Patient-derived solitary fibrous tumour xenografts predict high sensitivity to doxorubicin/dacarbazine combination confirmed in the clinic and highlight the potential effectiveness of trabectedin or eribulin against this tumour

被引:27
作者
Stacchiotti, S. [1 ]
Saponara, M. [1 ]
Frapolli, R. [2 ]
Tortoreto, M. [3 ]
Cominetti, D. [3 ]
Provenzano, S. [1 ]
Negri, T. [4 ]
Dagrada, G. P. [4 ]
Gronchi, A. [5 ]
Colombo, C. [5 ]
Vincenzi, B. [6 ]
Badalamenti, G. [7 ]
Zuco, V. [3 ]
Renne, S. L. [8 ]
Collini, P. [8 ]
Morosi, C. [9 ]
Tos, A. P. Dei [10 ]
Bello, E. [2 ]
Pilotti, S. [4 ]
Casali, P. G. [1 ,11 ]
D'Incalci, M. [2 ]
Zaffaroni, N. [3 ]
机构
[1] Fdn IRCCS Ist Nazl Tumori, Med Oncol Unit 2, Adult Mesenchymal Tumours, Milan, Italy
[2] IRCCS Ist Ric Farmacol Mario Negri, Dept Oncol, Milan, Italy
[3] Fdn IRCCS Ist Nazl Tumori, Dept Expt Oncol & Mol Med, Mol Pharmacol Unit, Milan, Italy
[4] Fdn IRCCS Ist Nazl Tumori, Dept Diagnost Pathol & Lab, Lab Expt Mol Pathol, Milan, Italy
[5] Fdn IRCCS Ist Nazl Tumori, Dept Surg, Melanoma & Sarcoma Unit, Milan, Italy
[6] Univ Campus Biomed, Dept Oncol, Via Alvaro del Portillo 21, Rome, Italy
[7] Univ Palermo, Sect Med Oncol, Dept Surg Oncol & Oral Sci, Palermo, Italy
[8] Fdn IRCCS Ist Nazl Tumori, Dept Diagnost Pathol & Lab Med, Soft Tissue & Bone Pathol Histopathol & Pediat Pa, Milan, Italy
[9] Fdn IRCCS Ist Nazl Tumori, Dept Radiol, Milan, Italy
[10] Gen Hosp Treviso, Dept Anat Pathol, Treviso, Italy
[11] Univ Milan, Dept Oncol, Milan, Italy
关键词
Sarcoma; Solitary fibrous tumour; Treatment; Metastasis; Chemotherapy; Anthracycline; Doxorubicin; Ifosfamide; Dacarbazine; Trabectedin; Eribulin; Xenograft; Mice model; SOFT-TISSUE SARCOMA; HEMANGIOPERICYTOMA; RECURRENT; CHEMOTHERAPY; IDENTIFICATION; TEMOZOLOMIDE; EXPRESSION; MECHANISM; MESYLATE; PHASE-2;
D O I
10.1016/j.ejca.2017.02.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Preclinical models that mimic pathological and molecular features of solitary fibrous tumour (SFT) represent an important tool to select effective regimes and novel compounds to be tested in the clinic. This study was aimed at developing two preclinical models of SFT, assessing their predictive value in the clinic and selecting potential novel effective treatments. Material and methods: Two dedifferentiated-SFT (D-SFT) models obtained from patients' biopsies were grown in immunodeficient mice. The antitumour activity on these models of doxorubicin, dacarbazine (DTIC), ifosfamide (monotherapy or combination), trabectedin and eribulin was tested. Twelve SFT patients were treated with doxorubicin and DTIC. Response by RECIST, progression-free survival and overall survival were retrospectively evaluated, distinguishing malignant-SFT (M-SFT) and D-SFT. Results: Two D-SFT patient-derived xenografts (PDXs) that represent the first available pre clinical in vivo models of SFT were developed and characterised. Doxorubicin/DTIC, DTIC/ifosfamide, doxorubicin/ifosfamide combinations consistently induced better antitumour activity than the single-agents. Particularly, doxorubicin/DTIC combination caused a max tumour volume inhibition >80% in both models. Doxorubicin/DTIC combo showed activity also in the case-series. Best RECIST responses were: 6 responses (M-SFT = 2 of 7, D-SFT = 4 of 5), I stable disease, 5 progressions, with a 6-month median progression-free survival (M-SFT = 6, D-SFT = 10 months). The PDXs were very sensitive to trabectedin and eribulin. Conclusion: Doxorubicin plus DTIC combination was effective in our two D-SFT mice models and appeared to be active also in the clinic, especially in high-grade D-SFT patients. Among additional drugs tested in the PDXs, trabectedin and eribulin were highly effective, providing a rational to test these drugs in D-SFT patients. (C) 2017 Elsevier Ltd. All rights reserved.
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收藏
页码:84 / 92
页数:9
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