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本文引用的文献

1
Neoadjuvant chemoradiation compared to neoadjuvant radiation alone and surgery alone for Stage II and III soft tissue sarcoma of the extremities.新辅助放化疗对比新辅助放疗联合手术与单纯手术治疗肢体 II 期和 III 期软组织肉瘤。
Radiat Oncol. 2011 Aug 9;6:91. doi: 10.1186/1748-717X-6-91.
2
Randomized clinical trials in soft tissue sarcoma.软组织肉瘤的随机临床试验。
Surg Oncol Clin N Am. 2010 Jan;19(1):1-11. doi: 10.1016/j.soc.2009.09.006.
3
Primary tumor necrosis predicts distant control in locally advanced soft-tissue sarcomas after preoperative concurrent chemoradiotherapy.原发肿瘤坏死可预测术前同步放化疗后局部晚期软组织肉瘤的远处控制。
Int J Radiat Oncol Biol Phys. 2010 Mar 15;76(4):1147-53. doi: 10.1016/j.ijrobp.2009.03.015. Epub 2009 Jul 4.
4
Pathologic response to preoperative therapy: does it mean what we think it means?术前治疗的病理反应:它的含义是我们所认为的那样吗?
Ann Surg Oncol. 2009 Jun;16(6):1465-79. doi: 10.1245/s10434-009-0374-z. Epub 2009 Mar 27.
5
Why do patients with low-grade soft tissue sarcoma die?低度恶性软组织肉瘤患者为何会死亡?
Ann Surg Oncol. 2008 Dec;15(12):3550-60. doi: 10.1245/s10434-008-0163-0. Epub 2008 Oct 1.
6
Selection of response criteria for clinical trials of sarcoma treatment.肉瘤治疗临床试验反应标准的选择。
Oncologist. 2008;13 Suppl 2:32-40. doi: 10.1634/theoncologist.13-S2-32.
7
SARC-CTOS imaging symposium: introduction to the problem from a clinical perspective.SARC-CTOS成像研讨会:从临床角度介绍该问题
Oncologist. 2008;13 Suppl 2:1-3. doi: 10.1634/theoncologist.13-S2-1.
8
Histologic response of dose-intense chemotherapy with preoperative hypofractionated radiotherapy for patients with high-risk soft tissue sarcomas.高风险软组织肉瘤患者术前大分割放疗联合剂量密集化疗的组织学反应
Cancer. 2008 Jun;112(11):2432-9. doi: 10.1002/cncr.23478.
9
Opportunities for improving the therapeutic ratio for patients with sarcoma.改善肉瘤患者治疗比率的机会。
Lancet Oncol. 2007 Jun;8(6):513-24. doi: 10.1016/S1470-2045(07)70169-9.
10
Evidence-based recommendations for local therapy for soft tissue sarcomas.软组织肉瘤局部治疗的循证医学推荐意见。
J Clin Oncol. 2007 Mar 10;25(8):1003-8. doi: 10.1200/JCO.2006.09.8525.

新辅助放疗后的完全病理缓解可预测软组织肉瘤患者的肿瘤学结局。

Complete pathologic response to neoadjuvant radiotherapy is predictive of oncological outcome in patients with soft tissue sarcoma.

机构信息

Division of Surgical Oncology, University of California Davis Medical Center, Sacramento, CA, USA.

出版信息

Anticancer Res. 2012 Sep;32(9):3911-5.

PMID:22993336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4153787/
Abstract

UNLABELLED

We sought to determine if complete pathological necrosis (pathCR) predicts favorable oncological outcome in soft tissue sarcoma (STS) patients receiving pre-operative radiation monotherapy (RT).

PATIENTS AND METHODS

We evaluated 30 patients with primary STS treated with neoadjuvant RT followed by definitive resection, from 2000 to 2010 at our institution. We defined ≥ 95% tumor necrosis as pathCR.

RESULTS

There were 22 STS of the extremities (73%), 7 of the retroperitoneum (23%), and 1 (4%) of the trunk. The median pathological percentage of tumor necrosis was 35% (range 5-100%) with three tumors (10%) demonstrating pathCR. With a median follow-up of 40 months, the 5-year local recurrence-free survival (LRFS), distant recurrence-free survival (DRFS), and overall survival (OS) for the entire cohort were 100%, 61% ± 11%, and 69% ± 11%, respectively. Among patients with pathCR, 3-year DRFS was 100% compared to 63±11% in patients without pathCR (p=0.28).

CONCLUSION

Following neoadjuvant RT for STS, pathCR is associated with a clinically but not statistically significant 37% improvement in 3-year DRFS.

摘要

未标记

我们试图确定软组织肉瘤(STS)患者接受术前放射单药治疗(RT)时,完全病理性坏死(pathCR)是否预测良好的肿瘤学结果。

患者和方法

我们评估了 2000 年至 2010 年在我院接受新辅助 RT 后行确定性切除的 30 例原发性 STS 患者。我们将≥95%的肿瘤坏死定义为 pathCR。

结果

有 22 例 STS 位于四肢(73%),7 例位于腹膜后(23%),1 例位于躯干(4%)。肿瘤坏死的中位数病理百分比为 35%(范围 5-100%),其中 3 例(10%)表现为 pathCR。中位随访 40 个月时,全队列的 5 年局部无复发生存率(LRFS)、远处无复发生存率(DRFS)和总生存率(OS)分别为 100%、61%±11%和 69%±11%。在 pathCR 患者中,3 年 DRFS 为 100%,而无 pathCR 患者为 63%±11%(p=0.28)。

结论

在 STS 接受新辅助 RT 后,pathCR 与 3 年 DRFS 临床显著但无统计学意义的 37%改善相关。