Hysterectomy is the most common major surgery with almost 400,000 cases for benign indications performed in the United States annually.1 Compared with abdominal hysterectomies, minimally invasive approaches confer a lower risk of perioperative complications and quicker recovery.2 However, smaller incisions present the challenge of removing large specimens. The practice of morcellation has been used for decades, but the introduction of electromechanical morcellators facilitated the removal of tissue during endoscopic procedures.3 The practice has come under scrutiny as a result of concerns over the inadvertent dissemination of occult malignancies of presumed benign tissue.4,5 Doing so may worsen the prognosis of uterine sarcoma and confer the need for additional treatment.6,7 This has led the U.S. Food and Drug Administration (FDA) to issue a safety communication “discouraging the use of power morcellation” and has resulted in changes in surgical practice.8,9
The incidence of occult sarcoma in women undergoing hysterectomy is unclear with rates ranging from 1 in 204 to 1 in 667 in women with presumed myomas.10,11 Risk estimates from the FDA and American College of Obstetricians and Gynecologists range from 1 in 352 to 1 in 500, respectively, for women undergoing surgery for presumed myomas.12,13 A recent study examining 6,360 women undergoing hysterectomy for benign indications found a 1 in 500 risk of sarcoma in this broader group of women.14 To guide patient counseling and clinical practice, we sought to estimate the frequency of unsuspected sarcoma identified in women undergoing hysterectomy for presumed benign conditions at our institution.
MATERIALS AND METHODS
After approval from the University of Texas Southwestern Medical Center institutional review board, all cases of hysterectomy performed for benign gynecologic indications from September 2000 to December 2014 at the University of Texas Southwestern Medical Center and Parkland Memorial Hospital were identified from a prospectively maintained departmental billing database, which includes all surgeries performed on our campus by the University of Texas Southwestern faculty. The database is maintained with quality assurance by a database specialist and is searchable through International Classification of Diseases codes, Current Procedural Terminology codes, and faculty names. The database was queried for all hysterectomies performed during this time period. Cases performed for obstetric purposes and for malignancy or suspected malignancies were excluded.
As a designated Academic Comprehensive Cancer Program by the American College of Surgeons' Commission on Cancer, we utilized the tumor registry of each hospital at the University of Texas Southwestern to identify all cases of uterine sarcoma. The tumor registry, which maintains records of all patients with cancer diagnosed and treated at the hospital, was queried using the search terms “leiomyosarcoma,” “endometrial stromal sarcoma,” “adenosarcoma,” “undifferentiated sarcoma,” and “uterine sarcoma, not otherwise specified.” Carcinosarcoma (previously known as malignant mixed Müllerian tumor) was excluded from this analysis because it is no longer considered pure sarcoma and is considered poorly differentiated carcinoma.
For all uterine sarcoma cases, data regarding clinical presentation, preoperative evaluation, intraoperative findings, and pathology were systematically reviewed from the medical record. Unexpected sarcomas were defined as cases in which uterine sarcoma was confirmed on surgical pathology but did not have clinical preoperative suspicion or indication of malignancy. Because the staging system for uterine sarcoma changed during our study period, we assigned International Federation of Gynecology and Obstetrics 2009 sarcoma and adenosarcoma staging systems to all identified occult sarcomas. Relevant clinical and pathologic data were collected from the medical record including symptoms, family history of cancer, preoperative diagnosis, uterine size, imaging studies, surgeon subspecialty, surgical procedure, pathologic findings, further treatment, interventions, or both, and survival status. Demographics and patient characteristics were summarized using descriptive statistics and Wilcoxon rank-sum test was used to compare uterine weights by sarcoma type. Exact Clopper-Pearson (closed form) was used to calculate confidence limits.15 Data analyses were performed using SAS 9.3. P<.05 was considered statistically significant.
A total of 10,119 hysterectomies for benign gynecologic indications were performed during this time period, including abdominal (59.4%), laparoscopic or robotic-assisted (21.6%), and vaginal approaches (18.9%). Among these, nine patients were found to have an unexpected uterine sarcoma with an overall rate of 1 in 1,124 (95% confidence interval [CI] 1/592–1/2,457). These malignancies included five leiomyosarcomas, two endometrial stromal sarcomas, and two uterine adenosarcomas. Thus, in our population, the rate of unexpected leiomyosarcomas is 1 in 2,024 (95% CI 1/909–1/6,250) and 1 in 5,060 (95% CI 1/401–1/41,841) for endometrial stromal sarcomas and adenosarcomas.
The most common primary indications for hysterectomy were leiomyomata (37%), abnormal uterine bleeding (28%), and pelvic organ prolapse (11%). In the cohort of women with occult sarcoma, hysterectomy was performed as a primary indication for abnormal bleeding (77.8%) and leiomyomas (22.2%). Seven of nine (77.8%) patients did report either a pelvic mass or uterine myomas as a first or secondary indication.
The average age of women undergoing hysterectomy for benign indications was 45.3 years. In the cohort of women found to have an unanticipated sarcoma at the time of hysterectomy, the median age at diagnosis was 39 years (range 25–53 years); none were postmenopausal. The ethnic makeup was mixed: four were Hispanic, three were non-Hispanic white, and two were black. Median body mass index (calculated as weight [kg]/[height (m)]2) was 27 (range 20–46).
Regarding known or proposed risk factors that may be associated with sarcomas, two women were known to have taken combined oral contraceptives, one had been on progesterone-only pills, four were not on hormones, and the status of two women was unobtainable from chart review. Three women had been given leuprolide acetate preoperatively; two women (one with leiomyosarcoma, one with endometrial stromal sarcoma) experienced improved bleeding and only one woman (found to have a leiomyosarcoma) experienced a size reduction in her uterus. None of the women had a history of tamoxifen use or pelvic irradiation, and all denied a family history of cancer. Only one patient gave a history of rapid uterine growth; she was a 25-year-old woman with increasing abdominal girth over 6 months who was found to have a 52-cm uterus on imaging, ultimately diagnosed with leiomyosarcoma postoperatively.
Preoperative evaluation of the patients included up-to-date cervical cancer screening in all cases. Two patients had an atypical squamous cells of undetermined significance Pap smear with negative high-risk human papillomavirus testing. Preoperative imaging was obtained in eight of nine participants; six had pelvic ultrasonography, one sonohysterogram, and one computed tomography scan. None of these imaging studies were suspicious for malignancy. Five women had preoperative endometrial sampling, four with normal findings and one with insufficient tissue.
All women with occult sarcoma were operated on by obstetrician–gynecologist specialists. No cases in which an occult sarcoma was identified was performed by a subspecialist such as female pelvic reconstruction, reproductive endocrinology, or gynecologic oncology subspecialists. The cases included six total abdominal hysterectomies (TAH), two total vaginal hysterectomies, and one abdominal supracervical hysterectomy. One patient undergoing TAH required manual morcellation of a large bulky uterus. Electromechanical morcellation was not used in any of the cases (Table 1).
The one patient who underwent morcellation of an occult sarcoma was a 53-year-old found to have a stage IB leiomyosarcoma who underwent TAH and bilateral salpingo-oophorectomy (BSO) with uncontained manual morcellation of a bulky 1,692-g uterus. During the procedure, a suspicious-appearing uterine mass was noted and sent for frozen section, which suggested leiomyosarcoma. Intraoperative gynecologic oncology was requested, and the abdominal cavity was thoroughly explored, with no findings of suspicious disease. She was not upstaged as result of the morcellation. The patient was subsequently treated with six cycles of gemcitabine and docetaxel. As of January 2015, she is alive, well, and has had no evidence of disease 3 years since her surgery.
The two uteri found to have endometrial stromal sarcoma weighed 90 g and 93 g. The two uteri with adenosarcoma uteri weighed 116 g and 225 g. The five uteri found to have leiomyosarcoma were significantly larger with a median weight of 1,692 g (range 144–13,062 g; P=.03). The five women with leiomyosarcoma were stage IA (one) and IB (four); the two adenosarcomas were stage IB (one) and II (one); the two endometrial stromal sarcomas were stage IA.
Three patients did not receive any additional surgery or treatments outside of observation. Three patients underwent subsequent BSO, one with additional pelvic and paraaortic lymphadenectomy for IB adenosarcoma identified after total vaginal hysterectomy. Three patients with stage IB leiomyosarcoma underwent chemotherapy with gemcitabine and docetaxel.
Two patients had recurrent disease. One patient with stage IA endometrial stromal sarcoma found after total vaginal hysterectomy had a subsequent BSO and received postoperative megestrol acetate but was found to have a distant recurrence with pulmonary metastases 7 months after her index hysterectomy and was treated with letrazole. She was alive with disease 23 months after her index surgery. One additional patient who underwent TAH and BSO found to have stage IB leiomyosarcoma also had a recurrence. She underwent posterior exenteration, chemotherapy with gemcitabine and docetaxel, radiation treatment, and died within 23 months after her index hysterectomy. The remaining seven patients with occult sarcomas, including the patient who underwent manual morcellation during TAH, were known to be alive with no evidence of disease over a median follow-up of 48 months (range 12–135 months).
Uterine sarcomas are a relatively rare, potentially aggressive, heterogeneous group of gynecologic malignancies. Sarcomas have been challenging to diagnose before surgery as a result of limitations in clinical and radiographic predictors. Because of the frequency with which hysterectomies are performed, accurate assessment of the incidence of occult malignancies encountered during surgery for suspected benign gynecologic conditions is important for various reasons, including counseling regarding the risks and benefits of surgical approach, appropriate surgical planning, and avoidance of iatrogenic complications.
Our finding of the incidence of unexpected sarcoma at the time of hysterectomy is on the lower end of estimates previously reported. This rate is lower than a recent report using a statewide database examining the occult malignancy rate in women undergoing hysterectomy in Michigan.14 The different findings likely reflect differences in the study populations. In both instances, the overall low rates of occult sarcoma may also be the result of inclusion of a broader group of patients undergoing hysterectomy, not limited to those only with presumed myomas.
Previously reported rates of occult sarcoma have ranged from 0 to 1 in 20411,16 in analyses limited to women with presumed myomas, which may confer a higher likelihood of sarcoma. When developing their recommendations, the FDA used available reports of occult sarcoma in a pooled analysis to derive an estimate of 1 in 352 risk of occult sarcoma in women undergoing hysterectomy or myomectomy for presumed myomas. Their estimate has been criticized based on concerns about the quality of the data of the nine studies included as well as the potential for publication bias and inclusion of only retrospectives studies.17–19 The largest study in the pooled analysis included only 1,429 patients. Furthermore, mixed populations including women undergoing hysterectomy and myomectomy were used to derive the risk estimate, and some studies also included referral patients, which may have elevated the risk. This methodology may have additional flaws because the indications for myomectomy are different from those for hysterectomy, and thus the populations, age distribution, and incidence of occult malignancy in the two groups vary.20,21 Although many of the studies used by the FDA in their pooled analysis were from university hospitals and referral centers much like ours, they were not able to describe clinically relevant factors such as preoperative evaluation and postoperative care and outcomes.18
During the study period, there were 64 cases of preoperatively clinically suspected uterine sarcoma in which the primary surgery was performed at our institution. Of the 64 uterine sarcomas, there were 28 leiomyosarcomas, 14 endometrial stromal sarcomas, 13 high-grade uterine sarcomas, and nine adenosarcomas. Sarcoma cases that were referred only for postoperative management were excluded from this analysis.
Of note, all occult sarcoma cases in our study were found in patients who were receiving their primary gynecologic care at our institution, not among women referred for subspecialty care. All patients had received up-to-date cervical cancer screening and in the majority of cases, women had received preoperative evaluation with either endometrial sampling or imaging, which did not suggest malignancy. Of the suggested risk factors for sarcoma, it is notable that none of the women we identified were postmenopausal, exposed to pelvic radiation or tamoxifen, nor had a family history of cancer. The average age of women undergoing hysterectomy at our institution was younger than that in the Michigan study, and our finding of a relatively young cohort of women with sarcoma is unexpected and contrary to expectations of age-related risks.13,21 The absence of these risk factors may be related to why these patients were not referred to gynecologic oncologists and were not suspected to have sarcomas preoperatively.
A strength of our study is that we were able to determine the postoperative outcomes of these patients to a median of 48 months after hysterectomy. Six of the nine patients underwent additional interventions with additional surgery, chemotherapy, radiation therapy, or a combination of these. Data are limited to guide the postoperative management of such occult cases; thus, management should be individualized to each case. Notably, the patient who did experience manual morcellation of a leiomyosarcoma completed six cycles of chemotherapy and has been followed to 49 months since her hysterectomy with no further evidence of disease. The major disadvantage of our study is it is retrospective with the inherent biases, including misclassification and missing data, which may limit the findings. Given the rarity of uterine sarcomas, prospective studies may be challenging to perform at a single institution.
The relatively low rates of occult uterine sarcoma derived from ours and other recent studies may be useful for counseling patients about management options and surgical planning during hysterectomy,14 yet it is important to stress that although low, the risk of encountering an occult sarcoma exists. Hence, ongoing efforts to identify potentially safer methods for tissue extraction are essential as are efforts to improve preoperative identification of malignancies.
In summary, occult uterine sarcoma was identified in 1 in 1,124 hysterectomies for benign indications in our population. The frequency is lower than the rate derived in earlier reports and by the FDA in their pooled analysis.
1. Rosero EB, Kho KA, Joshi GP, Giesecke M, Schaffer JI. Comparison of robotic and laparoscopic hysterectomy for benign gynecologic disease. Obstet Gynecol 2013;122:778–86.
2. Nieboer TE, Johnson N, Lethaby A, Tavender E, Curr E, Garry R, et al.. Surgical approach to hysterectomy for benign gynaecological disease. The Cochrane Database of Systematic Reviews 2009, Issue 3. Art. No.: CD003677. DOI: 10.1002/14651858.CD003677.pub4.
3. Steiner RA, Wight E, Tadir Y, Haller U. Electrical cutting device for laparoscopic removal of tissue from the abdominal cavity. Obstet Gynecol 1993;81:471–4.
4. Kho KA, Nezhat CH. Evaluating the risks of electric uterine morcellation. JAMA 2014;311:905–6.
5. Levitz J. Doctors eye cancer risk in uterine procedure. The Wall Street Journal December 18, 2013.
6. Park JY, Park SK, Kim DY, Kim JH, Kim YM, Kim YT, et al.. The impact of tumor morcellation during surgery on the prognosis of patients with apparently early uterine leiomyosarcoma. Gynecol Oncol 2011;122:255–9.
7. George S, Barysauskas C, Serrano C, Oduyebo T, Rauh-Hain JA, Del Carmen MG, et al.. Retrospective cohort study evaluating the impact of intraperitoneal morcellation on outcomes of localized uterine leiomyosarcoma. Cancer 2014;120:3154–8.
9. Desai VB, Guo XM, Xu X. Alterations in surgical technique after FDA statement on power morcellation. Am J Obstet Gynecol 2015;212:685–7.
10. Kamikabeya TS, Etchebehere RM, Nomelini RS, Murta EF. Gynecological malignant neoplasias diagnosed after hysterectomy performed for leiomyoma in a university hospital. Eur J Gynaecol Oncol 2010;31:651–3.
11. Leibsohn S, d'Ablaing G, Mishell DR Jr, Schlaerth JB. Leiomyosarcoma in a series of hysterectomies performed for presumed uterine leiomyomas. Am J Obstet Gynecol 1990;162:968–74.
14. Mahnert N, Morgan D, Campbell D, Johnston C, As-Sanie S. Unexpected gynecologic malignancy diagnosed after hysterectomy performed for benign indications. Obstet Gynecol 2015;125:397–405.
15. Clopper CJ, Pearson ES. The use of confidence or fiducial limits illustrated in the case of the binomial. Biometrika 1934;26:404–13.
16. Reiter RC, Wagner PL, Gambone JC. Routine hysterectomy for large asymptomatic uterine leiomyomata: a reappraisal. Obstet Gynecol 1992;79:481–4.
17. Kho KA, Anderson TL, Nezhat CH. Intracorporeal electromechanical tissue morcellation: a critical review and recommendations for clinical practice. Obstet Gynecol 2014;124:787–93.
18. Liu FW, Galvan-Turner VB, Pfaendler KS, Longoria TC, Bristow RE. A critical assessment of morcellation and its impact on gynecologic surgery and the limitations of the existing literature. Am J Obstet Gynecol 2015;212:717–24.
19. Pritts EA, Vanness DJ, Berek JS, Parker W, Feinberg R, Feinberg J, et al.. The prevalence of occult leiomyosarcoma at surgery for presumed uterine fibroids: a meta-analysis. Gynecol Surg 2015;12:165–77.
20. Wright JD, Tergas AI, Burke WM, Cui RR, Ananth CV, Chen L, et al.. Uterine pathology in women undergoing minimally invasive hysterectomy using morcellation. JAMA 2014;312:1253–5.
© 2016 by The American College of Obstetricians and Gynecologists. Published by Wolters Kluwer Health, Inc. All rights reserved.
21. Wright JD, Tergas AI, Cui R, Burke WM, Hou JY, Ananth CV, et al.. Use of electric power morcellation and prevalence of underlying cancer in women who undergo myomectomy. JAMA Oncol 2015;1:69–77.