Introduction

The vertical tumor thickness in cutaneous melanoma, first described by Alexander Breslow, correlates with long-term recurrence in most patients [1]. In 1989, we reported for the first time an association between tumor recurrence and vascularity assessed by blood flow measurement and histological vascular quantitation [2].

The adverse outcome of thick melanomas may be related to the degree of neovascularization. In the present work, we studied the association between the parameters of tumor blood flow and the long-term outcome, to see if the association demonstrated at 2 years persisted over a much longer period.

Patients and Methods

We have investigated the tumor vascularity in 71 primary melanomas in 67 patients (4 patients had 2 melanomas each), by the Doppler ultrasound flowmetry between March 1984 and December 1986. All new consecutive patients coming to Melanoma Clinic of the Department of Surgery, University Hospital of Wales, Cardiff, the UK, were selected after an informed consent. Of these, data on 63 patients were used for the prognostic assessment.

Four exclusions were as follows: One patient died of previously metastatic melanoma and one case had stage II melanoma at presentation (regional lymph node metastasis), and two patients moved out and were lost to follow-up. Four patients presented with two lesions each; in these four cases, the information on thicker lesions has been used for analysis (the thinner of the two lesions were three in situ melanomas and one superficial spreading melanoma of 0.68 mm thickness). The follow-up information is complete until December 2005.

Method of Recording Tumor Blood Flow

A thin pencil ultrasonic continuous wave transducer probe of 7 mm diameter was applied over the skin melanoma with a drop of ultrasonic coupling gel prior to any biopsy or surgery. The method has been described previously in detail [3]. The statistical analysis and variable coding are described in detail in Appendix.

Results

The mean age of patients was 56.20 (standard deviation 14.29; range 29–84) years. The median tumor thickness was 0.9 mm (interquartile range 0.3, 2.14 mm) and median peak systolic frequency was 2159.5 Hz (interquartile range 1476.5, 3440). Blood flow was detected in 41 lesions, and these were labeled “Doppler flow positive.” No blood flow was present in 22 lesions, and these were called “Doppler flow negative”. Among the Doppler-positive lesions, 13 lesions were ulcerated, whereas only one Doppler-negative lesion was ulcerated. The proportion of ulcerated lesions was statistically different in Doppler-positive and Doppler-negative groups (p = 0.023). Among the Doppler-positive group, 20 lesions were ≤1.5 mm in thickness and 21 were thicker than 1.5 mm. Among the Doppler-negative group, all except one (21/22) lesions were thinner than 0.75 mm (Table 1). In order to analyze the data according to Clark’s level, the data were categorized in category 1 (including Clark’s level I, II, and III) and category 2 (Clark’s level IV and V). Table 2 provides information on tumor thickness categories and result of Doppler flowmetry.

Table 1 Association of considered covariates with Doppler status
Table 2 Tumor thickness and doppler flowmetry

Doppler Status and Survival

The Doppler ultrasound flowmetry detected blood flow signals in 41 lesions. Among the Doppler flow-positive group, 39% of lesions were associated with death due to melanoma. In the remaining 22 lesions, no flow was detected. None of the 22 cases with a Doppler-negative lesion have died of melanoma or developed any local, lymph nodal, or systemic recurrence (Table 3) in 15 years. One patient with Doppler-negative lesion died on the 10th postoperative day due to coronary artery thrombosis (autopsy confirmed). Five more patients with a Doppler-negative tumor have died without any recurrence due to old age-related diseases.

Table 3 Survival status of patients in relation to results of doppler flowmetry

Results in Intermediate Thickness Lesions (0.751–4.0 mm Thick)

The results in this group are presented in Table 4. All patients with Clark’s level I tumor (8 cases) were flow negative. All except one case (24 cases) with Clark’s level IV and V lesions were flow positive. In 12 of 17, Clark’s level III and 5 of 13 lesions with Clark’s level II melanoma blood flow was detected by the Doppler flowmetry. Thirteen of 14 ulcerated lesions exhibited blood flow.

Table 4 Survival in patients with 0.751 mm to 4.0 mm thick melanomas

The peak systolic, mean systolic, and minimum diastolic frequencies were strongly correlated to each other. The correlation coefficient between the peak systolic and mean systolic frequencies was 0.83 and between the peak and diastolic frequencies was 0.78. The correlation coefficient between the mean systolic and minimum diastolic frequencies was 0.66. This correlation between potential predictor variables suggests collinearity. Hence, only peak systolic frequency has been used for further analysis.

The current outcome status is as follows: alive with no recurrence, 32 cases (50%); dead with local or systemic recurrence, 16 cases (25%); and dead with other causes without recurrence, 12 (19%). Nine patients developed a recurrence in the regional nodal basin, and all had a flow-positive lesion. Remaining 54 cases had no lymph node recurrence. Of these, 3 are alive after lymph node recurrence (treated by regional node dissection). Four patients developed local recurrence and all 4 had a Doppler-positive melanoma. Remaining 59 cases remain free from local recurrence; of these 22 had a Doppler-negative lesion and 37 had a Doppler flow-positive lesion. Fifteen patients developed systemic recurrence, and all these patients had presented with a Doppler flow-positive lesion. Remaining 48 cases were free from systemic recurrence and of these 22 had a flow-negative lesion and 26 cases had flow-positive lesion.

Survival Analysis

The median duration of follow-up of the patients was 144 months (range 0.4–252 months). A total of 28 (44.4%) patients died. Of 63 patients, only 16 (25.4%) died with recurrence. The 5-year overall survival of the patients was 76% (95% CI 64.1–84.9%) and 5-year cause-specific survival (melanoma-related death) was 77.4% (95% CI 64.9–86.0%). Figures 1 and 2 show the pattern of overall survival (all-cause deaths) and cause-specific deaths (melanoma-related), respectively, for the whole cohort. Figure 3 demonstrates the Kaplan-Meier survival probability curves for Doppler-positive and Doppler-negative cases.

Fig. 1
figure 1

Depicting Kaplan Meier survival probability curve for whole cohort for overall survival time in months

Fig. 2
figure 2

Showing Kaplan Meier survival probability curve for survival time for melanoma related death in months

Fig. 3
figure 3

Showing Kaplan Meier survival probability curve for doppler positive and doppler negative cases

Under univariate analysis of death due to melanoma, the variables such as ulcer, peak, tumor thickness category, and Clark’s level were found significant. The results under univariate Cox model are presented in Table 5. The patients who had the ulcer were 14 times more likely to die (HAZARD RATE 14.86; 95% CI 5.05–43.76) than those without an ulcer. The risk of death due to melanoma was 13 times more in case of thickness more than 1.5 mm (HAZARD RATE 13.3; 95% CI 5.05–43.76) as compared to cases with thin melanoma less than 1.5 mm thick.

Table 5 Hazard ratio of death on Cox regression analysis

Survival Analysis and Doppler Flowmetry

On univariate analysis, patients having higher peak systolic frequency (above 2,500 MHz) were more likely to die of melanoma than those with lower peak systolic frequency (HAZARD RATE 5.88; 95% CI 1.86–18.57; SE 3.45, z = 3.02; p = 0.003).

There was no melanoma-related death among Doppler-negative patients.

The following variables were included in the final stepwise Cox regression: peak systolic frequency category, thickness, and Clark’s level. Age category (>50 years and ≤50 years) was adjusted in the final model. The proportional hazard assumption was checked and was found to be satisfied. In the final multivariable Cox analysis, only thickness and peak systolic frequency category remained as significant factors. The patients with thickness more than 1.5 mm were five times more likely to have died in comparison to the patients with less than 1.5 mm thickness after adjusting other important covariates (HAZARD RATE 5.80; 95% CI 1.56–21.54). Similarly, the risk of death was five times more among the patients who had higher peak systolic frequency (above 2,500 MHz) after controlling other potential covariates (HAZARD RATE 5.99; 95% CI 1.55–23.16). Among the Doppler-positive cases, only these two factors (thickness category above 1.5 mm and peak systolic frequency category above 2,500 MHz) remained significant in multivariable Cox proportional hazard regression analysis for death due to melanoma.

Discussion

The vertical tumor thickness is established as the most important predictor of outcome in patients with malignant melanoma of skin. Why should thickness play such an important role in influencing the biological behavior of melanoma? Is it just an expression of increasing tumor volume or a surrogate for the increasing biologic aggressiveness with release of progressively increasing amounts of molecules causing tumor invasion and metastasis?

Several workers have shown a prognostic value of tumor vascularity in skin melanoma. In one study, angiogenin, vascular endothelial growth factor (VEGF), fibroblast growth factor (b-FGF), and interleukin-8 (IL-8) were measured in sera of 125 melanoma patients. Serum levels of angiogenin, VEGF, b-FGF, and IL-8 were significantly increased in patients with melanoma compared to healthy controls. Elevated serum levels of VEGF, b-FGF, and IL-8 were strongly associated with poor survival [4].

The tumor thickness was strongly correlated with peak systolic and mean systolic frequencies. Such strong correlation between the thickness and the frequency measurements indicates that with progressive tumor growth the blood flow velocity increases pari passu with thickness. The neovascular network with rapid blood flow offers a path for abundant supply of nutriments for rapid proliferation and opens up avenues for hematogenous dissemination. A high peak systolic frequency indicates high velocity of blood flow through the tumor.

Doppler flowmetry allows preoperative assessment of the biological aggressiveness and long-term outcome, whereas the vertical thickness information is available only after the tumor excision. In tumors with marked vascularity, it may help to administer preoperative chemotherapy or chemoradiation in a manner akin to neoadjuvant therapy in breast cancer. In this regard, newer agents such as tyrosine kinase inhibitors, angiostatin, or newer antimitotic drugs are worthy of trial. After two to three courses of chemotherapy, the response of the melanoma may be assessed and the same drugs may be used following excision. Serial assessment of the tumor vascularity may predict the response to therapy as profuse blood flow through the tumor tissue may enhance the delivery of drugs in the tumor. The overall response of surgery alone in thick tumors (>4 mm thick) is so poor that the proposed approach of neoadjuvant therapy is worthy of investigation.

Survival of all the patients with Doppler-negative tumors for more than 15 years with no death due to melanoma recurrence is a very significant biological finding. Such excellent outcome has been reported for the “horizontal growth phase melanomas” by Clark’s group [5, 6]. It is possible that the absence of “detectable blood flow” is a feature of horizontal growth phase lesions. Doppler flowmetry allows demarcation between two categories of lesions (horizontal growth phase and vertical growth phase lesions) preoperatively. The similar association between tumor vasculature and survival has been reported by other authors [7, 8]. Lassau et al. [8] in the largest study on color Doppler sonography (CDS) assessed the tumor vascularity in 111 skin melanomas before surgical resection and demonstrated intratumor vessels in 43 lesions. The neovascularization visualized with CDS was significantly linked to relapse. Similar to our observation, they found a strong correlation between the vascularization and Breslow tumor thickness. They reported that Breslow thickness and vascularity confer equivalent prognostic information.

We propose that a “tumor vascularity database” should be established in countries with a high prevalence of melanoma to prospectively record the tumor vascularity assessed by Laser and ultrasonic Doppler flowmetry in a large cohort of patients to evaluate its biological significance. The flow signals should be subjected to more detailed signal analysis, namely, time-averaged mean frequency, normalized area under the spectrum, and relative flow index, for a detailed insight in tumor vascularity.

Conclusion

Doppler flowmetry predicts long-term survival. It may help in planning neoadjuvant therapies aimed at inhibiting angiogenesis or targeting tumor vasculature.

We suggest that tumor vascularity should be included in the preoperative assessment of skin melanoma.