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👉What is the best dose of levothyroxine post total thyroidectomy ?
👉Thyroid hormone replacement dosing is variable in overweight and obese patients after a thyroidectomy
👉https://www.thyroid.org/patient-thyroid-information/ct-for-patients/january-2020/vol-13-issue-1-p-3-4/
👉This study suggests that the use of a standardized dose for prescribing the initial dose of levothyroxine after surgery based on the actual body weight frequently will result in either too high or too low thyroid levels.
👉In overweight and obese patients, a much lower mcg/kg body weight dose should be used, while a higher dose should be used in patients with a normal BMI.
👉These results will benefit patients after thyroid surgery as they may start taking a more appropriate dose of levothyroxine as soon as possible after thyroid surgery, and require fewer blood tests for dose adjustments.
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Classification
👉Multiple endocrine neoplasia type 2 (MEN2) is subclassified into two distinct syndromes: types 2A (MEN2A) and 2B (MEN2B).
👉Within MEN2A, there are four variants:
● Classical MEN2A
● MEN2A with cutaneous lichen amyloidosis (CLA)
● MEN2A with Hirschsprung disease (HD)
● Familial medullary thyroid cancer (FMTC)
👉In both MEN2A and MEN2B, there is an occurrence of multicentric tumor formation in all organs where the RET proto-oncogene is expressed.
👉The thyroid, parathyroid, adrenal glands, and accessory adrenals are at risk for developing tumors that may reduce life expectancy and quality of life.
Multiple endocrine neoplasia type 2A
Classical MEN2A
👉Classical multiple endocrine neoplasia 2A (MEN2A) is the most common MEN2A variant.
👉It is a heritable predisposition to medullary thyroid cancer (MTC), pheochromocytoma, and primary parathyroid hyperplasia.
👉The respective frequency of these tumors in classical MEN2A is over 90% for MTC, approximately 10% to 50% for pheochromocytoma, and 10% to 20% for multigland parathyroid hyperplasia.
👉The frequency of the development of MTC, pheochromocytoma, and parathyroid hyperplasia depends upon the specific RET mutation.
MEN2A with cutaneous lichen amyloidosis
👉CLA (also known as lichen planus amyloidosis [LPA]) has been described in some families with multiple endocrine neoplasia 2A (MEN2A), predominantly those with the RET codon 634 mutation, although it has also been reported in a patient with a codon 804 mutation.
👉The diagnosis of CLA may precede the onset of clinically evident MTC (Image).
👉Patients with this variant develop pheochromocytomas and parathyroid hyperplasia with a similar frequency as those with classical MEN2A.

MEN2A with Hirschsprung disease (HD)
👉HD is a motor disorder of the gut that is caused by the failure of neural crest cells (precursors of enteric ganglion cells) to migrate completely during intestinal development.
👉The resulting aganglionic segment of the colon fails to relax, causing a functional obstruction.
👉At least eight genetic mutations have been identified in patients with HD.
👉The predominant gene affected is the RET proto-oncogene.
👉RET malfunction accounts for at least 50% of familial and 20% of sporadic cases of HD.
👉In one study, the prevalence of HD in MEN2 was 7.5%.
👉The frequency of HD in MEN2A depends upon the specific RET mutation.
👉The co-occurrence of HD and MEN2A is predominantly associated with RET mutations involving codons 609, 611, 618, and 620.
👉In such patients, HD may be the first presentation of MEN2A.
👉Patients with this variant of MEN2A develop MTC, pheochromocytomas, and parathyroid hyperplasia with a similar frequency as those with classical MEN2A.
Familial medullary thyroid cancer
👉FMTC is a variant of MEN2A in which there is a strong predisposition to MTC but not the other clinical manifestations of MEN2A (or 2B).
👉The clinical distinction of FMTC from MEN2A may be difficult on statistical grounds in small families; even in some large kindreds, the clinical designation of FMTC has been changed to MEN2A after the diagnosis of pheochromocytoma or hyperparathyroidism in a family member.
👉Because FMTC is the most limited variant of MEN2, making the wrong diagnosis of FMTC could result in missing a pheochromocytoma in a patient with MEN2.
👉Therefore, an FMTC kindred should be defined using the following rigorous criteria:
● More than 10 carriers in the kindred
● Multiple carriers or affected members over the age of 50 years
● An adequate medical history, particularly in older family members
👉Why pheochromocytomas and hyperparathyroidism infrequently develop in these families is still unknown since many FMTC and MEN2A families carry identical RET mutations.
👉In rare families, both HD and FMTC appear to segregate.
👉In a report summarizing data from 250 Italian kindreds with hereditary MTC, the prevalence of the FMTC phenotype among RET mutation carriers was higher than MEN2A and MEN2B (57%, 34% and 6.8%, respectively).
👉This may be related to the introduction of RET screening in the work-up of apparently sporadic MTC and the more extensive search for RET mutations in non-hot spot regions of the gene.
Multiple endocrine neoplasia type 2B
👉The frequency of MEN2B has been estimated at roughly 6% of all MEN2 patients.
👉MEN2B shares the inherited predisposition to MTC and pheochromocytoma that occurs in MEN2A.
👉On the other hand, parathyroid hyperplasia is not a feature of this disorder.
👉There are additional important clinical differences.
👉Patients with MEN2B tend to have mucosal neuromas, typically involving the lips and tongue, and intestinal ganglioneuromas.
👉Disturbances of colonic function are common, including chronic constipation and megacolon.
👉Many of these patients have development abnormalities, a Marfanoid habitus, and myelinated corneal nerves.
👉MTC is the most common component of the MEN2B syndrome.
👉Furthermore, the tumor is often more aggressive and of earlier onset than in MEN2A; as a result, early diagnosis and prevention are particularly critical.









👉Capecitabine is often used to treat breast cancer, but the best use of capecitabine is open for discussion.
👉According to a large meta-analysis of the effects of capecitabine in early breast cancer, capecitabine improves disease-free and overall survival for patients with triple-negative breast cancer, but only when it is added to other systemic therapies and not when it is used as a substitute.
👉The results of the meta-analysis were presented at the 2019 San Antonio Breast Cancer Symposium (SABCS) by Marion van Mackelenbergh, MD, of the University of Kiel, Germany.
👉Overall survival was also improved when capecitabine was given in addition to other therapies.
👉There is no evidence supporting a predictive value of capecitabine-specific adverse events on outcome.
👉It can be concluded that the addition of capecitabine to other treatment may be recommended for patients with triple-negative.
👉The meta-analysis showed no data comparing the effects of capecitabine with carboplatin in triple-negative breast cancer.
👉One trial is recruiting patients to evaluate this in the post-neoadjuvant setting.
👉The effect of capecitabine compared with other systemic therapies, including carboplatin, remains to be investigated.
👉Capecitabine is approved by the U.S. Food and Drug Administration (FDA) for use as monotherapy or in combination with docetaxel in metastatic breast cancer.
👉The meta-analysis results addressed its use in early breast cancer.
👉Several randomized trials have evaluated the effect of capecitabine in early breast cancer, mainly in high-risk patients.
👉The German Breast Group investigators sought to examine the effect of capecitabine in patients with early breast cancer on disease-free survival as the primary objective; secondary endpoints included the effect of capecitabine on overall survival and to determine whether there was an interaction between capecitabine-specific toxicity and treatment effect.
👉Study Details👈
👉The meta-analysis included individual patient data from 15,457 patients enrolled in 12 randomized controlled trials; 7,983 patients with early breast cancer were treated with capecitabine, and 7,474 patients were in the control arms.
👉Five of the trials included in the meta-analysis addressed capecitabine given instead of other therapies, and seven evaluated the use of capecitabine in addition to other therapies.
👉The analysis was performed on the overall study population and in two predefined subsets: patients who received capecitabine in addition to other therapies and those who received capecitabine instead of another systemic treatment.
👉The median age of patients at initial diagnosis was 53 years.
👉Nearly three-quarters of patients had nodal involvement; 56% presented with tumor stage II disease; about 68% had hormone receptor–positive disease; 45% had high-grade disease; 15% had HER2-positive breast cancer.
👉About 80% of the patients were treated in the adjuvant setting and almost 20%, in the neoadjuvant setting.
👉Key Findings👈
👉Among the entire data set, there was no significant effect of capecitabine alone on disease-free survival, but a significant benefit was observed in the patients who received capecitabine in addition to other systemic therapies (hazard ratio [HR] = 0.888, 95% confidence interval [CI[ = 0.817–0.965).
👉Only the CREATE-X trial had positive results for disease-free survival, and no benefit of capecitabine on disease-free survival was observed when capecitabine was given instead of another treatment.
👉A slight benefit for capecitabine was observed in overall survival for the total data set (HR = 0.892, 95% CI = 0.824–0.965; P = .005), which was more pronounced when capecitabine was added to other systemic therapies (HR = 0.837, 95% CI = 0.751–0.933; P = .001).
👉Only the CREATE-X and USON 01062 trials were positive for overall survival.
👉There was no overall survival benefit [in the meta-analysis] when capecitabine was substituted for another systemic therapy.
👉In patients with triple-negative breast cancer, capecitabine improved disease-free survival by 18% when added to standard chemotherapy and overall survival by 22% (P = .004 for both analyses).
👉Only benefit of capecitabine was observed in the triple-negative breast cancer overall cohort and when capecitabine was added [to another therapy].
👉No benefit was observed in triple-negative breast cancer when capecitabine was given instead of another systemic therapy.
👉The most common grade 3 and 4 toxicities associated with capecitabine were mucositis, hand-foot syndrome, and diarrhea.
👉No significant associations were reported between capecitabine-specific toxicities and treatment benefit.
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👉Functional adrenocortical cancers have worse long-term survival vs. non-functional tumors.
👉Read more at: https://www.sciencedirect.com/science/article/pii/S0039606019305471?via%3Dihub
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👉Platica sobre diagnósticos moleculares de nódulos tiroideos
👉Thyroseq primera prueba molecular en MEXICO para nódulos tiroideos indeterminados
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👉REFERENCES










👉REFERENCES









👉Interested in the utility of autofluorescence imaging for parathyroid glands?
👉Check out this study: https://www.sciencedirect.com/science/article/pii/S0039606019305604?via%3Dihub
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