Clinical outcomes of brain metastasectomy from soft tissue and bone sarcomas: a systematic review

被引:2
|
作者
Wang, Ying [1 ]
Delisle, Megan [2 ]
Smith, Denise [3 ]
Alshamsan, Bader [4 ,5 ]
Srikanthan, Amirrtha [4 ,6 ,7 ]
机构
[1] Univ British Columbia, Dept Med, Div Med Oncol, Vancouver, BC V5Z 4E6, Canada
[2] Ottawa Hosp, Div Surg, Ottawa, ON K1H 8L6, Canada
[3] McMaster Univ, Hlth Sci Lib, 1280 Main St West, Hamilton, ON L8S 4L8, Canada
[4] Univ Ottawa, Dept Med, Div Med Oncol, Ottawa, ON K1H 8L6, Canada
[5] Qassim Univ, Coll Med, Dept Med, Buraydah, Saudi Arabia
[6] Ottawa Hosp Canc Ctr, Dept Med, Div Med Oncol, 501 Smyth Rd, Ottawa, ON K1H 8L6, Canada
[7] Ottawa Hosp Res Inst, Ottawa, ON K1Y 4E9, Canada
关键词
Metastasectomy; Brain metastasis; Sarcoma; Systematic review; RANDOMIZED-TRIAL; RADIOTHERAPY; MANAGEMENT; SURVIVAL; COMORBIDITY; PREVALENCE; PATTERNS; SURGERY; COHORT; IMPACT;
D O I
10.1007/s10147-022-02227-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Brain metastasis in sarcomas is associated with a poor prognosis. Data regarding prognostic factors and clinical outcomes of surgical resection of brain metastasis from sarcomas are limited. The objective of this systematic review was to evaluate survival outcomes post-brain metastasectomy for patients with soft tissue and bone sarcomas. Methods A systematic review was conducted examining survival outcomes among adults and children with soft tissue and bone sarcoma undergoing brain metastasectomy, in the English language from inception up to May 31, 2021. Two reviewers independently evaluated and screened the literature, extracted the data, and graded the included studies. The body of evidence was evaluated and graded according to the Newcastle-Ottawa Quality Assessment Scale for Cohort Studies and the Joanna Briggs Institute Critical Appraisal Checklist for Case Series. Results were synthesized using descriptive methods. A meta-analysis was not possible due to the low quality and heterogeneity of studies. Results Ten studies published between 1994 and 2020 were included: three were retrospective cohort studies and seven were case series. 507 patients were included, of whom 269 underwent brain metastasectomy. The median follow-up period ranged between 14 and 29 months. The median survival period after metastasectomy ranged from 7 to 25 months. The most common prognostic factors associated with survival included presenting performance status, age, number of brain metastases, presence of lung metastases, and peri-operative radiation therapy administration. Discussion Although the level of evidence is low, retrospective studies support that brain metastasectomy can be performed with reasonable post-operative survival in selected individuals.
引用
收藏
页码:1767 / 1779
页数:13
相关论文
共 50 条
  • [41] Clinical and Treatment Outcomes of Planned and Unplanned Excisions of Soft Tissue Sarcomas
    Arai, Eisuke
    Nishida, Yoshihiro
    Tsukushi, Satoshi
    Wasa, Junji
    Ishiguro, Naoki
    CLINICAL ORTHOPAEDICS AND RELATED RESEARCH, 2010, 468 (11) : 3028 - 3034
  • [42] Soft tissue sarcomas of the buttock: A systematic review and meta-analysis
    Sacco, Riccardo
    Lalevee, Matthieu
    Pellegrino, Pietro
    Ferro, Andrea
    Yasmine, Bendoukha
    Andre, Gillibert
    Matthieu, Gilleron
    Hamza, Amine
    Piana, Raimondo
    Dujardin, Franck
    SURGICAL ONCOLOGY-OXFORD, 2022, 45
  • [43] Proximal Row Carpectomy With Soft Tissue Interposition: A Systematic Review of Clinical Outcomes
    Aravinthan, Neveadan
    Siddiqui, Salwa
    Khan, Moin
    Moro, Jaydeep
    Pino, Paula A.
    Prada, Carlos
    HAND-AMERICAN ASSOCIATION FOR HAND SURGERY, 2024,
  • [44] Bone invasion in soft tissue sarcomas of the extremities: An underappreciated prognostic factor. Bone invasion in soft tissue sarcomas
    Yarih Garcia-Ortega, Dorian
    Alvarez-Cano, Alethia
    Angel Clara-Altamirano, Miguel
    Caro-Sanchez, Claudia
    De la Cruz Ruvalcaba-Gonzalez, Cuauhtemoc
    Cesar Cortes-Gonzalez, Carlo
    Luna-Ortiz, Kuauhyama
    SURGICAL ONCOLOGY-OXFORD, 2022, 40
  • [45] Clinical trials in soft tissue sarcomas
    Saxman, S
    Schoenfeldt, M
    ONCOLOGY-NEW YORK, 2002, 16 (10): : 1359 - 1360
  • [46] Clinical features of soft tissue sarcomas
    Johnson, CJD
    Pynsent, PB
    Grimer, RJ
    ANNALS OF THE ROYAL COLLEGE OF SURGEONS OF ENGLAND, 2001, 83 (03) : 203 - 205
  • [47] SOFT-TISSUE SARCOMAS - A REVIEW
    FIZAZI, K
    COJEAN, I
    LECESNE, A
    KAYITALIRE, L
    LECHEVALIER, T
    TURSZ, T
    SPIELMANN, M
    BULLETIN DU CANCER, 1994, 81 (10) : 835 - 852
  • [48] Assessment of Efficiency and Safety of Apatinib in Advanced Bone and Soft Tissue Sarcomas: A Systematic Review and Meta-Analysis
    Long, Zuoyao
    Huang, Mengquan
    Liu, Kaituo
    Li, Minghui
    Li, Jing
    Zhang, Hongmei
    Wang, Zhen
    Lu, Yajie
    FRONTIERS IN ONCOLOGY, 2021, 11
  • [49] CT and MRI radiomics of bone and soft-tissue sarcomas: an updated systematic review of reproducibility and validation strategies
    Gitto, Salvatore
    Cuocolo, Renato
    Huisman, Merel
    Messina, Carmelo
    Albano, Domenico
    Omoumi, Patrick
    Kotter, Elmar
    Maas, Mario
    Van Ooijen, Peter
    Sconfienza, Luca Maria
    INSIGHTS INTO IMAGING, 2024, 15 (01)
  • [50] Proton therapy in soft tissue and bone sarcomas
    Thariat, Juliette
    Tessonnier, Thomas
    Bonvalot, Sylvie
    Lerouge, Delphine
    Mammar, Hamid
    Bolle, Stephanie
    Claren, Audrey
    Duffaud, Florence
    Alapetite, Claire
    Vogin, Guillaume
    BULLETIN DU CANCER, 2018, 105 (09) : 830 - 838