Phase II Capecitabine, Oxaliplatin & Bevacizumab for Metastatic / Unresectable Neuroendocrine Tumors

Not Recruiting

Trial ID: NCT00398320


Given the lack of other viable treatment options for metastatic neuroendocrine tumors, contrasted with our positive anecdotal experience, and the relative tolerability of the treatment regimen for colorectal cancer patients, we propose a single-institution phase II trial investigating the efficacy of capecitabine, oxaliplatin and bevacizumab for patients with metastatic neuroendocrine tumors.

Official Title

A Phase II Study of Capecitabine, Oxaliplatin and Bevacizumab for Metastatic or Unresectable Neuroendocrine Tumors

Stanford Investigator(s)

George A. Fisher Jr.
George A. Fisher Jr.

Colleen Haas Chair in the School of Medicine


Inclusion Criteria: Subjects must be treated at Stanford University Medical Center for the
entire length of study participation.

   - Patients must have histologically or cytologically confirmed neuroendocrine tumor,
   including both well-differentiated tumors (carcinoid) or moderately to poorly
   differentiated tumors. Patients must be deemed unresectable due to involvement of
   critical vasculature, adjacent organ invasion, or presence of metastasis.

   - Patients with prior surgical resection who develop radiological or clinical evidence
   of metastatic cancer do not require separate histological or cytological confirmation
   of metastatic disease unless an interval of > 5 years has elapsed between the primary
   surgery and the development of metastatic disease. Clinicians should consider biopsy
   of lesions to establish diagnosis of metastatic disease if there is substantial
   clinical ambiguity regarding the nature or source of apparent metastases.

   - Prior chemotherapy will be permitted, although the patient may not have had prior

   - Patients must have a primary or metastatic lesion measurable in at least one dimension
   by Modified RECIST criteria (see Section 4.2) within 4 weeks prior to entry of study

   - Patients must have Eastern Cooperative Oncology Group (ECOG) performance status of 0
   to 2

   - Patients must be ≥ 18 years of age

   - Laboratory values ≤ 2 weeks prior to randomization:

      - Absolute Neutrophil Count (ANC) >=1500/mm3

      - Platelets (PLT) ≥ 100,000/mm3

      - Hemoglobin (Hgb) ≥ 9 g/dL

      - Serum creatinine ≤ 1.5 x upper limit of normal (ULN)

      - Serum bilirubin ≤ 1.5 x ULN (≤ 3.0 x ULN if liver metastases present)

      - Aspartate aminotransferase (AST/SGOT), alanine aminotransferase (ALT/SGPT), and
      alkaline phosphatase ≤ 3.0 x ULN (≤ 5.0 x ULN if liver metastases present). Note:
      Endoscopic retrograde cholangiopancreatogram (ERCP) or percutaneous stenting may
      be used to normalize the liver function tests.

   - Life expectancy ≥ 12 weeks

   - Ability to give written informed consent according to local guidelines

Exclusion Criteria:- Disease-Specific Exclusions

   1. Prior oxaliplatin for any reason.

   2. Prior full field radiotherapy ≤ 4 weeks or limited field radiotherapy ≤ 2 weeks prior
   to enrollment. Patients must have recovered from all therapy-related toxicities. The
   site of previous radiotherapy should have evidence of progressive disease if this is
   the only site of disease.

   3. Prior biologic or immunotherapy ≤ 2 weeks prior to registration. Patients must have
   recovered from all therapy-related toxicities

   4. Prior therapy with anti-vascular endothelial growth factor (VEGF) agents

   5. If history of other primary cancer, subject will be eligible only if she or he has:

      - Curatively resected non-melanomatous skin cancer

      - Curatively treated cervical carcinoma in situ

      - Other primary solid tumor curatively treated with no known active disease present
      and no treatment administered for the last 3 years

   6. Concurrent use of other investigational agents and patients who have received
   investigational drugs ≤ 4 weeks prior to enrollment.

      - General Medical Exclusions

1. Subjects known to have chronic or active hepatitis B or C infection 2. History of any
medical or psychiatric condition or laboratory abnormality that in the opinion of the
investigator may increase the risks associated with study participation or study drug
administration or may interfere with the conduct of the study or interpretation of study
results 3. Male subject who is not willing to use adequate contraception upon enrollment
into this study and for 6 months following the last dose of second-line treatment 4. Female
subject (of childbearing potential, post-menopausal for less than 6 months, not surgically
sterilized, or not abstinent) who is not willing to use an oral, patch or implanted
contraceptive, double-barrier birth control, or an intrauterine device (IUD) during the
course of the study and for 6 months following the last dose of second-line treatment 5.
Female subject who is breast-feeding or who has positive serum pregnancy test 72 hours
prior to randomization 6. Pleural effusion or ascites that causes respiratory compromise (≥
CTCAE grade 2 dyspnea) 7. Any of the following concurrent severe and/or uncontrolled
medical conditions within 24 weeks of enrollment which could compromise participation in
the study:

   - Unstable angina pectoris

   - Symptomatic congestive heart failure

   - Myocardial infarction ≤ 6 months prior to registration and/or randomization

   - Serious uncontrolled cardiac arrhythmia

   - Uncontrolled diabetes

   - Active or uncontrolled infection

   - Interstitial pneumonia or extensive and symptomatic interstitial fibrosis of the lung

   - Chronic renal disease

   - Acute or chronic liver disease (eg, hepatitis, cirrhosis) 8. Patients unwilling to or
   unable to comply with the protocol 9. Life expectancy of less than 12 weeks 10.
   Current, recent (within 4 weeks of the first infusion of this study), or planned
   participation in an experimental drug study other than a Genentech-sponsored
   bevacizumab cancer study

      - Bevacizumab-Specific Exclusions

         1. Inadequately controlled hypertension (defined as systolic blood pressure >
         150 and/or diastolic blood pressure > 100 mmHg on antihypertensive

         2. Any prior history of hypertensive crisis or hypertensive encephalopathy

         3. New York Heart Association (NYHA) Grade II or greater congestive heart
         failure (see Appendix E)

         4. History of myocardial infarction or unstable angina within 6 months prior to
         study enrollment

         5. History of stroke or transient ischemic attack within 6 months prior to
         study enrollment

         6. Known central nervous system (CNS) disease

         7. Significant vascular disease (eg, aortic aneurysm, aortic dissection)

         8. Symptomatic peripheral vascular disease

         9. Evidence of bleeding diathesis or coagulopathy

      10. Major surgical procedure, open biopsy, or significant traumatic injury
         within 28 days prior to study enrollment or anticipation of need for major
         surgical procedure during the course of the study

      11. Core biopsy or other minor surgical procedure, excluding placement of a
         vascular access device, within 7 days prior to study enrollment

      12. History of abdominal fistula, gastrointestinal perforation, or
         intra-abdominal abscess within 6 months prior to study enrollment

      13. Serious, non-healing wound, ulcer, or bone fracture

      14. Urine protein ≥ 2+ on urinalysis dipstick and ≥ 1.0 gram on 24-hour urine

      15. Known hypersensitivity to any component of bevacizumab


drug: Capecitabine

drug: Oxaliplatin

drug: Bevacizumab

Not Recruiting

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Heidi Kaiser

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