Induction Chemotherapy Using Doxorubicin and Cisplatin Followed by Combretastatin A4 Phosphate and Radiation Therapy in Treating Patients With Newly Diagnosed Regionally Advanced Anaplastic Thyroid Cancer

• Status: Terminated
• Trial end date: 2007-12-01
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Drugs used in chemotherapy, such as doxorubicin and cisplatin, work in different ways to stop tumor cells from dividing so they stop growing or die. Radiation therapy uses high-energy x-rays to damage tumor cells. Combretastatin A4 phosphate may stop the growth of cancer by stopping blood flow to the tumor. Combining doxorubicin and cisplatin with radiation therapy and combretastatin A4 phosphate may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving induction chemotherapy using doxorubicin and cisplatin together with radiation therapy and combretastatin A4 phosphate works in treating patients with newly diagnosed regionally advanced anaplastic thyroid cancer.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Case Comprehensive Cancer Center
• Collaborator: National Cancer Institute (NCI)
• Treatments: Cisplatin; Combretastatin; Doxorubicin; Fosbretabulin; Lenograstim; Liposomal doxorubicin

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed anaplastic or poorly differentiated variant thyroid carcinoma of either of the following:

• Regionally advanced disease

• Confined to the neck and/or superior mediastinum (i.e., above the level of the carina)

• Measurable or evaluable* disease

• Completely resected disease without measurable or evaluable disease NOTE: *At a minimum, abnormalities on physical exam or radiographic studies that may not be precisely measured but readily followed

• Must have original/diagnostic tumor blocks available to confirm histopathology and for tumor microvessel density immunohistochemistry

• Patients with no available original/diagnostic tumor blocks must have tumor accessible for pretreatment needle core biopsy

• Must undergo indirect and direct laryngoscopy to ensure patency of the trachea/airway if deemed inoperable, with bulky thyroid/neck masses and/or suspicion of airway obstruction

• No distant metastases, including but not limited to, brain metastases, disease below the level of the carina, pulmonary parenchyma, and hepatic or bony metastases

• Superior mediastinal disease (i.e., above the level of the carina) in addition to regional neck disease is allowed provided the disease can be contained in a single radiotherapy port

PATIENT CHARACTERISTICS:

Age

• 18 and over

Performance status

• ECOG 0-2

Life expectancy

• At least 12 weeks

Hematopoietic

• Absolute granulocyte count ≥ 1,500/mm^3

• Platelet count ≥ 75,000/mm^3

• Hemoglobin ≥ 8.5 g/dL

Hepatic

• Bilirubin ≤ 1.5 mg/dL

• ALT and AST ≤ 3.5 times upper limit of normal

Renal

• Creatinine ≤ 1.5 mg/dL

Cardiovascular

• LVEF ≥ 50% by echocardiogram

• EKG normal

• No prior angina

• No prior myocardial infarction (e.g., significant Q waves), QTc > 450 msec, or other clinically significant abnormalities on ECG

• No congestive heart failure

• No uncontrolled atrial arrhythmias or clinically significant arrhythmias, including any of the following:

• Conduction abnormality

• Nodal junctional arrhythmias and dysrhythmias

• Sinus bradycardia or tachycardia

• Supraventricular arrhythmias

• Atrial fibrillation or flutter

• Syncope or vasovagal episodes

• No significant heart wall abnormality or heart muscle damage by echocardiogram

• No uncontrolled hypertension (i.e., blood pressure consistently greater than 150/100 mm Hg irrespective of medication)

• Hypertension is allowed provided there is clinical documentation of controlled blood pressure for 2 months before study entry

• No symptomatic peripheral vascular disease or cerebrovascular disease

Other

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective contraception

• No uncontrolled hypokalemia or hypomagnesemia

• No concurrent serious infection

• No other nonmalignant uncontrolled medical illness or one whose control may be jeopardized by the complications of study therapy

• No grade 2 or greater pre-existing motor or sensory peripheral neuropathy

• No psychiatric disorder or other condition that would preclude study compliance

• No conditions associated with QTc prolongation

PRIOR CONCURRENT THERAPY:

Biologic therapy

• No concurrent biologic therapy

• No concurrent immunotherapy

Chemotherapy

• No prior chemotherapy

• No other concurrent chemotherapy

Endocrine therapy

• No concurrent hormonal therapy, except for the following:

• Gonadotropin-releasing hormone agonists for patients with hormone-refractory prostate cancer

• Hormone replacement therapy

• Oral contraceptives

• Megestrol for anorexia/cachexia

Radiotherapy

• No prior radiotherapy

• No concurrent radiotherapy

Surgery

• See Disease Characteristics

• Prior attempt at resection or cytoreduction (e.g., debulking) surgery irrespective of surgical margins allowed provided there are no distant metastases

• At least 1 week but no more than 8 weeks since prior surgery and recovered

Other

• No other concurrent cytotoxic therapy

• No other concurrent antineoplastic therapy

• No other concurrent investigational therapy

• No concurrent medications known to prolong the QTc interval unless the medication can be held for at least 4 days during each treatment course