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Case Reports

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Prolonged stable disease using pazopanib in recurrent and refractory uterine leiomyosarcoma: a proposal of “pazopanib beyond progression”

  • H. Ishibashi11
  • M. Takano2,*,
  • M. Miyamoto1
  • T. Aoyama1
  • T. Yoshikawa2
  • K. Furuya1

1Departments of Obstetrics and Gynecology, Tokorozawa (Japan)

2Clinical Oncology, National Defense Medical College, Tokorozawa (Japan)

DOI: 10.12892/ejgo3920.2018 Vol.39,Issue 5,October 2018 pp.821-824

Published: 10 October 2018

*Corresponding Author(s): M. Takano E-mail: mastkn@ndmc.ac.jp

Abstract

Background: To date, there is no standard therapy in patients with recurrent or refractory uterine leiomyosarcoma (LMS). A case with LMS that achieved prolonged stable disease using pazopanib beyond progression (PBP) is reported. Case Report: A 49-year-old patient with recurrent and refractory LMS that achieved long-term stable disease is reported. The patient had previously received three regimens before pazopanib therapy: combination chemotherapy with ifosfamide, doxorubicin, and cisplatin (IAP), gemcitabine monotherapy, and combination therapy with bevacizumab, temozolomide, and cabozantinib. Subsequently, oral administration of pazopanib was initiated at a dose of 400 mg daily. At the third week, the dose was reduced to 200 mg daily due to grade 1 hypothyroidism. At the ninth week, a new lesion in liver was detected; however, continuation of pazopanib was selected. At the 15th week, the patient developed moderate genital bleeding and received palliative radiotherapy (30 Gy) in addition to pazopaznib. The patient occasionally developed toxicities such as hypetension and diarrhea, which were manageable. At the 59th week, her general condition was suddenly worsened due to disease progression, and pazopanib treatment was discontinued. During the period of pazopanib, recurrent tumors showed stable disease, in spite of occurrence of new lesion at liver. Subsequently, the patient died of the disease 16 months after the initiation of pazopanib monotherapy. Conclusion: PBP could be a candidate for the patients with recurrent or refractory LMS.

Keywords

Uterus; Leiomyosarcoma; Pazopanib beyond progression (PBP).

Cite and Share

H. Ishibashi1,M. Takano,M. Miyamoto,T. Aoyama,T. Yoshikawa,K. Furuya. Prolonged stable disease using pazopanib in recurrent and refractory uterine leiomyosarcoma: a proposal of “pazopanib beyond progression”. European Journal of Gynaecological Oncology. 2018. 39(5);821-824.

References

[1] Amant F., Moerman P., Neven P., Timmerman D., Van Limbergen E., Vergote I: “Endometrial cancer”. Lancet, 2005, 366, 491.

[2] Raut C.P., Nucci M.R., Wang Q., Manola J., Bertagnolli M.M., Demetri G.D., et al.: ”Predictive value of FIGO and AJCC staging systems in patients with uterine leiomyosarcoma”. Eur. J. Cancer, 2009, 45, 2818.

[3] van der Graaf W.T., Blay J.Y., Chawla S.P., Kim D.W., Bui-Nguyen B., Casali P.G., et al.: “EORTC Soft Tissue and Bone Sarcoma Group; PALETTE study group. Pazopanib for metastatic soft-tissue sarcoma (PALETTE): a randomised, double-blind, placebo-controlled phase 3 trial”. Lancet, 2012, 379, 1879..

[4] Grothey A., Sugrue M.M., Purdie D.M., Dong W., Sargent D., Hedrick E., et al.: “Bevacizumab beyond first progression is associated with prolonged overall survival in metastatic colorectal cancer: results from a large observational cohort study (BRiTE)”. J. Clin. Oncol., 2008, 26, 5326.

[5] Reichardt P.: “The treatment of uterine sarcomas” Ann. Oncol., 2012, 23, x151.

[6] Arita S., Kikkawa F., Kajiyama H., Shibata K., Kawai M., Mizuno K., et al.: “Prognostic importance of vascular endothelial growth factor and its receptors in the uterine sarcoma”. Int J Gynecol Cancer, 2005, 15, 329.

[7] Sanci M., Dikis C., Inan S., Turkoz E., Dicle N., Ispahi C.: “Prognostic importance of vascular endothelial growth factor and its receptors in the uterine sarcoma”. Acta Histochem., 2011, 113, 317

[8] Naumov G.N., Nilsson M.B., Cascone T., Briggs A., Straume O., Akslen L.A., et al.: “Combined vascular endothelial growth factor receptor and epidermal growth factor receptor (EGFR) blockade inhibits tumor growth in xenograft models of EGFR inhibitor resistance”. Clin. Cancer Res., 2009, 15, 3484.

[9] Hensley M.L., Miller A., O’Malley D.M., Mannel R.S., Behbakht K., Bakkum-Gamez J.N., et al.: “Randomized phase III trial of gemcitabine plus docetaxel plus bevacizumab or placebo as first-line treatment for metastatic uterine leiomyosarcoma: an NRG Oncology/Gynecologic Oncology Group study”. J. Clin. Oncol., 2015, 33, 1180

[10] Takano M, Kikuchi Y, Susumu N, Kudoh K, Kita T, Kouta H, et al.: “Complete remission of recurrent and refractory uterine epithelioid leiomyosarcoma using weekly administration of bevacizumab and temozolomide” Eur. J. Obstet. Gynecol. Reprod. Biol., 2011, 157, 236

[11] Ebos J.M., Lee C.R., Cruz-Munoz W., Bjarnason G.A., Christensen J.G.,Kerbel R.S.: “Accelerated metastasis after short-term treatment with a potent inhibitor of tumor angiogenesis”. Cancer Cell, 2009, 15, 232.

[12] Bennouna J, Sastre J, Arnold D, Österlund P, Greil R, Van Cutsem E, et al: “ML18147 Study Investigators. Continuation of bevacizumab after first progression in metastatic colorectal cancer (ML18147): a randomised phase 3 trial”. Lancet Oncol., 2013, 14, 29.

[13] Pujade-Lauraine E, Hilpert F, Weber B, Reuss A, Poveda A, Kristensen G,, et al.: “Bevacizumab combined with chemotherapy for platinum-resistant recurrent ovarian cancer: The AURELIA openlabel randomized phase III trial”. J. Clin. Oncol., 2014, 32, 1302.

[14] Aghajanian C., Goff B., Nycum L.R., Wang Y.V., Husain A., Blank S.V.: “Final overall survival and safety analysis of OCEANS, a phase 3 trial of chemotherapy with or without bevacizumab in patients with platinum-sensitive recurrent ovarian cancer”. Gynecol. Oncol., 2015, 139, 10.

[15] Kawai A, Araki N, Hiraga H, Sugiura H, Matsumine A, et al: “A randomized, double-blind, placebo-controlled, Phase III study of pazopanib in patients with soft tissue sarcoma: results from the Japanese subgroup”. Jpn. J. Clin. Oncol., 2016, 46, 248.

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