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. 2016 Dec 3;8(2):3422–3429. doi: 10.18632/oncotarget.13788

Abdominal radical trachelectomy guided by sentinel lymph node biopsy for stage IB1 cervical cancer with tumors >2 cm

Xiangyun Deng 1,2,3, Ying Zhang 1,2,3, Dapeng Li 2,3, Xiaoling Zhang 2,3, Hui Guo 1,2,3, Fei Wang 1,2,3, Xiugui Sheng 2,3
PMCID: PMC5356892  PMID: 27926501

Abstract

Accuracy of prediction of pelvic lymph node status using sentinel lymph node biopsy (SLNB), and outcomes of SLNB-guided abdominal radical trachelectomy (ART) were assessed. Patients with stage IB1 (Figure 2009) cervical cancer and with tumors >2 cm were enrolled. Prior to fertility-sparing surgery 99mTc-labeled phytate was administered. SLNs were intraoperatively identified, excised, and assessed using fast-frozen sections. Systematic bilateral pelvic lymphadenectomy with or without para-aortic lymphadenectomy was subsequently undertaken. The SLN detection rate was 91.8% (45/49 patients); 8.2% (4/49) had radical hysterectomies because of metastatic primary SLNs. All SLNs received routine immunopathological examination to detect micrometastasis. Sensitivity, accuracy, and false negative rates were 100%, 100%, and 0%, respectively. ART was successfully completed in 45 patients (median follow-up, 61 [range, 4–149] months). Three of the 45 (6.7%) were lost to follow-up; two relapsed and one died of tumor progression. Overall 3-year survival and progression-free survival rates were 97.6% and 95.2%, respectively. Of the 19 patients who attempted to conceive after surgery, five achieved pregnancy, and one had a live birth in the third trimester. We concluded that SLNB using 99mTc-labeled phytate can accurately assess pelvic node status. SLNB-guided ART is safe and feasible in patients selected for fertility-sparing procedures.

Keywords: cervical cancer, tumor >2 cm, abdominal radical trachelectomy, sentinel lymph node, oncological outcomes

INTRODUCTION

Cervical cancer is the second most common gynecological malignancy, and the number of patients in their childbearing years that are diagnosed with the early stages of this cancer is increasing [1]. Preserving fertility is a common desire for young cervical cancer patients. When evaluating preservation of the uterus, tumor size is something to take into consideration. Larger lesions suggest an increased risk of recurrence [2, 3]. The 2015 National Comprehensive Cancer Network (NCCN) cervix cancer guidelines states that radial trachelectomy and pelvic lymph node (PLN) dissection, with or without para-aortic lymph node sampling, is an option for patients with stage IB1 disease that want to sustain their fertility. This is usually only performed in patients with tumors 2 cm in size or smaller. Tumors >2 cm in size are left to the surgeon's discretion. Some surgeons suggest that a 2-cm cutoff should be used for a vaginal trachelectomy and a 4-cm cutoff for an abdominal trachelectomy (e.g., laparotomy, laparoscopic and robotic) [4].

A major indicator in cervical cancer patients is PLN status; it affects clinical outcomes and decisions regarding treatment [5]. In stage IB cervical cancer, the prevalence of PLN metastasis has been estimated to be approximately 16.7% [6]. This means that the majority of early cervical cancer patients who undergo pelvic lymph node dissection will not gain any benefit from the procedure. They will also be subjected to a considerable number of complications such as lymphedema, lymphocyst, and vessel or nerve damage [7].

Sentinel lymph node (SLN) mapping is becoming more prominent in the management of cervical cancer. SLN mapping aims to identify cervical cancer patients who are SLN negative for metastases by using frozen sections; this approach avoids complete pelvic lymphadenectomy [8, 9]. SLN mapping is also used for the selection of candidates for fertility sparing treatment in young patients [1012]. Abdominal radical trachelectomy (ART) is a possible application of SLN mapping in patients who want to preserve fertility. However, it is unclear if it would be safe to use SLN biopsy (SLNB) intro-operatively to select candidates for ART among stage IB1 patients that have tumors larger than 2 cm.

To assess the feasibility and accuracy of the SLNB procedure in this study, we used 99mTc-labeled phytate to guide ART in patients with stage IB1 cervical cancer that had tumors larger than 2 cm in size. We also evaluated the safety of SNLB-guided ART by observing surgical, oncologic and fertility outcomes in patients who wished to preserve their fertility.

RESULTS

Forty-nine patients were identified and entered into the study group. Patient characteristics are summarized in Table 1.

Table 1. Characteristics of the 49 patients in our study.

Characteristics No. of patients
Mean age (range) 28.5 years (19-40)
Childbearing history
 0 20
 ≥1 29
Histology
 Squamous cell carcinoma 46
 Adenocarcinoma 3
Tumor size
 2 cm < Tumor size < 3 cm 20
 3 cm ≤ Tumor size ≤ 4 cm 29
Cell differentiation
 Well 17
 Moderate 17
 Poor 15
Total 49

Procedure details and complications

The proportion of patients who underwent ART was 91.8% (45/49); the remaining 8.2% (4/49) had radical hysterectomies as a result of positive primary SLNs. The median surgical time was 235 (range, 175–280) min; median blood loss was 450 (range, 300–1000) ml. Intraoperative complications included bladder muscle-layer injury in one of 49 (2.0%) patients. The patient with bladder muscle-layer injury received urethral catheterization for 2 weeks and bladder function finally recovered postoperatively. Postoperative complications included pelvic lymphocysts in seven of 49 (14.3%) patients and post-trachelectomy stenosis of the neo-cervix in three of 49 (6.1%) patients.

SLN detection results

We detected 1008 PLNs, including 145 SLNs in the population of 45 patients. The SLN detection rate was 91.8% (45/49) and the median number of SLNs identified per patient was 3.2. The obturator was the most common location for SLN detection, followed by the external and internal iliac and the common iliac (Table 2). Bilateral pelvic SLNs were detected in 69.4% (34/49) of patients. Intraoperatively, the SLNs of four (8.9%) patients were found to be positive on frozen sections; they then underwent immediate complete radical hysterectomies. In the other 41 (91.1%) patients, the intraoperative frozen SLN sections and bilateral ovarian biopsies were negative and ART was successfully completed. The results for the frozen sections and the permanent staining were identical. A routine pathologic examination revealed that all four patients with positive SLNs had metastatic PLNs. In this examination there were no false negative SLNs and there were no cases of metastasis in the non- SLNs (Figure 1). The sensitivity and accuracy rates were both 100%, and the false negative rate was 0%; the negative predictive value of the SLNs was 100% as well (Table 3). Results of anti-keratinose immunohistochemical staining indicated no missed micrometastases (lesions <2 mm) or isolated tumor cells (ITCs) in SLNs (data not shown).

Table 2. Localization and status of the SLNs.

Details of SLNs No. of patients (%)
SLNs detection 45/49 (93.8%)
Total number of SLNs 145
Localization of SLNs
 Common iliac 8/145 (5.5%)
 External and internal iliac 46/145 (31.7%)
Sacral 1/145 (0.7%)
 Obturator 89/145 (61.4%)
 Para-aortic 1/145 (0.7%)
Latus of pelvic SLNs
Unilateral 11/49 (22.4%)
Bilateral 34/49 (69.4%)

Figure 1. Outcome of sentinel lymph node biopsy in 49 patients with stage IB1 cervical cancer and tumors >2 cm in size.

Figure 1

Table 3. Diagnosis of lymph node involvement using SLNB, compared with full lymphadenectomy, in patients with stage IB1 cervical cancer with tumors > 2 cm.

Metastatic lymph node diagnosisa Lymphadenectomy
Yes No Total
SLN biopsyb
Yes 4 0 4
No 0 41 41
Total 4 41 45
a

Presence of macrometastasis, micrometastasis, and/or ITC.

b

Sensitivity: 100.0% (95% CI: 47.3–100.0%); accuracy: 100.0% (95% CI, 92.9–100.0%);

positive predictive value: 100.0% (95% CI: 47.3–100.0%); negative predictive value: 100.0% (95% CI: 92.9–100.0%).

Adjuvant therapy

In 45 (91.8%) patients who underwent ART, 16 (35.6%) received adjuvant therapy. Two of the patients showed three intermediate risk factors: poor differentiation, deep stromal invasion (DSI), and lymphovascular space invasion (LVSI). These patients were treated with concurrent chemotherapy. Chemotherapy treatment was prompted by the occurrence of any two intermediate risk factors in six patients and only one intermediate risk factor in eight patients. Of these patients, eight received chemotherapy involving combination PVB, five received PEB chemotherapy, and three adenocarcinoma patients received TC chemotherapy. Four patients who underwent radical hysterectomy received concurrent chemo-radiotherapy.

Outcomes of follow-up

ART was successfully completed in 45 patients with a median follow-up time of 61 months; the range of the follow-up time was 4-149 months. By July 2015, three of the 45 (6.7%) patients had been lost, leading to a follow-up rate of 93.3%. Of the three patients lost to follow-up, one was out of contact and the other two gave up reexaminations. They did not differ significantly from the patients remaining in the study in terms of age (P=0.215), tumor size (P = 0.147), preoperative conization (P = 0.437) or complications (P = 0.279). Of the remaining 42 patients, two (4.8%) suffered relapses with pelvic recurrences at 28 and 30 months after their initial diagnoses; they received four cycles and six cycles of combination PEB, respectively. One patient died of tumor progression at 34 months. The characteristics of the two patients with recurrence are summarized in Table 4. The other 40 patients were progression-free during the follow-up period. Their overall survival and progression-free survival rates at 3 years were 97.6% and 95.2%, respectively.

Table 4. Characteristics of patients who suffered recurrences.

No. Histology Tumor size Cell differentiation Deep stromal invasion Lymphovascular space invasion Progression-free survival (months) Adjuvant therapy Result
1 Squamous 3cm Poor < 1/2 Positive 28 6 cycles of combination PEB Death
2 Squamous 2.5cm Poor <1/2 Negative 30 4 cycles of combination PEB Alive

Of the 19 patients who wished to conceive, five succeeded, for a total of five pregnancies after surgery. Of these five pregnancies, one was a term delivery, one was a mid-trimester miscarriage and three were first-trimester miscarriages. The newborn developed well.

DISCUSSION

The results of the latest systematic review show the pooled detection rate of SLN mapping in early stage cervical cancers is 89.2% [7]. Although it has been reported that a larger tumor size (>2 cm) and a more advanced disease stage (>IB2) are associated with low detection rates and sensitivity [7, 13], a comparison of the subgroups regarding tumor size has not generally been pre-specified in the study protocol; hence, the reported results might be influenced by differences in disease stage and the prevalence of metastatic disease. The present study was focused on stage IB1 patients with tumors >2 cm in size. The results of the study suggest that SLN mapping may also be a sensitive method for detecting node metastases on stage IB1 cervical cancer patients under the conditions of tumor size being greater than 2 cm.

Lecuru et al. demonstrated that when the identification is bilateral, a negative SLN accurately predicts the absence of pelvic node involvement in early cervical cancer patients [5, 14]. The reported bilateral SLN detection rates were between 24% and 88%, as compared with 69.4% in our series [1517]. In the current study, a higher number of bilateral nodes was detected than in our previous study. This may suggest that the rate of SLN identification will improve significantly with time and experience. Because intracervical injection is technically more difficult, the learning curve effect for cervical cancer is likely to be in the range of 30 [18].

Studies have found that the sensitivity of SLN mapping is higher than that of full PLN dissection [19]. This can be explained by the detection of uncommon draining pathways (e.g., common iliac, presacral or para-aortic), which are not routinely included in systematic PLN dissection, complete SLN excision and the routine use of ultrastaging [20]. Data in the literature regarding the diagnostic value of SLNB varies greatly among different series, with sensitivity ranging from 33.3% to 100% [21, 22]. The main cause of the insufficient sensitivity was its inability to detect low volume metastatic disease (LVD): micrometastases and ITCs [23]. In our study, the results of anti-keratinose immuno-histochemical staining indicated that no LVDs were missed in the SLNs; the results that used frozen sections were identical to those that used permanent staining. Even so, we are of the opinion that the failure to detect LVD constitutes an important limitation of SLNB in clinical management. Micrometastases in cervical cancer have been reported to have a negative prognostic impact; they compromise the recurrence rate [24] and progression free survival [25]. They have also been found to be an independent prognostic factor for survival in a recent study. A 23% reduction in overall survival was reported in the patients with micrometastases as compared to those with negative nodes [19, 26]. It is necessary to strive for improvement regarding the methods of intra-operative assessment for the detection of micrometastasis. It appears that ITCs have no clinical significance, and their finding on definitive examination does not require modification of the therapeutic strategy [5, 27].

The abdominal approach for patients with tumors >2 cm in size permits a wider resection of the parametria and thus has the potential for the resection of larger tumors [28]. Wethington et al. [28] reported on 29 patients with tumors >2 cm in size, 22 of whom underwent ART. After a median follow-up time of 44 (range, 1–90) months, the authors reported no relapse or death. Litner et al. [29] followed up with 45 stage I cervical cancer patients with tumors >2 cm in diameter. Their 5-year survival rate (93.5%) was equal if not better than rates reported for patients treated by radical hysterectomies. Of the 42 patients who underwent definitive ART in the present study, two (4.8%) relapsed and one died from tumor progression. The other 40 patients achieved disease-free survival during a median follow-up time of 61 months. All of the data on survival seemed to support the feasibility and safety of fertility-sparing ART for selected patients with stage IB1 disease and tumors >2 cm in size.

There is a tremendous variation of recurrence rates among patients with tumors >2 cm in size, ranging from 0% to 29% [2831]. These differences could be attributable to variations in patient population and sample sizes, follow-up periods, degrees of surgical radicality and the accuracy of intraoperative and preoperative selection of high-risk cases. In a previous study, we reported on 86 patients with stage IA2 to IB1 cervical cancer who underwent ART. The recurrence rates of these patients after a median follow-up of 77 (range, 3–142) months was 4.4% (2/45) for tumors ≤2 cm in size, and 4.9% (2/41) for tumors >2 cm in size, which was not significantly different (P = 1). This suggests that tumors >2 cm in size are not a risk factor for oncologic outcomes after ART. In the present study, of the two patients with recurrence, one had poor tumor differentiation and deep stromal invasion (DSI) <1/2, and the other had poor tumor differentiation, DSI <1/2 and or lymphovascular space invasion (LVSI). Although the patient sample size was too small to provide statistically reliable data, these results are consistent with LVSI and poor tumor differentiation being important risk factors for recurrence.

In our series, of 19 patients who attempted to conceive, five (26.3%) became pregnant spontaneously. Three patients had first semester miscarriages, one patient had a second trimester miscarriage, and one patient had a live birth in the third trimester. There are several factors that can further affect fertility after ART including a higher risk of adhesions after the abdominal approach, a greater disruption of pelvic nerve innervations to the uterus, and abnormality of the fallopian tubes caused by larger resection of the paracervix tissue. Various approaches have been suggested in several case series for preventing preterm birth in women who experienced radical trachelectomies. Reproductive infertility specialists were also reported to be important in helping patients conceive. Unfortunately, there is limited data available about preterm delivery and there are no definite guidelines on the topic [32, 33].

In conclusion, although we embrace and endorse ART with SLNB as a feasible procedure for patients with IB1 cervical cancer and tumors >2 cm in size, further research is needed. New molecular techniques that offer preoperative assessment of SLNs are especially interesting. Strategies should be developed for the prevention of preterm birth in women who have undergone radical trachelectomies. Data regarding long-term safety, fertility, and neonatal outcome for this fertility-preserving concept are still needed.

MATERIALS AND METHODS

Patients

Patients diagnosed with stage IB1 (Figure 2009) cervical cancer with tumors >2 cm, who were treated at the Shandong Cancer Hospital and Institute between March 2003 and July 2015, were recruited into this study. Patients who met the institutional eligibility criteria (Table 5) were considered eligible to undergo ART with pelvic lymphadenectomy, with or without para-aortic lymphadenectomy. The study was approved by our institutional review board. All patients enrolled in the study provided written informed consent before surgery.

Table 5. Suggested clinical eligibility criteria for ART and transperitoneal pelvic lymphadenectomy.

Criteria
1. Histologic diagnosis of squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma
2. FIGO stage IB1 disease with tumors > 2 cm
3. Age ≤ 40 years
4. Desire to preserve fertility
5. No clinical evidence of impaired fertility
6. Preoperative magnetic resonance imaging (MRI) of pelvis and abdomen, or appropriate imaging protocol with no evidence of pelvic lymph node metastases, and confirmation of tumor limited to the cervix

SLN detection and surgical technique

SLNs were detected by means of an isotope injection into the uterine cervix. On the day before surgery, we injected fluid containing 2.5 ml (100.0 MBq) of 99mTc-labeled sulfur colloid submucosally into four quadrants of the cervix (3, 6, 9 and 12 o’clock positions). After systematic exploration of the peritoneal cavity, the SLNs were detected with a handheld gamma probe (Neoprobe, neo2000TM: AR-MED Ltd.) that was used to fully scan the pelvic sidewall, presacral area and para-aortic lymph beds. SLNs were identified based on the presence of radioactive hot nodes measuring >5-fold above the background level. The SLNs were then excised with safety margins and submitted for fast-frozen sectioning (adenocarcinoma patients received bilateral ovarian biopsies at this time). After removing the SLNs, patients routinely received bilateral pelvic lymphadenectomy to ensure the absence of PLN metastasis by analysis of frozen sections. If SLNs were identified in aberrant locations para-aortic lymphadenectomy was also conducted.

Intraoperative frozen section analysis of the SLNs was performed to guide the selection of surgical treatment. ART was performed if the SLNs and bilateral ovarian biopsies were negative. The round ligaments were transected and ligated laterally. Then paravesicle and pararectal spaces were developed with ligation of uterine arteries and preservation of ovarian vessels. The ureter was mobilized from the medial sheath of the broad ligament to the level of the cardinal ligament. A vessel loop was used to place traction on the ureter. Intraoperatively, the cervical canal was separated from the corpus uteri and opened through a longitudinal section at the 12 o’clock location. A frozen section was prepared 10 mm from the surgical margin to ensure a 10-mm negative endocervical margin. If frozen sections suggested tumor-free surgical margins, the uterus was reconstructed to the upper vagina with absorbable sutures. If the frozen section of the SLNs, bilateral ovarian sample and/or surgical margin was cancerous, radical hysterectomy and/or para-aortic lymphadenectomy was performed. After the incision was taken down and the specimen was removed, a cerclage suture (non-absorbable no. 10 silk suture) was performed in patients who underwent ART.

Surgical specimens were examined using routine hematoxylin and eosin staining. All SLNs were immuno-stained with anti-cytokeratin antibody to detect micrometastasis. The intensity of protein expression was evaluated using OPTIMAS 6.5 software.

Adjuvant therapy

Recommendations for postoperative chemotherapy or radiation therapy were based on high-risk pathological features, such as nodal metastasis or parametrial involvement, as well as for those with intermediate risk factors, such as adenocarcinoma, poor differentiation, DSI or LVSI. Specific treatment recommendations were at the discretion of the gynecological oncologist and radiation oncologist. Adjuvant chemotherapy included the following: a combination of cisplatin, vincristine and bleomycin (combination PVB); a combination of cisplatin, etoposide and bleomycin (combination PEB); or a combination of paclitaxel and carboplatin (combination TC). The radiation therapy regimen consisted of the following: external beam radiation planned using an ADAC Treatment Planning System; delivered using 15 MV X-rays from a Varian 21EX (Palo Alto, CA, USA); and designed based on CT scans. External irradiation was delivered in four fractions per week (2.0 Gy daily fractions) to a total dose of 50–55 Gy.

Follow-up

After surgery, all patients were followed up at regular intervals with clinical examinations, trans-vaginal ultrasound, Papanicolaou tests and squamous cell carcinoma antigen tests; combined oral contraceptives were recommended for sexually active patients. Survival, recurrence, pregnancy and childbearing information were obtained from personal contact with the patient or her family. Overall survival was calculated from the date of diagnosis. Surviving patients were censored on the date of last follow-up.

Statistical analysis

Continuous variables were compared using Student's t test; categorical variables were compared using the chi squared test or Fisher's exact test, as appropriate. A P value < 0.05 was considered significant. All analyses were performed using SPSS version 19.0 (SPSS Inc., Chicago, IL, USA).

Acknowledgments

The authors wish to acknowledge the appreciated contribution of Dr. Xiang Wang regarding the continuing patient follow-up. We also thank Dr. Yajie Yin and Dr. Nan Gao for manuscript preparation.

Footnotes

CONFLICTS OF INTEREST

The authors have declared no conflicts of interest.

GRANT SUPPORT

This study was supported by the Taishan Scholars Program of Shandong Province, China [NO. ts201511073].

REFERENCES

  • 1.Jemal A, Bray F, Center MM, Ferlay J, Ward E, Forman D. Global cancer statistics. CA Cancer J Clin. 2011;61:69–90. doi: 10.3322/caac.20107. [DOI] [PubMed] [Google Scholar]
  • 2.Lanowska M, Mangler M, Speiser D, Bockholdt C, Schneider A, Köhler C, Vasiljeva J, Al-Hakeem M, Vercellino GF. Radical vaginal trachelectomy after laparoscopic staging and neoadjuvant chemotherapy in women with early-stage cervical cancer over 2 cm: oncologic, fertility, and neonatal outcome in a series of 20 patients. Int J Gynecol Cancer. 2014;24:586–593. doi: 10.1097/IGC.0000000000000080. [DOI] [PubMed] [Google Scholar]
  • 3.Hertel H, Köhler C, Michels W, Possover M, Tozzi R, Schneider A. Laparoscopic-assisted radical vaginal hysterectomy (LARVH): prospective evaluation of 200 patients with cervical cancer. Gynecol Oncol. 2003;90:505–511. doi: 10.1016/s0090-8258(03)00378-0. [DOI] [PubMed] [Google Scholar]
  • 4.Li J, Wu X, Li X, Ju X. Abdominal radical trachelectomy: Is it safe for IB1 cervical cancer with tumors ≥ 2 cm? Gynecol Oncol. 2013;131:87–92. doi: 10.1016/j.ygyno.2013.07.079. [DOI] [PubMed] [Google Scholar]
  • 5.Martínez A, Mery E, Filleron T, Boileau L, Ferron G, Querleu D. Accuracy of intraoperative pathological examination of SLN in cervical cancer. Gynecol Oncol. 2013;130:525–529. doi: 10.1016/j.ygyno.2013.01.023. [DOI] [PubMed] [Google Scholar]
  • 6.Noguchi H, Shiozawa I, Sakai Y, Yamazaki T, Fukuta T. Pelvic lymph node metastasis of uterine cervical cancer. Gynecol Oncol. 1987;27:150–158. doi: 10.1016/0090-8258(87)90287-3. [DOI] [PubMed] [Google Scholar]
  • 7.Kadkhodayan S, Hasanzadeh M, Treglia G, Azad A, Yousefi Z, Zarifmahmoudi L, Sadeghi R. Sentinel node biopsy for lymph nodal staging of uterine cervix cancer: a systematic review and meta-analysis of the pertinent literature. Eur J Surg Oncol. 2015;41:1–20. doi: 10.1016/j.ejso.2014.09.010. [DOI] [PubMed] [Google Scholar]
  • 8.Roy M, Bouchard-Fortier G, Popa I, Grégoire J, Renaud MC, Têtu B, Plante M. Value of sentinel node mapping in cancer of the cervix. Gynecol Oncol. 2011;122:269–274. doi: 10.1016/j.ygyno.2011.04.002. [DOI] [PubMed] [Google Scholar]
  • 9.Levenback C. Intraoperative lymphatic mapping and sentinel node identification: gynecologic applications. Recent Results Cancer Res. 2000;157:150–158. doi: 10.1007/978-3-642-57151-0_13. [DOI] [PubMed] [Google Scholar]
  • 10.Du XL, Sheng XG, Jiang T, Li QS, Yu H, Pan CX, Lu CH, Wang C, Song QQ. Sentinel lymph node biopsy as guidance for radical trachelectomy in young patients with early stage cervical cancer. BMC Cancer. 2011;11:157. doi: 10.1186/1471-2407-11-157. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Abu-Rustum NR, Sonoda Y. Fertility-sparing surgery in early-stage cervical cancer: indications and applications. J Natl Compr Canc Netw. 2010;8:1435–1438. doi: 10.6004/jnccn.2010.0107. [DOI] [PubMed] [Google Scholar]
  • 12.Cibula D, Sláma J, Svárovský J, Fischerova D, Freitag P, Zikán M, Pinkavová I, Pavlista D, Dundr P, Hill M. Abdominal radical trachelectomy in fertility-sparing treatment of early-stage cervical cancer. Int J Gynecol Cancer. 2009;19:1407–1411. doi: 10.1111/IGC.0b013e3181b9549a. [DOI] [PubMed] [Google Scholar]
  • 13.Rob L, Robova H, Halaska MJ, Hruda M, Skapa P. Current status of sentinel lymph node mapping in the management of cervical cancer. Expert Rev Anticancer Ther. 2013;13:861–870. doi: 10.1586/14737140.2013.811147. [DOI] [PubMed] [Google Scholar]
  • 14.Lécuru F, Mathevet P, Querleu D, Leblanc E, Morice P, Daraï E, Marret H, Magaud L, Gillaizeau F, Chatellier G, Dargent D. Bilateral negative sentinel nodes accurately predict absence of lymph node metastasis in early cervical cancer: results of the SENTICOL study. J Clin Oncol. 2011;29:1686–1691. doi: 10.1200/JCO.2010.32.0432. [DOI] [PubMed] [Google Scholar]
  • 15.Li J, Li Z, Wang H, Zang R, Zhou Y, Ju X, Ke G, Wu X. Radical abdominal trachelectomy for cervical malignancies: surgical, oncological and fertility outcomes in 62 patients. Gynecol Oncol. 2011;121:565–570. doi: 10.1016/j.ygyno.2011.01.032. [DOI] [PubMed] [Google Scholar]
  • 16.Hauspy J, Beiner M, Harley I, Ehrlich L, Rasty G, Covens A. Sentinel lymph nodes in early stage cervical cancer. Gynecol Oncol. 2007;105:285–290. doi: 10.1016/j.ygyno.2007.02.008. [DOI] [PubMed] [Google Scholar]
  • 17.Levenback C, Coleman RL, Burke TW, Lin WM, Erdman W, Deavers M, Delpassand ES. Lymphatic mapping and sentinel node identification in patients with cervix cancer undergoing radical hysterectomy and pelvic lymphadenectomy. J Clin Oncol. 2002;20:688–693. doi: 10.1200/JCO.2002.20.3.688. [DOI] [PubMed] [Google Scholar]
  • 18.Plante M, Renaud MC, Têtu B, Harel F, Roy M. Laparoscopic sentinel node mapping in early-stage cervical cancer. Gynecol Oncol. 2003;91:494–503. doi: 10.1016/j.ygyno.2003.08.024. [DOI] [PubMed] [Google Scholar]
  • 19.Gortzak-Uzan L, Jimenez W, Nofech-Mozes S, Ismiil N, Khalifa MA, Dubé V, Rosen B, Murphy J, Laframboise S, Covens A. Sentinel lymph node biopsy vs. pelvic lymphadenectomy in early stage cervical cancer: is it time to change the gold standard? Gynecol Oncol. 2010;116:28–32. doi: 10.1016/j.ygyno.2009.10.049. [DOI] [PubMed] [Google Scholar]
  • 20.Rob L, Strnad P, Robova H, Charvat M, Pluta M, Schlegerova D, Hrehorcak M. Study of lymphatic mapping and sentinel node identification in early stage cervical cancer. Gynecol Oncol. 2005;98:281–288. doi: 10.1016/j.ygyno.2005.04.016. [DOI] [PubMed] [Google Scholar]
  • 21.Fader AN, Edwards RP, Cost M, Kanbour-Shakir A, Kelley JL, Schwartz B, Sukumvanich P, Comerci J, Sumkin J, Elishaev E, Rohan LC. Sentinel lymph node biopsy in early-stage cervical cancer: utility of intraoperative versus postoperative assessment. Gynecol Oncol. 2008;111:13–17. doi: 10.1016/j.ygyno.2008.06.009. [DOI] [PubMed] [Google Scholar]
  • 22.Di Stefano AB, Acquaviva G, Garozzo G, Barbic M, Cvjeticanin B, Meglic L, Kobal B, Rakar S. Lymph node mapping and sentinel node detection in patients with cervical carcinoma: a 2-year experience. Gynecol Oncol. 2005;99:671–679. doi: 10.1016/j.ygyno.2005.07.115. [DOI] [PubMed] [Google Scholar]
  • 23.Slama J, Dundr P, Dusek L, Cibula D. High false negative rate of frozen section examination of sentinel lymph nodes in patients with cervical cancer. Gynecol Oncol. 2013;129:384–388. doi: 10.1016/j.ygyno.2013.02.001. [DOI] [PubMed] [Google Scholar]
  • 24.Marchiolé P, Buénerd A, Benchaib M, Nezhat K, Dargent D, Mathevet P. Clinical significance of lympho vascular space involvement and lymph node micrometas- tases in early-stage cervical cancer: a retrospective case-control surgico-pathological study. Gynecol Oncol. 2005;97:727–732. doi: 10.1016/j.ygyno.2005.01.004. [DOI] [PubMed] [Google Scholar]
  • 25.Fregnani JH, Latorre MR, Novik PR, Lopes A, Soares FA. Assessment of pelvic lymph node micrometastatic disease in stages IB and IIA of carcinoma of the uterine cervix. Int J Gynecol Cancer. 2006;16:1188–1194. doi: 10.1111/j.1525-1438.2006.00519.x. [DOI] [PubMed] [Google Scholar]
  • 26.Horn LC, Hentschel B, Fischer U, Peter D, Bilek K. Detection of micrometastases in pelvic lymph nodes in patients with carcinoma of the cervix uteri using step sectioning: frequency, topographic distribution and prognostic impact. Gynecol Oncol. 2008;111:276–281. doi: 10.1016/j.ygyno.2008.07.017. [DOI] [PubMed] [Google Scholar]
  • 27.Cibula D, Abu-Rustum NR, Dusek L, Zikán M, Zaal A, Sevcik L, Kenter GG, Querleu D, Jach R, Bats AS, Dyduch G, Graf P, Klat J, et al. Prognostic significance of low volume sentinel lymph node disease in early-stage cervical cancer. Gynecol Oncol. 2012;124:496–501. doi: 10.1016/j.ygyno.2011.11.037. [DOI] [PubMed] [Google Scholar]
  • 28.Wethington SL, Sonoda Y, Park KJ, Alektiar KM, Tew WP, Chi DS, Leitao MM, Jr, Jewell EL, Barakat RR, Abu-Rustum NR. Expanding the indications for radical trachelectomy: a report on 29 patients with stage IB1 tumors measuring 2 to 4 centimeters. Int J Gynecol Cancer. 2013;23:1092–1098. doi: 10.1097/IGC.0b013e318296034e. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.Lintner B, Saso S, Tarnai L, Novak Z, Palfalvi L, G Del Priore, Smith JR, Ungar L. Use of abdominal radical trachelectomy to treat cervical cancer greater than 2 cm in diameter. Int J Gynecol Cancer. 2013;23:1065–1070. doi: 10.1097/IGC.0b013e318295fb41. [DOI] [PubMed] [Google Scholar]
  • 30.Dargent D, Franzosi F, Ansquer Y, Martin X, Mathevet P, Adeline P. [Extended trachelectomy relapse: plea for patient involvement in the medical decision] Bull Cancer. 2002;89:1027–1030. [PubMed] [Google Scholar]
  • 31.Marchiole P, Benchaib M, Buenerd A, Lazlo E, Dargent D, Mathevet P. Oncological safety of laparoscopic-assisted vaginal radical trachelectomy (LARVT or Dargent's operation): a comparative study with laparoscopic-assisted vaginal radical hysterectomy (LARVH) Gynecol Oncol. 2007;106:132–141. doi: 10.1016/j.ygyno.2007.03.009. [DOI] [PubMed] [Google Scholar]
  • 32.Kim CH, Abu-Rustum NR, Chi DS, Gardner GJ, Leitao MM, Jr, Carter J, Barakat RR, Sonoda Y. Reproductive outcomes of patients undergoing radical trachelectomy for early-stage cervical cancer. Gynecol Oncol. 2012;125:585–588. doi: 10.1016/j.ygyno.2012.03.014. [DOI] [PubMed] [Google Scholar]
  • 33.Kim CH, Abu-Rustum NR, Chi DS, Gardner GJ, Leitao MM, Jr, Carter J, Barakat RR, Sonoda Y. Reproductive outcomes of patients undergoing radical trachelectomy for early-stage cervical cancer. Gynecol Oncol. 2012;125:585–588. doi: 10.1016/j.ygyno.2012.03.014. [DOI] [PubMed] [Google Scholar]

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