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Gemcitabine - Cisplatin regimen
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Lung Cancer News |
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Lung Cancer |
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Abstract: Randomized phase III study of gemcitabine-cisplatin versus
etoposide-cisplatin in the treatment of locally advanced or metastatic non-small-cell
lung cancer.
PURPOSE: We conducted a randomized trial to compare gemcitabine-cisplatin
with etoposide-cisplatin in the treatment of patients with advanced non-small-cell
lung cancer (NSCLC). The primary end point of the comparison was response
rate. PATIENTS AND METHODS: A total of 135 chemotherapy-naive patients with
advanced NSCLC were randomized to receive either gemcitabine 1,250 mg/m2
intravenously (IV) days 1 and 8 or etoposide 100 mg/m2 IV days 1 to 3 along
with cisplatin 100 mg/m2 IV day 1. Both treatments were administered in
21-day cycles. One hundred thirty-three patients were included in the intent-to-treat
analysis of response. RESULTS: The response rate (externally validated)
for patients given gemcitabine-cisplatin was superior to that for patients
given etoposide-cisplatin (40.6% v 21.9%; P = .02). This superior response
rate was associated with a significant delay in time to disease progression
(6.9 months v 4.3 months; P = .01) without an impairment in quality of life
(QOL). There was no statistically significant difference in survival time
between both arms (8.7 months for gemcitabine-cisplatin v 7.2 months for
etoposide-cisplatin; P = .18). The overall toxicity profile for both combinations
of drugs was similar. Nausea and vomiting were reported more frequently
in the gemcitabine arm than in the etoposide arm. However, the difference
was not significant. Gemcitabine-cisplatin produced less grade 3 alopecia
(13% v 51%) and less grade 4 neutropenia (28% v 56% ) but more grade 3 and
4 thrombocytopenia (56% v 13%) than did etoposide-cisplatin. However, there
were no thrombocytopenia-related complications in the gemcitabine arm. CONCLUSION:
Compared with etoposide-cisplatin, gemcitabine-cisplatin provides a significantly
higher response rate and a delay in disease progression without impairing
QOL in patients with advanced NSCLC.
References
Cardenal F, Lopez-Cabrerizo MP, Anton A, Alberola V, Massuti B, Carrato
A, Barneto I, Lomas M, Garcia M, Lianes P, Montalar J, Vadell C, Gonzalez-Larriba
JL, Nguyen B, Artal A, Rosell R. Randomized phase III study of gemcitabine-cisplatin
versus etoposide-cisplatin in the treatment of locally advanced or metastatic
non-small-cell lung cancer.J Clin Oncol. 1999 Jan;17(1):12-8.
Sandler AB, Nemunaitis J, Denham C, von Pawel J, Cormier Y, Gatzemeier
U, Mattson K, Manegold C, Palmer MC, Gregor A, Nguyen B, Niyikiza C, Einhorn
LH. Phase III trial of gemcitabine plus cisplatin versus cisplatin alone
in patients with locally advanced or metastatic non-small-cell lung cancer.
J Clin Oncol. 2000 Jan;18(1):122-30.

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Gemcitabine....... 1000 mg / M2 IV days 1,8,15
Cisplatin....... 100 mg / M2 IV day 1
FREQUENCY every 28 days
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