Particle therapy in lung cancer: Where do we stand?

被引:15
|
作者
Pijls-Johannesmata, Madelon [1 ,2 ]
Grutters, Janneke P. C. [1 ]
Lambin, Philippe [1 ,2 ]
De Ruysscher, Dirk [1 ,2 ]
机构
[1] Maastricht Radiat Oncol MAASTRO Clin, NL-6229 ET Maastricht, Netherlands
[2] Univ Hosp Maastricht, Dept Radiat Oncol, GROW, NL-6202 AZ Maastricht, Netherlands
关键词
hadron; charged particles; proton; C-ion; radiotherapy; lung cancer;
D O I
10.1016/j.ctrv.2007.12.003
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: From a theoretical point of view, charged particles should lead to superior results compared to photons. In this review, we searched for clinical evidence that protons or C-ions are realty beneficial. to patients with tung cancer. Methods: A systematic literature review based on an earlier published comprehensive review was performed and updated until November 1st 2007. Results: Ten fully published series, all dealing with non-small cell lung cancer (NSCLC), mainly stage I, were identified. No phase III trials were found. On proton therapy, 2-5 year local tumor control rates varied between 87% and 57%. The 2 year/5 year overall. survival. and 2 year/5 year cause specific survival varied between 31-74%/23% and 58-86%/46%, respectively. Late side effects were observed in about 10% of the patients. For C-ion therapy, the local tumor control rate was 77%, while 95% when using a hypofractionated radiation schedule. The 5 year overall survival and cause specific survival rates were 42% and 60%, respectively. Slightly better results were reported when using hypofractionation, 50% and 76%, respectively. The reported late side effects for C-ions were 4%. Conclusion: The results with charged particles, at least for stage I disease, seem to be promising. A gain can be expected in reduction of late side effects, especially after treatment with C-ions. Available data demonstrate that particle therapy in general is a safe and feasible treatment modality. Although current results are promising, more evidence is required before particle therapy can become internationally the standard treatment for (subsets of) lung cancer patients. (c) 2007 Elsevier Ltd. All rights reserved.
引用
收藏
页码:259 / 267
页数:9
相关论文
共 50 条
  • [21] Lung volume reduction: where do we stand?
    Naunheim, KS
    [J]. SURGICAL CLINICS OF NORTH AMERICA, 2002, 82 (04) : 783 - +
  • [22] Targeted therapies for small cell lung cancer: Where do we stand?
    Arcaro, Alexandre
    [J]. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2015, 95 (02) : 154 - 164
  • [23] Particle therapy for non-small cell lung tumors: where do we stand? A systematic review of the literature
    Wink, Krista C. J.
    Roelofs, Erik
    Solberg, Timothy
    Lin, Liyong
    Simone, Charles B., II
    Jakobi, Annika
    Richter, Christian
    Lambin, Philippe
    Troost, Esther G. C.
    [J]. FRONTIERS IN ONCOLOGY, 2014, 4
  • [24] Gene therapy for arthritis - where do we stand?
    Chernajovsky, Y
    [J]. ARTHRITIS RESEARCH & THERAPY, 2005, 7 (06) : 227 - 229
  • [25] Phage therapy 2.0: where do we stand?
    Breederveld, Roelf S.
    [J]. LANCET INFECTIOUS DISEASES, 2019, 19 (01): : 2 - 3
  • [26] Electroconvulsive therapy in schizophrenia - where do we stand?
    Silva, J.
    Mota, J.
    Azevedo, P.
    [J]. EUROPEAN PSYCHIATRY, 2016, 33 : S262 - S263
  • [27] Photodynamic Therapy in Melanoma - Where do We Stand?
    Baldea, Ioana
    Giurgiu, Lorin
    Teacoe, Ioana Diana
    Olteanu, Diana Elena
    Olteanu, Florin Catalin
    Clichici, Simona
    Filip, Gabriela Adriana
    [J]. CURRENT MEDICINAL CHEMISTRY, 2018, 25 (40) : 5540 - 5563
  • [28] COMBINATION THERAPY IN HYPERTENSION: WHERE DO WE STAND
    Laurent, S.
    [J]. JOURNAL OF HYPERTENSION, 2010, 28 : E611 - E611
  • [29] Haemophilia gene therapy: where do we stand?
    Nathwani, Amit
    [J]. HUMAN GENE THERAPY, 2017, 28 (08) : A2 - A2
  • [30] Intrauterine therapy-where do we stand?
    Weber, Eva Christin
    Gottschalk, Ingo
    Bedei, Ivonne
    Berg, Christoph
    [J]. GYNAKOLOGIE, 2024, 57 (06): : 386 - 400