Advertisement

Needle Biopsies for Noninvasive Breast Cancer: Routine Analysis Wastes Millions

Advertisement

Key Points

  • Why not to reflexively test a core biopsy showing DCIS for hormone receptors: (1) Regardless of hormone receptor testing results, the U.S. standard of care after needle biopsy for DCIS is that the breast tissue remaining in the suspect area is excised by lumpectomy or mastectomy. (2) Almost 20% of the time, the excision reveals that the noninvasive DCIS that the core needle biopsy caught is accompanied by invasive breast cancer. (3) When the surgical excision contains DCIS alone and the core biopsy result was negative, most physicians would recommend retesting of the DCIS in the surgically excised specimen.
  • Unnecessary early receptor analysis cost about $140 per patient for preparing a trustworthy stained slide and for the pathologist's study of it; extrapolating that to the roughly 60,000 U.S. patients diagnosed with DCIS yearly puts the cost at about $8.5 million.

For patients with the most common type of noninvasive breast cancer, routine testing for estrogen and progesterone receptors in tissue taken at the first needle biopsy is both unnecessary and wasteful, according to results of a study led by Johns Hopkins pathologists. The results for people with ductal carcinoma in situ (DCIS) were persuasive enough that The Johns Hopkins Hospital ended the practice of routinely conducting so-called core needle biopsy hormone receptor testing last January.

“If you apply our local results nationally, these unnecessary initial hormone receptor tests currently come with an annual price tag of around $35 million,” said Pedram Argani, MD, Professor of Pathology and Oncology at the Johns Hopkins University School of Medicine and senior author of a study published by VandenBussche et al in the American Journal of Surgical Pathology. “Our results indicate that's an expense without any justification. If these tests were routinely eliminated, the savings would be substantial.” Dr. Argani also directs the Breast Pathology Service at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins.

Study Details

The study focused solely on people newly diagnosed with DCIS. The Hopkins team reviewed the pathology and medical records of 58 such patients who, within a 2-year period beginning in January 2011, had core needle biopsies showing DCIS and follow-up excision at The Johns Hopkins Hospital.

The rationale for doing the testing has always been that patients with hormone receptor–positive DCIS after excision can take relatively nontoxic medications such as tamoxifen to block the receptors and help prevent the DCIS from recurring.

However, there are multiple reasons not to reflexively test a core biopsy showing DCIS for hormone receptors, Dr. Argani explained. First, regardless of the core biopsy hormone receptor testing results, the standard of care in the United States after needle biopsy for DCIS is that the breast tissue remaining in the suspect area is excised by lumpectomy or mastectomy. Hence, the core biopsy hormone receptor results do not affect therapy.

Second, Dr. Argani added, “Almost 20% of the time, the excision reveals that the noninvasive DCIS that the core needle biopsy caught is actually accompanied by invasive breast cancer. So you have to receptor-test the invasive cancer that the core biopsy missed. That means the testing of the core biopsy with DCIS was useless.”

Third, when the surgical excision contains DCIS alone (as it does about 80% of the time) and the core biopsy result was negative, most physicians would recommend retesting of the DCIS in the surgically excised specimen, since hormone receptor expression can be heterogeneous and a small biopsy could miss a positive area.

While hormone-blocking therapy specifically for receptor-positive DCIS can modestly lower the chance of tumor recurrence, prior studies have shown that therapy ultimately has no effect on a patient's survival. Plus, hormone-disabling medications like tamoxifen carry side effects, including a higher-than-usual risk of blood clots.

“Two-thirds of our DCIS study patients did not receive hormone therapy,” Dr. Argani said, “even after excision confirmed their hormone receptor–positive DCIS status. So analyzing their needle biopsies or surgical excisions for receptors would have clearly been unnecessary for them.”

In the Hopkins study, unnecessary early receptor analysis cost about $140 per patient for preparing a trustworthy stained slide and for the pathologist's study of it.

“Extrapolating that to the roughly 60,000 U.S. patients diagnosed with DCIS yearly puts the cost at about $8.5 million,” Dr. Argani added. “The unnecessary cost of automatically testing DCIS in excisions when the information is not used is $26.5 million, which adds up to $35 million dollars per year in the United States.”

The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.


Advertisement

Advertisement




Advertisement