Əsas səhifə

Çap

Əks əlaqə

İnfo
Hyperbaric oxygenation for tumour sensitisation to radiotherapy

Mündəricat

Hyperbaric oxygenation for tumour sensitisation to radiotherapy

Sübutlu məlumatların xülasələri
11.05.2018 • Sonuncu dəyişiklik 11.05.2018
Editors

Breathing hyperbaric oxygen (HBO) during radiotherapy for cancer treatment may reduce the risk of death and local recurrence within five years for head and neck cancer.

The quality of evidence is downgraded by indirectness (differences in studied patients) and inconsistency (variability in results across studies).

Summary

A Cochrane review included 19 studies with a total of 2 286 subjects. With hyperbaric oxygenation therapy (HBOT), there was a reduction in mortality for head and neck cancers at both one year and five years after therapy (RR 0.83, 95% CI 0.70 to 0.98, number needed to treat (NNT)=11 and RR 0.82, 95% CI 0.69 to 0.98, NNT=5 respectively), as well as improved local tumour control immediately following irradiation (RR with HBOT 0.58, 95% CI 0.39 to 0.85, NNT=7). There was also a lower incidence of recurrence of tumour when using HBOT at both one and five years (RR at one year 0.66, 95% CI 0.56 to 0.78, NNTB=5; RR at 5 years 0.77, 95% CI 0.62 to 0.98, NNTB=6). The effect of HBO varied with different fractionation schemes. There was a significant increase in the rate of severe radiation reaction (RR 2.64, 95% CI 1.65 to 4.23), but not an increased risk of seizures from acute oxygen toxicity (RR 4.3, 95% CI 0.47 to 39.6).

For carcinoma of the uterine cervix and urinary bladder cancer, no benefits were observed with HBOT. When all cancer types were combined, there was an increased risk of severe radiation tissue injury during the course of radiotherapy (RR 2.45, 95% CI 1.85 to 3.24, NNTH=8) and of oxygen toxic seizures during treatment (RR with HBOT 6.8, 96% CI 1.2 to 39.3, NNTH = 22).

A Cochrane review included 19 studies with a total of 2286 subjects. With hyperbaric oxygenation therapy (HBOT), there was a reduction in mortality for head and neck cancers at both one year and five years after therapy (RR 0.83, P = 0.03, number needed to treat (NNT) = 11 and RR 0.82, P = 0.03, NNT = 5 respectively), as well as improved local tumour control at three months (RR with HBOT 0.58, P = 0.006, NNT = 7). The effect of HBO varied with different fractionation schemes. Local tumour recurrence was less likely with HBO at one year (head and neck, RR 0.66, P < 0.0001, NNT = 5), two years (uterine cervix RR 0.60, P = 0.04, NNT = 5) and five years (head and neck (RR 0.77, P = 0.01). There was a significant increase in the rate of both severe radiation tissue injury (RR 2.35, P < 0.0001, (number needed to harm (NNH) = 8. and the chance of seizures during therapy (RR 6.76, P = 0.03, NNH 22) with HBO. Comment: The quality of evidence is downgraded by indirectness (differences in studied patients) and inconsistency (variability in results across studies).

Note: The observed benefits may only occur with unusual fractionation schemes. In general, HBO exposure during irradiation was more beneficial when the total dose of radiation was delivered in low numbers of fractions (12 or fewer) than when a more conventional 20- to 25-fraction scheme was used.

Ədəbiyyat

  1. Bennett MH, Feldmeier J, Smee R et al. Hyperbaric oxygenation for tumour sensitisation to radiotherapy. Cochrane Database Syst Rev 2018;(4):CD005007. .