COMPARISON OF CONSOLIDATION STRATEGIES IN ACUTE MYELOID LEUKEMIA: STANDARD CHEMOTHERAPY VS AUTOLOGOUS HEMATOPOIETIC STEM CELL TRANSPLANTATION


Dikyar A., Yegin Z. A., Aydın Kaynar L., Can F., Özkurt Z. N., Yağcı A. M.

7th INTERNATIONAL CONGRESS ON LEUKEMIA, LYMPHOMA, MYELOMA, İstanbul, Türkiye, 3 - 04 Mayıs 2019, ss.38-39

  • Yayın Türü: Bildiri / Özet Bildiri
  • Basıldığı Şehir: İstanbul
  • Basıldığı Ülke: Türkiye
  • Sayfa Sayıları: ss.38-39
  • Gazi Üniversitesi Adresli: Evet

Özet

OP-012 Abstract Referance: 51

COMPARISON OF CONSOLIDATION STRATEGIES IN ACUTE

MYELOID LEUKEMIA: STANDARD CHEMOTHERAPY

VS AUTOLOGOUS HEMATOPOIETIC STEM CELL

TRANSPLANTATION

Asena Dikyar, Zeynep Arzu Yeğin, Lale Aydın Kaynar, Ferda Can, Zübeyde Nur Özkurt, Münci Yağcı

Gazi University School of Medicine, Department of Hematology

Background: Treatment of acute myeloid leukemia (AML) is based on

remission induction therapy and several consolidation approaches including

standard consolidation regimens such as high dose/intermediate dose

Ara-C (HIDAC/IDAC) and allogeneic hematopoietic stem cell transplantation

(HSCT) based on risk assessment models, particularly cytogenetics.

Autologous HSCT is considered as a feasible option for patients without

adverse cytogenetics and HLA-compatible donors. The aim of this study is

to compare the efficacy of HIDAC/IDAC regimens and autologous HSCT as

consolidation modalities in terms of relapse and overall survival (OS) in AML

patients.

Methods: A total of 101 patients [median age: 47(19-79) years; M/F: 51/50]

who were diagnosed as AML between in 2002 and 2019 were reviewed in

this retrospective study.

Results: After standard 7+3 remission induction therapy, 70 patients (69.3%)

continued with consolidation chemotherapy including 3 to 4 courses of

HIDAC/IDAC, while autologous HSCT was performed in 31 patients (30.7%)

after the first consolidation course. Patient characteristics are summarized

in Table 1. All patients were in complete remission before HSCT. G-CSF was used for median 8(1-16) days during stem cell mobilization. Median infused

CD34+ cell count was 4.47(2.2-5.86)x106/kg. Neutrophil and platelet engraftments

were achieved on day 12(9-27) and 13(10-202), respectively. Grade

1(1-3) mucositis was observed during peri-engraftment period. A total of

16 patients (51.6%) had neutropenic fever and 1patient (3.2%) had sinusoidal

obstruction syndrome. In chemotherapy group, 22 patients (31.4%)

experienced hematological relapse at median 330(60-2190) days after the

first remission, 4 of these patients (18.2%) underwent allogeneic HSCT for

salvage treatment. A total of 14 patients (45.2%) relapsed at median 225(60-

395) days after autologous HSCT and 12 patients (85.7%) underwent allogeneic

HSCT in this group. At a median follow-up of 915(30-4470) days, OS was

found to be better in autologous HSCT group compared to chemotherapy

group without statistical significance [79.2% vs 38.8%, p=0.054] (Figure 1).

Leukemia risk status at diagnosis was considered as the only prognostic

parameter for OS in Cox regression analysis (p=0.002).

Conclusions: In this study, the superiority of consolidative autologous HSCT

was demonstrated in AML patients compared to standard chemotherapy

arm, without statistical significance. This favourable issue, despite high and

early relapse rates after autologous HSCT, may be explained by the additive

positive impact of high percentage of salvage allogeneic HSCT in this group

of patients. Furthermore, patients in the chemotherapy arm were relatively

older and had more comorbidities compared to HSCT group. As leukemia

risk status at diagnosis was indicated to be the only statistically significant

factor for OS, the importance of patient-based treatment decisions in newly-

diagnosed AML patients should be underlined. Small sample size may

be another explanation for statistical inconvenience. Further studies are

required in order to standardize consolidation strategies in AML patients.

Keywords: Acute Myeloid Leukemia; Autologous Stem Cell Transplantation;

Consolidation Therapy; Prognosis