Age-Based Treatment of Aggressive Fibromatosis in the Head and Neck Region

被引:14
作者
Wang, Weiqi [1 ]
Koirala, Ujjwal [2 ]
Ma, Shufang [3 ]
Liu, Guicai [1 ]
Ding, Mingchao [1 ]
Hu, Xiaoguang [1 ]
Lei, Delin [1 ]
机构
[1] Fourth Mil Med Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, Xian 710032, Peoples R China
[2] Jiamusi Univ, Sch Stomatol, Dept Oral & Maxillofacial Surg, Jiamusi, Peoples R China
[3] Fourth Mil Med Univ, Sch Stomatol, Dept Pediat Dent, Xian 710032, Peoples R China
关键词
LOW-DOSE CHEMOTHERAPY; TRUNK DESMOID TUMORS; OF-THE-LITERATURE; PHASE-II TRIAL; RADIATION-THERAPY; COMBINATION CHEMOTHERAPY; RETROSPECTIVE ANALYSIS; PROGNOSTIC-FACTORS; LOCAL-CONTROL; METHOTREXATE;
D O I
10.1016/j.joms.2013.07.021
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Purpose: To review our experience regarding the difference in management and treatment outcomes of aggressive fibromatosis of the head and neck region in children and adults, emphasizing, in particular, the role of conservative surgery in comprehensive treatment strategies. Patients and Methods: A retrospective analysis of patients with aggressive fibromatosis was performed during a 5-year period (2008 to 2012). Nine patients were enrolled in the present study, including 5 children (age, < 18 years) and 4 adults (age, > 18 years). All patients underwent surgical intervention and were treated by surgical resection with different surgical margins. Adjuvant low-dose chemotherapy and radiotherapy were given to pediatric and adult patients, respectively, with macroscopically or microscopically positive surgical margins. Results: All 5 pediatric patients (3 females and 2 males) received low-dose chemotherapy after conservative surgical resection (in 4 patients, microscopically incomplete resection; and in 1 patient, macroscopic residual tumor). Of the 4 adults (3 females and 1 male), 2 underwent complete surgical resection and 2 underwent surgery and postoperative radiotherapy (1 patient had microscopically suspected residual tumor and 1 had macroscopic residual tumor). The patients were followed up for a period of 7 to 51 months. Two pediatric patients and one adult patient had disease progression after resection and became stable after continued adjuvant therapy. None of the patients had functional or cosmetic defects. All patients had good long-term outcomes, with no disease progression. Conclusions: For the treatment of aggressive fibromatosis, conservative resection with preservation of form and function should be given greater priority in all age groups. Also, postoperative adjuvant therapy is vital for patients with gross or microscopic residual tumor to obtain progression-free survival. (C) 2014 Published by Elsevier Inc on behalf of the American Association of Oral and Maxillofacial Surgeons
引用
收藏
页码:311 / 321
页数:11
相关论文
共 46 条
[1]  
Azzarelli A, 2001, CANCER, V92, P1259, DOI 10.1002/1097-0142(20010901)92:5<1259::AID-CNCR1446>3.0.CO
[2]  
2-Y
[3]   Radiation therapy in the management of desmoid tumors [J].
Ballo, MT ;
Zagars, GK ;
Pollack, A .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1998, 42 (05) :1007-1014
[4]   Desmoid tumor: Prognostic factors and outcome after surgery, radiation therapy, or combined surgery and radiation therapy [J].
Ballo, MT ;
Zagars, GK ;
Pollack, A ;
Pisters, PWT ;
Pollock, RA .
JOURNAL OF CLINICAL ONCOLOGY, 1999, 17 (01) :158-167
[5]   Recurrence and prognostic factors in patients with aggressive fibromatosis. The role of radical surgery and its limitations [J].
Bertani, Emilio ;
Testori, Alessandro ;
Chiappa, Antonio ;
Misitano, Pasquale ;
Biffi, Roberto ;
Viale, Giuseppe ;
Mazzarol, Giovanni ;
De Pas, Tommaso ;
Botteri, Edoardo ;
Contino, Gianmarco ;
Verrecchia, Francesco ;
Bazolli, Barbara ;
Andreoni, Bruno .
WORLD JOURNAL OF SURGICAL ONCOLOGY, 2012, 10
[6]   Multiple approach to the exploration of genotype-phenotype correlations in familial adenomatous polyposis [J].
Bertario, L ;
Russo, A ;
Sala, P ;
Varesco, L ;
Giarola, M ;
Mondini, P ;
Pierotti, M ;
Spinelli, P ;
Radice, P .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (09) :1698-1707
[7]   Pediatric aggressive fibromatosis - A retrospective analysis of 13 patients and review of the literature [J].
Buitendijk, S ;
van de Ven, CP ;
Dumans, TG ;
den Hollander, JC ;
Nowak, PJ ;
Tissing, WJ ;
Pieters, R ;
van den Heuvel-Eibrink, MM .
CANCER, 2005, 104 (05) :1090-1099
[8]   Mesenchymal Stromal Cell Mutations and Wound Healing Contribute to the Etiology of Desmoid Tumors [J].
Carothers, Adelaide M. ;
Rizvi, Hira ;
Hasson, Rian M. ;
Heit, Yvonne I. ;
Davids, Jennifer S. ;
Bertagnolli, Monica M. ;
Cho, Nancy L. .
CANCER RESEARCH, 2012, 72 (01) :346-355
[9]   Efficacy of Imatinib in Aggressive Fibromatosis: Results of a Phase II Multicenter Sarcoma Alliance for Research through Collaboration (SARC) Trial [J].
Chugh, Rashmi ;
Wathen, J. Kyle ;
Patel, Shreyaskumar R. ;
Maki, Robert G. ;
Meyers, Paul A. ;
Schuetze, Scott M. ;
Priebat, Dennis A. ;
Thomas, Dafydd G. ;
Jacobson, Jon A. ;
Samuels, Brian L. ;
Benjamin, Robert S. ;
Baker, Laurence H. .
CLINICAL CANCER RESEARCH, 2010, 16 (19) :4884-4891
[10]   Fibromatoses in childhood: The desmoid/fibromatosis complex [J].
Dormans, JP ;
Spiegel, D ;
Meyer, J ;
Asada, N ;
Alman, BA ;
Pill, SG ;
Himelstein, B ;
Womer, R .
MEDICAL AND PEDIATRIC ONCOLOGY, 2001, 37 (02) :126-131