Capecitabine and Docetaxel in Treating Patients With Recurrent or Progressive Metastatic Pancreatic Cancer

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Brief Title

Capecitabine and Docetaxel in Treating Patients With Recurrent or Progressive Metastatic Pancreatic Cancer

Official Title

A Multicenter Phase II Study of Capecitabine and Docetaxel for Previously Treated Pancreatic Cancer Patients "CapTere"

Brief Summary

      RATIONALE: Drugs used in chemotherapy, such as capecitabine and docetaxel, work in different
      ways to stop the growth of tumor cells, either by killing the cells or by stopping them from
      dividing. Giving more than one drug (combination chemotherapy) may kill more tumor cells.

      PURPOSE: This phase II trial is studying how well giving capecitabine together with docetaxel
      works in treating patients with recurrent or progressive metastatic pancreatic cancer.
    

Detailed Description

      OBJECTIVES:

      Primary

        -  Determine the overall (complete and partial) response rate in patients with recurrent or
           progressive metastatic pancreatic cancer treated with capecitabine and docetaxel.

      Secondary

        -  Determine the overall and progression-free survival of patients treated with the
           chemotherapy combination.

        -  Determine the duration of response (complete or partial) among patients who attain a
           response.

        -  Determine the frequency of patients having > 50% fall of CA19-9 from an initial level of
           > 100 U/mL in association with treatment with this regimen.

        -  Evaluate the toxicity associated with the administration of the combination in these
           patients.

      OUTLINE: This is a multicenter, open-label, nonrandomized study.

      Patients receive oral capecitabine twice daily on days 1-14 and docetaxel IV over 1 hour on
      days 1 and 8. Treatment repeats every 3 weeks in the absence of disease progression or
      unacceptable toxicity.

      After completion of study treatment, patients are followed every 3 months for up to 1 year.

      PROJECTED ACCRUAL: A total of 45 patients will be accrued for this study.
    

Study Phase

Phase 2

Study Type

Interventional


Primary Outcome

Rate of Participants Achieving Complete Response or Partial Response to Therapy.

Secondary Outcome

 Overall Surival (OS)

Condition

Pancreatic Cancer

Intervention

Capecitabine

Study Arms / Comparison Groups

 CapTere (Capecitabine + Docetaxel)
Description:  Capecitabine + Docetaxel (Taxotere)

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Drug

Estimated Enrollment

45

Start Date

July 2004

Completion Date

June 2010

Primary Completion Date

August 2008

Eligibility Criteria

        Inclusion Criteria:

          1. Participants or their authorized legally acceptable representative must consent to be
             in the study and must have signed and dated an approved consent form which conforms to
             federal and institutional guidelines.

          2. Patients must be 18 years or older.

          3. Participants must have recurrence or progression of histologically or cytologically
             documented pancreatic adenocarcinoma. Re-documentation of tumor histology or cytology
             prior to protocol therapy is not required if documented tumor was confirmed prior to
             initial therapy.

          4. Patients must have metastatic disease.

          5. Patients with metastatic disease to the brain if they have received radiation therapy
             or are stable, and are not receiving steroids or anticonvulsants.

          6. Participants must have received one prior gemcitabine based chemotherapy regimen (with
             or without radiation therapy). Participants must be 3 weeks or more beyond completion
             of prior chemotherapy (30 days beyond any experimental agent) and show recovery from
             toxicity to within the eligibility parameters of this protocol.

          7. Radiation for palliation and of the primary tumor must have been completed at least
             four weeks prior to initiation of protocol therapy.

          8. Patients must have measurable tumor by Response Evaluation Criteria in Solid Tumors
             (RECIST) (Therasse et al, 2000). Measurable disease includes any lesion ≥ 1 cm by
             spiral CT or ≥ 2 cm by non-spiral CT in longest diameter which can be repetitively
             assessed by radiographic measurement or any lesion ≥ 2 cm in longest diameter which
             can be repetitively assessed by physical examination. Positive bone scans,
             osteoblastic or osteolytic bone lesions, pleural effusions and positive bone marrow
             biopsies are not considered acceptable as either measurable or evaluable lesions.

          9. Participants must have Eastern Cooperative Oncology Group (ECOG) Performance Status
             Score of 0,1, or 2.

         10. Females of reproductive potential must not plan on conceiving children during the
             treatment period and must agree to use an effective medically accepted form of
             contraception. Patients will agree to continue contraception for 60 days from the date
             of the last study drug administration.

         11. Required initial laboratory data:

               -  Granulocytes ≥ 1,500/µl

               -  Platelets ≥ 100,000/µl

               -  Hg ≥ 8.0 g/dL

               -  Creatinine ≤ 2.0 mg/dL

               -  Creatine Clearance >30 ml/min as calculated with Cockroft-Gault equation

               -  Bilirubin ≤ Upper Limits of Normal (ULN)

               -  Pregnancy test for females with child-bearing potential: Negative within 7 days
                  of starting protocol

         12. Transaminases (SGOT and/or SGPT) may be up to 2.5 x institutional upper limit of
             normal (ULN) if alkaline phosphatase is ≤ ULN, or alkaline phosphatase may be up to 4
             x ULN if transaminases are ≤ ULN.

        Exclusion Criteria:

          1. Patient currently enrolled in another clinical trial.

          2. Pregnant or breast feeding women. With the exception of post-menopausal or infertile
             women, a negative blood test for pregnancy is mandatory before entry on study. Fertile
             persons refusing to use contraceptives may not participate.

          3. Participants may not have had capecitabine or docetaxel as part of prior therapy.

          4. No concurrent clinically evident malignancy is allowed except inactive non-melanoma
             skin cancer, low grade low stage bladder carcinoma followed off therapy, treated
             in-situ cervical cancer or lobular neoplasia of the breast.

          5. Participants with serious uncontrolled medical or psychiatric illness that would
             render chemotherapy unsafe are ineligible.

          6. Pregnant or breast-feeding at the time of proposed study entry.

          7. Clinical AIDS or known positive HIV serology.

          8. Peripheral neuropathy > grade 1

          9. Patients with a history of severe hypersensitivity reaction to drugs formulated with
             polysorbate 80 must be excluded.

         10. Prior unanticipated severe reaction to fluoropyrimidine therapy, or known sensitivity
             to 5-fluorouracil.

         11. Clinically significant cardiac disease (e.g. congestive heart failure, symptomatic
             coronary artery disease and cardiac arrhythmias not well controlled with medication)
             or myocardial infarction within the last 12 months.

         12. Lack of physical integrity of the upper gastrointestinal tract or malabsorption
             syndrome.

         13. Major Surgery within 4 weeks of the start of study treatment, without complete
             recovery.

         14. Unwillingness to participate or inability to comply with the protocol for the duration
             of the study.

         15. Patients with impaired renal function (estimated creatinine clearance < 30 ml/min as
             calculated by the Cockroft-Gault Equation).
      

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Caio Max S. Rocha Lima, MD, , 

Location Countries

United States

Location Countries

United States

Administrative Informations


NCT ID

NCT00290693

Organization ID

20030652

Secondary IDs

SCCC-2003099

Responsible Party

Sponsor

Study Sponsor

University of Miami


Study Sponsor

Caio Max S. Rocha Lima, MD, Principal Investigator, University of Miami


Verification Date

October 2017