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大剂量化疗及造血干细胞移植治疗炎性乳腺癌:病理反应与预后

High-dose chemotherapy and haematopoietic stem cell transplantation for inflammatory breast cancer: pathologic response and outcome.

作者信息

Viens P, Penault-Llorca F, Jacquemier J, Gravis G, Cowen D, Bertucci F, Houvenaeghel G, Blaise D, Maraninchi D

机构信息

Department of Medicine, Institut Paoli-Calmettes, Marseille, France.

出版信息

Bone Marrow Transplant. 1998 Feb;21(3):249-54. doi: 10.1038/sj.bmt.1701074.

DOI:10.1038/sj.bmt.1701074
PMID:9489647
Abstract

Inflammatory breast cancer still has a poor prognosis despite improvements related to the introduction of neoadjuvant chemotherapy. The purpose of this study was to evaluate pathologic response rate and outcome of patients receiving high-dose chemotherapy with haematopoietic stem cell support for IBC. Seventeen consecutive patients with IBC received an association of mitoxantrone (36 mg/m2), cyclophosphamide (120 mg/kg), melphalan (140 mg/m2), with stem cell transplantation (SCT) following four to five cycles of cyclophosphamide (1000 mg/m2), doxorubicin (75 mg/m2) and 5FU (500 mg/m2). Mastectomy was performed a median of 2 months (range 1.5-45) after high-dose chemotherapy and was followed by radiotherapy. Macroscopic and microscopic pathologic complete response rates were respectively 56 and 39%. With a median follow-up of 36 months (range 17-52) 10 patients remain alive free of disease and seven patients have relapsed. Two relapses occurred in the group of patients with pathologic CR and five in the group with residual tumour. These results show that high-dose chemotherapy (HDC) with alkylating agents followed by SCT allows a very high tumour eradication in inflammatory breast cancer, suggesting a possible global benefit in progression-free survival and survival which remains to be demonstrated prospectively.

摘要

尽管新辅助化疗的应用带来了一些改善,但炎性乳腺癌的预后仍然很差。本研究的目的是评估接受高剂量化疗联合造血干细胞支持治疗炎性乳腺癌患者的病理缓解率和预后情况。17例连续的炎性乳腺癌患者接受了米托蒽醌(36mg/m²)、环磷酰胺(120mg/kg)、美法仑(140mg/m²)联合治疗,并在接受四至五个周期的环磷酰胺(1000mg/m²)、阿霉素(75mg/m²)和5-氟尿嘧啶(500mg/m²)治疗后进行干细胞移植(SCT)。在高剂量化疗后中位2个月(范围1.5 - 45个月)进行乳房切除术,随后进行放疗。宏观和微观病理完全缓解率分别为56%和39%。中位随访36个月(范围17 - 52个月),10例患者无病存活,7例患者复发。病理完全缓解组有2例复发,残留肿瘤组有5例复发。这些结果表明,烷化剂联合高剂量化疗(HDC)后进行SCT可使炎性乳腺癌的肿瘤根除率非常高,提示在无进展生存期和总生存期方面可能有整体获益,这仍有待前瞻性研究证实。

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High-dose chemotherapy and haematopoietic stem cell transplantation for inflammatory breast cancer: pathologic response and outcome.大剂量化疗及造血干细胞移植治疗炎性乳腺癌:病理反应与预后
Bone Marrow Transplant. 1998 Feb;21(3):249-54. doi: 10.1038/sj.bmt.1701074.
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引用本文的文献

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Pathological complete response of adding targeted therapy to neoadjuvant chemotherapy for inflammatory breast cancer: A systematic review.新辅助化疗联合靶向治疗对炎性乳腺癌的病理完全缓解作用:系统评价。
PLoS One. 2021 Apr 16;16(4):e0250057. doi: 10.1371/journal.pone.0250057. eCollection 2021.
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Update on systemic treatment for newly diagnosed inflammatory breast cancer.炎性乳腺癌的新辅助治疗进展。
J Adv Res. 2020 Aug 29;29:1-12. doi: 10.1016/j.jare.2020.08.014. eCollection 2021 Mar.
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Long-Term Outcome of Inflammatory Breast Cancer Compared to Non-Inflammatory Breast Cancer in the Setting of High-Dose Chemotherapy with Autologous Hematopoietic Cell Transplantation.
与非炎性乳腺癌相比,炎性乳腺癌在高剂量化疗联合自体造血细胞移植情况下的长期预后。
J Cancer. 2017 Mar 25;8(6):1009-1017. doi: 10.7150/jca.16870. eCollection 2017.
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Prognostic impact of hormone receptor- and HER2-defined subtypes in inflammatory breast cancer treated with high-dose chemotherapy: a retrospective study.高剂量化疗治疗的炎性乳腺癌中激素受体和HER2定义的亚型的预后影响:一项回顾性研究
J Cancer. 2016 Oct 23;7(14):2077-2084. doi: 10.7150/jca.15797. eCollection 2016.
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Strategies to improve long-term outcome in stage IIIB inflammatory breast cancer: multimodality treatment including dose-intensive induction and high-dose chemotherapy.改善IIIB期炎性乳腺癌长期预后的策略:包括剂量密集诱导和大剂量化疗的多模式治疗。
Biol Blood Marrow Transplant. 2009 Aug;15(8):963-70. doi: 10.1016/j.bbmt.2009.04.018.
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Can sequential administration minimise the cost of high dose chemotherapy? An economic assessment in inflammatory breast cancer.序贯给药能否将高剂量化疗的成本降至最低?炎性乳腺癌的经济学评估。
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Dose-intensive chemotherapy for locally advanced breast cancer.局部晚期乳腺癌的剂量密集化疗。
Curr Oncol Rep. 1999 Sep;1(1):23-30. doi: 10.1007/s11912-999-0006-6.
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