de Graaf H, Willemse P H, de Vries E G, Sleijfer D T, Mulder P O, van der Graaf W T, Smit Sibinga C T, van der Ploeg E, Dolsma W V, Mulder N H
Department of Internal Medicine, University Hospital Groningen, The Netherlands.
Eur J Cancer. 1994;30A(2):150-3. doi: 10.1016/0959-8049(94)90076-0.
Patients with breast cancer and a high number of involved axillary lymph nodes have a poor prognosis, despite adjuvant chemotherapy. The 5-year disease-free survival (DFS) in this group amounts to 30-40% and the 10-year DFS is only 15-20%. Therefore, new treatment modalities are being sought for this group of patients. The aim of the present study was the evaluation of the efficacy of high-dose chemotherapy combined with autologous bone marrow support. 24 patients with a primary breast cancer with more than five involved axillary lymph nodes received, after surgery, six courses of induction chemotherapy followed by ablative chemotherapy and reinfusion of autologous bone marrow. All patients were premenopausal or less than 2 years postmenopausal. Induction chemotherapy consisted of methotrexate (MTX) 1.5 g/m2 intravenous (i.v.) and 5-fluorouracil (5-FU) 1.5 g/m2 i.v. on day 1, prednisone 40 mg/m2 orally on days 2-14, doxorubicin 50 mg/m2 i.v. and vincristine 1 mg/m2 i.v. on day 14. Courses were repeated six times every 4 weeks. 10 patients received cyclophosphamide 7 g/m2 i.v. and etoposide 1.5 g/m2 i.v. as intensive regimen, in 14 patients this comprised mitoxantrone 50 mg/m2 i.v. and thiotepa 800 mg/m2 i.v. Reinfusion of autologous marrow followed on day 7. Finally, patients received locoregional radiotherapy for extranodal disease and tamoxifen 40 mg daily orally over a period of 2 years. The median age of patients was 42 years, range 29-54. The median number of involved nodes was 10. During induction therapy, fever requiring i.v. antibiotics occurred in 4% of 144 courses, 14% of patients suffered from mucositis WHO grade 2-3, and the other patients had mucositis grade 1. During the ablative chemotherapy, 1 patient died, 6 developed septicaemia, 5 showed mucositis grade 3-4 and the other patients had mucositis grade 1 or 2. In the follow-up, 1 patient died from acute cardiac failure. Reversible radiation-induced pneumonitis occurred in 7 out of 14 irradiated patients; symptoms started directly following radiotherapy and lasted for several weeks, but disappeared in due course. During follow-up, 2 patients with six and > 10 positive nodes, respectively, have relapsed after 18 and 36 months, both in the cyclophosphamide/etoposide regimen. Median observation is 3 years, disease-free survival at 5 years is predicted to be 84%. Intensive treatment in these patients with high numbers of involved axillary lymph nodes is a toxic regimen, but may improve the chance of surviving free of disease.
尽管接受了辅助化疗,但患有乳腺癌且腋窝淋巴结受累数量较多的患者预后较差。该组患者的5年无病生存率(DFS)为30%-40%,10年DFS仅为15%-20%。因此,正在为该组患者寻找新的治疗方法。本研究的目的是评估大剂量化疗联合自体骨髓支持的疗效。24例原发性乳腺癌且腋窝淋巴结受累超过5个的患者在手术后接受了6个疗程的诱导化疗,随后进行清髓性化疗和自体骨髓回输。所有患者均为绝经前或绝经后不到2年。诱导化疗包括第1天静脉注射甲氨蝶呤(MTX)1.5 g/m²和5-氟尿嘧啶(5-FU)1.5 g/m²,第2-14天口服泼尼松40 mg/m²,第14天静脉注射多柔比星50 mg/m²和长春新碱1 mg/m²。疗程每4周重复6次。10例患者接受环磷酰胺7 g/m²静脉注射和依托泊苷1.5 g/m²静脉注射作为强化方案,14例患者的方案包括米托蒽醌50 mg/m²静脉注射和塞替派800 mg/m²静脉注射。自体骨髓在第7天回输。最后,患者接受了针对结外病变的局部放疗,并在2年期间每天口服40 mg他莫昔芬。患者的中位年龄为42岁,范围为29-54岁。受累淋巴结的中位数为10个。在诱导治疗期间,144个疗程中有4%出现需要静脉注射抗生素的发热,14%的患者发生WHO 2-3级粘膜炎,其他患者为1级粘膜炎。在清髓性化疗期间,1例患者死亡,6例发生败血症,5例出现3-4级粘膜炎,其他患者为1或2级粘膜炎。在随访中,1例患者死于急性心力衰竭。14例接受放疗的患者中有7例发生可逆性放射性肺炎;症状在放疗后立即出现,持续数周,但最终消失。在随访期间,分别有6个和>10个阳性淋巴结的2例患者在18个月和36个月后复发,均在环磷酰胺/依托泊苷方案组。中位观察时间为3年,预计5年无病生存率为84%。对这些腋窝淋巴结受累数量较多的患者进行强化治疗是一种毒性方案,但可能提高无病生存的机会。