首页> 外文期刊>International Journal of Radiation Oncology, Biology, Physics >Phase I study of escalating doses of low-dose-rate, locoregional irradiation preceding Cytoxan-TBI for patients with chemotherapy-resistant non-Hodgkin's or Hodgkin's lymphoma.
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Phase I study of escalating doses of low-dose-rate, locoregional irradiation preceding Cytoxan-TBI for patients with chemotherapy-resistant non-Hodgkin's or Hodgkin's lymphoma.

机译:I期研究在抗药性非霍奇金淋巴瘤或霍奇金淋巴瘤患者中,在Cytoxan-TBI之前逐步增加低剂量率局部区域照射的剂量。

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摘要

In patients in whom bone marrow transplantation (BMT) fails, recurrence often occurs at sites known to have contained disease before initiating BMT. The purpose of this study was to find the maximal tolerable dose of locoregional irradiation (LRT) between 1000 and 2000 cGy that could be integrated with our Cytoxan-total body irradiation (TBI) BMT conditioning regimen in the treatment of lymphoma.Patients had Hodgkin's or non-Hodgkin's lymphoma in chemotherapy-refractory relapse. All patients received LRT to a maximum of three sets of fields encompassing either all current or all previously known sites of disease. Cytoxan-TBI consisted of cyclophosphamide 50 mg/kg daily for 4 days followed by TBI of 1200 cGy given in four fractions.Twenty-one patients were enrolled. Radiation Therapy Oncology Group Grade 3 in-field acute toxicity was observed in 1 patient at each dose level up to 1500 cGy and in 3 of 6 patients receiving 2000 cGy. Clinically evident late toxicities were limited to hypothyroidism and onesecond malignancy occurring outside the LRT fields.Low-dose-rate, LRT with concurrent Cytoxan-TBI before BMT has acceptable rates of in-field toxicity for doses up to 1500 cGy in five fractions. This regimen safely permits the use of a total combined radiation dose of up to 2700 cGy during 2 weeks, with encouraging in-field response rates in treatment-refractory patients.
机译:在骨髓移植(BMT)失败的患者中,复发通常发生在开始BMT之前已知患有疾病的部位。这项研究的目的是寻找可以在1000至2000 cGy之间进行局部区域照射(LRT)的最大耐受剂量,该剂量可以与我们的Cytoxan全身照射(TBI)BMT调理方案相结合来治疗淋巴瘤。非霍奇金淋巴瘤的化疗难治性复发。所有患者最多接受三组视野的LRT,包括所有当前或所有先前已知的疾病部位。 Cytoxan-TBI由环磷酰胺每天50 mg / kg组成,持续4天,然后分四部分给予1200 cGy的TBI.21名患者入组。放射治疗肿瘤学小组在每个剂量水平高达1500 cGy的患者中观察到3级场内急性毒性,在接受2000 cGy的6例患者中有3例被观察到。临床上明显的晚期毒性仅限于甲状旁腺功能减退和LRT场外发生的一秒钟恶性肿瘤。低剂量率,LRT与并发Cytoxan-TBI并用BMT在剂量高达1500 cGy的情况下,在五个部分中具有可接受的场内毒性率。该方案安全地允许在2周内使用高达2700 cGy的总组合放射剂量,并在难治性患者中提高了现场应答率。

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