Trial Search Results

Radiation Therapy With or Without Chemotherapy in Treating Patients With High-Risk Malignant Salivary Gland Tumors That Have Been Removed By Surgery

The purpose of this trial is to study radiation therapy with or without chemotherapy to see how well it works in treating patients with high-risk malignant salivary gland tumors that have been removed by surgery.

Stanford is currently accepting patients for this trial.

Lead Sponsor:

Radiation Therapy Oncology Group

Collaborator: NRG Oncology

Stanford Investigator(s):

Intervention(s):

  • Drug: cisplatin
  • Radiation: 3-dimensional conformal radiation therapy
  • Radiation: intensity-modulated radiation therapy

Phase:

Phase 2

Eligibility


DISEASE CHARACTERISTICS:

   - Pathologically proven diagnosis of a malignant major salivary gland tumor or malignant
   minor salivary gland tumor of the head and neck of the following histologic subtypes:

      - Intermediate-grade adenocarcinoma or intermediate-grade mucoepidermoid carcinoma

      - High-grade acinic cell carcinoma or high-grade (>30% solid component) adenoid
      cystic carcinoma

   - Surgical resection with curative intent within 8 weeks prior to registration

   - All patients must have a Medical Oncology evaluation within 4 weeks prior to
   registration

   - Pathologic stage T3-4 or N1-3 or T1-2, N0 with a close (≤ 1mm) or microscopically
   positive surgical margin; patients must be free of distant metastases based upon the
   following minimum diagnostic workup:

      - History/physical examination within 8 weeks prior to registration

      - Radiologic confirmation of the absence of hematogenous metastasis within 12 weeks
      prior to registration; at a minimum, contrast CT imaging of the chest is required
      (PET/CT is acceptable)

   - No patients with residual macroscopic disease after surgery

   - No prior systemic chemotherapy or radiation therapy for salivary gland malignancy

PATIENT CHARACTERISTICS:

   - Zubrod performance status 0-1

   - Absolute neutrophil count (ANC) ≥ 1,800 cells/mm^3

   - Platelets ≥ 100,000 cells/mm^3

   - Hemoglobin ≥ 8.0 g/dL (the use of transfusion or other intervention to achieve
   hemoglobin ≥ 8.0 g/dL is acceptable)

   - Serum creatinine < 2.0 mg/dL

   - Total bilirubin < 2 x the institutional upper limit of normal (ULN)

   - Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) < 3 x the
   institutional ULN

   - Negative serum pregnancy test within 2 weeks prior to registration for women of
   childbearing potential

   - Women of childbearing potential and male participants who are sexually active must
   practice adequate contraception during treatment and for 6 weeks following treatment

   - Not pregnant or nursing

   - Patients must be deemed able to comply with the treatment plan and follow-up schedule

   - Patients must provide study specific informed consent prior to study entry, including
   consent for mandatory tissue submission for central review

   - No prior invasive malignancy (except non-melanomatous skin cancer) unless disease free
   for a minimum of 3 years (for example, carcinoma in situ of the breast, oral cavity,
   or cervix are all permissible)

   - No severe, active co-morbidity, defined as follows:

      - Unstable angina and/or congestive heart failure requiring hospitalization within
      the last 6 months

      - Transmural myocardial infarction within the last 6 months

      - Acute bacterial or fungal infection requiring intravenous antibiotics at the time
      of registration

      - Chronic Obstructive Pulmonary Disease exacerbation or other respiratory illness
      requiring hospitalization or precluding study therapy at the time of registration

      - Hepatic insufficiency resulting in clinical jaundice and/or coagulation defects
      (coagulation parameters are not required for entry into this protocol)

      - Acquired immune deficiency syndrome (AIDS) based upon current Centers for Disease
      Control (CDC) definition (HIV testing is not required for entry into this
      protocol)

         - Protocol-specific requirements may also exclude immunocompromised patients

      - Pre-existing ≥ grade 2 neuropathy

   - No significant pre-existing hearing loss, as defined by the patient or treating
   physician

PRIOR CONCURRENT THERAPY:

   - See Disease Characteristics

   - No prior systemic chemotherapy or radiation therapy for salivary gland malignancy
   (prior chemotherapy for a different cancer is allowable)

   - No prior radiotherapy to the region of the study cancer that would result in overlap
   of radiation therapy fields

   - No prior organ transplant

   - No concurrent hematopoietic growth factors (e.g., G-CSF or pegfilgrastim) during
   radiotherapy

   - No concurrent erythropoiesis-stimulating agents

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Now accepting new patients

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Amanda Simmons
650-724-4606
Recruiting