1. Department of Medical Oncology B, Regina Elena National Cancer Institute, Via Elio Chianesi 53, 00144, Rome, Italy, Rome, Italy.
2. Medical Oncology Unit ASL Frosinone, Via Armando Fabi, 03100, Frosinone, Italy.
J Cancer. 2014 Apr 25;5(6):398-405. doi: 10.7150/jca.9132. eCollection 2014.
Chemotherapy regimens containing anthracyclines and taxanes represent the landmark of neoadjuvant systemic therapy of breast cancer. In advanced breast cancer patients liposomal anthracyclines (LA) have shown similar efficacy and less cardiac toxicity when compared to conventional anthracyclines. We performed this retrospective analysis in order to evaluate the efficacy and tolerability of neoadjuvant regimens including LA outside of clinical trials in routine clinical practice.
Fifty operable or locally advanced, HER2 negative, breast cancer patients were retrospectively identified in 5 Italian cancer centres. Nineteen patients had received 4 cycles of non-pegylated liposomal doxorubicin (NPLD) and cyclophosphamide, followed by 4 cycles of docetaxel, every 3 weeks. In 25 patients the reverse sequence was employed, and a third subgroup of 6 patients received 4 cycles of NPLD/cyclophosphamide every 3 weeks followed by 4 cycles of weekly carboplatin and paclitaxel.
We observed 10 pathological complete responses (pCR) (20.0%, 95%CI, 9% to 31%), and 35 (70%, 95%CI, 57.3% to 82.7%) partial responses (pPR), whereas no patients progressed onto therapy. In the small subset of triple negative tumors the pCR rate was 37.5%, and in tumors expressing ER and/or PgR it was 16.7%. A pCR rate of 26.5% was observed in tumors with high Ki-67, whereas in tumors with low Ki-67 only one (6.2%) pCR was observed (p=0.14). Treatments were well tolerated. The most common toxicities were myelosuppression and palmar-plantar erytrodysesthesia; 4 asymptomatic and transient LVEF decrease have been recorded, without any case of clinical cardiotoxicity.
NPLD-cyclophosphamide and taxanes sequential regimens were proven effective and well tolerated in breast cancer patients with contra-indication to conventional anthracyclines undergoing neoadjuvant chemotherapy, even outside of clinical trials in everyday clinical practice.
含蒽环类和紫杉类药物的化疗方案代表了乳腺癌新辅助全身治疗的里程碑。在晚期乳腺癌患者中,与传统蒽环类药物相比,脂质体蒽环类药物(LA)显示出相似的疗效和较少的心脏毒性。我们进行了这项回顾性分析,以评估在临床试验之外的常规临床实践中使用包含 LA 的新辅助方案的疗效和耐受性。
在意大利的 5 个癌症中心,我们回顾性地确定了 50 例可手术或局部晚期、HER2 阴性的乳腺癌患者。19 例患者接受了 4 个周期的非聚乙二醇化脂质体多柔比星(NPLD)和环磷酰胺,随后每 3 周接受 4 个周期的多西他赛。在 25 例患者中采用了相反的顺序,第 3 组 6 例患者每 3 周接受 4 个周期的 NPLD/环磷酰胺,随后接受 4 个周期的每周卡铂和紫杉醇。
我们观察到 10 例病理完全缓解(pCR)(20.0%,95%CI,9%至 31%)和 35 例(70%,95%CI,57.3%至 82.7%)部分缓解(pPR),而没有患者进展到治疗。在三阴性肿瘤的小亚组中,pCR 率为 37.5%,在表达 ER 和/或 PgR 的肿瘤中为 16.7%。在高 Ki-67 的肿瘤中,pCR 率为 26.5%,而在低 Ki-67 的肿瘤中,只有 1 例(6.2%)pCR(p=0.14)。治疗耐受性良好。最常见的毒性是骨髓抑制和掌跖红斑感觉异常;记录到 4 例无症状和短暂的左心室射血分数降低,无任何临床心脏毒性病例。
NPLD-环磷酰胺和紫杉烷序贯方案在新辅助化疗中对有使用传统蒽环类药物禁忌证的乳腺癌患者有效且耐受良好,即使在临床试验之外的日常临床实践中也是如此。