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Vol. 108. Issue 9.
Pages 818-826 (November 2017)
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Vol. 108. Issue 9.
Pages 818-826 (November 2017)
Novelties in Dermatology
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Novel Additions to the AJCC's New Staging Systems for Skin Cancer
Los nuevos sistemas de estadificación del AJCC incorporan novedades en el cáncer cutáneo
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J. Cañuetoa,b,
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jcanueto@yahoo.es

Corresponding author.
, C. Román-Curtoa,b
a Servicio de Dermatología, Complejo Asistencial Universitario de Salamanca, Salamanca, España
b IBSAL Instituto de Investigación Biomédica de Salamanca, Complejo Asistencial Universitario de Salamanca, Salamanca, Spain
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Tables (5)
Table 1. Eighth Edition of the AJCC TMN Staging Manual: Merkel Cell Carcinoma.
Table 2. Comparison of the Seventh and Eighth Editions of the American Joint Committee on Cancer (AJCC) Staging Manual: Squamous Cell Carcinoma and Nonmelanoma Skin Cancer (NMSC) Other Than Merkel Cell Carcinoma Differences in the 4 T Categories.
Table 3. Eighth Edition of the TNM Staging Manual of the AJCC for Cutaneous Epidermal Carcinoma (SCC) of the Head and Neck and Nonmelanoma Skin Cancer Other Than Merkel Cell Carcinoma of the Head and Neck.
Table 4. Comparison of the Seventh and Eighth Editions of the American Joint Committee on Cancer (AJCC) Staging Manual for Melanoma.
Table 5. Eighth Edition of the AJCC TNM Staging Manual for Melanoma (Cutaneous).
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Abstract

The eighth edition of the staging manual of the American Joint Committee on Cancer incorporates important changes in the classification of skin cancers. Coming 40 years after the first edition, the latest manual preserves its specific system for Merkel cell carcinoma and takes into account recent publications on the prognosis of squamous cell carcinoma by defining a completely new T category for this neoplasm. Staging for squamous cell carcinoma considers head and neck tumors (excluding the eyelid) and does not offer solutions for other sites except the vulva, penis, and perianal region. Regarding melanoma, use of the mitotic index has been eliminated and the prognosis of the primary tumor is based on Breslow thickness and ulceration. In addition, thickness is now recorded to an accuracy of 0.1mm, and the T0 concept has been introduced to define those metastatic melanomas in which the primary tumor has regressed completely. In this new edition, changes have also been made to the N category of all the skin cancer staging systems, and M1d has been added to the M category for melanoma to refer to metastatic involvement of the central nervous system, which, up to now, had been included in the M1c category. This new system will need to be validated with patient series to determine if it adequately satisfies the objective of tumor risk stratification.

Keywords:
Staging
Skin cancer
Cutaneous squamous cell carcinoma
Melanoma
Merkel cell carcinoma
Resumen

Cuarenta años después de la publicación de la primera edición de la estadificación del American Joint Committee on Cancer, la octava edición se publica con cambios relevantes en el cáncer de piel. En el cáncer cutáneo no melanoma el American Joint Committee on Cancer mantiene un enfoque específico para el carcinoma de células de Merkel y tiene en cuenta algunos trabajos publicados recientemente sobre el pronóstico del carcinoma epidermoide cutáneo en la definición de una categoría T completamente nueva para este tumor. Por otra parte, la estadificación se contempla para el carcinoma epidermoide cutáneo de cabeza y cuello (excluyendo el párpado) y en otras localizaciones; únicamente ofrece soluciones para la estratificación de tumores de vulva, pene y región perineal. En relación con el melanoma, el valor del índice mitótico desaparece y el pronóstico del tumor primario se define basándose en el espesor de Breslow y la ulceración. Además, el espesor pasa a registrarse con una precisión de 0,1mm y aparece el concepto de T0 para los melanomas metastásicos en los que el primario ha regresado completamente. Existen diferencias en la categoría N de todos los sistemas de estadificación de cáncer cutáneo en esta nueva edición, y en relación con la categoría M, en el melanoma aparece la categoría M1d para hacer referencia a la afectación metastásica del SNC, que hasta el momento se incluía dentro de la categoría M1c. Será necesario validar este nuevo sistema con series de pacientes para valorar si efectivamente cumple con el objetivo de estratificar por riesgo los tumores de una manera adecuada.

Palabras clave:
Estadificación
Cáncer cutáneo
Carcinoma epidermoide cutáneo
Melanoma
Carcinoma de células de Merkel
Full Text
Introduction

Forty years after the publication by the American Joint Committee on Cancer (AJCC) of the first edition of its TNM staging manual1 the eight version has been published with substantial changes in the case of skin cancer.2 In nonmelanoma skin cancer (NMSC), the new manual preserves a specific system for Merkel cell carcinoma (MCC) and takes into account certain studies on the prognosis of squamous cell carcinoma (SCC) published in recent years, although SCC and other forms of NMSC (with the exception of MSC) still use the same system. That is, SCC and basal cell carcinoma are staged in the same way. In the case of melanoma, the mitotic index is now longer used as a modifier of the T category, which is stratified only by the Breslow thickness and the presence of ulceration.

Nonmelanoma Skin Cancer

Since the first edition of the manual in 1977,1 major progress has been made in assessing NMSC prognosis, leading to progressive changes in successive editions up until the current edition, published in 20172 and to be implemented in clinical practice on January 1, 2018. In reality, up to the sixth edition of the AJCC TNM staging manual,2 and despite several relevant studies in the 1990s,4–19 the changes in the T category of NMSC have been very subtle. With small differences between some of the systems, basically the tumor was considered T1 if its greater dimension measured less than 2cm, T2 if it measured between 2 and 5cm, T3 if it measured more than 5cm, and T4 if bone, muscle, or cartilage invasion was present.1,11–14 Studies were published that recognized the influence of different factors on SCC prognosis.15–23 Some of these studies explicitly highlighted the need for an improvement in the staging system.18,21

Merkel Cell Carcinoma

In 2010, the seventh edition of the AJCC TNM staging manual incorporated significant novelties in NMSC classification.24 For the first time, a separate staging system was introduced for Merkel cell carcinoma (MCC), which until then had been classified with the same staging system as other NMSC. This means that all forms of NMSC other than MCC should be classified according to the criteria for SCC. TNM classification for MCC has been modified in the most recent edition2 in light of a study that assessed clinical outcomes in a large series of patients.25 In reality, T categorization has not been changed, but there are significant changes in N categorization and stratification of stages I-IV.2,25 Furthermore, clinical and pathologic staging are separated out in this eight edition of the manual.2,25 In the T category, MCC is classified as T1 if it measures 2cm or less in the largest dimension, T2 if it measures between 2 and 5cm in the largest dimension, T3 if it measures more than 5cm, and T4 if it invades deep structures (bone, muscle, fascia, or cartilage).2,25

Within the N category, a tumor is considered N1 if metastasis to the regional lymph nodes is present, N2 if in transit metastasis is present without metastasis to the regional lymph nodes, and N3 if both in transit and lymph node metastases are present. With regards the corresponding pathologic staging within the N category, a distinction is made between the N1a subtype (clinically occult, detected by lymph node dissection), N1a(sn) subtype (clinically occult, detected by selective lymph node biopsy), and N1b subtype (detected clinically and radiologically and confirmed by biopsy). In the case of the M category, M1a is used for skin or distant subcutaneous involvement (not in transit metastasis, which would be covered within the N category) or involvement of distant lymph nodes (not regional ones); category M1b refers to lung involvement and M1c to involvement of viscera other than the kidney. If microscopic confirmation is obtained, the tumor is considered pM1, with its corresponding subclassification. Table 1 summarizes the current staging system for MCC.

Table 1.

Eighth Edition of the AJCC TMN Staging Manual: Merkel Cell Carcinoma.

Classification System for Merkel Cell Carcinoma (Eighth Edition)
T  TX  Primary tumor cannot be assessed (after curretage) 
  T0  No evidence of primary tumor 
  Tis  Carcinoma in situ 
  T1  Greatest tumor dimension 2cm 
  T2  Greatest tumor dimension >2cm but 5cm 
  T3  Greatest tumor dimension>5cm 
  T4  Primary tumor invades tissues such as fascia, muscle, cartilage or bones. 
NNX:  Nearby lymph nodes cannot be assessed (prior resection for another reason, body habitus...) 
N0No involvement of nearby lymph nodes as determined clinically/radiologically 
pN0 (absence of lymph node involvement on biopsy) 
N1Metastasis to regional lymph nodes 
pN1 (confirmed in biopsy) 
pN1a (clinically occult, detected by lymph node dissection) 
pN1a(sn) (clinically occult, detected by SLNB) 
pN1b (detected clinically or radiologically and confirmed in biopsy) 
N2In transit metastasis without lymph node metastasis 
pN2 (in transit metastasis confirmed in biopsy without lymph node metastasis) 
N3In transit metastasis with regional lymph node metastasis 
pN3 (in transit metastasis with regional lymph node metastasis confirmed in biopsy) 
MM0  No clinical/radiological evidence of distant metastasis 
M1M1a (cutaneous or subcutaneous distant metastasis or distant but not regional lymph node metastasis) 
M1b (pulmonary metastasis) 
M1c (metastasis in other viscera) 
AJCC TMN Staging System for Merkel Cell Carcinoma (Eighth Edition)
Tis  N0  M0  Stage 0 
T1  N0  M0  Stage I 
T2-3  N0  M0  Stage IIA 
T4  N0  M0  Stage IIB 
T1-4  N1a(sn) or N1a  M0  Stage IIIA 
T0  N1b  M0  Stage IIIB 
T1-T4  N1b-N3  M0  Stage IIIC 
T0-4  N0-N3  M1  Stage IV 

We have taken into account pathologic staging. In boldface, aspects most relevant to staging.

Abbreviation: SLNB, sentinel lymph node biopsy

Squamous Cell Carcinoma of the Head and Neck and Nonmelanoma Skin Cancer Other than Merkel Cell Carcinoma

In the case of the staging system for SCC, the seventh edition included a series of high risk factors that permitted modification of the T category of a primary tumor regardless of the horizontal size (this represented an important advance compared with previous editions) (Table 2).24 Specifically, the manual recognized poor degree of histological differentiation, perineural infiltration, vertical depth of more than 2mm, Clark levels iv and v, and the involvement of the ear or lower lip, along with the horizontal size of the tumor as risk factors defining the T category of the primary tumor: a) a tumor measuring <2cm with <2 risk factors was T1; b) a tumor measuring >2cm or measuring <2cm with 2 or more risk factors was considered T2; c) T3 or T4 corresponded to bone invasion: T3 corresponded to invasion of the maxillary, mandibular, orbital, or temporal bones, while T4 corresponded to invasion of other bones or perineural infiltration of the base of the cranium.24 However, not all risk factors were included and, as validation studies were performed, deficiencies emerged. The main criticism was that the T2 category encompassed a range of heterogeneous patients in terms of risk and prognosis.26–31 The seventh edition of the staging manual seemed to focus on the poor prognosis of SCC in T2 tumors.32,33 In fact, in a cohort of 1818 patients, only 6 cases of T3-T4 tumors were detected and most adverse outcomes occurred in tumors classified as T2 (72% of local relapses, 82% of lymph node metastases, and 67% of disease-specific deaths).32

Table 2.

Comparison of the Seventh and Eighth Editions of the American Joint Committee on Cancer (AJCC) Staging Manual: Squamous Cell Carcinoma and Nonmelanoma Skin Cancer (NMSC) Other Than Merkel Cell Carcinoma Differences in the 4 T Categories.

Classification System for Squamous Cell Carcinoma and Non-Merkel NMSC
T  Seventh Edition of AJCC Manual  Eighth Edition of AJCC Manual 
T1  Greatest dimension up to 2cm and <2 high risk factors  Greatest dimension up to 2cm 
T2  Greatest dimension > 2cm or 2 or more high risk factorsa  Greatest tumor dimension>2cm but <4cm 
T3  Invasion of maxillary, orbital, mandibular, temporal bone  Greatest dimension of tumor4cm or minimal erosion of the bone or perineural invasion or deep invasionb 
T4  Other bones (including axial skeleton), perineural infiltration of the base of the cranium  Tumor with extensive cortical or medullary bone involvement (T4a), invasion of the base of the cranium or invasion through the foramen of the base of the cranium (T4b) 
a

Thickness greater than 2mm, poor degree of differentiation, perineural infiltration, involvement of the ear or lower lip, Clark level iv-v invasion.

b

Deep invasion defined as thickness greater than 6mm or invasion deeper than subcutaneous fat. For a tumor to be classified as T3, perineural invasion should be present in nerves greater than 0.1mm, deeper than the dermis, or clinical and radiological involvement of affected nerves without involvement or invasion of the base of the cranium.

The eight edition of the AJCC2 seems to have taken into account some studies that had focused, on the one hand, on assessing the influence of thickness on prognosis,21 and on the other the influence of thickness of the involved nerve branch that infiltrates the tumor and the depth of invasion of the SCC32 for stratification of the T category (Table 2). N stratification is based on the system shared with other head and neck tumors. Moreover, for the first time, SCC of the head and neck is given its own independent section (in previous editions, NMSC referred in general to any site) and includes SCC of the lower lip given its relationship with UV radiation. However, it excludes a site on the eyelid and all tumors located outside the head and neck. Although for the special sites of the eyelid, vulva, penis, and perineal region, the AJCC manual offers solutions, it does not define any system for classification of tumors located outside the area of the head and neck, and so does not cover these particular sites. This is clearly a drawback and means, for example, that an SCC on the dorsum of the hand cannot be classified according to the eighth edition of the AJCC TNM staging manual. On the other hand, forms of NMSC other than SCC and MCC follow the same criteria as SCC (as was the case in previous editions).

Regarding the T category, the eighth edition of the AJCC considers a tumor measuring less than 2cm in greatest dimension as T1, one measuring 2 to 4cm as T2, and one greater than 4cm as T3. So far, this category is similar to editions prior to 2010. However, a tumor is also T3 if it has a thickness greater than 6cm, if it shows perineural infiltration of nerve branches of more than 0.1cm, if invasion extends beyond the fatty tissue, or if it shows minimal bone erosion. The tumor is classified as T4 if it invades the bone more extensively, as well as if it invades the base or foramen of the cranium.2 Thus, tumors with poor prognosis should tend to be categorized as T3. In view of the study by O’Brien et al,34 the expert panel of the AJCC considered staging patients also in accordance with progressive lymph node involvement. The N category is based on a system shared with other tumors of the head and neck. A tumor is considered N1 if it involves an isolated ipsilateral lymph node, is less than 3cm in diameter, and is without extracapsular extension, N3 if there is metastasis to a major lymph node and it is more than 6cm in diameter or any size if there is extracapsular extension. N2 is used for intermediate situations between N1 and N3 (Table 3). On the other hand, involvement of other organs is defined as M1 (without establishing any subgroups). Table 3 summarizes classification of SCC of the head and neck according to the latest edition of the TNM AJCC staging manual.

Table 3.

Eighth Edition of the TNM Staging Manual of the AJCC for Cutaneous Epidermal Carcinoma (SCC) of the Head and Neck and Nonmelanoma Skin Cancer Other Than Merkel Cell Carcinoma of the Head and Neck.

AJCC TNM Staging Manual for Squamous Cell Carcinoma of the Head and Neck (Eighth Edition)
T  TX  Primary tumor cannot be assessed (after curettage...) 
  T0  No evidence of primary tumor 
  Tis  Carcinoma in situ 
  T1  Greatest dimension up to 2cm 
  T2  Greatest tumor dimension>2cm but<de 4cm 
  T3  Greatest tumor dimension 4cm or minimal erosion of the bone or perineural invasion or deep invasiona 
  T4  Tumor with extensive cortical or medullary bone involvement (T4a), invasion of the base of the cranium or invasion through the foramen of the base of the cranium (T4b) 
NNX:  Nearby lymph nodes cannot be assessed (prior resection for another reason, body habitus...) 
N0  No involvement of nearby lymph nodes as determined clinically/radiologically 
N1  Metastasis in an isolated ipsilateral lymph node ≤3cm in greatest dimension, ENE (–) 
N2N2a: metastasis in an isolated ipsilateral lymph node 3-6cm in greatest dimension, ENE (–) 
N2b: metastasis in multiple ipsilateral lymph nodes less than 6cm, ENE (–) 
N2c: metastasis in bilateral or contralateral lymph nodes, less than 6cm, ENE (–) 
N3N3a: metastasis in a lymph node greater than 6cm, ENE (–) 
N3b: metastasis in any lymph node(s) and ENE (+) 
MM0  Absence of distant metastasis 
M1  Distant metastasis 
AJCC TNM Staging System for SCC of Head and Neck (Eighth Edition)
T1  N0  M0  Stage i 
T2  N0  M0  Stage ii 
T3  N0, N1  M0  Stage iii 
T1  N1  M0  Stage iii 
T2  N1  M0  Stage iii 
T1-T3  N2  M0  Stage iv 
Any T  N3  M0  Stage iv 
T4  Any N  M0  Stage iv 
Any T  Any N  M1  Stage iv 

Sites on the lower lip are included, eyelid carcinoma is excluded. Tumors of the vulva, pens, perineal region, and other sites other than the head and neck are excluded.

In boldface, aspects most relevant to staging.

Abbreviations: ENE extranodal or extracapsular extension defined as extension through the lymph node capsule in the surrounding connective tissue with or without stromal reaction; SCC squamous cell carcinoma; SLNB sentinel lymph node biopsy.

a

Deep invasion defined as thickness greater than 6mm or invasion deeper than subcutaneous fat. For a tumor to be T3, perineural invasion should be present in nerves greater than 0.1mm, deeper than the dermis, or clinical and radiological involvement of affected nerves without involvement or invasion of the base of the cranium.

The following criticisms could be made: 1) Omission of certain risk factors; 2) lack of a specific staging system for basal cell carcinoma or for other forms of NMSC (excluding MCC, which has its own staging system since 2010); 3) exclusion of sites other than the head and neck, which means that some cases cannot be staged according to the eighth edition of TNM of the AJCC. However, the system seems to have improved significantly compared with previous editions and at least considers relevant factors that had been ignored in the past, although validation series would be necessary for confirmation.

Melanoma

Melanoma has also undergone some important changes. In the case of the T category, the discrepancy resides in stratification of the thinner melanomas (Table 4). The changes throughout the different staging systems for melanoma have been more noteworthy than in the case of NMSC (due mainly to series of patients studied more extensively with more robust methodology and increasing evidence concerning risk factors that is not available for other forms of skin cancer). Since the appearance of the original article by Alexander Breslow in 1970,35 support for the impact of melanoma thickness (in mm, measured from the granular layer) has become increasingly solid. Although initially the intention was not to displace but rather complement melanoma prognosis according to degree of Clark invasion,35 from the first edition of the AJCC TNM staging manual, the so-called Breslow index already figured with a similar weight to Clark invasion,1,11,12 and this was maintained until the sixth and seventh editions removed reference to Clark invasion.24,36 Ulceration, another of the classic prognostic factors in melanoma, whose influence is known since before introduction of the Breslow index,37 is another of the parameters that has been retained in the successive staging systems.1,3,11–14,24

Table 4.

Comparison of the Seventh and Eighth Editions of the American Joint Committee on Cancer (AJCC) Staging Manual for Melanoma.

T Category for Melanoma
Seventh Edition of the AJCCEighth Edition of the AJCC
T1=1mma (without ulceration and <1 mitosis/mm2=1mma (<0.8 without ulceration) 
b (with ulceration or 1 ormoremitosis/mm2b (<0.8mm with ulceration or 0.8-1mm with or without ulceration) 
T21.01-2.0mma (without ulceration)  > 1mm-2mma (without ulceration) 
b (with ulceration)  b (with ulceration) 
T32.01-4mma (without ulceration)  >2mm-4mma (without ulceration) 
b (with ulceration)  b (with ulceration) 
T4>4mma (without ulceration)  > 4mma (without ulceration) 
b (with ulceration)  b (with ulceration) 

Differences are established for the T1 category. The mitotic index disappears from the T category in the eighth edition and stratification is based exclusively on the Breslow index and presence or absence of ulceration

Later on, in the seventh edition, mitosis was introduced as a useful system for stratifying prognosis in melanomas of less than 1mm thick,38 and then went on to replace the level of Clark invasion for stratification of these fine melanomas.24,36 In T1 tumors, ulceration, presence of mitosis, and thickness were the factors that had greatest impact on patient survival.36 However, the influence of mitosis on the prognosis of melanoma was important not only in tumors of less than 1mm thick (T1) but also in general in localized melanomas.39–41 Studies emerged that demonstrated its prognostic value in melanomas more than 1mm thick and as predictive factors of positive sentinel lymph node biopsy,42 thus reducing its specificity in the prognosis of fine melanomas. On the other hand, certain variability between observers was noted along with a low reproducibility of the mitotic index. This made it necessary for 3 to 5 serial sections to be taken for the assessment of mitosis to be reliable,43 and it was therefore not considered a good parameter for making therapeutic decisions.44 In fact, some multivariate analyses were unable to demonstrate its true prognostic relevance.45,46

In the eight edition of AJCC staging manual, once again, the main points of contention lie in fine tumors.2 Mitosis is no longer used to stratify T1 tumors and the focus is exclusively on the thickness and presence of ulceration.2 Thus, a tumor is classified as T1a if it measures less than 0.8mm thick and is not ulcerated and T1b if it measures less than 0.8mm thick and is ulcerated or measures 0.8-1mm thick, regardless of whether ulceration is present or not.2 Measures of thickness should be recorded with a precision of 0.1mm (instead of 0.01mm, as proposed in the seventh edition). Tumors of up to 1mm thick can be measured with a precision of 0.01mm if this turns out to be more practical, but the value should be rounded up or down such that the thickness is recorded to one decimal place.2 For the T category, the eighth edition of AJCC staging manual also includes the concept of T0, which is applied in those cases in which melanoma has fully regressed. T0 is not used for cases of partial regression of the primary tumor and starts with distant involvement,2 that is, for cases of metastatic melanoma and primary unknown tumor.

There are also changes regarding stratification within the N and M categories, as well as in the staging itself. Thus, an N1c tumor is defined by the presence of in transit, satellite, or microsatellite metastases without lymph node involvement (lesions which were N2c in the previous edition) and N2c is now reserved for the presence of metastases in a lymph node associated with in transit metastases. The N3 category is also stratified into N3a, N3b, and N3c (unlike in the previous edition).2 The M category is also modified, and M1d is now used to refer to melanomas that develop metastases in the central nervous system; until now these were included in the M1c category. LDH levels are used for stratification of the M category, although this does not affect staging.2 There are no substantial changes up to stage IIC or in stage IV although there are some changes in stage III, which is now more complex.2Table 5 summarizes the characteristics of TNM staging according to the latest edition of the AJCC manual.

Table 5.

Eighth Edition of the AJCC TNM Staging Manual for Melanoma (Cutaneous).

Classification System for Melanoma (Eighth Edition)
TTX  Primary tumor cannot be assessed (after curettage...)
T0  No evidence of primary tumor
Tis  Melanoma in situ
T1=1mma (<0.8 without ulceration) 
b (<0.8mm with ulceration or 0.8-1mm with or without ulceration) 
T2>1mm-2mma (without ulceration) 
b (with ulceration) 
T3>2mm-4mma (without ulceration) 
b (with ulceration) 
T4> 4mma (without ulceration) 
b (with ulceration) 
NNX:  Nearby lymph nodes cannot be assessed (prior resection for another reason, body habitus...)
N0  No involvement of nearby lymph nodes as determined clinically/radiologically
N1N1a: micrometastasis in a lymph node (clinically occult)
N1b: clinically detected lymph node
N1c: in transit, satellite, or microsatellite metastasis without lymph node involvement
N2N2a: micrometastasis in 2 or 3 lymph nodes (clinically occult)
N2b: metastasis in 2 or 3 lymph nodes
N2c: metastasis in a lymph node (occult or clinically detected) and in transit, satellite, or microsatellite metastasis
N3N3a: 4 or more micrometastases in lymph nodes
N3b: 4 or more metastases in lymph nodes, at least one of them clinically evident or presence of matted lymph nodes
N3c: 2 or more micrometastases or clinically detectable lymph node metastases or presence of matted lymph nodes and in transit, satellite, or microsatellite metastasis
MM0  No evidence of lymph node metastasis
M1M1a: distant metastasis in skin, soft tissue (including muscle), and/or nonregional lymph nodes
- M1a(0): Normal LDH
- M1a(1): Elevated LDH
M1b: pulmonary metastasis with/without M1a
- M1b(0): Normal LDH
- M1b(1): Elevated LDH
M1c: distant metastasis in organs other than the CNS with/without M1a and M1b
- M1c(0): Normal LDH
- M1c(1): Elevated LDH
M1d: metastasis of the CNS with/without M1a, M1b, or M1c
- M1d(0): Normal LDH
- M1d(1): Elevated LDH
AJCC TNM Staging System for Melanoma (Eighth Edition)
Tis  N0  M0  Stage 0 
T1a-T1b  N0  M0  Stage IA 
T2a  N0  M0  Stage IB 
T2b-T3a  N0  M0  Stage IIA 
T3b-T4a  N0  M0  Stage IIB 
T4b  N0  M0  Stage IIC 
T0  N1b/1c  M0  Stage IIIB 
T0  N2b/2c, N3b/3c  M0  Stage IIIC 
T1a/b-T2a  N1a, N2a  M0  Stage IIIA 
T1a/b-T2a  N1b/1c, N2b  M0  Stage IIIB 
T2b/T3a  N1a-N2b  M0  Stage IIIB 
T1a/T3a  N2c/N3a,b,c  M0  Stage IIIC 
T3b/T4a  N1-N3  M0  Stage IIIC 
T4b  N1a-N2c  M0  Stage IIIC 
T4b  N3a/b/c  M0  Stage IIID 
Any T, Tis  Any N  M1  Stage iv 

In boldface, aspects most relevant to staging.

The most recent edition of the AJCC staging manual for melanoma places greatest relevance on Breslow thickness and ulceration. Changes are made to the N and M category, as well as staging. Series will be needed to validate whether the predictive capacity of this new staging system is better than previous ones.

Ethical ResponsibilitiesProtection of human and animal subjects

The authors declare that no experiments were performed on humans or animals for this investigation.

Confidentiality of data

The authors declare that they have followed their hospital's protocol on the publication of data concerning patients.

Right to privacy and informed consent

The authors declare that patient data do not appear in this article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

J.C. received partial funding for this study through Project GRS1342/A/16 and the Intensification program of the Castile-Leon Regional Health Authority (INT/M/16/17).

References
[1]
Manual for Staging of Cancer.,
[2]
AJCC Cancer Staging Manual, 8th ed.,
[3]
AJCC Cancer Staging Manual, 6th ed.,
[4]
D.E. Rowe, R.J. Carroll, C.L. Day Jr..
Prognostic factors for local recurrence, metastasis, and survival rates in squamous cell carcinoma of the skin, ear, and lip Implications for treatment modality selection.
J Am Acad Dermatol., 26 (1992), pp. 976-990
[5]
H. Breuninger, B. Black, G. Rassner.
Microstaging of squamous cell carcinomas.
Am J Clin Pathol., 94 (1990), pp. 624-627
[6]
D.G. Brodland, J.A. Zitelli.
Surgical margins for excision of primary cutaneous squamous cell carcinoma.
J Am Acad Dermatol., 27 (1992), pp. 241-248
[7]
M.A. Weinstock.
Nonmelanoma skin cancer mortality in the United States, 1969 through 1988.
Arch Dermatol., 129 (1993), pp. 1286-1290
[8]
E. Tavin, M. Persky.
Metastatic cutaneous squamous cell carcinoma of the head and neck region.
Laryngoscope., 106 (1996), pp. 156-158
[9]
A. Eroglu, U. Berberoglu, S. Berreroglu.
Risk factors related to locoregional recurrence in squamous cell carcinoma of the skin.
[10]
G. Petter, U.F. Haustein.
Squamous cell carcinoma of the skin--histopathological features and their significance for the clinical outcome.
J Eur Acad Dermatol Venereol., 11 (1998), pp. 37-44
[11]
Manual for Staging of Cancer, 2nd edition,
[12]
Manual for Staging of Cancer, Third Edition,
[13]
Manual for Staging of Cancer, 4th ed.,
[14]
AJCC Cancer Staging Manual, Fifth Edition,
[15]
B.S. Cherpelis, C. Marcusen, P.G. Lang.
Prognostic factors for metastasis in squamous cell carcinoma of the skin.
Dermatol Surg., 28 (2002), pp. 268-273
[16]
G.L. Clayman, J.J. Lee, F.C. Holsinger, X. Zhou, M. Duvic, A.K. El-Naggar, et al.
Mortality risk from squamous cell skin cancer.
J Clin Oncol., 23 (2005), pp. 759-765
[17]
B.A. Moore, R.S. Weber, V. Prieto, A. El-Naggar, F.C. Holsinger, X. Zhou, et al.
Lymph node metastases from cutaneous squamous cell carcinoma of the head and neck.
Laryngoscope., 115 (2005), pp. 1561-1567
[18]
S.M. Dinehart, S. Peterson.
Evaluation of the American Joint Committee on Cancer staging system for cutaneous squamous cell carcinoma and proposal of a new staging system.
Dermatol Surg., 31 (2005), pp. 1379-1384
[19]
M.J. Veness, C.E. Palme, G.J. Morgan.
High-risk cutaneous squamous cell carcinoma of the head and neck: results from 266 treated patients with metastatic lymph node disease.
Cancer., 106 (2006), pp. 2389-2396
[20]
A.S. Ross, F.M. Whalen, R. Elenitsas, X. Xu, A.B. Troxel, C.D. Schmults.
Diameter of involved nerves predicts outcomes in cutaneous squamous cell carcinoma with perineural invasion: an investigator-blinded retrospective cohort study.
Dermatol Surg., 35 (2009), pp. 1859-1866
[21]
K.D. Brantsch, C. Meisner, B. Schonfisch, B. Trilling, J. Wehner-Caroli, M. Rocken, et al.
Analysis of risk factors determining prognosis of cutaneous squamous-cell carcinoma: a prospective study.
Lancet Oncol., 9 (2008), pp. 713-720
[22]
A.S. Weinberg, C.A. Ogle, E.K. Shim.
Metastatic cutaneous squamous cell carcinoma: an update.
Dermatol Surg., 33 (2007), pp. 885-899
[23]
A. Kyrgidis, T.G. Tzellos, N. Kechagias, A. Patrikidou, P. Xirou, K. Kitikidou, et al.
Cutaneous squamous cell carcinoma (SCC) of the head and neck: risk factors of overall and recurrence-free survival.
Eur J Cancer., 46 (2010), pp. 1563-1572
[24]
AJCC cancer staging manual (7th ed),
[25]
K.L. Harms, M.A. Healy, P. Nghiem, A.J. Sober, T.M. Johnson, C.K. Bichakjian, et al.
Analysis of Prognostic Factors from 9387 Merkel Cell Carcinoma Cases Forms the Basis for the New 8th Edition AJCC Staging System.
Ann Surg Oncol., 23 (2016), pp. 3564-3571
[26]
A. Jambusaria-Pahlajani, P.A. Kanetsky, P.S. Karia, W.T. Hwang, J.M. Gelfand, F.M. Whalen, et al.
Evaluation of AJCC tumor staging for cutaneous squamous cell carcinoma and a proposed alternative tumor staging system.
JAMA Dermatol., 149 (2013), pp. 402-410
[27]
L. Hutchinson.
Skin cancer: Setting the stage for cutaneous SCC.
Nature reviews Clinical oncology., 11 (2014), pp. 63
[28]
S.J. Miller.
Staging cutaneous squamous cell carcinoma.
JAMA Dermatol., 149 (2013), pp. 472-474
[29]
N.D. Brougham, E.R. Dennett, R. Cameron, S.T. Tan.
The incidence of metastasis from cutaneous squamous cell carcinoma and the impact of its risk factors.
J Surg Oncol., 106 (2012), pp. 811-815
[30]
H. Breuninger, K. Brantsch, T. Eigentler, H.M. Hafner.
Comparison and evaluation of the current staging of cutaneous carcinomas.
Journal der Deutschen Dermatologischen Gesellschaft=Journal of the German Society of Dermatology: JDDG., 10 (2012), pp. 579-586
[31]
C.D. Schmults, P.S. Karia, J.B. Carter, J. Han, A.A. Qureshi.
Factors predictive of recurrence and death from cutaneous squamous cell carcinoma: a 10-year, single-institution cohort study.
JAMA Dermatol., 149 (2013), pp. 541-547
[32]
P.S. Karia, A. Jambusaria-Pahlajani, D.P. Harrington, G.F. Murphy, A.A. Qureshi, C.D. Schmults.
Evaluation of American Joint Committee on Cancer. International Union Against Cancer, and Brigham and Women's Hospital tumor staging for cutaneous squamous cell carcinoma.
J Clin Oncol., 32 (2013), pp. 327-334
[33]
A.R. Schmitt, J.D. Brewer, J.S. Bordeaux, C.L. Baum.
Staging for cutaneous squamous cell carcinoma as a predictor of sentinel lymph node biopsy results: meta-analysis of American Joint Committee on Cancer criteria and a proposed alternative system.
JAMA Dermatol., 150 (2014), pp. 19-24
[34]
C.J. O’Brien, E.B. McNeil, J.D. McMahon, I. Pathak, C.S. Lauer, M.A. Jackson.
Significance of clinical stage, extent of surgery, and pathologic findings in metastatic cutaneous squamous carcinoma of the parotid gland.
Head Neck., 24 (2002), pp. 417-422
[35]
A. Breslow.
Thickness, cross-sectional areas and depth of invasion in the prognosis of cutaneous melanoma.
Ann Surg., 172 (1970), pp. 902-908
[36]
C.M. Balch, J.E. Gershenwald, S.J. Soong, J.F. Thompson, M.B. Atkins, D.R. Byrd, et al.
Final version of 2009 AJCC melanoma staging and classification.
J Clin Oncol., 27 (2009), pp. 6199-6206
[37]
W.J. Williams, K. Davies, W.M. Jones, M.M. Roberts.
Malignant melanoma of the skin: prognostic value of histology in 89 cases.
Br J Cancer., 22 (1968), pp. 452-460
[38]
A.B. Francken, H.M. Shaw, J.F. Thompson, S.J. Soong, N.A. Accortt, M.F. Azzola, et al.
The prognostic importance of tumor mitotic rate confirmed in 1317 patients with primary cutaneous melanoma and long follow-up.
Ann Surg Oncol., 11 (2004), pp. 426-433
[39]
J.J. Baker, M.O. Meyers, A.M. Deal, J.F. Frank, K.B. Stitzenberg, D.W. Ollila.
Prognostic significance of tumor mitotic rate in T2 melanoma staged with sentinel lymphadenectomy.
J Surg Oncol., 111 (2015), pp. 711-715
[40]
H. Eriksson, M. Frohm-Nilsson, J. Jaras, L. Kanter-Lewensohn, P. Kjellman, E. Mansson-Brahme, et al.
Prognostic factors in localized invasive primary cutaneous malignant melanoma: results of a large population-based study.
Br J Dermatol., 172 (2015), pp. 175-186
[41]
R. Betti, R. Santambrogio, A. Cerri, R. Vergani, L. Moneghini, S. Menni.
Observational study on the mitotic rate and other prognostic factors in cutaneous primary melanoma arising from naevi and from melanoma de novo.
J Eur Acad Dermatol Venereol., 28 (2014), pp. 1738-1741
[42]
M. Mandala, F. Galli, L. Cattaneo, B. Merelli, E. Rulli, S. Ribero, et al.
Mitotic rate correlates with sentinel lymph node status and outcome in cutaneous melanoma greater than 1 millimeter in thickness: A multi-institutional study of 1524 cases.
J Am Acad Dermatol., 76 (2017), pp. 264-73e2
[43]
S.R. Knezevich, R.L. Barnhill, D.E. Elder, M.W. Piepkorn, L.M. Reisch, G. Pocobelli, et al.
Variability in mitotic figures in serial sections of thin melanomas.
J Am Acad Dermatol., 71 (2014), pp. 1204-1211
[44]
C. Garbe, T.K. Eigentler, J. Bauer, N. Blodorn-Schlicht, L. Cerroni, F. Fend, et al.
Mitotic rate in primary melanoma: interobserver and intraobserver reliability, analyzed using H&E sections and immunohistochemistry.
Journal der Deutschen Dermatologischen Gesellschaft=Journal of the German Society of Dermatology: JDDG., 14 (2016), pp. 910-915
[45]
M.J. Speijers, E. Bastiaannet, S. Sloot, A.J. Suurmeijer, H.J. Hoekstra.
Tumor mitotic rate added to the equation: melanoma prognostic factors changed?.: a single-institution database study on the prognostic value of tumor mitotic rate for sentinel lymph node status and survival of cutaneous melanoma patients.
Ann Surg Oncol., 22 (2015), pp. 2978-2987
[46]
A. Tejera-Vaquerizo, E. Nagore, E. Herrera-Acosta, A. Martorell-Calatayud, P. Martin-Cuevas, V. Traves, et al.
Prediction of sentinel lymph node positivity by growth rate of cutaneous melanoma.
Arch Dermatol., 148 (2012), pp. 577-584

Please cite this article as: Cañueto J, Román-Curto C. Los nuevos sistemas de estadificación del AJCC incorporan novedades en el cáncer cutáneo. Actas Dermosifiliogr. 2017;108:818–826.

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