Logo Medical Science Monitor

Call: +1.631.470.9640
Mon - Fri 10:00 am - 02:00 pm EST

Contact Us

Logo Medical Science Monitor Logo Medical Science Monitor Logo Medical Science Monitor

16 December 2015: Clinical Research  

Correlation Between Platelet and Hemoglobin Levels and Pathological Characteristics and Prognosis of Early-Stage Squamous Cervical Carcinoma

Xiaowei Li ABC , Cheng Tan BC , Wanxuan Zhang DE , Jingyi Zhou AC , Zhiqi Wang DF , Shijun Wang EF , Jianliu Wang ACD , Lihui Wei CE

DOI: 10.12659/MSM.895016

Med Sci Monit 2015; 21:3921-3928

0 Comments

Abstract

BACKGROUND: We sought to determine the effect of pre-operative hemoglobin (HGB) and platelet (PLT) levels on the clinical features and prognosis of early-stage squamous cervical carcinoma (SCC).

MATERIAL AND METHODS: We performed a retrospective analysis of 380 patients with SCC who underwent hysterectomy and pelvic lymphadenectomy. SCC was confirmed post-operatively by pathological diagnosis. The relations between HGB and PLT levels and clinicopathological characteristics were observed, and a Cox regression analysis was performed to determine their influence on survival.

RESULTS: There were significant differences in tumor staging, tumor diameter, and lymphatic metastasis between the 69 patients with PLT levels >300×109/L and the 311 patients with PLT levels ≤300×109/L (P<0.05). Tumor staging, extent of differentiation, and lymphatic metastasis were significantly different between 134 patients with HGB levels <120 g/L and 246 patients with HGB levels ≥120 g/L (P<0.05). The overall survival rate in the group with PLT levels >300×109/L was lower than that in the group with PLT levels ≤300 × 109/L, but this difference was not significant. The overall survival rate in the group with HGB levels <120 g/L was significantly lower than that in the group with HGB levels ≥120 g/L (P<0.05), and the overall survival rate in the group with PLT levels >300×109/L and HGB levels <120 g/L was significantly lower than that in the group with PLT levels ≤300×109/L and HGB levels ≤120 g/L (P<0.05). According to Cox regression analysis, a pre-operative HGB level <120 g/L was considered a separate risk factor affecting prognosis.

CONCLUSIONS: Close attention must be paid to pre-operative PLT and HGB levels, and anemia should be remedied to facilitate the treatment of cervical carcinoma.

Keywords: Carcinoma, Squamous Cell - surgery, Hemoglobins - analysis, Lymph Node Excision, Platelet Count, Uterine Cervical Neoplasms - surgery

Background

Thrombocytosis and anemia are 2 factors adversely affecting prognosis for patients with malignant cervical tumors [1–4]. Thrombocytosis in patients with malignant tumors may be related to the invasion and metastasis of the tumor and can produce a series of biological responses related to thrombocytosis [1,5]. Most patients with malignant tumors have anemia primarily because of variations in iron metabolism due to the insufficiency of endogenous hematopoietin and blood loss. Anemia and hypoxemia can enhance angiopoiesis, promote tumor cell proliferation and metastasis, reduce the response of tumor cells to apoptotic cell signals, and influence curative effects [6].

A host of current, related studies have focused on the relations among platelet (PLT) or hemoglobin (HGB) level, the curative effects of cervical carcinoma treatment, and prognosis, with particular focus on advanced cervical carcinoma [1,7–9]. However, there have been few studies focusing on the relations among combined PLT-HGB levels, clinical features, and prognosis of early-stage cervical carcinoma [10]. Here, we aimed to study the relations between pre-operative PLT and HGB levels and the clinical features and prognosis of patients with early-stage squamous cervical carcinoma (SCC).

Material and Methods

GENERAL DATA:

We carried out a retrospective analysis of 380 patients with SCC treated from June 2000 to July 2013. This study was conducted in accordance with the Declaration of Helsinki. This study was conducted with approval from the Ethics Committee of Peking University People’s Hospital. Written informed consent was obtained from all participants before the operation. All patients underwent radical hysterectomy with pelvic lymphadenectomy, and SCC was verified by post-operative pathological diagnosis. Tumor staging was based on the 2009 International Federation of Gynecology and Obstetrics (FIGO) staging system. We retrospectively reviewed pre-operative HGB and PLT levels, age, tumor stage, tumor differentiation, lymphatic metastasis, depth of tumor invasion into the cervical mesenchyme, parametrial metastasis, vessel infiltration, and tumor size. No patient had acute or chronic liver or kidney injury, bleeding, thromboembolic disease, heart disease, or other infectious diseases. Those who took anticoagulant or coagulant drugs within the preceding month or with a previous history of malignant tumor, radiotherapy, chemotherapy, or immunological therapy were excluded. All patients were followed for 12 to 175 months, with a median follow-up period of 62 months and a lost-to-follow-up rate of 3.4%.

STATISTICAL METHODS:

SPSS 16.0 (SPSS Inc., Chicago, IL, USA) was used for data processing. All tests were 2-sided, with significance set at p<0.05. The measurement data are presented as means ± standard deviation, and inter-group comparisons were performed with the Student’s t-test. Enumerated data are presented as cases (constituent ratio), and inter-group comparisons were performed with the Pearson chi-squared test or Fisher exact test. The log-rank test was used for the single-factor analysis of the influence of pre-operative PLT, HGB, and combined PLT-HGB levels on the post-operative long-term survival of patients, and the Kaplan-Meier method was used to determine survival curves. Cox regression analysis of pre-operative PLT and HGB levels on the post-operative long-term survival of patients with SCC was also performed.

CLINICAL GROUPING:

Patients with PLT levels >300×109/L were classified as having thrombocytosis [11], and patients were divided into 2 groups based on this PLT level for comparison of clinical features and 5-year survival rates. Patients with HGB levels <120 g/L were classified as having anemia, and patients were divided into 2 groups based on this HGB level for comparison of clinical features and 5-year survival rates. Based on the survival analysis, the effects of PLT, HGB, and combined PLT-HGB levels on the prognosis of cervical carcinoma were then evaluated.

Results

RELATIONS BETWEEN PLT LEVEL AND THE CLINICAL FEATURES OF CERVICAL CARCINOMA:

Patients with PLT levels >300×109/L accounted for 18.2% (69/380) of the study group, and, compared with patients with PLT levels ≤300×109/L, had a more advanced tumor stage (P<0.05), larger tumor size (P<0.05), and higher incidence of positive lymph node (P<0.05). There was no statistical difference between these 2 groups in terms of age, extent of differentiation, depth of cervical invasion, existence of cancer embolus in the vessel, parametrial positivity, or 5-year survival rate (Table 1).

RELATIONS BETWEEN HGB LEVEL AND CLINICAL FEATURES OF CERVICAL CARCINOMA:

There were 134 patients with HGB levels <120 g/L. Compared with patients with HGB levels ≥120 g/L, they had a more advanced tumor stage (P<0.05), worse differentiation (P<0.05), higher incidence of positive lymph node (P<0.05), and a higher 5-year survival rate (P<0.05). There were no statistical differences between these 2 groups in terms of age, depth of cervical invasion, existence of cancer embolus in the vessel, or parametrial positivity (Table 2).

RELATIONS BETWEEN PLT, HGB, AND COMBINED PLT-HGB LEVELS AND OVERALL SURVIVAL RATE:

The log-rank test was performed for the single-factor analysis of the influence of pre-operative PLT, HGB, and combined PLT-HGB levels on the post-operative long-term survival of patients, while the Kaplan-Meier method was used to determine the survival curves. The overall survival rate of the group with PLT levels >300×109/L was lower than that of the group with PLT levels ≤300×109/L (Figure 1), but this difference was not significant. The overall survival rate of the group with HGB levels <120 g/L was significantly lower than that of the group with HGB levels ≥120 g/L (P<0.05) (Figure 2). The overall survival rate of the group with PLT levels >300×109/L and HGB levels <120 g/L was significantly lower than that of the group with PLT levels ≤300×109/L and HGB levels ≥120 g/L (P<0.05) (Figure 3).

RELATIONS BETWEEN PLT AND HGB LEVELS AND CERVICAL CARCINOMA PROGNOSIS:

Cox regression analysis of the factors with the potential to influence prognosis of patients with SCC revealed that age, tumor differentiation, tumor size, lymphatic metastasis, and FIGO stage were the independent risk factors for patients’ survival and that HGB level was a protective factor (Table 3).

RELATIONS BETWEEN COMBINED PLT-HGB LEVEL AND CERVICAL CARCINOMA PROGNOSIS:

The Cox regression analysis with combined PLT-HGB level as a factor influencing tumor prognosis revealed that combined pre-operative anemia and thrombocytosis and pre-operative anemia were independent risk factors for patients’ survival (Table 4).

Discussion

RELATIONS BETWEEN PLT AND HGB LEVELS AND CERVICAL CARCINOMA CLINICAL FEATURES:

According to the literature, patients with thrombocytosis account for 14–38% of all patients with malignant tumors [12]. Malignant cells often produce cytokines and growth factors able to induce platelets, which in turn can secrete growth factors that stimulate cancer cell proliferation, angiogenesis, and distant progression [1,5,13]. Platelets are a rich source of both platelet-derived growth factor, which is a potent mitogen, and thrombospondin, which supports the adhesion of tumor cells to the endothelium through an increased expression of urokinase-type plasminogen activator [5,13]. Hernandez et al. [1] performed an analysis of 294 patients with stage IIB–IVA cervical carcinoma who had no aortic lymph node metastasis and did not undergo standard radiotherapy or chemotherapy with hydroxyurea or misonidazole. Compared with the patients with normal PLT levels, the patients with thrombocytosis had tumors with a greater volume and were more likely to have bilateral parametrial infiltration, tumors fixed to the pelvic wall, and positive cavum pelvis lymph nodes. Zhao’s [14] research on the influence of PLT level on early-stage cervical carcinoma showed that 25.5% of patients had thrombocytosis; thrombocytosis had positive correlations with tumor staging, tumor size, and tumor recurrence rate; and thrombocytosis tended to occur among patients with advanced cervical carcinoma. Thus, there appears to be a negative correlation between thrombocytosis and tumor characteristics [15,16].

In this study, 18.1% of patients had pre-operative thrombocytosis, in line with the rate reported in the literature. Our results show that a higher PLT level is associated with later clinical stages, greater tumor volume, and a higher positive lymph node rate; however, thrombocytosis was not significantly associated with 5-year survival rate, perhaps related to unmeasured difference in the patients, as well as the sample size. This non-significant result is in contrast to results from the study noted above.

For patients with cervical carcinoma, anemia can directly influence the effects of radiotherapy [3]. About 30% of patients with cervical carcinoma have pre-operative anemia [17]. In this study, 35.3% of patients had pre-operative anemia. The present research showed that such actions as blood transfusion prior to the operation would not improve the prognosis for patients with cervical carcinoma, indicating that the tumor has a highly invasive nature among patients with anemia, and may imply poor prognosis. Therefore, anemia may indicate high tumor risk [18].

RELATIONS BETWEEN PLT AND HGB LEVELS AND SURVIVAL OF CERVICAL CARCINOMA:

A meta-analysis by Yu et al. showed that 12 out of 14 studies confirmed a negative correlation between thrombocytosis and the 5-year survival rate [7]. The results of Hernandez et al. [1] showed that, among patients with advanced cervical carcinoma with negative cavum pelvis lymph nodes, there was a negative correlation between thrombocytosis and survival rate. In contrast, a study by Gadducci et al. [8] showed that pre-operative PLT and HGB levels were unrelated to the 5-year survival rate of the patients. Shin’s [19] research showed that patients with anemia had a lower survival rate compared with that of patients without anemia, but the difference was not significant. The present study indicated that pre-operative HGB level was significantly correlated with the overall survival rate, although there was no significant association between pre-operative PLT level and overall survival, despite the fact that the overall survival was lower for the group with PLT levels >300×109/L compared with that for the group with PLT levels ≤300×109/L. We found that overall survival for the group with both PLT levels >300×109/L and HGB levels <120 g/L was significantly lower than that for the group with both PLT levels ≤300×109/L and HGB levels ≥120 g/L (P<0.05). However, at present, no other reported study has evaluated the overall survival rate with the combined PLT-HGB levels as the predictor; therefore, a larger study is needed to confirm these results.

RELATIONS BETWEEN PLT AND HGB LEVELS AND CERVICAL CARCINOMA PROGNOSIS:

Several studies have confirmed that the pre-operative PLT level is an independent factor influencing cervical carcinoma prognosis [1,20]; however, some studies have also denied it [14,21]. The present study showed that the pre-operative PLT level was not an independent factor that influenced prognosis. Many recent studies indicate that, among patients with cervical carcinoma undergoing new adjuvant chemotherapy and radical hysterectomy, HGB level could influence prognosis [9,18]; however, there are conflicting reports as to whether it is an independent factor that influences prognosis. According to Choi’s report [22], a low pre-operative HGB level was an independent factor that influences the prognosis of some patients with advanced cervical carcinoma. The research of Shin et al. showed that a low HGB level was an independent factor influencing the survival rate of patients with early-stage cervical carcinoma [19]. However, the research of Angiolo et al. denied this association. The present study showed that pre-operative HGB level might be an independent factor that influences prognosis. The reason for the reported differences may be due to differences in the participants, different tumor staging, or different therapeutic methods.

This study also analyzed the combined pre-operative PLT-HGB level as a potential factor influencing prognosis and revealed that PLT levels >300×109/L combined with HGB levels <120 g/L may be an independent factor influencing prognosis, although there has been no similar previous research and the results remain to be verified in a study with a larger sample size.

Conclusions

Measuring the HGB and PLT levels of patients pre-operatively is a simple and affordable means to predict disease stage and recurrence. In particular, the HGB level could be an independent factor that influences prognosis in early-stage cervical carcinoma. Therefore, attention should be paid to the pre-operative PLT and HGB levels and to correcting any observed anemia, which may have a positive effect in the treatment of cervical carcinoma. The study did not investigate the impact on the clinical features and prognosis by means of correcting anemia or/and thrombocytosis in the preoperative setting, which needs further research.

References

1. Hernandez E, Donohue KA, Anderson LL, The significance of thrombocytosis in patients with locally advanced cervical carcinoma: a Gynecologic Oncology Group study: Gynecol Oncol, 2000; 78; 137-42, pmid: 10926792

2. Dunst J, Kuhnt T, Strauss HG, Anemia in cervical cancers: impact on survival, patterns of relapse, and association with hypoxia and angiogenesis: Int J Radiat Oncol Biol Phys, 2003; 56; 778-87, pmid: 12788185

3. Winter WE, Maxwell GL, Tian C, Association of hemoglobin level with survival in cervical carcinoma patients treated with concurrent cisplatin and radiotherapy: a Gynecologic Oncology Group Study: Gynecol Oncol, 2004; 94; 495-501, pmid: 15297194

4. Serkies K, Badzio A, Jassem J, Clinical relevance of hemoglobin level in cervical cancer patients administered definitive radiotherapy: Acta Oncol, 2006; 45; 695-701, pmid: 16938812

5. Anderberg C, Li H, Fredriksson L, Paracrine signaling by platelet-derived growth factor-CC promotes tumor growth by recruitment of cancer-associated fibroblasts: Cancer Res, 2009; 69; 369-78, pmid: 19118022

6. Van Belle SJ, Cocquyt V, Impact of haemoglobin levels on the outcome of cancers treated with chemotherapy: Crit Rev Oncol Hematol, 2003; 47; 1-11, pmid: 12853095

7. Yu M, Liu L, Zhang BL, Pretreatment thrombocytosis as a prognostic factor in women with gynecologic malignancies: a meta-analysis: Asian Pac J Cancer Prev, 2012; 13; 6077-81, pmid: 23464407

8. Gadducci A, Cosio S, Zola P, Pretreatment platelet and hemoglobin levels are neither predictive nor prognostic variables for patients with locally advanced cervical cancer treated with neoadjuvant chemotherapy and radical hysterectomy: Int J Gynecol Cancer, 2010; 20; 1399-404, pmid: 21051984

9. Fuso L, Mazzola S, Marocco F, Pretreatment serum hemoglobin level as a predictive factor of response to neoadjuvant chemotherapy in patients with locally advanced squamous cervical carcinoma: a preliminary report: Gynecol Oncol, 2005; 99; S187-91, pmid: 16185756

10. Wang D, Wu M, Ren T, Effects of pre-chemotherapy hemoglobin and platelet levels in patients with stage Ib2-IIb cervical cancer treated with neoadjuvant chemotherapy followed by radical hysterectomy: Zhonghua Fu Chan Ke Za Zhi, 2012; 47; 577-81, pmid: 23141176

11. Metindir J, Bilir Dilek G, Preoperative hemoglobin and platelet count and poor prognostic factors in patients with endometrial carcinoma: J Cancer Res Clin Oncol, 2009; 135; 125-29, pmid: 18542999

12. Hwang SG, Kim KM, Cheong JH, Impact of pretreatment thrombocytosis on blood-borne metastasis and prognosis of gastric cancer: Eur J Surg Oncol, 2012; 38; 562-67, pmid: 22592098

13. Dabrow MB, Francesco MR, McBrearty FX, The effects of platelet-derived growth factor and receptor on normal and neoplastic human ovarian surface epithelium: Gynecol Oncol, 1998; 71; 29-37, pmid: 9784315

14. Zhao K, Deng H, Qin Y, Prognostic significance of pretreatment plasma fibrinogen and platelet levels in patients with early-stage cervical cancer: Gynecol Obstet Invest, 2015; 79; 25-33, pmid: 25278089

15. Gungor T, Kanat-Pektas M, Sucak A, Mollamahmutoglu L, The role of thrombocytosis in prognostic evaluation of epithelial ovarian tumors: Arch Gynecol Obstet, 2009; 279; 53-56, pmid: 18470520

16. Ikeda M, Furukawa H, Imamura H, Poor prognosis associated with thrombocytosis in patients with gastric cancer: Ann Surg Oncol, 2002; 9; 287-91, pmid: 11923136

17. Barkati M, Fortin I, Mileshkin L, Hemoglobin level in cervical cancer: a surrogate for an infiltrative phenotype: Int J Gynecol Cancer, 2013; 23; 724-29, pmid: 23446376

18. Lim S, Lee CM, Park JM, An association between preoperative anemia and poor prognostic factors and decreased survival in early stage cervical cancer patients: Obstet Gynecol Sci, 2014; 57; 471-77, pmid: 25469335

19. Shin NR, Lee YY, Kim SH, Prognostic value of pretreatment hemoglobin level in patients with early cervical cancer: Obstet Gynecol Sci, 2014; 57; 28-36, pmid: 24596815

20. Rodriguez GC, Clarke-Pearson DL, Soper JT, The negative prognostic implications of thrombocytosis in women with stage IB cervical cancer: Obstet Gynecol, 1994; 83; 445-48, pmid: 8127540

21. De Jonge ET, Viljoen E, Lindeque BG, The prognostic significance of p53, mdm2, c-erbB-2, cathepsin D, and thrombocytosis in stage IB cervical cancer treated by primary radical hysterectomy: Int J Gynecol Cancer, 1999; 9; 198-205, pmid: 11240767

22. Choi YS, Yi CM, Sin JI, Impact of hemoglobin on survival of cervical carcinoma patients treated with concurrent chemoradiotherapy is dependent on lymph node metastasis findings by magnetic resonance imaging: Int J Gynecol Cancer, 2006; 16; 1846-54, pmid: 17009981

In Press

Clinical Research  

Institutional and Regional Variations in Access to Clinical Trials and Next-Generation Sequencing in Turkis...

Med Sci Monit In Press; DOI: 10.12659/MSM.951027  

Clinical Research  

Low-Intensity Blood Flow-Restricted Multi-Joint Exercise Improves Muscle Function in Patients With Patellof...

Med Sci Monit In Press; DOI: 10.12659/MSM.950516  

Review article  

Musculoskeletal Ultrasound and MRI in the Evaluation of Chemotherapy-Induced Peripheral Neuropathy: A Review

Med Sci Monit In Press; DOI: 10.12659/MSM.951283  

Clinical Research  

Sensory Processing, Dissociation, and Affective Symptoms in Misophonia: A Cross-Sectional Study of 35 Adults

Med Sci Monit In Press; DOI: 10.12659/MSM.950938  

Most Viewed Current Articles

17 Jan 2024 : Review article   10,187,196

Vaccination Guidelines for Pregnant Women: Addressing COVID-19 and the Omicron Variant

DOI :10.12659/MSM.942799

Med Sci Monit 2024; 30:e942799

0:00

13 Nov 2021 : Clinical Research   3,708,487

Acceptance of COVID-19 Vaccination and Its Associated Factors Among Cancer Patients Attending the Oncology ...

DOI :10.12659/MSM.932788

Med Sci Monit 2021; 27:e932788

0:00

14 Dec 2022 : Clinical Research   2,341,643

Prevalence and Variability of Allergen-Specific Immunoglobulin E in Patients with Elevated Tryptase Levels

DOI :10.12659/MSM.937990

Med Sci Monit 2022; 28:e937990

0:00

16 May 2023 : Clinical Research   706,524

Electrophysiological Testing for an Auditory Processing Disorder and Reading Performance in 54 School Stude...

DOI :10.12659/MSM.940387

Med Sci Monit 2023; 29:e940387

0:00

Your Privacy

We use cookies to ensure the functionality of our website, to personalize content and advertising, to provide social media features, and to analyze our traffic. If you allow us to do so, we also inform our social media, advertising and analysis partners about your use of our website, You can decise for yourself which categories you you want to deny or allow. Please note that based on your settings not all functionalities of the site are available. View our privacy policy.

Medical Science Monitor eISSN: 1643-3750
Medical Science Monitor eISSN: 1643-3750