TY - JOUR
T1 - Improved clinical trial enrollments for uterine leiomyosarcoma patients after gynecologic oncology partnership with a sarcoma center
AU - Lange, S. E.S.
AU - Liu, J.
AU - Adkins, D. R.
AU - Powell, M. A.
AU - Van Tine, B. A.
AU - Mutch, D. G.
N1 - Publisher Copyright:
© 2015 Elsevier Inc.
PY - 2016
Y1 - 2016
N2 - Objective A retrospective chart review was performed to determine patient outcomes before and after partnership by gynecologic oncologists (GYN/ONC) with a sarcoma center (SC) for patients with recurrent unresectable/metastatic (RM) uterine leiomyosarcoma (uLMS). Methods 58 RM patients, identified from medical records of uLMS patients cared for by either GYN/ONC service and/or the SC between 1/1/2000-4/1/2014, were audited for patient and tumor characteristics, outcomes, and clinical trials enrollments. Results Of the 58 patients, 26 patients (48%) were treated by GYN/ONC alone and 32 were treated by a combination of GYN/ONC and SC (52%). Age, race, tumor size, grade, presence of lymphovascular invasion, cervical involvement, and FIGO stage at diagnosis were not statistically different between the two groups. There was a significant difference between the number of clinical trial enrollments (0.07 vs 0.84 trials/patient, p < 0.001) and the number of chemotherapy regimens prescribed (2.67 vs 4.29/patient, p = 0.03) by GYN/ONC vs SC; the latter was driven by the number of clinical trial enrollments by the SC. Sixty-nine percent of patients referred to the SC were enrolled in at least one clinical trial, while just 8% of patients in the GYN/ONC group were enrolled in at least one clinical trial, a difference that is significant (p < 0.0001). Conclusions Referral of RM uLMS patients by GYN/ONC to a dedicated clinical trials-based SC resulted in an increase in the number of chemotherapy regimens prescribed and clinical trial enrollments. Partnership between GYN/ONC and a dedicated SC with access to clinical trials should be encouraged for all RM uLMS patients.
AB - Objective A retrospective chart review was performed to determine patient outcomes before and after partnership by gynecologic oncologists (GYN/ONC) with a sarcoma center (SC) for patients with recurrent unresectable/metastatic (RM) uterine leiomyosarcoma (uLMS). Methods 58 RM patients, identified from medical records of uLMS patients cared for by either GYN/ONC service and/or the SC between 1/1/2000-4/1/2014, were audited for patient and tumor characteristics, outcomes, and clinical trials enrollments. Results Of the 58 patients, 26 patients (48%) were treated by GYN/ONC alone and 32 were treated by a combination of GYN/ONC and SC (52%). Age, race, tumor size, grade, presence of lymphovascular invasion, cervical involvement, and FIGO stage at diagnosis were not statistically different between the two groups. There was a significant difference between the number of clinical trial enrollments (0.07 vs 0.84 trials/patient, p < 0.001) and the number of chemotherapy regimens prescribed (2.67 vs 4.29/patient, p = 0.03) by GYN/ONC vs SC; the latter was driven by the number of clinical trial enrollments by the SC. Sixty-nine percent of patients referred to the SC were enrolled in at least one clinical trial, while just 8% of patients in the GYN/ONC group were enrolled in at least one clinical trial, a difference that is significant (p < 0.0001). Conclusions Referral of RM uLMS patients by GYN/ONC to a dedicated clinical trials-based SC resulted in an increase in the number of chemotherapy regimens prescribed and clinical trial enrollments. Partnership between GYN/ONC and a dedicated SC with access to clinical trials should be encouraged for all RM uLMS patients.
KW - Clinical trials
KW - Gynecologic oncology
KW - Medical oncology
KW - Overall survival
KW - Sarcoma center
KW - Uterine leiomyosarcoma
UR - http://www.scopus.com/inward/record.url?scp=84952021029&partnerID=8YFLogxK
U2 - 10.1016/j.ygyno.2015.12.016
DO - 10.1016/j.ygyno.2015.12.016
M3 - Article
C2 - 26718726
AN - SCOPUS:84952021029
SN - 0090-8258
VL - 140
SP - 307
EP - 312
JO - Gynecologic oncology
JF - Gynecologic oncology
IS - 2
ER -