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随机Hypofractionated 前列腺癌放疗(HYPRO)试验急性期的患者报告结局。

Patient-Reported Outcomes in the Acute Phase of the Randomized Hypofractionated Irradiation for Prostate Cancer (HYPRO) Trial.

机构信息

Department of Radiotherapy, Erasmus MC Cancer Institute, Rotterdam, The Netherlands; Rwanda Cancer Centre, Rwanda Military Hospital, Kigali, Rwanda.

Department of Radiotherapy, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.

出版信息

Int J Radiat Oncol Biol Phys. 2022 Mar 15;112(4):870-879. doi: 10.1016/j.ijrobp.2021.10.139. Epub 2021 Nov 3.

Abstract

PURPOSE

Many patients experience bowel and bladder toxicity during the acute phase of radiation therapy for prostate cancer. Recent literature indicates that hypofractionation (HF) might increase this acute response but little is known on patient-reported outcome during this phase with HF. We evaluated the course of patient-reported acute symptoms during HF versus standard fractionated (SF) radiation therapy within the hypofractionated irradiation for prostate cancer (HYPRO) trial.

METHODS AND MATERIALS

In the HYPRO trial patients were treated with either 64.4 Gy (HF) in 19 fractions (3 times per week) or 78 Gy (SF) in 39 fractions (5 times per week). Normalized total dose for 2 Gy/fractions (NTD)for acute toxicity (α/β ratio of 10) for HF was 72.1 Gy with a similar dose rate of 10.2 Gy per week. Among the 794 patients who were previously eligible for acute grade ≥2 toxicity assessment, 717 had filled out ≥1 symptom questionnaires. For each maximum symptom, we scored "any complaint" and "moderate-severe complaint." Differences were tested by χ test, and associations with clinical factors were tested using logistic regression. Significance was set at P ≤ .008 to adjust for multiple testing.

RESULTS

We observed significantly higher rates of moderate-severe painful defecation (HF 10.8%, SF 5.3%), any mucus discharge (HF 47.1%, SF 37.4%), any rectal blood loss (HF 16.1%, SF 9.3%), increased daily stool frequency ≥4 and ≥6 (HF 34.6%/13.8%, SF 25.6%/7.0%), and any urinary straining (HF 69.9%, SF 58.0%). At 3 months postradiation therapy, rates dropped considerably with similar levels for HF and SF. Hormonal treatment was associated with less acute gastrointestinal symptoms.

CONCLUSION

The increased patient-reported acute rectal symptoms with HF confirmed the previously reported results on acute grade ≥2 rectal toxicity. The increase in bladder symptoms with HF was not identified previously. These observations contradict the NTD calculations. We observed no patterns of persisting complaints with HF after the acute period; therefore, HF is well tolerated and only associated with a temporary increase of symptoms.

摘要

目的

许多前列腺癌患者在放射治疗的急性期会出现肠道和膀胱毒性。最近的文献表明,分次剂量降低(HF)可能会增加这种急性反应,但对于 HF 期间患者报告的急性期结果知之甚少。我们在 HYPRO 试验中评估了 HF 与标准分割(SF)放疗期间患者报告的急性症状的进展。

方法和材料

在 HYPRO 试验中,患者接受 64.4 Gy(HF)19 次(每周 3 次)或 78 Gy(SF)39 次(每周 5 次)治疗。HF 急性毒性的归一化总剂量(2 Gy/fraction 的 NTD)(α/β 比为 10)为 72.1 Gy,每周剂量率相似,为 10.2 Gy。在之前有资格进行急性 2 级以上毒性评估的 794 名患者中,有 717 名患者填写了至少 1 份症状问卷。对于每个最大症状,我们记录“任何投诉”和“中度至重度投诉”。通过 χ 检验测试差异,使用逻辑回归测试与临床因素的关联。设 P≤0.008 以调整多重检验。

结果

我们观察到中度至重度疼痛性排便(HF 10.8%,SF 5.3%)、任何黏液排出(HF 47.1%,SF 37.4%)、任何直肠出血(HF 16.1%,SF 9.3%)、每日排便次数增加≥4 次和≥6 次(HF 34.6%/13.8%,SF 25.6%/7.0%)和任何排尿困难(HF 69.9%,SF 58.0%)的发生率明显更高。放射治疗后 3 个月,HF 和 SF 的发生率均大幅下降,但水平相似。激素治疗与急性胃肠道症状较轻有关。

结论

HF 导致的患者报告的急性直肠症状增加证实了先前关于急性 2 级以上直肠毒性的报告结果。HF 导致的膀胱症状增加以前没有报道过。这些观察结果与 NTD 计算结果相矛盾。我们没有观察到 HF 后急性期持续投诉的模式;因此,HF 耐受良好,仅与症状的暂时增加有关。

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