Literature DB >> 12009230

Hypofractionated irradiation for non-small cell lung cancer.

Raymond P Abratt1, Jeffrey A Bogart, Alistair Hunter.   

Abstract

Large radiation fractions are an effective way of killing tumour cells but have generally been avoided in curative treatment of patients because of concerns of a disproportionate increase in late normal tissue toxicity. Radiobiological modelling of the effect of radiation on lung tumours and late-reacting normal tissues, which are more sensitive to large radiation fractions, has been undertaken. The biological effect of radiation on tumours is increased as the overall treatment time is shortened but this is not true for late-reacting normal tissue. Sample data are shown in which the relative increases in radiation effect on the tumour and late-reacting normal tissues are similar after hypofractionation. A favourable therapeutic ratio can be achieved because the bulk of normal tissue will receive a lower dose of radiation at a lower dose per fraction than the tumour, especially with current techniques where the volume of normal tissue irradiated can be sharply reduced. The clinical evidence confirms that lung toxicity is volume-dependent. It is the small Stage I and II tumours which are most likely to benefit from hypofractionated regimens, as the volumes to be treated are smaller and they have a lower incidence of distant metastases. Patients with Stage III tumours with favourable prognostic factors are nowadays treated with combined chemotherapy and radiotherapy and so for this group more conservative hypofractionation regimens are being explored. However, more advanced tumours may be treated with hypofractionation to lower total doses to achieve palliation and a modest degree of survival benefit.

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Mesh:

Year:  2002        PMID: 12009230     DOI: 10.1016/s0169-5002(02)00020-x

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   5.705


  5 in total

1.  Experimental verification of the utility of positron emitter nuclei generated by photonuclear reactions for X-ray beam monitoring in a phantom.

Authors:  Teiji Nishio; Taku Inaniwa; Kazumasa Inoue; Aya Miyatake; Keiichi Nakagawa; Kiyoshi Yoda; Takashi Ogino
Journal:  Radiat Med       Date:  2007-12-25

2.  Simultaneous Integrated Boost for Radiation Dose Escalation to the Gross Tumor Volume With Intensity Modulated (Photon) Radiation Therapy or Intensity Modulated Proton Therapy and Concurrent Chemotherapy for Stage II to III Non-Small Cell Lung Cancer: A Phase 1 Study.

Authors:  Melenda D Jeter; Daniel Gomez; Quynh-Nhu Nguyen; Ritsuko Komaki; Xiaodong Zhang; Xiaorong Zhu; Michael O'Reilly; Frank V Fossella; Ting Xu; Xiong Wei; Hui Wang; Wenjuan Yang; Anne Tsao; Radhe Mohan; Zhongxing Liao
Journal:  Int J Radiat Oncol Biol Phys       Date:  2017-11-03       Impact factor: 7.038

3.  Accelerated hypofractionated radiation therapy compared to conventionally fractionated radiation therapy for the treatment of inoperable non-small cell lung cancer.

Authors:  Arya Amini; Steven H Lin; Caimiao Wei; Pamela Allen; James D Cox; Ritsuko Komaki
Journal:  Radiat Oncol       Date:  2012-03-15       Impact factor: 3.481

4.  Hypofractionated stereotactic body radiation therapy for elderly patients with stage IIB-IV nonsmall cell lung cancer who are ineligible for or refuse other treatment modalities.

Authors:  Sana D Karam; Zachary D Horne; Robert L Hong; Don McRae; David Duhamel; Nadim M Nasr
Journal:  Lung Cancer (Auckl)       Date:  2014-10-03

5.  Absence of toxicity with hypofractionated 3-dimensional radiation therapy for inoperable, early stage non-small cell lung cancer.

Authors:  Sergio L Faria; Luis Souhami; Lorraine Portelance; Marie Duclos; Te Vuong; David Small; Carolyn R Freeman
Journal:  Radiat Oncol       Date:  2006-11-01       Impact factor: 3.481

  5 in total

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