Journal List > Tuberc Respir Dis > v.66(2) > 1001334

Ban, Chi, Park, Kim, Kim, Kim, Ju, Kwon, Oh, Kim, Lim, and Kim: Efficacy of Darbepoetin alfa in Anemia Developed during Chemotherapy for Lung Cancer

Abstract

Background

Anemia is quite common in lung cancer patients and known to decrease the quality of life. Darbepoetin alfa is an erythropoiesis-stimulating protein approved for administration to cancer patients. This study examined the efficacy and safety of darbepoetin alfa in lung cancer patients with a hemoglobin concentration <10 g/dl during chemotherapy.

Methods

Lung cancer patients (n=178) received darbepoetin alfa at doses of 1.91 µg/kg per week until the hemoglobin concentration increased to >10 g/dl. The efficacy and safety were measured by comparing the hemoglobin concentration and assessing the adverse events.

Results

After chemotherapy, the hemoglobin concentration decreased to 9.03±0.64 g/dl. With the darbepoetin alfa treatment, the hemoglobin concentration increased to 10.09±1.17 g/dl after 4 weeks reaching a peak hemoglobin concentration of 10.45±1.18 g/dl. The changes in hemoglobin after 4 and 8 weeks with treatment were 1.08±1.24 g/dl and 1.38±1.59 g/dl (p<0.01). At least a 1 g/dl or more increase in hemoglobin was observed in 62.4% of patients. There were no serious adverse effects except for some mild reactions.

Conclusion

Darbepoetin alfa administered to lung cancer patients appears to be an effective, well-tolerated treatment for chemotherapy induced anemia.

Figures and Tables

Figure 1
Change of hemoglobin concentration before and after administrations of darbepoetin alfa. Darbepoetin alfa administered every 1 week significantly increased mean hemoglobin levels in chemotherapy induced anemia. Increased hemoglobin levels after administration of darbepoetin alfa were shown over the course of the study period.
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Figure 2
The comparison of hemoglobin concentration changes between darbepoetin alfa responders and non-responders. The hemoglobin levels were significantly different between responders and non-responders after darbepoetin alfa administration. Also non-responders at 2 weeks have no change of hemoglobin levels at 4 weeks.
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Table 1
The clinicopathological characteristics of the 178 lung cancer patients
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SCLC: small cell lung cancer; ADC: adenocarcinoma; SQC: squamous cell lung cancer; NSCLC: non-small cell lung cancer.

Table 2
Concentration of hemoglobin before and after treatment with darbepoetin alfa
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Table 3
The comparsion of clinicopathologic factors between darbepoetin alfa responders and non-responders
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SCLC: small cell lung cancer; ADC: adenocarcinoma; SQC: squamous cell lung cancer; NSCLC: non-small cell lung cancer. *Hemoblobin increased>1 g/dL with darbepoetin alpha, independent T test.

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