| Literature DB >> 34553851 |
Wen Liu1, Xuejing Yan2, Ruochuan Cheng1.
Abstract
Due to exponential increases in incidences, low risk papillary thyroid microcarcinoma (PTMC) has become a clinical and social issue in recent years. An active surveillance (AS) management approach is an alternative to immediate surgery for patients with low risk PTMC. With decreased doubts about the safety and validity due to evidence from a large number of studies, the AS approach has become increasingly popular worldwide. However, Chinese thyroid surgeons still lag behind other countries in their knowledge of clinical practices and research related to AS. To promote the implementation of AS in China, thyroid surgeons should understand the implications, advantages, and disadvantages of management approaches for AS, and should also consider the willingness of Chinese patients, the impact on the medical billing system, and the enthusiasm of doctors. Thus, a management approach for AS based on the Chinese population should be developed to reduce the risk of disease progression and enhance patient adherence. Herein, we summarize the recent research achievements and deficiencies in AS approaches, and describe the initial experiences regarding AS in the Chinese population, in order to assist Chinese thyroid surgeons in preparing for AS management in the era of PTMC precision medicine.Entities:
Keywords: Papillary thyroid carcinoma; active surveillance; microcarcinoma; observation
Year: 2021 PMID: 34553851 PMCID: PMC9196058 DOI: 10.20892/j.issn.2095-3941.2021.0058
Source DB: PubMed Journal: Cancer Biol Med ISSN: 2095-3941 Impact factor: 5.347
Updates of the guidelines, and consensus on the recommendation of active surveillance management for low risk papillary thyroid microcarcinomas after active surveillance outcomes from Kuma Hospital were published in 2014†
| Affiliation | Publication year | Statement type | Active surveillance | Immediate surgery | Reference |
|---|---|---|---|---|---|
| BTA | 2014 | Guideline | ○ | ● |
|
| ATA | 2015 | Guideline | ● | ○ |
|
| Netherlands | 2015 | Guideline | ○ | ● |
|
| CATO | 2016 | Consensus | ◑ | ● |
|
| UK national multidisciplinary | 2016 | Guideline | ○ | ● |
|
| KTA | 2016 | Guideline | ● | ● |
|
| NHCC | 2018 | Guideline | ○ | ● |
|
| Italian‡ | 2018 | Consensus | ● | ● |
|
| Polish§ | 2018 | Guideline | ○ | ● |
|
| JAES | 2018 | Guideline | ● | ○ |
|
| ESMO | 2019 | Guideline | ● | ○ |
|
| SEOM | 2019 | Guideline | ○ | ● |
|
| NCCN | 2019 | Guideline | ● | ○ |
|
| African | 2019 | Guideline | ● | ● |
|
| AAES | 2020 | Guideline | ● | ○ |
|
CATO, Chinese Association of Thyroid Oncology; ATA, American Thyroid Association; AAES, American Association of Endocrine Surgeons; BTA, British Thyroid Association; ESMO, European Society for Medical Oncology; JAES, Japan Associations of Endocrine Surgeons; KTA, Korean Thyroid Association; NCCN, National Comprehensive Cancer Network; NHCC, National Health Commission of China; SEOM, Spanish Society for Medical Oncology. ○ Not Recommended; ● recommended; ◑ selective under strict conditions. †For search strategies, see Supplement 1. ‡Joint statements of six Italian societies: the Italian Thyroid Association, the Medical Endocrinology Association, the Italian Society of Endocrinology, the Italian Association of Nuclear Medicine and Molecular Imaging, the Italian Society of Unified Endocrine Surgery and the Italian Society of Anatomic Pathology and Diagnostic Cytology. §Joint statements of Polish national societies: the Polish Endocrine Society, Polish Society of Oncology, Polish Thyroid Association, Polish Society of Pathologists, Society of Polish Surgeons, Polish Society of Surgical Oncology, Polish Society of Clinical Oncology, Polish Society of Radiation Oncology, Polish Society of Nuclear Medicine, Polish Society of Pediatric Endocrinology, Polish Society of Pediatric Surgeons, Polish Society of Ultrasonography.
Clinical studies of active surveillance for patients with low risk papillary thyroid carcinomas
| Author, year | Affiliation | Patients | Age(range), year | Tumor diameter (range), mm | Inclusion criteria | F-U protocol | F-U period(range), months | Tumor size enlargement (≥ 3 mm) | Tumor volume increase (> 50%) | Newly developed LNM | Non-progression surgery, cases | FU period after delayed surgery(range), months | Outcomes of delayed surgery |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ito et al.[ | Kuma Hospital, Japan | 1235 | NA | 324 tumors ≤ 5, 686 tumors 5–8, 225 tumors 8–10 | Diagnosed PTMC by FNAB, cN0M0, without invasion to the RLN or trachea, without high-grade malignancy findings, tumor location not adjacent to the RLN or trachea | US Q 6 to 12 months, FNAB for suspicious lymph node | Mean, 60(18–227) | 4.7% in total, 4.9% in 5 years, 8.0% in 10 years | NA | 1.5% in total, 1.7% in 5 years, 3.8% in 10 years | NA | Mean, 75(1–246) | 1 case residual lobe recurrence |
| Fukuoka et al.[ | Cancer institute Hospital, Japan | 384‡ | Mean, 54.0(23–84) | NA | Diagnosed PTMC by FNAB, cT1aN0M0 (asymptomatic and lymph node < 10 mm) | Clinical exam and US Q 6 to 12 months, chest imaging Q 12–24 months | Mean, 81.6 | 6.0% in total, 6.3% in 5 years, 7.3% in 10 years | NA | 1.0% | NA | NA | NA |
| Sakai et al.[ | Cancer institute Hospital, Japan | 61 | Mean, 54.4(32–78) | Mean, 11.7(11–16) | Diagnosed PTC by FNAB, cT1bN0M0 (asymptomatic and lymph node < 10 mm), take age, tumour size and other risk factor into account | Clinical exam and US q 6 to 12 months, chest imaging Q 12–24 months | Mean, 94.8(12–204) | 6.6% in total, 5% in 5 years§12% in 5 years§ | 11.5% | 3.3% | 5 | NA | No differences in surgical procedures, complications, or recurrence compared with immediate surgery¶ |
| Tuttle et al.[ | Memoria Sloan Kettering Cancer centre, America | 291†† | Median, 51(20–86) | 232 tumours ≤ 10, 59 tumours 11–15 | Bethesda category V or VI, ≤ 15 mm, without evidence of ETE, cN0M0, TSH level within the reference range | US Q 6 to 12 months for 2 years, then annually | Median, 25(6–166) | 3.8% in total,2.5% in 2 years,12.1% in 5 years | 12.4% in total, 11.5% in 2 years24.8% in 5 years | 0% | 5 | Mean, 7.3(3–32) | No biochemical or structural persistence or recurrence |
| Oh et al.[ | Multicenter‡‡, South Korea | 370 | Mean, 51.1 | Mean, 5.9 | Diagnosed PTMC by FNAB or CNB, without aggressive variant subtype, without evidence of ETE, cN0M0, tumour location not adjacent to the RLN | Clinical exam and US Q 6 to 12 months, FNAB and thyroglobulin washout for suspicious lymph node | Median, 32.5 (IQR21.5–47.6) | 3.5% in total, 0.6% in 2 years, 6.4% in 5 years, 12.0% in 6 years | 23.2% in total, 6.9% in 2 years, 36.2% in 5 years, 47.5% in 6 years | 1.4% | 28 | Median, 18.7(IQR7.7–32.2) | No recurrence |
| Sanabria[ | Medellin, Colombia | 57 | Mean, 51.9(24–85) | Mean, 9.7 | Bethesda category V or VI, < 15 mm, encapsulated, cN0 | US, the interval not disclosed | Median, 13.3(0–54) | 3.5% | NA | 0% | 2 | NA | NA |
| Rosario et al.[ | Belo Horizonte, Brazil | 77 | Mean, 52(23–81) | 69 tumors ≤ 10, 8 tumors 11–12 | ≥ 20 years, Bethesda category V or VI, ≤ 12 mm, without evidence of ETE, cN0, | US Q 6 months, maintain TSH between 0.5–2.0 mIU/L in patients with TSH > 2.5 mIU/L | Mean, 24.4(6–42)§§ | 1 case suspicious capsular invasion (after F-U 30 months) | NA | 0% | 2 | NA | NA |
| Molinaro et al.[ | University Hospital of Pisa, Italy | 93 | Mean, 44 | Mean, 9.4 | ≥ 18 years, Bethesda category V or VI, ≤ 13 mm, single malignant (or suspicious) nodule, without evidence of ETE, cN0M0, without hyperthyroidism or concomitant antithyroid drugs, without previous history of thyroid surgery | US Q 6 to 12 months for 2 years, then annually | Mean, 19(6–54) | 2.2% | 16% | 1.1% | 19 | Median, 18(6–36) | Excellent response |
CNB, core needle biopsy; ETE, extrathyroidal extension; FNAB, fine-needle aspiration biopsy; F-U, follow-up; IQR, interquartile range; LNM, lymph node metastases; NA, not available; Q, quaque (every); RLN, recurrent laryngeal nerve; TSH, thyrotropin; US, ultrasonography. †Both studies were from the cohort of the Cancer Institute Hospital, Japan. ‡Included 480 lesions from 384 patients with PTMC. §Overall disease progression rate at 5 years and 10 years, including tumor enlargement > 3 mm and new LNM appearance. ¶All of < 15 mm cases were not recurrence. ††Included 5 patients who was inappropriate for observation (3 for suspicious minor ETE into overlying strap muscles and 2 for suspicious subcentimeter LNM), afterwards, 2 patients were treated with delayed surgery for an increase in tumor size and volume after 12 and 18 months of AS, respectively. ‡‡Asan Medical Center, Samsung Medical Center, and Seoul St. Mary’s Hospital. §§Inference was based on the number of follow-up visits for cases.
Indications of inactive surveillance from the Japanese Endocrine Surgery Association consensus statements for papillary thyroid microcarcinomas[48]
| Indication of non-AS | |
|---|---|
| 1. | Presence of clinical lymph node metastasis or distant metastasis (rare) |
| 2. | Clinically apparent invasion into the RLN or trachea |
| 3. | Diagnosis of aggressive subtype of papillary thyroid carcinoma on cytology (rare) |
| 4. | Tumors adherent to the trachea, possibly invading |
| 5. | Tumors located along the course of the RLN |
| 6. | Associated with other thyroid or parathyroid disease requiring surgery |
| 7. | Age < 20 years (no current evidence) |
AS, Active surveillance; JAES, Japan Associations of Endocrine Surgeons; RLN, Recurrent laryngeal nerve.