Presentation on theme: "IVD Validation and Regulation in Rx/Dx Combinations"— Presentation transcript:
1IVD Validation and Regulation in Rx/Dx Combinations FDA/Industry Statistics WorkshopClassifiers in Combination Rx/Dx SubmissionsRobert L. Becker, Jr, MD, PhDU.S. Food and Drug AdministrationCenter for Devices and Radiological HealthOffice of In Vitro Diagnostic Device Evaluation and Safety
2SettingCoordinated, interdependent development and use of diagnostic devices and therapeutics is both needed and happening now.Preclinical drug developmentFocusing drug trialsShaping drug indications (test, then treat)Measuring drug effect (treat, then test…)
3Practical Constraints Diagnostic devices measuring biomarkers have technical characteristics and limitations, demonstrated from experience, that inform their use.Biomarker measurement is a messy affair, with challenges that affect the ease of Rx/Dx application.Study designs for biomarker/IVD validation, and clearance or approval, present trade-offs.Regulatory approach must accommodate all of the above.
8Tumor Associated Antigen Immunological Test System “Measurement of tumor-associated antigen levels may aid in the monitoring of patients for disease progression or response to therapy or for the detection of recurrent or residual disease. Tumor-associated antigen immunoassay systems intended for use in screening for the early detection or diagnosis of cancer in either the general population or in a high risk population, or in disease staging, are not included.”
9TAA Uses and Impacts Diagnosis Monitoring Prognosis Prediction ScreeningConfirmatory initial diagnosisResidual or recurrent diseaseMonitoringChange in tumor burden over timePrognosisLikely outcome (e.g. natural history), given a set of featuresPredictionMarker-dependent change in outcome, given a new or changed therapy
12A Few IHC Complications Non-linear amplification, signal “development”Antigen recovery, variationAntibody specificity, affinity, avidityReadout variates (distribution, intensity, prevalence)As a result, analytical (and hence clinical) sensitivity and specificity are highly dependent on technique.
13FISH vs IHC Techniques FISH probes and ligands usually better defined FISH uses less layering or amplificationFISH cytologic features more discrete; possibly easier readoutMultiple (e.g. two) markers readily accomodatedTechnique aside, what is clinical import? Less widely studied, but this is changing.
14Immunohistological Markers Long and wide (TNTC) experience with markers of tumor histogenesis – generally Class 1 exemptLong but narrower (e.g. down-classified ER/PR) experience with markers for prognosis or predictionRecent experience with a few markers intended to help guide chemotherapy selection.
16Immunohistochemical Applications “Class I IHC’s provide the pathologist with adjunctive diagnostic information that may be incorporated into the pathologist’s report, but that is not ordinarily reported to the clinician as an independent finding.”“Class II IHC’s are intended for the detection and/or measurement of certain target analytes by immunological techniques in order to provide prognostic and predictive data that are not directly confirmed by routine histopathologic internal and external congtrol specimens. These IHC’s provide the pathologist with diagnostic information that is ordinarily reported as independent diagnostic information to the ordering clinician, and the claims associated with these data are widely accepted and supported by valid scientific evidence.”“[Class III IHC’s] are IHC’s that do not meet the criteria for class I or class II, or are IHC’s that meet those criteria but raise new issues of safety and effectiveness.”
17Three Recent PMA IHC Applications CD 117 (c-kit) for imatinib (Gleevec) treatment of gastrointestinal stromal tumorHer2/neu for trastuzumab (Herceptin) treatment of metastatic breast cancerEGFR for cetuximab (Erbitux) or panitumumab (Vectibix) treatment of metastatic colorectal cancerNone of these applications included a prospective trial of the device for its ability to predict drug response.
18Absent a BM+/BM- Drug Trial… Biomarker predictive value for drug effect is incompletely evaluated at best.Rely on BM-dependent drug effect within BM+ patients.Risk exclusion of potentially responsive patients.Cannot dissect BM predictive power from prognostic power.How much confidence in the BM IVD cut-off? In the assay to meet it?Post-approval study commitments? Fulfillable?What non-trial evidence suffices to conclude non-response for BM- patients?Larger problem when BM+ fraction is small.Some combination of practical benefits to trial execution.Lower cost?More power?Fewer adverse events?
19CD 117 and Gleevec for GIST“…indicated as an aid in the diagnosis of GIST within the context of the patient’s clinical history, tumor morphology, and other diagnostic tests… …may be used after the diagnosis of GIST as an aid in the selection of GIST patients who may qualify for imatinib mesylate (Gleevec) therapy.”Any specific staining is a positive result.Main utility is in helping to identify GIST, not in selecting the drug.
20Her-2/neu IHC and Herceptin for Breast Ca “…indicated as an aid in the assessment of patients for whom HERCEPTIN (Trastuzumab) treatment is being considered…”Graded staining result (2+ vs 3+ makes a difference)Technique and read-out variations, in deployed performance, may decrease effectiveness – FISH back-up for IHC 2+ cases.
21EGFR and Erbitux for Colorectal CA “…indicated as an aid in identifying colorectal cancer patients eligible for treatment with ERBITUX…”No sign of clinical response dependence on IHC signal strengthPost-market suggestions that IHC “negative” patients respond similar to “positives”Ambiguity as to what is a “negative” result
22Some Issues to AddressAnalytical validation of IHC tests, the earlier the better, especially wrt definition and performance near cut-off points.Trial designs such that clinical validity is assessed across the full range of test results (i.e. including “negative” patients).Retention and access to clinical trial samples so that later tests (either same or different technique) can be properly evaluated.
23Why worry?Multiple modalities for tumor assessment aimed at drug selection are emerging – EGFR for NSCLC as an example.Other markers further complicate the picture.Numerous non-comparable, low-power studies.Risk that biomarkers will be unfairly dismissed, or relied on without justification.
24Why hope?Issues, though complex and controversial, can at least be defined.Continually improving coordination between stakeholders.With large stakes, continuing interest seems assured.