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局部晚期乳腺癌术前每周两次紫杉醇联合同步放疗,随后手术及术后基于阿霉素的化疗:一项I/II期试验

Preoperative twice-weekly paclitaxel with concurrent radiation therapy followed by surgery and postoperative doxorubicin-based chemotherapy in locally advanced breast cancer: a phase I/II trial.

作者信息

Formenti Silvia C, Volm Matthew, Skinner Kristin A, Spicer Darcy, Cohen Deidre, Perez Edith, Bettini Anna C, Groshen Susan, Gee Conway, Florentine Barbara, Press Michael, Danenberg Peter, Muggia Franco

机构信息

Kaplan Comprehensive Cancer Center, New York University School of Medicine, New York, NY, USA.

出版信息

J Clin Oncol. 2003 Mar 1;21(5):864-70. doi: 10.1200/JCO.2003.06.132.

Abstract

PURPOSE

Preoperative chemotherapy is the conventional primary treatment in locally advanced breast cancer (LABC). We investigated the safety and efficacy of primary twice-weekly paclitaxel and concurrent radiation (RT) before modified radical mastectomy followed by adjuvant doxorubicin-based chemotherapy.

PATIENTS AND METHODS

Stage IIB (T3N0) to III LABC patients were eligible. Primary chemoradiation consisted of paclitaxel, 30 mg/m(2) delivered intravenously for 1 hour twice weekly for a total of 8 to 10 weeks, and concurrent RT (45 Gy at 1.8 Gy/fraction). Modified radical mastectomy was performed at least 2 weeks after completion of chemoradiation or on recovery of skin toxicity. Postoperatively, patients who responded to paclitaxel and RT received four cycles of doxorubicin/paclitaxel, whereas patients who did not respond received doxorubicin/cytoxan.

RESULTS

Forty-four patients were accrued. Toxicity from paclitaxel/RT included grade 3 skin desquamation (7%), hypersensitivity (2%), and stomatitis (2%). Postsurgery complications occurred in six patients (14%). The only grade 4 toxicity of postmastectomy chemotherapy was hematologic (10%). Grade 3 toxicities were leukopenia (24%), infection (22%), peripheral neuropathy (17%), arthralgia and pain (17%), stomatitis (12%), fatigue (10%), esophagitis (5%), and nausea (2%). Overall clinical response rate to preoperative paclitaxel and RT was 91%. Thirty-four percent of patients achieved a pathologic response in the mastectomy specimen: 16% pathologic complete responses (clearance of invasive cancer in the breast and axillary contents) and 18% pathologic partial responses (< 10 residual microscopic foci of invasive breast cancer).

CONCLUSION

Twice-weekly paclitaxel with concurrent RT is a feasible and effective primary treatment for LABC. Future studies should compare primary chemoradiation to chemotherapy in LABC.

摘要

目的

术前化疗是局部晚期乳腺癌(LABC)的传统主要治疗方法。我们研究了在改良根治性乳房切除术之前,每周两次使用紫杉醇联合同步放疗(RT),随后进行基于阿霉素的辅助化疗的安全性和有效性。

患者与方法

IIB期(T3N0)至III期LABC患者符合条件。主要放化疗包括紫杉醇,静脉注射30mg/m²,每周两次,每次1小时,共8至10周,同步放疗(45Gy,每次1.8Gy)。在放化疗完成后至少2周或皮肤毒性恢复后进行改良根治性乳房切除术。术后,对紫杉醇和放疗有反应的患者接受四个周期的阿霉素/紫杉醇治疗,而无反应的患者接受阿霉素/环磷酰胺治疗。

结果

共纳入44例患者。紫杉醇/放疗的毒性包括3级皮肤脱屑(7%)、超敏反应(2%)和口腔炎(2%)。6例患者(14%)发生术后并发症。乳房切除术后化疗唯一的4级毒性是血液学毒性(10%)。3级毒性包括白细胞减少(24%)、感染(22%)、周围神经病变(17%)、关节痛和疼痛(17%)、口腔炎(12%)、疲劳(10%)、食管炎(5%)和恶心(2%)。术前紫杉醇和放疗的总体临床缓解率为91%。34%的患者在乳房切除标本中达到病理反应:16%为病理完全缓解(乳腺和腋窝内容物中浸润性癌清除),18%为病理部分缓解(浸润性乳腺癌残留微观病灶<10个)。

结论

每周两次紫杉醇联合同步放疗是LABC的一种可行且有效的主要治疗方法。未来的研究应比较LABC中主要放化疗与化疗的效果。

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