首页> 外文期刊>Bone marrow transplantation >Cardiac sequelae of doxorubicin and paclitaxel as induction chemotherapy prior to high-dose chemotherapy and peripheral blood progenitor cell transplantation in women with high-risk primary or metastatic breast cancer.
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Cardiac sequelae of doxorubicin and paclitaxel as induction chemotherapy prior to high-dose chemotherapy and peripheral blood progenitor cell transplantation in women with high-risk primary or metastatic breast cancer.

机译:高危原发性或转移性乳腺癌妇女在大剂量化疗和外周血祖细胞移植之前先进行阿霉素和紫杉醇的心脏后遗症作为诱导化疗。

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Doxorubicin plus paclitaxel has been shown to be an active regimen for metastatic breast cancer and is now frequently used as adjuvant therapy for high-risk primary breast cancer. Initial studies reported a higher than expected rate of cardiac toxicity with this regimen. We studied 105 patients with either high-risk primary breast cancer or metastatic breast cancer who were treated with doxorubicin (60 mg/m2) and 3-h infusions of paclitaxel (175 mg/m2) cycled every 3 weeks. Patients received three cycles of chemotherapy for high-risk primary or four cycles for metastatic disease. Patients then proceeded to high-dose chemotherapy (HDC) (STAMP I cyclophosphamide, cisplatin and carmustine) and peripheral blood progenitor cell transplantation (PBPCT). Patients underwent radionuclide multi-gated angiograms (MUGA) before and following induction chemotherapy and following HDC. During induction chemotherapy 40 (38%) of the patients had a reduction in left ventricular ejection fraction (LVEF). Fourteen had a decrease of 20% or greater and two were mildly symptomatic from CHF. There was additional reduction in the LVEF after HDC with a median value for LVEF of 59% (range, 20-78%). During HDC 10 patients developed clinical signs of congestive heart failure (CHF). Five patients responded to diuretic therapy and did not require any additional treatment. Four patients responded to vasodilation and/or digoxin with improvement in cardiac function. A clinically significant decrease in cardiac function was found in a small number of patients after induction chemotherapy and HDC with PBPCT. The majority of the patients tolerated this regimen without problems. Although there was a decline in LVEF as measured by radionuclide MUGA this did not prevent the majority of patients from proceeding with HDC. Bone Marrow Transplantation (2000).
机译:阿霉素加紫杉醇已被证明是转移性乳腺癌的有效治疗方案,现在经常被用作高危原发性乳腺癌的辅助治疗。最初的研究报道,该方案的心脏毒性高于预期。我们研究了105名患有高危原发性乳腺癌或转移性乳腺癌的患者,这些患者接受阿霉素(60 mg / m2)和每3周一次的3小时紫杉醇(175 mg / m2)输注治疗。对于高危原发患者,患者接受了三个周期的化疗,对于转移性疾病,患者接受了四个周期。然后,患者进行了大剂量化疗(HDC)(STAMP I环磷酰胺,顺铂和卡莫司汀)和外周血祖细胞移植(PBPCT)。患者在诱导化疗之前和之后以及在HDC之后接受了放射性核素多选血管造影(MUGA)。在诱导化疗期间,有40名患者(38%)的左心室射血分数(LVEF)降低。 14人的CHF降低了20%或更大,其中2人有轻度症状。 HDC后LVEF进一步降低,LVEF中位数为59%(范围为20-78%)。在HDC期间,有10位患者出现了充血性心力衰竭(CHF)的临床体征。五例患者对利尿剂治疗有反应,不需要任何其他治疗。四名患者对血管舒张和/或地高辛的反应改善了心脏功能。在使用PBPCT进行诱导化疗和HDC后,在少数患者中发现了心脏功能的临床显着下降。大多数患者耐受该方案而没有问题。尽管通过放射性核素MUGA测得的LVEF下降,但这并不能阻止大多数患者进行HDC。骨髓移植(2000年)。

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