View Clinical Trial (Medical Research Study)
A Phase I/II Study of Radiation Therapy, Paclitaxel Poliglumex and Cetuximab in Advanced Head and Neck Cancer
| City: |
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Syracuse |
| State: |
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New York |
| Zip Code: |
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13210 |
| Conditions: |
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Carcinoma, Squamous Cell |
| Purpose: |
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This study involves two phases. Phase I of this study is designed to find out the maximum
dose of paclitaxel poliglumex which can be safely given to subjects when combined with
cetuximab and radiotherapy in head and neck cancer. Once the maximum safe dose of
paclitaxel poliglumex is found, Phase II of the study will continue to find out whether the
addition of paclitaxel poliglumex increases tumor response and survival compared to
treatment with cetuximab and radiotherapy alone.
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| Study Summary: |
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Patients with locally advanced (stage III and IV) head and neck cancer are often managed by
radiotherapy with or without chemotherapy because most of them have unresectable tumor,
require too extensive surgery, or are medically unfit to go through radical surgery.
However, the treatment results from conventionally fractionated radiotherapy for locally
advanced head and neck cancers are poor in terms of local control and survival. Therefore,
combinations of radiation and chemotherapy have been studied to improve treatment results.
Sequential radiation-chemotherapy (most given in neo-adjuvant setting) has been studied
extensively in prospective pilot and large randomized trials. So far, a survival advantage
over standard radiotherapy has not been demonstrated, but organ preservation has been
achieved in many patients. Response rates to chemotherapy are high, and decrease in distant
metastases has been demonstrated in some trials. Despite a high response rate in trials
comparing neoadjuvant chemotherapy and radiotherapy to radiotherapy alone, improved
locoregional control (LRC) has not been shown. Concurrent radiation and cisplatin-based
chemotherapy has shown survival advantage over radiotherapy alone in meta-analysis.
However, the administration of cisplatin-based chemotherapy is associated with significantly
increased local and systemic toxic effects, which may preclude many patients from proceeding
with combined therapy. Therefore, there is a great interest in defining an active regimen
that does not contain cisplatin.
An alternative approach to concurrent chemotherapy and radiotherapy has emerged with the
development of molecular targeted agents. A recently reported randomized phase III study
demonstrated improved duration of control of locoregional disease and overall survival with
the addition of the antibody against the epidermal growth factor receptor, cetuximab, to
definitive radiotherapy in patients with squamous cell carcinoma of the head and neck.
Importantly, cetuximab administration did not increase radiation-related toxicity.
The most commonly used chemotherapy other than cisplatin chemotherapy for the treatment of
advanced head and neck cancer is paclitaxel. There are many studies showing improvement of
tumor control when paclitaxel was added to the radiotherapy. Paclitaxel poliglumex (PPX,
CT-2103, Xyotax) is a macromolecule that consists of a biodegradable, water-soluble polymer
of glutamic acid, a naturally-occurring amino acid, linked to paclitaxel. Preclinical
studies suggest increased tumor uptake of PPX compared with paclitaxel, resulting in
enhanced tumor cell kill. PPX may potentiate tumor radiocurability without affecting acute
normal tissue injury. Moreover, a synergistic increase in tumor cell death was observed
when paclitaxel poliglumex was administered with cetuximab in a preclinical tumor model.
The proposed study will assess the rational combination of PPX with radiotherapy and
cetuximab. This regimen is of great interest and has the potential to improve the
therapeutic ratio compared with an approach of either cisplatin-based chemoradiotherapy or
radiotherapy and cetuximab.
There is also an optional tissue submission component of this study, in which subjects who
require surgery following their treatment can give permission for a block of tumor tissue
removed at the time of their surgery to be sent to Cell Therapeutics, Inc. (the manufacturer
of PPX) for evaluation of PPX accumulation, level of cathepsin B, and estrogen receptor
expression. This information will be used to correlate the tumor response and survival of
patients in the future.
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| Criteria: |
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Inclusion Criteria:
- Patients with histological proof (from the primary lesion and/or cervical lymph node)
of squamous carcinoma of the oral cavity, oropharynx, hypopharynx, larynx, or unknown
primary.
- Patients should have stage III or IV disease
- Patients must have ECOG Performance Status of 0-1
- Patients must be >/= 18 years of age
- Patients must have measurable disease
- Patients should have adequate bone marrow function defined as an absolute peripheral
granulocyte count (AGC) of >/= 1500 cells/mm3, platelet count of >/= 100,000 cells/
mm3; adequate hepatic function with bilirubin </= 1.5mg/dl, AST and ALT </= 2x the
upper limit of normal; serum creatinine </= 1.5mg/dl, creatinine clearance >/= 50
ml/min and INR 0.8 - 1.2
- Patients must sign a study specific informed consent form prior to study entry
Exclusion Criteria:
- Histology other than squamous cell carcinoma
- Evidence of metastases (below the clavicle or distant) by clinical or radiographic
examinations for phase II study subjects
- History of malignancy other than non-melanoma skin cancer
- Prior chemotherapy or anticancer biologic therapy for any type of cancer, or prior
radiotherapy to the head and neck region except for radioactive iodine therapy
- Prior history of allergy or hypersensitivity to cetuximab or paclitaxel
- Weight loss > 10% in the past three months
- Patients with uncontrolled intercurrent disease
- Patients with currently active malignancy
- Pregnant or lactating women
- Female patients of childbearing potential who are unwilling to practice adequate
contraception during study treatment and for two months after the last administration
of study drug
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| NCT ID: |
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NCT00660218 |
| Primary Contact: |
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Principal Investigator
Seung Shin Hahn, MD
State University of New York - Upstate Medical University
Dena R Martin, CRA
Phone: 315-464-5262
Email: martind@upstate.edu
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| Backup Contact: |
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N/A |
| Location Contact: |
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Syracuse, New York 13210
United States
There is no listed contact information for this specific location.
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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May 25, 2013 |
| Modifications to this listing: |
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