Introduction
The morbidity and mortality of cervical cancer rank 4th among female malignant tumors worldwide [
1]. Globally, approximately 527,600 new cervical cancer cases and 265,700 cervical cancer-related deaths are reported annually [
1]; among them, more than 80% of cases come from developing countries. According to statistics, 98,900 new cervical cancer cases and 30,500 deaths occurred in China in 2015 [
2]. Currently, the International Federation of Gynecology and Obstetrics (FIGO) classification system is mainly used to judge the clinical prognosis of cervical cancer. However, the FIGO classification system is restricted in judging the prognosis of cervical cancer patients. So, other indexes must be applied (such as hematological indexes, pathological type, histological grade, tumor infiltration depth or scope, and lymph node metastasis (LNM) staging) to comprehensively judge the patient prognosis.
In recent years, hematological indexes have attracted extensive attention regarding their predictive value in malignant tumors [
3,
4]. In cervical cancer, the neutrophil/lymphocyte ratio (NLR), platelet/lymphocyte ratio (PLR), monocyte/lymphocyte ratio (MLR) and systemic inflammation response index (SIRI) are closely related to the prognosis of cervical cancer patients [
5]. Recent studies have indicated that the MPV/PC ratio based on the mean platelet volume (MPV) and platelet count (PC) can predict the prognosis of multiple malignant tumors [
6‐
12]. However, the prognostic value of MPV/PC in cervical cancer has not yet been investigated. Therefore, this study aimed to explore the influencing factors for the prognosis of cervical cancer patients, evaluate the prognostic values of MPV/PC, NLR, PLR and MLR in cervical cancer, and construct a prognostic nomogram for resectable cervical cancer patients on this basis. Additionally, the prognostic prediction accuracy of this model was compared with that of the FIGO classification system to guide clinical practice and improve the clinical outcomes of cervical cancer patients.
Materials and methods
Clinical data of patients
Together, 283 patients who received radical surgery for cervical cancer at the Second Affiliated Hospital of Soochow University from 2009 to 2017 were retrospectively analyzed. The inclusion criteria were as follows: 1. patients pathologically diagnosed with primary cervical squamous carcinoma with FIGO stage IA-IIA; 2. patients with no chronic heart, liver, kidney disease, diabetes, or severe infection; 3. patients who did not take antiplatelet agents or receive anticoagulation therapy within 1 month before examination; 4. patients with complete clinical and follow-up data; and 5. patients who did not receive neoadjuvant chemotherapy (NCT) or radiotherapy. The follow-up plan after initial treatment comprised re-examinations every 3 months within 1–2 years after surgery, every 6 months within 3–5 years and yearly thereafter. The follow-up examinations mainly included interrogation, gynecological examination, cervical cytological examination, transvaginal ultrasonography, and CT or MRI. Overall survival (OS) was defined as the time from the date of surgery to the date of death from any cause or the last follow-up for the survivors or those lost to follow-up (censor). The last follow-up was conducted on June 30th, 2019, and the median follow-up period was 72 (range, 4–129) months. Additionally, 125 cervical cancer patients who had undergone radical resection at the Kunshan First People’s Hospital were recruited as the validation cohort. The study design conformed to the Declaration of Helsinki and was approved by the Ethics Committee of the Second Affiliated Hospital of Soochow University (2009-KY-043). All the patients provided written informed consent.
Data collection
The clinical information, clinicopathological parameters and preoperative routine blood tests of the patients were collected. Clinical information included patient age, FIGO stage, postoperative therapeutic scheme, smoking history, medical complications and surgical complications. Pathological features mainly included pelvic lymph node (PLN) metastasis status, tumor size, histological grade, tumor invasion depth, lymphovascular invasion and surgical margin. The routine blood tests at 1 week before surgery included those to evaluate WBC, Hb, monocytes, neutrophils, lymphocytes, PC, MPV and the platelet distribution width (PDW), along with NLR, PLR, MLR and MPV/PC calculated based on the abovementioned results. Additionally, the optimal cutoff values of some continuous variables were determined by the receiver operating characteristic (ROC) curve to convert them into categorical variables [
12].
Statistical analysis
The intergroup differences in variable data were analyzed by chi-squared test or t-test. The Kaplan–Meier curve was adopted for survival analysis and tested using the log-rank test. To evaluate the discriminating ability of MPV/PC, NLR, PLR and MLR in cervical cancer prognosis, ROC curves were plotted to preliminarily evaluate the area under the curve (AUC). Next, the prognostic factors for patients were evaluated using the univariate Cox proportional hazard regression model. Later, the multivariate Cox proportional hazard model was constructed using the reverse step-by-step deletion method. Afterward, the variables selected by the multivariate Cox model were used to construct the nomogram. Typically, the C-index and AUC were mainly used to assess the performance of the nomogram. Bootstrap sampling was repeated 1000 times for nomogram verification and evaluation calibration. The rms module of the R programming language, SPSS 22.0 and GraphPad Prism 5 were employed for statistical analysis. All p values were two-sided, and a difference of P < 0.05 indicated statistical significance.
Discussion
Since scholars first reported the increased platelet count in cancer patients in 1872 [
13], the platelet changes in blood from patients with malignant tumors at different sites have been successively investigated. Platelets are one of the bioactive visible blood components produced by mature megakaryocytes in bone marrow and affect the inflammatory response and immune regulation in the body [
14,
15]. Platelets extensively exist in the peripheral blood circulation and exert their role in tumor invasion, hematogenous metastasis and distal organ colonization through surface molecules or secreting related factors [
16,
17]. PC and MPV are the two most important indices to evaluate platelet function, and their combination in the MPV/PC index has recently been used in the prognosis evaluation of malignant tumor patients. MPV/PC was first used as the prediction index for long-term mortality after myocardial infarction [
18]. Recently, Cho et al. revealed the expression level and diagnostic value of MPV/PC in hepatocellular carcinoma (HCC) patients [
6]. Subsequently, Gu et al. found that the OS of HCC patients with high MPV/PC was significantly poorer [
11]. In lung carcinoma, Inagaki et al. found that MPV was expressed at low levels in lung carcinoma patients, while PC was highly expressed. The OS of non-small cell lung cancer (NSCLC) patients with low MPV/PC was significantly superior to that of patients with high MPV/PC, and MPV/PC was an independent prognostic factor for locally advanced NSCLC [
7]. In colorectal cancer (CRC), the low MPV/PC in patients suggests a low TNM stage and less LNM [
9]. We confirmed that cervical cancer patients with high MPV/PC had a poor prognosis, and MPV/PC was an independent prognostic factor for cervical cancer patients. The ROC curve revealed that MPV/PC showed higher prognostic value than NLR, PLR and MLR in cervical cancer. Afterward, multivariate analysis identified the clinicopathological variables MPV/PC, FIGO stage and lymphovascular invasion, which were incorporated to construct the nomogram. The nomogram exhibited a high accuracy in predicting survival (C-index = 0.78) and a significantly higher predictive ability in the survival of the primary cohort than the FIGO classification system. These results were then verified by a group of independent external verification cohort data. MPV/PC may serve as a prognostic and therapeutic marker that contributes to the early formulation of a more accurate and timelier individualized therapeutic scheme.
Malignant tumors may result in alterations in platelet parameters, but the mechanism by which MPV/PC can be used to predict the prognosis of malignant tumors has not yet been completely illustrated and may be related to the following factors. Bone marrow hyperplasia is active in malignant tumor patients, tumor cells produce thrombogenic factors, and the body fluid environment concentration that promotes the generation of bone marrow megakaryocytes is elevated in the blood circulation [
15]. The number of cytokines that promote tumor growth is increased in tumor patients. Additionally, these cytokines, such as interleukin (IL)-1, IL-3, IL-6, IL-17, IL-18 and tumor necrosis factor-α (TNF-α), specifically stimulate increased production of platelets, [
19,
20]. Stone et al. revealed that IL-6 promotes the secretion of more thrombogenic factors by the liver, while ovarian cancer cells secrete IL-6, which causes an increased amount of thrombogenic factors to act on the bone marrow, resulting in increased platelet production and a changed platelet morphology [
21]. Furthermore, malignant tumor cells secrete granulocyte macrophage-colony stimulating factors, thus accelerating megakaryocyte production and thrombosis [
15]. Malignant tumors consume a large amount of patient energy; thus, tumor patients may develop chronic blood loss, malnutrition and tissue necrosis, which affect platelet morphological parameters [
15]. Malignant tumor cells can secrete and stimulate increased platelets to release transforming growth factor (TGF), directly stimulating the growth of certain tumor cells; however, proliferating tumor tissues produce more stimulating factors to accelerate bone marrow megakaryocyte production, thus forming a vicious cycle [
15].
This study has certain limitations. (1) This study was a retrospective single-center study, which might be associated with selection bias. (2) Heterogeneity existed in the treatments that patients received after surgical resection, likely affecting different clinical outcomes. (3) The cutoff values in this study were not verified in other cohorts. Thus, more large-scale, multicenter clinical studies are warranted to verify our research results.
Conclusion
As a noninvasive, lost-cost, simple and repeatable index, MPV/PC is a novel independent prognostic index for patients with resectable cervical cancer. Compared with the traditional FIGO classification system, the nomogram that integrates MPV/PC maybe reliably predict the survival of cervical cancer patients after radical surgery.
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