Effective Treatment of Elderly Acute Myeloid Leukaemia (AML) with Continuous Combined Granulocyte Colony Stimulating Factor (G-CSF) and Single Oral Chemotherapeutic Agents.

Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 4515-4515
Author(s):  
Jennifer L. Curnow ◽  
Francesco Piccolo ◽  
Christopher M. Ward ◽  
Luke Coyle ◽  
Keith Fay ◽  
...  

Abstract Advanced age is a poor prognostic factor in acute myeloid leukaemia (AML). There is evidence that continuous low-dose chemotherapy with oral agents can achieve partial remission in AML and may be suitable as palliative therapy in elderly patients. Such low-dose treatment is usually complicated by drug-related neutropenia and thrombocytopenia. Granulocyte colony stimulating factor (G-CSF) may lessen the associated neutropenia and some anecdotal reports suggest G-CSF alone may be able to induce remission in AML. The study aim was to assess the benefits of combining an oral chemotherapeutic agent with continuous G-CSF. We describe a retrospective audit of 12 elderly patients with AML, diagnosed between 2000 and 2002, who were deemed to be either unfit for induction chemotherapy or who had failed to respond to intravenous chemotherapy. Patients were treated with continuous oral mercaptopurine, thioguanine, or hydroxyurea with concomitant G-CSF on three to seven days/week. The median age at diagnosis was 80 years (range 70–89 years). Eight (67%) had a preceding myelodysplastic syndrome. Eleven of the twelve patients died within the study period described, with a median survival of 9 months (95%CI 4.32–13.75). Eleven patients (92%) had a response to treatment, with blast disappearance obtained within 14 days of starting treatment. All patients achieved an increase in neutrophil count >0.5x109/L. Neutrophil recovery was attained within a mean of 13 days of treatment. From the onset of treatment, patients had neutrophils greater than 0.5 x109/L for 71% of the time, despite being on continuous cytotoxic treatment. Five patients (42%) had a platelet response with a rise in count above 100x109/L. A total of nine (75%) patients experienced a period of platelet transfusion independence and four (33%) patients became red cell transfusion independent for a mean of 4.6 and 4.8 months respectively. The analysis of this small cohort suggests that G-CSF administered in combination with one of the above oral chemotherapeutic agents, may be a novel way of providing treatment to elderly patients with AML which is both tolerable and of potential survival benefit.

1970 ◽  
Vol 18 (2) ◽  
pp. 155-160
Author(s):  
AR Biswas ◽  
M Begum ◽  
MA Khan ◽  
MJ Rahman

Context: This study was designed to observe the course of neutropenia that is onset of absolute neutropenia, depth of neutropenia and recovery pattern of neutropenia following induction chemotherapy and effect of granulocyte colony stimulating factor (G-CSF) on the course of neutropenia in adult acute myeloid leukaemia (AML) patients. Methods: A total of 34 newly diagnosed, adult, de novo AML patients opted to receive induction chemotherapy were enrolled for this study. All of them were given induction chemotherapy with cytarabine and daunorubicin as per 2+5 protocol. Four of them were dropped from this study; 2 due to early death and 2 due to resistant disease so were treated with early alternative chemotherapy regimen. So the ultimate sample of this study was 30 patients. Out of them 13 were given G-CSF following chemotherapy. Absolute Neutrophil count (ANC) of all patients were followed up until full recovery. Results: The difference in day of onset of absolute neutropenia (day 8 in G-CSF group vs. day 9 in no G-CSF group, P=.078) and number of day to reach nadir (day 11 in G-CSF treated group vs. day 12 in no G-CSF group, P=.688) was not significant between two group. The depth of neutropenia did not differ significantly as well (mean ANC 66/mm3 vs. 102/mm3, P=.184). However, recovery from absolute neutropenia was significantly (4 days) earlier in G-CSF treated patients (day 18 vs. day 22, P<.001). G-CSF treated patients also showed earlier attainment of ANC e"1,000/mm3 (day 20 vs. day 25, P<.001) and ANC e"1,500/mm3 (day 21 vs. day 27, P<.001). Duration of severe neutropenia was significantly shorter (9.6 days vs. 12.8 days P=.001) in G-CSF treated group. Key words: Acute myeloid leukaemia (AML); neutropenia; Granulocyte colony stimulating factor (G-CSF) DOI: 10.3329/jdmc.v18i2.6278 J Dhaka Med Coll. 2009; 18(2) : 155-160


2007 ◽  
Vol 25 (18_suppl) ◽  
pp. 7067-7067
Author(s):  
S. Qian ◽  
J. Li ◽  
S. Zhang

7067 Background: To evaluate the efficacy and toxicity of low-dose cytarabine and aclarubicin in combination with granulocyte colony-stimulating factor (G-CSF) protocol in elderly patients with acute myeloid leukemia (AML). Methods: A total of fifty-two elderly patients were enrolled. Twenty-eight patients were male, and 24 were female, with ages ranging from 60 to 81 years (median, 65 years). Complete remission (CR) had not been achieved in five patients after 2 courses of a standard induction regimen including daunorubicin and cytarabine or an equivalent anthracycline-based regimen. Cytogenetic analysis was performed in 40 patients, and unfavourable cytogenetic aberrations were showed in 10 patients. All patients were treated with CAG regimen including low-dose cytarabine (10 mg/m2 per 12 hours, days 1 to 14), aclarubicin (10 mg per day, days 1 to 8), and G-CSF priming (200 μg/m2 per day, days 1 to 14). Results: The overall response rate was 69.2%, and 29 of 52 (55.8%) patients achieved CR, including 23 of 35 (65.8%) patients with previously untreated AML, 6 of 17 (35.2% ) patients with refractory, relapsed and secondary AML, 4 of 9 (44.4%) patients aged over 70 years, 4 of 10 (40.0%) patients with unfavourable cytogenetic aberrations. The early death rate was 7.6%. The median overall survival duration 14 months. Myelosuppression was mild to moderate, severe nonhematologic toxicity was not observed. Conclusions: CAG priming regimen as the induction therapy is well tolerable and effective in elderly patients with AML. No significant financial relationships to disclose.


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