Clinical Trial: Study of Zoledronic Acid Versus Observation on Bone Mineral Density and Incidence of Micrometastasis in Women Undergoing Pelvic Radiation for Cervical Cancer

Study Status: Terminated
Recruit Status: Terminated
Study Type: Interventional

Official Title: Randomized Phase II Study of Zoledronic Acid vs Observation on Bone Mineral Density and Incidence of Micrometastasis in Women Undergoing Pelvic Radiation for Cervical Canc

Brief Summary: The treatment of cervical cancer with chemotherapy and radiation will make women post menopausal (no estrogen from the ovaries), if a woman is not already in menopause. Estrogen plays a key role in maintaining bone health. Therefore, these women are at higher risk of getting osteoporosis (decrease minerals in the bone) and bone fractures. The overall purpose of this research is to look at the effects of zoledronic acid (Zometa) on preventing bone loss. Studies have also shown that zoledronic acid may prevent metastasis to the bone which can occur in women with cervical cancer. Zometa is investigational (not approved by the Food and Drug Administration (FDA)) in this study to prevent metastasis to the bone in women with cervical cancer. Therefore, the goal of this study is to also look at the effects of zoledronic acid (Zometa) on circulating tumor cells in the bone marrow and blood. This study is being done to find a way to prevent bone loss and metastasis to the bone in women undergoing chemotherapy and radiation for cervical cancer. An additional component of the study is to assess the importance of stress on immune markers in blood during standard treatment.

Detailed Summary:

OBJECTIVES

  • To determine the incidence of disseminated tumor cells (DTCs) in bone marrow and circulating tumor cells (CTCs) in the blood of women with cervical cancer at diagnosis and 3 to 9 months after chemotherapy and pelvic radiation with and without Zometa.
  • To determine the change in biochemical markers of bone turnover from diagnosis to 9 months after radiation in women receiving chemoradiation for cervical cancer with and without Zometa.
  • To determine change in bone mineral density from diagnosis to 9 month after chemoradiation with and without Zometa.
  • To determine if depressed and anxious mood are associated with greater impairment of adaptive immunity (ratio of Th1/Th2) and higher levels of angiogenesis (VEGF) in peripheral blood of cervical cancer patients.
  • To examine the relationship of standardized uptake values (SUV)Max and metabolic heterogeneity in the primary tumor and evidence of persistent/recurrent disease on the 3 and 9 month Fludeoxyglucose (FDG)-Positron Emission Tomography (PET) scans with DTCs and CTCs.

Sponsor: Washington University School of Medicine

Current Primary Outcome:

  • Incidence of Circulating Tumor Cells (CTCs) [ Time Frame: At time of diagnosis, 3 months after completion of treatment, and 9 months after completion of treatment ]
  • Incidence of Disseminated Tumor Cells in Bone Marrow [ Time Frame: At time of diagnosis, 3 months after completion of treatment, and 9 months after completion of treatment ]


Original Primary Outcome:

  • FDG-PET Metabolic Response [ Time Frame: Assessed qualitatively, at 3 and 9 months. ]
  • Circulating Tumor Cells (CTC) [ Time Frame: Once at randomization and 3, 6, and 9 months after completion of radiation ]
  • Quality of life and stress response [ Time Frame: Pre-treatment, 6 and 9 months post radiation ]
  • Bone mineral density [ Time Frame: At baseline and post treatment - a DEXA scan will be performed at the baseline screening visit and the end of study visit to measure bone mineral density ]
  • Disseminated tumor cells in Bone Marrow [ Time Frame: At baseline, 3 and 9 months post radiation ]


Current Secondary Outcome:

  • Change in Bone Mineral Density [ Time Frame: At the time of diagnosis and 9 months after completion of treatment ]
  • Change in Biochemical Markers of Bone Turnover [ Time Frame: At the time of diagnosis and 9 months after completion of treatment ]
  • If Depressed and Anxious Moods Are Associated With Greater Impairment of Adaptive Immunity and Higher Levels of Angiogenesis in Peripheral Blood [ Time Frame: At diagnosis, 6 months after completion of treatment, and 9 months after completion of treatment ]
  • Relationship of SUVmax and Metabolic Heterogeneity in the Primary Tumor and Evidence of Persistent/Recurrent Disease [ Time Frame: 3 months after completion of treatment and 9 months after completion of treatment ]


Original Secondary Outcome:

Information By: Washington University School of Medicine

Dates:
Date Received: August 18, 2009
Date Started: August 2009
Date Completion:
Last Updated: August 10, 2015
Last Verified: August 2015