Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis

Weeks, Kristin S.; Herbach, Emma; McDonald, Megan; Charlton, Mary; Schweizer, Marin L.

doi:https://doi.org/10.1155/2020/2374716

Obstetrics and Gynecology International

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Abstract Introduction Materials and Methods Results Discussion Conclusions Appendix Data Availability Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2020 | Article ID 2374716 | https://doi.org/10.1155/2020/2374716

Meta-Analysis of VTE Risk: Ovarian Cancer Patients by Stage, Histology, Cytoreduction, and Ascites at Diagnosis

Kristin S. Weeks,^1,2Emma Herbach,¹Megan McDonald,³Mary Charlton,¹and Marin L. Schweizer^2,4

Academic Editor: Diego Raimondo

Received30 Jun 2020

Revised07 Aug 2020

Accepted18 Aug 2020

Published03 Sept 2020

Abstract

Venous thromboembolisms (VTEs) have been a leading secondary cause of death among ovarian cancer patients, prompting multiple studies of risk factors. The objective of this meta-analysis is to quantify the associations between VTE and the most commonly reported risk factors among ovarian cancer patients. PubMed, Embase, and Cumulative Index to Nursing and Allied Health Literature (CINAHL) were used to identify observational studies. Two reviewers independently abstracted data and assessed quality via the Newcastle–Ottawa tool. A random effects model was used to calculate the pooled odds ratios for VTE with each of the following exposures: advanced cancer stage, clear cell histology, serous histology, ascites at diagnosis, and complete cytoreduction. The I² and Q tests were used to evaluate heterogeneity. Twenty cohort studies with 6,324 total ovarian cancer patients, 769 of whom experienced a VTE, were included. The odds of VTE in ovarian cancer patients were higher among patients with cancer stage III/IV (versus cancer stage I/II, pooled odds ratio (OR) 2.73; 95% CI 1.84–4.06; I²= 64%), clear cell (versus nonclear cell) histology (OR 2.11; 95% CI 1.55–2.89; I² = 6%), and ascites (versus no ascites) at diagnosis (OR 2.12; 95% CI 1.51–2.96; I² = 32%). Serous (versus nonserous) histology (OR 1.26; 95% CI 0.91–1.75; I² = 42%) and complete (versus incomplete) cytoreduction (OR 1.05; 95% CI 0.27–4.11; I² = 88%) were not associated with VTE. This meta-analysis quantifies the significantly elevated odds of VTE in ovarian cancer patients with advanced stage at diagnosis, clear cell histology, and ascites at diagnosis. Further studies are needed to account for confounders and inform clinical decision-making tools.

1. Introduction

Venous thromboembolisms (VTEs), including deep vein thromboses (DVTs) and pulmonary embolisms (PEs), are a major complication of the hypercoagulative state caused by cancer [1, 2]. Ovarian cancer patients have one of the highest rates of VTEs among all cancer patients [3–10]. Additionally, VTEs are a leading secondary cause of death for ovarian cancer patients and can cause significant morbidity and decreased quality of life [9, 11–17].

There are many reasons ovarian cancer patients are at high risk for VTEs [8]. First, eighty percent of women with ovarian cancer are diagnosed at an advanced cancer stage with regional or distant metastasis [18]. Large tumor growth and accumulated ascites at diagnosis can compress the pelvic veins in women leading to hemostasis and increased risk of thrombosis [19, 20]. Moreover, advanced stage at diagnosis and the associated abdominal ascites are thought to contribute to VTE events through cellular mechanisms, vessel wall irritation, inflammation, and thrombocytosis [8, 19, 21]. Secondly, certain ovarian cancer histologies, such as clear cell carcinoma, are also thought to contribute to hypercoagulability and endothelial risk [19, 22]. The grade, aggressiveness, and cellular-level mechanisms associated with specific histological types of ovarian cancer are thought to influence VTE risk through the upregulation of tissue factor, VIIa, biomarkers, and macrophages [9, 15, 18, 19, 23, 24]. Further, the aggressive surgical and chemotherapy treatment of ovarian cancer likely causes high thrombosis rates [16, 19, 25–27]. Complete cytoreductive surgery, the recommended surgical treatment for ovarian cancer, requires extensive surgical steps involving lymph node sampling, tumor removal, and organ removal [28, 29].

Estimates of the odds of VTE in ovarian cancer patients by common tumor, clinical presentation, and treatment factors have sparsely been reported over the last three decades, most often only including unadjusted odds ratios or raw numbers. The odds of VTEs in ovarian cancer patients by the most frequently discussed tumor, clinical presentation, and treatment factors need to be quantified by meta-analysis in order to further our understanding of VTE hazard in this high-risk population [30]. This meta-analysis of observational studies aims to examine the risk of VTE in ovarian cancer patients by the exposures of advanced stage at diagnosis, serous histology, clear cell carcinoma histology, ascites at diagnosis, and complete cytoreductive surgery.

2. Materials and Methods

2.1. Data Sources and Searches

Human studies published before April 17, 2019, detailing risk factors associated with VTE in ovarian cancer patients were identified from PubMed, Embase, and Cumulative Index to Nursing and Allied Health Literature (CINAHL). Reference lists were reviewed, although this only provided duplicates. The primary index terms used were “ovarian neoplasm,” “carcinoma, ovarian epithelial,” and “venous thromboembolism.” A medical librarian assisted in creating our search strategy (Appendix A). We did not restrict by date; however, the terms were created in the databases in 1974. No studies published prior to 1990 were found. Published conference abstracts were included in our search. Unpublished studies were not sought, and no authors were contacted. Studies were not restricted by language.

2.2. Study Selection

Studies eligible for inclusion met the following criteria: women; exclusively malignant ovarian cancer patients; multiple (>2) histologies represented; all four cancer stages represented; and pulmonary embolisms, deep vein thromboses, a combination of both, or generalized VTEs as an outcome. Only observational studies were included. Studies were excluded if they provided only aggregate results for multiple cancer types, compared ovarian cancer patients to noncancer patients, and investigated an experimental intervention beyond standard of care. Other exclusion criteria included the lack of at least one exposure of interest, the inability to calculate an odds ratio, and spontaneous arterial thrombosis.

The exposures of interest (and the comparator groups) were cancer stage III/IV (cancer stage I/II), serous histology (nonserous histology), clear cell histology (nonclear cell histology), cytoreduction with total removal of the tumor (cytoreduction without total removal of the tumor), and significant ascites of the abdomen at diagnosis (unremarkable ascites of the abdomen). Ascites was defined as any volume measurement cutoff or by the clinical judgement of the physicians in the study.

2.3. Data Abstraction

The variables in the abstraction form included authors, publication year, study location, study design, the number of healthcare centers included, interventions received, anticoagulation, how VTE was diagnosed (whether by presentation with symptoms or screening), time period of study, VTE type, timing of the VTE in the treatment/diagnosis course, the average age of those with and without the outcome, frequencies and/or effect estimates (unadjusted and adjusted), and two-by-two contingency tables for each exposure and the outcome. Abstraction forms were piloted by one reviewer ahead of abstraction.

One investigator determined eligibility of studies. Two investigators independently extracted the data. Each investigator was blinded to the other investigator’s codes. A third investigator reviewed the differences and recorded the number of disagreements. The abstractors reviewed and revised their responses independently. All the remaining disagreements were reconciled by consensus. Each study’s quality was evaluated using the Newcastle-Ottawa risk of bias assessment tool for cohort studies.

2.4. Statistical Analysis

Unadjusted odds ratios and raw numbers were primarily reported in articles; thus, this study pooled unadjusted odds ratios. Pooled odds ratios for VTE in ovarian cancer patients by each exposure were computed using random effects models with inverse-variance weighting. The I² and Cochrane Q tests were used to assess heterogeneity. The potential for publication bias was evaluated using funnel plots. Clear cell carcinoma was the only exposure that had more than one reported multivariable odds ratio. We completed a sensitivity analysis in which we pooled adjusted odds ratio results for clear cell carcinoma (versus other histologies).

Results were stratified by those that diagnosed VTE at least partially by screening asymptomatic patients versus diagnosed only symptomatic patients. If three or more articles within each stratum assessed an exposure, a stratified analysis was conducted. If less than three articles were in each stratum, we conducted a subgroup analysis; this was completed for the serous histology exposure. This stratification scheme was chosen a priori for clinical relevance.

3. Results

3.1. Literature Search and Study Characteristics

There were 733 articles identified in the database search; 106 full-text articles were reviewed, and 20 articles met eligibility criteria (Figure 1) [13–15, 23, 26, 31–47]. The included studies were performed in the following countries: Japan (N = 7), the United States (6), China (2), Italy (2), England (1), Ireland (1), and Germany (1) (Table 1). The majority (16) were single-institution, retrospective cohort studies of moderate quality (Table 2). The earliest period when a patient was diagnosed with ovarian cancer in any study was 1990 and the latest was 2017. There was variability in the proportion of each study population that received anticoagulation, as well as the length, type, and timing of anticoagulation used. Treatment received, method of VTE identification, and the timing of VTE events in relation to treatment and/or diagnosis also varied among studies. The retrospective studies primarily assessed VTE after surgical treatment with or without chemotherapy concurrence. The four prospective studies assessed presurgery VTE events (Table 1).

There were 6,324 ovarian cancer patients included in the main analysis and 769 patients experienced a VTE. It was not possible to calculate an average age across studies because it was not always reported, but most studies estimated a mean age of around 60 years of age. There were three separate instances of overlapping study populations (Sakurai and Satoh, Tateo and Mereu, and Wagner and Mokri). If the overlapping studies evaluated one of the same exposures, the study with the larger sample size was used in that exposure analysis. The smaller study was used when the larger overlapping study did not assess an exposure.

3.2. Meta-Analysis Results

Ovarian cancer patients with cancer stage III/IV at diagnosis had 2.73 times greater pooled odds of having a VTE than patients with ovarian cancer stage I/II at diagnosis (95% confidence interval (CI) 1.84–4.06, number of studies (N) = 15) (Figure 2). Overall, the exposure had moderate-to-high heterogeneity (I² = 64%). Stratified analyses were significantly different (). The publications that diagnosed VTE by screening asymptomatic patients had lower heterogeneity (I² = 35% vs. 55%) than the symptomatic subgroup and a nonsignificant pooled odds ratio (OR 1.23, 95% CI 0.63–2.40, N = 4). The stratum of articles with symptomatic patients had a significantly elevated pooled odds ratio (OR 3.42, 95% CI 2.31–5.06, N = 11).

The overall pooled odds of VTE in ovarian cancer patients with a serous histology were nonsignificant at 1.26 times greater odds of VTE than other histologies (95% CI 0.91–1.75, N = 10) (Figure 3). Heterogeneity overall was moderate (I² = 42%) for serous histology. The subgroup analysis (N = 8, removed Kawaguchi and Sakurai) of articles with VTE diagnosed in symptomatic patients was significant (OR 1.35, 95% CI 1.05–1.72). Subgroup heterogeneity was mildly reduced to I² of 32% (not shown).

The pooled odds of VTE in ovarian cancer patients with a clear cell carcinoma histology were 2.11 (95% CI 1.55–2.89, N = 16) times greater than ovarian cancer patients without that histology (Figure 4). Heterogeneity overall was minimal (I² = 6%). Odds of VTE by clear cell histology were not significantly different between patients diagnosed by screening and by symptomatic presentation (), and both had odds ratios significantly greater than one. The pooled odds ratio for the articles with asymptomatic VTE diagnoses was 3.28 (95% CI 1.54–6.98), while it was 1.70 (95% CI 1.18–2.46) for the articles with symptomatic diagnoses. The clear cell carcinoma stratum with subclinical diagnosis (N = 5) had greater heterogeneity (I² = 48% vs. 0%) than the symptomatic stratum (N = 11). The sensitivity analysis using only multivariable odds ratios found elevated risk, with clear cell carcinoma having 6.29 times greater odds of VTE than other histologies (95% CI 3.08–12.85, N = 4).

There was no significant difference in the odds of VTE related to whether the patient had complete tumor removal with cytoreductive surgery (OR 1.05, 95% CI 0.27–4.11, N = 5) versus did not have total tumor removal (Figure 5). Substantial heterogeneity was present (I² = 88%).

Ovarian cancer patients with ascites at diagnosis had 2.12 (95% CI 1.51–2.96, N = 8, I² = 32%) times greater odds of having a VTE than patients without ascites at diagnosis (Figure 6). Within publications with subclinical VTE diagnoses, there was low-to-moderate heterogeneity and a nonsignificant pooled odds ratio (OR 1.56, 95% CI 0.73–3.34, N = 3, I² = 35%). The publications with symptomatic VTEs had low-to-moderate heterogeneity and a significantly elevated pooled odds ratio (2.33, 95% CI 1.61–3.37, N = 5, I² = 34%).

3.3. Publication Bias

All funnel plots showed mild asymmetry, meaning publication bias could not be ruled out (Supplemental Figure 1).

4. Discussion

The results of this meta-analysis suggest that advanced cancer stage, clear cell carcinoma histology, and ascites at diagnosis are significant risk factors for VTE events in ovarian cancer patients. The odds ratios for advanced cancer stage and ascites at diagnosis were significant overall and for publications where only symptomatic patients were diagnosed with VTE. It is possible that the results of asymptomatic patients were limited by the few studies available or represent a racial difference as these results were all from Japan. Given that the asymptomatic stratums had uneven distributions in their funnel plots, it is possible that publication bias could have contributed to the limited number of studies. Finally, these results may suggest that advanced cancer stage and ascites at diagnosis increase the odds of severe VTEs that cause symptoms, such as pain, swelling, and dyspnea versus the odds of all coagulopathy.

Histologically, clear cell carcinoma significantly increased the odds of VTE in both publications that diagnosed VTE in asymptomatic patients and symptomatic patients. This finding has been supported by cellular-level mechanism studies of genes, tissues factors, and inflammatory activation [48–52]. The moderate-to-high heterogeneity seen among the subclinical stratum may have been caused by variability in ultrasound technician skills, equipment used, patient population BMI differences, or study quality. Given the large number of studies and the absence of heterogeneity among publications, it is likely that across various countries, treatments, and patient populations, clear cell carcinoma histology increases the odds of VTE in ovarian cancer patients. Finally, our sensitivity analysis suggests that the true independent odds of VTE attributed to clear cell carcinoma are likely even greater than the pooled bivariate results.

There was no significant difference in the overall pooled odds of VTE related to serous histology. This aligns with prior literature [33, 35]. There may be no association between serous histology and VTE risk. The significant finding for symptomatic patients may be due to confounding by stage at diagnosis [53]. Serous histology has the highest likelihood of being diagnosed at a distant stage and the lowest likelihood of being diagnosed at a local stage compared to other epithelial histologies and nonepithelial histologies [53]. A multivariable analysis assessing the risk of VTE for women with serous histology cancers would be helpful.

There was no significant difference in the pooled odds of VTE associated with receipt of complete cytoreduction. There was a high degree of heterogeneity between the pooled studies. Variability in postoperative anticoagulation, lengths of surgeries, and hospitalization rates/lengths could have affected the magnitude of the effect detected. The insignificant results may be due to a lack of association between complete cytoreduction and VTE. However, they may also be due to study limitations, including a small number of studies investigating this exposure, the use of unadjusted odds ratios, large heterogeneity between studies, and likely publication bias. Future studies are needed investigating this relationship that control for treatment differences, tumor factors, and hospital care variables.

This meta-analysis includes studies of moderate quality. The strengths of the studies included in this meta-analysis were that they independently linked their outcome to exposures through medical records and included many countries (with diverse racial/ethnic compositions), years of diagnosis, and treatment methods. The major limitations of the studies included are the temporality of the exposures and outcome, limited generalizability, and failure to control for residual confounding. Only five studies screened patients to ensure they did not have VTEs prior to the period of outcome assessment and/or excluded persons with medical conditions, falls, or surgeries that would have independently caused VTEs prior to diagnosis. Moving forward, a prospective, multicenter cohort study that screens for VTEs with questionnaires or ultrasounds at time of diagnosis could be useful. The majority of the included studies were performed at a single tertiary institution or academic teaching center. These findings may not be applicable to patients in a community hospital population or a true community population. The majority of results presented by the studies in this meta-analysis are bivariate, unadjusted results. Comprehensive patient, tumor, and clinical treatment/intervention variables, including chemotherapy variables, need to be collected and analyzed independent of other exposures in a multivariable analysis.

Our results quantify the difference in pooled odds of VTE in ovarian cancer patients by the most commonly reported exposures. An estimated 5%–25% of ovarian cancer patients will have a VTE within the first two years after their cancer diagnosis [13, 17, 54, 55]. These women will likely have lower survival rates than their counterparts without VTEs [13, 17, 54, 55]. There is a critical and urgent need to investigate the clinically relevant VTE risk factors of ovarian cancer patients in order to compile a comprehensive understanding of which ovarian cancer patients are most at risk of VTEs. These findings need to be translated into clinical decision-making tools that can improve the timeliness of detection of VTEs and subsequently reduce the risk of thrombosis-related mortality in this vulnerable population. Furthermore, these findings need to be translated into anticoagulation decision-making tools for pre- and postoperative ovarian cancer patients. The most commonly used anticoagulation risk assessment tools for ovarian cancer patients are nonspecific or do not include important variables such as histology [56–62]. Most tools were created for generalized abdominal/pelvic surgery or oncology patients [56–59, 61]. Risk assessment tools specific to ovarian cancer patients that have ascites at diagnosis, stage at diagnosis, and histology of tumor may be useful [62, 63]. In the meantime, robust multidisciplinary team efforts should consider the benefits and risks of various pre- and postoperative anticoagulation regimens [19].

5. Conclusions

Advanced cancer stage, clear cell carcinoma, and ascites at diagnosis significantly increased the pooled odds of VTE in ovarian cancer patients. Further studies are needed to account for confounders and inform clinical decision-making tools and anticoagulation recommendations. The possibility of publication bias could not be excluded as a limitation of this meta-analysis.

Appendix

A. Database Search Terms Used without Explosion of Mesh Terms

PubMed search: 546 results on 4/17/19 ((((“Ovarian Neoplasms”[Mesh:noexp]) OR “Carcinoma, Ovarian Epithelial”[Mesh])) OR (“ovarian cancer” OR “ovarian cancers” OR “ovarian neoplasm” OR “ovarian neoplasms” OR “ovary neoplasm” OR “ovary neoplasms” OR “ovary cancer” OR “ovary cancers” OR “cancer of the ovary” OR “cancer of ovary”)) AND ((((“venous thrombosis” OR “venous thromboses” OR “deep vein thrombosis” OR “deep vein thromboses” OR “deep-venous thrombosis” OR “deep-venous thromboses” OR “deep venous thrombosis” OR “deep venous thromboses”)) OR (“venous thromboembolism” OR “pulmonary embolism” OR “pulmonary embolisms” OR “pulmonary thromboembolisms” OR “pulmonary thromboembolism”)) OR (((((“Venous Thromboembolism”[Mesh]) OR “Pulmonary Embolism”[Mesh:noexp]) OR “Embolism”[Mesh:noexp]) OR “Thromboembolism”[Mesh]) OR “Thrombosis”[Mesh])) Embase search: 87 results on 4/17/19 (((((((“ovary”/exp OR ovary) AND (“cancer”/exp OR cancer) OR cancer) AND (“ovary”/exp OR ovary) OR malignant) AND (“ovary”/exp OR ovary) AND (“tumor”/exp OR tumor) OR malignant) AND (“ovary”/exp OR ovary) AND (“tumour”/exp OR tumour) OR ovarial) AND (“cancer”/exp OR cancer) OR ovarian) AND (“cancer”/exp OR cancer) OR “ovarium”/exp OR ovarium) AND (“cancer”/exp OR cancer) AND (((((((venous AND (“thromboembolism”/exp OR thromboembolism) OR thromboembolism) AND venous OR “vein”/exp OR vein) AND (“thromboembolism”/exp OR thromboembolism) OR deep) AND (“vein”/exp OR vein) AND (“thrombosis”/exp OR thrombosis) OR lower) AND (“extremity”/exp OR extremity) AND deep AND (“vein”/exp OR vein) AND (“thrombosis”/exp OR thrombosis) OR “lung”/exp OR lung) AND (“embolism”/exp OR embolism) OR upper) AND (“extremity”/exp OR extremity) AND deep AND (“vein”/exp OR vein) AND (“thrombosis”/exp OR thrombosis) OR lower) AND (“extremity”/exp OR extremity) AND deep AND (“vein”/exp OR vein) AND (“thrombosis”/exp OR thrombosis) CINAHL: 100 results on 4/17/19 (venous thromboembolism OR deep vein thrombosis OR deep vein thrombosis OR deep venous thrombosis OR deep-venous thromboses OR pulmonary embolism OR pulmonary thromboembolism) AND (ovarian cancer OR ovarian cancer OR ovary cancer OR ovarian neoplasm OR carcinoma, ovarian epithelial OR cancer of the ovary OR cancer of ovary).

Data Availability

Appendix A should be referenced to obtain all the underlying data supporting the results.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

The authors would like to thank Kurayi Mahachi (MPH), Dinesh Voruganti (MD, MPH), and Heather Healy (MA, MLS) for their contributions to this manuscript. The authors acknowledge the National Institute of Health for their funding of the University of Iowa Medical Scientist Training Program (NIH T32GM007337).

Supplementary Materials

Supplemental Figure 1: funnel plots of all included exposures. This figure shows the funnel plots for all exposures. There is mild asymmetry indicating publication bias cannot be ruled out. (Supplementary Materials)

References

S. Ikushima, R. Ono, K. Fukuda, M. Sakayori, N. Awano, and K. Kondo, “Trousseau’s syndrome: cancer-associated thrombosis,” Japanese Journal of Clinical Oncology, vol. 46, no. 3, pp. 204–208, 2016.
View at: Publisher Site | Google Scholar
E. Donnellan and A. A. Khorana, “Cancer and venous thromboembolic disease: a review,” The Oncologist, vol. 22, no. 2, pp. 199–207, 2017.
View at: Publisher Site | Google Scholar
A. Graul, N. Latif, X. Zhang et al., “Incidence of venous thromboembolism by type of gynecologic malignancy and surgical modality in the national surgical quality improvement Program,” International Journal of Gynecological Cancer, vol. 27, no. 3, pp. 581–587, 2017.
View at: Publisher Site | Google Scholar
R. A. Sheth, A. Niekamp, K. B. Quencer et al., “Thrombosis in cancer patients: etiology, incidence, and management,” Cardiovascular Diagnosis and Therapy, vol. 7, no. S3, pp. S178–S185, 2017.
View at: Publisher Site | Google Scholar
T. Wun and R. H. White, “Epidemiology of cancer-related venous thromboembolism,” Best Practice & Research Clinical Haematology, vol. 22, no. 1, pp. 9–23, 2009.
View at: Publisher Site | Google Scholar
L. A. Norris, F. A. Martin, S. A. O’Toole, F. A. Saadeh, and N. Gleeson, “PO-24-determinants of thrombin generation in gynaecological malignancies,” Thrombosis Research, vol. 140, p. S185, 2016.
View at: Publisher Site | Google Scholar
R. L. Metcalf, D. J. Fry, R. Swindell et al., “Thrombosis in ovarian cancer: a case control study,” British Journal of Cancer, vol. 110, no. 5, pp. 1118–1124, 2014.
View at: Publisher Site | Google Scholar
Y. Hisada and N. Mackman, “Cancer-associated pathways and biomarkers of venous thrombosis,” Blood, vol. 130, no. 13, pp. 1499–1506, 2017.
View at: Publisher Site | Google Scholar
N. Yokota, S. Koizume, E. Miyagi et al., “Self-production of tissue factor-coagulation factor VII complex by ovarian cancer cells,” British Journal of Cancer, vol. 101, no. 12, pp. 2023–2029, 2009.
View at: Publisher Site | Google Scholar
N. Levitan, A. Dowlati, S. C. Remick et al., “Rates of initial and recurrent thromboembolic disease among patients with malignancy versus those without malignancy: risk analysis using medicare claims data,” Medicine, vol. 78, no. 5, pp. 285–291, 1999.
View at: Publisher Site | Google Scholar
W. Ghanima, H. S. Wik, M. Tavoly, T. Enden, and L.-P. Jelsness-Jørgensen, “Late consequences of venous thromboembolism: measuring quality of life after deep vein thrombosis and pulmonary embolism,” Thrombosis Research, vol. 164, pp. 170–176, 2018.
View at: Publisher Site | Google Scholar
I. M. van Korlaar, C. Y. Vossen, F. R. Rosendaal et al., “The impact of venous thrombosis on quality of life,” Thrombosis Research, vol. 114, no. 1, pp. 11–18, 2004.
View at: Publisher Site | Google Scholar
A. Bakhru, “Effect of ovarian tumor characteristics on venous thromboembolic risk,” Journal of Gynecologic Oncology, vol. 24, no. 1, pp. 52–58, 2013.
View at: Publisher Site | Google Scholar
Y. Ebina, M. Uchiyama, H. Imafuku, K. Suzuki, Y. Miyahara, and H. Yamada, “Risk factors for deep venous thrombosis in women with ovarian cancer,” Medicine, vol. 97, no. 23, p. e11009, 2018.
View at: Publisher Site | Google Scholar
W. Zhang, X. Liu, H. Cheng, Z. Yang, and G. Zhang, “Risk factors and treatment of venous thromboembolism in perioperative patients with ovarian cancer in China,” Medicine, vol. 97, no. 31, 2018.
View at: Publisher Site | Google Scholar
M. B. Streiff, “Association between cancer types, cancer treatments, and venous thromboembolism in medical oncology patients,” Clinical Advances in Hematology & Oncology: H&O, vol. 11, no. 6, pp. 349–357, 2013.
View at: Google Scholar
M. S. Tetsche, M. Nørgaard, L. Pedersen, T. L. Lash, and H. T. Sørensen, “Prognosis of ovarian cancer subsequent to venous thromboembolism: a nationwide Danish cohort study,” BMC Cancer, vol. 6, no. 1, p. 189, 2006.
View at: Publisher Site | Google Scholar
Surveillance E, and end results (SEER) Program, SEER∗Stat Database: Incidence-SEER 9 Regs Research Data, Nov 2018 Sub (1975–2016) <Katrina/Rita Population Adjustment>-Linked to County Attributes-Total U.S., 1969–2017 Counties, National Cancer Institute, Bethesda, MD, USA, 2019, http://www.seer.cancer.gov.
A. Cohen, C. S. Lim, and A. H. Davies, “Venous thromboembolism in gynecological malignancy,” International Journal of Gynecologic Cancer, vol. 27, no. 9, pp. 1970–1978, 2017.
View at: Publisher Site | Google Scholar
T.-F. Wang, A. Li, and D. Garcia, “Managing thrombosis in cancer patients,” Research and Practice in Thrombosis and Haemostasis, vol. 2, no. 3, pp. 429–438, 2018.
View at: Publisher Site | Google Scholar
A. N. Davis, V. Afshar-Kharghan, and A. K. Sood, “Platelet effects on ovarian cancer,” Seminars in Oncology, vol. 41, no. 3, pp. 378–384, 2014.
View at: Publisher Site | Google Scholar
Z. Ma, T. Zhang, R. Wang et al., “Tissue factor-factor VIIa complex induces epithelial ovarian cancer cell invasion and metastasis through a monocytes-dependent mechanism,” International Journal of Gynecologic Cancer, vol. 21, no. 4, pp. 616–624, 2011.
View at: Publisher Site | Google Scholar
T. Satoh, A. Oki, K. Uno et al., “High incidence of silent venous thromboembolism before treatment in ovarian cancer,” British Journal of Cancer, vol. 97, no. 8, pp. 1053–1057, 2007.
View at: Publisher Site | Google Scholar
C. Ay, I. Pabinger, and A. T. Cohen, “Cancer-associated venous thromboembolism: burden, mechanisms, and management,” Thrombosis and Haemostasis, vol. 117, no. 2, pp. 219–230, 2017.
View at: Publisher Site | Google Scholar
M. M. Piróg, R. Jach, and A. Undas, “Thromboprophylaxis in women undergoing gynecological surgery or assisted reproductive techniques: new advances and challenges,” Ginekologia Polska, vol. 87, no. 11, pp. 773–779, 2016.
View at: Publisher Site | Google Scholar
F. A. Saadeh, L. Norris, S. O’Toole, and N. Gleeson, “Venous thromboembolism in ovarian cancer: incidence, risk factors and impact on survival,” European Journal of Obstetrics & Gynecology and Reproductive Biology, vol. 170, no. 1, pp. 214–218, 2013.
View at: Publisher Site | Google Scholar
A. Pant, D. Liu, J. Schink, and J. Lurain, “Venous thromboembolism in advanced ovarian cancer patients undergoing frontline adjuvant chemotherapy,” International Journal of Gynecologic Cancer, vol. 24, no. 6, pp. 997–1002, 2014.
View at: Publisher Site | Google Scholar
I. Ray-Coquard, P. Morice, D. Lorusso et al., “Non-epithelial ovarian cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up,” Annals of Oncology, vol. 29, no. 4, pp. iv1–iv18, 2018.
View at: Publisher Site | Google Scholar
N. Bacalbasa, S. Dima, I. Balescu, L. David, V. Brasoveanu, and I. Popescu, “Results of primary cytoreductive surgery in advanced-stage epithelial ovarian cancer: a single-center experience,” Anticancer Research, vol. 35, no. 7, pp. 4099–4104, 2015.
View at: Google Scholar
G. H. Lyman, A. A. Khorana, A. Falanga et al., “American Society of Clinical Oncology guideline: recommendations for venous thromboembolism prophylaxis and treatment in patients with cancer,” Journal of Clinical Oncology, vol. 25, no. 34, pp. 5490–5505, 2007.
View at: Publisher Site | Google Scholar
L. R. Duska, L. Garrett, M. Henretta, J. S. Ferriss, L. Lee, and N. Horowitz, “When “never-events” occur despite adherence to clinical guidelines: the case of venous thromboembolism in clear cell cancer of the ovary compared with other epithelial histologic subtypes,” Gynecologic Oncology, vol. 116, no. 3, pp. 374–377, 2010.
View at: Publisher Site | Google Scholar
S. Tateo, L. Mereu, S. Salamano et al., “Ovarian cancer and venous thromboembolic risk,” Gynecologic Oncology, vol. 99, no. 1, pp. 119–125, 2005.
View at: Publisher Site | Google Scholar
X. Wu, X. Xue, J. Tang et al., “Evaluation of risk factors for venous thromboembolism in Chinese women with epithelial ovarian cancer,” International Journal of Gynecologic Cancer, vol. 23, no. 1, pp. 65–72, 2013.
View at: Publisher Site | Google Scholar
M. Sakurai, K. Matsumoto, M. Gosho et al., “Expression of tissue factor in epithelial ovarian carcinoma is involved in the development of venous thromboembolism,” International Journal of Gynecologic Cancer, vol. 27, no. 1, pp. 37–43, 2017.
View at: Publisher Site | Google Scholar
B. Mokri, A. Mariani, J. A. Heit et al., “Incidence and predictors of venous thromboembolism after debulking surgery for epithelial ovarian cancer,” International Journal of Gynecologic Cancer, vol. 23, no. 9, pp. 1684–1691, 2013.
View at: Publisher Site | Google Scholar
L. Mereu, S. Tateo, C. Klersy, E. Martinotti Gabellotti, and F. Polatti, “Stratification of venous thromboembolism risk in ovarian cancer patients during chemotherapy,” International Journal of Gynecologic Cancer, vol. 19, no. 1, pp. 79–83, 2009.
View at: Publisher Site | Google Scholar
O. M. Heath, H. J. van Beekhuizen, V. Nama et al., “Venous thromboembolism at time of diagnosis of ovarian cancer: survival differs in symptomatic and asymptomatic cases,” Thrombosis Research, vol. 137, pp. 30–35, 2016.
View at: Publisher Site | Google Scholar
C. C. Gunderson, E. D. Thomas, K. N. Slaughter et al., “The survival detriment of venous thromboembolism with epithelial ovarian cancer,” Gynecologic Oncology, vol. 134, no. 1, pp. 73–77, 2014.
View at: Publisher Site | Google Scholar
D. Black, A. Iasonos, H. Ahmed, D. Chi, R. Barakat, and N. Aburustum, “Effect of perioperative venous thromboembolism on survival in ovarian, primary peritoneal, and fallopian tube cancer,” Gynecologic Oncology, vol. 107, no. 1, pp. 66–70, 2007.
View at: Publisher Site | Google Scholar
N. Suzuki, N. Yoshioka, T. Ohara et al., “Risk factors for perioperative venous thromboembolism: a retrospective study in Japanese women with gynecologic diseases,” Thrombosis Journal, vol. 8, no. 1, p. 17, 2010.
View at: Publisher Site | Google Scholar
J. Kodama, N. Seki, C. Fukushima et al., “Elevated preoperative plasma D-dimer levels and the incidence of venous thromboembolism in Japanese females with gynecological cancer,” Oncology Letters, vol. 5, no. 1, pp. 299–304, 2013.
View at: Publisher Site | Google Scholar
R. Kawaguchi, N. Furukawa, and H. Kobayashi, “Cut-off value of D-dimer for prediction of deep venous thrombosis before treatment in ovarian cancer,” Journal of Gynecologic Oncology, vol. 23, no. 2, pp. 98–102, 2012.
View at: Publisher Site | Google Scholar
C. Fotopoulou, A. Karavas, R. Trappe, R. Chekerov, W. Lichtenegger, and J. Sehouli, “Venous thromboembolism in recurrent ovarian cancer-patients: a systematic evaluation of the north-eastern German society of gynaecologic oncology ovarian cancer study group (NOGGO),” Thrombosis Research, vol. 124, no. 5, pp. 531–535, 2009.
View at: Publisher Site | Google Scholar
D. M. Chavan, Z. Huang, K. Song et al., “Incidence of venous thromboembolism following the neoadjuvant chemotherapy regimen for epithelial type of ovarian cancer,” Medicine, vol. 96, no. 42, Article ID e7935, 2017.
View at: Publisher Site | Google Scholar
P. S. Greco, A. A. Bazzi, K. McLean et al., “Incidence and timing of thromboembolic events in patients with ovarian cancer undergoing neoadjuvant chemotherapy,” Obstetrics & Gynecology, vol. 129, no. 6, pp. 979–985, 2017.
View at: Publisher Site | Google Scholar
B. E. Wagner, C. L. Langstraat, M. E. McGree et al., “Beyond prophylaxis: extended risk of venous thromboembolism following primary debulking surgery for ovarian cancer,” Gynecologic Oncology, vol. 152, no. 2, pp. 286–292, 2019.
View at: Publisher Site | Google Scholar
K. Uno, S. Homma, T. Satoh et al., “Tissue factor expression as a possible determinant of thromboembolism in ovarian cancer,” British Journal of Cancer, vol. 96, no. 2, pp. 290–295, 2007.
View at: Publisher Site | Google Scholar
F. Abu Saadeh, L. Norris, S. O’Toole et al., “Tumour expresion of tissue factor and tissue factor pathway inhibitor in ovarian cancer- relationship with venous thrombosis risk,” Thrombosis Research, vol. 132, no. 5, pp. 627–634, 2013.
View at: Publisher Site | Google Scholar
S. Koizume, S. Ito, Y. Yoshioka et al., “High-level secretion of tissue factor-rich extracellular vesicles from ovarian cancer cells mediated by filamin-A and protease-activated receptors,” Thrombosis and Haemostasis, vol. 115, no. 2, pp. 299–310, 2016.
View at: Publisher Site | Google Scholar
S. Koizume, T. Takahashi, M. Yoshihara et al., “Cholesterol starvation and hypoxia activate the FVII gene via the SREBP1-GILZ pathway in ovarian cancer cells to produce procoagulant microvesicles,” Thrombosis and Haemostasis, vol. 119, no. 7, pp. 1058–1071, 2019.
View at: Publisher Site | Google Scholar
J. Cuff, K. Salari, N. Clarke et al., “Integrative bioinformatics links HNF1B with clear cell carcinoma and tumor-associated thrombosis,” PLoS One, vol. 8, no. 9, Article ID e74562, 2013.
View at: Publisher Site | Google Scholar
J. G. Cohen, E. Prendergast, J. E. Geddings et al., “Evaluation of venous thrombosis and tissue factor in epithelial ovarian cancer,” Gynecologic Oncology, vol. 146, no. 1, pp. 146–152, 2017.
View at: Publisher Site | Google Scholar
A. C. Society, Special Section: Ovarian Cancer. Cancer Facts & Figures 2018, American Cancer Society, Atlanta, GA, USA, 2018.
E. H. Shinn, D. J. Lenihan, D. L. Urbauer et al., “Impact of cardiovascular comorbidity on ovarian cancer mortality,” Cancer Epidemiology Biomarkers & Prevention, vol. 22, no. 11, pp. 2102–2109, 2013.
View at: Publisher Site | Google Scholar
A. O. Rodriguez, T. Wun, H. Chew, H. Zhou, D. Harvey, and R. H. White, “Venous thromboembolism in ovarian cancer,” Gynecologic Oncology, vol. 105, no. 3, pp. 784–790, 2007.
View at: Publisher Site | Google Scholar
J. A. Caprini, “Thrombosis risk assessment as a guide to quality patient care,” Disease-a-Month, vol. 51, no. 2-3, pp. 70–78, 2005.
View at: Publisher Site | Google Scholar
J. A. Caprini, J. I. Arcelus, and J. e. J. Reyna, “Effective risk stratification of surgical and nonsurgical patients for venous thromboembolic disease,” Seminars in Hematology, vol. 38, no. 5, pp. 12–19, 2001.
View at: Publisher Site | Google Scholar
E. A. Akl, I. Terrenato, M. Barba, F. Sperati, P. Muti, and H. J. Schünemann, “Extended perioperative thromboprophylaxis in patients with cancer. A systematic review,” Thrombosis and Haemostasis, vol. 100, no. 6, pp. 1176–1180, 2008.
View at: Publisher Site | Google Scholar
M. H. Einstein, E. A. Pritts, and E. M. Hartenbach, “Venous thromboembolism prevention in gynecologic cancer surgery: a systematic review,” Gynecologic Oncology, vol. 105, no. 3, pp. 813–819, 2007.
View at: Publisher Site | Google Scholar
W. Stroud, J. M. Whitworth, M. Miklic et al., “Validation of a venous thromboembolism risk assessment model in gynecologic oncology,” Gynecologic Oncology, vol. 134, no. 1, pp. 160–163, 2014.
View at: Publisher Site | Google Scholar
A. Kuk, M. Magnowska, W. Suchy et al., “Retrospective evaluation of thromboembolism risk in ovarian cancer patients treated with bevacizumab,” Targeted Oncology, vol. 12, no. 4, pp. 495–503, 2017.
View at: Publisher Site | Google Scholar
G. T. Gerotziafas, A. Taher, H. Abdel-Razeq et al., “A predictive score for thrombosis associated with breast, colorectal, lung, or ovarian cancer: the prospective COMPASS-cancer-associated thrombosis study,” The Oncologist, vol. 22, no. 10, pp. 1222–1231, 2017.
View at: Publisher Site | Google Scholar
E. L. Barber and D. L. Clarke-Pearson, “The limited utility of currently available venous thromboembolism risk assessment tools in gynecological oncology patients,” American Journal of Obstetrics and Gynecology, vol. 215, no. 4, pp. 445–449, 2016.
View at: Publisher Site | Google Scholar

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Copyright © 2020 Kristin S. Weeks et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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