首页> 美国卫生研究院文献>Cancers >Serial Assessment of Therapeutic Response to a New Radiosensitization Treatment Kochi Oxydol-Radiation Therapy for Unresectable Carcinomas Type II (KORTUC II) in Patients with Stage I/II Breast Cancer Using Breast Contrast-Enhanced Magnetic Resonance Imaging
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Serial Assessment of Therapeutic Response to a New Radiosensitization Treatment Kochi Oxydol-Radiation Therapy for Unresectable Carcinomas Type II (KORTUC II) in Patients with Stage I/II Breast Cancer Using Breast Contrast-Enhanced Magnetic Resonance Imaging

机译:使用乳房造影增强磁共振成像技术对I / II期乳腺癌患者进行的对新的放射增敏治疗(高知二氧化铀放射治疗II型不能切除的癌症KORTUC II)的治疗反应的系列评估

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摘要

Background: We have developed a new radiosensitization treatment called Kochi Oxydol-Radiation Therapy for Unresectable Carcinomas, Type II (KORTUC II). Using KORTUC II, we performed breast-conserving treatment (BCT) without any surgical procedure for elderly patients with breast cancer in stages I/II or patients refusing surgery. Since surgery was not performed, histological confirmation of the primary tumor region following KORTUC II treatment was not possible. Therefore, to precisely evaluate the response to this new therapy, a detailed diagnostic procedure is needed. The goal of this study was to evaluate the therapeutic response to KORTUC II treatment in patients with stage I/II breast cancer using annual breast contrast-enhanced (CE) magnetic resonance imaging (MRI). Methods: Twenty-one patients with stage I/II breast cancer who were elderly and/or refused surgery were enrolled in this study. All patients underwent MRI prior to and at 3 to 6 months after KORTUC II, and then approximately biannually thereafter. Findings from MRI were compared with those from other diagnostic modalities performed during the same time period. Results: KORTUC II was well tolerated, with minimal adverse effects. All of 21 patients showed a clinically complete response (cCR) on CE MRI. The mean period taken to confirm cCR on the breast CE MRI was approximately 14 months. The mean follow-up period for the patients was 61.9 months at the end of October 2014. Conclusions: The therapeutic effect of BCT using KORTUC II without surgery could be evaluated by biannual CE MRI evaluations. Approximately 14 months were required to achieve cCR in response to this therapy.
机译:背景:我们已经开发出一种新的放射增敏治疗方法,称为II型不可切除癌的高知氧合放射疗法。使用KORTUC II,我们对I / II期的老年乳腺癌患者或拒绝手术的老年患者进行了不采取任何外科手术的保乳治疗(BCT)。由于未进行手术,因此不可能对KORTUC II治疗后的原发肿瘤区域进行组织学确认。因此,为了精确评估对这种新疗法的反应,需要详细的诊断程序。这项研究的目的是使用年度乳房造影剂(CE)磁共振成像(MRI)评估I / II期乳腺癌患者对KORTUC II治疗的治疗反应。方法:本研究招募了21例年龄较大和/或拒绝手术的I / II期乳腺癌患者。所有患者均在KORTUC II之前和之后3至6个月接受MRI检查,然后大约每半年进行MRI检查。将来自MRI的结果与同一时期进行的其他诊断方式的结果进行比较。结果:KORTUC II耐受性良好,不良反应最小。所有21例患者均在CE MRI上显示出临床完全缓解(cCR)。在乳腺CE MRI上确认cCR的平均时间约为14个月。截至2014年10月,患者的平均随访期为61.9个月。结论:可以通过每两年进行一次CE MRI评估来评估使用KORTUC II无需手术的BCT的治疗效果。响应此疗法,需要约14个月才能达到cCR。

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