (MTD), and pharmacokinetics of ABI-007.

Experimental Design: ABI-007 was administered in the outpatient setting, as a 30-min infusion without premedications. Doses of ABI-007 ranged from 135 (level 0) to 375 mg/m2 (level 3). Sixteen patients participated in pharmacokinetic studies.

Results: Nineteen patients were treated. No acute hypersensitivity reactions were observed during the infusion period. Hematological toxicity was mild and not cumulative. Dose-limiting toxicity, which occurred in 3 of 6 patients treated at level 3 (375 mg/m2), consisted of sensory neuropathy (3 patients), stomatitis (2 patients), and superficial keratopathy (2 patients). The MTD was thus determined to be 300 mg/m2 (level 2). Pharmacokinetic analyses revealed paclitaxel Cmax and area under the curveinf values to increase linearly over the ABI-007 dose range of 135–300 mg/m2. Cmax and area under the curveinf values for individual patients correlated well with toxicity.

Conclusions: ABI-007 offers several features of clinical interest, including rapid infusion rate, absence of requirement for premedication, and a high paclitaxel MTD. Our results provide support for Phase II trials to determine the antitumor activity of this drug.

INTRODUCTION

Paclitaxel is a chemotherapeutic agent with a wide spectrum of antitumor activity when used as monotherapy or in combination chemotherapy regimens (1) . The drug is used extensively in the treatment of advanced carcinomas of the breast, ovary, head and neck, and lung. Research into its activity in prostate cancer and urothelial tumors is ongoing as well. On the basis of early reports suggesting a dose-response phenomenon (2 , 3) , and in keeping with standard medical oncology practice, attempts are generally made to maintain paclitaxel doses at or near the MTD.3 Several schedules of administration have been studied, each demonstrating a slightly different toxicity profile. Short infusions of 1–3 h result in peripheral neuropathy as a dose-limiting toxicity, whereas longer, continuous infusion schedules produce a higher incidence of neutropenia (2 , 4, 5, 6) . Other common side effects include alopecia, mucositis, arthralgias, myalgias, and mild nausea.

The paclitaxel preparation in clinical use (Taxol; Bristol-Myers Squibb, Princeton, NJ) is formulated in the nonionic surfactant Cremophor EL (polyoxyethylated castor oil) and ethanol to enhance drug solubility (7) . Cremophor EL may add to paclitaxel’s toxic effects by producing or contributing to the well-described hypersensitivity reactions that commonly occur during infusion, affecting 25–30% of treated patients (8 , 9) . To minimize the incidence and severity of these reactions, premedication with histamine 1 and 2 blockers, as well as glucocorticoids (usually dexamethasone), has become standard practice (10) . The cumulative side effects of dexamethasone used as a premedication may add to treatment-related morbidity and, in some instances, result in early discontinuation of therapy. Cremaphor EL may also contribute to chronic paclitaxel toxic effects, such as peripheral neuropathy (11) . An additional problem arising from the Cremophor and ethanol solvent is the leaching of plasticizers from PVC bags and infusion sets in routine clinical use (12) . Consequently, Taxol must be prepared and administered in either glass bottles or non-PVC infusion systems and with in-line filtration. These problematic issues have spurred interest in the development of taxanes with improved solubility in aqueous solutions (13) .

ABI-007 is a novel Cremophor-free formulation of paclitaxel (14) . It is prepared by high-pressure homogenization of paclitaxel in the presence of human serum albumin, resulting in a nanoparticle colloidal suspension. Like Taxol, ABI-007 dosage is determined by the paclitaxel content of the formulation, making direct comparison of the two drugs possible. ABI-007 can be reconstituted in normal saline at concentrations of 2–10 mg/ml, compared with 0.3–1.2 mg/ml for Taxol. Thus, the volume and time required for administration is reduced. In the absence of Cremophor EL, the risk of hypersensitivity reactions should decrease significantly, and patients receiving ABI-007 might thus avoid premedication. Moreover, there is no danger of leaching plasticizers from infusion bags or tubing, and conventional PVC infusion systems may be safely used.

To explore the potential clinical utility of ABI-007, we have conducted a Phase I study of this drug for patients with advanced solid tumors. The objectives of this trial were to determine the toxic effects, MTD, and pharmacokinetic profile of this unique paclitaxel preparation.

PATIENTS AND METHODS

Patient Eligibility and Evaluation on Study.

Eligible patients included those with a diagnosis of an advanced solid tumor, having failed standard therapy. Requirements included a Zubrod performance status of 0–3, an expected survival of >6 weeks, hemoglobin ≥ 9 g/dl, ANC ≥ 1,500/mm3, platelet count ≥ 100,000/mm3, serum creatinine < 2 mg/dl, and serum bilirubin < 1.5 mg/dl. Patients with prior exposure to taxanes were eligible for the study.

Pretreatment evaluations included a complete blood count with differential and platelet count, serum chemistry profile, chest radiograph, and electrocardiogram. Baseline imaging studies and serum tumor marker levels were obtained at the discretion of the treating physician. Brain imaging by computerized tomography or magnetic resonance imaging was required for patients with symptoms suggestive of central nervous system involvement. Evaluations performed during the study included a complete blood count with differential and platelet count at least once weekly and a chemistry profile prior to each course. Restaging was performed after every 2nd or 3rd cycle of therapy. Patients were removed from the study for progression of disease, unacceptable toxicity, or at the patient’s request.

Study Design.

This Phase I study was conducted at The University of Texas M. D. Anderson Cancer Center and was approved by the M. D. Anderson Institutional Review Board. Informed consent was obtained from all subjects. Toxicity was graded according to National Cancer Institute Common Toxicity Criteria. Dose levels of ABI-007 are shown in Table 1⇓ . Dose escalation followed the standard “3 + 3” rule. Briefly, 3 patients were accrued at the starting dose level. If no toxic effects greater than grade 2 were observed, 3 patients were entered at the next dose level. If, at any level, one of the first 3 patients experienced a grade 3 or 4 toxic effect, 3 additional patients were entered at that dose level. The MTD was defined as one dose level below that at which ≥2 patients experienced grade 3 or 4 toxic effects. Six patients were to be treated at the MTD. Patients were permitted to escalate to the next higher dose level if no significant toxic effects were observed after the first 2 cycles of therapy. Patients with toxicity greater than grade 2 were permitted to reduce dosage by one dose level and remain on therapy at the discretion of the treating physician.

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Table 1

Dose levels

Treatment.

ABI-007 was supplied by American Bioscience, Inc. (Santa Monica, CA). All therapy was administered in the outpatient treatment center of the M. D. Anderson Cancer Center, with the exception of patients participating in pharmacokinetic studies, which required an overnight hospital stay. The prescribed dose of ABI-007 was prepared in 100–150 ml of 0.9% saline. The drug was administered i.v. without in-line filtration and without premedication. For the first 3 patients on study, the total dose of ABI-007 was administered at a rate of 1.4 mg/kg/h or roughly over 3 h. If no acute hypersensitivity reactions were noted, the remainder of the patients were to receive treatment over 30 min. One cycle of therapy was 21 days.

Pharmacokinetic Studies.

Pharmacokinetic studies were performed in 16 patients, with at least 3 patients representing each dose level. Whole blood samples of 5 ml each were taken to determine the pharmacokinetics of ABI-007 at 13 time points: 0, 0.25, 0.5, 1, 1.5, 2, 4, 6, 8, 12, 18, 24, and 48 h. Paclitaxel was extracted from whole blood samples using protein precipitation with acetonitrile, followed by solid phase extraction. The sample extracts were analyzed for paclitaxel using liquid chromatography atmospheric pressure ionization tandem mass spectrometry. The limit of quantitation for paclitaxel is 5 ng/ml, and the range of reliable response is 5–1000 ng/ml.

Pharmacokinetic parameters were determined from each patient’s whole blood/plasma paclitaxel concentration profile. Analysis was performed by the noncompartmental routine using WinNonlin software (Pharsight Corp., Mountain View, CA). The peak or maximum paclitaxel concentration (Cmax) and the corresponding peak time (tmax) were observed values. The elimination constant (λ12z) was obtained by log-linear regression analysis of the terminal phase of the whole blood/plasma concentration versus time profile. The elimination half-life (T1/2) was determined by taking the ratio of natural log of 2 and λ12z. The AUC from time 0 to time infinity (AUCinf) was obtained by summation of AUClast (AUC from time 0 to last measurable concentration, calculated by the linear trapezoidal rule) and AUCext (extrapolated area, estimated by taking the ratio between the last measurable concentration and λ12z). The dose area relationship (i.e., total ABI-007 dose divided by AUCinf) was used to determine total body CL. The volume of distribution (Vz) was determined by taking the ratio between CL and λ12z.

Descriptive statistics (mean, median, SD, coefficient of variation, maximum, and minimum) were computed for pertinent pharmacokinetic parameters by ABI-007 dose. Regression analysis of mean AUCinf versus dose was performed to gain an appreciation of pharmacokinetic linearity, if evident, for the dose range evaluated in this trial. Differences in the means of Cmax and AUCinf between groups of patients were analyzed for significance using a two-tailed, two-sample t test. Pearson’s correlation coefficient was used to examine the correlation between degree of myelosuppression and Cmax or AUCinf.

RESULTS

Patients.

Twenty patients were enrolled in the trial. One of these chose not to be treated after signing an informed consent. Therefore, 19 patients received drug and were evaluable for toxic effects. Patient characteristics are summarized in Table 2⇓ .

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Table 2

Patient characteristics

Treatment and MTD Determination.

All treatment was administered without dexamethasone or histamine 1 or 2 blockers. The first 3 patients received infusions of ABI-007 over 2–3 h. No hypersensitivity reactions were observed. Therefore, all subsequent infusions were administered over 30 min. Even at the faster infusion rate, there were no instances of acute hypersensitivity to the ABI-007 preparation.

Three patients were entered initially at level 0, receiving 135 mg/m2 over 3 h. One of these experienced progression of disease over the next several weeks, with rapid clinical deterioration, making it difficult to ascertain toxic effects of ABI-007 in this individual. To verify toxicity data at this dose level and ascertain the safety of administering the drug over a short infusion period, a 4th patient was entered at level 0 and was the first patient to receive drugs over 30 min. There were no instances of grade 3 or 4 toxicity observed at dose levels 0 or 1 (200 mg/m2). At dose level 2 (300 mg/m2), 1 of the first 3 patients developed grade 3 sensory neuropathy. Three more patients were accrued at this level, with no additional observations of dose-limiting toxicity. At dose level 3 (375 mg/m2), during the 1st cycle of treatment, one of the first 3 patients experienced grade 3 sensory neuropathy, grade 3 stomatitis, and a visual disturbance diagnosed as superficial keratopathy, also grade 3. An additional 3 patients were accrued at level 3. One patient from this second cohort experienced a similar spectrum of grade 3 toxic effects, including sensory neuropathy, stomatitis, and superficial keratopathy; this patient developed grade 3 vomiting and diarrhea and thrombocytopenia as well. An additional case of sensory neuropathy, this time as an isolated grade 3 toxic effect, was observed in a 3rd patient at level 3. The study was thus terminated. The MTD for ABI-007 administered as a 30-min infusion every 21 days, as determined by this study, was 300 mg/m2. The dose-limiting toxic effects were sensory neuropathy, stomatitis, and superficial keratopathy. Specific toxic effects are described below.

Hematological Toxicity.

Hematological toxicity was dose dependent but remained modest throughout the study (Table 3)⇓ . Of the 96 treatment cycles administered, only 7 (7.3%) resulted in an ANC nadir < 500/mm3, 6 of which occurred above the MTD at dose level 3. There was one hospital admission for febrile neutropenia. In only one case did the platelet count drop below 75,000/mm3. The patient, who was found to have a platelet nadir of 25,000/mm3 during her 1st cycle of therapy at level 3, also developed a constellation of grade 3 nonhematological toxic effects. This was the only individual who required a platelet transfusion during the study. No patients received growth factors for granulocyte support.

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Table 3

Median absolute neutrophil and platelet nadirs by dose level

Nonhematological Toxicity.

Table 4⇓ summarizes the nonhematological toxic effects observed during the first 2 cycles of therapy at each dose level. The majority of these were grades 1 and 2; no patient manifested grade 4 toxicity. Nausea, vomiting, and muscle and joint aches were common but mild. Skin toxicity was also mild, consisting of dry skin or localized vesicular or pustular rash. Alopecia was universal. Peripheral neuropathy, absent at the lower dose levels, was common with higher doses, appearing in 11 of 12 patients treated at levels 2 and 3. The neuropathy occurred in a typical stocking/glove distribution and was manifested by numbness or pain. Six patients with peripheral neuropathy developed peri-oral numbness as well. As described above, the most severe nonhematological adverse effects occurred in 2 patients at dose level 3, consisting of a complex of peripheral neuropathy, stomatitis, and superficial keratopathy, all grade 3.

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Table 4

Nonhematologic toxicity by dose levela

A variety of ocular side effects was observed, the severity of which appeared to be dose dependent. One patient, entered at level 0, complained of dry eyes but noted no visual disturbance. No ocular complaints were registered by patients treated at level 1. Four patients developed ocular toxicity at level 2. One noted intermittent “smoky” vision, and another experienced blurred vision, both occurring with cycle 1 and both presenting as grade 1. Two other patients at dose level 2 noted “flashing lights” and photosensitivity during their third course of treatment. One went on to develop grade 2 superficial keratopathy during course 4. The other experienced a reversible decrease in visual acuity without specific abnormalities on ophthalmologic exam. At level 3, 2 patients complained of mild dry eyes throughout therapy but did not experience visual disturbances. Two other patients at dose level 3 developed grade 3 superficial keratopathy during their 1st cycle of treatment, as described above. All cases of keratopathy received full ophthalmologic evaluation, and all resolved with the use of topical lubricating drops and ointments. No patient developed a permanent loss of vision or experienced any other permanent ocular sequellae.

Occurrences of new types of toxic effects after the first 2 cycles of therapy were rare. Furthermore, it was uncommon for toxic effects to increase in grade after the first 2 treatment cycles. Therefore, cumulative toxicity did not appear to be a significant problem.

Response.

Partial responses were observed in two breast cancer patients, both of whom had prior exposure to Taxol. The first patient, entered at dose level 2, experienced a 68% decrease in the size of pulmonary metastases. This response lasted a total of 15 months, including 9 months after discontinuation of therapy for toxicity. The 2nd patient, who was also treated at dose level 2, had significant improvement in soft tissue disease involving the chest wall. Because of toxic effects, she was taken off treatment on the date of her response. Disease progression was noted 6 weeks later.

Pharmacokinetic Studies.

Sixteen of the 19 patients entered into the study contributed analyzable pharmacokinetic profiles. Three of these received ABI-007 as a 180-min infusion; the remaining 13 were treated over 30 min. A semilog plot of the mean values of the whole blood paclitaxel concentration for each dose level versus time is shown in Fig. 1⇓ . The maximum paclitaxel concentrations were observed at the termination of ABI-007 infusion; the decline from maximum was biphasic.

Fig. 1.
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Fig. 1.

Pharmacokinetic profile of ABI-007 showing mean whole blood paclitaxel concentrations at increasing doses of ABI-007 versus time. All infusions were given over 30 min except for the first 3 patients who received 135 mg/m2 over 180 min.

A summary of the pharmacokinetic parameter values derived by noncompartmental methods is shown in Table 5⇓ . The pharmacokinetics of ABI-007 administered over 30 min appeared to be linear across the three lower dose levels, which included the MTD (Fig. 2)⇓ . Calculations from the data in Table 5⇓ reveal a 2.2-fold increase in Cmax and a 2.7-fold increase in AUCinf over the 2.2-fold increase in dose from 135 to 300 mg/m2. The decline in CL estimates over this range is 0.8-fold (16.1%). If the highest dose level of 375 mg/m2 is included, nonlinearity becomes evident (Fig. 2)⇓ . Individual Cmax and AUCinf values versus dose are shown in Fig. 3, a and b⇓ , respectively.

Fig. 2.
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Fig. 2.

Correlation between the mean AUCinf and dose level. The data have been fit using a linear regression and an exponential regression function.

Fig. 3.
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Fig. 3.

Individual values of Cmax (a) and AUCinf (b) versus dose for patients receiving 30-min infusions of ABI-007.

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Table 5

Summary of noncompartmental pharmacokinetic parameters, mean (% coefficient of variation) values by dosea

The group of 13 patients who received 30-min infusions and for whom pharmacokinetic profiles were obtained included 3 who experienced grade 3 nonhematological toxic effects (neuropathy with or without stomatitis and keratopathy). The Cmax and AUCinf for these 3 patients relative to those of the remaining 10 patients are plotted in Fig. 4⇓ . The differences in mean Cmax and mean AUCinf between the two groups were significant (P = 0.034 and 0.007, respectively). The effect of ABI-007 exposure on myelosuppression was also examined in this group of patients. The percentage of decrease in ANC from baseline to nadir was found to correlate positively with both Cmax (r = 0.610, P = 0.027) and AUCinf (r = 0.614, P = 0.025).

Fig. 4.
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Fig. 4.

Individual values of Cmax (a) and AUCinf (b) for patients who experienced grade 3 nonhematological toxic effects (“yes”) and those who did not (“no”). In the “yes” category, the solid diamond symbols (♦) represent 2 patients with multiple grade 3 toxicities, whereas the open circle (○) represents the patient with only grade 3 neuropathy.

DISCUSSION

This clinical trial was conducted to examine the pharmacokinetic properties and spectrum of toxic effects associated with ABI-007. Because ABI-007 is not formulated in a Cremophor-containing solvent, we anticipated that hypersensitivity reactions would be diminished or absent. Our results show that ABI-007 can indeed be administered safely as a short infusion without dexamethasone or antihistamine premedication. Thus, when considering the process of drug administration, ABI-007 appears to offer advantages in terms of safety (avoidance of hypersensitivity reactions), morbidity (avoidance of dexamethasone premedication), and patient convenience and comfort (less time spent in the treatment center). These advantages could ultimately translate into an overall decrease in cost of therapy.

It must be pointed out that, although the absence of Cremophor is clearly desirable with respect to toxicity, this same compound has been proposed to enhance the efficacy of cytotoxic drugs through reversal of the multidrug resistance phenotype (15) . Plasma concentrations of Cremophor attainable during Taxol infusions are sufficient to inhibit P-glycoprotein effects in vitro (16) . However, there have been questions raised as to whether these Cremophor concentrations are relevant to solid tumors, as pharmacokinetic studies demonstrate the compound’s distribution to be limited to the central plasma compartment (17) . This issue should be clarified with the completion of ongoing Phase II trials of ABI-007. If the response rate of ABI-007 is not less than that of Taxol and if responses are seen in patients who are previous taxane failures, the therapeutic contribution of Cremophor to paclitaxel can be considered negligible.

In terms of treatment-related toxicity, a lower incidence of myelosuppression was observed than that which we anticipated based on the dose of paclitaxel administered. In this regard, hematological toxicity was mild and played virtually no role in dose and treatment decisions made in this trial. Although direct comparisons to Taxol administered at this dose range and schedule are not possible, the myelosuppression induced by ABI-007 appeared to be similar to or less severe than that reported for 1-h Taxol infusions at lower doses (18) . Otherwise, the spectrum of toxic effects produced by ABI-007 resembled that of high-dose short-infusion Taxol reported in early Phase I trials, with sensory neuropathy and mucositis becoming dose limiting (19 , 20) . A third dose-limiting toxic effect, superficial keratopathy, was also observed. We were unable to find any prior report of superficial keratopathy as a consequence of paclitaxel administration. In our Phase I trial, this side effect appeared to be related to dose and presented at the level of grade 3 only above the MTD, at a dose of 375 mg/m2. Superficial keratopathy secondary to ABI-007 was similar to that most commonly recognized in association with 1-β-D-arabinofuranosylcytosine, although any type of ocular surface irritation, including dry eye syndrome, can result in similar corneal findings (21) . Other ocular complications of taxane therapy have been reported. The most common adverse ocular effects of Taxol are photopsia and blurred vision, usually reported by patients during the infusion period (22 , 23) . Cases of optic nerve disturbances have also been documented (24) . Cases of grade 2 conjunctivitis necessitating dose reduction and treatment delay have been reported during weekly therapy with docetaxel (25) . Similar to our findings, reported ocular effects from paclitaxel have been noted only at higher doses and are usually transient. Although all cases of keratopathy in this study resolved completely and without permanent sequellae, in the ensuing Phase II trial, patients will be aggressively monitored for the development of ophthalmologic abnormalities.

Pharmacokinetic analysis of ABI-007 revealed interesting similarities and differences relative to Taxol, based on published data. Disappearance from the blood is biphasic for both drugs (19) . ABI-007 displays linear pharmacokinetics over the clinically relevant dose range of 135–300 mg/m2; over a similar dose range, Taxol AUCinf is nonlinear (26, 27, 28) . In comparing the AUCinf values of ABI-007 infused over 30 min to those reported for Taxol infused over 1 or 3 h, ABI-007 in general showed lower AUCinf values over a similar range of doses (26, 27, 28) . Although several explanations are possible for the differences in AUCinf, it is reasonable to hypothesize that ABI-007 may be distributed more rapidly out of the vascular compartment, a suggestion supported by the difference in formulation between the two drugs. A substantial amount of solvent (Cremophor/ethanol) is infused with Taxol, and the partition of paclitaxel from the vascular compartment to the tissues may thus be relatively slow. In contrast, ABI-007 is formulated with human serum albumin at a concentration of 3–4%, similar to the concentration of albumin in the blood. Because paclitaxel has a very limited solubility in an aqueous albumin solution (<30 μg/ml), it may partition more efficiently into the tissues in the case of ABI-007. Furthermore, lipid, macromolecular, and nanoparticle drug carriers have been known to preferentially accumulate in tumor beds and tissues in what is known as enhanced permeation and retention effect (29) . These factors may facilitate the partition of ABI-007 into tissues.

The MTD of ABI-007 was found in this study to be 300 mg/m2 when given as a short infusion on a 21-day cycle. Although the usual dose range for Taxol is 135–200 mg/m2, doses as high as 250 mg/m2 are occasionally administered. Therefore, the MTD established by this trial represents a moderate increase over that of Taxol. The issue of whether one can achieve uniform and repeated dosing of ABI-007 at the MTD will need to be addressed in Phase II trials.

In conclusion, ABI-007 appears to represent an improvement in paclitaxel formulation in that it can be administered rapidly and safely without the risk of hypersensitivity reactions, eliminating the need for steroid and antihistamine premedication. Furthermore, the increased MTD and favorable toxicity profile of ABI-007 may ultimately prove advantageous in terms of rate and quality of response. Although several interesting pharmacokinetic properties were noted for ABI-007, the small number of patients in this study renders comparisons with Taxol preliminary, and additional studies will need to be conducted to fully appreciate differences in pharmacokinetic behavior. The partial responses seen in 2 patients with prior exposure to Taxol are encouraging and support a continued effort to explore the spectrum of activity for this drug. We are currently conducting a Phase II trial of ABI-007 for patients with metastatic breast cancer to establish the antitumor activity of this novel paclitaxel formulation.

Acknowledgments

We thank Drs. Timothy Madden and Laura Boehnke Michaud for their critical reviews of the manuscript.

Footnotes

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

  • ↵1 Supported by American Bioscience, Inc., Santa Monica, CA.

  • ↵2 To whom requests for reprints should be addressed, at Department of Molecular and Cellular Oncology, Box 79, M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Houston, TX 77030. Phone: (713) 792-8990; Fax: (713) 794-0209; E-mail: jaellerh{at}mail.mdanderson.org

  • ↵3 The abbreviations used are: MTD, maximum tolerated dose; ANC, absolute neutrophil count; AUC, area under the curve; CL, clearance; PVC, polyvinyl chloride.

  • Received September 25, 2001.
  • Revision received January 23, 2002.
  • Accepted February 1, 2002.

References

  1. ↵
    Crown J., O’Leary M. The taxanes: an update. Lancet, 355: 1176-1178, 2000.
    OpenUrlCrossRefPubMed
  2. ↵
    Eisenhauer E. A., ten Bokkel Huinink W. W., Swenerton K. D., Gianni L., Myles J., van der Burg M. E. L., Kerr I., Vermorken J. B., Buser K., Colombo N., Bacon M., Santabarbara P., Onetto N., Winograd B., Canetta R. European-Canadian randomized trial of paclitaxel in relapsed ovarian cancer: high-dose versus low-dose and long versus short infusion. J. Clin. Oncol., 12: 2654-2666, 1994.
    OpenUrlAbstract/FREE Full Text
  3. ↵
    Nabholtz J. M., Gelmon K., Bontenbal M., Spielmann M., Catimel G., Conte P., Klaassen U., Namer M., Bonneterre J., Fumoleau P., Winograd B. Multicenter randomized comparative study of two doses of paclitaxel in patients with metastatic breast cancer. J. Clin. Oncol., 14: 1858-1867, 1996.
    OpenUrlAbstract/FREE Full Text
  4. ↵
    Smith R. E., Brown A. M., Mamounas E. P., Anderson S. J., Lembersky B. C., Atkins J. H., Shibata H. R., Baez L., DeFusco P. A., Davila E., Tipping S. J., Bearden J. D., Thirlwell M. P. Randomized trial of 3-hour versus 24-hour infusion of high-dose paclitaxel in patients with metastatic or locally advanced breast cancer: National Surgical Adjuvant Breast and Bowel Project Protocol B-26. J. Clin. Oncol., 17: 3403-3411, 1999.
    OpenUrlAbstract/FREE Full Text
  5. ↵
    Wiernik P. H., Schwartz E. L., Einzig A., Strauman J. J., Lipton R. B., Dutcher J. P. Phase I trial of taxol given as a 24-hour infusion every 21 days: responses observed in metastatic melanoma. J. Clin. Oncol., 5: 1232-1239, 1987.
    OpenUrlAbstract/FREE Full Text
  6. ↵
    Socinski M. A., Mudd P. N., Radomski K. M., Steagall A., Lawrence P., Bernard S., Letrent S. P., Gonzalez P., Brouwer K. L. R. Phase I trial of a 96 h paclitaxel infusion with filgrastim support in refractory solid tumor patients. Anticancer Drugs, 9: 611-619, 1998.
    OpenUrlCrossRefPubMed
  7. ↵
    Dorr R. T. Pharmacology and toxicology of Cremophor EL diluent. Ann. Pharmacother., 28: S11-S14, 1994.
  8. ↵
    Weiss R. B., Donehower R. C., Wiernik P. H., Ohnuma T., Gralla R. J., Trump D. L., Baker J. R., Jr., Van Echo D. A., Von Hoff D. D., Leyland-Jones B. Hypersensitivity reactions from taxol. J. Clin. Oncol., 8: 1263-1268, 1990.
    OpenUrlAbstract
  9. ↵
    Rowinsky E. K., Donehower R. C. Paclitaxel (taxol). N. Eng. J. Med., 332: 1004-1014, 1995.
    OpenUrlCrossRefPubMed
  10. ↵
    Finley R. S., Rowinsky E. K. Patient care issues: the management of paclitaxel-related toxicities. Ann. Pharmacother., 28: S27-S30, 1994.
  11. ↵
    Windebank A. J., Blexrud M. D., de Groen P. C. Potential neurotoxicity of the solvent vehicle for cyclosporine. J. Pharmacol. Exp. Ther., 268: 1051-1056, 1994.
    OpenUrlAbstract/FREE Full Text
  12. ↵
    Waugh W. N., Trissel L. A., Stella V. J. Stability, compatibility, and plasticizer extraction of taxol (NSC-125973) injection diluted in infusion solutions and stored in various containers. Am. J. Hosp. Pharm., 48: 1520-1524, 1991.
    OpenUrlAbstract
  13. ↵
    Hidalgo M., Aylesworth C., Hammond L. A., Britten C. D., Weiss G., Stephenson J., Jr, Schwartz G., Patnaik A., Smith L., Molpus K., Felton S., Gupta E., Ferrante K. J., Tortora A., Sonnichsen D. S., Skillings J., Rowinsky E. K. Phase I and pharmacokinetic study of BMS-184476, a taxane with greater potency and solubility than paclitaxel. J. Clin. Oncol., 19: 2493-2503, 2001.
    OpenUrlAbstract/FREE Full Text
  14. ↵
    Desai N. P., Louie L., Ron N., Magdassi S., Soon-Shiong P. Protein-based nanoparticles for drug delivery of paclitaxel. Trans. World Biomater. Congr., 1: 199 2000.
  15. ↵
    Woodcock D. M., Jefferson S., Linsenmeyer M. E., Crowther P. J., Chojnowski G. M., Williams B., Bertoncello I. Reversal of the multidrug resistance phenotype with cremophor EL, a common vehicle for water-insoluble vitamins and drugs. Cancer Res., 50: 4199-4203, 1990.
    OpenUrlAbstract/FREE Full Text
  16. ↵
    Webster L., Linsenmeyer M., Millward M., Morton C., Bishop J., Woodcock D. Measurement of cremophor EL following taxol: plasma levels sufficient to reverse drug exclusion mediated by the multidrug-resistant phenotype. J. Natl. Cancer Inst. (Bethesda), 85: 1685-1690, 1993.
    OpenUrlAbstract/FREE Full Text
  17. ↵
    Sparreboom A., Verweij J., van der Burg M. E., Loos W. J., Brouwer E., Vigano L., Locatelli A., de Vos A. I., Nooter K., Stoter G., Gianni L. Disposition of cremophor EL in humans limits the potential for modulation of the multidrug resistance phenotype in vivo. Clin. Cancer Res., 4: 1937-1942, 1998.
    OpenUrlAbstract
  18. ↵
    Hainsworth J. D., Greco F. A. Paclitaxel administered by 1-hour infusion. Preliminary results of a phase I/II trial comparing two schedules. Cancer (Phila.), 74: 1377-1382, 1994.
    OpenUrlCrossRefPubMed
  19. ↵
    Wiernik P. H., Schwartz E. L., Strauman J. J., Dutcher J. P., Lipton R. B., Paietta E. Phase I clinical and pharmacokinetic study of taxol. Cancer Res., 47: 2486-2493, 1987.
    OpenUrlAbstract/FREE Full Text
  20. ↵
    Donehower R. C., Rowinsky E. K., Grochow L. B., Longnecker S. M., Ettinger D. S. Phase I trial of taxol in patients with advanced cancer. Cancer Treat. Rep., 71: 1171-1177, 1987.
    OpenUrlPubMed
  21. ↵
    Ritch P. S., Hansen R. M., Heuer D. K. Ocular toxicity from high-dose 1-β-D-arabinofuranosylcytosine. Cancer (Phila.), 51: 430-432, 1983.
    OpenUrlCrossRefPubMed
  22. ↵
    Tan W. W., Walsh T. Ocular toxicity secondary to paclitaxel in two lung cancer patients. Med. Pediatr. Oncol., 31: 177 1998.
    OpenUrlCrossRefPubMed
  23. ↵
    Seidman A. D., Barrett S., Canezo S. Photopsia during 3-hour paclitaxel administration at doses ≥ 250 mg/m2. J. Clin. Oncol., 12: 1741-1742, 1994.
    OpenUrlFREE Full Text
  24. ↵
    Al-Tweigeri T., Nabholtz J. M., Mackey J. R. Ocular toxicity and cancer chemotherapy. Cancer (Phila.), 78: 1359-1373, 1996.
    OpenUrlCrossRefPubMed
  25. ↵
    Burstein H. J., Younger J., Bunnell C. A., Matulonis U. A., Garber J. E., Shulman L. N., Parker L. M., Scheib R., Clarke K., Fowler K., Gelman R., Winer E. P. Weekly docetaxel (Taxotere) for metastatic breast cancer: a phase II trial. Proc. Am. Soc. Clin. Oncol., 18: 127 1999.
    OpenUrl
  26. ↵
    Kearns C. M. Pharmacokinetics of taxanes. Pharmacotherapy, 17: 105S-109S, 1997.
    OpenUrlPubMed
  27. ↵
    Mross K., Hollander N., Hauns B., Schumacher M., Maier-Lenz H. The pharmacokinetics of a 1-h paclitaxel infusion. Cancer Chemother. Pharmacol., 45: 463-470, 2000.
    OpenUrlCrossRefPubMed
  28. ↵
    Gianni L., Kearns C. M., Giani A., Capri G., Vigano L., Locatelli A., Bonadonna G., Egorin M. J. Nonlinear pharmacokinetics and metabolism of paclitaxel and its pharmacokinetic/pharmacodynamic relationships in humans. J. Clin. Oncol., 13: 180-190, 1995.
    OpenUrlAbstract/FREE Full Text
  29. ↵
    Maeda H., Wu J., Sawa T., Matsumura Y., Hori K. Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. J. Control Release, 65: 271-284, 2000.
    OpenUrlCrossRefPubMed
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May 2002
Volume 8, Issue 5
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Phase I and Pharmacokinetic Study of ABI-007, a Cremophor-free, Protein-stabilized, Nanoparticle Formulation of Paclitaxel
Nuhad K. Ibrahim, Neil Desai, Sewa Legha, Patrick Soon-Shiong, Richard L. Theriault, Edgardo Rivera, Bita Esmaeli, Sigrid E. Ring, Agop Bedikian, Gabriel N. Hortobagyi and Julie A. Ellerhorst
Clin Cancer Res May 1 2002 (8) (5) 1038-1044;

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Phase I and Pharmacokinetic Study of ABI-007, a Cremophor-free, Protein-stabilized, Nanoparticle Formulation of Paclitaxel
Nuhad K. Ibrahim, Neil Desai, Sewa Legha, Patrick Soon-Shiong, Richard L. Theriault, Edgardo Rivera, Bita Esmaeli, Sigrid E. Ring, Agop Bedikian, Gabriel N. Hortobagyi and Julie A. Ellerhorst
Clin Cancer Res May 1 2002 (8) (5) 1038-1044;
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