Download Single-Agent Paclitaxel in Advanced Non–Small

Single-Agent Paclitaxel in Advanced Non–Small-Cell Lung Cance
Published on Cancer Network (http://www.cancernetwork.com)
Single-Agent Paclitaxel in Advanced Non–Small-Cell Lung
Cancer
Review Article [1] | September 01, 1999 | Lung Cancer [2]
By Ulrich Gatzemeier, MD [3]
Despite the availability of combination chemotherapy, response rates are poor in patients with
non–small-cell lung cancer. Recently, phase II trials have been undertaken with single-agent
paclitaxel (Taxol). Good results have
Introduction
reatment results in patients with advanced non–small-cell lung cancer are still unsatisfactory. In
single-institution trials, combination chemotherapy regimens have produced responses in the 20% to
43% range; however, the impact on median survival time is minimal.[1] To improve these results,
new cytotoxic agents are needed.
Paclitaxel (Taxol) is one of the new antineoplastic agents with a unique mechanism of action and a
wide spectrum of clinical activity. Significant antitumor efficacy has been reported in patients with
ovarian and breast cancer. Paclitaxel has also shown activity in patients with lung cancer, including
non–small-cell lung cancer and small-cell lung cancer. Single-agent paclitaxel chemotherapy has
been investigated in a number of trials in advanced non–small-cell lung cancer using different
dosages and schedules (Table 1).
T
Phase II Studies of Single-Agent Paclitaxel
Long Infusion (24 h)
Two trials of single-agent paclitaxel were conducted in previously untreated patients with advanced
non–small-cell lung cancer.[2,3] In one trial conducted by the Eastern Cooperative Oncology Group
(ECOG), 250 mg/m² of paclitaxel was administered by 24-hour infusion. In a second trial conducted
at M. D. Anderson Cancer Center, 200 mg/m² of paclitaxel was administered by 24-hour infusion.
The overall response rate in the Eastern Cooperative Oncology Group trial was 21%, with a 1-year
survival rate of 42%. The second trial conducted at M. D. Anderson confirmed these data, with an
overall response rate of 24% and a 1-year survival rate of 38%. The results of these two trials
generated a lot of interest and several other investigators initiated trials to further explore the
activity of paclitaxel in the treatment of patients with advanced non–small-cell lung cancer.
A later trial using a 24-hour infusion of paclitaxel was published by Tan.[4] In this trial, 11 patients
were pretreated with cisplatin-containing regimens and the response rate was 16%.
The median survival time in these trials ranges from 24 to 40 weeks with a 1-year survival rate of
approximately 40%.
Short Infusion (3 h)
It has been shown that the administration of paclitaxel by a 3-hour infusion significantly reduces
hematologic toxicity, in particular, neutropenia. Consequently, four other phase II trials using a
3-hour infusion schedule have been published by Gatzemeier,[5] Rosell,[6] Furuse,[7] and
Millward.[8] The paclitaxel dosages ranged from 175 mg/m² up to 225 mg/m². The response rates
were between 24% and 32%. An Australian trial reported a 10% response rate. However, in this trial
57% of the patients had received prior radiotherapy, but more importantly, the investigators had
used a different formulation of paclitaxel.[8]
Again the median survival time published to date was in the range of 30 to 40 weeks. The
1-year-survival ranged from 22% to 47%.
Short Infusion (1 h)
In one trial published by Hainsworth,[9] between 135 mg/m² and 200 mg/m² of paclitaxel was
administered as a 1-hour infusion. The response rate on this trial was 25%, with a median survival
time of 33 weeks, and the 1-year-survival probability was 33%.
Page 1 of 3
Single-Agent Paclitaxel in Advanced Non–Small-Cell Lung Cance
Published on Cancer Network (http://www.cancernetwork.com)
Weekly Administration
In a study by Akerley,[10] a weekly schedule of 100 mg/m² and up to 175 mg/m² of paclitaxel as a
3-hour infusion yielded a response rate of 38%. The study included 21 patients–all with stage IV
disease. Survival data are not available to date.
Toxicity
Looking at the toxicity data suggested that the frequency and intensity of the myelosuppressive side
effects are correlated with the infusion length of the paclitaxel administration (Table 2). Episodes of
febrile neutropenia have been reported only with the use of the 24-hour schedule. The incidence of
grade IV granulocytopenia was found to be significantly less with the 3- or 1-hour infusion schedules
compared with the 24-hour schedule. Excluding the Japanese trial, all 3- and 1-hour infusion trials
showed a very low level of grade IV neutropenia. Thrombocytopenia (Table 3) was rarely reported
with almost no incidence of World Health Organization (WHO) grade II, III, or IV toxicity. The infusion
length has no impact on the frequence or severity of thrombocytopenia. Neurotoxicity is usually mild
to moderate. It is noteworthy that grade IV neurotoxicity has not been reported in any trials (Table 4
).
No major differences were demonstrated between the different trials based on schedule and infusion
length. The different dosages and schedules did not lead to differences in the incidence and severity
of nausea and vomiting (Table 5). Overall, very few patients experienced WHO grades III and IV
gastrointestinal toxicity. Myalgia and arthralgia (Table 6) was usually mild to moderate and was
reported in 40% to 50% of the patients. Very few patients experienced WHO grades III and IV
myalgia and arthralgia, again without any difference between the schedules.
Discussion
Paclitaxel is one of the most active agents in advanced non–small-cell lung cancer, with response
rates of approximately 22%. The data are very consistent and are based on about 400 patients in
phase II trials. In comparison to older drugs,[1] the response rate is in the upper range of the
effective drugs. Myelosuppression is the major dose-limiting toxicity, especially when paclitaxel is
used as a 24-hour schedule. The incidence of grade IV granulocytopenia was found to be significantly
less with the 3- and 1-hour infusion schedules compared with the 24-hour schedule.
The 40% 1-year survival rate of single-agent paclitaxel is double that achieved by the combination of
cisplatin and etoposide, which has shown a 1-year survival rate of approximately 20% in several
previous studies. Paclitaxel as a single agent is an active drug in non–small-cell lung cancer.
References:
1. Ettinger DS: Overview of paclitaxel (Taxol) in advanced lung cancer. Semin Oncol 20(suppl
3):46-49, 1993.
2. Murphy WK, Winn RJ, Fossella FV, et al: Phase II study of Taxol in patients with non–small-cell lung
cancer (NSCLC). J Natl Cancer Inst 85:384-388, 1993.
3. Chang AY, Kim K, Glick J, et al: Phase II-study of Taxol, merbarone and piroxantrone in stage IV
non–small-cell lung cancer. The Eastern Co-operation Oncology Group results. J Natl Cancer Inst
85:388-394, 1993.
4. Tan V, Herrera C, Einzig AL, et al: Taxol is active as a 3/h or 24/h infusion in non–small-cell lung
cancer (NSCLC)(abstract 1122). Proc Am Soc Clin Oncol 14:366A, 1995.
5. Gatzemeier UR, Neuhauss I, Schlüter, et al: Single-agent paclitaxel as a 3-hour infusion. Semin
Oncol 23(suppl 16):94-97, 1996.
6. Rosell R, Gonzalez-Larriba JL, Alberola V, et al: Three-hour infusion of single-agent paclitaxel in the
treatment of non–small-cell lung cancer. Proc 5th Int Congress on Anti-cancer chemotherapy, Paris
1995.
7. Furuse K, Naka N, Ariyoshi Y, et al: Phase II-Study of 3-hour infusion of paclitaxel in patients with
previously untreated non-small-cell lung cancer (abstract 1072). Eur J Can 31A(suppl 5):224, 1995.
Page 2 of 3
Single-Agent Paclitaxel in Advanced Non–Small-Cell Lung Cance
Published on Cancer Network (http://www.cancernetwork.com)
8. Millward MJ, Bishop JF, Friedlander M, et al: Phase II trial of a 3-hour infusion of paclitaxel in
previously untreated patients with advanced non-small-cell lung cancer. J Clin Oncol 14:142-148,
1996.
9. Hainsworth JD, Thompson DS, Greco FA: Paclitaxel by 1-hour infusion. An active drug in metastatic
non–small-cell lung cancer. J Clin Oncol 13:1609-1614, 1995.
10. Akerley WL, Choy H, Rege V, et al: A Phase-I Trial of weekly paclitaxel administered as a 3-hour
infusion for metastatic non–small-cell lung cancer (abstract 1170). Proc Am Soc Clin Oncol 378A,
1995.
Source URL:
http://www.cancernetwork.com/review-article/single-agent-paclitaxel-advanced-non%E2%80%93sma
ll-cell-lung-cancer
Links:
[1] http://www.cancernetwork.com/review-article
[2] http://www.cancernetwork.com/lung-cancer
[3] http://www.cancernetwork.com/authors/ulrich-gatzemeier-md
Page 3 of 3