Leading the Way in Life Science Technologies

GEN Exclusives

More »

Feature Articles

More »
Jun 15, 2009 (Vol. 29, No. 12)

Banked-Specimen Retrospective Studies

A Clinical Validation Shortcut or a Lengthy Detour?

  • Click Image To Enlarge +
    MammaPrint identifies patients with early metastasis, providing doctors with a clear rationale to assess the benefit of chemotherapy in addition to other clinical information and pathology tests, according to Agendia.

    Many marketing applications for in vitro diagnostics (IVDs) need to be supported by clinical data. This is especially likely for new analytes or new intended uses. In some instances, the only means to gather the requisite data is by conducting a prospective study. Sometimes, only freshly collected specimens can be used to generate the necessary data due to the nature of the disease or the assay. Moreover, collecting specimens prospectively gives the applicant the most control over the study design. The applicant, for example, can make sure the clinical specimens are collected in a manner that precisely matches the proposed intended use. 

    Prospective studies, however, often suffer the drawback of taking too long to conduct. This is particularly true for predictive or prognostic tests for conditions which manifest themselves, progress, or recur over prolonged periods. These patients may need to be followed for years to assess the IVD’s clinical performance.

    There is an obvious shortcut: use banked specimens to conduct a retrospective study.  By testing specimens that were gathered years ago, a company may be able to dramatically accelerate its clinical validation program.

    Can retrospective studies ever support a 510(k) clearance or a premarket approval application (PMA)? The answer is yes.  FDA has already cleared or approved a number of applications based on testing banked samples, such as Agendia’s MammaPrint and Pathwork Diagnostics’ Tissue of Origin Test.

    Of course, utilizing banked specimens is no panacea. This approach can present multiple obstacles. Before embarking on a retrospective study to support an IVDs marketing, the company must be sure it can overcome these scientific, legal, and regulatory challenges.

    In general, an FDA applicant must obtain the written informed consent of subjects before they can participate in a clinical study. For retrospective studies where specimens were obtained years ago, obtaining consent to participate in a post-collection study is often impossible. 

    Recognizing this problem, FDA has established a policy permitting the use of remnant samples for IVD studies. Entitled “Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens that Are Not Individually Identifiable,” this policy allows companies to rely upon stored samples, provided that certain conditions are met. FDA adopted this policy in recognition of it sometimes being “difficult, if not impossible, to locate the donor and obtain consent.”

    In order to qualify for the exemption, the study must meet multiple criteria. These include that the specimens are “remnants of specimens collected for routine care or analysis that would have been discarded”; the specimens cannot be individually identified by the sponsor or investigator (meaning that coded specimens can be used); the individuals caring for the patients do not conduct the investigation; and any clinical data accompanying the specimens do not allow the source of the specimen to be identified. This “de-identification” must be irreversible. A study where the IVD results would be reported back to the subject’s healthcare provider would be ineligible under this policy.

    One other issue that must be considered is whether the new study is consistent with the informed consent provided by the patients when the sample was collected. It may be that there is no consent form documentation relating to the issue of subsequent use of tissue. The IVD sponsor should be able to use the specimens under this scenario if the banked specimens otherwise meet FDA’s policy. However, sometimes the consent form states that the specimen is to be used only for a specified purpose, e.g., a named study, or the form affirmatively excludes certain uses, e.g., genetic research.

    This clear expression of intent generally controls, even if the samples are “de-identified” so that the applicant does not know the patient’s name. The patient’s explicit intent to limit the use of his or her biological materials will ordinarily prevail.

    A related issue is whether the patient has any ownership claim to the specimen.  Biological materials may turn out to be valuable, and the patients who provided the specimens may feel that they deserve a share of the proceeds. This is a complex topic, which has been the subject of litigation. In general, a biological specimen collected from a patient is medical waste, and the patient has no legal claim to any intellectual property or other rights stemming from the specimens.

    Specific factual circumstances, though, may allow one or more patients to allege that they are entitled to share in the IVD company’s earnings. It is prudent to verify that there is no basis by which patients can plausibly claim that they also have an ownership or other interest in the specimens being used to evaluate the performance of the IVD product, or to address this issue in the Clinical Trial Agreement with the study site.

Related content

Be sure to take the GEN Poll

Drug Price Hikes

Novum Pharma recently raised the price of an acne cream by over 3,900% in less than a year-and-a-half and Mylan increased price of EpiPen from $100 to $608 . Do you think pharmaceutical companies need to be subjected to price controls?

More »