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同步放化疗联合或不联合诱导化疗用于治疗原发灶不明的颈部淋巴结转移癌。

Concurrent chemoradiotherapy with or without induction chemotherapy for the management of cervical lymph node metastasis from unknown primary tumor.

作者信息

Khan Mohsin, Siddiqui Shahid A

机构信息

Department of Radiotherapy, Jawaharlal Nehru Medical College, Aligarh Muslim University, Aligarh, Uttar Pradesh, India.

出版信息

J Cancer Res Ther. 2018 Jul-Sep;14(5):1117-1120. doi: 10.4103/0973-1482.203594.

Abstract

BACKGROUND

To determine the impact of concurrent chemoradiotherapy (CCRT) with or without induction chemotherapy over radiation alone for the treatment of patients of cervical lymph node metastasis from an unknown primary tumor.

MATERIALS AND METHODS

A total of 96 patients with squamous cell histology of cervical lymph node metastases from unknown primary tumor were retrospectively reviewed. About 12 patients were treated with radiation alone (RT alone), 45 with CCRT, and 39 with induction chemotherapy followed by CCRT (ICCRT).

RESULTS

Overall response rate (ORR) obtained with RT alone arm was 75%, whereas for CCRT, it was 86.7%. About 15.4% had a complete response (CR) after induction chemotherapy with 92.3% ORR after the completion of CCRT. At 2 years, the disease free survival (DFS) was 50% in RT alone, 73% with CCRT, and 62% with ICCRT, while the corresponding rates at 5 years were 50% for RT alone, 45% with CCRT, and 54% in ICCRT arm.

CONCLUSION

Though we obtained a high ORR with concurrent or induction chemotherapy arm over RT alone, there is no clear advantage in the DFS. The nonrandomized nature of this trial and the potential for selection bias should definitely be taken into account while drawing comparisons from this trial.

摘要

背景

确定同步放化疗(CCRT)联合或不联合诱导化疗相对于单纯放疗在治疗原发灶不明的颈部淋巴结转移患者中的影响。

材料与方法

回顾性分析96例原发灶不明的颈部淋巴结转移鳞状细胞组织学患者。约12例患者接受单纯放疗(单纯RT),45例接受同步放化疗,39例接受诱导化疗后同步放化疗(ICCRT)。

结果

单纯放疗组的总缓解率(ORR)为75%,同步放化疗组为86.7%。诱导化疗后约15.4%达到完全缓解(CR),同步放化疗完成后的ORR为92.3%。2年时,单纯放疗组的无病生存率(DFS)为50%,同步放化疗组为73%,ICCRT组为62%,而5年时单纯放疗组、同步放化疗组和ICCRT组的相应比率分别为50%、45%和54%。

结论

尽管与单纯放疗相比,同步或诱导化疗组获得了较高的ORR,但在DFS方面没有明显优势。在从本试验进行比较时,应充分考虑本试验的非随机性质和选择偏倚的可能性。

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