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Home: Oncology Leader Commentary: David Krag, MD

Click on the topic below for comments by Dr David Krag to comment on. You will also find links to related articles and clinical trials.

NSAPB sentinel node trial: Eligibility
NSAPB study
Immunohistochemistry
NSABP sentinel node trial: Survival endpoints
NSABP sentinel node trial: Morbiditiy endpoints
Morbidity of axillary dissection
NSABP sentinel node trial: Training surgeons to participate
Rationale for axillary dissection
NSABP sentinel node trial: Accrual
Should Sentinel node biopsies be done outside a clinical trial setting?
American College of Surgeons sentinel node trial

Immunohistochemistry

Interview with Neil Love, MD from Breast Cancer Update for Surgeons, Program 2000

Play Audio Below:

There are two ways to find small metastasis in a node: Either by multiple cut serial sections or by enhanced staining procedures, immunohistochemistry. And so we know since 1948 that if you cut through in serial sections you’re going to upstage anywhere from 15 to 30%. So it’s really nothing new, the numbers have not changed since before I was born. So what’s happened is we just never documented, in sufficient ways, levels in a perspective study whether this is meaningful for survival. So for this study we will have enough patients to demonstrate if there is a survival difference, we’ll be able to demonstrate that. So, since we know that the most important is in the 1 to 2 millimeter range, as a cut-off that these are definitively shown to be pathologically meaningful, we’re doing serial sections at the participating site. The pathologist will cut the node in layers. That will be used clinically. But then, those nodes are negative with that initial serial section analysis, with H&E, will then be sent to University of Vermont in a blinded fashion and have immunohistochemistry performed.

And we think the conversion rate’s probably going to be around 10%.

Relevant Articles:

Kronz, J. D.; Westra, W. H., and Epstein,J.I.Cancer.86(11):2426-2435,1999Dec 1.

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