Skinner K A, Silberman H, Florentine B, Lomis T J, Corso F, Spicer D, Formenti S C
Department of Surgery, Kenneth Norris Comprehensive Cancer Center, and the University of Southern California, Los Angeles 90033, USA.
Ann Surg Oncol. 2000 Mar;7(2):145-9. doi: 10.1007/s10434-000-0145-3.
Approximately 15% of breast cancer patients present with large tumors that involve the skin, the chest wall, or the regional lymph nodes. Multimodality therapy is required, to provide the best chance for long-term survival. We have developed a regimen of paclitaxel, with concomitant radiation, as a primary therapy in patients with locally advanced breast cancer.
Eligible patients had locally advanced breast cancer (stage IIB or III). After obtaining informed consent, patients received paclitaxel (30 mg/m2 during 1 hour) twice per week for 8 weeks and radiotherapy to 45 Gy (25 fractions, at 180 cGy/fraction, to the breast and regional nodes). Patients then underwent modified radical mastectomy followed by postoperative polychemotherapy.
Twenty-nine patients were enrolled. Of these, 28 were assessable for clinical response and toxicity, and 27 were assessable for pathological response. Objective clinical response was achieved in 89%. At the time of surgery, 33% had no or minimal microscopic residual disease. Chemoradiation-related acute toxicity was limited; however, surgical complications occurred in 41% of patients.
Preoperative paclitaxel with radiotherapy is well tolerated and provides significant pathological response, in up to 33% of patients with locally advanced breast cancer, but with a significant postoperative morbidity rate.
约15%的乳腺癌患者表现为肿瘤较大,累及皮肤、胸壁或区域淋巴结。需要采用多模式治疗,以提供最佳的长期生存机会。我们已制定了一种紫杉醇联合放疗的方案,作为局部晚期乳腺癌患者的主要治疗方法。
符合条件的患者患有局部晚期乳腺癌(IIB期或III期)。在获得知情同意后,患者每周接受两次紫杉醇(30mg/m²,持续1小时),共8周,并接受45Gy的放疗(25次分割,每次180cGy,照射乳房及区域淋巴结)。患者随后接受改良根治性乳房切除术,然后进行术后多药化疗。
共纳入29例患者。其中,28例可评估临床反应和毒性,27例可评估病理反应。客观临床反应率为89%。手术时发现,33%的患者无或仅有微小残留病灶。放化疗相关的急性毒性有限;然而,41%的患者出现手术并发症。
术前紫杉醇联合放疗耐受性良好,在高达33%的局部晚期乳腺癌患者中可产生显著的病理反应,但术后发病率较高。