Literature DB >> 25828068

Longitudinal study of acute haematologic toxicity in cervical cancer patients treated with chemoradiotherapy.

He Zhu1, Kaveh Zakeri1, Florin Vaida2, Ruben Carmona1, Kaivan K Dadachanji1, Ryan Bair3,4, Bulent Aydogan3,4, Yasmin Hasan3, Catheryn M Yashar1, Loren K Mell1.   

Abstract

INTRODUCTION: Acute hematologic toxicity (HT) limits optimal delivery of concurrent chemoradiotherapy (CRT) for patients with pelvic malignancies. We tested the hypothesis that pelvic bone marrow (PBM) dose-volume metrics were associated with weekly reductions in peripheral blood cell counts in cervical cancer patients undergoing CRT.
METHODS: We included 102 cervical cancer patients treated with concurrent cisplatin (40 mg/m(2) /week) and pelvic radiotherapy treated at three US centres. No patient received granulocyte-monocyte colony stimulating factor (GM-CSF) or platelet transfusions. Using linear-mixed effects modelling, we analysed weekly reductions in log-transformed peripheral blood cell counts as a function of time (weeks), mean PBM dose and the PBM volume receiving ≥10 Gy (V(10)), 20 Gy (V(20)), 30 Gy (V(30)) and 40 Gy (V(40)).
RESULTS: Increases in mean PBM radiation dose, V(20), V(30) and V(40) were all significantly associated with a greater weekly reduction in white blood cell (WBC) and absolute neutrophil counts (ANCs). We estimated that with every 1 Gy increase in mean PBM dose, ln(ANC) was reduced by 9.6/μL per week (95% confidence interval, 1.9-17.3, P = 0.015). Subregion analysis also identified significant associations between weekly reductions in ln(WBC) and ln(ANC) within lumbosacral spine, ischium and proximal femora, as opposed to ilium.
CONCLUSIONS: PBM radiation dose-volume metrics are significantly associated with weekly reductions in peripheral blood cell counts in cervical cancer patients undergoing CRT, particularly within the lower pelvis and lumbosacral spine.
© 2015 The Royal Australian and New Zealand College of Radiologists.

Entities:  

Keywords:  acute hematologic function; cervical cancer; chemoradiotherapy; longitudinal analysis

Mesh:

Year:  2015        PMID: 25828068      PMCID: PMC6373449          DOI: 10.1111/1754-9485.12297

Source DB:  PubMed          Journal:  J Med Imaging Radiat Oncol        ISSN: 1754-9477            Impact factor:   1.735


  9 in total

1.  Lumbar-sacral bone marrow dose modeling for acute hematological toxicity in anal cancer patients treated with concurrent chemo-radiation.

Authors:  Pierfrancesco Franco; Riccardo Ragona; Francesca Arcadipane; Massimiliano Mistrangelo; Paola Cassoni; Nadia Rondi; Mario Morino; Patrizia Racca; Umberto Ricardi
Journal:  Med Oncol       Date:  2016-11-04       Impact factor: 3.064

2.  Dosimetric predictors of acute hematologic toxicity during concurrent intensity-modulated radiotherapy and chemotherapy for anal cancer.

Authors:  P Franco; R Ragona; F Arcadipane; M Mistrangelo; P Cassoni; N Rondi; M Morino; P Racca; U Ricardi
Journal:  Clin Transl Oncol       Date:  2016-04-01       Impact factor: 3.405

3.  The absolute volume of PET-defined, active bone marrow spared predicts for high grade hematologic toxicity in cervical cancer patients undergoing chemoradiation.

Authors:  Y M Zhou; C Freese; T Meier; D Go; K Khullar; M Sudhoff; M Lamba; J Kharofa
Journal:  Clin Transl Oncol       Date:  2017-10-26       Impact factor: 3.405

4.  Clinical and dosimetric factors associated with the development of hematologic toxicity in locally advanced cervical cancer treated with chemotherapy and 3D conformal radiotherapy.

Authors:  Miguel Ángel Souto-Del Bosque; Miguel Ángel Cervantes-Bonilla; Gerardo Del Carmen Palacios-Saucedo
Journal:  Rep Pract Oncol Radiother       Date:  2018-08-13

5.  Feasibility of bone marrow sparing volumetric modulated arc therapy to spare active bone marrow in cervical and vaginal cancer patients: a retrospective dosimetric analysis.

Authors:  Michaela Beavan; Kylie Dundas; Felicity Hudson; Yolanda Surjan; Annie Lau; Shrikant Deshpande; Karen Lim; Viet Do
Journal:  J Med Radiat Sci       Date:  2021-07-19

6.  Which Bone Marrow Sparing Strategy and Radiotherapy Technology Is Most Beneficial in Bone Marrow-Sparing Intensity Modulated Radiation Therapy for Patients With Cervical Cancer?

Authors:  De-Yang Yu; Yan-Ling Bai; Yue Feng; Le Wang; Wei-Kang Yun; Xin Li; Jia-Yu Song; Shan-Shan Yang; Yun-Yan Zhang
Journal:  Front Oncol       Date:  2020-12-17       Impact factor: 6.244

7.  Correlation between changes of pelvic bone marrow fat content and hematological toxicity in concurrent chemoradiotherapy for cervical cancer.

Authors:  Cong Wang; Xiaohang Qin; Guanzhong Gong; Lizhen Wang; Ya Su; Yong Yin
Journal:  Radiat Oncol       Date:  2022-04-07       Impact factor: 3.481

8.  Comparison of Hematologic Toxicity and Bone Marrow Compensatory Response in Head and Neck vs. Cervical Cancer Patients Undergoing Chemoradiotherapy.

Authors:  Lucas K Vitzthum; Elena S Heide; Helen Park; Casey W Williamson; Paige Sheridan; Minh-Phuong Huynh-Le; Igor Sirak; Lichun Wei; Rafal Tarnawski; Umesh Mahantshetty; Cammie Nguyen; Jyoti Mayadev; Catheryn M Yashar; Assuntina G Sacco; Loren K Mell
Journal:  Front Oncol       Date:  2020-07-21       Impact factor: 6.244

9.  The volume of 99m Tc sulfur colloid SPET-defined active bone marrow can predict grade 3 or higher acute hematologic toxicity in locally advanced cervical cancer patients who receive chemoradiotherapy.

Authors:  Shan-Bing Wang; Jia-Pei Liu; Kai-Jian Lei; Yu-Ming Jia; Yan Xu; Jin-Feng Rong; Chun-Xiu Wang
Journal:  Cancer Med       Date:  2019-10-16       Impact factor: 4.452

  9 in total

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