Abstract
Background: The literature reports conflicting results regarding the effect of human papillomavirus (HPV) genotype 16 (HPV-16)/18 (HPV-18) positivity on cervical cancer (CC) prognosis.
Aim: To conduct a meta-analysis to examine the effect of HPV-16/18 positivity on the prognosis of patients with CC.
Methods: PubMed, Embase, and the Cochrane Library were searched for available papers published up to March 2020. The main outcome was the hazard ratio (HR) of overall survival (OS) or disease-free survival (DFS) comparing HPV-16 or HPV-18 positivity and negativity. The random-effects model was used for synthesizing survival outcomes.
Results: Nine studies and 2,028 patients were included. Four studies reported OS in HPV-16 positivity, and no association was found between HPV-16 positivity and OS to CC (HR = 0.79, 95% CI: 0.26–2.39, P = 0.675). Three studies reported DFS in HPV-16 positivity, and no association was found between HPV-16 positivity and DFS to CC (HR = 0.80, 95% CI: 0.30–2.11, P = 0.654). Two studies reported DFS in HPV-18 positivity, and no association was found between HPV-18 positivity and DFS to CC (HR = 0.99, 95% CI: 0.55–1.78, P = 0.984). One study reported progression-free survival (PFS) in HPV-18 positivity, and an association was observed between HPV-18 positivity and PFS to CC (HR = 2.66, 95% CI: 1.44–4.94, P = 0.002). The sensitivity analyses showed that one study biased the analysis of the association between HPV-16 and OS, and another study biased the association between HPV-16 and DFS.
Conclusion: The presence of HPV-16 and HPV-18 positivity appears to have no significant association with prognosis in CC in either OS or PFS. The presence of HPV-16 or HPV-18 positivity has no significant association with prognosis in CC in either OS or PFS.
Introduction
Cervical cancer (CC) is a malignancy originating in the transformation zone of the cervix, most commonly in squamous cells (). It is the second most common cancer in women worldwide, with an estimated 569,847 new cases in 2018, and the third most common cause of female cancer mortality, with 311,365 deaths (, ). CC has a strong tendency to affect young women, and the peak incidence is in the 40–49 age group (, ).
Infection with high-risk human papillomavirus (HPV) is a major risk factor for the development of CC (, –). It is now well-recognized that the majority of CC is associated with HPV genotypes 16 (HPV-16) and 18 (HPV-18) (, –). HPV, an epitheliotropic double-stranded DNA oncovirus, typically infects the basal layer of the epithelium through small tears in the mucosa resulting from sexual activity. Active papillomavirus infection occurs when infected basal cells replicate and fill the area. HPV synthesizes six early proteins (E1–E7) and two late capsid proteins (L1 and L2) during replication, and those proteins have immortalizing and transforming properties (). Persistent HPV infection results in squamous intraepithelial lesions that are graded as cervical intraepithelial neoplasia (CIN) 1, CIN 2, and CIN 3 according to how much epithelium is impacted. The progression from cervical dysplasia to invasive cancer may take years or decades but has been reported to take <1 year in about 10% of patients ().
Nevertheless, despite the sound pathogenic effect of HPV-16 and HPV-18 for CC, the prognosis of HPV-16 and HPV-18 positivity in patients with CC has not been established. A recent meta-analysis revealed that HPV DNA positivity is associated with good overall survival (OS) and disease-free survival (DFS) in patients with CC (). Similar meta-analyses reported that HPV positivity was an indicator of favorable prognosis in head and neck cancers (, ), but there are studies that failed to support the relationship between HPV-16 or HPV-18 positivity and prognosis of CC (), and some even indicate that CC associated with HPV-16/18 has a worse survival ().
Gaining a more comprehensive insight into how the HPV type affects survival is important. We herein hypothesized that HPV-16/18 positivity is associated with poorer prognosis in patients with CC. To test our hypothesis, we conducted this meta-analysis and systematically reviewed the existing literature.
Methods
Literature Search
This meta-analysis was conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (). The search was based on the PICO principle (), followed by screening using a prespecified protocol and eligibility criteria: () population: patients with CC who had a record of HPV genotype; () exposure: HPV-16 or HPV-18 positivity; () controls: HPV-16 or HPV-18 negativity; () outcome: survival; and () full text available in English. PubMed, Embase, and the Cochrane Library were searched for available papers published up to March 2020 using the MeSH term “Uterine Cervical Neoplasms,” as well as relevant keywords.
Data Extraction
The study characteristics (authors, year of publication, country where the study was performed, median follow-up time, sample size, and mean age in each group), treatment parameters [The International Federation of Gynecology and Obstetrics (FIGO) stage of CC, histology, detection method of HPV genotype, reported HPV genotype, the operation the patients underwent, the endpoint of the study, type of specimens that were used, and covariates if a multivariable model was used], and outcome (OS and DFS) were extracted by two authors independently. Any discrepancy was solved by discussion.
Outcomes
The main outcome was the hazard ratio (HR) of OS or DFS comparing HPV-16 or HPV-18 positivity and negativity on DFS or OS.
Quality of the Evidence
The quality level of evidence of all articles was assessed independently by two authors according to the Newcastle–Ottawa scale (NOS) for cohort study (). Discrepancies in the assessment were resolved through discussion until a consensus was reached.
Data Synthesis
The risk estimates of each study were reported as HR or relative risk (RR). We treated RRs as HRs. When possible, multi-adjusted HRs were used in the meta-analysis.
Statistical Analysis
All analyses were performed using STATA SE 14.0 (StataCorp, College Station, Texas, USA). HRs and corresponding 95% confidence intervals (CIs) were used to compare the outcomes. Statistical heterogeneity among studies was calculated using Cochran's Q-test and the I2 index. An I2 > 50% and a Q-test P < 0.10 indicated high heterogeneity, and the random-effects model was used; otherwise, the fixed-effects model was applied. P < 0.05 were considered statistically different. We did not assess potential publication bias by funnel plots and Egger's test because the numbers of studies included in each quantitative analysis were <10, in which case, the funnel plots and Egger's test could yield misleading results ().
Results
Selection of the Studies
Figure 1 presents the selection flowchart. In the initial search, 184 records were retrieved, and 166 were screened after removing the duplicates. From them, 44 were excluded because of the publication type (notes, conference abstracts, and reviews). Then, 122 full-text papers were assessed and 113 were excluded because of study aim/design (n = 34), outcome (n = 9), population (n = 48), exposures (n = 8), full text not accessible (n = 2), meta-analyses (n = 2), and non-English (n = 10).
Figure 1
Therefore, nine studies were included (, , –) (Table 1). Those studies included a total of 2,028 patients. The mean age range was 47–57 years. The median follow-up ranged from 33 to 136 months. Four studies scored 7 on the NOS (, –), four studies scored 8 (, , , ), and one study scored 9 () (Supplementary Table 1).
Table 1
| Reference | Country | FIGO stage | Histology | Method of detecting HPV | HPV genotype reported | Surgical operation if mentioned | n | Age (Exposure/ control) | Median follow-up | Endpoint | Type of specimens | Covariates in the model |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| () | Korea | ALL | SCC, AC, ASC | PCR | HPV 16 | Laparoscopic or robotic radical hysterectomy with pelvic and/or para-aortic lymphadenectomy | 248 | 51.4 ± 11.5 | 59 | DFS | Fresh | Age, FIGO stage, tumor size, lymph node metastasis |
| () | China | ALL | SCC, AC, ASC | PCR | HPV 16, HPV 18 | Radical hysterectomy with pelvic lymphadenectomy | 306 | 48 (26–71) | 54 | OS | fresh | Age, FIGO stage, treatment |
| () | Korea | IB–IIA | SCC, AC, ASC | PCR | HPV 18 | Radical hysterectomy with pelvic lymphadenectomy | 204 | 47.4 ± 11.8/ 49.5 ± 11.7 | NR | PFS | Fresh | Histology, stage, tumor size, lymph node metastasis |
| () | Korea | IIA–IVB | SCC, AC, ASC | PCR | HPV 18 | NR | 181 | 57 (23–80) | 33 | DFS | paraffin | Age, stage nodal status, histologic grade, histologic type, tumor size, smoking |
| () | Russia | III | NR | PCR | HPV 16 | Chemo- and radiotherapy or radiotherapy alone | 92 | NR | NR | DFS | fresh | NA |
| () | Taiwan | I–IV | AC, ASC | PCR | HPV 16 | Primary definitive surgery | 452 | 48.3 (27.5–89.2) | 136 | DFS | paraffin | Age, FIGO stage, grade |
| () | Japan | ALL | SCC, AC, ASC, SCCC | PCR | HPV 16 | NR | 137 | 49.2 ± 14.8 | 102.5 | OS | fresh | Age, FIGO stage, histology |
| () | Germany | I–II | SCC, AC, ASC | PCR | HPV 16 | Radical hysterectomy and pelvic lymphadenectomy | 121 | 48.1 | 42 | OS | Paraffin | Depth of invasion, tumor grade, node metastases, HPV in histologically confirmed cancer-free pelvic lymph nodes |
| () | Germany | I–IIa | SCC, AC, ASC, SCCC | SBH+PCR | HPV 16 | Intracavitary radiotherapy, radical hysterectomy and pelvic lymphadenectomy | 287 | NR | NR | OS | fresh | Age, histology, hospital |
Literature search and study characteristic.
SCC, squamous cell carcinoma; AC, adenocarcinoma; ASC, adeno-adenosquamous carcinoma; SCCC, small cell carcinoma of the cervix; HPV, human papillomavirus; FIGO, The International Federation of Gynecology and Obstetrics; DFS, disease-free survival; OS, overall survival; PFS, progression-free survival.
Survival According to Human Papillomavirus Subtype 16
Four studies reported OS in HPV-16 positivity (, , , ), and no association was found between HPV-16 positivity and OS to CC (HR = 0.79, 95% CI: 0.26–2.39, P = 0.675; I2 = 91.6%, Pheterogeneity < 0.001) (Figure 2, Table 2). Three studies reported DFS in HPV-16 positivity (, , ), and no association was found between HPV-16 positivity and DFS to CC (HR = 0.80, 95% CI: 0.30–2.11, P = 0.654; I2 = 87.6%, Pheterogeneity < 0.001; Figure 3, Table 2).
Figure 2
Table 2
| N | HR (95% CI) | P | I-square | P (Heterogeneity) | |
|---|---|---|---|---|---|
| HPV16 | |||||
| OS | 4 | 0.79 (0.26, 2.39) | 0.675 | 91.6 | <0.001 |
| DFS | 3 | 0.80 (0.30, 2.11) | 0.654 | 87.6 | <0.001 |
| HPV18 | |||||
| DFS | 2 | 0.99 (0.55, 1.78) | 0.984 | 0.0 | 0.853 |
| PFS | 1 | 2.66 (1.44, 4.94) | 0.002 | ||
Results from the meta-analysis. HPV genotype positive vs. negative.
HPV, human papillomavirus; DFS, disease-free survival; OS, overall survival; PFS, progression-free survival; HR, hazard ratio.
Figure 3
Survival According to Human Papillomavirus Subtype 18
Two studies reported DFS in HPV-18 positivity (, ), and no association was found between HPV-18 positivity and DFS to CC (HR = 0.99, 95% CI: 0.55–1.78, P = 0.984; I2 = 0.0%, Pheterogeneity = 0.853; Figure 4, Table 2). One study reported progression-free survival (PFS) in HPV-18 positivity (), and an association was observed between HPV-18 positivity and PFS to CC (HR = 2.66, 95% CI: 1.44–4.94, P = 0.002; Figure 4, Table 2).
Figure 4
Sensitivity Analyses
Regarding the association between HPV-16 and OS, the sensitivity analysis showed that omitting Pilch et al. () affected the conclusion (Figure 5). Regarding the association between HPV-16 and DFS, the sensitivity analysis showed that omitting Kiseleva et al. () affected the conclusion (Figure 6).
Figure 5
Figure 6
Discussion
The literature reports conflicting results regarding the effect of HPV-16/18 positivity on CC prognosis. Therefore, this meta-analysis aimed to examine the effect of HPV-16/18 positivity on the prognosis of patients with CC. The results suggest that the presence of HPV-16 and HPV-18 positivity appears to have no significant association with prognosis in CC in either OS or PFS. The presence of HPV-16 or HPV-18 positivity has no significant association with the prognosis of CC (either OS or PFS). This is in contradiction to the aggressive feature of HPV-16/18-positive lesions during the development of CIN to CC.
In HPV-associated CC, tumorigenesis is driven by the E6 and E7 oncogenes from the viral DNA integrated into the host cells (), but in HPV-negative CC, tumorigenesis is driven by the intrinsic oncogenes (), and the two types of CC could be distinct diseases (). A recent meta-analysis showed that pretreatment HPV DNA positivity in patients with CC was associated with a better prognosis in Mongoloids and Caucasians (). Similar results were observed for head and neck cancers (, ), but these previous meta-analyses did not examine the HPV types.
It is now well-known that the different HPV types differ widely in terms of epidemiology and potential for CIN and CC (–). Among them, HPV-16 and HPV-18 are generally considered as being those at the highest risk of CC (–). Available studies suggest a positive effect of HPV16/18 positivity on CC outcomes (, , ), a negative effect (, ), or no effect (, ). A nationwide study that was not eligible for the present meta-analysis showed that patients with CC positive for a high-risk HPV type had a better prognosis than patients negative for such types (), but other non-eligible studies also report conflicting results (, –). Indeed, Cuschieri et al. () showed that patients with CC and HPV-16/18 had better survival than those without HPV-16/18. Wang et al. () showed that CC caused by both HPV α-7 (which includes HPV-18) and HPV α-8 (which includes HPV-16) had a better prognosis than CC caused by HPV α-7 alone. Dahlgren et al. () reported a better prognosis for CC with HPV-16, but Lai et al. () reported a worse prognosis for HPV-18. When considering the eligible studies, the present meta-analysis suggests that there is no association between HPV-16/18 positivity and CC outcomes.
The results of the present meta-analysis must be considered in light of its limitations. We failed to conclude the prognostic effect of HPV-16 and HPV-18 in CC because the eligible studies had conflicting results. Of note, a number of studies could not be included because they did not report results specifically for HPV-16 or HPV-18. To our knowledge, there are only a few studies that investigated the prognostic effect of HPV-16 and HPV-18 in patients with CC, and the survival outcomes in each study were reported differently. Nevertheless, the non-eligible studies also had conflicting conclusions. Despite that nine studies were included in the meta-analysis, never more than four studies were analyzed together for a given outcome. One study reported the risk estimates as RR instead of HR. We treated the RR as HR for the analysis purpose, but it could introduce a bias. The nine studies were all observational studies, decreasing the strength of the conclusion, but a randomized control trial is not possible in this context. In addition, false-negatives could not be taken into account because of nonuniform reporting or non-reporting among the included studies. Finally, the risk estimates of survival outcomes were not reported at the same duration after the patients were discharged from the hospital.
In conclusion, the presence of HPV-16 and HPV-18 positivity appears to have no significant association with prognosis in CC in either OS or PFS, but the sensitivity analysis indicated that the study by Pilch et al. () has a strong impact on the outcome. Eliminating this study from the analysis would lead to a conclusion of a better prognosis of HPV-16 positivity in CC. Despite the limitations, the present meta-analysis observed different results on the prognostic effect of HPV-16 and HPV-18 among the existing studies. Future studies with larger numbers of patients in different countries and various ethnicities should be encouraged.
Statements
Data availability statement
All datasets generated for this study are included in the article/Supplementary Material.
Author contributions
XC substantially contributed to conception or design, contributed to acquisition, analysis, or interpretation of data, drafted the manuscript for important content, critically revised the manuscript for important intellectual content, and gave final approval. PZ substantially contributed to conception or design, contributed to acquisition, analysis, or interpretation of data, drafted the manuscript for important content, and critically revised the manuscript for important intellectual content. SC contributed to acquisition, analysis, or interpretation of data. HZ drafted the manuscript for important content. XDC gave final approval. All authors contributed to the article and approved the submitted version.
Funding
This work was supported by grants from the Zhejiang Provincial Natural Fund Public Welfare Technology Applied Research Funding Project (LGF20H160022).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fonc.2020.01733/full#supplementary-material
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Summary
Keywords
human papillomavirus 16, human papillomavirus 18, uterine cervical neoplasms, prognosis, meta-analysis
Citation
Chen X, Zhang P, Chen S, Zhu H, Wang K, Ye L, Wang J, Yu J, Mei S, Wang Z and Cheng X (2020) Better or Worse? The Independent Prognostic Role of HPV-16 or HPV-18 Positivity in Patients With Cervical Cancer: A Meta-Analysis and Systematic Review. Front. Oncol. 10:1733. doi: 10.3389/fonc.2020.01733
Received
30 April 2020
Accepted
03 August 2020
Published
07 October 2020
Volume
10 - 2020
Edited by
Angeles Alvarez Secord, Duke University, United States
Reviewed by
Lorenzo Gerratana, University of Udine, Italy; Luigi Pedone Anchora, Catholic University of the Sacred Heart, Italy
Updates
Copyright
© 2020 Chen, Zhang, Chen, Zhu, Wang, Ye, Wang, Yu, Mei, Wang and Cheng.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xiaodong Cheng chenxing@enzemed.com
This article was submitted to Women's Cancer, a section of the journal Frontiers in Oncology
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