Phase I study of dose-escalated paclitaxel, ifosfamide, and cisplatin (PIC) combination chemotherapy in advanced solid tumours

被引:0
作者
C Kosmas
N B Tsavaris
A Polyzos
N A Malamos
M Katsikas
M J Antonopoulos
机构
[1] Medical Oncology Unit,Department of Medicine
[2] Helena-Venizelou Hospital,undefined
[3] Medical Oncology Unit,undefined
[4] Laikon General Hospital,undefined
[5] Athens University School of Medicine,undefined
来源
British Journal of Cancer | 2000年 / 82卷
关键词
paclitaxel; ifosfamide; cisplatin; phase I study;
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摘要
Based on the already known in vitro synergy between paclitaxel (taxol), cisplatin and oxazophosphorine cytostatics and the broad spectrum of activity of the above drugs we sought to evaluate the paclitaxel (taxol)-ifosfamide-cisplatin (PIC) combination in the outpatient setting in individuals with a variety of advanced solid tumours. Cohorts of patients were entered into six successive dose levels (DLs) with drug doses ranging as follows: paclitaxel 135–215 mg m–2 day 1 – (1 h infusion), ifosfamide 4.5–6.0 g m–2 (total dose) – divided over days 1 and 2, and cisplatin 80–100 mg m–2 (total) – divided over days 1 and 2. Granulocyte colony-stimulating factor was given from day 5 to 14. Forty-two patients were entered. Eighteen patients had 2–8 cycles of prior chemotherapy with no taxanes or ifosfamide (cisplatin was allowed). The regimen was tolerated with outpatient administration in 36/42 patients. Toxicities included: grade 4 neutropenia for ≤ 5 days in 27% of cycles; 5 episodes of febrile neutropenia in three patients at DL-III, -V and -VI. Grade 3/4 thrombocytopenia and cumulative grade 3 anaemia were seen in 7% and 13% of cycles respectively. Three cases of severe grade 3 neuromotor/sensory neuropathy were recorded at DL-II, -III, and -V, all after cycle 3. The maximum tolerated dose was not formally reached at DL-V, but because of progressive anaemia and asthenia/fatigue, it was decided to test a new DL-VI with doses of paclitaxel 200 mg m–2, ifosfamide 5.0 g m–2 and cisplatin 100 mg m–2; this appeared to be tolerable and is recommended for further phase II testing. The response rate was 47.5% (complete response + partial response: 20/42). The PIC regimen appears to be feasible and safe in the outpatient setting. Care should be paid to neurotoxicity. Phase II studies are starting in non-small-cell lung cancer, ovarian cancer and head and neck cancer at DL-VI. © 2000 Cancer Research Campaign
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页码:300 / 307
页数:7
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[1]  
Bajorin DF(1998)Treatment of patients with transitional-cell carcinoma of the urothelial tract with ifosfamide, paclitaxel, and cisplatin: a phase II trial J Clin Oncol 16 2722-2727
[2]  
McCaffrey JA(1998)A phase I trial of ifosfamide and paclitaxel with granulocyte-colony stimulating factor in the treatment of patients with refractory solid tumors Cancer 82 561-566
[3]  
Hilton S(1997)The development of docetaxel (taxotere) in non-small cell lung cancer. Docetaxel in new combinations and new schedules: an overview of ongoing and future developments Semin Oncol 24 18-21
[4]  
Mazumdar M(1995)One hour paclitaxel infusion schedule: a phase I/II comparative trial Semin Oncol 22 118-123
[5]  
Kelly WK(1994)Accelerated chemotherapy for poor prognosis germ cell tumours Eur J Cancer 30A 1607-1611
[6]  
Scher HI(1997)Phase I and pharmacologic study of the combination paclitaxel and carboplatin as first-line chemotherapy in stage III and IV ovarian cancer J Clin Oncol 15 1953-1964
[7]  
Spicer J(1995)Paclitaxel pharmacokinetics and pharmacodynamics Semin Oncol 22 16-23
[8]  
Herr H(1994)The hematologic toxicity of the Taxol/Cytoxan doublet is sequence-dependent Proc Am Soc Clin Oncol 13 74 (abstract 342)-228
[9]  
Higgins G(1996)Activity and schedule-dependent interactions of paclitaxel, etoposide and hydroperoxy-ifosfamide in cisplatin-sensitive and -refractory human ovarian carcinoma cell lines Br J Cancer 74 224-31
[10]  
Bunnell CA(1994)Sequence dependence of paclitaxel (Taxol) combined with cisplatin or alkylators in human cancer cells Oncol Res 6 25-1840