|
Tuberculosis:
An Old Disease Needs New Cures
By
Martha Bedelu
Doctors without Borders
(Khayelitsha,
South Africa)- The World Health Organization released its global
tuberculosis figures on World Tuberculosis
Day [March 24, 2005], and much was made of the news that incidence
rates are declining or stable in five of the six regions of the
world.
Yet the global
incidence rate is still rising, and every day, tuberculosis kills
5,000 people, nearly all of them in underdeveloped countries. We
are still losing the battle against the disease, and it is time
to admit that prescribing more of the same just won't work.
A big part
of the problem is the increasing number of patients with the deadly
combination of TB and H.I.V., which renders both diagnosis and treatment
more difficult. From my native Ethiopia to Cambodia, tuberculosis
is the No. 1 killer of people with H.I.V. and AIDS. In Khayelitsha,
the poor township where I work, one in every four adults is infected
with H.I.V. Tuberculosis incidence rates here are 1,122 per 100,000
people per year, nearly 10 times the global rate.
Often, the
only diagnostic tool I have is the sputum test, a procedure invented
in 1882. In ideal conditions and in the absence of H.I.V. infection,
the sputum test detects 75 percent of pulmonary tuberculosis infections.
But for children, people with extra-pulmonary tuberculosis, and
the majority of H.I.V. patients with TB, the test is virtually useless.
Like the sputum
test, the only available medicines to treat the disease are from
another era. They were invented three to five decades ago, and require
patients to take four to six pills every day for up to eight months.
In many countries,
patients have to go to separate clinics run by national tuberculosis
programs several times a week to receive their medicines, and then
wait for a counselor to watch them swallow their pills. This direct
observation is intended to prevent the development of multidrug-resistant
strains of tuberculosis, an especially grave concern since no new
drugs are yet available to counter it.
If the patients
are also being treated for H.I.V. they must go through all of this
in addition to their daily regimen of antiretroviral therapy. These
burdens cause many patients to abandon treatment.
I refuse to
believe that we cannot find better methods of diagnosis and treatment.
We urgently need an easy-to-use blood, urine or sweat test that
quickly detects active tuberculosis.
We have to
make a regimen that is simpler for patients, creating innovative
ways of improving treatment adherence and reducing the need for
direct observation, as we have done here with antiretroviral therapy
for the treatment of H.I.V. It should also be standard practice
to integrate tuberculosis and H.I.V. care so patients receive their
medicines for both diseases in one place, as they can at our clinic
in Khayelitsha.
In the longer
term, we need newer, more potent medicines that shorten the duration
of treatment. Patients with multidrug-resistant tuberculosis, for
example, have to endure up to two years of hospitalized treatment
with expensive drugs whose severe side effects can include acute
psychosis. Research and development of new drugs over the last 35
years has been nearly nonexistent.
To this end,
the World Health Organization and governments need to create a research
and development program based on public health needs as an alternative
to the pharmaceutical companies, which are motivated by profit.
When the commercial
interests of pharmaceutical companies threaten to hamper the development
of potential TB treatments, governments should step in by finding
ways to make promising tuberculosis compounds available to groups
willing to develop them into medicines.
Promises will
not be enough to tackle this resurgent scourge. In an age of unparalleled
medical advances, we must refuse to accept that millions of people
will be left to perish at the hands of this antique disease."
Excerpts
from a Statement on World TB Day from the National Institute
of Allergy and Infectious Diseases, National Institutes of Health
|
"Recently,
two new TB vaccine candidates entered human clinical trials
in the United States and the United Kingdom; a third candidate
is scheduled to undergo human testing shortly in the United
States. These new TB vaccine candidates are the first to
be tested in people in the United States in more than six
decades.
"The
development of a new and improved TB vaccine is critical,
because the currently available TB vaccine, Bacille Calmette-Guérin
(BCG), offers protection against TB only in infants
and young children, with limited effectiveness against the
most contagious form of the disease, TB of the lung.
"The
development of new TB drugs is proceeding apace. A promising
drug candidate developed by public/private partners with
contributions by NIAID is completing preclinical evaluation
and is expected to undergo FDA review later this year for
approval to be tested in humans. This candidate is a new
member of a class of chemicals known as nitroimidazoles,
which have the potential to be effective against both the
drug-resistant and drug-sensitive forms of TB."
|
[Editor's
Note: Development and approval of new drugs to treat tuberculosis,
if successful, will likely require at least 3-5 years. A vaccine
would require even longer to develop]
03/28/05
Sources
M Bedelu. An Old Disease Needs New Cures (Op Ed). The New York
Times. March 26, 2005.
A Fauci and
C F Sizemore. Statement on World TB Day from the National Institute
of Allergy and Infectious Diseases National Institutes of Health.
March 22, 2005.
Additional
Articles on Tuberculosis
Tuberculosis:
An Old Disease Needs New Cures -
3/28/05
Short-Course
Therapy with Rifampin plus Isoniazid, Compared with Standard Therapy
with Isoniazid, for Latent Tuberculosis Infection -
2/14/05
Incidence of Immune
Reconstitution Syndrome in HIV-Tuberculosis Coinfected
Patients in India -
2/11/05
Roche
Issues Drug Interaction Warning on Hepatocellular Toxicity in
Healthy Volunteers Receiving TB Drug Rifampin and Saquinavir/Ritonavir
- 2/09/05
Cotrimoxazole
Prophylaxis for TB Effectively Reduces Adult Death Rates
in Rural South Africa - 2/09/05
The Risk of Acquiring Tuberculosis
(TB) Increases Rapidly After Infection with HIV -
1/05/05
The
Extraordinary Hope of Antiretroviral Therapy in South Africa (Even
for Patients with Tuberculosis or Kaposi Sarcoma!)
-
1/03/05
Two 8-month
Regimens of Chemotherapy for Treatment of Tuberculosis
Found Inferior to 6-month Standard Regimen - 10/25/04
Adjunctive
Dexamethasone Improves Survival in Tuberculous Meningitis
- 10/22/04
Outcome of HIV-Associated Tuberculosis
in the HAART Era -
10/13/04
Does Tuberculosis Increase HIV
Load? -
10/13/04
Combined TB/HIV Care Could Save
500,000 Lives in Africa Every Year, UN Says -
09/22/04
Paradoxical Reactions Are Common During
Tuberculosis Treatment -
09/10/04
Safety and Effectiveness of Efavirenz
with and without Rifampicin for the Treatment of Antiretroviral-naïve
Patients Coinfected with Tuberculosis and HIV -
09/01/04
Use
of Prednisolone in HIV-associated Tuberculous Pleurisy
Is Not Recommended -
08/16/04
Paradoxical
Reactions During Treatment of Tuberculosis in Patients
with and without HIV Infection - 08/06/04
Isoniazid
Prophylaxis Has an Early and Significant Survival Benefit and
Reduces TB in HIV Positive Children in Africa -
07/21/04
Strategy
for Successful Treatment of TB and HIV -
07/19/04
Incidence
of Tuberculosis Pre and Post Introduction of ART in a Setting
of High Tuberculosis-HIV Co-morbidity 7-12-04
Efavirenz
600 mg/day Versus 800 mg/day in HIV-infected Patients with Tuberculosis
7-12-04
Incidence
of Tuberculosis Pre and Post Introduction of ART in a Setting
of High Tuberculosis-HIV Co-morbidity - 07/12/04
Lopinavir-Ritonavir
Dose Adjustment and Therapeutic Drug Monitoring and Monitoring
of Liver Function May Allow Concomitant Use of Rifampin in HIV
Patients with Tuberculosis - 06/18/04
HIV Coinfection Does Not Alter Initial
Clinical Presentation of Tuberculosis 03/03/04
Clinical and Radiographic Features of
HIV-related Tuberculosis 02/06/04
Rifampin-indinavir-ritonavir Combination
Markedly Lowers Indinavir Level 02/04/04
Improved
Outcomes in HIV Positive Adults with Tuberculosis in the
HAART Era 01/07/04
HIV
-driven Tuberculosis Epidemics: Is Prevention Better Than
Cure? 11/21/03
Virological
and Immunological Impact of Tuberculosis on HIV Disease
-
10/17/03
Secondary
Prophylaxis Prevents TB Recurrence in HIV Patients
-
10/17/03
Toxicity
Data and Revised CDC Recommendations Against the Use of Rifampin
and Pyrazinamide for Treatment of Latent Tuberculosis Infection
-
08/20/03
In
Areas Where HIV Is Endemic, TB Recurrence Can Be Reduced
by Administration of Rifampin-based Treatment for at Least 6 Months
-
08/11/03
Tuberculosis
Does Not Accelerate HIV Disease Progression -
06/27/03
Outbreak
of Tuberculosis Among Homeless Persons Coinfected with
HIV -
06/02/03
|