Tumor invasion depth is a useful pathologic assessment for predicting outcomes in cervical squamous cell carcinoma after neoadjuvant radiotherapy
© Lv et al. 2015
Received: 19 August 2015
Accepted: 9 October 2015
Published: 4 November 2015
To evaluate whether tumor invasion depth can be a reliable and easily applicable pathologic assessment strategy to predict outcomes using surgically resected cervical squamous cell carcinoma specimens from patients who have received neoadjuvant radiotherapy (RT) or concurrent chemoradiotherapy (CCRT).
We included 173 patients with cervical squamous cell carcinoma who received neoadjuvant CCRT (n = 125) or RT (n = 48) and underwent subsequent radical hysterectomy. Data for the pre-operative clinical International Federation of Gynecology and Obstetrics (FIGO) stage, post-operative pathologic FIGO stage, World Health Organization (WHO) double diameter measurement evaluation, response evaluation criteria in solid tumors (RECIST 1.1) criteria, tumor necrosis rate (TNR), and tumor regression grade (TRG) were investigated to identify correlations with outcomes related to distant metastasis and survival. The tumor invasion depth (TID) and the tumor invasion depth with cytokeratin immunostaining correction (TIDC) at the cervical internal surface were measured to assess their relations to patients’ outcomes.
Based on measurements taken via transvaginal ultrasound, the pre-operative clinical and post-operative pathologic FIGO staging as well as the WHO double diameter measurement evaluation and RECIST 1.1 criteria were predictive of distant metastasis and survival-related outcomes. Also, lymph node involvement was found to be an independent prognostic factor for recurrence and distant metastasis. Finally, univariate analysis showed both the TID and TIDC were highly related to distant metastasis, overall survival, and progression-free survival, irrespective of the clinical stage of carcinomas.
The TID or TIDC measured at the cervical internal surface is a useful and easily applied pathologic prognostic factor for distant metastasis and survival outcomes in patients with cervical squamous cell carcinoma treated with neoadjuvant RT or CCRT.
Cervical squamous cell carcinoma is one of the most common gynecological malignancies, affecting the health of women worldwide [1, 2]. In China, cervical carcinoma is the second most common gynecological malignancy . The treatment strategy for cervical carcinoma has been changed significantly in the past two decades [4, 5]. For International Federation of Gynecology and Obstetrics (FIGO) stage Ib and II patients, treatment involving neoadjuvant therapies plus surgery have been shown to achieve more benefits than surgery alone [6–8]. In addition, just as we have observed in our clinical practice, previous studies also have confirmed that even FIGO stage III b cervical carcinoma patients who receive neoadjuvant therapies are able to endure surgical treatment with better outcomes [9–11]. Moreover, the use of neoadjuvant radiotherapy (RT) alone or with concomitant chemoradiotherapy (CCRT) is effective for achieving excellent cervical carcinoma control along with surgical resection [12, 13].
Pathologic findings in resected specimens of cervical carcinoma can be the basis for extremely accurate assessment of the extent of disease [14, 15]. However, as neoadjuvant RT and CCRT are applied in increasingly more cervical carcinoma patients, the need for a useful and easily applied pathologic assessment becomes increasingly critical.
In the present study, we conducted a retrospective analysis of 173 cervical squamous cell carcinoma patients who received neoadjuvant RT or CCRT with the objective of determining whether the tumor invasion depth could be an objectively, reproducibly, and quantitatively measured pathologic parameter to predict these patients’ outcomes.
Between April 2006 and June 2011, 173 FIGO stage Ib2–IIIb cervical carcinoma patients underwent radical hysterectomy and pelvic lymph node dissection after neoadjuvant RT (n = 48) or CCRT (n = 125) in the Xijing Hosptial, Fourth Military Medical University. The interval between pre-operative RT or CCRT and radical surgery was typically 2–3 weeks. The pathologic subtype in all cases was squamous cell carcinoma. Patients’ complete information was recorded in our department, and follow-up information was obtained from electronic medical records or by telephone interviews of patients between April 2006 and December 2014.
And all the researches, including the different treatments, the name of the patients and their outcomes, were performed with the approval of an appropriate ethics committee of Fourth Military Medical University.
Cervical carcinoma staging
We evaluated target lesions via physical examination and transvaginal ultrasound (TVS) examination, and tumor size was measured according to images taken before surgery. Based on the 2009 FIGO staging system [16, 17], the pre-operative clinical staging data included primarily the size of the imaged tumor and observations from physical examinations.
After surgery, tumor size and extent were evaluated by pathologic examination. Post-operative staging was carried out as “y” Pathologic stage according to 2009 FIGO staging system.
Tumor neoadjuvant treatment response evaluation
The tumor size was measured by TVS examination before RT and again before surgery, and the data were used for evaluation by World Health Organization (WHO) double diameter measurement  and the response evaluation criteria in solid tumors (RECIST) 1.1 criteria . The microscopic residual tumor size was used to evaluate the tumor necrosis rate (TNR)  and tumor regression grade (TRG) evaluation.
Considering the change in tumor burden as an important feature in the clinical evaluation of cancer therapeutics, the WHO double diameter measurement was obtained as previously described . Complete response (CR) is defined as the disappearance of all target lesions, and any pathological lymph nodes must be reduced to having a short axis <10 mm. Partial response (PR) is defined as at least a 50 % decrease in the products of bidimensional lesion measurements of target lesions. Progressive disease (PD) is defined as at least a 25 % increase and stable disease (SD) is defined as tumor shrinkage not sufficient to qualify as PR or tumor growth not sufficient to qualify as PD.
The response evaluation criteria in solid tumors (RECIST) 1.1 criteria  use a unidimensional measure (the longest diameter) assessment of one or more target lesions with summation of unidimensional assessments of many lesions to quantify measurable tumor lesions. CR requires a complete absence of disease, whereas PR indicates a more than 30 % decrease in the sum of the largest diameters. PD is defined by an increase in the sum of the largest diameters by more than 20 %, and SD represents all the outcomes between PR and PD.
The TNR  is defined as the presence of microscopic coagulative necrosis, and the presence of necrosis on gross examination was not considered. The extent of tumor necrosis was assessed in a semiquantitative manner at low magnification (magnification, ×40) of all available tumor blocks. The TRG was recorded according to a 5-grade scale: TRG 1 indicates absence of residual cancer; TRG 2 indicates few residual cancer cells; TRG 3 indicates a considerable number of residual cancer cells; TRG 4 indicates outgrowth of residual cancer; and TRG 5 indicates a lack of regressive changes.
Neoadjuvant RT and chemotherapy regimens
Pre-operative pelvic RT was delivered using three-dimensional conformal radiation techniques and 6.0 or 15.0 medium voltage photons using a linear accelerator (Clinac 23EX or 600 C/D; Varian Medical Systems, Palo Alto, CA, USA). Patients were immobilized in the supine position using a custom vacuum mattress and first underwent a computed tomography (CT) simulation scan (PQS + AcQSim; Philips, Amsterdam, The Netherlands) with intravenous contrast, using 5.0-mm slice thickness. Simulation images extended from L1 to 5.0 cm below the ischial tuberosities. The treatment planning was designed and computed using the Plato system version 2.7.5 (Varian, Salt Lake City, UT, USA). The pelvic irradiation dose was 40–50 Gy in 20–25 fractions.
CCRT was administered to 121 patients via weekly intravenous infusion of cisplatin (40 mg/m2) during pelvic external beam RT. Patients received either three (n = 30, 25 %), four (n = 46, 38 %), or five (n = 45, 37 %) cycles of cisplatin. Chemotherapy was withheld under the following conditions: white blood cell count <2.0 × 109/L, absolute neutrophil count <1.0 × 109/L, platelet count <50 × 109/L, or grade 3–4 radiation enteritis or cystitis.
The interval between pre-operative RT or CCRT and radical surgery was 3 weeks for 71 (41.0 %) patients, 2 weeks for 93 (53.8 %) patients, and 1 week for only 9 (5.2 %) patients.
Histopathologic examination and immumohistochemical staining
The histopathologic response to neoadjuvant therapy was evaluated based on pathologic examination of resected specimens, including uterine tissue, the vaginal cuff, the parametrium, bilateral adnexa, and pelvic lymph nodes. The status of resected lymph nodes was described in terms of lymph-node involvement (involved or not involved).
The pan-cytokeratin antibody (AE1/AE3) (Dako, Glostrup, Denmark) was used in immunohistochemical staining to identify any invisible residual tumor cells.
Measurement of TID
Quantitative variables are presented as frequencies and percentages, and the Chi-square test and Spearman test were applied to assess associations between categorical variables. Univariate analysis was first performed to identify factors of strongest significance, followed by step-wise stratified analysis and complemented with multivariate analysis to define the best statistically significant combination of these factors. Then multivariate Cox proportional hazard models were applied to assess the independent impacts of combined variables with distant metastasis, progression-free survival (PFS), and overall survival (OS), followed by step-wise stratified analysis beginning with the strongest factors.
Receiver operating characteristic (ROC) curves were calculated to represent the relationship between true positive events (sensitivity) and false positive events (100 – specificity) for different cut-off points. Such ROC curves for sensitivity and specificity are often used to assess the performance of diagnostic tests, prognostic factors, and classifiers.
Therefore, ROC curves were constructed for quantitative variables to determine the best cut-off point values discriminating between groups with good or poor prognosis and to define the distinctions between groups with differing prognosis.
OS and PFS were calculated from the date of diagnosis to the date of the last follow-up. Death events in the absence of disease progression were censored in the calculation of PFS. Survival probabilities were calculated by the Kaplan–Meier method and compared by the log-rank test. A P-value of less than 0.05 was considered statistically significant in all tests, and all statistical analyses were performed using SPSS version 19.0 software (IBM, Armonk, NY, USA).
The characteristics of 173 patients with FIGO stages Ib-IIIb cervical squamous cell carcinoma before and after the radical hysterectomy and results of correlation analyses
Number of patients, n (%)
Median age, years (range)
Distant metastasis, n (%)
Recurrence, n (%)
The death events within 5 years, n (%)
Lymph node metastasis
Outcomes according to existing tumor staging systems and evaluation standards
Outcomes according to TID and TIDC
Patient characteristics according to TID and TIDC cut-off values and results of correlation analyses
Invasion depth (mm)
Number of patients, n (%)
Median age, years (range)
Distant metastasis, n (%)
Lymph node metastasis, n (%)
The death events in 5 years, n (%)
104 (60.1 %)
4 (3.8 %)
12 (11.5 %)
1 (1.0 %)
1 (1.0 %)
69 (39.9 %)
14 (20.2 %)
8 (11.6 %)
4 (5.8 %)
10 (14.5 %)
100 (57.8 %)
4 (4.0 %)
12 (12.0 %)
1 (1.0 %)
1 (1.0 %)
73 (42.2 %)
14 (19.2 %)
8 (11.0 %)
4 (5.5 %)
10 (13.7 %)
TID or TIDC values less than the cut-off values could represent two different situations: (1) a complete lack of residual tumor cells, and (2) a measurable invasion depth less than the cut-off point. Correlation analysis indicated that there were no statistical differences in outcomes related to survival (P = 0.254) or distant metastasis (P = 0.212) between these situations. The same results were obtained for TIDC, with no differences in outcomes related to survival (P = 0.823) and distant metastasis (P = 0.412).
In this study, we assessed the prognostic value of different clinical and pathologic assessment parameters using data of 173 cervical squamous cell carcinoma patients who underwent neoadjuvant RT or CCRT prior to radical hysterectomy. Although no standard procedures for neoadjuvant therapy plus surgery have been confirmed yet and more supporting data are still needed, especially data regarding CCRT, some studies have suggested that pre-operative CCRT is associated with significantly improved PFS and OS compared with RT alone [21, 22], whereas other studies have provided evidence suggesting almost the same clinical outcomes following these different treatment modalities [13, 23]. Our data also did not show significant differences in the outcomes of patients who received RT alone or CCRT, which is consistent with the results of the study by Keys et al. . Moreover, improvement of the 5-year OS rate with neoadjuvant CCRT over that achieved with RT alone remains to be proven. In our study, the 60.0 % 5-year survival rate of stage IIIb patients is similar to the rates previously reported, whereas the 96.7 % 5-year survival rate of stage IIb patients in our study seems to be higher than rates previously reported (e.g., 71.0 %) [25, 26]. These findings may suggest the benefit of neoadjuvant RT or CCRT, but further studies are still needed to draw such conclusions.
Before radical hysterectomy, we obtained the tumor size measurements used in the clinical FIGO staging system and WHO and RECIST 1.1 evaluation criteria by TVS examination, which has been shown to be highly accurate for detecting tumor presence and evaluating the local extension of cervical carcinoma [27, 28]. Because this imaging technique is faster, cheaper, and more widely available than other imaging techniques [27, 28], its use is consistent with our objective of establishing prognostic criteria for cervical carcinoma underwent neoadjuvant treatment that are easily applied in most hospitals. However, TVS is a painful and time-consuming procedure, especially for the patients who have undergone RT or CCRT.
The FIGO staging system [16, 17], especially the revised FIGO (2009) staging system, is widely used in standard clinical and pathologic staging procedures for many types of cancer, including cervical carcinoma. Similar to the results of previous clinicopathologic studies on cervical carcinoma , our data demonstrate that the clinical FIGO staging prior to radical hysterectomy serves as a valuable independent predictor of distant metastasis and survival outcomes (Table 1 and Fig. 2) in patients with FIGO stage III carcinomas, whereas it is not a very effective predictor of outcomes for stage I and II carcinomas. In addition, our results showed that post-operative pathologic FIGO staging is a less effective predictor compared with the clinical stage. Use of the FIGO staging system both before and after surgical treatment are dependent on the assessment of tumor size and invasion of the parametrium and pelvic side wall as well as the evaluation of adjacent organs and lymph node involvement . Thus, high accuracy of FIGO staging prior to radical hysterectomy for cervical carcinoma prognosis is not easily obtainable and depends heavily on accurate clinical examinations [28–32].
The WHO (double diameter measurement evaluation) criteria and RECIST 1.1 criteria are widely used and also were found to be effective in our study (Table 1 and Additional file 2: Figure S2 & Additional file 3: Figure S3). However, these two sets of criteria clearly state that tumor lesions situated in a previously irradiated area, or in an area subjected to other loco-regional therapy, are not usually considered measurable unless evidence of progression in the lesion has been demonstrated . Moreover, both sets of criteria also suggest the ultrasound examinations should not be used for imaging-based evaluation measurements, because ultrasound is regarded as operator dependent and therefore of limited reliability . However, the effective application of these two sets of criteria in our study indicated that the use of TVS is more reliable than ordinary ultrasound examination with respect to the accuracy of the results.
In our study, to find useful prognostic factors for cervical carcinoma treated with neoadjuvant RT or CCRT, we also included the TNR in our analyses and showed that the TNR cannot be considered an effective prognostic factor (Table 1). This is likely because the degree of necrosis within tumor tissue is not apparent until some time after treatment. Moreover, TNR also can be easily affected by tumor heterogeneity, artery dilatation, and vascular proliferation within the tumor . We also applied the 5-point TRG scoring system to determine whether the TRG is correlated with outcomes in these patients. Based on the hypothesis that a shorter tumor cell doubling time indicates a more aggressive tumor, the regression grade is in general considered to be related to patients’ prognosis. However, the TNR is a subjective criterion not based on an objective measurement and thus does not offer good reproducibility, and our results showed no clear prognostic significance for patients with cervical carcinoma treated with neoadjuvant therapy (Table 1).
Residual tumor cells are generally considered aggressive, and the area containing such cells may be important for the determination of invasive and metastatic capacity. Dipen et al. proposed “tumor thickness” as a new prognostic factor for therapy response and survival outcome in patients with resected hepatic colorectal metastases , and other studies also indicated that the tumor thickness remains the most important determinant of melanoma patient survival [35, 36]. For cervical carcinoma, tumor diameter and volume, as determined by pre-surgery imaging examinations, can predict progression-free survival , and previous studies confirmed that the tumor size on T2-weighted magnetic resonance images is a useful index for evaluating parametrial involvement of cervical carcinoma with full-thickness stromal invasion . Therefore, based on the hypothesis that the existence of residual tumor cells correlates with the outcomes of patients, the TID was designed to measure the length perpendicular to the cervical internal surface in the maximal cutting plane. Measurement of this dimension was less time consuming and more reproducible, because few parameters are considered and major parts of the tumor cannot be disregarded [34, 39].
In practice, nest-like or cord-like scattered tumor cells and continuous tumor tissue invading to different depths with different degrees of necrosis and inflammatory reactions can be identified easily under a microscope. Also, the reproducibility of such objective measurements could not be easily influenced by the pathologist’s experience. In the present study, cytokeratin immunostaining was used to identify some uncertain residual tumor tissue and obtain TIDC measurements. The positive results demonstrated the existence of residual tumor tissue and inevitably changed the measured invasion depth. Even after we eliminated the major influence of patients’ pre-operative clinical FIGO stages on survival outcomes, both the TID and TIDC were found to be significantly correlated with distant metastasis and survival outcomes in cervical squamous cell carcinoma patients who had undergone adjuvant RT or CCRT.
Pre-operative clinical FIGO staging as well as the WHO double diameter measurement evaluation and RECIST 1.1 criteria, according to tumor size assessed by TVS examination, were found to be useful predictive indicators of patient outcomes following radical hysterectomy in cervical squamous carcinoma patients who underwent neoadjuvant RT or CCRT. However, in addition to these previously reported assessment standards and methods, our results also provide evidence that the TID or TIDC at the cervical internal surface is a useful and easily applied prognostic factor for distant metastasis and survival outcomes in these patients, irrespective of pre-operative FIGO staging.
This work was supported in part by grants from the National Natural Science Foundation of China (Nos. 30771120, 81272651, 81570180 and 81072103).
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