Microculture Kinetic (MiCK) Apoptosis Test Results With Drug Treatment Results in Cancer Patients (MiCK)

Correlation of the Microculture Kinetic (MiCK) Apoptosis Test Results With Drug Treatment Results in Cancer Patients

The purpose of this study is to correlate the results of the MICK assay with short- and long-term results of treatments in cancer patients and evaluate the role of the MiCK assay in guiding chemotherapy of cancer patients.

Study Overview

• Status: Completed
• Conditions: Cancer

Detailed Description

Identification of those patients with cancer who will or will not respond to a specific chemotherapy is important for making decisions regarding chemotherapy regimens as well as alternative management approaches. A laboratory test that could help to determine the sensitivity of an individual patient's tumor cells to specific chemotherapeutic agents would be valuable in choosing the optimal chemotherapy regimen for that patient with an expectation of increasing the response rate to the therapy. Several types of in vitro assays that measure tumor cell survival following exposure to cytotoxic agents have been evaluated for their ability to predict chemotherapy outcomes. As a group, these assays are referred to as drug resistance assays. In a resistance assay, the surviving tumor cells can be detected directly by their exclusion or metabolism of specific dyes. Alternatively, since some of tumor cells are proliferating, their survival can be detected by measurement of DNA synthesis by radiolabeled precursor incorporation or demonstration of clonogenic potential by growth into colonies in semi-solid culture medium. In several clinical studies, these assays were useful in detecting drug resistance and in predicting a poor prognosis for cancer patients. However, these resistance assays cannot detect sensitivity of an individual patient's tumor cells to a specific drug. Therefore, new methods determining drug-sensitivity of the tumor cells of an individual patient and, thus, capable of both predicting a positive treatment outcome and guiding chemotherapy, would be of significant value.

Recently, an automated microculture kinetic (MiCK) assay for measuring drug induced apoptosis in tumor cells has been developed1-4. Apoptosis is a distinct mode of cell death which occurs under physiological conditions and yet can be induced in malignant cells by chemical and physical factors including antitumor drugs5-7. During the last decade, it has been recognized that chemotherapeutic agents exert their antitumor activity by triggering apoptosis in susceptible tumor cells8-17. This implies that the MiCK assay for apoptosis provides a mechanism-based approach to studying effects of cytotoxic agents on tumor cells. Unlike "resistance" assays that measure a fraction of cells surviving drug exposure, the MiCK assay measures a fraction of tumor cells killed by a chemotherapeutic agent via mechanism of apoptosis. Therefore the MiCK assay determines drug sensitivity, rather than resistance. Recently the MiCK assay has been shown to predict complete remission rate and survival in acute myeloid leukemia patients better than clinical criteria did18-20. In a limited study, the MiCK assay has been used to direct chemotherapy of the leukemia patients 21.

The MiCK assay has also been used to study drug-induced apoptosis in solid tumors, including neuroblastoma and colon adenocarcinoma cell lines22-23. More recent data accumulated by DiaTech has demonstrated that the MiCK assay can detect drug induced apoptosis in primary cultures of tumor cells isolated from patients with ovarian carcinoma, gastric carcinoma, metastatic breast cancer and high grade soft tissue sarcoma. The purpose of this study is to correlate the results of the MICK assay with short- and long-term results of treatments in cancer patients and evaluate the role of the MiCK assay in guiding chemotherapy of cancer patients.

• Study Type: Observational
• Enrollment (Actual): 300

Contacts and Locations

Study Locations

• Canada
  • Quebec
    • Montreal, Quebec, Canada, H2X 3P9
      • DiaTech Oncology
• United States
  • California
    • La Verne, California, United States, 91750
      • Wilshire Oncology Medical Group, Inc
  • Florida
    • Tampa, Florida, United States, 33606
      • Tampa General Hospital
  • Tennessee
    • Brentwood, Tennessee, United States, 37027
      • DiaTech Oncology
    • Crossville, Tennessee, United States, 38555
      • Cumberland Medical Center
    • Murfreesboro, Tennessee, United States, 37219
      • Middle Tennessee Medical Center
    • Nashville, Tennessee, United States, 37203
      • Baptist Hospital
    • Nashville, Tennessee, United States, 37203
      • Nashville Oncology Associates
    • Nashville, Tennessee, United States, 37203
      • St. Thomas Research Institute, LLC
    • Nashville, Tennessee, United States, 37203
      • Tennessee Breast Specialists
    • Nashville, Tennessee, United States, 37205
      • Tennessee Toracic Surgical Specialists

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Child; Adult; Older Adult
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

• Sampling Method: Non-Probability Sample

Study Population

Cancer Patients for whom chemotherapy is planned.

Description

Inclusion Criteria:

• 3.1.1 Patients with pathological diagnoses of cancer or leukemia
• 3.1.2 Patients must have tumor which is accessible for biopsy and agree to undergo tumor biopsy, or drainage of malignant effusion, and the specimen must be submitted for MiCK assay.
• 3.1.3 Patients for whom chemotherapy is planned.

Exclusion Criteria:

• 3.2.1 Patients with symptomatic/uncontrolled parenchymal brain or meningeal metastasis and tumors not accessible for biopsy.
• 3.2.2 Patients who are pregnant. Pregnancy. During the course of the study, all patients of childbearing potential should be instructed to contact the treating physician if they suspect they might have conceived a child; for females, a missing or late menstrual period should be reported to the treating physician. If pregnancy is confirmed by a pregnancy test, the patient must not receive chemotherapy in this study and must not be enrolled into the study or, if already enrolled, must be withdrawn from the study. If a male patient is suspected of having fathered a child while on the study, the pregnant female partner must be notified and counseled regarding the risk to the fetus. Pregnancy during the course of this study will be reported to the Principal Investigator as a serious adverse event. Women of child bearing potential are defined to include any female who has experienced menarche and has not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation, or bilateral oophorectomy) or is not post-menopausal (defined as amenorrhea for more than 12 consecutive months); these includes also females using oral, implanted, or injectable contraceptive hormones, mechanical devices, or barrier methods to prevent pregnancy.

Study Plan

How is the study designed?

Number of groups / cohorts

2

Cohorts and Interventions

Group / Cohort
1; Patients with pathological diagnoses of cancer or leukemia
2; 3.1.3 Patients for whom chemotherapy is planned.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
To evaluate the ability of the MiCK assay to guide chemotherapy of cancer patients, with emphasis on patients failing primary treatment, patients with unknown primary tumors, and patients with tumors difficult to treat such as carcinoma of lung.	one year

Secondary Outcome Measures

Outcome Measure	Time Frame
Correlate the MiCK assay results with objective response rates, symptom response rates, time to progression and survival of cancer patients treated with chemotherapy.	one year

Collaborators and Investigators

• Sponsor: Pierian Biosciences
• Investigators: Study Director: Cary Presant, MD, Pierian Biosciences; Principal Investigator: Dirk Davidson, MD, Cumberland Medical Center; Principal Investigator: Karl Rogers, MD, Nashville Oncology Associates; Principal Investigator: Swapnil P. Rajurkar, MD, Wilshire Oncology Medical Group, Inc.; Principal Investigator: Laura Lawson, MD, Tennessee Breast Specialists; Principal Investigator: L. James Wudel Jr., MD, Tennessee Thoracic Surgical Specialists; Principal Investigator: Raymond F Bluth, MD, Baptist Hospital Nashville; Principal Investigator: Peter F Jelsma, MD, St. Thomas Research Institute, LLC; Principal Investigator: Richard D Michaelson, MD, Middle Tennessee Medical Center; Principal Investigator: Jorge E Marcet, MD, Tampa Gerneral Hospital

Publications and helpful links

General Publications

• Bosserman L, Rogers K, Willis C, Davidson D, Whitworth P, Karimi M, Upadhyaya G, Rutledge J, Hallquist A, Perree M, Presant CA. Application of a drug-induced apoptosis assay to identify treatment strategies in recurrent or metastatic breast cancer. PLoS One. 2015 May 29;10(5):e0122609. doi: 10.1371/journal.pone.0122609. eCollection 2015.

Study record dates

Study Major Dates

• Study Start: December 1, 2008
• Primary Completion (Actual): November 1, 2012
• Study Completion (Actual): November 1, 2012

Study Registration Dates

• First Submitted: May 12, 2009
• First Submitted That Met QC Criteria: May 12, 2009
• First Posted (Estimate): May 13, 2009

Study Record Updates

• Last Update Posted (Estimate): November 14, 2012
• Last Update Submitted That Met QC Criteria: November 12, 2012
• Last Verified: November 1, 2012

More Information

Terms related to this study

• Keywords: Chemosensitivity, chemotherapy, all cancers, personalized chemotherapy, personalized cancer treatment; Cancer Patients for whom chemotherapy is planned.
• Other Study ID Numbers: Master Study DiaTech Oncology