Literature DB >> 20472367

Distribution of proliferating bone marrow in adult cancer patients determined using FLT-PET imaging.

James A Hayman1, Jason W Callahan, Alan Herschtal, Sarah Everitt, David S Binns, Rod J Hicks, Michael Mac Manus.   

Abstract

PURPOSE: Given that proliferating hematopoietic stem cells are especially radiosensitive, the bone marrow is a potential organ at risk, particularly with the use of concurrent chemotherapy and radiotherapy. Existing data on bone marrow distribution have been determined from the weight and visual appearance of the marrow in cadavers. 18F-fluoro-L-deoxythymidine concentrates in bone marrow, and we used its intensity on positron emission tomography imaging to quantify the location of the proliferating bone marrow. METHODS AND MATERIALS: The 18F-fluoro-L-deoxythymidine positron emission/computed tomography scans performed at the Peter MacCallum Cancer Centre between 2006 and 2009 on adult cancer patients were analyzed. At a minimum, the scans included the mid-skull through the proximal femurs. A software program developed at our institution was used to calculate the percentage of administered activity in 11 separately defined bony regions.
RESULTS: The study population consisted of 13 patients, 6 of whom were men. Their median age was 61 years. Of the 13 patients, 9 had lung cancer, 2 had colon cancer, and 1 each had melanoma and leiomyosarcoma; 6 had received previous, but not recent, chemotherapy. The mean percentage of proliferating bone marrow by anatomic site was 2.9%±2.1% at the skull, 1.9%±1.2% at the proximal humeri, 2.9%±1.3% at the sternum, 8.8%±4.7% at the ribs and clavicles, 3.8%±0.9% at the scapulas, 4.3%±1.6% at the cervical spine, 19.9%±2.6% at the thoracic spine, 16.6%±2.2% at the lumbar spine, 9.2%±2.3% at the sacrum, 25.3%±4.9% at the pelvis, and 4.5%±2.5% at the proximal femurs.
CONCLUSION: Our modern estimates of bone marrow distribution in actual cancer patients using molecular imaging of the proliferating marrow provide updated data for optimizing normal tissue sparing during external beam radiotherapy planning.
Copyright © 2011 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2010        PMID: 20472367     DOI: 10.1016/j.ijrobp.2009.11.040

Source DB:  PubMed          Journal:  Int J Radiat Oncol Biol Phys        ISSN: 0360-3016            Impact factor:   7.038


  34 in total

1.  A prospective phase II study of magnetic resonance imaging guided hematopoietical bone marrow-sparing intensity-modulated radiotherapy with concurrent chemotherapy for rectal cancer.

Authors:  Wang Jianyang; Tian Yuan; Tang Yuan; Wang Xin; Li Ning; Ren Hua; Fang Hui; Feng Yanru; Wang Shulian; Song Yongwen; Liu Yueping; Wang Weihu; Li Yexiong; Jin Jing
Journal:  Radiol Med       Date:  2015-11-27       Impact factor: 3.469

2.  Vertebral lesion distribution in multiple myeloma--assessed by reduced-dose whole-body MDCT.

Authors:  Georg Bier; Christopher Kloth; Christoph Schabel; Malte Bongers; Konstantin Nikolaou; Marius Horger
Journal:  Skeletal Radiol       Date:  2016-01       Impact factor: 2.199

3.  Dosimetric predictors of acute haematological toxicity in oesophageal cancer patients treated with neoadjuvant chemoradiotherapy.

Authors:  Jie Lee; Jhen-Bin Lin; Fang-Ju Sun; Kuo-Wei Lu; Chou-Hsien Lee; Yu-Jen Chen; Wen-Chien Huang; Hung-Chang Liu; Meng-Hao Wu
Journal:  Br J Radiol       Date:  2016-08-24       Impact factor: 3.039

Review 4.  The functional interplay between systemic cancer and the hematopoietic stem cell niche.

Authors:  Amber J Giles; Christopher D Chien; Caitlin M Reid; Terry J Fry; Deric M Park; Rosandra N Kaplan; Mark R Gilbert
Journal:  Pharmacol Ther       Date:  2016-09-02       Impact factor: 12.310

5.  Mapping Bone Marrow Response in the Vertebral Column by Positron Emission Tomography Following Radiotherapy and Erlotinib Therapy of Lung Cancer.

Authors:  Azadeh Abravan; Hanne Astrid Eide; Ayca Muftuler Løndalen; Åslaug Helland; Eirik Malinen
Journal:  Mol Imaging Biol       Date:  2019-04       Impact factor: 3.488

6.  (2S,4R)-4-[18F]Fluoroglutamine as a PET Indicator for Bone Marrow Metabolism Dysfunctional: from Animal Experiments to Clinical Application.

Authors:  Hua Zhu; Fei Liu; Yan Zhang; Jianhua Yang; Xiaoxia Xu; Xiaoyi Guo; Teli Liu; Nan Li; Lin Zhu; Hank F Kung; Zhi Yang
Journal:  Mol Imaging Biol       Date:  2019-10       Impact factor: 3.488

7.  Bone marrow sparing in intensity modulated proton therapy for cervical cancer: Efficacy and robustness under range and setup uncertainties.

Authors:  Eric Dinges; Nicole Felderman; Sarah McGuire; Brandie Gross; Sudershan Bhatia; Sarah Mott; John Buatti; Dongxu Wang
Journal:  Radiother Oncol       Date:  2015-05-13       Impact factor: 6.280

8.  Predictors of Hematologic Toxicity and Chemotherapy Dose Intensity in Patients Undergoing Chemoradiation for Pancreatic Cancer.

Authors:  Talha Shaikh; Lora S Wang; Brian Egleston; Meher Burki; John P Hoffman; Steven J Cohen; Joshua E Meyer
Journal:  Am J Clin Oncol       Date:  2018-01       Impact factor: 2.339

9.  Cervical cancer treated with reduced-volume intensity-modulated radiation therapy base on Sedlis criteria (NCCN VS RTOG).

Authors:  Hua-Chun Luo; Gui-Shan Lin; Shao-Guang Liao; Feng-Mei Wang; Hui-Hua Cheng; Jing Feng; Qin Yin; Qun-Hua Chen; Jin-Feng Zhu; Jian-Feng Xu; Dian Wang; Zhi-Chao Fu
Journal:  Br J Radiol       Date:  2017-12-05       Impact factor: 3.039

10.  Thoracic Vertebral Body Irradiation Contributes to Acute Hematologic Toxicity During Chemoradiation Therapy for Non-Small Cell Lung Cancer.

Authors:  Matthew P Deek; Brian Benenati; Sinae Kim; Ting Chen; Inaya Ahmed; Wei Zou; Joseph Aisner; Salma K Jabbour
Journal:  Int J Radiat Oncol Biol Phys       Date:  2015-09-25       Impact factor: 7.038

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.