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ORIGINAL RESEARCH article

Front. Endocrinol., 01 August 2022
Sec. Thyroid Endocrinology
This article is part of the Research Topic Thermal Ablation of Thyroid Nodules View all 8 articles

Long-term outcome of microwave ablation for benign thyroid nodules: Over 48-month follow-up study

Jia-Rui DuJia-Rui Du1Wen-Hui LiWen-Hui Li1Cheng-Hai QuanCheng-Hai Quan2Hui Wang*&#x;Hui Wang1*†Deng-Ke Teng*&#x;Deng-Ke Teng1*†
  • 1Department of Ultrasound, China-Japan Union Hospital of Jilin University, Changchun, China
  • 2Department Of Oncology, Hospital of Jilin Bureau of Geologic Exploration and Mineral Development, Changchun, China

Objectives: The short-term effects of microwave ablation (MWA) for the treatment of benign thyroid nodules (BTNs) were satisfactory in previous studies. However, as a slowly progressing disease, the long-term efficacy of MWA for BTNs at present is not clear. Our study aim was to assess the long-term results of MWA for BTNs after a 48-month follow-up.

Methods: From June 2015 to September 2017, 148 patients had 148 BTNs. All patients were from the China-Japan Union Hospital of Jilin University. Careful ultrasound examinations were performed 1 day, 1 month, 3 months, 6 months, 12 months, and every 6 months after MWA. The volume, volume reduction rate (VRR), recurrence rate of the ablated area and thyroid function were recorded.

Results: The mean volumes of the 148 nodules were 15.6 ± 9.4 cm3 (range: 1.3-48.9 cm3) and 0.6 ± 0.6 cm3 (range: 0-3.5 cm3) before and 48 months after MWA, respectively, with a nodule VRR of 96.9 ± 2.5% (range: 90.4-100%). Two patients (1.35%) had recurrence after MWA. Compared with thyroid function before MWA, no significant variation was observed after MWA. Five patients experienced complications (3.38%): two patients (1.35%) had bleeding, two patients (1.35%) had ear pain and toothache during MWA, and one patient (0.68%) had hoarseness after MWA. No cases of oesophageal injury, tracheal injury, infection, skin burns, etc., were reported during or after MWA.

Conclusions: Based on a long-term follow-up, MWA is an effective method for treating BTNs and is expected to be a potential first-line treatment.

Introduction

In recent years, the detection rate of thyroid nodules has been as high as 65%, and more than 90% of nodules are benign (1, 2). Only a few of these benign nodules require treatment, due to nodules tend to grow and/or associated pressure and/or clinically symptomatic etc. Although surgery is a widely used and effective treatment regimen, it is traumatic, that results in a slow recovery and affects the appearance of the patient. Moreover, some patients must be placed on long-term thyroid hormone replacement therapy after surgery (35). Therefore, in recent years, several scholars have sought minimally invasive treatment (MIT) methods to treat benign thyroid nodules (BTNs).

One such method is ultrasound (US)-guided percutaneous microwave ablation (MWA) (6). MWA is a promising thermal ablation technique that has been used in tumours of the liver and kidney (7, 8) due to its continuously higher intratumor temperature and greater ablation range in a shorter ablation time (9, 10). In recent years, the short-term (less than 12 months) effects of MWA for the treatment of BTNs have been verified by some scholars with encouraging results, with a volume reduction rate (VRR) that ranges from 45.99% to 85.97% (6, 9, 11). However, as a slowly progressing disease (12), the real efficacy of MWA treatment for BTNs should be observed in a long-term follow-up of more than 12 months. Therefore, this study aimed to clarify the efficacy of MWA for the treatment of BTNs in a follow-up of at least 48 months.

Materials and methods

Study oversight

This retrospective study was approved by the Ethics Committee of the China-Japan Union Hospital of Jilin University, and all patients signed an informed consent form before undergoing MWA. All patients were confirmed to have BTNs by core-needle biopsy (CNB).

Patients

The inclusion criteria were as follows (met all of the criteria) (1): benign nodules with once clear pathological result by CNB (Bethesda category: class II, benign), US imaging findings without malignant suspicious features (2); the longest diameter of the lesion is ≥2 cm (3); large nodules (the largest diameter > 4 cm) causing compressive or structural symptoms or psychological anxiety or that affected the appearance of the patient (4); only a single nodule of the thyroid gland (5); refusal to undergo surgical treatment or intolerance for surgery; and (6) normal thyroid functionality.

Patients must meet one of the following exclusion criteria (1): no clear pathological diagnosis or inaccurate CNB results (Nondiagnostic or Unsatisfactory; Atypia of Undetermined Significance or Follicular Lesion of Undetermined Significance; Follicular Neoplasm or Suspicious for a Follicular Neoplasm or Specify if Hurthle cell type) (2); pregnancy or lactation (3); severe abnormal blood coagulation (4); severe abnormal heart or lung function causing inability to tolerate MWA (5); nodules accompanied by macrocalcifications (>1 cm); and (6) infraclavicular goiters.

From June 2015 to September 2017, 153 patients with 153 lesions at our hospital underwent ultrasound-guided MWA for the treatment of BTN. Five patients with 5 lesions were lost to follow-up, and the remaining 148 patients with 148 lesions were ultimately included in this study. Among them, there were 33 males and 115 females with an average age of 41.2 ± 10.7 years (range: age 25-72 years).

Equipment

A Siemens S2000 (Siemens Mountainview, USA) and MINDRAY® DC-8Exp (MINDRAY, Shenzhen, China) colour Doppler ultrasonic diagnostic instrument was employed for ultrasonic image acquisition and MWA guidance. The probe was a 4-9 MHz linear array probe for detecting the superficial organs. An ECO-100A1 microwave treatment instrument (YIGAO Microwave System Engineering Co., Ltd., Nanjing, Jiangsu Province, China) and ECO-100AI3 superficial organ ablation needle (16 G, total length: 10 cm, microwave transmitter away from the shaft tip: 3 mm) were used for MWA.

Pre-MWA procedures

Image collection included observing and recording the size, location, composition, echogenicity, margin, shape, echogenic foci, blood flow, etc., of the lesion. All images were collected by a senior doctor (with more than 10 years of experience in thyroid ultrasound examination). Contrast-enhanced ultrasonography (CEUS) was performed before MWA to obtain the scope and blood supply of the nodules and to design a corresponding MWA plan, which was designed by two experienced doctors (with more than 5 years of experience in MWA). The volume of the lesion was calculated using V =πabc∕6 (V: volume, a: maximum diameter, b and c: the other two perpendicular diameters). A thyroid function test was performed before MWA and at 1 month, 6 months, 12 months, and every 12 months thereafter.

Symptom and cosmetic scores and the Hospital Anxiety and Depression Scale (HADS) were evaluated before and after MWA. We used a visual analogue scale (with scores ranging from 0 to 10) to evaluate neck compression symptoms and dysphagia. The experienced physician evaluated the cosmetic appearance with a score from 1 to 4: 1: no palpable mass; 2: palpable but invisible mass; 3: cosmetic problems when swallowing; 4: cosmetic problems (6, 11). Patients with psychological anxiety about their disease were asked to complete the Anxiety Subscale (HADS-a) questionnaire of the Hospital Anxiety and Depression Scale (HADS), which was used to assess the degree of anxiety. The HADS-a consists of 7 items pertaining to anxiety (with scores ranging from 0 to 21). If the anxiety subscale values exceed seven, anxiety is indicated in the patients (13, 14).

MWA procedure

The patient was laid supine with the neck fully exposed, and local infiltration anaesthesia with 1% lidocaine was administered. For lesions close to high-risk areas, e.g., near the trachea, oesophagus, recurrent laryngeal nerve and neck vasculature, normal saline was used as an isolation fluid to separate the high-risk area from the lesion to prevent damage to the surrounding important organs or tissues (1517).

According to Teng’s puncture method, a 16 G sharp needle 4 cm in length was used to puncture the skin. When the needle was pulled out, a tunnel was created, through which the antenna was inserted and placed into the thyroid nodule by US guidance (18). On the MWA instrument, ablation mode was initiated with 25 W-30 W power. Using moving-shot techniques (19) during MWA, according to the volume, location and blood supply of the nodule, ablation was performed layer by layer from the upper pole to the lower pole or from the lower pole to the upper pole of the thyroid, following the “from far to near” or “from deep to shallow” principle (19). When the MWA process was performed near the recurrent laryngeal nerve, the operator verbally communicated intermittently with the patient to quickly detect any hoarseness. During the MWA process, the isolation fluid should be quickly replenished if it is absorbed.

A CEUS examination was performed immediately after MWA. If the ablation range was satisfactory, i.e., the “black hole” without contrast filling completely covered the tumour, then the ablation was considered complete; if the ablation range was not satisfactory, i.e., CEUS showed contrast filling the nodules, then supplemental ablation was performed.

Follow-up

Careful ultrasound examinations were performed at 1 day, 1 month, 3 months, 6 months, 12 months, and then every 6 months after MWA. The volume and volume reduction rate (VRR) of the MWA area were observed and recorded using the following formula: VRR (%) = ([initial volume–final volume] × 100%)/initial volume. Recurrence was defined as an abnormal nodular echo found in the internal or marginal ablation area, a gradually growing nodular echo or abundant blood flow signals inside the nodule during follow-up; and then, a BTN was confirmed by CNB.

Statistical analysis

SPSS 20.0 was used for statistical analysis. The size of the nodule and the age of the patient were described using the mean ± standard deviation (SD). The volume changes before and after MWA were measured by the paired samples t–test.

Result

Lesion characteristics

A total of 148 lesions were confirmed by CNB pathology to be BTNs. Among them, 81 were located in the right lobe, and 67 were located in the left lobe. The average maximum diameter of the nodules was 3.6 ± 0.8 cm (range: 2.0-5.8 cm), and the mean volume was 15.6 ± 9.4 cm3 (range: 1.3-48.9 cm3). Of the nodules, 46 (31.1%), 95 (64.2%), and 7 (4.7%) had volumes ≤10, 10–30, and ≥ 30 cm3, respectively. The mean ablation time was 456 ± 318 s. The baseline characteristics of the BTNs are presented in Table 1.

TABLE 1
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Table 1 The clinical features of patients and nodules.

MWA procedure and complications

During MWA, all 148 patients tolerated the local anaesthesia well, and none required other analgesic drugs after MWA.

Five patients (3.38%) had complications in the peri-MWA period: major complications (0.68%) were observed in one patient (one with hoarseness), and minor complications (2.70%) were observed in four patients (two with bleeding and two with earache and toothache). No cases of oesophageal injury, tracheal injury, infection, skin burns, etc., were reported during or after MWA.

Of the two patients (1.35%) who had bleeding during MWA, 5 minutes of compression stopped the bleeding for one but not for the other, as confirmed by colour Doppler ultrasound at the bleeding site. For the other patient, the bleeding site was burned for 1 minute with an ablation power of 40 W, which successfully stopped the bleeding. None of the patients who had bleeding required surgical haemostasis.

Two patients (1.35%) experienced earache or toothache on the same side as the lesion during MWA, and the pain was relieved within two hours after MWA.

One patient (0.68%) had hoarseness after MWA and recovered 3 months after MWA. The nodule in this patient was larger than that in the other patients, measuring 5.8 cm×3.5 cm×4.6 cm, with a volume of 48.9 cm3, and was located adjacent to the dorsal thyroid gland.

Two patients (1.35%) had recurrence after MWA. Two recurrent nodules showed regrowth at the marginal region of the previous nodule at the 18-month and 24-month follow-ups. Both of them were diagnosed with a BTN by CNB and underwent a second MWA procedure. After the secondary procedure, two nodules were decreased in size and did not recur during the follow-up period, which continued for more than 24 months and 30 months.

Follow-up

The follow-up duration of the 148 patients was more than 48 months. 48 months after MWA, the mean volume of the 148 nodules significantly decreased from 15.6 ± 9.4 cm3 (range: 1.3-48.9 cm3) to 0.6 ± 0.6 cm3 (range: 0-3.5 cm3) (P <0.0001) (Figure 1), with a VRR of 96.9 ± 2.5% (range: 90.4-100%) (Figure 2). At 48 months, 44 nodules (29.7%) were completely absorbed. The changes in the volume of the nodules before MWA and at each follow-up time point are summarized in Table 2. Different VRRs were observed in different subgroups at the 48-month follow-up (Table 3). For small nodules with a volume ≤ 10 cm3, the VRR at the 48-month follow-up was 99.1 ± 2.0%, and for medium nodules with a volume of 10–30 cm3, the VRR at the 48-month follow-up was 95.9 ± 1.9%. For large nodules with a volume of ≥30 cm3, the VRR at the 48-month follow-up was 94.2 ± 1.6%.

FIGURE 1
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Figure 1 Variation in the mean volume before and after MWA at each follow-up point.

FIGURE 2
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Figure 2 A 52-year-old woman with a diagnosis of a benign thyroid nodule in the left thyroid lobe. The images show the nodule before and during follow-up after MWA. (A) Before MWA, the nodule measures 4.6 cm × 3.1 cm × 3.5 cm in size and 26.1 cm3 in volume. (B) CEUS shows uniform low enhancement of the nodule before MWA. (C) 1 month after MWA, the ablation area measures 4.4 cm × 2.8 cm × 3.3 cm in size and 21.3 cm3 in volume. (D) 3 months after MWA, the ablation area measures 3.8 cm × 2.2 cm × 3.3 cm and 14.4 cm3 in volume. (E) 6 months after MWA, the ablation area measures 3.4 cm × 2.1 cm × 2.3 cm and 8.6 cm3 in volume. (F) 12 months after MWA, the ablation area measures 3.0 cm × 1.8 cm × 2.0 cm and 5.7 cm3 in volume. (G) 18 months after MWA, the ablation area measures 2.5 cm × 1.3 cm × 1.5 cm and 2.6 cm3 in volume. (H) 24 months after MWA, the ablation area measures 1.7 cm × 1.0 cm × 1.4 cm and 1.2 cm3 in volume. (I) 30 months after MWA, the ablation area measures 1.3 cm × 0.6 cm × 1.0 cm and 0.4 cm3 in volume. (J) 36 months after MWA, the ablation area has vanished.

TABLE 2
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Table 2 Mean volume, volume reduction rate and absorption rate of the nodules after MWA.

TABLE 3
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Table 3 Nodule characteristics and the effects of MWA at different sizes.

All 148 patients underwent thyroid function examination before MWA and at 1 month, 6 months, 12 months, and then every 12 months after MWA, and there was no significant variation in thyroid function in any of the patients after MWA compared with thyroid function before MWA.

Symptomatic, cosmetic and anxiety problems

The symptom and cosmetic scores were 4.1 ± 1.3 (range: 0-8) and 2.1 ± 0.8 (range: 1-4) before MWA, respectively. 48 months later, it was significantly decreased to 0.7 ± 0.5 (range: 0-2) (P<0.0001) and 1.0 ± 0.2 (range: 1-2) (P=0.0002), respectively. Prior to MWA, 27.0% (40/148) of the patients complained of psychological anxiety. At the 48-month follow-up, the HADS-a scores of those patients significantly decreased from 8.8 ± 1.3 (range: 8-13) to 4.1 ± 1.8 (range: 1-7) (P<0.0001). All of the discomfort and anxiety problems mentioned above were completely resolved at the 48-month follow-up. (Figure 3)

FIGURE 3
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Figure 3 At each follow-up time point, the symptoms and cosmetic scores and HADS-a varied with thyroid nodule shrinkage.

Discussion

In this study, 148 nodules in 148 patients were treated with MWA, and the patients were followed-up for 48 months. The long-term follow-up results of the study showed that MWA was effective and safe for the treatment of BTNs. In previous research (6, 9, 11, 20, 21), the follow-up duration after MWA was 6-12 months, and the mean VRR of the nodules was 45.99%-85.97%. However, BTNs are slow progressing, and a short-term follow-up may not be enough to accurately determine recurrence after MWA (12).

In this study, MWA was used to treat BTNs and achieved good therapeutic effects according to the long-term follow-up. After the 48 months of follow-up after MWA, the nodule volume was significantly reduced, with a VRR of 96.9 ± 2.5% (range: 90.4-100%). Similar to Luo et al. (22) and Liu et al. (23), the mean VRR of the nodules was 93.2% and 97.1%, respectively, in two 3-year follow-ups. Meanwhile, nodule shrinkage was also accompanied by improvements in symptoms and cosmesis, and MWA for the treatment of BTNs in this study significantly alleviated the patients’ symptoms and cosmetic problems at the time of the last follow-up. Interestingly, although the previous literature (2428) had a shorter follow-up period than our study, we found similar results: the volume reduction rapidly increased in the first 6-12 months, and the symptoms and cosmetic problems improved as the nodule volume decreased.

After 48 months of follow-up after MWA, among all 148 nodules, 44 nodules were completely absorbed (13 were mainly solid nodules and 31 were mainly cystic nodules), and the complete disappearance rate was 29.7%. Similar to Yue’s study (27), the complete disappearance rate was 30.7%. However, 104 nodules were not completely absorbed among the cohort in our study. The mean VRR of these nodules was 95.3 ± 1.7% (range 90.4-98.7%) after more than 48 months of follow-up. The nodules (mean volume 19.69 ± 7.77 cm3) that were not completely absorbed in our study were larger (P<0.000), more solid and less cystic (P=0.004) than the nodules (mean volume 6.04 ± 4.63 cm3) that were completely absorbed. At the same time, Yue’s study (23, 27) also confirmed that mixed and cystic nodules were better absorbed after ablation. Therefore, we speculate that the volume and components of the nodules may be the main factors affecting their absorption after MWA.

Our study revealed a recurrence rate of 1.35% (2/148), which was lower than that in Cheng’s (11), Lim’s (29) and Deandrea’s (30) studies, in which the recurrence rates were 7.7% (51/664), 5.6% (7/126) and 4.1% (9/215), respectively. We hypothesize three reasons for the low recurrence rate after MWA in this study. First, the application of CEUS helped to quickly detect the presence of residual nodules after MWA and to minimize or avoid recurrence through timely supplemental ablation. Second, during MWA, the supplying blood vessel was usually located at the edge of the nodule; thus, the marginal area of the nodule should be fully ablated. Third, careful planning before MWA and strict implementation of the plan during MWA were crucial for preventing recurrence after MWA.

This study showed that MWA was safe for the treatment of BTNs. Five patients (3.38%) in this study had complications in the peri-MWA period, which was similar to Lim’s (29) study, and the overall complication rate in Lim’s study was 3.6% (4/111).

In our study, two patients (1.35%) experienced bleeding in the anterior neck space of the thyroid capsular, which may be caused by damage to the thyroid capsule and its surrounding blood vessels by the puncture path. During the MWA procedure in our study, the bleeding risk rate was lower than that in previous studies on MWA and RFA for the treatment of BTNs, such as studies by Liu et al. (10), Korkusuz et al. (31) and Deandrea et al. (32), who found bleeding risk rates of 3.4%, 7.1% and 15%, respectively. The lower bleeding risk rate in this study was attributed to the following reasons. First, careful observation with colour Doppler prior to puncture could avoid some bleeding, which was caused by damage to the small blood vessels during the puncture process. Second, colour Doppler ultrasound was used to locate the bleeding site quickly and accurately, and MWA could be used to perform haemostasis with 1 minute of ablation at a power of 40 W.

One patient (0.68%) experienced hoarseness that recovered after 3 months, which was lower than Zhi Xi’s (3) study (3.6%) and Cheng’s (11) report (5.8%), but is similar to that in Deandrea’s (32) study (0.4%). Our experience shows that the treatment of BTNs should comprise full ablation under the premise of safety. Therefore, when ablating BTNs, heat injury of the peripheral nerves should be avoided as much as possible. When the duration of ablation is too long, it is important to quickly replenish the isolation liquid to prevent a nerve injury (3335).

Our study also demonstrated other advantages. The thyroid function of all 148 patients was reviewed 48 months after MWA, showing no significant variation compared with that before MWA. This shows that MWA does not cause hypothyroidism in patients, which is a very important advantage of MWA for BTNs.

This research also has some limitations. First, this research had a small sample size. Second, this study was conducted at a single centre; a multicentre study with a larger sample should be conducted in the future to further verify the results. Finally, although CNB was performed in all 148 nodules in this study to reduce the occurrence of false negatives, this cannot be completely avoided.

In conclusion, over 48-month follow-up, MWA for the treatment of BTNs is effective and safe and is expected to be a potential first-line treatment.

Data availability statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.

Ethics statement

The studies involving human participants were reviewed and approved by Ethics Committee of the China-Japan Union Hospital of Jilin University. The patients/participants provided their written informed consent to participate in this study. Written informed consent was obtained from the individual(s) for the publication of any potentially identifiable images or data included in this article.

Author contributions

HW and D-KT contributed to the study conception and design. The first draft of the manuscript was written by J-RD. Material preparation, data collection and analysis were performed by W-HL and C-HQ, and all authors commented on previous versions of the manuscript. All authors read and approved the final manuscript.

Funding

This work was supported by the Department of Science and Technology of Jilin Province (Grant No. 20190303140SF), the Jilin Provincial Health and Family Planning Commission (Grant No. 2019SCZ027) and the China Postdoctoral Science Foundation (Grant No. 2019M661219).

Acknowledgments

The authors would like to thank Xue-Qing Feng for her encouragement and support of this study.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Abbreviations

MWA, microwave ablation; BTNs, benign thyroid nodules; RFA, radiofrequency ablation; VRR, volume reduction rate; CNB, core-needle biopsy; CEUS, contrast-enhanced ultrasonography.

References

1. Guth S, Theune U, Aberle J, Galach A, Bamberger CM. Very high prevalence of thyroid nodules detected by high frequency (13 MHz) ultrasound examination. Eur J Clin Invest (2009) 39(8):699–706. doi: 10.1111/j.1365-2362.2009.02162.x

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Durante C, Grani G, Lamartina L, Filetti S, Mandel SJ, Cooper DS. The diagnosis and management of thyroid nodules a review. JAMA (2018) 319(9):914–24. doi: 10.1001/jama.2018.0898

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Zhi X, Zhao N, Liu Y, Liu JB, Teng C, Qian L. Microwave ablation compared to thyroidectomy to treat benign thyroid nodules. Int J Hyperthermia (2018) 34(5):644–52. doi: 10.1080/02656736.2018.1456677

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Zheng BW, Wang JF, Ju JX, Wu T, Tong G, Ren J. Efficacy and safety of cooled and uncooled microwave ablation for the treatment of benign thyroid nodules: a systematic review and meta-analysis (Review). Endocrine (2018) 62(2):307–17. doi: 10.1007/s12020-018-1693-2

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Yan J, Qiu T, Lu J, Wu Y, Yang Y. Microwave ablation induces a lower systemic stress response in patients than open surgery for treatment of benign thyroid nodules. Int J Hyperthermia (2018) 34(5):606–10. doi: 10.1080/02656736.2018.1427286

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Feng B, Liang P, Cheng Z, Yu X, Yu J, Han Z, et al. Ultrasound-guided percutaneous microwave ablation of benign thyroid nodules: experimental and clinical studies. Eur J Endocrinol (2012) 166(6):1031–7. doi: 10.1530/eje-11-0966

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Liang P, Wang Y, Yu X, Dong B. Malignant liver tumors: treatment with percutaneous microwave ablation–complications among cohort of 1136 patients. Radiology (2009) 251(3):933–40. doi: 10.1148/radiol.2513081740

PubMed Abstract | CrossRef Full Text | Google Scholar

8. Yu J, Liang P, Yu XL, Cheng ZG, Han ZY, Zhang X, et al. US-Guided percutaneous microwave ablation versus open radical nephrectomy for small renal cell carcinoma: intermediate-term results. Radiology (2014) 270(3):880–7. doi: 10.1148/radiol.13130275

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Wu W, Gong X, Zhou Q, Chen X, Chen X, Shi B. US-Guided percutaneous microwave ablation for the treatment of benign thyroid nodules. Endocr J (2017) 64(11):1079–85. doi: 10.1507/endocrj.EJ17-0152

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Liu YJ, Qian LX, Liu D, Zhao JF. Ultrasound-guided microwave ablation in the treatment of benign thyroid nodules in 435 patients. Exp Biol Med (Maywood) (2017) 242(15):1515–23. doi: 10.1177/1535370217727477

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Cheng Z, Che Y, Yu S, Wang S, Teng D, Xu H, et al. US-Guided percutaneous radiofrequency versus microwave ablation for benign thyroid nodules: A prospective multicenter study. Sci Rep (2017) 7(1):9554. doi: 10.1038/s41598-017-09930-7

PubMed Abstract | CrossRef Full Text | Google Scholar

12. Durante C, Costante G, Lucisano G, Bruno R, Meringolo D, Paciaroni A, et al. The natural history of benign thyroid nodules. JAMA (2015) 313:926–35. doi: 10.1001/jama.2015.0956

PubMed Abstract | CrossRef Full Text | Google Scholar

13. Zigmond AS, Snaith RP. The hospital anxiety and depression scale. Acta Psychiatr Scand (1983) 165:8e15. doi: 10.1111/j.1600-0447.1983.tb09716.x

CrossRef Full Text | Google Scholar

14. Yuan Q, Zheng L, Hou J, Xu G, Yang Q, Xu R, et al. Intraoperative radiofrequency ablation for contralateral benign nodules in unilateral thyroid cancer patients to relieve anxiety. J Surg Res (2022) 276:347–53. doi: 10.1016/j.jss.2022.03.012

PubMed Abstract | CrossRef Full Text | Google Scholar

15. Lee SJ, Jung SL, Kim BS, Ahn KJ, Choi HS, Lim DJ, et al. Radiofrequency ablation to treat loco-regional recurrence of well-differentiated thyroid carcinoma. Korean J Radiol (2014) 15:817–26. doi: 10.3348/kjr.2014.15.6.817

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Park HS, Baek JH, Park AW, Chung SR, Choi YJ, Lee JH. Thyroid radiofrequency ablation: updates on innovative devices and techniques. Korean J Radiol (2017) 18:615–23. doi: 10.3348/kjr.2017.18.4.615

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Shin JH, Baek JH, Ha EJ, Lee JH. Radiofrequency ablation of thyroid nodules: basic principles and clinical application. Int J Endocrinol (2012) 2012:919650. doi: 10.1155/2012/919650

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Teng D, Ding L, Wang Y, Liu C, Xia Y, Wang H. Safety and efficiency of ultrasound-guided low power microwave ablation in the treatment of cervical metastatic lymph node from papillary thyroid carcinoma: a mean of 32 months follow-up study. Endocrine (2018) 62(3):648–54. doi: 10.1007/s12020-018-1711-4

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Kim JH, Baek JH, Lim HK, Ahn HS, Baek SM, Choi YJ, et al. 2017 thyroid radiofrequency ablation guideline: Korean society of thyroid radiology. Korean J Radiol (2018) 19(4):632–55. doi: 10.3348/kjr.2018.19.4.632

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Yue W, Wang S, Wang B, Xu Q, Yu S, Yonglin Z, et al. Ultrasound guided percutaneous microwave ablation of benign thyroid nodules: safety and imaging follow-up in 222 patients. Eur J Radiol (2013) 82(1):e11–16. doi: 10.1016/j.ejrad.2012.07.020

PubMed Abstract | CrossRef Full Text | Google Scholar

21. Yue WW, Wang SR, Lu F, Sun LP, Guo LH, Zhang YL, et al. Radiofrequency ablation vs. microwave ablation for patients with benign thyroid nodules: a propensity score matching study. Endocrine (2017) 55(2):485–95. doi: 10.1007/s12020-016-1173-5

PubMed Abstract | CrossRef Full Text | Google Scholar

22. Luo F, Huang L, Gong X, Han Z, Liu F, Cheng Z, et al. Microwave ablation of benign thyroid nodules: 3-year follow-up outcomes. Head Neck (2021) 43(11):3437–47. doi: 10.1002/hed.26842

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Liu LH, Yang BB, Liu Y, Wang JL, Wang DD, Ding HY, et al. Factors related to the absorption rate of benign thyroid nodules after image-guided microwave ablation: a 3-year follow-up. Int J Hyperthermia (2022) 39(1):8–14. doi: 10.1530/EJE-18-0685

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Li J, Xue W, Xu P, Deng Z, Duan C, Zhang D, et al. Efcacy on radiofrequency ablation according to the types of benign thyroid nodules. Sci Rep (2022) 11:22270. doi: 10.1038/s41598-021-01593-9

CrossRef Full Text | Google Scholar

25. Abd El-Galil MS, Ali AH, Botros RM, Abd El-Khaleq Y, Hetta OMA. Efficacy and safety of ultrasound (US)-guided radiofrequency ablation of benign thyroid nodules. Egyptian J Radiol Nucl Med (2021) 52:57. doi: 10.1186/s43055-021-00435-y

CrossRef Full Text | Google Scholar

26. Escobedo RR, Tames GM, Iglesias SL, Felgueroso CA, Garcia AMM, Fernandez AP, et al. Efficacy in size and symptom reduction of radiofrequency ablation of benign non-functioning thyroid nodules. Endocrinol Diabetes y Nutr (2022) 69:194—200. doi: 10.1016/j.endien.2022.02.018

CrossRef Full Text | Google Scholar

27. Russ G, Hamou AB, Poirée S, Ghander C, Ménégaux F, Leenhardt L, et al. Learning curve for radiofrequency ablation of benign thyroid nodules. Int J Hyperthermia (2021) 38:55–64. doi: 10.1080/02656736.2021.1871974

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Nguyen VB, Nguyen TX, Nguyen VVH, Nguyen HT, Nguyen DT, Le CV. Efficacy and safety of single-session radiofrequency ablation in treating benign thyroid nodules: A short-term prospective cohort study. Int J Endocrinol (2021) 2021:P7556393 1687–8337. doi: 10.1155/2021/7556393

CrossRef Full Text | Google Scholar

29. Lim HK, Lee JH, Ha EJ, Sung JY, Kim JK, Baek JH. Radiofrequency ablation of benign non-functioning thyroid nodules: 4-year follow-up results for 111 patients. Eur Radiol (2013) 23(4):1044–9. doi: 10.1007/s00330-012-2671-3

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Deandrea M, Trimboli P, Garino F, Mormile A, Magliona G, Ramunni MJ, et al. Long-term efficacy of a single session of RFA for benign thyroid nodules: A longitudinal 5-year observational study. J Clin Endocrinol Metab (2019) 104:3751–6. doi: 10.1210/jc.2018-02808

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Korkusuz H, Nimsdorf F, Happel C, Ackermann H, Grunwald F. Percutaneous microwave ablation of benign thyroid nodules. functional imaging in comparison to nodular volume reduction at a 3-month follow-up. Nuklearmedizin Nucl Med (2015) 54(1):13–9. doi: 10.3413/Nukmed-0678-14-06

CrossRef Full Text | Google Scholar

32. Deandrea M, Garino F, Mormile A, Garberoglio R, Rossetto R, Bonelli N, et al. Radiofrequency ablation for benign thyroid nodules according to different US features: an Italian multicentre prospective study. Eur J Endocrinol (2018) 180:79–87. doi: 10.1530/EJE-18-0685

CrossRef Full Text | Google Scholar

33. Teng DK, Li HQ, Sui GQ, Lin YQ, Luo Q, Fu P, et al. Preliminary report of microwave ablation for the primary papillary thyroid microcarcinoma: a large-cohort of 185 patients feasibility study. Endocrine (2019) 64(1):109–17. doi: 10.1007/s12020-019-01868-2

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Lee MK, Baek JH, Chung SR, Choi YJ, Lee YM, Kim TY, et al. Effectiveness of injecting cold 5% dextrose into patients with nerve damage symptoms during thyroid radiofrequency ablation. Endocrinol Metab (Seoul) (2020) 35(2):407–15. doi: 10.3803/EnM.2020.35.2.407

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Dong P, Wu XL, Sui GQ, Luo Q, Du JR, Wang H, et al. The efficacy and safety of microwave ablation versus lobectomy for the treatment of benign thyroid nodules greater than 4 cm. Endocrine (2021) 71(1):113–21. doi: 10.1007/s12020-020-02338-w

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: thyroid, benign nodules, thermal ablation, ultrasound, microwave ablation

Citation: Du J-R, Li W-H, Quan C-H, Wang H and Teng D-K (2022) Long-term outcome of microwave ablation for benign thyroid nodules: Over 48-month follow-up study. Front. Endocrinol. 13:941137. doi: 10.3389/fendo.2022.941137

Received: 11 May 2022; Accepted: 12 July 2022;
Published: 01 August 2022.

Edited by:

Laura Sterian Ward, State University of Campinas, Brazil

Reviewed by:

Erivelto Martinho Volpi, Centro de referencia no ensino do diagnóstico por imagem (CETRUS), Brazil
Alfio Jose Tincani, State University of Campinas, Brazil

Copyright © 2022 Du, Li, Quan, Wang and Teng. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Hui Wang, whui66@jlu.edu.cn; Deng-Ke Teng, tengdk@jlu.edu.cn

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.