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Published in: International Cancer Conference Journal 1/2019

01-01-2019 | Case report

Uterine leiomyosarcoma well-controlled with eribulin mesylate

Authors: Etsuko Fujimoto, Kazuhiro Takehara, Tamaki Tanaka, Takanori Yokoyama, Katsuyuki Tomono, Mika Okazawa-Sakai, Shinichi Okame, Yoshifumi Sugawara, Norihiro Teramoto

Published in: International Cancer Conference Journal | Issue 1/2019

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Abstract

Uterine leiomyosarcoma is a rare type of malignant gynecological tumor and has a poor prognosis; therefore, this tumor is often difficult to treat. Some new drugs have been approved during the past several years in Japan and are expected to be efficacious. Eribulin, one of these drugs, is a natural product of halichondrin B, which is isolated from a marine sponge. A recent clinical trial comparing eribulin with dacarbazine to target liposarcoma and leiomyosarcoma indicated that overall survival (OS) was prolonged by treatment with eribulin. We report a case of uterine progressive leiomyosarcoma that responded to eribulin. A 57-year-old woman was suspected of having leiomyosarcoma based on an endometrial biopsy and imaging examinations. Although the tumor grew toward the uterine artery on the right side of the uterine cervix, we performed a total abdominal hysterectomy and bilateral salpingo-oophorectomy to obtain an outcome of no gross residual disease. However, the margin of the right side of the uterine cervix was histologically positive, so leiomyosarcoma stage IIB (pT2bcN0cM0, FIGO2008) was diagnosed. Gemcitabine and docetaxel therapy was administered postoperatively. However, after three cycles, the residual tumor progressed. Other anticancer drugs were administered but were ineffective. We administered eribulin (1.4 mg/m2) as a fourth-line regimen, and the mass decreased by 32% after four cycles. However, the residual tumor continued to grow after eight cycles. The only adverse event associated with eribulin treatment was mild, grade 2 neutropenia. For our patient, eribulin was effective for her recurrent leiomyosarcoma. In selecting chemotherapy, there are currently no fixed guidelines; we should consider the characteristics and adverse events associated with each drug and patient performance status and comorbidities. In this patient, eribulin was associated with few adverse events, an easy route of administration and a good quality of life. Therefore, eribulin is expected to be efficacious for the treatment of gynecologic sarcoma.
Literature
1.
go back to reference Schöffski P, Chawla S, Maki RG et al (2016) Eribulin versus dacarbazine in previously treated patients with advanced liposarcoma or leiomyosarcoma. Lancet 387:1629–1637CrossRefPubMed Schöffski P, Chawla S, Maki RG et al (2016) Eribulin versus dacarbazine in previously treated patients with advanced liposarcoma or leiomyosarcoma. Lancet 387:1629–1637CrossRefPubMed
2.
go back to reference WHO classification of tumors of Female Reproductive Organs; 2014:139–141 WHO classification of tumors of Female Reproductive Organs; 2014:139–141
3.
go back to reference Seagle BL, Sobecki-Rausch J, Strohl AE et al (2017) Prognosis and treatment of uterine leiomyosarcoma: a National Cancer Database study. Gynecol Oncol 145:61–70CrossRef Seagle BL, Sobecki-Rausch J, Strohl AE et al (2017) Prognosis and treatment of uterine leiomyosarcoma: a National Cancer Database study. Gynecol Oncol 145:61–70CrossRef
4.
go back to reference Omura GA, Major FJ, Blessing JA et al (1983) A randomized study of Adriamycin with and without dimethyl triazenoimidazole carboxamide in advanced uterine sarcomas. Cancer 52:626–632CrossRefPubMed Omura GA, Major FJ, Blessing JA et al (1983) A randomized study of Adriamycin with and without dimethyl triazenoimidazole carboxamide in advanced uterine sarcomas. Cancer 52:626–632CrossRefPubMed
5.
go back to reference Look KY, Sandler A, Blessing JA et al (2004) PhaseII trial of gemcitabine as second-line chemotherapy of uterine leiomyosarcoma: a Gynecologic Oncology Group (GOG) Study. Gynecol Oncol 92:644–647CrossRefPubMed Look KY, Sandler A, Blessing JA et al (2004) PhaseII trial of gemcitabine as second-line chemotherapy of uterine leiomyosarcoma: a Gynecologic Oncology Group (GOG) Study. Gynecol Oncol 92:644–647CrossRefPubMed
6.
go back to reference Sutton GP, Blessing JA, Barrett RJ et al (1992) Phase II trial of ifosfamide and mesna in leiomyosarcoma of the uterus: a Gynecologic Oncology Group study. Am J Obstet Gynecol 166:556–559CrossRefPubMed Sutton GP, Blessing JA, Barrett RJ et al (1992) Phase II trial of ifosfamide and mesna in leiomyosarcoma of the uterus: a Gynecologic Oncology Group study. Am J Obstet Gynecol 166:556–559CrossRefPubMed
7.
go back to reference Sutton G, Blessing JA, Park R et al (1996) Ifosfamide treatment of recurrent or metastatic endometrial stromal sarcoma previously unexposed to chemotherapy: a study of the Gynecologic Oncology Group. Obstet Gynecol 87:747–750CrossRefPubMed Sutton G, Blessing JA, Park R et al (1996) Ifosfamide treatment of recurrent or metastatic endometrial stromal sarcoma previously unexposed to chemotherapy: a study of the Gynecologic Oncology Group. Obstet Gynecol 87:747–750CrossRefPubMed
8.
go back to reference Hensley ML, Blessing JA, Mannel R et al (2008) Fixed-dose rate gemcitabine plus docetaxel as first-line therapy for metastatic uterine sarcoma: a Gynecologic Oncology Group phase II trial. Gynecol Oncol 109:329–334CrossRefPubMedPubMedCentral Hensley ML, Blessing JA, Mannel R et al (2008) Fixed-dose rate gemcitabine plus docetaxel as first-line therapy for metastatic uterine sarcoma: a Gynecologic Oncology Group phase II trial. Gynecol Oncol 109:329–334CrossRefPubMedPubMedCentral
9.
go back to reference Hensley ML, Blessing JA, Degreest K et al (2008) Fixed-dose rate gemcitabine plus docetaxel as second-line therapy for metastatic uterine leiomyosarcoma: a Gynecologic Oncology Group phase II study. Gynecol Oncol 109:323–328CrossRefPubMedPubMedCentral Hensley ML, Blessing JA, Degreest K et al (2008) Fixed-dose rate gemcitabine plus docetaxel as second-line therapy for metastatic uterine leiomyosarcoma: a Gynecologic Oncology Group phase II study. Gynecol Oncol 109:323–328CrossRefPubMedPubMedCentral
11.
go back to reference Seddon B, Strauss S, Whelan J et al (2017) Gemcitabine and docetaxel versus doxorubicin as first-line treatment in previously untreated advanced unresectable or metastatic soft-tissue sarcomas(GeDDiS): a randomised controlled phase 3 trial. Lancet Oncol 18:1397–1410CrossRefPubMedPubMedCentral Seddon B, Strauss S, Whelan J et al (2017) Gemcitabine and docetaxel versus doxorubicin as first-line treatment in previously untreated advanced unresectable or metastatic soft-tissue sarcomas(GeDDiS): a randomised controlled phase 3 trial. Lancet Oncol 18:1397–1410CrossRefPubMedPubMedCentral
13.
go back to reference Van der Graaf WT, Blay JY, Chawla SP et al (2012) Pazopanib for metastatic soft-tissue sarcoma (PALETTE): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet 379:1879–1886CrossRefPubMed Van der Graaf WT, Blay JY, Chawla SP et al (2012) Pazopanib for metastatic soft-tissue sarcoma (PALETTE): a randomised, double-blind, placebo-controlled phase 3 trial. Lancet 379:1879–1886CrossRefPubMed
14.
go back to reference Kawai A, Araki N, Sugiura H et al (2015) Trabectedin monotherapy after standard chemotherapy versus best supportive care in patients with advanced, translocation-related sarcoma: a randomised, open-label, phase 2 study. Lancet 16:406–416CrossRefPubMed Kawai A, Araki N, Sugiura H et al (2015) Trabectedin monotherapy after standard chemotherapy versus best supportive care in patients with advanced, translocation-related sarcoma: a randomised, open-label, phase 2 study. Lancet 16:406–416CrossRefPubMed
15.
go back to reference Kawai A, Yonemori K, Takahashi S et al (2017) Systemic therapy for soft tissue sarcoma: Proposals for the optimal use of pazopanib, trabectedin, and eribulin. Adv Ther 34:1556–1571CrossRefPubMedPubMedCentral Kawai A, Yonemori K, Takahashi S et al (2017) Systemic therapy for soft tissue sarcoma: Proposals for the optimal use of pazopanib, trabectedin, and eribulin. Adv Ther 34:1556–1571CrossRefPubMedPubMedCentral
16.
go back to reference Kuznetsov G, TenDyke K, Yu MJ et al (2007) Antiproliferative effects of halichondrin B analog eribulin mesylate (E7389) against paclitaxel-resistant human cancer cells in vitro. [abstract C58]. Proc Am Assoc Cancer Res 48:275 Kuznetsov G, TenDyke K, Yu MJ et al (2007) Antiproliferative effects of halichondrin B analog eribulin mesylate (E7389) against paclitaxel-resistant human cancer cells in vitro. [abstract C58]. Proc Am Assoc Cancer Res 48:275
17.
go back to reference Funahashi Y, Okamoto K, Adachi Y et al (2014) Eribulin mesylate reduces tumor microenvironment abnormality by vascular remodeling in preclinical human breast cancer models. Cancer Sci 105:1334–1342CrossRefPubMedPubMedCentral Funahashi Y, Okamoto K, Adachi Y et al (2014) Eribulin mesylate reduces tumor microenvironment abnormality by vascular remodeling in preclinical human breast cancer models. Cancer Sci 105:1334–1342CrossRefPubMedPubMedCentral
Metadata
Title
Uterine leiomyosarcoma well-controlled with eribulin mesylate
Authors
Etsuko Fujimoto
Kazuhiro Takehara
Tamaki Tanaka
Takanori Yokoyama
Katsuyuki Tomono
Mika Okazawa-Sakai
Shinichi Okame
Yoshifumi Sugawara
Norihiro Teramoto
Publication date
01-01-2019
Publisher
Springer Japan
Published in
International Cancer Conference Journal / Issue 1/2019
Electronic ISSN: 2192-3183
DOI
https://doi.org/10.1007/s13691-018-0350-1

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