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拉帕替尼联合吉西他滨治疗晚期乳腺癌的I期药理试验

Phase I and pharmacological trial of lapatinib in combination with gemcitabine in patients with advanced breast cancer.

作者信息

van der Noll R, Smit W M, Wymenga A N M, Boss D S, Grob M, Huitema A D R, Rosing H, Tibben M M, Keessen M, Rehorst H, Beijnen J H, Schellens J H M

机构信息

Department of Clinical Pharmacology, The Netherlands Cancer Institute, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.

Department of Internal Medicine, Medisch Spectrum Twente, P.O. Box 50 000, 7500 KA, Enschede, The Netherlands.

出版信息

Invest New Drugs. 2015 Dec;33(6):1197-205. doi: 10.1007/s10637-015-0281-z. Epub 2015 Sep 11.

Abstract

BACKGROUND

Lapatinib has proven efficacy as monotherapy and in combination with capecitabine in patients with metastatic breast cancer (MBC) overexpressing HER2 and/or EGFR. Gemcitabine also has anti-tumor activity in MBC and a favourable toxicity profile. In this phase I study lapatinib and gemcitabine were combined.

METHODS

Female patients with advanced BC were given lapatinib once daily (QD) in 28-day cycles with gemcitabine administered on day 1, 8 and 15. Physical examinations, vital signs and blood sampling for hematology, clinical chemistry and pharmacokinetics (PK) and radiological assessments of disease were performed at regular intervals.

RESULTS

In total, 33 patients were included. Six dose-limiting toxicities were observed, mostly grade 3 increases in liver function tests. Most common toxicities were fatigue (73%), nausea (70%), diarrhea (58%), increases in ALAT and ASAT (55 and 52%, respectively) and rash (46%). The maximum tolerated dose was lapatinib 1250 mg QD with gemcitabine 1000 mg/m(2). Lapatinib and gemcitabine PK did not appear to be influenced by each other. Anti-tumor activity was observed with one patient (4%) showing complete response and six (23%) partial response.

CONCLUSION

Despite a slightly increased toxicity profile compared to their respective monotherapies, lapatinib and gemcitabine can be safely combined while showing signs of anti-tumor activity.

摘要

背景

拉帕替尼已被证明在过表达HER2和/或EGFR的转移性乳腺癌(MBC)患者中作为单一疗法以及与卡培他滨联合使用时具有疗效。吉西他滨在MBC中也具有抗肿瘤活性且毒性特征良好。在这项I期研究中,拉帕替尼与吉西他滨联合使用。

方法

晚期乳腺癌女性患者接受拉帕替尼每日一次(QD)给药,每28天为一个周期,吉西他滨在第1、8和15天给药。定期进行体格检查、生命体征监测以及血液学、临床化学和药代动力学(PK)血液采样和疾病的放射学评估。

结果

总共纳入了33例患者。观察到6例剂量限制性毒性,主要是肝功能检查中3级升高。最常见的毒性是疲劳(73%)、恶心(70%)、腹泻(58%)、丙氨酸转氨酶和天冬氨酸转氨酶升高(分别为55%和52%)以及皮疹(46%)。最大耐受剂量是拉帕替尼1250 mg QD联合吉西他滨1000 mg/m²。拉帕替尼和吉西他滨的药代动力学似乎不受彼此影响。观察到抗肿瘤活性,1例患者(4%)显示完全缓解,6例(23%)部分缓解。

结论

尽管与各自的单一疗法相比毒性略有增加,但拉帕替尼和吉西他滨可以安全联合使用,同时显示出抗肿瘤活性迹象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e56f/4648969/982449a73781/10637_2015_281_Fig1_HTML.jpg

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