Hyperbaric oxygen therapy for late radiation-induced tissue toxicity: prospectively patient-reported outcome measures in breast cancer patients

被引:27
作者
Teguh, David N. [1 ,2 ]
Raap, Rene Bol [1 ]
Struikmans, Henk [3 ,4 ]
Verhoef, Cees [5 ]
Koppert, Linetta B. [5 ]
Koole, Arne [1 ]
Huang, Yadi [7 ]
van Hulst, Rob A. [1 ,6 ]
机构
[1] Hyperbaar Geneeskundig Ctr Rijswijk, Treubstr 5a, NL-2288 EG Rijswijk, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Surg Hyperbar Med, Treubstr 5a, NL-2288 EG Rijswijk, Netherlands
[3] Leiden Univ, Dept Radiat Oncol, Med Ctr, Leiden, Netherlands
[4] Med Ctr Haaglanden, Radiotherapy Ctr West, The Hague, Netherlands
[5] Erasmus MC Canc Inst, Dept Surg Oncol, Rotterdam, Netherlands
[6] Univ Amsterdam, Acad Med Ctr, Dept Anesthesiol Hyperbar Med, Treubstr 5a, NL-2288 EG Rijswijk, Netherlands
[7] Univ Leuven, Treubstr 5a, NL-2288 EG Rijswijk, Netherlands
来源
RADIATION ONCOLOGY | 2016年 / 11卷
关键词
Breast cancer; Radiotherapy; Radiation toxicity; Fibrosis; Pain; QUALITY-OF-LIFE; INTENSITY-MODULATED RADIOTHERAPY; LYMPH-NODE DISSECTION; DOUBLE-BLIND; RISK-FACTORS; TRIAL; PREVENTION; PRIORITIES; SURVIVORS; SURGERY;
D O I
10.1186/s13014-016-0700-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: This study examines patient reported outcome measures of women undergoing hyperbaric oxygen treatment (HBOT) after breast-conserving therapy. Method: Included were 57 women treated with HBOT for late radiation-induced tissue toxicity (LRITT) referred in the period January 2014-December 2015. HBOT consisted of (on average) 47 sessions. In total, 80 min of 100 % O-2 was administered under increased pressure of 2.4 ATA. Quality of life was assessed before and after treatment using the European Organization for Research and Treatment of Cancer (EORTC) QLQ-BR23, and a NRS pain score. Results: Fifty-seven women were available for evaluation before and after treatment. Before HBOT, patients had severe complaints of pain in the arm/ shoulder (46 %), swollen arm/ hand (14 %), difficulty to raise arm or move it sideways (45 %), pain in the area of the affected breast (67 %), swollen area of the affected breast (45 %), oversensitivity of the affected breast (54 %), and skin problems on/in the area of the affected breast (32 %); post HBOT, severe complaints were still experienced in 17, 7, 22, 15, 13, 15, and 11 % of the women, respectively. Differences were all significant. The NRS pain score improved at least 1 point (range 0-10) in 81 % of the patients (p < 0.05). Conclusion: In these breast cancer patients treated with HBOT for LRITT, the patient-reported outcomes were positive and improvements were observed. HBOT was a well-tolerated treatment for LRITT and its side-effects were both minimal and reversible.
引用
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页数:6
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