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Acute toxicity of chemo-radiotherapy for cervical cancer: the Addenbrooke's experience.

机译:化学放射疗法对子宫颈癌的急性毒性:Addenbrooke的经验。

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AIMS: An audit of acute treatment-related toxicity during chemo-radiotherapy for cervical cancer was carried out to assess its tolerance outside research settings. MATERIALS AND METHODS: Between May 1999 and April 2003, 74 patients with carcinoma of the cervix were treated with radical radiotherapy given concurrently with weekly cisplatin chemotherapy. Fifty-nine (79.7%) patients received chemo-radiotherapy as primary radical treatment, 10 (13.5%) patients were treated adjuvantly for poor-prognosis features after radical surgery, and the remaining five (6.8%) were given chemo-radiotherapy for pelvic recurrences after previous surgery. Acute treatment-related toxicity was graded prospectively at weekly intervals during chemo-radiotherapy using the National Cancer Institute Common Toxicity Criteria. RESULTS: The most common adverse effects were diarrhoea (80.6%), malaise (66.7%) and nausea (62.5%). The most common haematological toxicity was anaemia, with 41.7% patients developing grade 1 or 2 toxicity. Only three (4.2%) patients had grade 3 or 4 toxicity. One patient had grade 3 thrombocytopenia, another had grade 4 neutropenia and the third patient had grade 3 diarrhoea. A statistically significant correlation was found between maximum treatment-related toxicity, larger treatment volumes (P = 0.006) and disease stage (P = 0.04). A total of 97.3% of patients completed external beam radiotherapy without any interruptions for treatment-related toxicity. Only two patients (3.4%) experienced a delay in brachytherapy for treatment-related toxicity. Two patients died during external beam radiotherapy, and one patient suffered a fatal pulmonary embolism 1 week after completing brachytherapy treatment. A total of 70.2% patients completed the planned number of chemotherapy cycles, with a further 20.3% receiving at least three cycles. The most common reason for failure to complete chemotherapy as planned was gastrointestinal toxicity. There was no correlation between failure to complete planned chemotherapy and patient age, disease stage, radiotherapy treatment volumes or postoperative treatment. CONCLUSION: Our study has shown that cisplatin-based chemo-radiotherapy for carcinoma of the cervix is well tolerated when given to a largely unselected population of patients outside research settings. The effectiveness of the treatment should therefore mirror the efficacy obtained in clinical trials.
机译:目的:对宫颈癌化学放疗过程中与急性治疗相关的毒性进行了审计,以评估其在研究环境之外的耐受性。材料与方法:在1999年5月至2003年4月之间,对74例宫颈癌患者进行了放疗,并每周进行顺铂化疗。 59例(79.7%)患者接受了化学放疗作为主要的根治性治疗,其中10例(13.5%)接受了根治性手术后预后不良的辅助治疗,其余5例(6.8%)接受了盆腔化学放疗先前手术后复发。使用美国国家癌症研究所的通用毒性标准,在化学放疗期间每周一次对与急性治疗相关的毒性进行前瞻性分级。结果:最常见的不良反应是腹泻(80.6%),不适(66.7%)和恶心(62.5%)。最常见的血液学毒性是贫血,有41.7%的患者发生1级或2级毒性。只有三名(4.2%)患者具有3或4级毒性。一名患者患有3级血小板减少症,另一名患者患有4级中性粒细胞减少症,第三名患者患有3级腹泻。在最大的治疗相关毒性,更大的治疗量(P = 0.006)和疾病阶段(P = 0.04)之间发现了统计学上显着的相关性。总计97.3%的患者完成了外部束放射疗法,而未因治疗相关的毒性而中断治疗。只有两名患者(3.4%)因治疗相关毒性而接受了近距离放射治疗的延迟。两名患者在外部放射线治疗期间死亡,一名患者在完成近距离放射治疗后1周遭受致命的肺栓塞。总计70.2%的患者完成了计划的化疗周期数,另外20.3%的患者接受了至少三个周期。未能按计划完成化疗的最常见原因是胃肠道毒性。未能完成计划的化学疗法与患者年龄,疾病阶段,放疗治疗量或术后治疗之间没有相关性。结论:我们的研究表明,当在研究环境之外接受大量未经选择的患者治疗时,以顺铂为基础的化学放射治疗子宫颈癌的耐受性良好。因此,治疗的有效性应反映在临床试验中获得的功效。

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