Adjuvant Cytokine Therapy to Treat Pulmonary Mycobacterium Avium Complex Infection



Status:Completed
Conditions:Infectious Disease, Infectious Disease
Therapuetic Areas:Immunology / Infectious Diseases
Healthy:No
Age Range:18 - Any
Updated:4/21/2016
Start Date:May 2005
End Date:August 2010

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A Study of Adjuvant Cytokine Therapy in Pulmonary Mycobacterium Avium Complex and Other Pulmonary Nontuberculous Mycobacterial Infections

Mycobacterium avium complex (MAC) are ubiquitous organisms that cause isolated pulmonary
disease in otherwise healthy patients with yet undefined susceptibilities. Patients
typically present with a history of chronic cough, eventually progressing to hemoptysis,
fever, and hypoxia. With half or more of all patients failing standard three-drug therapy,
this is an insidious disease with a poor prognosis. Under the natural history protocol of
nontuberculous mycobacterial infection (NTM; #01-I-0202), 46 patients with diagnosed
pulmonary MAC disease are being studied. Numerous studies have suggested that a
dysregulation in cytokine production may make these patients susceptible to mycobacterial
infection. Cytokines are particularly important in the activaction of macrophages, which
help to clear mycobacterial infection. Interferon gamma 1b (Actimmune) and GM-CSF (Leukine)
are two cytokine therapies that have been approved in the treatment of chronic granulomatous
disease and post-transplantation hematopoietic reconstitution, respectively. A number of in
vitro studies suggest that either or both of these therapies may help to clear MAC
infection. Given the poor outcomes of therapy and the persistent, debilitating nature of the
disease, new therapies are desperately needed, and many are being tried without benefit of
scientific foundation. Currently, there are no prospective trials that show any effect of
these drugs in the lung delivered subcutaneously. This protocol proposes to perform a pilot
study to evaluate the effects, if any, of these macrophage stimulating cytokines in the
context of ongoing pulmonary MAC infection.

Aims:

To determine the local and systemic effect, if any, of adjuvant IFN gamma and GM-CSF in
pulmonary MAC patients.

Methods:

Fifteen patients will be randomized into three treatment groups of five patients each. The
first group will receive a standard drug regimen, based on the 1997 ATS guidelines. The
second and third groups, in addition to receiving the standard therapy, will also receive
three months of (IFN{gamma}) and GM-CSF, respectively. All patients will undergo
bronchoscopy with bronchoalveolar lavage (BAL) at the beginning of the study, after three
months, and at six months.

In addition to obtaining traditional subjective and objective clinical measures, both
proteomic and genomic analysis of the BAL will be performed to determine if cytokine therapy
effects any detectable change in the lungs. In vitro studies on typ...

Mycobacterium avium complex (MAC) and other pulmonary nontuberculous mycobacteria (P-NTM)
are ubiquitous organisms that cause isolated pulmonary disease in otherwise healthy patients
with yet undefined susceptibilities. Patients typically present with a history of chronic
cough, eventually progressing to hemoptysis, fever, and hypoxia. With half or more of all
patients failing standard three-drug therapy, this is an insidious disease with a poor
prognosis. Under the natural history protocol of nontuberculous mycobacterial infection
(NTM; #01-I-0202), 46 patients with diagnosed pulmonary MAC disease, 20 patients with M.
abscessus disease, and 14 with other types of mycobacteria (M. fortuitum, M. massiliense, M.
mucogenicum and M. chelonae) are being studied.

Numerous studies have suggested that a dysregulation in cytokine production may make these
patients susceptible to mycobacterial infection. Cytokines are particularly important in the
activation of macrophages, which help to clear mycobacterial infection. Interferon gamma 1b
(Actimmune) and GM-CSF (Leukine) are two cytokine therapies that have been approved in the
treatment of chronic granulomatous disease and post-transplantation hematopoietic
reconstitution, respectively. A number of in vitro studies suggest that either or both of
these therapies may help to clear MAC infection. Given the poor outcomes of therapy and the
persistent, debilitating nature of the disease, new therapies are desperately needed, and
many are being tried without benefit of scientific foundation. Currently, there are no
prospective trials that show any effect of these drugs in the lung delivered subcutaneously.
This protocol proposes to perform a pilot study to evaluate the effects, if any, of these
macrophage stimulating cytokines in the context of ongoing pulmonary mycobacterial
infection.

Aims:

To determine the local and systemic effect, if any, of adjuvant IFN gamma and GM-CSF in
P-NTM patients.

Methods:

Fifteen patients will be randomized into three treatment groups of five patients each. The
first group will receive a standard drug regimen, based on the 1997 ATS guidelines. The
second and third groups, in addition to receiving the standard therapy, will also receive
three months of (IFN{gamma}) and GM-CSF, respectively. All patients will undergo
bronchoscopy with bronchoalveolar lavage (BAL) at the beginning of the study, after, after
three months, and at six months.

In addition to obtaining traditional subjective and objective clinical measures, both
proteomic and genomic analysis of the BAL will be performed to determine if cytokine therapy
effects any detectable change in the lungs, In vitro studies on type II alveolar macrophages
culled from these patients before and after cytokine therapy will also be performed.

- INCLUSION CRITERIA:

To be eligible for this protocol, a patient must meet the following five criteria:

Diagnosed with M. avium complex (MAC) lung disease or other pulmonary mycobacterial
infection based on the 1997 version of American Thoracic Society (ATS) diagnostic criteria
and have positive AFB smear or culture for mycobacterial infection at least three months
prior to the date of enrollment. Patients with only histological evidence of mycobacterial
infection without positive smear or culture will not qualify for this protocol even if
they meet the ATS diagnostic criteria for nontuberculous mycobacterial lung infection.

A patient must have radiographic evidence on high resolution computerized tomography of
changes that are consistent with pulmonary mycobacterial infection. These include, but are
not limited to: multiple small nodules (less than 5 mm), and cylindrical bronchiectasis.

The patient must be on a treatment regimen based on ATS guidelines that has been stable
for at least three months. By stable, we mean that the patient has been tolerating the
regimen without any significant adverse reactions, and that no new agents have been begun
in the last three months.

The patient must be female and can be post-menopausal (either through natural menopause or
surgical removal of her ovaries) or menstruating. If the patient is still menstruating and
randomized to a study group receiving a cytokine she must agree to monthly pregnancy
testing, while on study, as well as to utilizing a barrier type of contraception or
abstinence. She must not be under 40 years of age at the time of enrollment in the study.

The patient must be enrolled in protocol # 01-I-0202 ("Natural History, Genetics,
Phenotype, and Treatment of Non-Tuberculoid Mycobacterial Infections").

EXCLUSION CRITERIA:

Patients with pulmonary MAC disease who do not meet the above entry criteria.

Patients with any of the following preexisting medical conditions:

1. HIV positive

2. asthma

3. active cancer requiring treatment

4. hepatic disease (defined as either a history of cirrhosis, or grade 3 or 4 hepatic
toxicity by the Toxicity Table in Appendix II of protocol)

Patients who are unable to tolerate bronchoscopy. This will be defined by the following
criteria:

1. A pulse oximetry reading less than 100% when given supplemental oxygen at 100% FiO2.

2. Clinically significant reactive airway disease that does not respond to
bronchodilators.

Patients with the following laboratory abnormalities:

1. creatinine greater than 1.5 mg/dL

2. Hemoglobin less than 9 mg/dL

3. WBC less than 3,000

4. Platelets less than 150,000

5. ALT greater than 82 U/L, or AST greater than 78 U/L.

6. Bilirubin greater than 2.0 mg/dL

7. Alkaline phosphates greater than 232 U/L

Patients with a preexisting allergy or history of allergic reactions to study or protocol
medications. These include, but are not necessarily limited to: IFN-gamma, GM-CSF,
azithromycin/ clarithromycin, ethambutol, rifampin/ rifabutin, anesthetic agents employed
in bronchoscopy, or any yeast-derived products.

Patients who are unable to maintain the described follow up schedule. Likewise, patients
who are unable to give informed consent are excluded from the study.

Patients with clinical diagnosis of cystic fibrosis.

Patients who are either currently smoking, or have a previous history of smoking that
exceeds 20 pack years.

Patients with prior treatment with either IFN-gamma or GM-CSF within the last three
months.

Patients with known history of cardiac, endocrine, neurologic or other medical conditions
that the principal investigator deems dangerous or unsuitable for enrollment will be
excluded.

Patients who are either pregnant or lactating. Also, menstruating patients who are
randomized to a study group receiving a cytokine and refuse to use appropriate barrier
forms of contraception or abstinence during this trial be excluded.

Patients who, at any time during this trial, have an active lung infection caused by
either Staphylococcus or a gram negative rod are excluded from this trial until this
infection has been successfully treated.

Patients that need to use supplemental oxygen.

Patients who have a Forced Vital Capacity less than 40% predicted.

Patients who are unable to walk and participate in the 6MWT.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
?
mi
from
Bethesda, MD
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