Factors associated with parametrial involvement in patients with stage IB1 cervical cancer: Who is suitable for less radical surgery?

Article information

Obstet Gynecol Sci. 2018;61(1):88-94
Publication date (electronic) : 2017 December 15
doi : https://doi.org/10.5468/ogs.2018.61.1.88
1Department of Obstetrics and Gynecology, Gil Medical Center, Gachon University of Medicine and Science, Incheon, Korea.
2Department of Pathology, Gil Medical Center, Gachon University of Medicine and Science, Incheon, Korea.
Corresponding author: Soyi Lim. Department of Obstetrics and Gynecology, Gil Medical Center, Gachon University of Medicine and Science, 21 Namdong-daero 774-beon-gil, Namdong-gu, Incheon 21565, Korea. soyilim@gmail.com
Received 2017 April 10; Revised 2017 June 22; Accepted 2017 July 06.

Abstract

Objective

To detect the possible clinicopathologic factors associated with parametrial involvement in patients with stage IB1 cervical cancer and to identify a cohort of patients who may benefit from less radical surgery.

Methods

We retrospectively reviewed 120 patients who underwent radical hysterectomy and pelvic lymphadenectomy as treatment for stage IB1 cervical cancer.

Results

Overall, 18 (15.0%) patients had parametrial tumor involvement. Tumor size larger than 2 cm, invasion depth greater than 1 cm, presence of lymphovascular space involvement (LVSI), corpus involvement, and positive lymph nodes were statistically associated with parametrial involvement. Multivariate analysis for other factors showed invasion depth >1 cm (P=0.029), and corpus involvement (P=0.022) were significantly associated with parametrial involvement. A subgroup with tumor size smaller than 2 cm showed no parametrial involvement, regardless of invasion depth or presence of LVSI.

Conclusion

Tumor size smaller than 2 cm showed no parametrial involvement, regardless of invasion depth or presence of LVSI. Invasion depth >1 cm and corpus involvement were significantly associated with parametrial involvement in multivariate analysis. These finding may suggest that tumor size may a strong predictor of parametrial involvement in International Federation of Gynecology and Obstetrics stage IB1 cervical cancer, which can be used to select a subgroup population for less radical surgery.

Introduction

Women with stage IB1 cervical cancer are typically treated by radical hysterectomy and bilateral lymph node dissection. Radical hysterectomy includes removal of the parametrial tissue, as well as a third to half of the upper vagina. The removal of parametrial tissue is important in the treatment of cervical cancer because this area is the most frequently affected site of cancer spread. The tumor can spread to the parametrium through either direct microscopic extension or by tumor embolization from the primary lesion to lymph nodes in the parametrial tissue. The incidence of pathological parametrial involvement has been reported to be between 6% and 31% [123]. Important prognostic factors in cervical cancer include tumor size, parametrial disease spread, lymphovascular space involvement (LVSI), and lymph node metastasis. However, parametrectomy is the main cause of postoperative complications which may include bladder dysfunction, sexual dysfunction, and anorectal mobility disorders attributable to partial denervation of the autonomic nerve supply to the pelvic organs which may occur during parametrial resection. Although, in the randomized controlled trial about nerve-sparing surgery to minimize these complications, nerve-sparing radical surgery was effective in preserving bladder function without sacrificing oncologic safety [4], more data is necessary for this issue.

Some authors suggested that less radical surgery should be applied in patient populations with favorable prognostic factors and low risk of parametrial involvement. Kim et al. [5] reported that stage IB1 patients with superficial invasion (<5 mm) have very low risk of parametrial involvement and thus, less radical surgery may be performed. Kodama et al. [6] also demonstrated that stage IB1 patients with depth of invasion (DOI) less than 10 mm, no LVSI, and less than 50 years of age should be considered as potential recipients of modified radical hysterectomy, or simple hysterectomy with pelvic lymphadenectomy.

In the present study, we evaluated the clinicopathologic factors associated with pathologic parametrial involvement in patients with stage IB1 cervical cancer. In addition, we identified those patients at low risk for parametrial involvement who may benefit from less radical surgery.

Materials and methods

A retrospective study was performed using a database of patients who underwent type III radical hysterectomy between January 2002 and December 2007 with the approval of the Institutional Review Board. We found that 120 consecutive patients diagnosed with International Federation of Gynecology and Obstetrics (FIGO) stage IB1 were treated with type III radical hysterectomy and pelvic lymph node dissection, either with or without para-aortic lymph node dissection. Patients who received primary radiotherapy and chemotherapy were excluded from our study. Patients with microinvasive carcinoma and patients treated by type I simple hysterectomy or type II modified radical hysterectomy, were also excluded.

The histological diagnosis was made using either punch biopsy or cone excision. Tumor diameter was obtained from the pathological measurements at conization or using the hysterectomy specimen. Radical hysterectomy included complete resection of cervical fascia (anterior parametrium), and uterosacral and rectovaginal ligaments (lateral and posterior parametrium). The pelvic lymphadenectomy consisted of systematic dissection of the common iliac, internal and external iliac vessels, and the obturator nodes both above and below the obturator nerves. Para-aortic lymph node dissection was performed from the level of the aortic bifurcation to the inferior mesenteric artery. The para-aortic nodes were dissected if suspicious pelvic nodes were detected. Pathologic data was collected by review of the pathology report. All hysterectomy specimens were collected and processed in a routine manner. The parametrium was usually defined as the connective tissue of the pelvic floor extending laterally from the fibrous subserous coat between the layers of the broad ligament in the supracervical part of the uterus. The parametrial tissue from all excised specimens was processed and examined to evaluate possible microscopic tumor spread. Abstracted pathologic data included: histologic subtype, depth of tumor invasion, LVSI, parametrial tumor involvement, vaginal or uterine corpus involvement, lymph node status, and status of the margins of resection. DOI and tumor size after conization were not added to those of hysterectomy specimens.

The associations between these pathologic factors and parametrial tumor involvement were evaluated using either χ2 or Fisher exact tests. Multivariate analysis was performed using stepwise logistic regression analysis. A P-value under 0.05 was taken to indicate statistical significance, and all tests were 2-sided. The statistical analysis was performed using SPSS version 12.0 (SPSS Inc., Chicago, IL, USA).

Results

The study population consisted of 120 women with FIGO stage IB1 who underwent radical hysterectomy, and pelvic and/or para-aortic lymph node dissection. Patient characteristics are shown in Table 1. Overall, 18 (15.0%) cases were observed to include parametrial tumor involvement. The median follow-up period was thirty-seven months (range, 1–81).

Clinical characteristics of patients

Patients with tumors larger than 2 cm had a 22.5% risk of parametrial involvement, compared with 0% for patients with tumors 2 cm or smaller (P=0.002). Cases with invasion depths greater than 1 cm were significantly associated with parametrial spread. Patients with invasion depths greater than 1 cm had a 32.7% probability for parametrial tumor spread, while those with invasion depths lesser than or equal to 1 cm had only a 1.5% probability for tumor spread (P<0.001). Uterine corpus involvement was also significantly associated with parametrial spread. Patients with uterine corpus involvement had a 70.0% probability of parametrial tumor spread, as compared to 10.0% for those without uterine involvement (P<0.001). Lymph node status correlated highly with parametrial involvement. Parametrial involvement was associated with lymph node metastasis in 52.9% of patients, as compared to 8.7% association with negative lymph nodes (P<0.001). Patients with LVSI had a 24.0% risk of parametrial involvement as compared to 8.6% of patients with negative LVSI (P=0.038). Histologic grade and histology subtype had no significant effect on parametrial involvement (Table 2). However, we had many missing data in histologic grade.

Variables associated with parametrial involvement

Tumor size more than 2 cm was considered for major factors associated with parametrial involvement, because a subgroup with tumor size smaller than 2 cm showed no parametrial involvement regardless of invasion depth or presence of LVSI. Therefore, multivariate analysis was performed for other clinicopathologic factors most associated with parametrial involvement except tumor size. After controlling for confounding factors, multivariate analysis for other factors showed invasion depth more than 1 cm (odds ratio [OR], 11.5; P=0.029), and uterine involvement (OR, 10.1; P=0.022), were significantly associated with parametrial involvement (Table 3).

Multivariate analysis of the risk factors for parametrial involvement

We identified a cohort of women with low risk for parametrial involvement using preoperatively accessible risk factors including tumor size, DOI, and LVSI (Table 4). There was no parametrial spread for any of the 40 patients with tumor size less than or equal to 2 cm. However, one patient with a tumor size lesser than or equal to 2 cm, an invasion depth more than 10 mm and positive LVSI, had lymph node metastasis. Among the 80 patients with tumor size greater than 2 cm, 20 patients suffered an invasion depth less than or equal to 10 mm, negative LVSI and no parametrial involvement. One patient with a tumor size greater than 2 cm, an invasion depth less than or equal to 10 mm, and positive LVSI, suffered parametrial spread. Among 47 patients with tumor size greater than 2 cm and invasion depth greater than 10 mm, 17 patients had parametrial involvement regardless of LVSI.

Relationship of depth of invasion, tumor size, and lymphovascular space involvement to parametrial disease and lymph node metastasis

Discussion

In the present study, we found that parametrial involvement occurred with an incidence of 15.0% in patients with FIGO stage IB1 cervical cancer. These findings are higher than those of previous studies which reported parametrial involvement incidences of 8.4%–10.7% in similar patient groups. It is plausible that the higher incidence of parametrial involvement observed in the present study results from the two third of patients (80 out of 120) having a tumor size greater than 2 cm, and patients with less advanced stage IA were included in the results of other studies. In the present study, the portion of chemotherapy only (30.8%) was higher than that of radiotherapy only (9.2%). The patients who received chemotherapy only were patients with intermediate risk factors of Sedlis criteria. According to the National Comprehensive Cancer Network guidelines, in case of absence of high-risk factors, observation or pelvic radiation with or without chemotherapy is recommended as post-operative adjuvant therapy. It is caused by the pattern of our institution for adjuvant treatment in cervical cancer patients with intermediate risk factors after radical surgery.

Spread of disease to parametrial tissue is associated with the size of the primary tumor. Winter et al. [7] observed that the rate of parametrial involvement increased from 6.7% to 33.0% in tumors 5–20 mL in volume. Therefore, many patients with stage IB1 cervical cancer may be over treated with radical surgery. There is no evidence tying the extent of parametrium resection with prevention of recurrence. Large numbers of IB1 patients with small lesions or favorable prognostic factors are being prescribed unnecessary overtreatment. Kim et al. [5] reported that stage IB1 patients with DOI less than or equal to 5 mm are at very low risk for parametrial involvement, and those patients are candidates for less radical surgery, omitting parametrectomy. Identification of useful predictors or factors associated with parametrial involvement allows clinicians to decrease the use of parametrial resection and reduce the occurrence and severity of its resultant complications. Using univariate analysis, our study showed that parametrial involvement was indicated with preoperative observations including, a tumor size more than 2 cm, an invasion depth greater than 1 cm, uterine involvement, lymph node metastasis, and positive LVSI. Patients with small tumors, negative LVSI, and invasion depth 1cm or less had a 0% risk for parametrial involvement in the subgroup analysis.

Previous studies including stage IA1–IIA patients have reported that large tumor size, higher histologic grade, presence of LVSI, and positive pelvic lymph nodes are associated with parametrial involvement in early stage of cervical cancer [689101112]. Large tumor size strongly correlated with parametrial involvement in most previous studies. Kamimori et al. [9] evaluated parametrial involvement in patients with stage IB1 disease and reported a 5.6% incidence. They suggested that parametrial involvement was found less frequently in patients with tumor diameter 20 mm or less, and preoperative tumor diameters imaged by magnetic resonance imaging (MRI) correlated well with parametrial involvement and other pathologic prognostic factors associated with FIGO stage IB1 cervical cancer. Most previous studies demonstrated that patients with parametrical involvement were more likely to have a primary tumor with a size larger than 2 cm [9101112]. Wright et al. [11] found that the incidence of parametrial involvement was only 0.4% in patients with negative nodes, no LVSI, and tumor size less than 2 cm. Frumovitz et al. [10] also found that there was no evidence of parametrial involvement in patients with primary tumor size less than 2 cm and no LVSI. In the present study, patients with tumor size less than or equal to 2 cm had no parametrial disease involvement, and only one patient with an invasion depth greater than 10 mm and positive LVSI, resulted with lymph node metastasis. A previous study reported that patients with an invasion depth greater than 5 mm had no parametrial disease [5]. Other investigators have presented 10 mm of invasion depth as the limit associated with parametrial spread [1613]. They showed that the incidence of parametrial involvement was only 0.6%–1.1% in a subset of patients with 10 mm DOI, and without other prognostic factors.

Positive lymph nodes have been previously reported as predictive of parametrial involvement [16810111314]. However, our study found that lymph node status was not associated with parametrial involvement by multivariate analysis, yet univariate indicated that lymph node status was associated with parametrial spread. It might be because there are several routes of parametrial involvement such as parametrial lymphovascular invasion, direct invasion, and parametrial lymphatic metastasis in cervical cancer [15]. van den Tillaart et al. [16] have found that only 50% of the parametrial invasion lesions are caused by direct invasion, whereas the other 50% of the lesions are not connected with primary lesions, which are distributed over the parametrium randomly. In the group of patients with lesions of pulsatility index that are not connected with primary tumors, van den Tillaart et al. [16] have found that the metastasis lesions are often in lymph nodes and/or lymph vessels, but are rarely in the blood vessels or isolated lesions. And small number of the present study may be another reason of no association of lymph node metastasis and parametrial involvement in multivariate analysis. Covens et al. [1] demonstrated that age and grade are also prognostic of parametrial invasion. However in our study, age and histologic grade did not have an association with parametrial disease spread.

Many authors have attempted to identify a cohort of women with early stage cervical cancer who are at low risk for parametrial involvement, and who are potential candidates for less radical surgery [19101112]. Most of these subsets have tumor sizes smaller than 2 cm, negative lymph nodes, invasion depth less than 10 mm, and negative LVSI. These findings were confirmed by our study. We chose subgroup criteria for parametrial spread to include tumor size, DOI, and LVSI, because these factors can be preoperatively assessed by pathological examination of the cone biopsy specimen or imaging study. We showed that patients with tumor size less than 2 cm had no parametrial disease, regardless of invasion depth or presence of LVSI. Therefore, if clinicians may know the tumor size before surgery by imaging study, it may be helpful to decide less radical surgery. Further investigation is needed.

The justification for complete parametrectomy in stage IB1 disease for all tumor sizes is the assumption that parametrial metastases can occur equally in both the lateral and medial parametrial [21718]. Less radical surgery, such as type I or II hysterectomy with lymph node dissection, may be a possible alternative in low risk candidates with clinical observations such as small tumor size, negative lymph node, superficial invasion, and negative LVSI. The primary goal of decreasing radical surgery is to prevent intraoperative complications such as ureteric injury, fistulas, blood loss, and long-term complications such as urinary dysfunction [19]. A randomized study of type II and III radical hysterectomy cases demonstrated no difference in recurrence and survival rate, but the type II hysterectomy group had fewer postoperative complications [20]. There are other advantages for patients in receiving less radical surgery in terms of shorter operative duration, lower volume of blood transfusion, shorter length of hospital stay, and reduced perioperative morbidity risk [21].

The limitation of this study is the retrospective nature. Although, retrospective finding of parametrium involvement factor after surgery may be meaningful, these factors are already well-known. And more important point is to find out the factors associated with parametrial involvement before surgery such as preoperative tumor size on MRI.

In conclusion, this study shows the association of parametrial involvement with tumor size, lymph node status, invasion depth, uterine involvement, and LVSI, an association that has also been suggested in many other previous studies. Also, a subgroup with tumor size smaller than 2 cm showed no parametrial involvement, regardless of invasion depth or presence of LVSI, and therefore patients with these observations may be considered for less radical surgery. Stage IB1 patients should be evaluated in a larger, prospective study to include assessment of preoperatively accessible predictors of parametrial involvement, the extent of radical surgery performed, and postoperative complications.

Notes

Conflict of interest: No potential conflict of interest relevant to this article was reported.

References

1. Covens A, Rosen B, Murphy J, Laframboise S, DePetrillo AD, Lickrish G, et al. How important is removal of the parametrium at surgery for carcinoma of the cervix? Gynecol Oncol 2002;84:145–149. 11748991.
2. Benedetti-Panici P, Maneschi F, D'Andrea G, Cutillo G, Rabitti C, Congiu M, et al. Early cervical carcinoma: the natural history of lymph node involvement redefined on the basis of thorough parametrectomy and giant section study. Cancer 2000;88:2267–2274. 10820348.
3. Delgado G, Bundy BN, Fowler WC Jr, Stehman FB, Sevin B, Creasman WT, et al. A prospective surgical pathological study of stage I squamous carcinoma of the cervix: a Gynecologic Oncology Group Study. Gynecol Oncol 1989;35:314–320. 2599466.
4. Roh JW, Lee DO, Suh DH, Lim MC, Seo SS, Chung J, et al. Efficacy and oncologic safety of nerve-sparing radical hysterectomy for cervical cancer: a randomized controlled trial. J Gynecol Oncol 2015;26:90–99. 25872890.
5. Kim MK, Kim JW, Kim MA, Kim HS, Chung HH, Park NH, et al. Feasibility of less radical surgery for superficially invasive carcinoma of the cervix. Gynecol Oncol 2010;119:187–191. 20663542.
6. Kodama J, Kusumoto T, Nakamura K, Seki N, Hongo A, Hiramatsu Y. Factors associated with parametrial involvement in stage IB1 cervical cancer and identification of patients suitable for less radical surgery. Gynecol Oncol 2011;122:491–494. 21703671.
7. Winter R, Haas J, Reich O, Koemetter R, Tamussino K, Lahousen M, et al. Parametrial spread of cervical cancer in patients with negative pelvic lymph nodes. Gynecol Oncol 2002;84:252–257. 11812083.
8. Puente R, Guzman S, Israel E, Poblete MT. Do the pelvic lymph nodes predict the parametrial status in cervical cancer stages IB-IIA? Int J Gynecol Cancer 2004;14:832–840. 15361191.
9. Kamimori T, Sakamoto K, Fujiwara K, Umayahara K, Sugiyama Y, Utsugi K, et al. Parametrial involvement in FIGO stage IB1 cervical carcinoma diagnostic impact of tumor diameter in preoperative magnetic resonance imaging. Int J Gynecol Cancer 2011;21:349–354. 21721193.
10. Frumovitz M, Sun CC, Schmeler KM, Deavers MT, Dos Reis R, Levenback CF, et al. Parametrial involvement in radical hysterectomy specimens for women with early-stage cervical cancer. Obstet Gynecol 2009;114:93–99. 19546764.
11. Wright JD, Grigsby PW, Brooks R, Powell MA, Gibb RK, Gao F, et al. Utility of parametrectomy for early stage cervical cancer treated with radical hysterectomy. Cancer 2007;110:1281–1286. 17654664.
12. Smith AL, Frumovitz M, Schmeler KM, dos Reis R, Nick AM, Coleman RL, et al. Conservative surgery in early-stage cervical cancer: what percentage of patients may be eligible for conization and lymphadenectomy? Gynecol Oncol 2010;119:183–186. 20708227.
13. Stegeman M, Louwen M, van der Velden J, ten Kate FJ, den Bakker MA, Burger CW, et al. The incidence of parametrial tumor involvement in select patients with early cervix cancer is too low to justify parametrectomy. Gynecol Oncol 2007;105:475–480. 17292460.
14. Steed H, Capstick V, Schepansky A, Honore L, Hiltz M, Faught W. Early cervical cancer and parametrial involvement: is it significant? Gynecol Oncol 2006;103:53–57. 16516279.
15. Cândido EB, Silva-Filho AL, Triginelli SA, Pedrosa MS, Macarenco R, Porto L, et al. Histopathological and immunohistochemical (cytokeratins AE1/AE3) study of the parametrium of patients with early stage cervical cancer. Eur J Obstet Gynecol Reprod Biol 2008;141:58–63. 18938023.
16. van den Tillaart SA, Trimbos JB, Dreef EJ, Jordanova ES, Fleuren GJ. Patterns of parametrial involvement in radical hysterectomy specimens of cervical cancer patients. Int J Gynecol Pathol 2011;30:185–192. 21293280.
17. Girardi F, Lichtenegger W, Tamussino K, Haas J. The importance of parametrial lymph nodes in the treatment of cervical cancer. Gynecol Oncol 1989;34:206–211. 2753426.
18. Burghardt E, Pickel H. Local spread and lymph node involvement in cervical cancer. Obstet Gynecol 1978;52:138–145. 683652.
19. Chen GD, Lin LY, Wang PH, Lee HS. Urinary tract dysfunction after radical hysterectomy for cervical cancer. Gynecol Oncol 2002;85:292–297. 11972390.
20. Landoni F, Maneo A, Cormio G, Perego P, Milani R, Caruso O, et al. Class II versus class III radical hysterectomy in stage IB-IIA cervical cancer: a prospective randomized study. Gynecol Oncol 2001;80:3–12. 11136561.
21. Panici PB, Angioli R, Palaia I, Muzii L, Zullo MA, Manci N, et al. Tailoring the parametrectomy in stages IA2-IB1 cervical carcinoma: is it feasible and safe? Gynecol Oncol 2005;96:792–798. 15721427.

Article information Continued

Table 1

Clinical characteristics of patients

Characteristics Patients (n=120)
Age (yr) 46 (22–77)
DOI (mm) 9 (2–28)
Tumor size (mm) 19 (4–75)
Histologic subtype
Squamous cell carcinoma 100 (83.3)
Adenocarcinoma 15 (12.5)
Adenosquamous 5 (4.2)
No. of lymph nodes removed 34 (12–96)
LVSI 50 (41.7)
Parametrial involvement 18 (15.0)
Lymph node metastasis 17 (14.2)
Positive resection margin 4 (3.3)
Uterine involvement 10 (8.3)
Vaginal involvement 11 (9.2)
Adjuvant treatment
None 45 (37.5)
Radiotherapy 11 (9.2)
Chemotherapy 37 (30.8)
Chemoradiation 27 (22.5)

Values are presented as median (range) or number (%).

DOI, depth of invasion; LVSI, lymphovascular space involvement.

Table 2

Variables associated with parametrial involvement

Variables Parametrium P-value
Negative (n=102) Positive (n=18)
Mean age (yr) 52.3 (22–71) 55.1 (31–77) 0.543
Tumor size (cm) 0.002
≤2 40 (100.0) 0
>2 62 (77.5) 18 (22.5)
DOI (cm) <0.001
≤1 67 (98.5) 1 (1.5)
>1 35 (67.3) 17 (32.7)
Corpus involvement <0.001
Negative 99 (90.0) 11 (10.0)
Positive 3 (30.0) 7 (70.0)
Vaginal involvement 0.060
Negative 95 (87.2) 14 (12.8)
Positive 7 (63.6) 4 (36.4)
Resection margins 0.096
Negative 100 (86.2) 16 (13.8)
Positive 2 (50.0) 2 (50.0)
Lymph nodes <0.001
Negative 94 (91.3) 9 (8.7)
Positive 8 (47.1) 9 (52.9)
LVSI 0.038
Negative 64 (91.4) 6 (8.6)
Positive 38 (76.0) 12 (24.0)
Histologic grade 0.395
Grade 1 27 (90.0) 3 (10.0)
Grade 2 30 (78.9) 8 (21.1)
Grade 3 5 (100.0) 0
NA 47
Histologic subtype 0.302
SCC 83 (83.0) 17 (17.0)
Non-SCC 19 (95.0) 1 (5.0)

Values are presented as median (range) or number (%).

DOI, depth of invasion; LVSI, lymphovascular space involvement; NA, not availabale; SCC, squamous cell carcinoma.

Table 3

Multivariate analysis of the risk factors for parametrial involvement

Variables OR 95% CI P-value
Invasion depth >1 cm 11.460 1.290–101.792 0.029
Corpus involvement 10.113 1.400–73.066 0.022
Lymph node metastasis 3.499 0.826–14.823 0.089
LVSI 1.925 0.502–7.386 0.340

OR, odds ratio; CI, confidence interval; LVSI, lymphovascular space involvement.

Table 4

Relationship of depth of invasion, tumor size, and lymphovascular space involvement to parametrial disease and lymph node metastasis

Variables (cm) No. Parametrial involvement Lymph node metastasis
Tumor size ≤2 DOI ≤1 LVSI (−) 26 0 0
LVSI (+) 9 0 0
DOI >1 LVSI (−) 1 0 0
LVSI (+) 4 0 1
Tumor size >2 DOI ≤1 LVSI (−) 20 0 1
LVSI (+) 13 1 1
DOI >1 LVSI (−) 23 6 5
LVSI (+) 24 11 9

DOI, depth of invasion; LVSI, lymphovascular space involvement.