Journal of Clinical Oncology, Vol 22, No 1 (January 1), 2004: pp. 45-52
© 2004 American Society of Clinical Oncology.
DOI: 10.1200/JCO.2004.05.039
Phase I Trial of Combined-Modality Therapy for Localized Esophageal Cancer: Escalating Doses of Continuous-Infusion Paclitaxel With Cisplatin and Concurrent Radiation Therapy
Baruch Brenner,
David H. Ilson,
Bruce D. Minsky,
Manjit S. Bains,
William Tong,
Mithat Gonen,
David P. Kelsen
From the Gastrointestinal Oncology Service, Department of Medicine, the Department of Radiation Oncology, the Thoracic Service, Department of Surgery, and the Department of Epidemiology & Biostatistics, Memorial Sloan-Kettering Cancer Center, and the Weill School of Medicine, Cornell University, New York, NY
Address reprint requests to David P. Kelsen, MD, the Gastrointestinal Oncology Service, Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021; e-mail: kelsend{at}mskcc.org
PURPOSE: To define the maximum-tolerated dose (MTD) of paclitaxel when given as a weekly 96-hour infusion with cisplatin and radiotherapy for patients with esophageal cancer.
PATIENTS AND METHODS: Thirty-four patients with locally advanced esophageal cancer and three patients with local recurrence or positive resection margins were treated. Weekly paclitaxel doses of 10, 20, 30, 40, 60, and 80 mg/m2, given as a continuous 96-hour infusion, were administered with weekly cisplatin, 30 mg/m2 on day 1, weeks 1 to 6, and concurrent radiation (50.4 Gy). Plasma paclitaxel steady-state levels were measured.
RESULTS: Dose-limiting toxicity, defined as a treatment break longer than 2 weeks for toxicity, occurred in one patient in the 80-mg/m2/wk dose level. Major causes for any (including 2 weeks) treatment breaks were mediport complications and neutropenic fever, which occurred mostly at that dose level. At a paclitaxel dose of 60 mg/m2/wk, myelosuppression, mostly neutropenia, was relatively mild and transient; stomatitis, esophagitis, diarrhea. and peripheral neuropathy were uncommon and usually of grade 2 or less. Therefore, the MTD was established at 60 mg/m2/wk. The mean steady-state concentration of paclitaxel at the MTD was 17.2 nmol/L. Complete (R0) resection was possible in 16 (73%) of 22 patients who underwent subsequent surgery, and the pathologic complete response rate was 24%.
CONCLUSION: Weekly, 96-hour infusion of paclitaxel 60 mg/m2/wk, given with concurrent cisplatin and radiotherapy, is a safe and tolerable regimen for patients with localized esophageal cancer. Preliminary efficacy data are encouraging. This regimen is the basis of ongoing Radiation Therapy Oncology Group phase II randomized trials in esophageal and gastric cancers.
Supported in part by grant no. U01 CA69913 from the National Cancer Institute, Bethesda, MD.
Authors' disclosures of potential conflicts of interest are found at the end of this article.

CiteULike Complore Connotea Del.icio.us Digg Facebook Reddit Technorati Twitter What's this?
This article has been cited by other articles:

|
 |

|
 |
 
D.G. Power and D.H. Ilson
Review: Integration of targeted agents in the neo-adjuvant treatment of gastro-esophageal cancers
Therapeutic Advances in Medical Oncology,
November 1, 2009;
1(3):
145 - 165.
[Abstract]
[PDF]
|
 |
|

|
 |

|
 |
 
G. K. Schwartz, K. Winter, B. D. Minsky, C. Crane, P. J. Thomson, P. Anne, H. Gross, C. Willett, and D. Kelsen
Randomized Phase II Trial Evaluating Two Paclitaxel and Cisplatin-Containing Chemoradiation Regimens As Adjuvant Therapy in Resected Gastric Cancer (RTOG-0114)
J. Clin. Oncol.,
April 20, 2009;
27(12):
1956 - 1962.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
J. A. Ajani, K. Winter, R. Komaki, D. P. Kelsen, B. D. Minsky, Z. Liao, J. Bradley, M. Fromm, D. Hornback, and C. G. Willett
Phase II Randomized Trial of Two Nonoperative Regimens of Induction Chemotherapy Followed by Chemoradiation in Patients With Localized Carcinoma of the Esophagus: RTOG 0113
J. Clin. Oncol.,
October 1, 2008;
26(28):
4551 - 4556.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. H. Ilson
Combined Modality Therapy for Gastric, Esophageal, and Gastroesophageal Junction Cancers
ASCO Educational Book,
January 1, 2008;
2008(1):
177 - 182.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
D. Ilson, R. Wadleigh, L. Leichman, and D. Kelsen
Paclitaxel given by a weekly 1-h infusion in advanced esophageal cancer
Ann. Onc.,
May 1, 2007;
18(5):
898 - 902.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
W. P. Tew, D. P. Kelsen, and D. H. Ilson
Targeted Therapies for Esophageal Cancer
Oncologist,
September 1, 2005;
10(8):
590 - 601.
[Abstract]
[Full Text]
[PDF]
|
 |
|

|
 |

|
 |
 
F. Pasini, G. de Manzoni, C. Pedrazzani, A. Grandinetti, E. Durante, M. Gabbani, A. Tomezzoli, C. Griso, A. Guglielmi, G. Pelosi, et al.
High pathological response rate in locally advanced esophageal cancer after neoadjuvant combined modality therapy: dose finding of a weekly chemotherapy schedule with protracted venous infusion of 5-fluorouracil and dose escalation of cisplatin, docetaxel and concurrent radiotherapy
Ann. Onc.,
July 1, 2005;
16(7):
1133 - 1139.
[Abstract]
[Full Text]
[PDF]
|
 |
|
|