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The Current State of Mohs Surgery for the Treatment of

Melanoma: A Nationwide Cross-Sectional Survey of


Mohs Surgeons
Spyros M. Siscos, MD, Brett C. Neill, MD, Edward W. Seger, MD, MS, Tyler A. Hooton, BS,
and Thomas L. H. Hocker, MD*

BACKGROUND The increased use of Mohs micrographic surgery (MMS) to treat melanoma has been
accompanied by wide variations in practice patterns and a lack of best practice guidelines.

OBJECTIVE The present study was a nationwide cross-sectional survey of Mohs surgeons to elucidate
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commonalities and variations in their use of MMS to treat melanoma.

MATERIALS AND METHODS A cross-sectional analysis was performed using survey responses of Mohs
surgeons with membership in the American College of Mohs Surgery.

RESULTS A total of 210/513 (40.9%) participants used MMS to treat melanoma of any subtype and 123/210
(58.6%) participants within this group treated invasive T1 melanoma (AJCC Eighth Edition) with MMS. A total
of 172/210 (81.9%) participants debulked melanoma in situ (MIS). Average margin size of the first Mohs stage
for MIS was 4.96 6 1.74 mm. A total of 149/210 (71.0%) participants used immunohistochemical stains, with
145/149 (97.3%) using melanoma antigen recognized by T-cells 1 (MART-1) in 96.5% of melanoma cases treated
with MMS.

CONCLUSION Over half of surveyed Mohs surgeons treating melanoma with MMS are treating early inva-
sive melanoma with MMS. Most Mohs surgeons treating melanoma with MMS debulk MIS and virtually all use
MART-1 when excising invasive melanoma with MMS.

The authors have indicated no significant interest with commercial supporters. IRB Approval Status: Reviewed
and approved by KUMC IRB and ACMS Executive Committee.

elanoma is the fifth most common malignant


M neoplasm in the United States, with 100,350
new cases estimated to be diagnosed in 2020.1 Mohs
across the United States without the development of
best practice guidelines.6 Lack of consensus on the
MMS approach to treating melanoma may be due, in
micrographic surgery (MMS) is emerging as 1 of the part, to differences in the fellowship training of Mohs
most effective treatment modalities for melanoma surgeons, ongoing debates in the literature, concerns
in situ (MIS) and invasive melanoma, with recent with interpreting frozen sections of melanoma, newer
studies demonstrating lower recurrence rates and rapid immunohistochemical (IHC) staining protocols,
improved/noninferior survival outcomes compared and surgeon preference. Given its increased use for
with wide local excision (WLE).2–5 Since 2001, the use melanoma combined with the lack of best practice
of MMS for melanoma has more than tripled within guidelines, this nationwide cross-sectional survey of
the United States.6 However, this increase has been Mohs surgeons sought to investigate commonalities
accompanied by wide variations in practice patterns and variations in the use of MMS to treat melanoma.

*All authors are affiliated with the Division of Dermatology, University of Kansas Medical Center, Kansas City, Kansas

Supplemental digital content is available for this article. Direct URL citations appear in the printed text and are provided
in the HTML and PDF versions of this article on the journal’s Web site (www.dermatologicsurgery.org).

© 2020 by the American Society for Dermatologic Surgery, Inc. Published by Wolters Kluwer Health, Inc. All rights reserved.
· ·
ISSN: 1076-0512 Dermatol Surg 2020;46:1267–1271 DOI: 10.1097/DSS.0000000000002645

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THE CURRENT STATE OF MOHS SURGERY

Methods without fellowship exposure (p < .001). Among the


participants with fellowship exposure who treated mel-
This study was a cross-sectional survey of Mohs sur-
anoma with MMS in current practice, 56.9%
geons with membership in the American College of
reported $35 cases and 43.1% reported 1 to 34 cases of
Mohs Surgery (ACMS). An anonymous 35-item
melanoma treated with MMS during fellowship. Par-
multiple-choice survey was developed using REDCap
ticipants who currently treated melanoma with MMS
(Vanderbilt University, TN) and distributed to all
were more likely to have received fellowship training on
ACMS members during October 2019 through
melanocytic IHC stains (61.1% with IHC fellowship
December 2019 using ACMS mailing lists. Mohs
training vs 34.0% without IHC fellowship training,
micrographic surgery was defined as Mohs surgery
p < .001). Male participants treating melanoma with
with intraoperative frozen section analysis. Excisional
MMS were older (age 49.0 [male] vs age 41.5 [female],
surgery with en face permanent section analysis (“slow
p < .001) and had more time in practice (15.2 years
Mohs”) was not considered as MMS for the purposes
[male] vs 9.87 years [female], p = .003). Age and time in
of this study. Fellowship exposure in MMS for mela-
practice did not vary significantly among same-sex par-
noma was defined as the completion of $1 melanoma
ticipants treating versus not treating melanoma with
case treated with MMS during fellowship. Participants
MMS. Among all participants, no significant differences
currently treating melanoma with MMS were queried
were found between sexual identity (male vs female) and
on melanoma subtypes treated (primary tumor [T],
fellowship exposure in MMS for melanoma, number of
AJCC Eighth Edition), anatomic locations treated,
melanoma cases treated with MMS during fellowship, or
initial margin size (the total distance beyond the clin-
fellowship training in melanocytic IHC staining.
ically apparent tumor after excision of the first MMS
stage), processing of debulked melanoma specimens,
Melanoma Types Treated
and IHC staining. The study was approved by the
ACMS executive committee and the institutional Among the 210 participants treating melanoma with
review board of the University of Kansas. Data anal- MMS, the vast majority treated both lentigo maligna
ysis was conducted using SAS, version 9.4 (SAS Insti- (97.5%) and other melanoma in situ subtypes (91.4%).
tute, Inc.). Chi square, Fisher exact test, and t-tests A slight majority (n = 123, 58.6%) reported treating
were used to compare differences between groups, invasive T1 melanoma, and 43 participants (20.5%)
with p < .05 considered statistically significant. reported treating invasive T2 and/or higher stage mela-
noma with MMS (See Supplemental Digital Content 2,
Results Table S2, http://links.lww.com/DSS/A452). Invasive T2
and/or higher stage melanoma was treated by a greater
Demographic Comparisons percentage of participants in academic hospitals com-
pared with other practice settings (30.2% vs 18.1%,
A total of 513 participants completed the survey (average
p = .041). Participants in a nonacademic hospital setting
age 45 6 11 years; 320 [62.4%] men; 365 [71.2%] in
were more likely to treat melanoma in situ (MIS) on the
private practice) (See Supplemental Digital Content 1,
trunk and extremities (excluding the hands and feet) than
Table S1, http://links.lww.com/DSS/A451). Among all
participants in academic hospitals (p = .01) (See Sup-
participants, 210 (40.9%) reported using MMS to treat
plemental Digital Content 2, Table S2, http://links.lww.
melanoma of any subtype. Participants who were older
com/DSS/A452). The number of yearly MIS cases trea-
(age 46.9 vs age 44.1, p < .001), had more time in practice
ted with MMS did not vary significantly between prac-
(13.9 years vs 10.9 years, p < .001), and men (49.4%
tice settings.
men vs 26.9% women, p < .001) were more likely to treat
melanoma with MMS. Over half of all participants (n =
Surgical/Processing Techniques
266, 51.9%) received fellowship exposure in MMS for
melanoma. Most (57.5%) participants with fellowship When treating MIS with MMS, 172 participants
exposure treated melanoma with MMS in current (81.9%) reported initially excising the clinically visible
practice, in contrast with only 23.1% of participants tumor (debulking) before excising the initial Mohs

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SISCOS ET AL

stage, with virtually all (171/172 [99.4%]) sharply melanoma with MMS. The percentage (40.9%) of
debulking MIS with a scalpel (See Supplemental Mohs surgeons treating melanoma with MMS was
Digital Content 3, Table S3, http://links.lww. similar compared with a study conducted in 2012
com/DSS/A453). Over half (100/171 [58.5%]) of (38.5%).7 However, ACMS membership has increased
surgeons who sharply debulk MIS submit the entire from 1,095 members in 2012 to 1,630 members in
debulked specimen for permanent vertical (bread-loaf) 2019, suggesting an overall increase in the number of
sectioning. A minority (18/171 [10.5%]) submit the Mohs surgeons treating melanoma with MMS. In
entire debulked specimen for frozen vertical section- addition, with its increased use for treatment of mela-
ing, and 49/171 (28.7%) submit portions of the noma, Mohs surgeons who previously treated MIS with
debulked specimen for both permanent and frozen MMS may be increasingly doing so and/or expanding
vertical sectioning. When treating MIS with MMS, the their scope of treatment to include invasive melanoma.
average initial margin size (debulk margin if applica- The present study highlights the importance of fellow-
ble + initial Mohs stage margin i.e. total distance ship exposure to MMS and IHC staining for mela-
beyond the clinically apparent tumor) was 4.96 6 noma. In addition, the creation of postfellowship
1.74 mm. The average initial margin size did not vary training opportunities in MMS and IHC staining for
significantly between practice settings nor among melanoma may help broaden its use among Mohs
participants using versus not using IHC stains. surgeons who received inadequate fellowship exposure.
In this study, male Mohs surgeons were more likely to
Immunohistochemical Staining use MMS to treat melanoma compared with female
Mohs surgeons. Although this finding may be due to a
More than half (149/210 [71%]) of participants treating variety of factors, our data demonstrated similar fel-
melanoma with MMS reported using melanocytic IHC lowship exposure to MMS for melanoma and IHC
stains (See Supplemental Digital Content 3, Table S3, stains among male and female Mohs surgeons. Male
http://links.lww.com/DSS/A453). Participants using IHC Mohs surgeons were older and had more time in
stains were younger (age 45 vs age 52, p < .01) and practice, although it is unclear how these factors may
reported less time in practice (12.3 years vs 18.0 years, influence the use of MMS for melanoma.
p < .01). Virtually all (145/149 [97.3%]) participants
using melanocytic IHC stains reported using melanoma The American Academy of Dermatology/American
antigen recognized by T-cells 1 (MART-1) as their pri- College of Mohs Surgery/American Society for Der-
mary IHC stain. Regarding frequency of use, participants matologic Surgery Association/American Society for
who use IHC stains used MART-1 in 96.5% of their Mohs Surgery Ad Hoc Task Force on Appropriate Use
melanoma cases treated with MMS (See Supplemental Criteria for Mohs surgery8 does not currently offer
Digital Content 3, Table S3, http://links.lww. specific recommendations on the use of MMS for
com/DSS/A453). A greater percentage (78.9%) of par- invasive melanoma. In this study, over half (58.6%) of
ticipants treating invasive melanoma used MART-1 Mohs surgeons treating melanoma with MMS treated
compared with the 51.9% of participants exclusively invasive melanoma. This finding may be due, in part,
treating noninvasive melanoma (p < .001). Participants in to upstaging during the MMS procedure and the
private practice were more likely to use hand staining increasing evidence demonstrating improved survival
versus automated staining compared with participants in of early-invasive melanoma treated with MMS com-
academic hospitals (81.7% vs 53.5%, p < .001). Tradi- pared with WLE.2,4 In addition, the advent of mela-
tional IHC staining protocols (53.2%) and rapid IHC nocytic IHC stains, particularly MART-1, has
staining protocols (51.4%) were used at a similar rate. improved the accuracy of interpreting frozen sections
of melanoma, with MART-1 providing equivalent
information on frozen sections of melanoma com-
Discussion
pared with that obtained in MART-1 permanent sec-
In this nationwide cross-sectional survey, less than half tions.9–13 Furthermore, recent studies have
of surveyed Mohs surgeons reported treating demonstrated that MMS aided by MART-1 achieves

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THE CURRENT STATE OF MOHS SURGERY

low local recurrence rates for MIS and invasive mel- aiming to preserve cosmesis and function. In this
anoma compared with published recurrence rates regard, MMS fills a gap in the treatment of melanoma.
achieved with WLE.5,14 In this study, most Mohs
surgeons reported using IHC stains (almost exclu- On average, Mohs surgeons in the present study repor-
sively MART-1), with MART-1 being used by a ted using initial margins for MIS treated with MMS that
greater percentage of Mohs surgeons treating invasive are at the lower end of the 0.5 to 1.0 cm range for WLE
melanoma with MMS compared with Mohs surgeons recommended by the National Comprehensive Cancer
exclusively treating noninvasive melanoma with Network and American Academy of Dermatology.17,18
MMS. Despite growing evidence supporting the use of
IHC stains with MMS for melanoma, 29% of sur- In this study, most Mohs surgeons reported submitting a
veyed Mohs surgeons treating melanoma with MMS debulked MIS specimen for breadloafing to evaluate for
are not using IHC stains. Mohs micrographic surgery deeper tumor invasion. Although we did not assess for
without IHC has been associated with as high as a margins used when debulking MIS, debulking the visible
33% recurrence rate.15 This may be due, in part, to the tumor with a peripheral margin of at least 2 to 3 mm of
difficulty visualizing atypical melanocytes on frozen clinically normal-appearing skin has previously been
sections, particularly on sun-damaged skin, where advocated.14 Breadloafing the debulked specimen allows
prominent single melanocytes may reside in the for accurate measurement of Breslow depth.19 In
absence of disease.15 Concerns regarding the wide- addition, breadloafing the debulked specimen with fro-
spread use of MMS for melanoma are legitimate when zen sections allows for timely detection of upstaging to
important variations in practice patterns exist.6 facilitate sentinel lymph node biopsy, if applicable,
before tissue rearrangement and disruption of lymphatic
Recent studies have demonstrated a higher likeli- drainage from reconstruction.14 Breadloafing addition-
hood of melanoma being treated with MMS at ally provides a positive control and enables precise
academic centers.2,4 Although the reasons behind evaluation of the relationship between the clinical and
this finding are unclear,2,4 our analysis found no pathologic surgical margins.14 The information obtained
association between a Mohs surgeon’s practice set- from breadloafing debulked specimens of melanoma
ting and treating noninvasive melanoma with MMS. may be useful when interpreting a Mohs layer with
In addition, Mohs surgeons working in academic heavily sun-damaged skin. It is unclear why a minority of
hospitals did not report a significantly higher annual surveyed Mohs surgeons reported not debulking MIS.
number of MIS cases treated with MMS compared Prior studies have demonstrated a wide range of MIS
with Mohs surgeons working in other practice set- lesions on initial biopsy which were subsequently
tings. However, Mohs surgeons working in aca- upstaged to invasive melanoma after histological review
demic hospitals were more likely to treat invasive T2 of the entire lesion.20,21 These staging discrepancies
and/or higher stage melanoma with MMS, a factor may stem from initial subtotal biopsies which can
which likely broadens the spectrum of melanoma misrepresent the depth of both MIS and invasive
subtypes treated with MMS at academic institu-
melanoma. Histologic evaluation of debulked mela-
tions. These findings suggest that academic institu-
noma specimens during MMS is recommended for
tions may be treating a greater percentage of
optimal staging, treatment, and follow-up.18,22
invasive melanomas with MMS.
Limitations and Future Directions
A recent study suggested that if comprehensive margin
assessment surgery (e.g. MMS) is not used, initial Limitations of this study include the response rate
surgical margins of at least 10-mm for primary (513/1,630 [31.5%]), which was similar compared
trunk/extremity and 12-mm for head/neck melanomas with a previous survey of the ACMS membership
should be used to achieve histologically negative (378/1,095 [34.5%]).7 In addition, responses may be
margins 97% of the time.16 These initial margins may biased and overstate the percentage of Mohs surgeons
not always be desirable or feasible, particularly when treating melanoma with MMS. The data in the present

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SISCOS ET AL

study provide a cross-sectional view exclusively of the 7. Trimble JS, Cherpelis BS. Rapid immunostaining in Mohs: current
applications and attitudes. Dermatol Surg 2013;39(1 Pt 1):56–63.
ACMS membership and do not represent all derma-
8. Ad Hoc Task F, Connolly SM, Baker DR, Coldiron BM, et al.
tologists who may utilize MMS. Anatomic site, num- AAD/ACMS/ASDSA/ASMS 2012 appropriate use criteria for Mohs
ber of cases treated with MMS per year, initial margin micrographic surgery: a report of the American Academy of
Dermatology, American College of Mohs surgery, American Society for
size and debulking characteristics pertain to MIS only. Dermatologic Surgery Association, and the American Society for Mohs
This study did not investigate margin sizes used when surgery. J Am Acad Dermatol 2012;67:531–50.

debulking melanoma. Future research may help better 9. Albertini JG, Elston DM, Libow LF, Smith SB, et al. Mohs
micrographic surgery for melanoma: a case series, a comparative study
define and characterize margin size variations during of immunostains, an informative case report, and a unique mapping
the first Mohs stage. In addition, this study did not technique. Dermatol Surg 2002;28:656–65.

investigate initial margins for invasive melanoma 10. Blessing K, Sanders DS, Grant JJ. Comparison of immunohistochemical
staining of the novel antibody melan-A with S100 protein and HMB-45
treated with MMS or the depth of the initial Mohs in malignant melanoma and melanoma variants. Histopathology 1998;
stage. Future studies investigating these important 32:139–46.

parameters are warranted and may help to further 11. Cherpelis BS, Moore R, Ladd S, Chen R, et al. Comparison of MART-1
frozen sections to permanent sections using a rapid 19-minute protocol.
guide treatment. Dermatol Surg 2009;35:207–13.

12. Miller CJ, Sobanko JF, Zhu X, Nunnciato T, et al. Special stains in
Mohs surgery. Dermatol Clin 2011;29:273–86, ix.
Conclusion
13. Zalla MJ, Lim KK, Dicaudo DJ, Gagnot MM. Mohs micrographic
excision of melanoma using immunostains. Dermatol Surg 2000;26:
To our knowledge, this study is the largest cross- 771–84.
sectional survey to date to examine the practice pat-
14. Etzkorn JR, Sobanko JF, Elenitsas R, Newman JG, et al. Low recurrence
terns of Mohs surgeons currently treating melanoma rates for in situ and invasive melanomas using Mohs micrographic
surgery with melanoma antigen recognized by T cells 1 (MART-1)
with MMS. These findings update and add to the immunostaining: tissue processing methodology to optimize pathologic
limited information previously available regarding the staging and margin assessment. J Am Acad Dermatol 2015;72:840–50.

use of MMS for melanoma in the United States.6,23 As 15. Walling HW, Scupham RK, Bean AK, Ceilley RI. Staged excision versus
Mohs micrographic surgery for lentigo maligna and lentigo maligna
the use of MMS to treat melanoma increases, we hope
melanoma. J Am Acad Dermatol 2007;57:659–64.
this analysis will help to reduce variations in practice
16. Ellison PM, Zitelli JA, Brodland DG. Mohs micrographic surgery for
patterns and ultimately help guide the development of melanoma: a prospective multicenter study. J Am Acad Dermatol 2019;
81:767–74.
best practice guidelines.
17. NCCN. Melanoma (Version 3.2018). Available at: https://www.nccn.
org/professionals/physician_gls/default.aspx. Accessed January 8, 2020.
Acknowledgments The authors thank Jo Wick, PhD
18. Swetter SM, Tsao H, Bichakjian CK, Curiel-Lewandrowski C, et al.
for assisting with the statistical analysis in this study. Guidelines of care for the management of primary cutaneous
melanoma. J Am Acad Dermatol 2019;80:208–50.

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