A phase I trial of docetaxel and pulse-dose 17-allylamino-17-demethoxygeldanamycin in adult patients with solid tumors.
A phase I trial of docetaxel and pulse-dose 17-allylamino-17-demethoxygeldanamycin in adult patients with solid tumors.
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DOI:
10.1007/s00280-011-1789-3
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发表时间:
2012-04
影响因子:
3
通讯作者:
Solit, David B.
中科院分区:
文献类型:
--
作者:
Iyer, Gopa;Morris, Michael J.;Rathkopf, Dana;Slovin, Susan F.;Steers, Macaulay;Larson, Steven M.;Schwartz, Lawrence H.;Curley, Tracy;DeLaCruz, Anthony;Ye, Qing;Heller, Glenn;Egorin, Merrill J.;Ivy, S. Percy;Rosen, Neal;Scher, Howard I.;Solit, David B.
To define maximum tolerated dose (MTD), clinical toxicities, and pharmacokinetics of 17-allylamino-17-demethoxygeldanamycin (17-AAG) when administered in combination with docetaxel once every 21 days in patients with advanced solid tumor malignancies. Docetaxel was administered over 1 h at doses of 55, 70, and 75 mg/m2. 17-AAG was administered over 1–2 h, following the completion of the docetaxel infusion, at escalating doses ranging from 80 to 650 mg/m2 in 12 patient cohorts. Serum was collected for pharmacokinetic and pharmacodynamic studies during cycle 1. Docetaxel, 17-AAG, and 17-AG levels were determined by high-performance liquid chromatography. Biologic effects of 17-AAG were monitored in peripheral blood mononuclear cells by immunoblot. Forty-nine patients received docetaxel and 17-AAG. The most common all-cause grade 3 and 4 toxicities were leukopenia, lymphopenia, and neutropenia. An MTD was not defined; however, three dose-limiting toxicities were observed, including 2 incidences of neutropenic fever and 1 of junctional bradycardia. Dose escalation was halted at docetaxel 75 mg/m2-17-AAG 650 mg/m2 due to delayed toxicities attributed to patient intolerance of the DMSO-based 17-AAG formulation. Of 46 evaluable patients, 1 patient with lung cancer experienced a partial response. Minor responses were observed in patients with lung, prostate, melanoma, and bladder cancers. A correlation between reduced docetaxel clearance and 17-AAG dose level was observed. The combination of docetaxel and 17-AAG was well tolerated in adult patients with solid tumors, although patient intolerance to the DMSO formulation precluded further dose escalation. The recommended phase II dose is docetaxel 70 mg/m2 and 17-AAG 500 mg/m2.
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影响因子:
8
作者:
Chandarlapaty, S.;Scaltriti, M.;Angelini, P.;Ye, Q.;Guzman, M.;Hudis, C. A.;Norton, L.;Solit, D. B.;Arribas, J.;Baselga, J.;Rosen, N.
通讯作者:
Rosen, N.
影响因子:
4.8
作者:
SEPPLORENZINO, L;MA, ZP;ROSEN, N
通讯作者:
ROSEN, N
影响因子:
45.3
作者:
Grem, JL;Morrison, G;Wilson, RH
通讯作者:
Wilson, RH
影响因子:
11.5
作者:
Ramanathan, RK;Trump, DL;Egorin, MJ
通讯作者:
Egorin, MJ
影响因子:
45.3
作者:
Sequist, Lecia V.;Gettinger, Scott;Natale, Ronald
通讯作者:
Natale, Ronald