Abstract
While it is known that positive surgical margins increase the risk of cervical cancer recurrence, little is known about the effect of close surgical margins (CSM). Therefore, we set out to determine the impact of margin status on recurrence and survival in patients with early-stage cervical cancer. A retrospective review was conducted of patients undergoing radical hysterectomy from 2000 to 2010 with Stage IA2-IIA cervical cancer. CSM were defined as ≤5mm; association with other clinicopathologic factors as well as recurrence and survival was evaluated. Of the 119 patients, 75 (63%) with CSM had a recurrence rate of 24% compared to 9% without CSM. Though not independently associated with recurrence, CSM were significantly associated with positive lymph nodes (44% vs. 18%), positive parametria (33.3% vs. 2.3%), larger tumors (3.5 vs. 2.5cm), greater depth of stromal invasion (DOI) (84% vs. 33%), and lymphovascular space invasion (LVSI) (61.3% vs. 34.1%). We failed to find an association between adjuvant therapy and recurrence in those with CSM. Exploratory analysis revealed that a surgical margin of ≤2mm was significantly associated with an increased risk of overall recurrence (36% vs. 9%, p=0.009) as well as loco-regional recurrence (22% vs. 4%, p=0.0034). Surgical margins of ≤5mm on radical hysterectomy specimens are often associated with other high or intermediate risk factors for recurrence. While not a proven independent risk factor, the distance to surgical margin may warrant further investigation as an intermediate risk factor along with tumor size, DOI and LVSI.
MeSH Terms
Adult
Female
Humans
Hysterectomy
Middle Aged
Neoplasm Invasiveness
Neoplasm Recurrence, Local/etiology,pathology
Neoplasm Staging
Retrospective Studies
Uterine Cervical Neoplasms/mortality,pathology,surgery
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
McCann Georgia A
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Taege Susanne K
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Boutsicaris Christina E
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Phillips Gary S
Center for Biostatistics, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Eisenhauer Eric L
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Fowler Jeffrey M
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
O'Malley David M
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Copeland Larry J
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Cohn David E
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA.
Salani Ritu
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, The Wexner Medical Center at the Ohio State University, Columbus OH, USA. Electronic address: ritu.salani@osumc.edu.
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