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米托蒽醌/长春瑞滨方案的诱导化疗能否使可手术的局部区域性乳腺癌患者接受保乳治疗?法国北部肿瘤学组对105例患者的试验。法国北部肿瘤学组

Does induction chemotherapy with a mitoxantrone/vinorelbine regimen allow a breast-conservative treatment in patients with operable locoregional breast cancer? A French Northern Oncology Group trial in 105 patients. French Northern Oncology Group.

作者信息

Adenis A, Vanlemmens L, Fournier C, Hecquet B, Bonneterre J

机构信息

French Northern Oncology Group, Centre Oscar Lambert (Northern France Cancer Center), Lille, France.

出版信息

Breast Cancer Res Treat. 1996;40(2):161-9. doi: 10.1007/BF01806211.

Abstract

BACKGROUND

In recent years, induction chemotherapy has been tested by several investigators in the management of operable breast cancer.

PATIENTS AND METHODS

Our current study was aimed to evaluate, pragmatically, in patients (74 stage II and 30 stage III) whose treatment would have been mastectomy, the percentage of them in whom a conservative treatment can be performed if primarily treated with a mitoxantrone/vinorelbine regimen.

RESULTS

67/104 patients (64%; 95% CI: 55-74%) had a conservative treatment (lumpectomy: 54, radiation therapy: 12, radiation therapy then lumpectomy: 1) Neutropenia was the major dose-limiting side effect, with grade 3 or 4 neutropenia registered in 83% of patients and 53.3% of the 442 cycles. Overall, a grade 3 or 4 non hematologic side effect occurred in 19.8% of patients and in 9.1% of cycles. One toxic death was observed after 2 cycles in a patient with aplasia who developped septicemia. Seventy one per cent of the patients experienced nausea and vomiting but grade 3 were observed in only 12% of the patients. Other side effects, including stomatitis, asthenia, alopecia, and constipation, were generally mild and uncommon.

CONCLUSIONS

This mitoxantrone/vinorelbine regimen is an efficient induction treatment with only neutropenia as a noticeable side effect. It allows 64% of conservative treatment in patients whose treatment would have been mastectomy.

摘要

背景

近年来,几位研究者对诱导化疗在可手术乳腺癌治疗中的应用进行了测试。

患者与方法

我们当前的研究旨在实际评估,如果对原本计划行乳房切除术的患者(74例II期和30例III期)首先采用米托蒽醌/长春瑞滨方案进行治疗,其中能够接受保乳治疗的患者比例。

结果

104例患者中有67例(64%;95%置信区间:55 - 74%)接受了保乳治疗(乳房肿瘤切除术:54例,放射治疗:12例,先放射治疗后乳房肿瘤切除术:1例)。中性粒细胞减少是主要的剂量限制性副作用,83%的患者出现3级或4级中性粒细胞减少,442个周期中有53.3%出现该情况。总体而言,19.8%的患者和9.1%的周期出现3级或4级非血液学副作用。1例发育不全患者在2个周期后发生败血症,出现1例毒性死亡。71%的患者出现恶心和呕吐,但仅12%的患者出现3级症状。其他副作用,包括口腔炎、乏力、脱发和便秘,通常较轻且不常见。

结论

这种米托蒽醌/长春瑞滨方案是一种有效的诱导治疗方案,仅有中性粒细胞减少这一明显副作用。对于原本计划行乳房切除术的患者,它能使64%的患者接受保乳治疗。

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