Blood transfusion during radical chemo-radiotherapy does not reduce tumour hypoxia in squamous cell cancer of the head and neck

被引:19
作者
Welsh, Liam [1 ,2 ,3 ]
Panek, Rafal [1 ,2 ,3 ]
Riddell, Angela [1 ,2 ]
Wong, Kee [1 ,2 ,3 ]
Leach, Martin O. [1 ,2 ,3 ]
Tavassoli, Mahvash [4 ]
Rahman, Durdana [4 ]
Schmidt, Maria [1 ,2 ,3 ]
Hurley, Tara [1 ,2 ]
Grove, Lorna [1 ,2 ]
Richards, Thomas [1 ,2 ,3 ]
Koh, Dow-Mu [1 ,2 ,3 ]
Nutting, Christopher [1 ,2 ,3 ]
Harrington, Kevin [1 ,2 ,3 ]
Newbold, Kate [1 ,2 ,3 ]
Bhide, Shreerang [1 ,2 ,3 ]
机构
[1] Royal Marsden Hosp, Fulham Rd, London SW3 6JJ, England
[2] Royal Marsden Hosp, Downs Rd, Sutton SM2 5PT, Surrey, England
[3] Inst Canc Res, 123 Old Brompton Rd, London SW7 3RP, England
[4] Kings Coll London, Floor 2,Hodgkin Bldg, London SE1 9RT, England
基金
英国工程与自然科学研究理事会;
关键词
head and neck cancer; anaemia; MRI; blood transfusion; radiotherapy; HEMOGLOBIN CONCENTRATION; INDUCTION CHEMOTHERAPY; PROGNOSTIC VALUE; CARCINOMA; RADIOTHERAPY; ANEMIA; OXYGENATION; THERAPY; CHEMORADIATION; RADIATION;
D O I
10.1038/bjc.2016.386
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Patients with head and neck squamous cell carcinoma (HNSCC) undergoing radical chemo-radiation (CRT) frequently receive transfusion with packed red cells (PRCT) during radiotherapy on the basis that PRCT increases tumour oxygenation and overcomes hypoxia-induced radio -resistance. This is likely to be a significant oversimplification given the fact that tumour hypoxia is the result of several intrinsic and extrinsic factors, including many that are not directly related to serum haemoglobin (Hb). Therefore, we have studied the effect of PRCT on tumour oxygenation in a prospective cohort of patients who developed low Hb during radical CRT for HNSCC. Methods: This was a prospective study of 20 patients with HNSCC receiving radical CRT undergoing PRCT for Hb <11.5 g dl (-1). Patients underwent pretransfusion and posttransfusion intrinsic susceptibility-weighted (SWI) MRI and dynamic contrast-enhanced (DCE) MRI. Blood samples were obtained at the time of MRI scanning and two further time points for measuring Hb and a panel of serum cytokine markers of tumour hypoxia. 3D T-2* and K-trans maps were calculated from the MRI data for primary tumours and cervical lymph node metastases. Results: PRCT produced no change (11 patients) or reduced (1 patient) T-2* (tumour oxygenation) in 12 of the 16 (75%) evaluable primary tumours. Three of the four patients with improved tumour oxygenation progressed or had partial response following treatment completion. There were variable changes in k(trans) (tumour perfusion or vessel permeability) following PRCT that were of small magnitude for most tumours. Pre-and Post-PRCT levels of measured cytokines were not significantly different. Conclusions: This study suggests that PRCT during radical CRT for HNSCC does not improve tumour oxygenation. Therefore, oncologists should consider changing practice according to NICE and American Association of Blood Banks guidelines on PRCT for anaemia.
引用
收藏
页码:28 / 35
页数:8
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