Advances in the Management of Relapsed/Refractory Multiple Myeloma
Can older refractory and relapsed AML patients...
Transcript of Can older refractory and relapsed AML patients...
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Paradigm Change: Can older refractory and relapsed AML
patients undergo a successful
stem cell transplant without entering
complete remission first?
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Joseph Jurcic, MD, Chair
Director, Hematologic Malignancies Section, Hematology/Oncology Division,
Professor of Medicine at Columbia University Medical Center; Attending
Physician, New York-Presbyterian Hospital
Participants:
Mark Frattini, MD, PhD, Director of Research for Hematologic Malignancies
Section, Associate Professor of Medicine at Columbia University Medical
Center; Associate Attending Physician, New York-Presbyterian Hospital
Sergio Giralt, MD, Chief, Adult BMT Service, Memorial Sloan Kettering
Cancer Center
Markus Mapara, MD, PhD, Director, BMT Program, Columbia University
Medical Center; Professor of Medicine; Attending Physician, New York-
Presbyterian Hospital
Peter Maslak, MD, Chief, Hematology Laboratory Service, Memorial Sloan
Kettering Cancer Center
Sebastian Mayer, MD, Assistant Professor of Medicine, Weill Cornell
Medical College; Assistant Attending Physician, New York-Presbyterian
Hospital
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Agenda
• AML background
• Current treatment approaches
• Radioimmunotherapy before HCT
Iomab-B overview
Clinical results to date
• Proposed phase III trial
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Normal Hematopoiesis Leukemogenesis
Development of AML
Neutrophil
Leukemia
oncogene
Second
hit
AML
1. Lack of Differentiation
2. Increased Proliferation
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AML Survival by Age
Juliusson G et al. Blood 2009;113:4179-4187.
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2012 AML Incidence by Age Group
Source: NCI SEER US Cancer Database, AML.
6% 7% 7%
12%
16%
20%
23%
10%
0%
5%
10%
15%
20%
25%
<20 20-34 35-44 45-54 55-64 65-74 75-84 85+
% o
f To
tal In
cid
en
ce
Age of Diagnosis
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AML: Cytogenetics Determines Survival
Bloomfield CD et al. Cancer Res 1998;58:4173-4179.
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Risk Status Based on Cytogenetic and
Molecular Abnormalities
Risk Status Cytogenetics Molecular Abnormalities
Better-risk inv(16) or t(16;16)
t(8;21)
t(15;17)
Normal cytogenetics:
NPM1 mutation in the
absence of FLT3-ITD
or isolated biallelic CEBPA
mutation
Intermediate-risk Normal cytogenetics
+8 alone
t(9;11)
Other non-defined
t(8;21), inv(16), t(16;16):
with c-KIT mutation
Poor-risk Complex (≥ 3 clonal abnormalities)
Monosomal karyotype
-5, 5q-, -7, 7q-
11q23 – non t(9;11)
inv(3), t(3;3)
t(6;9)
t(9;22)
Normal cytogenetics:
with FLT3-ITD mutation
NCCN Guidelines Version 2.2013.
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Phases of Leukemia Therapy
• Induction
– Cytarabine + anthracycline
• Postremission
– Consolidation chemotherapy
– Hematopoietic cell transplantation (HCT)
– Maintenance therapy
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Treatment Outcome by Age
Age < 56 yo 56-65 yo 66-75 yo >75 yo
No. of patients 368 246 274 80
Response, no. (%)
CR
Resistant disease
235 (64)
99 (27)
113 (46)
91 (37)
108 (39)
101 (37)
26 (33)
29 (36)
Median survival, mo.
(95% CI)
18.8
(14.9-22.6)
9.0
(8.1-10.2)
6.9
(5.4-7.7)
3.5
(1.4-6.1)
Median DFS, mo.
(95% CI)
21.6
(15.8-25.5)
7.4
(65.-8.8)
8.3
(6.3-10.2)
8.9
(5.8-10.8)
Appelbaum FR et al. Blood 2006; 107:3481-3485.
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Managing Relapsed AML
Hematopoietic
Cell Transplant
(HCT)
Salvage Therapy
Supportive
Care
Consolidation
Maintenance
CR
No CR
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Salvage Therapy for Relapsed AML
• No FDA-approved regimens
• Standard chemotherapy
High-dose cytarabine
Etoposide/mitoxantrone ± cytarabine (MEC)
Fludarabine/cytarabine/G-CSF ± idarubicin (FLAG-Ida)
Hypomethylating agents
• Investigational therapy
Antibodies, drug conjugates
Histone deacetylase inhibitors
Small molecule inhibitors (e.g., flt-3, IDH, etc.)
Others
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Response to Salvage Chemotherapy
for Relapsed AML
CR1 duration< 1 year or
1o refractory
< 1 year or
1o refractory
1-2
years
> 2
years
# prior salvage
attempts >1 0 0 0
N 58 160 30 15
CR Rate <1% 14% 47% 73%
Estey E et al. Blood 1996; 88:756.
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Hematopoietic Cell Transplant
Procedure
http://biomed.brown.edu/Courses/BI108/BI108_2007_Groups/group07/stemcells/stcell04.html
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Conditioning Regimens for
Allogeneic HCT
Myelosuppression
Minimal Short Long Irreversible
Ste
m c
ell
su
pp
ort
req
uir
ed
?
No
Yes
Myeloablative
MA
Reduced-Intensity Conditioning
RIC
Non-ablative
NMA
Bacigalupo A et al. Biol Blood Marrow Transplant 2009;15:1628-33.
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Stem Cell Sources for
Allogeneic HCT
• Sibling donor (HLA-matched)
• Matched unrelated donor
• Umbilical cord donor
• Haploidentical donor
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Outcome of HCT in CR2
• OS after HCT in CR2 for
patients 18-50 yo:
6 m: ~80%
12 m: ~70%
2 y: ~60%
BUT:
• Only ~15% enter CR2,
so OS for all patients is:
6 m: ~12%
12 m: ~10%
2 y: ~10%
Foreman SJ, Rowe JM. Blood 2013; 121:1077-1082.
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Impact of Disease Burden on
HCT Outcomes
Disease burdenNo. of
patients
Median
survival
(mos.)
Median
PFS
(mos.)
Morphologic & cytogenetic
remission8 10.4 7.8
Morphologic remission only 6 4.6 2.9
Overt relapse 33 5.9 2.8
Kebriaei P et al. Bone Marrow Transplant 2005; 965-970.
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Effect of TBI Dose on
HCT Outcomes
Relapse Probability Mortality Probability
Clift RA et al. Blood 1990; 76:1867-71.
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Relationship Between BM Dose
and Relapse
FHCRC data
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Rationale for RIT in HCT Regimens
• AML is highly radiosensitive.
• TBI is effective in HCT regimens at
high doses.
• TBI cannot be safely dose escalated.
• RIT can increase radiation doses to
leukemia cells and normal bone
marrow without increasing doses to
normal tissues.
• Iomab-B consists of an anti-CD45
mAb that targets lympho-
hematopoietic cells and the β-particle
emitting radionuclide 131I.
Tumor
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Iomab-B Biodistribution
Pagel JM et al. Blood 2009; 114:5444-5453.
Treatment at MTD (24 Gy to liver) delivers ~36 Gy to marrow and ~100 Gy to spleen.
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Outcomes after Iomab-B at MTD
Pagel JM et al. Blood 2009; 114:5444-5453.
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• Non-relapse mortality (NRM):
– Day 100: 10%
– Overall: 20% (46% with
myeloablative conditioning)
Compelling Results Enable Pivotal Phase III Trial
N = Number of patients treated
Iomab-B results from FHCRC clinical trials
Current BMT and Chemotherapy results from MD Anderson outcomes analysis.
• Complete response rate: 100%
• Engraftment by Day 28: 100%
• Transplant related mortality:
14% (same as RIC)
All relapsed/refractory AML patients > 50 Rel/ref AML pts > 50 with poor cytogenetics
30%
19%
10%
0%
10%
0%0%
5%
10%
15%
20%
25%
30%
35%
1 year 2 years
Pe
rce
nta
ge S
urv
iva
l
Iomab-B BMT (N=27)
Current BMT (N=10)
Chemotherapy (N=61)
33%
16%
3%
0%
3%
0%0%
5%
10%
15%
20%
25%
30%
35%
1 year 2 years
Pe
rce
nta
ge S
urv
iva
l
Iomab-B BMT(N=18)
Current BMT (N=19)
Chemotherapy (N=95)
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Iomab-B Pivotal Trial Schema
Control Arm
Chemotherapy,
excluding
hydroxyurea &
hypomethylating
agents
Maintenance
CR
No CR NMA/RIC
HCT
Consolidation
Screening,
including
HLA typing
Not
enrolledFail
R
A
N
D
O
M
I
Z
E
Pass Crossover
CR
No CR
Study Arm
Iomab-B HCT
Enrolled
Observation
Off Study
ObservationPrimary Endpoint: Durable CR rate, lasting at least 6 months.
Bone marrow aspirate and biopsy performed in all patients at ~1 and/or 2 months after the
last day of intervention to determine response and at 6 months after CR has been established
to confirm CR duration in groups labeled with .
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Conclusions
• Poor response and toxicity of conventional
salvage chemotherapy are barriers to HCT.
• Iomab-B can potentially increase anti-leukemic
effects of conditioning without added toxicity.
• Phase III study will address whether RIT-based
conditioning for HCT is superior to conventional
management for relapsed/refractory AML.