AML NCCN guidelines 2009 Presented by CR 謝燿宇. Introduction Treatment of AML: age, hx of prior...

AML NCCN guidelines 2009

Presented by CR謝燿宇

Introduction Treatment of AML: age, hx of prior MDS or

cytotoxic therapy and performance status The most predictable factor for disease free

survival: cytogenetic status 60 y/o: divergence point (Frederick R. et. al. Blood 2006 107: 3481-3485.)

P’ts < 60 y/o: induction

Standard induction: < 60 y/o p’ts without antedecent hematologic disease

Anthracycline [daunorubicin or idarubicin (more intracellular retension time)] + Cytarabine, no benefit of adding etoposide

Dose intensive v.s. standard: more treatment related morbidity and mortality, but longer remission duration (SWOG, ALSG)

Neurotoxicity and renal toxocity

SWOG study

CALGB study

CALGB trial: 44% remission rate with SDCA + Daunorubicin plus high dose cytarabine consolidation

High dose cytarabine induction: may be influenced by consolidation strategy, fewer high dose cytarabine consolidation or for early going auto-HSCT (category 2B)

Induction therapy 20-45% p’ts will not enter remission, which is

strongly influenced by cytogenetics

EBMT trial in secondary AML or MDS

45%34%

Post induction therapy

Evaluation: 7~10 days after completion of induction

Both lymphoid and myeloid marker: may response to ALL therapy if failure to induction

Post remission therapy

3-4 courses of high dose consolidation: non-protocol standard for p’ts < 60 y/o and good or intermediate cytogenetic

CALGB trial Robert J. Mayer et. al., N Engl J Med 1995;

332:334-335, 44% 12% severe

neurotoxicity and 5% treatment related mortality, 60% disease free survival in good risk; 30% in intermediate risk; 12% in poor risk

Post remission One or more cycles of high dose

cytarabine followed by auto-HSCT or allo-HSCT?

Consider: expected relapse rate, transplantation related morbidity and mortality, salvage option, features of disease at diagnosis, numbers of cycles of induction to achieve remission


Good risk: no single preferred suggestion

Treatment related mortality 8-10%

Clara D. Bloomfield, et. al. CANCER RESEARCH 58. 4173-4179.

CBF: t(8;21) inv(16), t(16;16), and del(16)

50-60%

EORTC/GIMEMA-AML10 BLOOD, 2003 VOLUME 102, 1232-1240

No significance


Multiple cycles of dose intensive consolidation (category 1), one cycle of dose intensive consolidation followed by auto-HSCT (category 2B)

CBF mutation with c-Kit mutation (20-30%): high risk for relapse (60-70% v.s. 30%), but no impact on remission rate, consider clinical trial


Normal risk: transplant based (matched sibling or 1-2 cycles of dose intensive cytarabine followed by auto-HSCT), also multiple courses of high or intermediate dose of cytarabine

Normal karyotype with isolated NPM1 mutation: good prognosis

Normal karyotype with isolated FLT3-ITD mutation: poor prognosis


No significance

CALGB study Farag SS, et. al. JCO 2005;23:482-193


Poor risk: matched sibling or matched UR-HSCT, as well as clinical trial

Auto-HSCT v.s. chemotherapy: comparable with 18% DFS


Significance!

AML in elderly patient: induction therapy

60 y/o as divergence point P’ts > 75 y/o, 60-75 y/o with significant co-

morbidites, PS >2: especially poor

Intensive Chemotherapy in AML and MDS, Kantarjian et al. CANCER 2006;106:1090-1098

British MRC AML14 trial (Burnett et al. CANCER 2007;109:1114-1124)

low dose cytarabine: 30 days mortalities 26%

AML in elderly patient: induction therapy

Pancytopenia with modest marrow infiltration (20-40%): may wait cytogenetic if clinically stable

Remission rate: 25% in poor risk group with 25% mortality rate, highly suggest clinical trial; whereas 40~50% CR rate in normal karyotype (favor idarubicin) ALFA 9801 study, Blood, 2007;110:55a

Phase II Study of Decitabine for Front-line Treatment of Older Patients with AML

Patients age > 60, no prior therapy for AML Primary endpoint: complete remission rate Treatment with decitabine 20 mg/m2 iv x 5 days

q4 weeks All patients will be treated with 2 cycles unless

they have progression of peripheral blast count Patients with a complete or partial response

after 2 cycles can get additional cycles until progression

Phase II Study of Decitabine for Front-line Treatment of Older Patients with AML

Bone marrow collection at baseline, day 5 of cycle 1 and day 28 of cycle 2 for correlative studies RNA profiling as part of the Genomics of AML project DNA methylation profiling Pilot proteomics study

CR rate: 29%3 of 10 poor risk patients also have CR

Clofarabine: previously used in refractory pediatric ALL, proved to use in adult AML as well


Evaluation: 7-10 days after completion of induction

Full normalization of PB count often does not occurred in elderly patients due to previous antedecent myelodysplasia

CRi: marrow blast < 5% with mild residual cytopenia


ALFA 9803 trial v.s. CALGB trial: dose intensive cytarabine?

Myeloablative HSCT: too risky RIC HSCT: still of interest

28% v.s.17% in 2yrs DFS

Ambulatory better than single dose intensive therapy

ALFA 9803 trial, BLOOD, 2007;109:5129-5135

Elihu Estey et al. BLOOD, 2007;109:1395-1400

Post-remission surveillance and salvage Followed-up: CBC qM-q3M in the first two

years after completion of consolidation then q3M-q6M for total 5 years

BM study: only if abnormal CBC count noted or cytopenia

Transplantation in first CR or first relapse

Post-remission surveillance and salvage Gemtuzumab ozogomicin: single agent use,

29% of p’ts with CD33+ expression obtained marrow clearance and transfusion dependence

Fever, chills, hypotension during infusion, persistent thrombocytopenia without leukemia relapse, hepatotoxicity, increased VOD like syndrome if exposure within 3-4months after HSCT

Auto-HSCT only in non-APL patient with no allogenic donor, no suggested in poor risk patient

CNS leukemia

CNS leukemia: <3% involvement compared with ALL

No routine LP surveillance Neurological symptoms on diagnosis:

imaging for r/o mass effect, if negative, consider LP

May substitute high dose cytarabine for intrathecal

Do not combine R/T with high dose cytarabine!

Supportive care G-CSF: 抽 BM前七天要停輸血：照光加減白！ High dose cytarabine: monitor renal function,

correlated neurotoxiticy (nystagmus, ataxia, dysmetria), change all subsequent high dose to standard dose

Retinoic acid syndrome: fever, fluid retension, WBC > 10000, treat with dexamethasone 10mg bid for 3-5 days taper within 2 weeks, may restart ATRA later

Arsenic trioxide: QT prolong, EKG monitor, keep Ca 9.0, K 4.0, Mg 1.8≧ ≧ ≧

AML NCCN guidelines 2009 Presented by CR 謝燿宇. Introduction Treatment of AML: age, hx of prior...

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