Carboplatin plus paclitaxel and sequential radiation followed by consolidation carboplatin and paclitaxel in patients with previously untreated locally advanced NSCLC - A Hoosier Oncology Group (HOG) phase II study
被引:5
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作者:
Bhatia, S
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机构:Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
Bhatia, S
Hanna, N
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机构:Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
Hanna, N
Ansari, R
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机构:Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
Ansari, R
Einhorn, L
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机构:Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
Einhorn, L
Sandler, A
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机构:Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
Sandler, A
机构:
[1] Indiana Univ, Dept Med, Indianapolis, IN 46202 USA
[2] Walther Canc Inst, Hoosier Oncol Grp, Indianapolis, IN 46208 USA
[3] No Indiana Canc Res Consortium, South Bend, IN 46601 USA
[4] Vanderbilt Univ, Med Ctr, Div Hematol Oncol, Vanderbilt Clin 1956, Nashville, TN 37232 USA
locally advanced NSCLC;
chemoradiation;
sequential plus consolidative carboplatin and taxol;
toxicity;
D O I:
10.1016/S0169-5002(02)00146-0
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Chemo,radiation is standard treatment for patients with unresectable locally advanced non-small cell lung cancer (NSCLC). However, local and distant relapse rates remain high. It has been postulated that the addition of consolidation chemotherapy might further decrease the systemic relapse rate. We performed this phase 11 study to evaluate the toxicities and activity of two cycles of paclitaxel and carboplatin administered prior to and following thoracic radiation in patients with locally advanced, inoperable NSCLC. From April to December 1997, 25 patients were entered on study. Twenty-three patients were eligible and received paclitaxel 225 mg/m(2) intravenously over 3 It followed by carboplatin at an AUC (6) on days I and 22. Radiation consisted of 60 Gy given over 6 weeks beginning on day 43. Patients with non-progressive disease received two additional cycles of consolidation carboplatin and paclitaxel. Four of 23 patients progressed during induction chemotherapy. There were seven PR's and I I had SD after induction chemotherapy. Following radiation, the response changed to I I PR, four SD, and three had progressive disease. Of the 15 patients eligible to receive consolidation chemotherapy, three were excluded due to a poor performance status. Twelve patients were treated with consolidation chemotherapy with further improvement in two patients (SD to PR, PR to CR). All 12 patients who received consolidation chemotherapy developed grade 3 or 4 neutropenia, including three patients with neutropenic fever. The overall response rate was 52.1%. The median survival, 1-, and 2-year survival was 10.5 months, 45, and 17%, respectively. In conclusion, consolidation chemotherapy was associated with significant hematologic toxicity without an obvious improvement in survival in comparison to other studies utilizing chemoradiation alone. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
机构:
Univ Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Smith, David C.
Mackler, Niklas J.
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Univ Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Mackler, Niklas J.
Dunn, Rodney L.
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Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Dunn, Rodney L.
Hussain, Maha
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机构:
Univ Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Hussain, Maha
Wood, David
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机构:
Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Wood, David
Lee, Cheryl T.
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Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Lee, Cheryl T.
Sanda, Martin
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机构:
Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Boston, MA USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Sanda, Martin
Vaishampayan, Ulka
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Wayne State Univ, Detroit, MI USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Vaishampayan, Ulka
Petrylak, Daniel P.
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机构:
Columbia Presbyterian Med Ctr, New York, NY 10032 USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Petrylak, Daniel P.
Quinn, David I.
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Univ So Calif, Dept Med, Div Canc Med & Blood Dis, Los Angeles, CA USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Quinn, David I.
Beekman, Kathleen
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机构:
Univ Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
Beekman, Kathleen
Montie, James E.
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机构:
Univ Michigan, Sch Med, Dept Urol, Ann Arbor, MI 48109 USA
Univ Michigan, Ctr Comprehens Canc, Ann Arbor, MI USAUniv Michigan, Sch Med, Div Hematol Oncol, Dept Internal Med, Ann Arbor, MI 48109 USA
机构:
Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Hiroshima Asa City Hosp, Dept Med Oncol, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Kitaguchi, S.
Kagawa, M.
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Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Kagawa, M.
Yamaguchi, K.
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Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Yamaguchi, K.
Watanabe, M.
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机构:
Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Watanabe, M.
Ogawa, T.
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机构:
Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Ogawa, T.
Furonaka, O.
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Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Furonaka, O.
Sugahara, F.
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Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan
Sugahara, F.
Egawa, H.
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Hiroshima Asa City Hosp, Dept Resp Med, Hiroshima, JapanHiroshima Asa City Hosp, Dept Resp Med, Hiroshima, Japan