Abstract
Background:
The indications for sentinel lymph node biopsy (SLNB) for thin melanoma are still unclear. This meta-analysis aims to determine the positive rate of SLNB in thin melanoma and to summarize the predictive value of different high-risk features for positive results of SLNB.
Methods:
Four databases were searched for literature on SLNB performed in patients with thin melanoma published between January 2000 and December 2020. The overall positive rate and positive rate of each high-risk feature were calculated and obtained with 95% confidence intervals (CIs). Both unadjusted odds ratios (ORs) and adjusted ORs (AORs) of high-risk features were analyzed. Pooled effects were estimated using random-effects model meta-analyses.
Results:
Sixty-six studies reporting 38,844 patients with thin melanoma who underwent SLNB met the inclusion criteria. The pooled positive rate of SLNB was 5.1% [95% confidence interval (CI) 4.9%-5.3%]. Features significantly predicted a positive result of SLNB were thickness≥0.8 mm [AOR 1.94 (95%CI 1.28-2.95); positive rate 7.0% (95%CI 6.0-8.0%)]; ulceration [AOR 3.09 (95%CI 1.75-5.44); positive rate 4.2% (95%CI 1.8-7.2%)]; mitosis rate >0/mm2 [AOR 1.63 (95%CI 1.13-2.36); positive rate 7.7% (95%CI 6.3-9.1%)]; microsatellites [OR 3.8 (95%CI 1.38-10.47); positive rate 16.6% (95%CI 2.4-36.6%)]; and vertical growth phase [OR 2.76 (95%CI 1.72-4.43); positive rate 8.1% (95%CI 6.3-10.1%)].
Conclusions:
The overall positive rate of SLNB in thin melanoma was 5.1%. The strongest predictor for SLN positivity identified was microsatellites on unadjusted analysis and ulceration on adjusted analysis. Breslow thickness ≥0.8 mm and mitosis rate >0/mm2 both predict SLN positivity in adjusted analysis and increase the positive rate to 7.0% and 7.7%. We suggest patients with thin melanoma with the above high-risk features should be considered for giving an SLNB.
Introduction
The incidence of melanoma has been increasing rapidly over the past few decades, with 100,350 new cases diagnosed in America in 2020, most of which are thin melanoma (T1, ≤1.0 mm) (1). Although thin melanomas have a relatively good prognosis with a 10-year survival rate of more than 95%, the absolute number of deaths is notable because of the volume of the disease (2).
To identify melanoma with a poor prognosis and provide more precise treatment, sentinel lymph node biopsy (SLNB) was proposed by surgeons. SLNB is generally considered appropriate for melanoma of T2 or thicker, but the indications for sentinel lymph node biopsy for thin melanoma are still controversial. The positive rate of SLNB for thin melanoma reported by previous studies is approximately 5% (3–5). In addition, SLNB carries a false negative rate of 12.5% (6) and several unwanted complications, including infection (2.9%), seroma (5.1%), hematoma (0.5%), lymphoedema (1.3%), and nerve injury (0.3%) (7).
It is critical to recognize thin melanoma with high-risk pathologic features and to reduce unnecessary invasive manipulation. The mainstream view is that SLNB should be performed in thin melanomas only if high-risk features are indicating SLNB positivity and worse prognosis, such as Breslow thickness >0.75 mm, ulceration, Clark level IV/V, and/or high mitotic rate (4, 8). The American Joint Committee on Cancer (AJCC) 8th edition of the guidelines for melanoma published in 2018 is currently in wide clinical use. T1 melanoma was reclassified into T1a (<0.8 mm) and T1b (0.8-1.0 mm, or any ulceration ≤1 mm) (9). According to the National Comprehensive Cancer Network (NCCN) guidelines of cutaneous melanoma, SLNB is recommended for T1b melanoma or T1a lesions with mitosis rate ≥2/mm2, lymphovascular invasion, or other combination of risk factors (10). In the European consensus-based interdisciplinary guideline for melanoma, however, SLNB is recommended only for melanoma ≥0.8 mm with ulceration, mitosis rate ≥1/mm2, microsatellites, or other risk factors (11).
The purpose of this meta-analysis was to determine the positive rate of SLNB in thin melanoma and to summarize the predictive value of different clinical and high-risk pathological features for positive results of SLNB.
Methods
This meta-analysis followed and adhered to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines.
Search Strategy
We searched literature published between January 2000 and December 2020 from the PubMed, Embase, Web of Science, and Cochrane Library databases. English articles with “melanoma”, or “melanomas”, and “sentinel lymph node biopsy”, or “SLNB”, or “SNB” were screened. Through reviewing the titles and abstracts of the retrieved literature, we selected potentially eligible studies preliminarily and further reviewed the full texts to determine whether they met the inclusion criteria. Two authors (HHZ & FZY) reviewed all literature obtained and examined whether each of them met the inclusion criteria.
To reduce potential bias due to the small sample size, we set the included criteria, which require a sample size for each study to be larger than 50. The inclusion criteria were as follows: including patients with a pathologic diagnosis of thin melanoma (Breslow thickness ≤1.0 mm) in the study; performing SLNB for >50 patients with thin melanoma, and reporting an SLN positivity rate. Reference lists of included articles and related literature were manually searched to complete the deficiency of computer search.
When multiple studies reported overlapping or duplicate patient sources, only the most recent and comprehensive study was included. Studies that did not report negative sentinel lymph nodes (SLNs) or included a single isolated high-risk pathologic feature were excluded. Case reports, literature reviews, commentaries, editorials, letters, and conference abstracts were also excluded.
Data Extraction and Quality Assessment
The following data were extracted from studies: 1) study information, including first author and publication year; 2) patient characteristics, including the number of SLNBs performed in patients with thin melanoma, clinical feature (primary tumor location), high-risk pathologic features [Breslow thickness, mitosis rate, Clark Level, ulceration, regression, microsatellites, vertical growth phase, tumor-infiltrating lymphocytes (TIL) and lymphovascular invasion (LVI)]; 3) outcomes, including the number of positive SLNs found in patients with thin melanoma and number of patients with thin melanoma reporting both positive SLN and high-risk features; 4) adjusted odds ratio (OR) for each high-risk pathologic feature if available.
Two authors (HHZ & FZY) used the Newcastle Ottawa Scale (NOS) to assess the risk of bias in the included studies. The NOS evaluates literature quality in three aspects: selection, comparability, and outcomes. The maximum score was 9, and a score greater than 6 is considered to indicate a low risk of bias.
Statistical Analysis
The primary outcome was the positive rate of SLNB in thin melanoma (Breslow thickness ≤ 1.0 mm), and the pooled effect was calculated and obtained with 95% confidence intervals (CIs). Forest plots were constructed to visually represent the results. The secondary outcomes were the predictive value of high-risk pathologic and clinical features for positive results of SLNB. Unadjusted ORs and adjusted ORs were pooled and analyzed using a random-effects model. Additionally, pooled positive rates of SLNB in patients with each pathologic feature were calculated. Heterogeneity among studies was calculated by the I2 measure of inconsistency, and an I2>50% indicated significant heterogeneity. The presence of publication bias was investigated visually using a funnel plot. Meta-analysis was performed by Stata/MP software (version 16.0 for Windows, StataCorp LLC, College Station, TX77845, USA).
Results
Characteristics of Included Studies
The process of study selection is described in Figure 1. A total of 6424 articles were obtained through retrieval, and 66 of them met the inclusion criteria. All of the included studies were retrospective, reporting 38,844 patients with thin melanoma who underwent SLNB (Table 1) (8, 12–76). The number of included patients in each study ranged from 51 to 9186, with a median of 205. A total of 2117 (5.45%) positive SLN cases were found among all patients. Thirty-eight of the 66 included studies reported at least one high-risk pathologic feature that may be associated with SLN positivity. A median NOS score of 7 (range from 6 to 8) indicated that the risk of bias of the included studies was small. No study was excluded based on the NOS quality assessment. No significant publication bias among the included studies was found by funnel plot (Figure 2).
Figure 1
Table 1
| Study | Year | Total No. of thin melanoma patients undergoing SLNB | Total No. of thin melanoma patients with positive SLN (%) | High-risk features reported | Risk of bias Score (NOS) (Max=9) |
|---|---|---|---|---|---|
| Theile et al. (12) | 2020 | 240 | 14 (5.8%) | Thickness, ulceration | 6 |
| Skochdopole et al. (13) | 2020 | 4332 | 229 (5.3%) | Thickness | 6 |
| Kocsis et al. (14) | 2020 | 78 | 9 (11.5%) | Ulceration, regression | 7 |
| Hu et al. (15) | 2020 | 238 | 19 (8.0%) | Nil | 7 |
| Antonialli et al. (16) | 2020 | 399 | 27 (6.8%) | Nil | 7 |
| Tejera-Vaquerizo et al. (17) | 2019 | 1083 | 73 (6.7%) | Nil | 8 |
| Santos et al. (18) | 2019 | 137 | 10 (7.3%) | Thickness, ulceration, MR, TIL, regression, CL, microsatellites | 8 |
| Piazzalunga et al. (19) | 2019 | 1272 | 76 (6.0%) | Thickness, ulceration, MR, CL | 7 |
| Conic et al. (8) | 2019 | 9186 | 457 (5.0%) | thickness, ulceration, MR, regression, CL | 8 |
| Verver et al. (20) | 2018 | 1607 | 115 (7.2%) | Nil | 7 |
| Stiegel et al. (21) | 2018 | 326 | 25 (7.7%) | Nil | 8 |
| Nguyen et al. (22) | 2018 | 142 | 7 (4.9%) | Nil | 6 |
| Isaksson et al. (23) | 2018 | 1038 | 49 (4.7%) | Thickness, ulceration, MR | 6 |
| Herbert et al. (24) | 2018 | 1129 | 49 (4.3%) | thickness | 7 |
| Tejera-Vaquerizo et al. (25) | 2017 | 203 | 14 (6.9%) | MR, regression, microsatellites | 7 |
| Joyce et al. (26) | 2017 | 65 | 1 (1.5%) | Thickness, ulceration | 8 |
| Wat et al. (27) | 2016 | 171 | 15 (8.8%) | MR | 7 |
| Rubinstein et al. (28) | 2016 | 252 | 6 (2.4%) | Nil | 8 |
| Hieken et al. (29) | 2015 | 4410 | 283 (6.4%) | Nil | 7 |
| Voit et al. (30) | 2014 | 288 | 15 (5.2%) | Nil | 7 |
| Mitteldorf et al. (31) | 2014 | 207 | 38 (18.4%) | Thickness, ulceration, MR, regression, CL | 7.5 |
| Bartlett et al. (32) | 2014 | 781 | 29 (3.7%) | Thickness, ulceration, MR, TIL, regression, CL, LVI, microsatellites | 6.5 |
| Balch et al. (33) | 2014 | 1213 | 73 (6.0%) | Nil | 6 |
| Venna et al. (34) | 2013 | 484 | 34 (7.0%) | Thickness, ulceration, MR, TIL, CL, LVI | 6 |
| van den Broek et al. (35) | 2013 | 61 | 0 (0.0%) | Nil | 6 |
| Mozzillo et al. (36) | 2013 | 492 | 24 (4.9%) | Ulceration, MR | 8 |
| Han et al. (37) | 2013 | 1250 | 65 (5.2%) | Thickness, ulceration, MR, TIL, regression, CL, LVI, VGP | 7.5 |
| Cooper et al. (38) | 2013 | 189 | 3 (1.6%) | Ulceration, MR, CL | 7 |
| Chu et al. (39) | 2013 | 106 | 3 (2.8%) | Ulceration, MR, CL | 8 |
| Ponti et al. (40) | 2012 | 286 | 3 (1.0%) | Nil | 6 |
| Murali et al. (41) | 2012 | 432 | 29 (6.7%) | Thickness, ulceration, MR, CL, LVI, microsatellites | 7 |
| Koshenkov et al. (42) | 2012 | 72 | 6 (8.3%) | Ulceration, CL | 6 |
| Hinz et al. (43) | 2012 | 121 | 5 (4.1%) | Thickness, ulceration, CL | 8 |
| Han et al. (44) | 2012 | 271 | 22 (8.1%) | Thickness, ulceration, MR, TIL, regression, CL, VGP | 7 |
| Elsaesser et al. (45) | 2012 | 212 | 2 (0.9%) | Nil | 7 |
| Yonick et al. (46) | 2011 | 147 | 16 (10.9%) | Nil | 6 |
| Lowe et al. (47) | 2011 | 260 | 9 (3.5%) | Nil | 7 |
| Vermeeren et al. (48) | 2010 | 78 | 5 (6.4%) | Thickness, ulceration, CL | 7 |
| Socrier et al. (49) | 2010 | 68 | 9 (13.2%) | Regression | 6.5 |
| Santillan et al. (50) | 2010 | 72 | 5 (6.9%) | Nil | 7 |
| Mitra et al. (51) | 2010 | 320 | 24 (7.5%) | Nil | 6 |
| Kunte et al. (52) | 2010 | 147 | 11 (7.5%) | Thickness | 7 |
| Ellis et al. (53) | 2010 | 105 | 2 (1.9%) | Nil | 7 |
| Testori et al. (54) | 2009 | 358 | 4 (1.1%) | Nil | 7 |
| Wright et al. (55) | 2008 | 631 | 31 (4.9%) | Thickness, ulceration, CL | 6.5 |
| Roulin et al. (56) | 2008 | 51 | 3 (5.9%) | CL | 7 |
| Kaur et al. (57) | 2008 | 62 | 2 (3.2%) | Regression | 7.5 |
| Starz and Balda (58) | 2007 | 87 | 10 (11.5%) | Nil | 6.5 |
| Koskivuo et al. (59) | 2007 | 141 | 5 (3.5%) | Nil | 7 |
| Vaquerano et al. (60) | 2006 | 91 | 6 (6.6%) | Nil | 7 |
| Ranieri et al. (61) | 2006 | 184 | 12 (6.5%) | Thickness, ulceration, regression, CL, VGP | 7 |
| Nowecki et al. (62) | 2006 | 260 | 17 (6.5%) | Nil | 7 |
| Karakousis et al. (63) | 2006 | 882 | 38 (4.3%) | Thickness, ulceration, MR, regression, CL, VGP | 8 |
| Hershko et al. (64) | 2006 | 64 | 5 (7.8%) | CL | 7 |
| Cascinelli et al. (65) | 2006 | 145 | 6 (4.1%) | Nil | 7 |
| Rex et al. (66) | 2005 | 73 | 3 (4.1%) | Nil | 7 |
| Puleo et al. (67) | 2005 | 409 | 20 (4.9%) | CL | 7 |
| Kesmodel et al. (68) | 2005 | 181 | 9 (5.0%) | Thickness, ulceration, MR, CL | 7 |
| Stitzenberg et al. (69) | 2004 | 146 | 6 (4.1%) | Ulceration, regression, CL | 6 |
| Borgognoni et al. (70) | 2004 | 114 | 2 (1.8%) | Nil | 7 |
| Rousseau et al. (71) | 2003 | 388 | 4 (1.0%) | Nil | 6 |
| Oliveira Filho et al. (72) | 2003 | 77 | 6 (7.8%) | Ulceration, regression, CL, VGP | 7 |
| Jacobs et al. (73) | 2003 | 63 | 2 (3.2%) | CL | 6 |
| Bleicher et al. (74) | 2003 | 272 | 8 (2.9%) | Thickness | 6 |
| Agnese et al. (75) | 2003 | 91 | 1 (1.1%) | Nil | 7 |
| Statius Muller et al. (76) | 2001 | 104 | 7 (6.7%) | Thickness | 7 |
Characteristic of the 66 included studies.
SLNB, sentinel lymph node biopsy; CL, Clark level; MR, mitotic rate; TIL, tumor-infiltrating lymphocytes; VGP, vertical growth phase; LVI, lymphovascular invasion; PTL, primary tumor location.
Figure 2
Outcomes
For the primary outcome, a pooled positive rate of SLNB was estimated by applying the random effect model, calculated as 5.1% (95% CI, 4.5% to 5.6%, Figure 3). Significant heterogeneity between studies was detected (I2 = 73.6%, p<0.001). The unadjusted ORs and pooled positive rate of each high-risk pathologic and clinical feature for SLN positivity is shown in Table 2. Breslow thickness ≥0.8 mm, presence of ulceration, mitosis rate >0/mm2, Clark level IV/V, and vertical growth phase showed a significant association with SLN positivity in unadjusted analysis. All of the above pathologic features showed a pooled positive rate higher than 5.1% except for the presence of ulceration. Notably, we found the presence of microsatellites to be most strongly associated with SLN positivity, with an unadjusted OR of 3.8 (95% CI, 1.38 to 10.47) and a pooled positive rate of 16.6% (95% CI, 2.4% to 36.6%).
Figure 3
Table 2
| Predictor | No. of studies | No. of thin melanoma patients undergoing SLNB | No. of thin melanoma patients with positive SLN | No. of patients with positive SLN and predictor | Unadusted Odds Ratio (95%CI) | Pooled Positive Rate (95%CI) (%) |
|---|---|---|---|---|---|---|
| Breslow thickness <0.8mm | 23 | 23426 | 1228 | 469 | – | 2.9 (2.1–3.7) |
| Breslow thickness ≥0.8mm | 23 | 23426 | 1228 | 759 | 1.61 (1.42–1.82) | 7.0 (6.0–8.0) |
| Ulceration | 25 | 17768 | 1108 | 115 | 1.60 (1.30–1.97) | 4.2 (1.8–7.2) |
| Regression | 14 | 11065 | 585 | 119 | 0.89 (0.72–1.11) | 5.2 (2.9–8.1) |
| Clark Level IV/V | 24 | 15198 | 803 | 421 | 1.68 (1.45–1.95) | 6.6 (5.7–7.6) |
| Mitosis Rate >0/mm2 | 18 | 15002 | 801 | 584 | 2.22 (1.88–2.63) | 7.7 (6.3–9.1) |
| Tumor-infiltrating Lymphocytes | 5 | 1613 | 91 | 51 | 0.69 (0.43–1.10) | 4.3 (2.5–6.5) |
| Lymphovascular Invasion | 4 | 1973 | 119 | 6 | 2.39 (1.00–5.75) | 12.9 (0–37.4) |
| Microsatellites | 4 | 1411 | 77 | 5 | 3.80 (1.38–10.47) | 16.6 (2.4–36.6) |
| Vertical Growth Phase | 5 | 1821 | 112 | 91 | 2.76 (1.72–4.43) | 8.1 (6.3–10.1) |
| Primary Tumor Location (trunk vs others) | 20 | 17345 | 1025 | 432 | 1.10 (0.96–1.26) | 6.2 (4.5–8.2) |
| Primary Tumor Location (extremities vs others) | 20 | 17345 | 1025 | 457 | 0.98 (0.86–1.12) | 6.4 (4.4–8.7) |
Predictive value of high-risk pathologic and clinical features for sentinel lymph node biopsy positivity.
The adjusted ORs of pathologic features are shown in Table 3. There were only 11 studies that had adjusted OR data that could be analyzed. Pathologic features that were available for adjusted analysis were limited as the presence of ulceration, Breslow thickness ≥0.8 mm, mitosis rate >0/mm2, Clark level IV/V, and the presence of regression. Breslow thickness ≥0.8 mm, presence of ulceration, mitosis rate >0/mm2 showed a significant association with SLN positivity in the adjusted analysis, while Clark level IV/V did not show a significant correlation with SLN positivity. Among these, the presence of ulceration was the strongest predictor of positive SLNB results in the adjusted analysis, with an adjusted OR of 2.75 (95%CI, 1.65 to 4.60).
Table 3
| Predictor | No. of studies | No. of thin melanoma patients undergoing SLNB | Adjusted Odds Ratio | 95%CI |
|---|---|---|---|---|
| Ulceration | 8 | 14003 | 2.75 | 1.65–4.60 |
| Breslow thickness ≥0.8mm | 10 | 19381 | 1.94 | 1.28–2.95 |
| Mitosis Rate >0/mm2 | 8 | 12101 | 1.63 | 1.13–2.36 |
| Clark Level IV/V | 9 | 11924 | 1.24 | 0.84–1.84 |
| Regression | 7 | 9881 | 1.20 | 0.89–1.63 |
Pooled adjusted odds ratio of high-risk pathologic features.
The associations between SLN positivity and the primary tumor location, the absence or presence of regression, LVI, or TIL were found with insufficient evidence.
Discussion
It is critical to identify thin melanoma with a worse prognosis so that patients can be able to receive precise therapies. Researchers around the world have been interested in investigating an effective prediction for the prognosis of thin melanoma. Several pieces of research have been published in the past few years. This study is the most recent and most comprehensive meta-analysis to date. Compared with the previous meta-analysis, this study included 19 newly published research articles since 2015, reporting 26,308 patients in total who had a diagnosis of thin melanoma and underwent SLNB.
The pooled estimated positive rate of SLNB in thin melanoma in this study was 5.1%, with a 95% CI of 4.5% to 5.6%. This result is similar to those found in preexisting meta-analyses, which reported pooled positive rates of 5.6%, 4.5%, and 5.1% (3–5), but we got narrower confidence intervals. A 5% risk threshold is often used for surgeons suggesting to perform SLNB for a patient (37, 77). Generally, SLNB is offered to patients with primary melanoma with Breslow thickness ≥0.8 mm with additional risk factors. But different risk factors are recommended in different guidelines (10, 11). Therefore we analyzed the predictive value of multiple pathological and clinical features for the positive SLN.
In this study, we not only updated the predictive value of pathologic features explored in the previous meta-analysis but also paid attention to primary tumor location, which was reported to be correlated with a positive SLN (34). We yielded some different results. Ulceration, Clark level, and Breslow thickness were commonly recorded features in patients, reporting in 37.9%, 36.4%, and 34.8% of included studies, respectively. In the unadjusted analysis in our study, we recognized the same significant predictors as the previous meta-analysis and the primary tumor location was not significantly related to SLN positivity. And in the adjusted analysis in our study, however, the presence of ulceration was the most predictive factor for SLN positivity, while Clark level IV/V did not show a significant correlation with SLN positivity.
A limitation of the previous meta-analysis is the relatively small sample size of included studies. Only one study provided the data on the pathologic features of patients with a sample size larger than 1,000 for analysis. Several large-scale studies were published after 2015 which supplemented the insufficiency of the previous meta-analysis in the adjusted odds ratios analyses. In our study, 6 pieces of literature with a sample size larger than 1,000 were included. The largest one is the study of Conic, et al. published in 2019 with a sample size of 9,186, and it provided data on pathologic features that are available for both unadjusted and adjusted OR analyzing. Thus, we could obtain more accurate predictive values of pathologic and clinical features for SLN positivity. And the 95% CIs of unadjusted ORs for all features analyzed in our study were narrower than those reported in the previous meta-analysis.
The presence of microsatellites was recognized to have a 3.8-fold higher risk and positive rate of 16.6% for SLN positivity in our study, which means it is the strongest predictor among the pathologic features we analyzed. Microsatellites are a rarely present pathologic feature associated with poor prognosis and are more likely found in thicker melanoma (78). Four studies in our meta-analysis including 1411 patients with thin melanoma reported data on microsatellites (18, 25, 32, 41). Two of them demonstrated a remarkable increase in SLN positive rate when microsatellites were present, but none of the four studies found it statistically significant because of the infrequence of events. Adjusted analysis for microsatellites was not available because relevant researches were too few. And it is the same reason why the adjusted analysis was not done for the vertical growth phase. Regression in primary melanoma has been reported as a protective factor that relates to lower SLN positivity (79) and lower risk of death (80). A host immunologic response to the tumor is considered to play a role in the presence of regression. However, regression did not show significance relativity of SLN positivity in unadjusted analysis nor adjusted analysis in this study.
The pooled positive rate of SLNB in thin melanoma in this study was 5.1%. When patients were confirmed with melanomas of Breslow thickness ≥0.8 mm or mitosis rate >0/mm2, the pooled positive rate of SLNB would rise to 7.0% and 7.7%, respectively. Therefore, we suggest that surgeons should consider giving SLNB to such patients. And when a combination of high-risk features is found, the patient should be informed of the even higher rate of SLN positivity.
Our study has some limitations. All studies performed SLNB only in patients with thin melanoma when there was any high-risk feature; therefore, the overall positive rate of SLNB was undoubtedly higher than the true incidence of SLN positivity in all thin melanomas. Significant heterogeneity among the included studies (I2 = 73.6%, p<0.001) was found using a weight estimated random-effects model in the meta-analysis. This probably resulted from several included studies with a higher proportion of positive SLNs. The reporting of identical pathologic features, such as mitosis rate, differed in some of the included studies by defining different cutoff values. This may lead to bias in analyzing its odds ratio. Since this meta-analysis was based on the study level, this variation could also increase the heterogeneity. A patient-level meta-analysis may help to avoid this variation and assess adjusted ORs for more pathologic features. For pathologic features such as microsatellites and the vertical growth phase, more research is needed to clarify their predictive value with larger data sets. Besides the risk factors analyzed in this study, there are other factors that affect the prognosis of melanoma. Melanin pigmentation plays a role in regulating melanocyte and neighboring cells’ behavior (81). It protects melanocytes from UVR but at times accelerates the progression of melanoma and makes melanocytes resistant to different types of therapy (82–84). And as a result, melanin pigmentation shortens overall survival and disease-free survival in metastatic melanoma (82). However, no study has reported the relationship between melanin pigmentation and a positive sentinel lymph node. We look forward to future researches.
Conclusion
The overall positive rate of SLNB in thin melanoma in this study was 5.1%. The strongest predictor for SLN positivity identified was the presence of microsatellites on unadjusted analysis and the presence of ulceration on adjusted analysis. Breslow thickness ≥0.8 mm and mitosis rate >0/mm2 both predict SLN positivity in adjusted analysis and increase the positive rate to 7.0% and 7.7%. We suggest patients with thin melanoma with the above high-risk features should be considered for giving an SLNB.
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Statements
Data availability statement
The original contributions presented in the study are included in the article/supplementary material. Further inquiries can be directed to the corresponding authors.
Author contributions
JH and XL contributed to conception and design of the study. ZF and HH performed articles review and quality assessments. HH performed the data analyses and wrote the first draft of manuscript. JJ, ZF, and HH wrote sections of the manuscript. JJ, JH, and XL helped perform the analysis with constructive discussions. All authors contributed to manuscript revision, read, and approved the submitted version.
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.
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Summary
Keywords
thin melanoma, sentinel lymph node biopsy, positive rate, ulceration, microsatellites, Breslow thickness, mitosis rate
Citation
Huang H, Fu Z, Ji J, Huang J and Long X (2022) Predictive Values of Pathological and Clinical Risk Factors for Positivity of Sentinel Lymph Node Biopsy in Thin Melanoma: A Systematic Review and Meta-Analysis. Front. Oncol. 12:817510. doi: 10.3389/fonc.2022.817510
Received
18 November 2021
Accepted
10 January 2022
Published
27 January 2022
Volume
12 - 2022
Edited by
Sapna Patel, University of Texas MD Anderson Cancer Center, United States
Reviewed by
Andrzej T. Slominski, University of Alabama at Birmingham, United States; Simone Ribero, University of Turin, Italy
Updates
Copyright
© 2022 Huang, Fu, Ji, Huang and Long.
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: Jiuzuo Huang, hjz1983@126.com; Xiao Long, pumclongxiao@126.com
†These authors have contributed equally to this work and share first authorship
This article was submitted to Skin Cancer, a section of the journal Frontiers in Oncology
Disclaimer
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