Clinical study of apatinib in the treatment of stage IV osteogenic sarcoma after failure of chemotherapy

被引:12
作者
Liao, Zhichao [1 ]
Li, Ting [1 ]
Zhang, Chao [1 ]
Liu, Xinyue [1 ]
Xing, Ruwei [1 ]
Teng, Sheng [1 ]
Yang, Yun [1 ]
Zhao, Gang [2 ]
Bai, Xu [3 ,4 ,5 ,6 ]
Zhao, Jun [1 ]
Yang, Jilong [1 ]
机构
[1] Tianjin Med Univ, Canc Inst & Hosp, Dept Bone & Soft Tissue Tumor, Tianjin 300060, Peoples R China
[2] Tianjin Med Univ, Canc Inst & Hosp, Dept Pathol, Tianjin 300060, Peoples R China
[3] Tianjin Med Univ, Canc Inst & Hosp, Dept Radiol, Tianjin 300060, Peoples R China
[4] Natl Clin Res Ctr Canc, Tianjin 300060, Peoples R China
[5] Key Lab Canc Prevent & Therapy, Tianjin 300060, Peoples R China
[6] Tianjins Clin Res Ctr Canc, Tianjin 300060, Peoples R China
关键词
Apatinib; osteogenic sarcoma; progression-free survival; safety; PHASE-II; TYROSINE KINASE; DOUBLE-BLIND; OSTEOSARCOMA; INHIBITOR; SURVIVAL; THERAPY; ENDOSTATIN; SORAFENIB; TRIAL;
D O I
10.20892/j.issn.2095-3941.2019.0397
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: To analyze the efficacy and safety of apatinib in the treatment of stage IV osteogenic sarcoma after chemotherapy failure through a single-arm, prospective, and open clinical phase II study. Methods: Information on 34 patients with stage IV osteogenic sarcoma treated with apatinib after failure of chemotherapy in Tianjin Medical University Cancer Institute and Hospital between September 2015 and December 2019 was collected and analyzed. The participants included 23 males and 11 females, with an average age of 35.24 years (11-73 years). The objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), PFS rate (PFR), and overall survival (OS) were evaluated. The treatment-related adverse events (AEs) and safety of apatinib were also evaluated. Results: Of the 34 patients, 33 were able to be evaluated for efficacy. One patient received apatinib treatment for less than one cycle; therefore, only safety analysis was performed. The 12-week clinical evaluation showed that 2 patients had a partial response (PR), 24 patients had stable disease (SD), and 7 patients had progressive disease (PD). The ORR, DCR, and PFR at 12 weeks were 6.06% (2/33), 78.79% (26/33), and 82%, respectively. By the end of the follow-up, 6 patients had SD (18.18%, 6/33), 27 patients had PD (81.82%, 27/33), and 15 patients died because of disease progression (45.45%, 15/33). The ORR was 0 (0/33), the DCR was 18.18% (6/33), and the median PFS (mPFS) was 7.89 months (95% CI: 4.56-11.21). The median OS (mOS) was 17.61 months (95% CI: 10.85-24.37). The most common treatment-related AEs were hand-foot syndrome (35.29%, 12/34), proteinuria (32.35%, 11/34), and hypertension (32.35%, 11/34). Conclusions: Apatinib is effective and well tolerated in stage IV osteogenic sarcoma patients after chemotherapy failure.
引用
收藏
页码:501 / 512
页数:12
相关论文
共 39 条
[1]   Response of refractory Ewing sarcoma to pazopanib [J].
Alcindor, Thierry .
ACTA ONCOLOGICA, 2015, 54 (07) :1063-U184
[2]   Global surveillance of cancer survival 1995-2009: analysis of individual data for 25 676 887 patients from 279 population-based registries in 67 countries (CONCORD-2) [J].
Allemani, Claudia ;
Weir, Hannah K. ;
Carreira, Helena ;
Harewood, Rhea ;
Spika, Devon ;
Wang, Xiao-Si ;
Bannon, Finian ;
Ahn, Jane V. ;
Johnson, Christopher J. ;
Bonaventure, Audrey ;
Marcos-Gragera, Rafael ;
Stiller, Charles ;
Azevedo e Silva, Gulnar ;
Chen, Wan-Qing ;
Ogunbiyi, Olufemi J. ;
Rachet, Bernard ;
Soeberg, Matthew J. ;
You, Hui ;
Matsuda, Tomohiro ;
Bielska-Lasota, Magdalena ;
Storm, Hans ;
Tucker, Thomas C. ;
Coleman, Michel P. .
LANCET, 2015, 385 (9972) :977-1010
[3]   The Epidemiology of Sarcoma [J].
Burningham, Zachary ;
Hashibe, Mia ;
Spector, Logan ;
Schiffman, Joshua D. .
CLINICAL SARCOMA RESEARCH, 2012, 2
[4]   Cancer Statistics in China, 2015 [J].
Chen, Wanqing ;
Zheng, Rongshou ;
Baade, Peter D. ;
Zhang, Siwei ;
Zeng, Hongmei ;
Bray, Freddie ;
Jemal, Ahmedin ;
Yu, Xue Qin ;
He, Jie .
CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (02) :115-132
[5]   Randomized Double-Blind Phase II Study of Regorafenib in Patients With Metastatic Osteosarcoma [J].
Davis, Lara E. ;
Bolejack, Vanessa ;
Ryan, Christopher W. ;
Ganjoo, Kristen N. ;
Loggers, Elizabeth T. ;
Chawla, Sant ;
Agulnik, Mark ;
Livingston, Michael B. ;
Reed, Damon ;
Keedy, Vicky ;
Rushing, Daniel ;
Okuno, Scott ;
Reinke, Denise K. ;
Riedel, Richard F. ;
Attia, Steven ;
Mascarenhas, Leo ;
Maki, Robert G. .
JOURNAL OF CLINICAL ONCOLOGY, 2019, 37 (16) :1424-+
[6]   Significant partial response of metastatic intraabdominal and pelvic round cell liposarcoma to a small-molecule VEGFR-2 tyrosine kinase inhibitor apatinib A case report [J].
Dong, Min ;
Bi, Jingwang ;
Liu, Xiaohong ;
Wang, Baocheng ;
Wang, Jun .
MEDICINE, 2016, 95 (31)
[7]   New response evaluation criteria in solid tumours: Revised RECIST guideline (version 1.1) [J].
Eisenhauer, E. A. ;
Therasse, P. ;
Bogaerts, J. ;
Schwartz, L. H. ;
Sargent, D. ;
Ford, R. ;
Dancey, J. ;
Arbuck, S. ;
Gwyther, S. ;
Mooney, M. ;
Rubinstein, L. ;
Shankar, L. ;
Dodd, L. ;
Kaplan, R. ;
Lacombe, D. ;
Verweij, J. .
EUROPEAN JOURNAL OF CANCER, 2009, 45 (02) :228-247
[8]   The Multidisciplinary Management of Osteosarcoma [J].
Federman, Noah ;
Bernthal, Nicholas ;
Eilber, Fritz C. ;
Tap, William D. .
CURRENT TREATMENT OPTIONS IN ONCOLOGY, 2009, 10 (1-2) :82-93
[9]   Postrelapse survival in osteosarcoma of the extremities: Prognostic factors for long-term survival [J].
Ferrari, S ;
Briccoli, A ;
Mercuri, M ;
Bertoni, F ;
Picci, P ;
Tienghi, A ;
Del Prever, AB ;
Fagioli, F ;
Comandone, A ;
Bacci, G .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (04) :710-715
[10]   Antiangiogenesis in cancer therapy - endostatin and its mechanisms of action [J].
Folkman, J .
EXPERIMENTAL CELL RESEARCH, 2006, 312 (05) :594-607