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Cepheid GeneXpert clinical value and
product details
佑康公司 楊瑞萍 Kelly
The System Approach:
It’s All about the Efficiency
Product availability based on timing of FDA submission in US
*Exclusively distributed worldwide by Instrumentation Laboratories
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Cepheid GeneXpert Product offer
Oct.2009 – CE IVD Menu of Xpert Assays
•
•
•
•
•
•
Xpert MRSA , Preventing MRSA infections and transmission
Xpert MRSA/SA Nasal , Pre-surgical screening to prevent surgical site infection
Xpert MRSA/SA BC , Diagnosing S.aureus blood stream infections
Xpert MRSA/SA SSTI , Diagnosing S.aureus skin and soft tissues infections
Xpert C.difficile , Diagnosing CDI (Clostridium difficile infection)
Xpert vanA/vanB , Preventing VRE spread and outbreaks
• Xpert MTB/RIF , Diagnosing tuberculosis and drug resistance
• Xpert GBS , GBS screening to prevent neonatal Group B Strep disease
• Xpert EV , Diagnosing Enterovirus meningitis
• Xpert BCR ABL , CML treatment monitoring
• Xpert Factor II and V , Deep venous thrombosis
GeneXpert® Platform Strategic Reach
GeneXpert Module
GX-I
PAGE | 4
GX-IV
GX-XVI
Infinity
Our System Approach
Versus a random competitor
Gen-Probe
• Fixed Analyzer Format
• Old “batch” Technology
• 4 Assays On-board
• 1 ANALYZER
Test on Menu
• Narrow Future Menu Focus
• Single Technology (dated)
• Labor Intensive
• Low Test / m2
VS.
Cepheid
• Scalable Configuration
• Total Random Access
• Limited only by Menu
System
• 13 Tests on Menu
• Broad Future Menu
• Multiple Technologies
• Easy to Use
• High Tests / m2
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Patient Care Continuum
Triage
Time & Resources
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Dispo
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Patient Care Continuum
Overall Reduction
due to Elimination
of Waste
Triage
Time & Resources
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MRSA超菌 孩童鼻腔帶菌高
2011/04/19 中央社記者陳麗婷台北19日電
•
金黃色葡萄球菌是臨床上相當重要的致病菌,抗藥性金黃色葡萄球菌(MRSA)也被歸
類為超級細菌之一,近10年來曾在社區出現流行,尤其造成兒童感染嚴重病例不少,甚
至造成死亡。
•
林口長庚兒童醫院兒童感染科醫師陳志榮在2005到2008年研究,針對6000多名孩童採鼻
腔檢體分析,結果發現,台灣5歲(含)以下健康兒童,有7.8%鼻腔帶菌,且帶菌率在3
年間顯著上升。
•
值得注意的是,前陣子H1N1新型流感疫情高峰時,臨床發現患者續發細菌性肺炎也是近
10年來最嚴峻的,其中有些就是MRSA細菌感染引起。
•
此外,陳志榮分析院內2004年到2006年間重覆感染MRSA的病童與感染菌株,共有48位
孩童有2次以上MRSA感染,且7成是由同一株MRSA引起,甚至有病童在相隔超過11個
月後再次感染MRSA,仍是同一株細菌,顯示細菌未被根除,仍在鼻腔等處帶菌,等待
孩童免疫力低下時,又再度造成感染。
•
這項研究顯示,大多數的重複感染來自於病患自身所帶的細菌,因此,醫師積極主動篩
檢,並有效投藥去除帶菌,例如鼻腔抹藥或以特定殺菌劑讓患者洗澡,才是杜絕大部分
MRSA重複感染的有效方法。
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C.difficile
C.difficile (梭狀芽胞桿菌)是最常見可被辨識出來會導致感染愛滋病患者腹瀉的
細菌
• 細菌性腹瀉的發生率為每年每1000人中有7.2人,且直接和患者的免疫力被抑制有
關連
• 在引起疾病的有機物中,C.difficile (梭狀芽胞桿菌)佔了54%,,賀氏菌(Shigella
species)佔了14%
• 主要的復發危險因子有年紀增長,使用抗生素及住院治療
•
•
及時檢測成本效益: 降低抗生素使用、 減少腸道檢查 (結腸鏡檢查、 影像診斷學)以
及不必要手術干預
•
C.difficle感染平均將增加病患在醫院5-6天的留置時間,將增加病患在醫院的醫療
成本
•
Xpert C.difficle 除針對懷疑CDI感染患者作快速篩檢之外, 更能針對GDH(+)檢體
進行確認C.difficle產毒菌種是否存在
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Xpert MTB Agenda
•
Background: tuberculosis infection and disease
•
Current testing algorithms
•
Clinical value of Xpert MTB/RIF
•
Xpert MTB/RIF: product details
•
Xpert MTB/RIF: latest clinical experience
Tuberculosis: an important public health concern
• Bacterial disease, airborne – transmitted caused by
M.tuberculosis
• 1/3 world population latently infected: 2 billion people
• ~9.3 million of new cases in 2007 and 1.8 million deaths
• TB the second most deadly infectious disease
worldwide after HIV/AIDS.
• Most of the cases occur in the developing world.
PAGE | 11
TB burden, Taiwan
結核病一直是台灣最嚴重的傳染疾病,到國民所得已超過一萬三千美元的今天,每年
仍有將近約一萬三千名的新發個案,其嚴重性比所有其他傳染病的總和還大。
(行政院衛生署 結核病十年減半第二期計畫書)
PAGE | 12
How Much Does TB Cost?
20120.68元 (OPD)* ;166983.35 元(山地鄉)*
Average cost of treating a case of TB
X
14265
Annual incidence in Taiwan
=
$約2億8千7百萬 (OPD)
Annual cost in Taiwan
Sources:* 中國醫藥大學 馬作金強 助理教授-住院治療結核病患之成本效益評估研究
Tuberculosis infection versus active disease
Inhalation (1–5 μm Ø)
droplet infection
14265人/ 2008年TB新案數
10–30% infection 14265*1/3= 4755 人
No infection
90% LTBI
10% TB during lifetime
10% TB within 1 year if HIV+
HIV-
85% pulmonary TB
15% extrapulmonary TB
PAGE | 14
5–10% ACTIVE
TB within 2
years
4755*5%=237.75
HIV+
(2年新增開放性TB
病患)
33% pulmonary TB
33% extrapulmonary TB
33% both
1st line and 2nd line antibiotics
1st line therapy
2nd line therapy
Rifampicin (RMP)
Kanamycin, Capreomycin
Amikacin
Fluoroquinolones
Cycloserin
…
Isoniazid (INH)
Pyrazinamide (PZA)
Ethambutol (EMB)
Usual treatment regimens for new cases:
- 2 months therapy with 4 drugs: rifampicin + Isoniazid + pyrazinamide + ethambutol
- followed by a 4 months treatment with rifampicin + isoniazid
Drug resistant TB
• Jeopardizing TB control programmes
• MDR TB = Resistance to at least Isoniazid (INH) and Rifampicin (RIF)
• XDR TB = Resistance to al least isoniazid and rifampicin + any of the
fluoroquinolones + any of the three injectable drugs : Amikacin,
Capreomycin , Kanamycin
PAGE | 16
RIF resistance as surrogate marker for MDR TB
•
RIF resistance as a mono resistance not very
frequent (5-15% of them)
•
80-95% of RIF resistant strains are also
resistant to INH
PAGE | 17
Current diagnostics and patient management
Diagnostics
Day 1-3
Clinical judgement
3 Smear tests
+/- confirmation by PCR
4-6 weeks
Culture (liquid and solid)
Identification : TB, other
mycobacteria…
No drug susceptibility
Patient
management
Drug susceptibility testing
TB- : Patient released
TB- / TB+ confirmed
TB+:
1st line therapy initiated
Smear- TB: patient released
Smear+ TB: patient hospitalized
and isolated
MDR TB or XDR TB:
Therapy modified with 2nd / 3rd line
drugs
Patient placed in a negative
pressure room if available
The problem with current testing methods
•
Smear test (AFB):
Insensitive, WHO and national guidelines recommend 2
to 3 smear tests to be performed by suspected patient
• Requires highly skilled technician
• Time consuming: 1-2 hours
•
•
Culture
Highly sensitive
• Slow: 4 to 6 weeks
•
•
Current/previous Nucleic Acid Amplification methods:
Time consuming and requiring highly skilled personnel
• Highly specific
• Not optimal on clinical samples:
•
•
•
•
Very sensitive on culture:
•
•
PAGE | 19
Highly sensitive on smear positive samples (95-100%)
Until now not so sensitive on smear negative samples (60-75%)
For identification
For drug susceptibility testing
Lowënstein medium
Focus on PCR: new CDC recommendations
“CDC recommends that Nucleic Acid
Amplification testing be performed:
• on at least one respiratory specimen
• from each patient with signs and symptoms
of pulmonary TB for whom a diagnosis of
TB is being considered but has not yet
been established,
• and for whom the test result would alter
case management or TB control activities,
such as contact investigations.”1
1. MMWR. Updated Guidelines for the Use of Nucleic Acid Amplification
Tests in the Diagnosis of Tuberculosis. Jan 19, 2009
PAGE | 20
Unmet Needs
•
Early detection of disease
TB cases diagnosed without aetiology (smear-, current PCR not
sensitive enough)
• Limitation of spread
• Detection in HIV cases
•
•
Detection of MDR / XDR TB
•
•
•
PAGE | 21
Rapid implementation of the appropriate therapy
Limitation of spread of resistance
Optimisation of expensive isolation facilities
The value of Xpert MTB/RIF
Patient
management
Diagnostics
Day 1-3
Clinical judgement
1-3 Smear tests
Xpert MTB/RIF:
Smear+ / smear- TB confirmed
Rifampicin resistance
4-6 weeks
Culture (liquid and solid)
Identification : TB, other
mycobacteria…
Drug susceptibility testing
TB- : Patient released
TB- / TB+, MDR TB confirmed
TB+:
1st or 2nd line therapy initiated
Patient released or admitted
Isolation in regular or negative
pressure room
XDR TB:
Therapy modified
Patient placed in a negative
pressure room if available
The value of Xpert MTB/RIF:
•
Xpert MTB/RIF detects simultaneously the tuberculosis complex
and rifampicin resistance
•
Xpert MTB/RIF significantly enhances diagnosis and therapeutic
decision making in pulmonary tuberculosis
•
Xpert MTB/RIF combines rapidity and high sensitivity in a simply
performed test
PAGE | 23
The Xpert MTB/RIF Molecular Beacon Assay
C
A
5’3’-
D
-3’
-5’
rpoB gene
E
B
5 Probes bind to wild type
Probes do not bind to mutant sequence
1 Probe for SPC (B. globigii)
Molecular
Beacon
6 fluorescent dyes detected simultaneously
Target
Hybrid
PAGE | 24
Sensitivity and Specificity
Culture
Positive
Culture
Negative
Smear
Positive
Culture
Positive
70
5
275
7
289
0
Smear negative
Xpert
Positive
Xpert
Negative
• Sensitivity in smear negative, culture positive (S-C+) was 90.9% (70/77)
• Sensivity in smear positive, culture positive (S+C+). was 100% (275/275)
• Specificity of the assay was 98.3%
• Sensitivity observed for Rifampicin resistance was 96.7%
• Specificity observed for Rifampicin resistance was 98.6%
Specimen Processing
Routine Bacteriology
BSL2
Mycobacteriology
BSL3
2 min
Incubate 1-2 days
3 hrs (batch)
Incubate up to 8 wks
Culture Detection and Identification
Routine Bacteriology
BSL2
Mycobacteriology
BSL3
Myobacterial Culture Methods
MGIT liquid medium
7H11 agar
LJ slant
Specimen pellet
Average TTD: 3 wks
Automated Liquid Culture Systems
MGIT 960
320 tubes per unit
Positive
Average TTD: 7days
Drug Susceptibility Testing Methods for M. tuberculosis
Solid Media
MGIT 960
1. Absolute conc.
2. Proportion method
3. Resistance ratio
Average TAT: 8 wks
2-3 weeks
Specimen Processing is Required for NAATs
BSL3
2 hrs (batched)
Real-Time PCR
DNA extraction
Specimen Processing is Required for NAATs
BSL3
2 hrs (batched)
Real-Time PCR
DNA extraction
It’s About Time to Stop Transmission!
•
Approximately 20% of transmitted infections are caused by
smear-negative / culture positive patients1
•
Should the patient be isolated until culture results are available?
•
=> cost
Should the patient be released while awaiting culture results?
•
•
=> transmission risk
Sources:
1:Behr MA, Warren SA, Salamon H, et al. Transmission of Mycobacterium tuberculosis from patients smear-negative for acid-fast bacilli,
Lancet 1999; 353:444–449
GeneXpert® Module
Syringe Motor
Motherboard
Uniframe
I-CORE
Module
Door
Ultrasonic Horn
Valve Drive Motor
GeneXpert® Cartridge
PROCESSING CHAMBERS
REACTION TUBE
VALVE BODY
Cartridge Design and Operating Principle
Syringe
Barrel
RT-PCR
Tube
Rotary
Valve
Sonicator
Dome
PAGE | 37
Bead Format Reagents
Retaining
balls
Sample Processing Control bead:
Bacillus globigii spores; excipients
Enzyme reagent bead:
Taq polymerase; dNTPs; Buffers;
Mg 2+
Target-specific reagent bead:
primers; rpoB specific probes;
controls
PAGE | 38
Xpert MTB/RIF : biosafety levels required
PAGE | 39
Based on the CDC recommendations
Novel Technologies Combine Sample Processing
and Nucleic Acid Amplification
Sputum treated with “buffer” for 15 min
120 minutes
Amplification plot – TB positive/Rif sensitive
MTB Positive Medium, Rif Resistance NOT DETECTED
PAGE | 41
WHO statements
PAGE | 42
WHO endorses new rapid tuberculosis test A major milestone
for global TB diagnosis and care
•
2010.12.8 | London | Geneva - Today, WHO endorsed a new and novel
rapid test for tuberculosis (TB), especially relevant in countries most
affected by the disease. The test could revolutionize TB care and control
by providing an accurate diagnosis for many patients in about 100
minutes, compared to current tests that can take up to three months to
have results.
•
"This new test represents a major milestone for global TB diagnosis and
care. It also represents new hope for the millions of people who are at the
highest risk of TB and drug-resistant disease." said Dr Mario Raviglione,
Director of WHO's Stop TB Department. "We have the scientific evidence,
we have defined the policy, and now we aim to support implementation for
impact in countries."
PAGE | 43
NEJM – September 2010 – Rapid Molecular Detection of
Tuberculosis and Rifampin Resistance
•
Large press coverage followed the publication in the US, Europe, many
parts of the world
•
PAGE | 44
Dr Mario Raviglione, Director of the World Health
Organization's Stop TB Department, said: “The search for
faster and more effective means to diagnose TB, which is
the second greatest infectious killer of adults worldwide,
is a top priority for the global health community. Over the
next few days, WHO will convene independent experts to
review the full evidence about the field effectiveness of
this novel technology and propose it to country programs.
These results suggest that it has the potential to
revolutionize TB care, and WHO will treat it as a top
priority.”
Xpert® MTB/RIF Performance Highlighted in
Recent New England Journal Article
•
Rapid Molecular Detection of Tuberculosis and
Rifampin Resistance
Catharina Boehme, et al. New England Journal of Medicine, 1 Sept,
2010
Studied >1,700 Patients
• Peru, Azerbaijan, South Africa and India
• Smear Positive Patients
• 98.2% Sensitivity, 99.2% Specificity
• Smear Negative, Culture Positive
Patients
• 90.2% Sensitivity with Three Samples
• 72.5% Sensitivity with One Sample
• Patients with Rimfampin Resistance
• 97.6% Sensitivity, 98.1% Specificity
Xpert MTB/RIF – Romain Prieur
Impact of Multiple Samples on Sensitivity
Results – Detection of Rifampicin Resistance
Sensitivity
Specificity
Overall
99.1%
100%
Lima
100%
100%
Baku
98.1%
100%
Cape Town
93.8%
100%
Durban
100%
100%
Mumbai
99.2%
100%
After discrepant result resolution by sequencing
Results - Comparison with Other NAATs
•
The authors noted:
At sites performing alternative nucleic acid amplification testing, the sensitivity of
the automated molecular test performed directly on sputum was higher than that
of Amplicor (94.6% vs. 86.8%, P<0.01) and similar to that of ProbeTec (83.7%
vs. 83.9%, P = 0.96) performed on extracted DNA from sputum pellets.
• The specificity of the automated molecular test did not differ significantly from
that of Amplicor or Probetec
•
•
The Xpert MTB/RIF advantage over other NAATs
Rapid, simple set-up with little hands-on time
• Minimal risk of contamination
• Simultaneous rifampicin resistance result
• On-demand testing – no batch delays
•
JCM – January 2010 – Helb et al.
•
Part of the data from the pre-registration trials presented from
Vietnam and Uganda
•
107 sputum samples from suspected TB cases from Vietnam:
Sensitivity in smear + samples: 100% (n=29)
• Sensitivity in smear – samples: 71,7% (n=53) (smear – and
+ve by solid and liquid media)
• Specificity 100%
• 64 smear+ samples from Uganda:
•
Sensitivity of 98.4% for TB and 100% for RIF resistance
• Specificity for RIF resistance 100%
•
•
“The Xpert MTB/RIF assay offers the first technical opportunity
to bridge this gap, potentially bringing tests for both TB and drug
resistance to levels of the health system where many seek care.
PAGE | 49
ECCMID poster P2032 S. Naidoo (Johannesburg, ZA)
Evaluation of GeneXpert MTB/RIF assay on pulmonary and
extra-pulmonary samples in a high-throughput laboratory
•
Xpert MTB/RIF was tested on 1140 pulmonary and 361 extrapulmonary samples and compared to culture (MGIT) ; 970
culture positives
•
In pulmonary samples:
Sensitivity for TB complex = 99.8% ; specificity: 94.1%
• Sensitivity for RIF resistance: 99.4% ; spec: 98.8%
•
•
In non pulmonary samples:
Sensitivity: 93.5%
• Specificity: 99%
Link
•
PAGE | 50
Other posters presented at ECCMID 2010
P2048 T. Bodmer, A. Ströhle (Berne, CH) Diagnosing pulmonary
tuberculosis in a low prevalence setting – the Xpert MTB/RIF test
P2047 - J.S. Lin, C. Lin, R. Hsiao, L. Shih (Changhua, TW)
Evaluation of Xpert MTB/RIF assay and amplified Mycobacterium
tuberculosis direct test in direct detection of pulmonary M.
tuberculosis complex
P2076 K. Kart Yasar, F. Pehlivanoglu, G. Sengoz, E.R. Ince, S.
Sandikci (Istanbul, TR) Tuberculosis meningoencephalitis with
severe neurologic sequelae in an immigrant family’s child:
PAGE | 51
Poster presented at ASM 2010
Posters presented at ESM 2010
Detection of M. tuberculosis and rifampicin resistance using a commercial PCR real
time technique in respiratory and extrapulmonary samples (T.Tortola, N.Martin…Vall
d’Hebron Hosp. in Barcelona, Spain)
Preliminary evaluation of Xpert MTB RIF kit for tuberculosis detection in nonrespiratory specimens (M. Casal, M. Causse, Reina Sofia hosp in Cordoba, Spain)
Evaluation of GeneXpert MTB/RIF assay for Mycobacterium Tuberculosis detection
and Rifampicin resistance identification in patients with high clinical suspicion of
TB. (P.Ioannidis, D. Papaventsis, S. Nikolaou, National reference lab in Athens, Greece)
Molecular diagnosis of tuberculous meningitis: a three day experience (M. Peracchi,
L. Fallico, Padua, Italy) + oral presentation respiratory and non respitatory samples
Evaluation of Genexpert MTB/RIF assay for detection of Mycobacterium
Tuberculosis and Rifampicin resistance in a routine laboratory setting in Slovenia
(Manca Zolnir-Dovc, Golnik, Slovenia)
More to come at ICAAC 2010
Rapid and Efficient detection of Mycobactrium Tuberculosis by the Cepheid Xpert
MTB RIF assay (B. Malbruny...R. Leclercq, V. Cattoire, CHU Caen, France)
Effectiveness Analysis of Integrated Nucleic Acid Amplification System for the
Rapid Diagnosis of Smear-negative Pulmonary Tuberculosis (L.Muñoz,…F. Alcaide,
M. Santin, Hosp Univ. Bellvitge, Barcelona, Spain)
•
越短的時間得到正確的藥物治療,對結核病患有較佳的預後
•
在短時間得到治療,能減低傳染家人及社會的傳播壓力
•
病患短時間確診能改變TB及MDR-TB的傳播
•
及時確診是全球結核病控制的重要步驟
NEJM 363;11 Sep 9, 2010
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Delivering A Better Way
Delivering a Better Way to Realize the Benefits of Molecular Diagnostics
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