Bioengineering and World Health Lecture Thirteen.

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Presentation transcript:

Bioengineering and World Health Lecture Thirteen

Outline The burden of cancer How does cancer develop? Why is early detection so important? Strategies for early detection Example cancers/technologies Cervical cancer Ovarian cancer Prostate cancer

Importance of Early Detection Five Year Relative Survival Rates

Screening Use of simple tests in a healthy population Goal: Identify individuals who have disease, but do not yet have symptoms Should be undertaken only when: Effectiveness has been demonstrated Resources are sufficient to cover target group Facilities exist for confirming diagnoses Facilities exist for treatment and follow-up When disease prevalence is high enough to justify effort and costs of screening

How do we judge efficacy of a screening test? Sensitivity/Specificity Positive/Negative Predictive Value

Bioengineering and Cervical Cancer

Statistics on cervical cancer US data (2007) Incidence: 11,150 Mortality: 3,670 World data (2004) Incidence: 510,000 (80% developing world) Mortality 288,000 deaths per year worldwide

Global Burden of Cervical Cancer

Risk factors HPV infection HPV infection is the central causative factor in squamous cell carcinoma of the cervix Sexual behaviors Sex at an early age Multiple sexual partners Cigarette smoking

Human papilloma virus (HPV) Most common STD >70 subtypes Asymptomatic infections in 5-40% of women of reproductive age HPV infections are transient

HPV and cervical cancer

What Initiates Transformation?

Pathophysiology

HPV vaccine Virus-like particles (VLP) made from the L1 protein of HPV 16 approved for use in girls and women aged 9 to 26 years in the US not effective to women already exposed to HPV Effective on 4 HPV isotypes Recombinant technology Alternative prevention technique to screening?

How Do We Detect Early Cervical Cancer?

Pap Smear 50, ,000 cells/per slide Cytotechnologists review slides (<100/day) Se = 62%3% Sp = 78% $6B

Colposcopy and Biopsy Se = 95% Sp = 44% Colposcope Biopsy sections

Colposcopy and Treatment CIN 1/LGSIL CIN 2/HGSIL CIN 3/HGSIL Microinvasive CA Invasive CA

Detection and Treatment Screening: Pap smear Diagnosis: Colposcopy + biopsy Treatment: Surgery, radiotherapy, chemotherapy 5 year survival Localized disease: 92% (56% diagnosed at this stage)

Screening Guidelines, ACS  All women should begin cervical cancer screening about 3 years after they begin having vaginal intercourse, but no later than when they are 21 years old. Screening should be done every year with the regular Pap test or every 2 years using the newer liquid-based Pap test.  Beginning at age 30, women who have had 3 normal Pap test results in a row may get screened every 2 to 3 years with either the conventional (regular) or liquid- based Pap test.  Option for women over 30 is to get screened every 3 years with either the conventional or liquid-based Pap test, plus the HPV DNA test.

Trends in Screening Cervical Cancer

Challenge Developed and developing world Cost and infrastructure requirements for screening Need for appropriate technologies

New Detection Technologies Aims: Reduce the false positive and false negative rates Give instantaneous results Reduce the costs

New Technologies for Cervical Cancer Liquid Based Pap testing Automated Pap smear screening HPV Testing VIA HPV Vaccine

Liquid Based Pap Smear Rinse collection device in preservative fluid Process suspension of cells to deposit a monolayer of cells on a microscope slide Conventional Pap Liquid Based Pap

Liquid Based Pap Smear Gentle dispersion breaks up blood, mucous, non- diagnostic debris, and mixes sample Negative pressure pulse draws fluid through filter to collect a thin, even layer of cells Monitor flow through filter during collection to prevent cells from being too scant or too dense Cells then transferred to a glass slide

Automated Pap Smear Screening TriPath Care Technologies m/usproducts/index.htm m/usproducts/index.htm

HPV Testing The DNAwithPap Test is FDA-approved for routine adjunctive screening with a Pap test for women age 30 and older. Digene YLC %20VER%20X.mpg

1. Release Nucleic Acids Clinical specimens are combined with a base solution which disrupts the virus or bacteria and releases target DNA. No special specimen preparation is necessary. 2. Hybridize RNA Probe with Target DNA Target DNA combines with specific RNA probes creating RNA:DNA hybrids. 3. Capture Hybrids Multiple RNA:DNA hybrids are captured onto a solid phase coated with universal capture anbtibodies specific for RNA:DNA hybrids. 4. Label for Detection Captured RNA:DNA hybrids are detected with multiple antibodies conjugated to alkaline phosphatase. Resulting signal can be amplified to at least 3000-fold. 5. Detect, Read and Interpret Results The bound alkaline phosphatase is detected with a chemiluminescent dioxetane substrate. Upon cleavage by alkaline phosphatase, the substrate produces light that is measured on a luminometer in Relative Light Units (RLUs).

Sensitivity of HPV Testing Study of 5,671 women age >30 years ens.gif

Comparison of Various Techniques SensitivitySpecificity Pap smear60-80%45-70% Colposcopy90-100%20-50% Digene HPV Test80-90%57-89% VIA67-79%49-86%

Costs Pap Test$10-20 Liquid-based Pap$50 Automated Pap Smear Screening $20-60 HPV DNA test$90 HPV vaccine$360

Needle Biopsy Dichroic Mirror LED Source 10X UPLAPO Objective Image Guide Tube Lens CCD Camera Frame Grabber

Needle Biopsy

Summary of Cancer The burden of cancer Contrasts between developed/developing world How does cancer develop? Cell transformation  Angiogenesis  Motility  Microinvasion  Embolism  Extravasation Why is early detection so important? Treat before cancer develops  Prevention Accuracy of screening/detection tests Se, Sp, PPV, NPV

Summary of Cervical Cancer Cervical cancer 2 nd Leading cause of cancer death in women in world Caused by infection with HPV Precancer  cancer sequence Precancer is very common Screening & Detection Pap smear; colposcopy + biopsy Reduces incidence and mortality of cervical cancer Insufficient resources to screen in developing countries New technologies Automated reading of Pap smears  reduce FN rate HPV testing VIA

South Africa Screening 1X/Life Cost saving to <$50/YLS South Africa Screening 2X/Life $50-$250/YLS South Africa Screening 3X/Life $250-$500/YLS United States Pap + HPV Every 3 yrs. $60,000/YLS United States Pap + HPV Every 2 yrs. $174,000/YLS United States Pap + HPV Every Year $795,000/YLS 15 Weeks 1,000 Years! Global Inequities in Cancer Prevention