News
- A Report From Endo 2003
For
the 8th year, the CSRF exhibited at the annual meeting of The Endocrine
Society, Endo 2003. This year's meeting was held June 19-22 in Philadelphia.
The booth was staffed by Jane Ancharski, Renee Brooks, Karen Campbell,
Dori Middleman, Michelle Molen, and Louise Pace. Mary Walsh also
attended the conference. It was wonderful to have so many of us
together at one time. The booth was in an excellent location and
while booth traffic ebbed and flowed, we were generally very pleased
with the number of endocrinologists that stopped by.
This year's
conference had many talks and posters on Cushing's and related areas.
It is impossible to summarize all of the presentations, but here
are some highlights.
At both the
Endo 2003 and the Pituitary Congress, Dr. Anthony Heaney of Cedars
Sinai presented very, very interesting papers on a potential drug
treatment for ACTH secreting tumors. Three patients with failed
pituitary surgery for Cushing's and no response to ketoconazole
were given a drug usually used to treat type II diabetes, called
rosiglitazone. A favorable response was observed in two out of the
three patients. Given that previously no drug has shown promise
in treating ACTH secreting tumors, these results, while very preliminary
are encouraging. Rosigliazone also appears promising for other types
of pituitary tumors. A study protocol is under development at Cedars
Sinai.
Carol Woodburn,
CCRC, and Dr. Mary Lee Vance (Univ. of Virginia) presented the results
of a survey of 90 patients with confirmed Cushing's. Most patients
saw 2-4 doctors prior to diagnosis and most patients had Cushing's
for 3-5 years prior to diagnosis. Dr. Monica Starkman (Univ. of
Michigan) presented data relating to changes in brain structure
and improvements in depression, anxiety and learning 1 year after
successful treatment of Cushing's.
In a very well
attended Sunday morning Cushing's symposium chaired by Dr. J. Blake
Tyrrell (UCSF), Dr. Findling (St. Luke's, Milwaukee, WI) presented
the latest information on using night time salivary cortisol to
test for Cushing's. The salivary test was shown to be superior to
24 hour urinary cortisol and the overnight dex suppression test
for making the initial diagnosis of Cushing's, particularly in patients
in the earlier stages of Cushing's. In several instances, nighttime
salivary cortisol was the only test result that was abnormal. There
is now an FDA approved salivary cortisol test for the diagnosis
of Cushing's that is commercially available. Hopefully, wider usage
of this test will lead to earlier diagnosis. This work is included
in a recently published review article (Raff H, Findling JW, Annals
of Internal Medicine, 2003 June 17; 138(12):980-91). You can also
find more information on our web site under About
Cushing's - Testing.
In the same
session, as well as at the Pituitary Congress, Dr. Lynnette Nieman
(NIH) presented the latest information on determining the cause
of Cushing's. In patients with Cushing's due to an adrenal tumor,
ACTH values are usually below normal and the adrenal tumor visible
on an abdominal CT scan. In patients with higher ACTH values, the
diagnosis becomes more difficult. Of those with elevated ACTH, approximately
80% have a pituitary tumor (Cushing's disease) and 20% have ectopic
tumors. Up to 50% of those with pituitary tumors have a normal pituitary
MRI and approximately 10% of the normal population have small pituitary
tumors. Differentiation between pituitary and ectopic tumors is
further discussed in the Report From the Pituitary Congress also
in this newsletter.
Also in this
session, Dr. Bruno Allolio, (Medical University Klinik, Wuerzburg,
Germany) presented on Adrenocortical Cancer. Adrenal cancer has
an incidence of approximately 1-2 per million compared to current
estimates for Cushing's of 10-15 per million. A substantial number
of patients present with symptoms of hormone excess, such as Cushing's,
or virilization. Surgical removal of the tumor is the preferred
treatment when possible. Chemotherapy has been used in some cases
as has localized radiation, however more studies are necessary to
determine if these treatments are beneficial in minimizing recurrences.
Current chemotherapy agents appear limited in their ability to produce
remission and other chemotherapy agents are clearly needed. Adrenal
cancer is the subject of an upcoming consensus meeting in September
hosted by Dr. David Schteingart at the University of Michigan.
In a symposium
titled Advances in Endocrine Surgery, Dr. Geoffrey Thompson (Mayo
Clinic, Rochester, MN) presented a wonderful paper on Laparoscopic
Adrenalectomy, complete with a video of the surgery. Compared to
traditional open procedures, laparascopic adrenalectomies offer
shorter hospital stays, lower surgical complication rates and a
faster recovery. From 1992-2002, 290 patients underwent laparoscopic
adrenealecties at the Mayo Clinic. Cushing's tumors accounted for
25% and 16% of patients had bilateral adrenalectomies. Cure rates
for functional tumors using laparoscopy are identical to the open
procedure. Laparoscopic adrenalectomies do have a surgical learning
curve and are "safe and efficacious for adrenalectomy when
performed by endocrine surgeons with advanced laparoscopic skills."
Several other papers addressed surgical outcomes of pituitary surgery
for Cushing's Disease. Dr. Serhat Aytug (Univ. of Virginia) presented
data that when a pituitary source of Cushing's is confirmed with
petrosal sinus sampling, the rate of successful surgery does not
differ between patients who underwent sinus sampling and those who
did not. Dr. Sylvie Salenave of France reported on 49 patients with
confirmed Cushing's Disease. In the study group, 24 patients had
pituitary tumors that were visible on an MRI and 25 patients had
"normal" MRI's. The surgical outcome did not differ between
the two groups, thus "we recommend pituitary neurosurgical
exploration as the first line treatment in Cushing's disease provided
that the pituitary origin of ACTH secretion has been previously
checked by petrosal sampling in patients with normal MRI's."
The cardiovascular
risk (high blood pressure, obesity, diabetes, high cholesterol,
etc.) associated with Cushing's was the subject of numerous presentations
and posters. The area of Subclinical Cushing's, adrenal incidentalomas
and Cushing's in children were also addressed. Dr. Neiman (NIH)
and Dr. Grossman (St. Bartholomew's Hospital, London) both presented
Meet-the-Professor sessions on Cushing's where endocrinologists
had many opportunities to ask questions. You can check the abstracts
yourself after signing in at www.endo-society.org.
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