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. 2016 Mar 31;11(3):e0152459. doi: 10.1371/journal.pone.0152459

Prognostic Value of Overexpressed p16INK4a in Vulvar Cancer: A Meta-Analysis

Hanyu Cao 1, Si Wang 2, Zhenyu Zhang 3, Jiangyan Lou 3,*
Editor: Magdalena Grce4
PMCID: PMC4816296  PMID: 27031618

Abstract

Objective

This study aimed to examine the prognostic value of overexpressed p16INK4a in vulvar cancer. Although the tumor suppressor p16INK4a has been shown to be of prognostic value in a wide variety of cancers and precancerous lesions, its role in the vulvar cancer is still unclear.

Methods

All publications in English language on the association between p16INK4a and clinicopathological features of vulvar cancer were searched from Pubmed, Embase, and Web of Science, and those in Chinese language were identified manually and online from the China National Knowledge Infrastructure. Strict inclusion and exclusion criteria were followed. Odds ratios(ORs) or risk ratios(RRs) with 95% confidence intervals(CIs) were pooled to assess the strength of association. Publication bias was estimated using funnel plots and the Egger’s regression test.

Results

A total of 17 studies with 2309 patients were included. The p16INK4a overexpression was found to correlate significantly with the lower International Federation of Gynecology and Obstetrics stage(I+II vs III+IV; OR = 0.60,95%CI:0.41–0.86,P = 0.006),negative lymph node metastasis(negative vs positive; OR = 0.61,95%CI:0.39–0.95,P = 0.029),patient’s age<55(OR = 0.54,95%CI:0.31–0.96,P = 0.034),human papillomavirus–positive status(OR = 0.01,95%CI:0.00–0.11,P<0.001),and higher overall survival(RR = 0.53,95%CI = 0.35–0.80,P = 0.003).

Conclusion

The p16INK4a might be associated with a higher survival and indicates better prognosis of vulvar cancer.

Introduction

Vulvar cancer is the fourth most common malignancy in the female genital tract, accounting for 5% of all gynecological cancers[1].With an estimate of over 5000 new cases and over 1000 deaths in the United States each year, the incidence of vulvar cancer keeps on rising, particularly in young women [1,2].The most frequent histological type of vulvar cancer is squamous cell carcinoma(SCC), which represents 80%–90% of the cases and can be divided into two groups based on whether they are related to human papillomavirus (HPV) infection[3,4]. One is the HPV-associated type including the warty or basaloid SCC, and the other is the HPV-independent keratinizing SCC[5,6].Radical surgery is the main modality of treatment for vulvar cancer, sometimes in combination with presurgical or postsurgical radiotherapy or chemotherapy depending on the tumor size and invasion, but often causes overtreatment in early stage cases when patients present nonmetastasis of lymph node[7]. For this reason, tumor biological markers are needed to predict clinical behavior and metastatic potential of vulvar cancer.

The p16INK4a protein is a cyclin-dependent kinase inhibitor that can act on cyclin-dependent kinases(CDKs) and thus inactivate the cell cycle[8].The loss of p16ink4a expression seems to be an early event in carcinogenesis. Over the past decades, the prognostic value of p16INK4a protein has been evaluated in a wide variety of cancers [9–14].Among these, the study of Hellman et al[15] concluded that p16INK4A expression might be used as a marker for HPV positivity in vaginal carcinoma, which shares a very similar etiology with vulvar cancer. However, its role and the etiological effect of its combination with the HPV status in vulvar cancer remain somehow unclear. Tringler and Dong reported a significant association between p16INK4a and longer survival of vulvar cancer patients, while Trietsch denied its independent prognostic role[16–18].In this regard, the present study performed a meta-analysis to explore the prognostic value of the overexpressed p16INK4a in vulvar cancer.

Methods

Search strategy

To identify all articles that investigated the association of p16INK4a expression and vulvar cancer, a literature search of PubMed database, Embase, Web of Science, and China National Knowledge Infrastructure was conducted between January 1991 and August 2015. All relevant articles were retrieved using the following search terms: “p16 or p16INK4a” and “vulvar neoplasm or vulvar neoplasms”. References of the retrieved publications were also screened for other relevant studies. For multiple publications from the same population, only the largest-scale study was included. Study selection was achieved by two investigators independently, according to the inclusion and exclusion criteria, by screening the title, abstract, and full-text. Any dispute was solved by discussion. The language of publication was restricted to English and Chinese. Only research articles were included. If an article reported results including different studies, each study was treated as a separate comparison in the present meta-analysis.

Inclusion criteria

The following inclusion criteria were followed in selecting studies for the current meta-analysis: Studies in which the diagnosis of vulvar cancer was proven by histopathological methods; studies of p16INK4a expression that were based on vulvar cancer tissue (after either surgical excision or biopsy sampling);specimens examined by immunohistochemistry; and all studies on the correlation of p16INK4a expression with clinicopathological markers or with the HPV status and the association of p16INK4a overexpression on the overall survival (OS) or disease-free survival (DFS) or recurrence of vulvar cancer patients. For inclusion into the analysis, no limitation was set on the minimum number of patients of each study. In the case of multiple articles by the same group based on similar patients and using same detection methods, only the largest or the most recent article was included.

Exclusion criteria

The exclusion criteria were defined as follows: Studies based on serum or any other kinds of specimen, and studies using methods other than immunohistochemistry to examine specimens.

Data extraction

Three investigators (Hanyu Cao, Si Wang, and Zhenyu Zhang) extracted independently all articles complying with the aforementioned inclusion criteria. Any discrepancy was resolved by discussion until an agreement was reached between the investigators. The following information was collected from each publication: the first author’s name, publication year, patient’s country, tumor stage, technique, percentage of p16INK4a positive cells, number of patients, cutoff value of overexpression of p16INK4a in cases and controls.

Statistical analysis

Odds ratios(OR) and 95% confidence intervals (CIs) were pooled to evaluate the association between p16INK4a expression and clinical or histopathological features of vulvar cancer including histological grade, International Federation of Gynecology and Obstetrics (FIGO) stage, lymph node metastasis, age, and HPV status. Risk ratios(RRs) and 95% CIs were synthesized to determine the correlation between p16INK4a expression and 5-year OS. Heterogeneity was examined with I2 statistics interpreted as the proportion of total variation contributed by between-study variations. Heterogeneity was investigated by the Cochran’s chi-square Q test with a significance level of P<0.10 and I2>50%.In this case, the random-effects model was used to estimate the pooled ORs [19].Otherwise, the pooled ORs were estimated by the fixed-effects model. RRs were pooled to evaluate the association of p16INK4a expression and survival outcome data. The Engauge Digitizer Version 4.1 software (free software downloaded from http://sourceforge.net) was used when the survival data could not be extracted directly according to previous studies[20]. Begg’s funnel plots and the Egger’s linear regression test were performed to investigate publication bias [21]. All statistical tests were performed with the stata 12.0 software(Stata Corp, TX, USA).

Results

Study inclusion and characteristics

As shown in Fig 1, a total of 17 eligible studies comprising 2309 patients from different countries were included in this meta-analysis, with the number of patients ranging from 4 to 1287 per study[16–17,22–36].Among them, eight studies dealt with the FIGO stage, and six studies presented data on lymph node metastasis. Three studies presented data classified according to patients’ age (55 years), and seven studies reported histological grade. In addition, four studies reported the association between p16INK4a and the HPV status, whereas only one study[34] included the DFS and OS data concerning the HPV status. Moreover, only three studies provided sufficient data on OS related to p16INK4a expression. All of them used the immunohistochemistry method with different cut-off values. The main characteristics of these studies are summarized in Table 1.

Fig 1. Flow chart demonstrating studies processed for inclusion in the meta-analysis.

Fig 1

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Table 1. Main Characteristics of all Eligible Studies.

Study Year Patient's country Tumor stage Technique Percentage of p16INK4a positive cells (%) Number of patients Cutoff(IHC)
Chan MK 1998 China FIGO IHC 72 30 ND
Zheng 2000 China FIGO IHC 40.38 52 ND
Ma 2002 China FIGO IHC 64 25 Staining grade>2
Hao 2004 China ND IHC 40 30 ND
Knopp S 2004 Norway FIGO IHC 31 224 5%
Mauricio 2006 Brazil ND IHC 24.3 37 5%
Santos M 2006 Spain ND IHC 18 92 25%
van der Avoort 2006 The Netherlands ND IHC 75 16 25%
Tringler B 2007 Austria FIGO IHC 43 80 ND
Wei 2008 China FIGO IHC 29 21 ND
Alonso I 2011 Spain FIGO IHC 20 98 Diffuse staining
Guerrero D 2011 Spain TNM IHC 70 30 1%
de Sanjosé S 2013 39 Countries ND IHC 29 1287 ND
Ma HM 2013 China FIGO IHC 90.3 36 Staining grade>2
Lavorato-Rocha 2013 Brazil FIGO IHC 29 139 5%
Missaoui N 2014 Tunisia FIGO IHC 73 15 ND
Dong 2015 America ND IHC 52 97 70%
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FIGO, International Federation of Gynecology and Obstetrics; IHC, immunohistochemistry; ND, no data; TNM, tumor node metastases.

Correlation of p16INK4a expression with clinicopathological parameters

As shown in Fig 2, the overexpression of p16INK4a was significantly associated with the lower FIGO stage of I–II(OR = 0.60,95%CI:0.41–0.86,P = 0.006,fixed effect; Fig 2A), no lymph node metastasis(OR = 0.61,95%CI:0.39–0.95,P = 0.029,fixed effect; Fig 2B), patient’s age<55(OR = 0.54,95%CI:0.31–0.96,P = 0.034,fixed effect; Fig 2C), and HPV-positive status(OR = 0.01,95%CI:0.00–0.11,P<0.001,random effect; Fig 2D).However, the overexpression of p16INK4a was not correlated with the histological grade(OR = 0.99,95%CI:0.71–1.39,P = 0.953,fixed effect; Fig 2E).

Fig 2.

Fig 2

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Forest plot for the association between p16INK4a expression and clinicopathological markers(A) FIGO stage.(B) LN metastasis. (C) Patient's age. (D) HPV status. (E) Histological grade. FIGO, International Federation of Gynecology and Obstetrics; LN, lymph node; HPV, human papillomavirus.

Correlation of p16INK4a expression with OS

Five-year OS rates were extracted from three studies and were pooled in this meta-analysis using the method mentioned earlier. The overexpression of p16INK4a was significantly correlated with a higher OS(RR = 0.53,95%CI = 0.35,0.80,P = 0.003,fixed effect; Fig 3) with no heterogeneity(I2 = 0.0%,P = 0.636).

Fig 3. Forest plot for the association between p16INK4a expression and OS.

Fig 3

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Publication Bias

Begg’s funnel plots and Egger’s test were used to assess whether publication bias existed in the 5-year OS studies. No obvious evidence of asymmetry was found in the funnel plot of OS(P = 0.217; Fig 4).

Fig 4. A funnel plot analysis on the detection of publication bias in the meta-analysis of the prognostic value of p16ink4a in the OS of vulvar cancer.

Fig 4

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Discussion

P16INK4a,as a member of the INK4a family, is known to inactivate cell cycle progression and differentiation by interfering with cyclin D–CDK4/6 assembly and thus block the G1 to S transition[37].The functional loss of INK4a family has been found in variable human cancers. Some previous studies have provided evidences indicating that p16INK4a is a potential tumor suppressor whose overexpression can inhibit abnormal cell growth, whereas downregulation may lead to tumorigenesis[38]. Although p16INK4a has been shown to be of prognostic value in a wide variety of cancers and precancerous lesions such as gastrointestinal stromal tumor, non-small lung cancer, osteosarcoma, cervical cancer, and cervical intraepithelial neoplasia, evidence of correlation with vulvar cancer is lacking[12–13,39–41].

Vulvar cancer is uncommon but represents a certain group in the carcinoma of lower genital tract in female. As the treatment for vulvar cancer tends to be more conservative and individualized over the past decade, acquaintance with the prognostic factors seems more essential and is of great value for early diagnosis, but is still a challenge because of scanty evidence compared with other gynecological malignancies[42].It was found that FIGO stage, lymph node metastasis, and histological grade are the most important prognostic factors in vulvar cancer[43–45]. The age of patients is also a predominant and independent factor in the 5-year survival of vulvar cancer[46]. This study is perhaps the first meta-analysis that evaluated the prognostic value of p16INK4a in vulvar cancer.

The present meta-analysis using pooled ORs demonstrated that p16INK4a overexpression correlates significantly with the lower FIGO stage, negative lymph node metastasis, and younger age, consistent with its well-known function of suppressing tumor invasion[47–49].The pooled RR of OS reveals that p16INK4a overexpression indicates a better prognosis for patients diagnosed with vulvar cancer. The results indicate that p16INK4a may be a potential biomarker for the diagnosis and prognosis of vulvar cancer. Although evidence shows improved survival of HPV-induced and p16-positive carcinoma associated with head and neck cancer[50], no detailed studies are found presenting the survival data including both HPV status and p16INK4a.A very few studies presented recurrence rate related to p16 concerning vulvar squamous cell carcinoma (VSCC) after repeated searches for several times, which may be due to the low frequency of VSCC. Among the included studies, HPV-positive rate independent of p16INK4a ranges between 0% and 41% [23,25,27,34],which is in accordance with the fact that vulvar cancer presents an overall HPV infection rate of only 30%–40%[51–52].Moreover, the analysis outcome shows that p16ink4a overexpression correlates significantly with the HPV-positive status, strongly supporting the etiological role of HPV infection in the development of vulvar cancer. The E7 and E6 oncoproteins encoded by HPV can be integrated into the host genome, binding to the tumor suppressor proteins pRB and p53, respectively, and leading to their deregulation, which results in the overexpression of p16INK4A as a means of genetic instability control[53].All these may reasonably lead to the speculation that p16INK4a is only associated with HPV-induced vulvar carcinoma.

However, this study has some limitations that should be taken into consideration. First, this study included a small sample size. A total of 817 patients may not be able to provide statistical evidence convincing enough to prove the role of p16INK4a in vulvar cancer prognosis. In addition, studies concerning the survival rate of vulvar cancer are even less. Second, the arbitrarily selected cutoff value of positive p16INK4a expression varies in different studies. This may be caused by the lack of a standardized immunostaining point decided by a combination of intensity and the variable methodological factors in immunohistochemistry such as storage time, fixation method, and different antibodies[54], which may result in an inaccurate outcome. All studies were evaluated based on a review of the entire histological section, while some declared the evaluation of the immunostaining results by one or two pathologists at the same time according to previous experience and established criteria in vulvar neoplasia or for uterine cervix[55,56],which ensure their reliability. Third, treatment methods for each patient differed to a certain extent for their multiple kinds of clinical and histological features, which should not be ignored. For these reasons, further research with a larger sample size and more evidence are needed to confirm the findings of this study.

In conclusion, despite the limitations, the results of the present meta-analysis suggested that p16INK4a overexpression was associated with a favorable prognosis in patients with vulvar cancer. The assessment of p16INK4a expression is capable of providing better prognostic information for patients with vulvar cancer.

Supporting Information

S1 PRISMA Checklist. PRISMA 2009 Checklist.

(DOC)

Click here for additional data file. (66KB, doc)

Acknowledgments

All the authors were directly involved in the whole process, therefore it is disclosed that all the authors contributed equally towards the research. Thanks to the editors and anonymous reviewers. The software used in the analysis:stata 12.0 software(Stata Corp, College Station, TX)

Data Availability

Data are from the included studies whose authors may be contacted at doi: 10.1006/gyno.1997.4914, doi: 10.1097/pas.0000000000000454, doi: 10.1002/ijc.25629, doi: 10.1016/j.ygyno.2004.07.026, doi: 10.1007/s13277-013-0955-0, doi: Paor.2006.12.3.0153, doi: 10.1097/01.pai.0000213118.81343.32, Int J Gynecol Pathol. 2006 Jan;25(1):22-9. from Pubmed, Web of Science and Embase, Chinese articles from Sichuan Medical Journal (05):405-406,Maternal and Child Health Care of China (22):3168-3170., Master thesis: Qingdao University. hin J Clin Oncol Rehabil (01):6-8., Master thesis: China Medical University. from CNKI database.

Funding Statement

The authors have no support or funding to report.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

S1 PRISMA Checklist. PRISMA 2009 Checklist.

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Data Availability Statement

Data are from the included studies whose authors may be contacted at doi: 10.1006/gyno.1997.4914, doi: 10.1097/pas.0000000000000454, doi: 10.1002/ijc.25629, doi: 10.1016/j.ygyno.2004.07.026, doi: 10.1007/s13277-013-0955-0, doi: Paor.2006.12.3.0153, doi: 10.1097/01.pai.0000213118.81343.32, Int J Gynecol Pathol. 2006 Jan;25(1):22-9. from Pubmed, Web of Science and Embase, Chinese articles from Sichuan Medical Journal (05):405-406,Maternal and Child Health Care of China (22):3168-3170., Master thesis: Qingdao University. hin J Clin Oncol Rehabil (01):6-8., Master thesis: China Medical University. from CNKI database.

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