How to identify indolent thyroid tumors unlikely to recur and cause cancer death immediately after surgery—Risk stratification of papillary thyroid carcinoma in young patients

Current histopathological diagnosis methods cannot distinguish the two types of thyroid carcinoma: clinically significant carcinomas with a potential risk of recurrence, metastasis, and cancer death, and clinically insignificant carcinomas with a slow growth rate. Both thyroid tumors are diagnosed a...

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Veröffentlicht in:ENDOCRINE JOURNAL 2021, Vol.68(8), pp.871-880
Hauptverfasser: Kakudo, Kennichi, Liu, Zhiyan, Bai, Yanhua, Li, Yaqiong, Kitayama, Naomi, Satoh, Shinya, Nakashima, Masahiro, Jung, Chan Kwon
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container_title ENDOCRINE JOURNAL
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creator Kakudo, Kennichi
Liu, Zhiyan
Bai, Yanhua
Li, Yaqiong
Kitayama, Naomi
Satoh, Shinya
Nakashima, Masahiro
Jung, Chan Kwon
description Current histopathological diagnosis methods cannot distinguish the two types of thyroid carcinoma: clinically significant carcinomas with a potential risk of recurrence, metastasis, and cancer death, and clinically insignificant carcinomas with a slow growth rate. Both thyroid tumors are diagnosed as “carcinoma” in current pathology practice. The clinician usually recommends surgery to the patient and the patient often accepts it because of cancer terminology. The treatment for these clinically insignificant carcinomas does not benefit the patient and negatively impacts society. The author proposed risk stratification of thyroid tumors using the growth rate (Ki-67 labeling index), which accurately differentiates four prognostically relevant risk groups based on the Ki-67 labeling index, ≥30%, ≥10 and 5 and
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Both thyroid tumors are diagnosed as “carcinoma” in current pathology practice. The clinician usually recommends surgery to the patient and the patient often accepts it because of cancer terminology. The treatment for these clinically insignificant carcinomas does not benefit the patient and negatively impacts society. The author proposed risk stratification of thyroid tumors using the growth rate (Ki-67 labeling index), which accurately differentiates four prognostically relevant risk groups based on the Ki-67 labeling index, ≥30%, ≥10 and &lt;30%, &gt;5 and &lt;10%, and ≤5%. Indolent thyroid tumors with an excellent prognosis have the following four features: young age, early-stage (T1-2 M0), curatively treated, and low proliferation index (Ki-67 labeling index of ≤5%), and are unlikely to recur, metastasize, or cause cancer death. Accurate identification of these indolent tumors helps clinicians select more conservative treatments to avoid unnecessary aggressive (total thyroidectomy followed by radio-active iodine) treatments. 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Accurate identification of these indolent tumors helps clinicians select more conservative treatments to avoid unnecessary aggressive (total thyroidectomy followed by radio-active iodine) treatments. 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Institute</aucorp><aucorp>Department of Endocrine Surgery</aucorp><aucorp>Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education</aucorp><aucorp>Izumi City General Hospital</aucorp><aucorp>Department of Dermatology</aucorp><aucorp>Shandong Provincial Hospital Affiliated with Shandong First Medical University</aucorp><aucorp>Atomic Bomb Disease Institute</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>How to identify indolent thyroid tumors unlikely to recur and cause cancer death immediately after surgery—Risk stratification of papillary thyroid carcinoma in young patients</atitle><jtitle>ENDOCRINE JOURNAL</jtitle><addtitle>Endocr J</addtitle><date>2021-01-01</date><risdate>2021</risdate><volume>68</volume><issue>8</issue><spage>871</spage><epage>880</epage><pages>871-880</pages><artnum>EJ21-0018</artnum><issn>0918-8959</issn><eissn>1348-4540</eissn><abstract>Current histopathological diagnosis methods cannot distinguish the two types of thyroid carcinoma: clinically significant carcinomas with a potential risk of recurrence, metastasis, and cancer death, and clinically insignificant carcinomas with a slow growth rate. Both thyroid tumors are diagnosed as “carcinoma” in current pathology practice. The clinician usually recommends surgery to the patient and the patient often accepts it because of cancer terminology. The treatment for these clinically insignificant carcinomas does not benefit the patient and negatively impacts society. The author proposed risk stratification of thyroid tumors using the growth rate (Ki-67 labeling index), which accurately differentiates four prognostically relevant risk groups based on the Ki-67 labeling index, ≥30%, ≥10 and &lt;30%, &gt;5 and &lt;10%, and ≤5%. Indolent thyroid tumors with an excellent prognosis have the following four features: young age, early-stage (T1-2 M0), curatively treated, and low proliferation index (Ki-67 labeling index of ≤5%), and are unlikely to recur, metastasize, or cause cancer death. Accurate identification of these indolent tumors helps clinicians select more conservative treatments to avoid unnecessary aggressive (total thyroidectomy followed by radio-active iodine) treatments. Clinicians can alleviate the fears of patients by confirming these four features, including the low proliferation rate, in a pathology report immediately after surgery when patients are most concerned.</abstract><cop>Japan</cop><pub>The Japan Endocrine Society</pub><pmid>33980775</pmid><doi>10.1507/endocrj.EJ21-0018</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Death
Female
Growth rate
Humans
Iodine
Ki-67
Labeling
Male
Metastases
Middle Aged
Papillary thyroid carcinoma
Patient anxiety
Patients
Prognosis
Risk Assessment
Risk groups
Surgery
Thyroid
Thyroid cancer
Thyroid Cancer, Papillary - pathology
Thyroid Cancer, Papillary - surgery
Thyroid carcinoma
Thyroid Gland - pathology
Thyroid Gland - surgery
Thyroid Neoplasms - pathology
Thyroid Neoplasms - surgery
Thyroidectomy
Tumors
title How to identify indolent thyroid tumors unlikely to recur and cause cancer death immediately after surgery—Risk stratification of papillary thyroid carcinoma in young patients
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