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Modulation of Immune Response by Oral Zinc Supplementation in Chemotherapy for Colon Cancer

Primary Purpose

Adjuvant Chemotherapy, Colon Cancer, Immunity

Status
Unknown status
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
zinc
Placebo
Sponsored by
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Adjuvant Chemotherapy focused on measuring Humoral immunity, Neutrophil function, Gene expression

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Age greater than 18 years
  • Diagnostic histopathology of colon cancer stage III (Dukes' stage C)
  • Performance Scale Karnofsky greater or equal to 70%
  • Have been subjected to resection of the primary neoplastic lesion in more than 8 weeks before start of chemotherapy
  • Patient in the first cycle of chemotherapy in adjuvant XELOX regimen.

Exclusion Criteria:

  • Patients with a history of autoimmune or inflammatory disease, active infectious disease, liver disease, renal failure or diabetes mellitus
  • Patients with metastatic disease
  • Have previously received radiotherapy or chemotherapy
  • Use of GCSF-Granulokine ® (growth-stimulating factor granulocyte)
  • Use of immunosuppressive drugs, diuretics and supplements of zinc or copper.

Sites / Locations

  • Departament of Clinical Oncology, Sao Paulo University

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Placebo Comparator

Other

Other

Arm Label

Chemotherapy and zinc

Chemotherapy placebo

Control and zinc

Control Placebo

Arm Description

Patients in adjuvant chemotherapy supplemented with zinc

Patients in adjuvant chemotherapy with placebo

Healthy patients supplemented with zinc

Healthy volunteers received placebo

Outcomes

Primary Outcome Measures

Gene expression
Modulation of genes related to immune response

Secondary Outcome Measures

Humoral immunity and neutrophil function

Full Information

First Posted
December 16, 2010
Last Updated
December 16, 2010
Sponsor
University of Sao Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT01261962
Brief Title
Modulation of Immune Response by Oral Zinc Supplementation in Chemotherapy for Colon Cancer
Official Title
Modulation of Immune Response by Oral Zinc Supplementation in Adjuvant Chemotherapy for Colon Cancer: a Study of Global Gene Expression and Function of Humoral Immunity and Neutrophils
Study Type
Interventional

2. Study Status

Record Verification Date
December 2010
Overall Recruitment Status
Unknown status
Study Start Date
February 2011 (undefined)
Primary Completion Date
December 2011 (Anticipated)
Study Completion Date
August 2013 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University of Sao Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
In leukocytes of patients undergoing adjuvant chemotherapy for colon cancer treatment: a)identify genes modulated by oral supplementation of zinc; b) evaluate the effects of oral zinc supplementation on humoral immunity and neutrophil function. The study will be conducted on 30 adult patients aged grater than 18 years, of both genders who have undergone surgical resection of colonic neoplastic lesions without metastatic lesion. Patients will be randomized into two groups, with the first (Group QT Zn, n = 15) receive 70 mg/d of zinc for 16 weeks and the second will receive placebo (QT Placebo Group, n = 15). The study will also include 30 healthy volunteers who receive supplementation of 70 mg/d of Zn (C Zn group, n = 15) or placebo (Group C Placebo, n = 15). Zinc supplementation or placebo for all study groups will start two days before the volunteers received the pneumococcal vaccine, polyvalent 23. Fifteen days after vaccination, patients begin chemotherapy as pre-established criteria by the Oncology Service. Will be monitored the parameters of nutritional status (anthropometry, bioelectrical impedance, food intake, and laboratory tests) adverse effects, according to rules of the CTCAE. In the evaluation of humoral immunity, antibodies opsonization and in the pneumococcal polysaccharide will be measured. Will be evaluated the function of neutrophils by measuring DNA NETs and quantified calprotectin and elastase released in the culture supernatants of activated neutrophils. RT-qPCR will be done of genes differentially expressed(DEGS) on activated leukocytes. In six volunteers from each group will be analyzed global gene expression from RNA extracted from leukocytes by microarray; will be detected and correlated the molecular pathways modulated by zinc by MetaCore software (GeneGo). The DEGS will be validated by RT-qPCR.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Adjuvant Chemotherapy, Colon Cancer, Immunity
Keywords
Humoral immunity, Neutrophil function, Gene expression

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Chemotherapy and zinc
Arm Type
Experimental
Arm Description
Patients in adjuvant chemotherapy supplemented with zinc
Arm Title
Chemotherapy placebo
Arm Type
Placebo Comparator
Arm Description
Patients in adjuvant chemotherapy with placebo
Arm Title
Control and zinc
Arm Type
Other
Arm Description
Healthy patients supplemented with zinc
Arm Title
Control Placebo
Arm Type
Other
Arm Description
Healthy volunteers received placebo
Intervention Type
Dietary Supplement
Intervention Name(s)
zinc
Intervention Description
zinc sulfate, 35 mg twice daily for 4 months
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo, One capsule, twice daily for 4 months
Primary Outcome Measure Information:
Title
Gene expression
Description
Modulation of genes related to immune response
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Humoral immunity and neutrophil function
Time Frame
18 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Age greater than 18 years Diagnostic histopathology of colon cancer stage III (Dukes' stage C) Performance Scale Karnofsky greater or equal to 70% Have been subjected to resection of the primary neoplastic lesion in more than 8 weeks before start of chemotherapy Patient in the first cycle of chemotherapy in adjuvant XELOX regimen. Exclusion Criteria: Patients with a history of autoimmune or inflammatory disease, active infectious disease, liver disease, renal failure or diabetes mellitus Patients with metastatic disease Have previously received radiotherapy or chemotherapy Use of GCSF-Granulokine ® (growth-stimulating factor granulocyte) Use of immunosuppressive drugs, diuretics and supplements of zinc or copper.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Camila Bitu M. Braga, Msc
Phone
55-16-36023369
Email
camilabitu@usp.br
First Name & Middle Initial & Last Name or Official Title & Degree
Selma Freire C. Cunha, PhD
Phone
55-16-36013369
Email
sfreire@fmrp.usp.br
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Selma Freire C. Cunha, PhD
Organizational Affiliation
Sao Paulo University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Camila Bitu M. Braga, Msc
Organizational Affiliation
Sao Paulo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Departament of Clinical Oncology, Sao Paulo University
City
Ribeirao Preto
State/Province
Sao Paulo
ZIP/Postal Code
14049-900
Country
Brazil
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Camila Bitu M. Braga, Msc
Phone
55-16-36023369
Email
camilabitu@usp.br
First Name & Middle Initial & Last Name & Degree
Selma Freire C. Cunha, PhD
Phone
55-16-36023369
Email
sfreire@fmrp.usp.br
First Name & Middle Initial & Last Name & Degree
Fernanda Maris Peria, PhD
First Name & Middle Initial & Last Name & Degree
Camila Bitu M. Braga, Msc

12. IPD Sharing Statement

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Modulation of Immune Response by Oral Zinc Supplementation in Chemotherapy for Colon Cancer

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