Outcomes and Prognostic Factors for Adenocarcinoma/Adenosquamous Carcinomas Treated with Radical Hysterectomy and Adjuvant Therapy ()
1. Introduction
Adenocarcinoma/adenosquamous carcinomas (AC/ASC) are relatively uncommon histological subtypes of cervical cancer. Recently, AC/ASC has accounted for approximately 20% of all cervical cancer cases [1] -[3] . In general, the prognoses of patients with cervical AC/ASC are poorer than those of patients with cervical squamous cell carcinoma (SCC), because AC/ASC is more likely to grow aggressively and metastasize [4] [5] . This may be partly due to the lack of consensus on the optimal treatment for cervical AC/ASC [6] . The first-line treatment for AC/ASC is similar to that for SCC [7] [8] ; cervical cancer patients with AC/ASC that are classified as stage IB-IIB by the International Federation of Gynecologists and Obstetricians (FIGO) are often treated with radical hysterectomy [9] . However, there are conflicting reports about whether the prognoses of AC/ASC patients who undergo surgery or radiotherapy are worse than those of SCC patients [5] [10] -[13] .
To help resolve this issue, we aim to identify outcomes and prognostic factors in early-stage cervical AC/ ASC patients who are treated with radical hysterectomy and adjuvant therapy. This information may be useful in optimizing the treatment of these patients.
2. Patients and Methods
After obtaining approval from the Institutional Review Board of Niigata University Hospital, we retrospectively reviewed the medical records of 26 patients with FIGO stage IB-IIB cervical AC/ASC who were treated with radical hysterectomy and adjuvant therapy between January 2001 and April 2013. Fifteen patients received neoadjuvant chemotherapy with at least one cycle of cisplatin (10 mg/body on days 1 - 10 every four weeks) and 5-fluorouracil (250 mg/body on days 1 - 10 every four weeks) [14] . One patient received a cycle of paclitaxel (175 mg/m2 on day 1every three weeks) and cisplatin (75 mg/m2 on day 1every three weeks) [15] . The remaining patients did not receive any neoadjuvant therapy. All patients underwent type III Piver-Rutledge radical hysterectomy [16] and systematic pelvic lymphadenectomy.
Approximately four weeks after surgery, all patients received radiotherapy (RT), chemotherapy (CT), or concurrent chemoradiotherapy (CCRT) as adjuvant therapy. RT consisted of external whole pelvic irradiation with 50.4 Gy in 28 fractions. CT (docetaxel: 70 mg/m2 on day 1; carboplatin: area under the curve = 5 on day 1) was administered for at least three cycles at three-week intervals. CCRT consisted of concurrent RT and cisplatin alone (30 - 40 mg/m2 weekly) or cisplatin (50 mg/m2every three weeks) plus paclitaxel (50 mg/m2 weekly). The differential indications for these therapies were based on the presence or absence of risk factors for postoperative recurrence, such as lymph node metastasis, parametrial invasion, positive surgical margin, large tumor size (≥4 cm), lymphovascular space invasion (LVSI), and deep stromal invasion (≥2/3 thickness). For example, among patients without lymph node metastasis, five received CCRT and eight received either RT or CT alone. On the other hand, among patients with lymph node metastasis, four received CCRT and nine received either RT or CT alone.
Survival outcomes were examined using the Kaplan-Meier method and compared using the log-rank test. Multivariate analyses of overall survival (OS) and progression-free survival (PFS) were performed with the Cox proportional hazards regression model to determine the prognostic significance of clinical features. A p-value of less than 0.05 was considered statistically significant.
3. Results
Patient characteristics are shown in Table 1. The median age at the start of treatment was 48.0 years (range: 29 - 69 years). For all patients, the estimated five-year OS rate was 49.5% and the estimated five-year PFS rate was 36.5%. Disease recurrence occurred in 12 patients (46.2%) with a median time of 11 months (range: 2 - 57 months). All patients except one had at least one risk factor for postoperative recurrence. However, the patient
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Table 1. Clinicopathological characteristics of the 26 patients with cervical adenocarcinoma/adenosquamous carcinomas in this study.
who did not have any risk factors still received adjuvant RT because cervical adenocarcinoma has a high risk of recurrence.
As shown in Table 2, lymph node metastasis was a significant prognostic factor for both OS and PFS. In addition, LVSI was a significant prognostic factor for only OS and parametrial invasion was a significant prognostic factor for only PFS. When these prognostic factors were further assessed using the Cox multivariate proportional hazard model, lymph node metastasis was identified as an independent predictor of PFS (p = 0.021, risk ratio = 6.47, 95% confidence interval: 1.33 - 31.43).
The effects of different types of adjuvant therapy in patients with and in those without lymph node metastasis on OS and PFS are shown in Figure 1. In patients with lymph node metastasis, relapses occurred in 10 patients (seven who did not receive CCRT and three who received CCRT). Compared with CT or RT alone, the effects of CCRT on OS and PFS were not significant. In patients without lymph node metastasis, relapses only occurred in two patients who did not receive CCRT. However, compared with CT or RT alone, the effects of CCRT on OS and PFS were not significant.
4. Discussion
In this study, we demonstrated that lymph node metastasis is an independent predictor of PFS in patients with cervical AC/ASC who are treated with radical hysterectomy and adjuvant therapy. This result is consistent with several other studies that show that lymph node metastasis in patients with cervical AC/ASC is an independent predictor for survival [9] [17] [18] . However, the type of adjuvant therapy did not make any significant difference on either OS or PFS, regardless of lymph node metastasis.
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Table 2. Multivariate analysis of survival for patients with cervical adenocarcinoma/adenosquamous carcinomas.
Abbreviations: OS: overall survival, PFS: progression-free survival, LVSI: lymphovascular space invasion, RR: risk ratio, CI: confidence interval. *Parenthetical values indicate that all cases were assessed before year 5.
Since there is no agreement about the optimal treatment for cervical AC/ASC, patients with AC/ASC tend to be treated similarly to those with SCC, namely, radical hysterectomy followed by adjuvant therapy [13] . Rotman et al. [19] suggested that postoperative adjuvant therapy, particularly RT, may be more beneficial for AC/ASC than for SCC. However, there are conflicting reports in the literature about the effect of CCRT on cervical AC/ASC. Some studies have shown that CCRT is beneficial for cervical AC/ASC [20] -[23] , while other studies have reported that CCRT does not improve the survival of patients with risk factors, such as lymph node metastasis [22] [23] . In this study, we showed that CCRT did not improve the survival of patients compared with either RT or CT alone, regardless of lymph node metastasis (Figure 1). However, our small sample sizelimits the statistical power of this study. As a result, a larger study is needed to confirm the generality of this conclusion.
These results suggest that other adjuvant therapeutic strategies may be needed to improve the survival of patients with cervical AC/ASC. For example, Park et al. [24] suggested that adjuvant therapy should be tailored
according to postoperative risk factors in patients with early stage adenocarcinoma. Since CCRT has many adverse effects [15] [20] , personalizing adjuvant therapydepending on the presence or absence of lymph node metastasis to reduce adverse effectsmay be worth considering.
5. Conclusion
In conclusion, we found that lymph node metastasis was an independent prognostic factor for poor survival in cervical AC/ASC patients treated with radical hysterectomy and adjuvant therapy. In this study, CCRT does not improve patient survival, regardless of lymph node metastasis, which suggests that novel or personalized adjuvant therapeutic strategies with fewer adverse effects than existing strategies are needed.
NOTES
*Corresponding author.