Endocrine Society Releases Guidelines on Treatment of Cushing’s Syndrome

Posted on August 26, 2015 by MaryO

To lessen the risk for comorbidity and death, the Endocrine Society’s newly published guidelines on the treatment of Cushing’s syndrome focus on surgical resection of the causal tumor with the goal of normalizing cortisol levels. Furthermore, there is increased emphasis on individualizing treatment options when choosing a second-line treatment.

In July 2015, the Endocrine Society published treatment guidelines to assist endocrinologists in appropriately initiating treatment or referring patients with Cushing’s syndrome to treatment. A task force of experts compiled evidence from systematic reviews and graded the strength of the recommendations.

“We hope that it will lead to improved treatment of comorbidities both before and after definitive treatment of the syndrome, and to increased individualization of patient treatment,” said chair of the task force Lynnette Nieman, MD, who is chief of the Endocrinology Consultation Service at the National Institutes of Health Clinical Center.

“There are two new drugs that were approved in 2012, and so I think that is what prompted the review. Still, medications are not the first line of treatment, but we have some new therapeutic options, and I think the idea was to help people understand where to use them,” Julie Sharpless, MD, assistant professor and director of the UNC Multidisciplinary Pituitary Adenoma Program, told Endocrinology Advisor.

“The primary treatment is surgical resection of the causal tumor(s). If that cannot be done (because the tumor is occult or metastatic) or is not successful, then the choice of secondary treatment should be individualized to the patient. The comorbidities of Cushing’s syndrome, for example hypertension and diabetes, should be treated separately as well,” Nieman said.

For example, the guidelines recommend surgical removal of the causative lesion, with the exception of cases which are unlikely to cause a drop in glucocorticoids or in patients who are not surgical candidates.

Likewise, in patients with benign unilateral adrenal adenoma, adrenalectomy by an experienced surgeon has a high rate of cure in children and adults. Because of the poor prognosis associated with adrenal carcinoma, the guidelines highlight the need for complete resection and possibly medical treatment to stabilize cortisol levels.

Other first-line treatment options include recommending surgical resection of ectopic ACTH-secreting tumors; referring to an experienced pituitary surgeon for transsphenoidal selective adenomectomy; treatments to block hormone receptors in bilateral micronodular adrenal hyperplasia; and surgical removal in bilateral adrenal disorders.

The elevated mortality rate seen in patients with Cushing’s syndrome is due to infection, venous thrombosis and cardiovascular disease (CVD). Appropriately lowering cortisol levels improves hypertension, insulin resistance, dyslipidemia and obesity in patients with Cushing’s syndrome. Therefore, the guidelines highlight the need for restoring cortisol levels and treating the associated comorbidities.

Nevertheless, the task force specifically recommends against treatment without an established diagnosis or when there are no signs of Cushing’s syndrome and hypothalamic-pituitary-adrenal laboratory studies are borderline.

In patients who are not surgical candidates or in cases of noncurative resection, the decision on whether to consider second-line treatment options such as medical therapy, radiation, bilateral adrenalectomy or repeat transsphenoidal surgery should be based on several factors. For instance, the guidelines recommend taking into consideration location and size of the tumor, patient desires, goals of treatment and level of biochemical control.

The guidelines note medical therapy should be based on cost, efficacy and individualization of treatment. Endocrinologists can approach medical therapy with a goal of establishing normal cortisol levels or reducing cortisol levels to very low levels and replacing to achieve desired levels.

Remission in Cushing’s syndrome is associated with notable improvement; however, long-term follow-up is recommended for osteoporosis, CVD and psychiatric conditions.

After treatment, patients may experience reductions in weight, blood pressure, lipids and glucose levels that may allow reduction or discontinuation of medications. Even so, patients with a history of Cushing’s syndrome tend to have higher rates of hypertension, hyperlipidemia and diabetes. Likewise, rates of myocardial infarction are higher in this population, further emphasizing the need for treatment and management of diabetes and hypertension.

Sharpless highlighted that Cushing’s syndrome is rare.

“There are multiple studies that have shown that patients do better when they are treated in a specialty center where people see a lot of cases of this. So in that sense, treatment is not usually going to fall to the general practitioner,” she said.

She continued that the guidelines are helpful and provide guidance to endocrinologist who “can’t readily refer their patient to a pituitary center.”

Sharpless went on to describe the multidisciplinary care involved in Cushing’s syndrome including endocrinologists, neurosurgeons, radiologists, counselors and radiation oncologist.

“When the care is complicated, you want to ensure all of your providers have reviewed your case together and figured out the best plan.”

The guidelines were co-sponsored by the European Society of Endocrinology. Nieman received salary support for her work on the manuscript from the Intramural Research Program of the Eunice Kennedy Shiver Institute of Child Health and Human Development. Members of the task force reported multiple disclosures.

Reference

  1. Nieman LK et al. J Clin Endocrinol Metab. 2015;100(8):2807-2831.

From http://www.endocrinologyadvisor.com/adrenal/cushings-syndrome-endocrine-society-guidelines/article/434307/

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Apathy and Pituitary Disease: It Has Nothing to Do With Depression

Posted on August 22, 2015 by MaryO
Michael A. Weitzner, , M.D., Steven Kanfer, , M.D., Margaret Booth-Jones, , Ph.D.
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Increasingly, patients with pituitary disease are evaluated and treated at cancer centers. In many ways, these patients resemble patients with other malignant brain tumors. Although the majority of pituitary adenomas are benign, the physical, emotional, and cognitive changes that these patients experience on their well-being is malignant. Pituitary disease causes a variety of physical illnesses resulting from the alterations in the hypothalamic-pituitary-end organ axis. In addition, patients with pituitary diseases may experience many emotional problems, including depression, anxiety, behavioral disturbances, and personality changes, above and beyond the many reactions these patients may have to the myriad of adjustments that they must make in their lives. There is a growing understanding that pituitary patients may experience these emotional problems as a result of long-term effects that the pituitary tumor itself, treatment, and/or hormonal changes have on the hypothalamic-pituitary-end organ axis. The authors present a series of cases, in which patients with pituitary disease were diagnosed and treated for depression and showed little response to the treatment for depression. When the diagnosis of apathy syndrome was considered and treatment implemented, the patients’ condition improved. A review of the literature on apathy, hypothalamic-pituitary-end organ axis dysfunction, and treatment for apathy syndrome is included.

Patients who are diagnosed with pituitary disease experience many physical changes that have been well documented in the literature. These patients may have significant fluctuations in their weight as well as changes in their physical appearance, as seen in patients with adrenocorticotropic hormone-producing adenomas (ACTHomas), prolactinomas, and growth hormone-producing adenomas (GHomas). They may also experience changes in their sexual and reproductive functioning, such as amenorrhea, impotence, and impaired orgasm. Many patients with pituitary disease develop comorbid medical illnesses as a result of their pituitary dysfunction. The development of diabetes mellitus, hypertension, and coronary artery disease are a few examples.

In addition to the physical changes and comorbid medical conditions, there is a clear association between psychiatric illness and pituitary disease. In pituitary disease, one of the most common psychiatric manifestations is the presence of depressive symptoms significant enough to warrant diagnosis of a major depressive disorder.1 Cushing’s disease is probably the most frequently studied of the pituitary diseases. It has been shown that roughly 50% of patients with Cushing’s disease have depressive symptoms of a sufficient intensity to be diagnosed with a major depressive disorder. In addition to the depressive symptoms, these patients often demonstrate pronounced psychopathology associated with the depression, including lethargy, increased sleepiness, cyclic mood instability, impaired cognitive function (i.e., deficits in concentration and memory), and personality change.2,3 Similarly, patients with growth hormone deficiency (GHD) may experience a lack of energy and drive (i.e., motivation), as well as problems with memory and concentration.4

Patients with acromegaly have also been shown to have psychiatric disturbances. Up to 75% of patients experience personality changes, including depressive symptoms, other mood changes, anger, loss of motivation, and a decreased willingness to socialize.5 Patients with prolactinomas also have reported a higher frequency of depressive symptoms, anxiety, and feelings of hostility than a group of people with either amenorrhea associated with normal prolactin levels or healthy comparison subjects with normal prolactin levels.6 In addition, apathy was one of four neuropsychiatric signs and symptoms (i.e., asexuality, adiposity, headache).7

Few studies have attempted to quantify the overall impact that a variety of pituitary diseases has on social functioning and overall quality of life. One study reported that patients with adult-onset pituitary insufficiency experienced decreased quality of life. The patients who had adult-onset GHD experienced a lower sense of well-being and a decreased psychological reserve (i.e., coping reserve) than a reference population. They also had lower scores on measures of perceived health and social function than the reference population.4

Another study compared pituitary tumor patients based on treatments received (i.e., surgery either transfrontally or transsphenoidally and medical management) to a group of comparison subjects.8 The results showed that the patient groups who had received either transsphenoidal surgery or medical management rated themselves as having mild mood disturbance, poorer social adjustment, higher levels of emotional distress, and lower energy levels than comparison subjects. Although the transfrontal surgery patients rated themselves no differently than the comparison group, proxy assessment revealed these patients to be different from the comparison group as well. The investigators concluded that this discrepancy was related to the lack of insight associated with frontal lobe surgery and damage.

Pituitary patients who received radiotherapy have been shown to have lower quality of life scores, when compared to healthy subjects.9 Furthermore, in a study that compared the performance of pituitary tumor patients with and without radiotherapy, both pituitary tumor groups performed poorer than the comparison group, with similar degrees of dysfunction in executive functioning, verbal memory and visual memory for both tumor groups.10

Thus, given the paucity of research, studies across all pituitary diagnoses document the presence of depressive symptoms, mood instability, loss of motivation, and anxiety. It also appears that, when matched against comparison groups, these patients experience lower quality of life and more cognitive dysfunction if they receive radiotherapy. Clearly, there are limitations to the work that has been described. These studies have all involved small sample sizes, so a question of adequate power to detect meaningful differences between the groups comes into question. In addition, the majority of these studies has focused on all pituitary patients, and it appears that issues may be different for different pituitary diagnoses. Finally, the majority of these studies has not controlled for other factors that may interfere with interpretation of the results, such as comorbid medical illness. As a result, it is difficult to generalize the results regarding neurocognitive functioning.

Furthermore, the studies to date have focused on the presence of depressive symptomatology, as measured by self-report instruments. Thus, depression is not being defined on a syndromal level, as it would be if a structured diagnostic interview was used. Without the use of a structured diagnostic interview for depression, it would be difficult to separate clinical depression from a secondary mood disorder directly related to the hormonal effects of the pituitary tumor. Conclusions about concentration and memory difficulties, as well as lack of motivation, are also being made using patient self-report as opposed to neuropsychological assessment (Table 1).

The fact remains, however, that these patients self-report depressive symptoms, lack of motivation, and cognitive impairment. The question that emerges is whether the symptoms and concerns that appear to reflect major depression, chronic fatigue, or apathy are caused by the syndrome of major depression, are sequelae of fatigue or apathy, or are due to some third factor independent of depression, fatigue, or apathy.

Our premise is that patients with pituitary disease have a neurobiological illness with dysfunction in the cerebral hemispheres and the diencephalons that manifests as apathy and fatigue. We present four cases (Appendix) of patients with pituitary disease presenting to Moffitt Cancer Center with depressive symptoms, but who appear to meet criteria for chronic fatigue or apathy syndrome. In this article we will discuss chronic fatigue and apathy syndromes and their relationship to pituitary disease, as well as potential treatments for chronic fatigue and apathy syndrome that are applicable to pituitary disease.

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Case 1

Mr. A is a 48 year-old Anglo lawyer and architect, diagnosed with a pituitary adenoma (clinically nonfunctioning) and treated with a transsphenoidal resection in 1997. He first noted memory problems in 1991 that worsened over the years, causing problems such as concentration and focused attention. He reported problems such as getting lost in familiar places and forgetting the names of people he had known for many years. He believed his thinking process was slow and he was “not as quick on the uptake” as before. He reported that he had an excellent memory, never having to use a reminder book of any kind prior to these symptoms.

Case 2

Ms. B is a 55-year-old Anglo homemaker with a history of a prolactinoma, diagnosed 15 years before her psychiatric evaluation. She reported that her symptoms of the tumor were primarily mood swings, headache, and loss of menstrual periods. She underwent surgery followed by radiation therapy, ultimately developing panhypopituitarism. Since then, she has been managed on hormone replacement, but she began to notice short-term memory difficulties. She reported difficulty finding the right words to express her thoughts. She also noticed difficulty in concentration and focused attention. She reported occasional fatigue and depressed feelings. She reported intermittent suicidal thoughts when she reported the depressed mood, but no active plans of suicide were reported during those times.

Case 3

Ms C. is a 47-year-old Anglo woman, employed as a management supervisor and diagnosed with a pituitary macroadenoma (clinically nonfunctioning) in 1994. She underwent transfrontal surgical resection and did not receive any postoperative radiation treatment but did develop panhypopituitarism. Since 1996, several changes in her behavior and personality were noted. Prior to the tumor she was a very active person. She was able to do very well at work and maintain a leadership position. She could do multiple tasks at once and received a lot of satisfaction from her work. However, after her surgery and recovery, she noticed that she was no longer able to multitask. She was deriving less satisfaction from her work and experienced transient periods of sadness. However, she was most concerned about her lack of energy and motivation. When she was able to work, she had to organize her activities very thoroughly and continuously write down everything in order not to forget what her tasks were. It took a lot of mental energy to function, and after work she would often need to take a 2-hour nap when she returned home. She showed no motivation to adequately take care of her home, including normal household chores. She reported she was not able to muster up much enthusiasm to interact with her grandchild because she was concerned about her energy and drive.

Case 4

Ms. D is a 36-year-old married Anglo woman, employed as a nurse, diagnosed with an ACTH-producing pituitary microadenoma in 1992. She was treated surgically following a brief period of hormone deficiency. At the time of her psychiatric assessment, however, she had regained full hormonal function. Ms. D reported that since regaining her hormonal function she noticed some “dragginess.” She reported there were times when she did not feel very motivated, and she thought that it took much more energy for her to do her normal activities. She reported that when she would take pseudoephedrine for sinus problems, she would see things “with more clarity” and that she would be able to be more focused in her attention and her ability to complete her tasks. Otherwise she tended to procrastinate and get distracted from various tasks.

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These four cases illustrate an example of a neurobiological illness in which patients report symptoms that appear to be part of the syndrome of depression but, in fact, are not. Instead, these symptoms encompass an overlapping problem with clinical depression, namely fatigue and apathy, which is very responsive to stimulant medications.

Fatigue has been defined as a clinical syndrome characterized with generalized weakness, and there is also an interrelationship between physical, emotional, and mental fatigue.11 Physical fatigue is a state in which individuals experience a sustained sense of exhaustion and decreased capacity for physical and mental work that can be restored with rest and support.12 The emotional effects of fatigue are well known in psychiatry. Numerous psychiatric illnesses, including major depressive disorder, generalized anxiety disorder, and dysthymia are frequently associated with fatigue. In fact, more than two thirds of patients with clinical depression present with signs of fatigue that may include low energy and listlessness.13 It has been proposed that the syndromes of fatigue and depression may represent overlapping constructs, sharing similar underlying mechanisms,13–15 a hypothesis that is supported by observations that patients with clinical depression, who respond to antidepressant medication, may continue to experience residual fatigue.16

Fatigue, as a mental state, displays a complex interaction of subjective feelings, tissue impairment and diminished performance.17 In fact, chronic fatigue, such as that observed in chronic fatigue syndrome, shares a number of cardinal symptoms with major depression, including profound fatigue; decreased, nonrestorative sleep; and decreased concentration and memory.18 However, these syndromes are associated with significantly different physiological abnormalities.19,20 In addition, unlike depressed patients, patients with chronic fatigue do not seem to respond to antidepressant medications.21,22 Such was the case for the subjects described in this report.

Furthermore, it has been shown that chronic fatigue patients consistently report lower mean scores on depression inventories than depressed patients, although their scores were still within the depressed range.23 Edwards et al.23 also showed that depressed patients scored significantly higher on the self-reproach or cognitive symptoms, including feelings of guilt, low self-esteem, and suicidal ideation, accounting for the differences in the groups. Another study expanded on these findings, comparing clinically depressed patients, depressed patients with chronic fatigue syndrome, nondepressed patients with chronic fatigue syndrome, and healthy comparison subjects.18 The clinically depressed group had significantly lower self-esteem, increased cognitive distortions across all situations, and was more likely to attribute their illness to psychological factors. The chronic fatigue patients rated their current health status lower, had a strong illness identity, and attributed their illness to external factors. Their distortions in thinking were specific to somatic experiences and they were more likely than depressed patients to cope with their illness by limiting stress and activity levels. The subjects in our report also stated specifically that their emotional and cognitive symptoms were attributable to their underlying medical illness and that their medical illness was something that was outside of their control.

The above observations suggest that what chronic fatigue patients, including our patients with pituitary disease, experience is not depression. However, what these patients experience also needs to be differentiated from demoralization, another psychological state. Demoralization is experienced as a persistent inability to cope, together with associated feelings of helplessness, hopelessness, meaninglessness, subjective incompetence, and diminished self-esteem.24 When coping is insufficient and the person is at a point when he or she does not know how to proceed, distress and helplessness result. While clinical depression is characterized primarily by anhedonia,25,26 demoralization is characterized by a feeling of subjective incompetence and helplessness. Any number of events can threaten a person’s sense of independence and competence, including both physical and mental illness.27 Chronic illness can threaten the integrity of the body and mind, challenging a person’s mastery and control. Patients often need to reduce social roles, depriving them of a sense of satisfaction and competence. With reduction of personal efficacy, and uncertain prognosis, comes a sense of demoralization.28,29 Our patients did not feel helpless or incompetent. In fact, they continued to actively seek help from different physicians because they knew that there was something wrong with their bodies that no one was addressing.

While fatigue affects physical, emotional, and mental areas of functioning, it also affects cognitive function by affecting the ability to focus or pay attention. The ability to focus and concentrate is essential for effective functioning in daily life.30 Directed attention is the capacity to inhibit or block competing stimuli or distractions during purposeful activity. Directed attention is what helps us function in goal-directed activities and regulates behavior to meet desired goals. Intense or prolonged demands on attentional capacity can lead to a decline in the ability to maintain directed attention, thus causing attentional fatigue. In healthy adults attentional fatigue has been associated with impaired ability to perceive, interpret and respond to environmental information and distressing affective states.31

The construct of fatigue, as described above, shares many similarities with the concept of apathy. There are three components to apathy: observable behavior, emotional content, and thought content.2,32 As in fatigue, all three components are affected simultaneously. It is not simply the lack of emotion that defines apathy; it is the diminished emotional responsiveness to goal-related events and decreased emotional distress that define apathy.2,32 Recent neurophysiological and neurocognitive research have provided a greater appreciation of the functional neuroanatomy of fatigue and apathy.33–35 Regarding fatigue, the frontal lobes, posterior parietal lobes, and the reticular formation are primarily involved in attention control. The posterior parietal cortex is associated with shift in attention focus from one spatial location to another and from one stimulus to another.36 The frontal lobes are associated with controlling selection of stimuli from competing inputs and exercising inhibitory control over other brain areas to perform complex tasks. In addition, the subcortical system, including the reticular formation in the brain stem, is responsible for alertness and waking states.36

Other areas that may play a role in fatigue and apathy include the medial dorsal nucleus of the thalamus, caudate nucleus, nucleus accumbens and globus pallidus.2 Thus, the circuit most implicated in this syndrome is the cortical-striatal-thalamic-cortical circuit. This circuit helps elucidate the mechanism behind fatigue and apathy, in general. How does this pertain to patients with pituitary disease? The hypothalamic-pituitary tract provides significant afferent input to the mediodorsal nucleus of the thalamus and any perturbation in hypothalamic-pituitary function will affect the frontal-subcortical circuits and cause apathy syndrome.2 However, when thinking of pituitary tumors and psychiatric disturbances, the deficits are related to the direct and indirect effects of the tumor and the hormonal alterations caused by the tumor. The neuropsychological impairment caused by these tumors has been documented to cause problems with executive functioning, verbal reasoning, and visual memory.2

In apathy syndrome it is believed that mesocortical tract hypoactivity causes impaired executive functioning and that mesolimbic tract hypoactivity is responsible for the affective component of apathy.2 Norepinephrine systems in the brain have been linked to attentional operations. Medications that increase noradrenergic activity enhance concentration, and disturbing this system has been shown to interfere with attention.36 The functioning of the frontal lobes and norepinephrine’s effect on attention constitute the primary relationship between fatigue and apathy syndrome.

Methylphenidate is a medication well known for its use in the treatment of Attention Deficit Hyperactivity Disorder (ADHD)/Attention Deficit Disorder (ADD).37 Preclinical studies have shown that stimulants, including methylphenidate, block the reuptake of dopamine and norepinephrine into the presynaptic neurons and increase the release of these neurotransmitters into the extraneuronal space.38 In ADD, a hypoperfusion of the striatum and hyperperfusion to the primary sensory regions were demonstrated by Xenon inhalation techniques.39 However, after the addition of methylphenidate, the striatal and posterior periventricular regions had increased blood flow. Conversely, after the addition of methylphenidate the primary sensory regions showed decreased blood flow. Additionally, after administration of methylphenidate PET scans have shown an increase in blood flow to the mesencephalon and basal ganglia, and conversely, motoric cortical areas have shown a decrease in blood flow.39 These changes mentioned above could provide the mechanism for improvement in children with ADHD taking methylphenidate.

The patients in our case series meet the criteria of apathy syndrome because of their impaired cognitive and affective functioning. As mentioned earlier, pituitary tumors can cause apathy syndrome by their influence on frontal-subcortical pathways. In our patients, we observed improvement after they started taking methylphenidate. Subjective improvements were described as increased ability to focus, increased memory, increased functioning at work, improved confidence, and improved mental stamina. These patients showed improvements in: new learning of verbal and nonverbal information; sustained effortful output as assessed with a verbal fluency task; executive function across tasks tapping novel problem solving; the ability to inhibit responding, sequencing, and mental flexibility; and psychomotor speed. Through intervention with methylphenidate the patients appeared to show significant improvement subjectively and objectively.

Many physicians have used stimulants to help with patients suffering from brain tumors and cognitive slowing. One case study suggested that methylphenidate improved severe neurobehavioral slowing caused by frontal and brain stem dysfunction due to cancer and cancer treatment.40 The patients in this study showed improvement in arousal, attention, and speed on initiation of tasks and were able to concentrate on tasks longer. Another study tested the effect of methylphenidate on patients with primary gliomas who had neurobehavioral slowing affecting their level of functioning.41 These patients showed an improvement in cognitive and daily functioning while taking methylphenidate. They also showed improvement in visual motor speed, verbal memory, expansive speech, and executive functioning, as well as improvement in cognition and mood.41 It is important to review, with the patient, the risks and benefits of treatment with methylphenidate, determining that the patient does not have uncontrolled hypertension, recent myocardial infarction, or glaucoma. A review of the potential for abuse, while extremely low as compared to the amphetamines, is also necessary.

In summary, apathy is an emerging concept in neuropsychiatry, and major depressive disorder and chronic fatigue syndrome are important syndromes from which apathy must be differentiated. As was demonstrated by our series of cases, these patients with pituitary disease appeared to be suffering from depression, given their constricted affect. However, when asked about their mood, all stated that they were not depressed but, instead, stated that they had chronic fatigue and lack of motivation. All responded well to methylphenidate and not to antidepressants. As more and more patients with pituitary disease present to cancer centers for evaluation and treatment, it is incumbent on the psychosocial staff to closely scrutinize the pituitary patient for mood changes. Since many of these patients will appear depressed, yet deny depressed mood and anhedonia, it is important to keep apathy syndrome in mind, particularly when these patients do not respond or their depression appears refractory to traditional antidepressants. Apathy syndrome is easily treated with stimulant medications, leading to increased energy and mood.

 

Table

Table

 

APPENDIX Common Clinical Observations for All Four Cases
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Table

Table

 

TABLE 1. Neuropsychological Assessment Battery
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Received September 30, 2002; revised July 7, 2003; accepted July 24, 2003. From the Department of Psychiatry and Behavioral Medicine, University of South Florida College of Medicine, Tampa, Florida; and the Psychosocial and Palliative Care Program, H. Lee Moffitt Cancer Center, Tampa, Florida. Address correspondence to Dr. Weitzner, Medical Director, Helios Pain & Psychiatry Center, 3262 Cove Bend Dr., Tampa, FL 33613; (E-mail).

References
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40. Weitzner MA, Meyers CA, Valentine AD: Methylphenidate in the treatment of neurobehavioral slowing associated with cancer and cancer treatment. J Neuropsychiatry and Clin Neurosciences 1995; 7:347–350 Abstract, Medline
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From http://neuro.psychiatryonline.org/doi/full/10.1176/jnp.17.2.159

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Pituitary Incidentaloma Treatment Guideline

Posted on August 22, 2015 by MaryO

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It is unclear how many people have pituitary incidentaloma, but imaging and autopsy studies indicate they are quite common and occur in up to one-third of patients. Fortunately, the vast majority of these serendipitously discovered tumors are clinically insignificant.

A management guideline in the Annals of Endocrinology brings endocrinologists up to date on current thinking about pituitary incidentaloma management.   Endocrinologists classify these tumors as micro- or macro-. Microincidentalomas are discovered in around 10% of patients, often upon CT after a fall, and are less than 1 cm in diameter. They may grow, but only 5% proceed to macroincidentaloma.

Currently, experts recommend assessing nonfunctioning (NF) microincidentaloma clinically for signs of hypersecretion (hyperprolactinemia, acromegaly or Cushing’s syndrome), with subsequent systematic prolactin and IGF-1 assay.   Pituitary incidentalomas that are larger than 1 cm at discovery—macroincidentalomas—are more likely to grow, with 25% and 24%-40% of patients having larger tumors at 4 and 8 years after diagnosis respectively.

Concerns escalate and closer surveillance is needed if a macroadenoma is in contact with the optic chiasm. With any NF macroincidentaloma, experts recommend assessing patients for signs of hormonal hypersecretion or hypopituitarism. Then, laboratory screening for hypersecretion or hormonal deficiency is needed, as is ophthalmologic assessment (visual acuity and visual field) if the lesion is near the optic chiasm (OC).   Surveillance differs by tumor size, with 5 mm the cutoff for NF microincidentaloma.

Tumors smaller than that require no surveillance, and those larger need to be monitored with MRI at 6 months and then 2 years. Endocrinologists should revisit macroincidentaloma distant from the optic chiasm with MRI at 1 year and conduct hormonal exploration (for anterior pituitary deficiency), then monitor every 2 years.   Proximity to the optic chiasm often creates a need for surgery or increased vigilance. MRI is recommended at 6 months, with hormonal and visual assessment, then annual MRI and hormonal and visual assessment every 6 months.

Specific types of pituitary incidentaloma call for surgery: evolutive NF microincidentaloma, NF macroincidentaloma associated with hypopituitarism or showing progression, incidentaloma compressing the optic chiasm, possible malignancy, non-compliant patient, pregnancy desired in the short-term, or context at risk of apoplexy.

Few guidelines are published for pituitary incidentaloma, and this one is enhanced with a decision tree that walks endocrinologist through the recommendations. –

See more at: http://www.hcplive.com/medical-news/pituitary-incidentaloma-treatment-guideline#sthash.0DqxeTru.dpuf

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Cortendo plans tax-fuelled shift to Dublin

Posted on August 6, 2015 by MaryO

Cortendo, a Swedish-American biopharmaceutical company that has invested millions developing treatments for rare conditions such as Cushing’s syndrome, is the latest global drug company to propose a move to Ireland for tax reasons.

The company operates from Pennsylvania, is listed in Norway but is incorporated in Sweden.

In recent days it told its investors it had submitted a prospectus to the Central Bank relating to the establishment of a Dublin-based public limited company.

Cortendo is proposing that the new Dublin company would become the parent of the group, replacing its current Swedish domicile. The Irish company would buy all of the outstanding stock in the current Cortendo parent, paying investors with an issuance of depositary receipts.

Depositary receipts have become popular financial instruments in the biopharma industry, and are typically used by non-US drug companies that want to trade in over-the-counter and traditional US markets.

Cortendo told its shareholders the move to Ireland “will have the effect of facilitating tax-efficient allocations of capital [and] tax-efficient returns of capital to shareholders”.

“Furthermore, the board expects that certain features of Irish company law will enable the Cortendo group to operate more flexibly and efficiently,” the company said.

Cortendo had not yet responded to a request prior to publication for details on what, if any, staff or operations would be shifted to Dublin as part of the move.

The company last month indicated it may seek to list its shares in the United States, although it did not discuss a valuation. It set up its Irish unit in May, according to company filings.

The company focuses on developing drugs to treat rare endocrine diseases, including the potentially fatal Cushing’s and acromegaly, inflammation of the hands and feet that can lead to diabetes.

Its main drugs have not yet been commercialised but it has high hopes for its treatment for Cushing’s , which is at a late stage of development. The company’s latest annual report shows an operating loss of about €8 million.

From http://www.irishtimes.com/business/health-pharma/swedish-drug-firm-plans-tax-fuelled-shift-to-dublin-1.2307007

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BLA Instead of Second Pituitary Surgery

Posted on July 31, 2015 by MaryO

One of the problems that can arise with a BLA (bilateral adrenalectomy) instead of a repeat pituitary surgery for Cushing’s recurrence is Adrenal Insufficiency.  Another is Nelson’s Syndrome.

Nelson’s syndrome is a rare disorder that occurs in some patients with Cushing’s disease patients as a result of removing both adrenal glands. In Nelson’s syndrome, the pituitary tumor continues to grow and release the hormone ACTH.

This invasive tumor enlarges, often causing visual loss, pituitary failure and headaches. One key characteristic of Nelson’s disease is dark skin pigmentation, resulting from the skin pigment cells responding to the release of ACTH.

AnchorNelson’s Syndrome: Physiology

Nelson’s syndrome can develop as a result of a specific treatment (bilateral adrenalecomy) for the pituitary disease called Cushing’s disease. The harmful effects of Cushing’s disease are due to the excessive amount of the hormone cortisol produced by the adrenal glands.

To treat Cushing’s disease, your doctor may recommend removing the adrenal glands, during a procedure called a bilateral adrenalectomy. The procedure will stop cortisol production and provide relief. However, the procedure does not treat the actual tumor. Rapid growth of the pituitary tumor can occur.

In about 15-25 percent of patients who had a bilateral adrenalectomy, Nelson’ syndrome develops within one to four years.

Darkening of Skin Color - Nelson's Syndrome SymptomAnchor

Nelson’s Syndrome: Symptoms

The most obvious symptom of Nelson’s syndrome is the darkening of the skin color (hyperpigmentation).

Macroadenomas

Macroadenomas are large pituitary tumors. Large tumors can compress surrounding structures, primarily the normal pituitary gland and optic (visual) pathways, causing symptoms. The symptoms that result from the compression are independent of the effects of excess growth hormone secretion.
This may result in vision problems:

  • Vision loss. This occurs when macroadenomas grow upward into the brain cavity, compressing the optic chiasm.
  • A loss of the outer peripheral vision, called a bitemporal hemianopsia Bitemporal Hemianopsia - Symptom of Nelson's Syndrome
    • When severe, a patient can only see what is directly in front of them.
    • Many patients do not become aware of their visual loss until it is quite severe.
  • Other visual problems can include:
    • Loss of visual acuity (blurry vision), especially if the macroadenoma grows forward and compresses an optic nerve.
    • Colors not perceived as bright as usual

Pituitary Failure or Hypopituitarism

Increased compression of the normal gland can cause hormone insufficiency, called hypopituitarism. The symptoms depend upon which hormone is involved.

AnchorNelson’s Syndrome: Diagnosis

Most patients with Nelson’s syndrome have undergone a bilateral adrenalectomy for the treatment of Cushing’s disease

Diagnostic testing includes:

  • Hormone testing. Typically, the blood ACTH levels are very elevated. Learn more about hormone testing at the UCLA Pituitary Tumor Program.
  • MRI imaging. Magnetic resonance imaging (MRI) scan of the pituitary gland can detect the presence of an adenoma, a pituitary tumor.

AnchorNelson’s Syndrome: Treatment Options

Surgery for Nelson's Syndrome

Treating Nelson’s syndrome effectively requires an experienced team of experts. Specialists at the UCLA’s Pituitary Tumor Program have years of experience managing the complex coordination and care for treatment of Nelsons’ syndrome.

Treatment options include:

AnchorSurgery for Nelson’s Syndrome

Surgical removal of the pituitary adenoma is the ideal treatment; however, it is not always possible. Surgical removal requires advanced surgical approaches, including delicate procedures involving the cavernous sinus.

If surgery is required, typically the best procedure is through a nasal approach. Our neurosurgeons who specialize in pituitary tumor surgery are experts in the minimally invasive expanded endoscopic endonasal technique. This procedure removes the tumor while minimizing complications, hospital time and discomfort. This advanced technique requires specialized training and equipment.

Very large tumors that extend into the brain cavity may require opening the skull (craniotomy) to access the tumor. Our surgeons are also experts in the minimally invasive “key-hole” craniotomy, utilizing a small incision hidden in the eyebrow.

AnchorRadiation Therapy for Nelson’s Syndrome

Radiation Therapy for Nelson's SyndromeRadiation therapy can be effective in controlling the growth of the tumor. However, if you received radiation therapy in the past, additional radiation may not be safe.

Our Pituitary Tumor Program offers the latest in radiation therapy, including stereotactic radiosurgery. This approach delivers a highly focused dose of radiation to the tumor while leaving the surrounding brain structures unharmed (with the exception of the normal pituitary gland).

One consequence of radiation treatment is that it can cause delayed pituitary failure. This typically occurs several years after treatment, and continued long-term follow-up with an endocrinologist is important. You may require hormone replacement therapy.

Medical Therapy for Nelson’s Syndrome

Medication for Nelson's SyndromeMedical therapies for the treatment of Nelson’s syndrome are currently limited, but include:

  • Somatostatin-analogs (SSAs). These medications are typically used to treat acromegaly. A small number of Nelson’s syndrome patients may respond.
  • Cabergoline. This medication is typically used to treat prolactinomas; you may require a very high dose.
  • Temozolomide. This is a type of chemotherapy used to treat primary brain tumors called glioblastoma.

If you require medication to treat Nelson’s syndrome, our endocrinologists will monitor you closely.

From http://pituitary.ucla.edu/body.cfm?id=53

 

Filed under: adrenal, adrenal crisis, Cushing's, pituitary, Rare Diseases, Treatments | Tagged: , , , , , , , , | Leave a comment »

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