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Adjuvant therapy for high‐grade, uterus‐limited leiomyosarcoma

dc.contributor.authorHensley, Martee L.en_US
dc.contributor.authorWathen, J. Kyleen_US
dc.contributor.authorMaki, Robert G.en_US
dc.contributor.authorAraujo, Dejka M.en_US
dc.contributor.authorSutton, Gregoryen_US
dc.contributor.authorPriebat, Dennis A.en_US
dc.contributor.authorGeorge, Suzanneen_US
dc.contributor.authorSoslow, Robert A.en_US
dc.contributor.authorBaker, Laurence H.en_US
dc.date.accessioned2013-05-02T19:35:12Z
dc.date.available2014-05-23T15:04:20Zen_US
dc.date.issued2013-04-15en_US
dc.identifier.citationHensley, Martee L.; Wathen, J. Kyle; Maki, Robert G.; Araujo, Dejka M.; Sutton, Gregory; Priebat, Dennis A.; George, Suzanne; Soslow, Robert A.; Baker, Laurence H. (2013). "Adjuvant therapy for high‐grade, uterus‐limited leiomyosarcoma ." Cancer 119(8): 1555-1561. <http://hdl.handle.net/2027.42/97490>en_US
dc.identifier.issn0008-543Xen_US
dc.identifier.issn1097-0142en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/97490
dc.description.abstractBACKGROUND: Between 30% and 50% of women who have high‐grade uterine leiomyosarcoma (uLMS) limited to the uterus at diagnosis remain progression‐free at 2 years. Adjuvant pelvic radiation does not improve outcome. The objective of the current study was to determine the 2‐year and 3‐year progression‐free survival (PFS) among a prospective cohort of women who received adjuvant gemcitabine plus docetaxel followed by doxorubicin. METHODS: Women with uterus‐limited, high‐grade uLMS and adequate organ function were eligible. Within 12 weeks of complete resection and after confirmation that they had no evidence of disease on computed tomography (CT) images, the patients received 4 cycles of fixed‐dose‐rate gemcitabine plus docetaxel. Those who were confirmed disease‐free on CT scans after cycle 4 received 4 cycles of doxorubicin. CT imaging for recurrence was performed every 3 months for 2 years, then every 6 months for 3 years. RESULTS: In total, 47 women were enrolled (46 evaluable) in 3 years. Characteristics included a median age of 53 years; 1988 International Federation of Gynecology and Obstetrics stage I disease in 81% of patients, stage II disease in 15%, and serosa‐only stage IIIA disease in 4%; American Joint Committee on Cancer stage II disease in 13% of patients and stage III disease in 87%; a median tumor size of 8 cm (range, 2.5‐30 cm); and a median mitotic rate of 18 mitoses per 10 high‐power fields (range, 5‐83 mitoses per 10 high‐power fields). At a median follow‐up of 39.8 months, 21 of 46 patients developed recurrent disease (45.7%). The median time to recurrence was 27.4 months (range, 3‐40 months). Seventy‐eight percent of patients (95% confidence interval, 67%‐91%) were progression‐free at 2 years, and 57% (95% confidence interval, 44%‐74%) were progression‐free at 3 years. The median PFS was not reached and exceeded 36 months. CONCLUSIONS: Among women with high‐grade, uterus‐limited uLMS who received treatment with adjuvant gemcitabine plus docetaxel followed by doxorubicin, 78% remained progression‐free at 2 years, and 57% remained progression‐free at 3 years. A randomized trial of adjuvant chemotherapy versus observation to determine whether adjuvant chemotherapy can improve survival in women with uterus‐limited uLMS is underway. Cancer 2013. © 2013 American Cancer Society. Among women with high‐grade, uterus‐limited leiomyosarcoma who receive treatment with adjuvant gemcitabine plus docetaxel followed by doxorubicin, 78% remain progression‐free at 2 years, and 57% remain progression‐free at 3 years.en_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherSurvivalen_US
dc.subject.otherLeiomyosarcomaen_US
dc.subject.otherUterineen_US
dc.subject.otherChemotherapyen_US
dc.subject.otherAdjuvanten_US
dc.titleAdjuvant therapy for high‐grade, uterus‐limited leiomyosarcomaen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelPublic Healthen_US
dc.subject.hlbsecondlevelOncology and Hematologyen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDivision of Hematology and Oncology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michiganen_US
dc.contributor.affiliationotherSection of Hematology/Oncology, Washington Cancer Instituteen_US
dc.contributor.affiliationotherDepartment of Medicine, Gynecologic Medical Oncology Service, Memorial Sloan‐Kettering Cancer Center, New York, New Yorken_US
dc.contributor.affiliationotherWeill Cornell Medical College, New York, New Yorken_US
dc.contributor.affiliationotherJanssen Research and Development, LLC, Titusville, New Jerseyen_US
dc.contributor.affiliationotherPediatric Hematology/Oncology Division, Mt. Sinai Medical Center, New York, New Yorken_US
dc.contributor.affiliationotherSarcoma Medical Oncology Division, University of Texas MD Anderson Cancer Center, Houston, Texasen_US
dc.contributor.affiliationotherDepartment of Surgery, Gynecologic Oncology, St. Vincent's Hospital, Indianapolis, Indianaen_US
dc.contributor.affiliationotherDepartment of Medical Oncology, Center for Sarcoma and Bone Oncology, Dana‐Farber Cancer Institute, Boston, Massachusettsen_US
dc.contributor.affiliationotherDepartment of Pathology, Memorial Sloan‐Kettering Cancer Center, New York, New Yorken_US
dc.contributor.affiliationotherDepartment of Medicine, Gynecologic Medical Oncology Service, Memorial Sloan‐Kettering Cancer Center, 300 East 66th Street, Suite 1355, New York, NY 10065en_US
dc.identifier.pmid23335221en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/97490/1/27942_ftp.pdf
dc.identifier.doi10.1002/cncr.27942en_US
dc.identifier.sourceCanceren_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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