Primary tumor surgery improves survival in non-metastatic primary urethral carcinoma patients: a large population-based investigation
BMC Cancer volume 21, Article number: 857 (2021)
Primary urethral carcinoma (PUC) is a rare genitourinary malignancy with a relatively poor prognosis. The aim of this study was to examine the impact of surgery on survival of patients diagnosed with PUC.
A total of 1544 PUC patients diagnosed between 2004 and 2016 were identified based on the SEER database. The Kaplan-Meier estimate and the Fine and Gray competing risks analysis were performed to assess overall survival (OS) and cancer-specific mortality (CSM). The multivariate Cox regression model and competing risks regression model were used to identify independent risk factors of OS and cancer-specific survival (CSS).
The 5-yr OS was significantly better in patients who received either local therapy (39.8%) or radical surgery (44.7%) compared to patients receiving no surgery of the primary site (21.5%) (p < 0.001). Both local therapy and radical surgery were each independently associated with decreased CSM, with predicted 5-yr cumulative incidence of 45.4 and 43.3%, respectively, compared to 64.7% for patients receiving no surgery of the primary site (p < 0.001). Multivariate analyses demonstrated that primary site surgery was independently associated with better OS (local therapy, p = 0.037; radical surgery, p < 0.001) and decreased CSM (p = 0.003). Similar results were noted regardless of age, sex, T stage, N stage, and AJCC prognostic groups based on subgroup analysis. However, patients with M1 disease who underwent primary site surgery did not exhibit any survival benefit.
Surgery for the primary tumor conferred a survival advantage in non-metastatic PUC patients.
Primary urethral carcinoma (PUC) is a rare genitourinary malignancy with a relatively poor prognosis [1,2,3]. In 2020, it was estimated that in the United States there are 3970 new diagnoses of cancer of the ureter and other urinary organs, and 1010 will die of these diseases . The 5-yr overall survival rate in PUC patients is reported to be 42% [4, 5]. Disease management of PUC is based on tumor stage, patient sex and tumor location [2, 6, 7]. Surgery, chemotherapy or radiation therapy are standard treatment options for patients diagnosed with PUC [8,9,10]. Unfortunately, owing to its rare nature, there is a lack of large-scale investigations to support the treatment strategies. The aim of this study was to examine the impact of surgery on survival of patients diagnosed with PUC using a large population-based cancer database.
Selection of patient cohort
We searched Surveillance, Epidemiology, and End Results (SEER) public-access database covering around 27.8% of the U.S. population from 2004 to 2016 and identified patients diagnosed with PUC based on the International Classification of Diseases-O-3 (ICD-O-3) codes C68.0. Only patients who met the following criteria were included: (1) urethra was the primary site; (2) survival time was ≥1 month; and (3) adequate tumor data were available. Data were extracted from the SEER database using SEER*Stat Software (version 8.3.6).
Data collection and variable definition
Parameters of interest included race, sex, age at diagnosis, the American Joint Commission on Cancer (AJCC) TNM Staging system, histology, tumor size, and grade. Therapy and follow-up information including type of surgical procedure, radiation, chemotherapy, survival months, and vital status were also collected. Surgical codes 30 (Simple/partial surgical removal of primary site), 40 (Total surgical removal of primary site; enucleation), 50 (Surgery stated to be “debulking”), and 60 (Radical surgery) for PUC were merged and collectively defined as “radical surgery”. Transurethral resection and other local tumor destruction or excision procedures (Surgical codes 10 and 20) were merged and collectively defined as “local therapy”. Surgical codes 00 (no surgery of primary site or autopsy only) was defined as “No surgery of primary site”. The overall survival (OS) months for PUC were defined as the time from diagnosis to any cause of death or last follow-up, with patients still alive censored at the last follow-up. For cancer-specific mortality (CSM), deaths not due to PUC were considered as competing risks.
Pearson’s chi-square was applied to compare the distribution of categorical data. Kaplan-Meier survival curves and log-rank tests were utilized to perform survival analysis. The Fine and Gray competing risk analysis was used to evaluate CSM [11, 12]. Multivariate Cox regression and competing risk regression analysis were utilized to identify independent risk factors to predict OS and cancer-specific survival (CSS) of PUC patients. All tests were two sided with a statistical significance set at p < 0.05. Statistical analyses were performed using R version 3.5.2 (the R foundation for Statistical Computing, Vienna, Austria).
Demographic and clinical characteristics of PUC patients
A total of 1544 PUC patients were identified. The demographic and clinical characteristics of the patient cohort are listed in Table 1. The majority of PUC patients were white (1164, 75.4%), male (971, 62.9%), with stage I (432, 28.2%) or IV (392, 25.6%) TNM stage, and III/ IV grade (833, 54.0%). Among 1544 PUC patients, 642 patients have precise tumor sizes, and the median size was 38.27 mm. Median age at diagnosis was 69.54 years. The pathological types comprised squamous cell carcinoma (437, 28.3%), transitional cell carcinoma (660, 42.7%), adenocarcinoma (252, 16.3%), and other pathological types (195, 12.6%). With regard to therapy, most patients underwent a surgical procedure (1114, 72.2%), and did not receive radiation (1141, 73.9%) or chemotherapy (1067, 69.1%).
Survival analyses in the overall patient cohort stratified by surgical procedure
Among the 1544 PUC patients, 403 (26.1%) did not undergo any surgery to the primary tumor, 532 (34.5%) received local therapy (transurethral or transvaginal resection), and 582 (37.7%) underwent radical surgery (urethrectomy). Patient characteristics stratified by surgical procedure are also presented in Table 1. The 5-yr OS was significantly better in patients undergoing either local therapy (39.8%; 95% CI: 35.3–44.7) or radical surgery (44.7%; 95% CI: 40.1–49.7) compared to patients receiving no surgery of the primary site (21.5%; 95% CI: 17.4–26.7) (p < 0.001) (Fig. 1 and Table 4). In addition, undergoing local therapy or radical surgery was each independently associated with decreased CSM, with predicted 5-yr cumulative incidence of 45.4 and 43.3%, respectively, compared to 64.7% for patients receiving no surgery of the primary site (p < 0.001) (Fig. 1 and Table 4).
Multivariate cox regression analysis and multivariable competing risks regression analysis
Based on the univariate and multivariate Cox regression model; older age, advanced T stage, lymph node involvement, metastatic disease, and larger tumor size were identified as independent risk factors associated with poorer OS (Table 2). Using a multivariable competing risks regression model, the factors independently associated with increased CSM for PUC patients were identified, included; older age, metastatic disease, advanced AJCC stage groups, and larger tumor size (Table 3). Notably, surgery of the primary site was independently associated with better OS (local therapy, p = 0.037; radical surgery, p < 0.001) and decreased CSM (p = 0.003).
Subgroup survival analyses based on the risk factors
Subgroup analyses were performed to further evaluate survival benefit of surgery for PUC patients among groups based on age (< 70 vs ≥ 70 years), tumor size (< 30 vs ≥ 30 mm) or sex. Patients who underwent surgery of the primary site showed significant survival advantage in both age subgroups (Supplementary Figure 1 and Table 4). The benefit of surgery was more marked in patients aged < 70 years, with median survival months of 105 and 84 for local therapy and radical surgery, respectively, compared to 21 for patients receiving no surgery of the primary site. Patients who underwent radical surgery exhibited higher OS and decreased CSM regardless of tumor size (Supplementary Figure 2 and Table 4). In contrast there were no significant differences in survival between patients who received local therapy or no surgery of the primary site in either tumor size subgroup. Subset analyses based on sex also revealed that surgery of the primary site brought significant survival benefit regardless of sex (Supplementary Figure 3 and Table 4). To determine whether higher cancer stage affected survival among surgery groups, subset analyses were also performed based on AJCC stage groups. Patients who underwent radical surgery exhibited higher OS and decreased CSM regardless of stage groups (Supplementary Figure 4 and Table 4). Local therapy did not result in significantly greater OS compared to no surgery of the primary site in the I/II stage (p = 0.392) or the III/IV stage group (p = 0.053), but did result in longer median survival (52 months) compared to no surgery (30 months) in the I/II stage group. Patients who underwent surgery of the primary site showed significant survival advantage in M0 disease, but did not exhibit any benefit in M1 disease (Supplementary Figure 5 and Table 4).
Cox’s and competing risks’ proportional hazard analyses
Finally, Cox’s and competing risks’ proportional hazard analyses were performed to assess the prognostic value of surgery in PUC patients (Fig. 2). Surgery of the primary site independently predicted statistically significantly higher OS and CSS in both age group (< 70 years, OS: p < 0.001, CSS: p < 0.001; ≥ 70 years, OS: p < 0.001, CSS: p < 0.001), both AJCC T stages (T0/T1/T2, OS: p < 0.001, CSS: p < 0.001; T3/T4, OS: p < 0.001, CSS: p < 0.001), both AJCC N stages (N0, OS: p < 0.001, CSS: p < 0.001; N1/N2, OS: p < 0.001, CSS: p < 0.001), both AJCC stage groups (I/ II, OS: p = 0.013, CSS: p < 0.001; III /IV, OS: p < 0.001, CSS: p = 0.034), both sexes (male, OS: p < 0.001, CSS: p < 0.001; female, OS: p < 0.001, CSS: p < 0.001), the larger tumor size group (OS: p < 0.001, CSS: p < 0.001), and the M0 group (OS: p < 0.001, CSS: p < 0.001), but surgery of the primary site was not an independent risk factor in the M1 group (OS: p = 0.374, CSS: p = 0.640) or the other histology group (OS: p = 0.074, CSS: p = 0.067). Notably, surgery of the primary site was an independent risk factor in the smaller tumor size group based only on the competing risks’ proportional hazard analyses (p = 0.002).
PUC is an aggressive and rare carcinoma, comprising < 1% of all genitourinary malignancies [7, 13]. The disease management of PUC requires multimodal therapy to improve functional outcome and quality of life. According to the National Comprehensive Cancer Network (NCCN) and European Association of Urology (EAU) guidelines, partial urethrectomy or urethra-sparing surgery is a valid treatment option for localized distal tumors (I/II stage), and Ta-Tis-T1 PUC can also be treated with a repeat transurethral or transvaginal resection. For patients with locally advanced disease (III/IV stage), multimodal treatment strategies are needed to optimize local control and prognosis. Chemotherapy followed by surgery or radiation therapy and concurrent chemoradiation with or without surgery have been shown to lead to an improvement in survival [2, 7, 14, 15]. However, given the rarity of PUC, there are few prospective multi-institutional studies to compare the effectiveness of various multimodal therapies, and the role of surgery in the management of PUC remains contentious.
To our knowledge, this is the first large population-based study to investigate the benefit of surgery for PUC patients. Our results demonstrated that PUC patients who underwent radical surgery or local therapy had a higher 5-yr OS and decreased CSM compared with patients who did not receive surgery of the primary site. Subgroup analysis based on TNM stage also demonstrated that survival of PUC patients who underwent surgery of the primary site was improved regardless of T stage, N stage, or AJCC prognostic group. In terms of M stage, PUC patients with metastatic disease were less likely to benefit from surgery. Notably, PUC patients with early TNM stage (I/II) who received radical surgery showed a more marked survival benefit, indicating that these patients were optimal candidates for urethrectomy.
We noted that factors independently associated with poor OS and increased CSM in PUC patients other than advanced TNM stage included age ≥ 70 years and tumor size ≥30 mm. Subset analyses revealed that patients < 70 years and tumor size ≥30 mm had a notably better survival benefit from surgery. Nevertheless, surgery of the primary site independently predicted significantly better prognosis in both age subgroups. Several studies have demonstrated anatomic differences between male and female PUC patients that contribute to variations in clinicopathological characteristics, including tumor location and histology [10, 16, 17]. In contrast we did not observe any difference in survival between males and females, and surgery of the primary site independently predicted statistically significantly higher OS and decreased CSM in both male and female PUC patients. SCC, TCC and AC together comprised approximately 90% of the histological types of PUC, and previous studies have demonstrated poorer survival in rare PUC pathological types [2, 18]. Subset analyses in our study demonstrated that PUC patients with the predominant histological types who underwent surgery of the primary site showed a significant survival advantage, while PUC patients with rare histological types were less likely to benefit from surgery. The results underscore the continued importance of improved guidelines for management of patients with rare PUC pathological types.
Despite several promising results, this registry-based study has unavoidable limitations. First, limitations of SEER-based studies included the absence of detail with regard to individual information about chemotherapy regimen and radiotherapy doses/fields. Thus, it was not possible to examine the effects of combined surgery and chemotherapy or radiotherapy on patient survival. Second, SEER also lacked information regarding the location of PUC, a significant prognostic factor that undoubtedly influences the treatment strategy. Moreover, this study is a retrospective analysis, and selection bias could not be completely avoided.
Despite the limitations of this study, our results suggest that surgery for the primary tumor conferred a survival advantage in non-metastatic PUC patients regardless of sex, age, T stage, and N stage. Furthermore, the surgical benefit was more marked in patients with early TNM stage (I/II) disease, patients < 70 years, and those with tumor size ≥30 mm.
Availability of data and materials
The data that support the findings of this study are openly available in the Surveillance, Epidemiology and End Results (SEER) database of the National Cancer Institute.
Primary urethral carcinoma
The Surveillance, Epidemiology and End Results database
The International Classification of Diseases-O-3
American Joint Committee on Cancer
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We sincerest thank the editor and reviewers for careful review and valuable comments. The manuscript has certainly benefited from these insightful revision suggestions.
This work was supported by the National Natural Science Foundation of China (Project 81772706).
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OS and CSM in PUC patients stratified by surgical procedure and age. (a) Patients aged < 70 years, (b) patients aged ≥70 years.
OS and CSM in PUC patients stratified by surgical procedure and tumor size. (a) Tumor size < 30 mm, (b) tumor size ≥30 mm.
OS and CSM in PUC patients stratified by surgical procedure and sex. (a) Male, (b) female.
OS and CSM in PUC patients stratified by surgical procedure and AJCC stage groups. (a) I/II stage, (b) III/IV stage.
OS and CSM in PUC patients stratified by surgical procedure and M stage. (a) Stage M0, (b) stage M1.
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Wu, J., Wang, YC., Luo, WJ. et al. Primary tumor surgery improves survival in non-metastatic primary urethral carcinoma patients: a large population-based investigation. BMC Cancer 21, 857 (2021). https://doi.org/10.1186/s12885-021-08603-z