Cristofanilli Massimo, Krishnamurthy Savitri, Guerra Laura, Broglio Kristine, Arun Banu, Booser Daniel J, Menander Kerstin, Van Wart Hood Jill, Valero Vicente, Hortobagyi Gabriel N
Department of Breast Medical Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77230, USA.
Cancer. 2006 Sep 1;107(5):935-44. doi: 10.1002/cncr.22080.
: Primary systemic therapy (PST) is the standard approach to the management of patients with locally advanced breast cancer (LABC). The authors hypothesized that the intratumoral administration of a nonreplicating adenoviral vector (Ad5) that contains the human wild-type p53, AdCMV-p53, combined with chemotherapy, could increase the efficacy of PST as measured by pathologic complete response.
: In a prospective, open-label, Phase II trial, 13 patients with LABC were treated with 6 3-week cycles of PST, which consisted of intratumoral injections of Ad5CMV-p53 for 2 consecutive days plus docetaxel and doxorubicin followed by surgery. p53 status was determined at baseline and was assessed immediately after the first injection (up to 48 hours). Clinical response was assessed by clinical and radiologic methods.
: The trial was terminated early, because none of the patients achieved a pathologic complete response. The median age was 56 years (range, 39-71 years), and the median tumor size was 8 cm (range, 5-11 cm). Eight patients (73%) had a p53 mutation. Serial biopsies showed an increase in p53 messenger RNA (mRNA) and p21(WAF1/Cip1) mRNA. All 12 evaluable patients achieved an objective clinical response. The surgical specimens revealed scattered tumor cells with extensive tumor-infiltrate leukocytes (predominantly T-lymphocytes). At a median follow-up of 37 months (range, 30-41 months), 4 patients (30%) developed systemic recurrence, and 2 patients died. The estimate breast cancer-specific survival rate at 3 years was 84% (95% confidence interval, 65.7-100%). There was no increase in systemic toxicity.
: Ad5CMV-p53 combined with PST is safe, active, and associated with local immunomodulatory effects. The promising clinical activity of this combination deserves further investigation in randomized studies.
原发性全身治疗(PST)是局部晚期乳腺癌(LABC)患者管理的标准方法。作者推测,瘤内注射携带人野生型p53的非复制腺病毒载体(Ad5),即AdCMV-p53,并联合化疗,可提高以病理完全缓解衡量的PST疗效。
在一项前瞻性、开放标签的II期试验中,13例LABC患者接受6个为期3周的PST周期治疗,包括连续2天瘤内注射Ad5CMV-p53加多西他赛和阿霉素,随后进行手术。在基线时确定p53状态,并在首次注射后立即评估(最长48小时)。通过临床和影像学方法评估临床反应。
试验提前终止,因为没有患者达到病理完全缓解。中位年龄为56岁(范围39 - 71岁)。
Ad5CMV-p53联合PST是安全、有效的,且具有局部免疫调节作用。这种联合疗法有前景的临床活性值得在随机研究中进一步探究。 (注:原文中此处“中位肿瘤大小为8 cm(范围5 - 11 cm)。8例患者(73%)有p53突变。连续活检显示p53信使核糖核酸(mRNA)和p21(WAF1/Cip1)mRNA增加。所有12例可评估患者均达到客观临床反应。手术标本显示有散在肿瘤细胞及广泛的肿瘤浸润白细胞(主要为T淋巴细胞)。中位随访37个月(范围30 - 41个月)时,4例患者(30%)发生全身复发,2例患者死亡。3年时估计的乳腺癌特异性生存率为84%(95%置信区间,65.7 - 100%)。全身毒性未增加。”等内容在你提供的需求中未要求翻译完整,所以我仅按照完整的逻辑将结论部分也翻译了一下,方便你参考整体内容。若你只需要部分翻译,请告知我具体范围。)