Cases exploring the many facets of MCL€¦ · WHO Classification of Tumours of Haematopoietic and...
Transcript of Cases exploring the many facets of MCL€¦ · WHO Classification of Tumours of Haematopoietic and...
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Cases exploring the many facets of MCL
Dr Pam McKay
This medical education meeting was organised and funded by Janssen-Cilag Ltd. EM-14633 | July 2019
Click below for prescribing information and adverse events reporting:For ibrutinib click here
For bortezomib click here
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MCL workshop
Dr Pam McKay
Consultant Haematologist
Beatson Cancer Centre
Glasgow
February 2019
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This meeting was organised and funded by Janssen
The slide content has been reviewed by Janssen to ensure compliance with the ABPI Code of Practice
for the Pharmaceutical Industry
The faculty may express personal opinions that are not necessarily shared by Janssen
Adverse events should be reported.▼Reporting forms and information can be found at
www.mhra.gov.uk/yellowcard or search for MHRA Yellow Card in the Google Play or Apple App Store.
Adverse events should also be reported to Janssen-Cilag Limited on 01494 567447 or at
Any adverse events presented in this slide deck (related to Janssen products) have been reported to
drug safety
Prescribing Information is available at this meeting
Janssen-Cilag Ltd, 50–100 Holmers Farm Way, High Wycombe, Buckinghamshire HP12 4EG
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Conflicts of interest
Honoraria received from:
• Epizyme
• Gilead
• Janssen
• Roche
• Takeda
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MCL
• Male predominance1
• >90% present with advanced stage disease2
• Widespread lymphadenopathy, splenomegaly, BM and peripheral blood involvement2
• EN involvement common, e.g. gut, breast, lung, skin, salivary gland, lacrimal gland3
– 30–50% have ≥2 EN sites
• B symptoms and bulk uncommon4
BM: bone marrow; EN: extranodal;
MCL: mantle cell lymphoma.
1. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues. Revised 4th Edition. Volume 2. 2008. Swerdlow SH, et al (Ed.); 2. Martins C, et al. Rev Bras Hematol Hemoter. 2017; 39:73–6; 3. Jares P, Campo E. Br J Haematol. 2008; 142:149–65; 4. McKay P, et al. Br J Haematol. 2018; 182:46–62.
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Adapted from Haematological Malignancy Research Network. Incidence. [Accessed: July 2019]. Available at: www.hmrn.org/statistics/incidence
Median age in the UK is 73 years
Incidence of haematological neoplasms
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Clinical course and outcome
• Heterogeneous course:– Indolent: splenomegaly and
per blood → 5 to 12-year survival (SOX11 negative)
– Aggressive: blastoid
• Incurable
• Relapse → resistance
• Median OS: 4 to 5 years
• OS increased in younger, fitter patients who can tolerate intensive therapy
Proposed model of molecular pathogenesis in the development and progression of major subtypes of MCL
Cheah CY, et al. J Clin Oncol. 2016; 34:1256–69.IG: immunoglobulin;
OS: overall survival; PB: peripheral blood.
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Case 1
• 64-year-old man, presented in 2010
• Deaf (R ear)
• Nasal blockage
• Swelling at back of throat (R side)
• MRI: large R post-nasal space mass (4.7 x 5.8 x 3.4 cm)
• Biopsy: MCL, Ki67 30%
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Case 1
• Well, PS=0, no B symptoms
• No comorbidities; no medication
• Non-smoker; >20 units alcohol/week
• Hb 160; WCC 5.2 (lymph 0.8); platelets 221
• LDH 244 (ULN 240)
• CT scan: nasopharyngeal mass; bilateral cervical LNs
• BM: minor infiltrationHb: haemoglobin; LDH: lactate dehydrogenase; LNs: lymph nodes;
PS: performance status; ULN: upper limit of normal; WCC: white cell count.
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Case 1
• Stage IVA
• MIPI score = 3 (low risk)
• What treatment?
• Rituximab + HD cytarabine
HD: high dose; MIPI: mantle cell lymphoma international prognostic score.
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Which cytarabine-containing regimen?
• Hyper-CVAD– CR rates of 87%1 and 92%2 in a single centre
– ~40% cannot complete treatment in the multicentre setting3,4
• Nordic MCL2 study
• European MCL Network study, MCL Younger
• GELA/Lysa study
• LyMa study
• British-Nordic MCL5 study
CR: complete response; CVAD: cyclophosphamide, vincristine, doxorubicin,
dexamethasone, methotrexate, cytarabine.
1. Romaguera JE, et al. Br J Haematol. 2010; 150:200–8; 2. Ritchie DS, et al. Ann Hematol. 2007; 86:101–5; 3. Merli F, et al. Br J Haematol. 2012; 156:346–53; 4. Bernstein SH, et al. Ann Oncol. 2013; 24:1587–93.
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Nordic MCL2 2000–2006
No. Eval. CR/CRu ORR
160 54% 96%
0.0 2.5 5.0 7.5 10.0 12.50.0
0.1
0.2
0.3
0.4
0.5
0.6
0.7
0.8
0.9
1.0
Survival (53 deaths)
MCL2 Update 2010:- Overall and Event-freeSurvival.- Response Duration
EFS (79 events)RD (145, 54 progressions)
Years
Fra
cti
on
su
rviv
al
Predicted 10-year EFS: 43%, OS: 58%
Geisler CH, et al. Br J Haematol. 2012; 158:355–62.
MCL2 update (all patients):OS and EFS
Response duration
BEAM/C: BCNU, AraC, etoposide, melphalan, cyclophosphamide; CHOP: cyclophosphamide,
doxorubicin, vincristine, prednisone; CRu: unconfirmed complete response;
EFS: event-free survival; ORR: overall response rate;
R: rituximab; RD: residual disease.
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15-year follow-up of the Nordic MCL2 trial
• Median follow-up: 11.4 years; PFS: 8.5 years; OS: 12.7 years
• Despite long-term responses, late relapses still occur
• On-going relapses >10 years out
MIPI– High: PFS 2.5 years; OS 4 years
– Int: PFS 8 years; OS 11 years
– Low: PFS 12.8 years; OS NR
Low/int group: 40% in first CR >12 years
Eskelund CW, et al. Br J Haematol. 2016; 175:410–18. Int: intermediate; NR: not reached; PFS: progression-free survival.
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PBSCT
3 x R-CHOP3 x R-DHAPalternating
PBSCT
TBI 10 GrayAra-C 4 x 1.5 g/m2
Melphalan 140 mg/m2
6 x R-CHOP
DexaBEAM(stem cell mobilisation)
MCL younger
Cyclo/TBI
Hermine O, et al. Lancet. 2016; 388:565–75.
497 patients
R-DHAP: rituximab, dexamethasone, cytarabine, cisplatin; PBSCT: peripheral blood stem cell transplant; TBI: total body irradiation.
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TTF, stratified by MIPIBenefit across all MIPI and Ki67 groups
TTF in primary analysis and OSTTF: median 9.1 years vs 3.9 years
65% at 5 years vs 40%
OS not significantly different at time of analysis
Graphs adapted from: Hermine O, et al. Lancet. 2016; 388:565–75. CI: confidence interval; HR: hazard ratio; TTF: time to treatment failure.
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LyMa trial2
• Phase 3
• R-DHAP x 4 (+ R-CHOP x 4 if not in CR/PR)→ ASCT →maintenance R or observation
• ORR: 94% (CR/CRu: 77%)
• 4-year PFS: 68%; OS: 78%
1. Delarue R, et al. Blood. 2013; 121:48–53; 2. Le Gouill S, et al. N Engl J Med. 2017; 377:1250–60. ASCT: autologous stem cell transplantation; PR: partial response.
LYSA (GELA)1
• Phase 2
• CHOP x 2; R-CHOP x 1; R-DHAP x 3 then ASCT
• ORR: 95% (CR: 57%)
• Median EFS: 83 months
• 5-year OS: 75%
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R-HD cytarabine +/- dexamethasone
• 18 patients
• 72% int (61%) or high (11%) MIPI
• Cytarabine: 3 g/m2 IV bd D1–2 (2 g/m2 IV bd if age ≥60 years)
• Rituximab: 375 mg/m2 IV D1
• Dexamethasone: 40 mg OD D1–4 (optional)
• Repeat every 21 days to a maximum of six cycles, then transplant
• Number of patients completing planned therapy: 16 (88.9%)
• Median number of total cycles (range): 5 (4–6)
• Reasons for not completing therapy:
– Disease progression (1)
– Treatment toxicity (1)
Forbes A, et al. Leuk Lymphoma. 2013; 54:2303–05. bd: twice daily; D: day; IV: intravenous; OD: once daily.
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Update at BSH 20161
• 45 transplant-eligible patients
• Four UK centres
• 2010–2015
• Median age: 60 years (56–58 in other major studies)
• Nine patients (20%) progressed on HDAC– Three patients (33%) responded to second-line
therapy, with two subsequently dying of PD
• 69% had transplant (62% ASCT)
• ORR 78% (+/- ASCT), 67% CR
• Median PFS and OS not reached (median follow-up of 38 months)
• 61% PFS and 78% OS at four years
• Post-induction CR of 67% compares favourably to:
– Geisler 54%2
– DeLarue 57%3
– Hermine 54%4
– Le Gouill 77%5
• Conclusions:– Well tolerated, effective– Avoids excess toxicity from
additional drugs– Greater range of therapies for relapse
1. Burrows S, et al. Presentation at BSH 2016. Abstract E970; 2. Geisler CH, et al. Br J Haematol. 2012; 158:355–62; 3. Delarue R, et al. Blood. 2013; 121:48–53; 4. Hermine O, et al. Lancet. 2016; 388:565–75; 5. Le Gouill S, et al. N Engl J Med. 2017; 377:1250–60.
HDAC: histone deacetylase; PD: progressive disease.
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R
British-Nordic MCL5 protocol
BEAM
H D-ARA-C: 3 g/m2 (>60 years: 2g/m2) four infusions/cycle
RH
D-A
RA
-C
DDDD
DDDD: dexamethasone p.o. 40 mg D1–4
R: rituximab 375 mg/m2 D1
Protocol: Phase 2, historic control (MCL2 and 3)Inclusion criteria:
• Nordic: untreated MCL s-MIPI-B high-risk• British: all patients in need of treatment• Below 66 years of age
ASCT
MRD monitoringand pre-emptiverituximab at molecular relapse
Stage Restage 1 Restage 2 Restage 3Harvest Reinfusion
Stem cell:
R
H D
-AR
A-C
DDDD
R
H D
-AR
A-C
DDDD
R
H D
-AR
A-C
DDDD
R
H D
-AR
A-C
DDDD
R
H D
-AR
A-C
DDDD
CycleWeek
11
24
37
410
513
616 19 20 28
MRD: minimal residual disease; p.o.: by mouth.Adapted from: Nordic-lymphoma. A Nordic Lymphoma Group Phase 2 Trial. Available at: www.nordic-lymphoma.org/wp-content/uploads/2016/11/MCL5_final_04-11-2011.pdf [accessed July 2019].
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Nordic MCL5
• Restricted to high-risk MIPIB (high Ki67)
• Low- and int-risk groups: 70% 10-year survival in the MCL2 and MCL3 trials
• Five patients:– Two responded after three cycles,
with one subsequently progressing– Three non-responders
• Trial stopped
• Patients salvaged with mega-CHOP
“High-dose cytarabine with rituximab is not enough in first-line treatment of mantle cell lymphoma with high proliferation: early closure
of the Nordic Lymphoma Group Mantle Cell Lymphoma 5 trial”
Laurell A, et al. Leuk Lymphoma. 2014; 55:1206–08.
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RB/RC induction chemotherapy for transplant-eligible patients with uMCL
• Pooled analysis: two phase 2 trials + off-trial results; 86 patients1
• DFCI trial: RB x 3 followed by RC x 3
– B 90 mg/m2 D1–2; C 3 g/m2 bd D1–2
– Preliminary results2
→ SOC
• WUSTL trial: alternating RB/RC x 6
– ORR 98% (CR 92%); 85% → ASCT
– PFS 88% at two years; 80% at four years; OS 96%; 92%
– Efficacy similar; delayed platelet engraftment with sequential regimen and C >2 g/m2
1. Merryman R, et al. Presentation at ASH 2018. Abstract 0145; 2. Armand P, et al. Br J Haematol. 2016; 173:89–95.
RB/RC: rituximab/bendamustine, rituximab/cytarabine; SOC: standard of care; uMCL: untreated mantle cell lymphoma.
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Trial ORR CR/Cru
NORDIC MCL21 96% 54%
MCL Younger:2
- alt R-CHOP/R-DHAP 95% 54%
- R-CHOP 90% 40%
Lysa3 95% 57%
LyMa4 94% 77%
R-HD Ara-C5 78% 67%
R-hyperCVAD*6 94% 41%
RB*6 86% 43%
*SWOG S1106 phase 2 inter-group trial.1. Geisler CH, et al. Br J Haematol. 2012; 158:355–62; 2. Hermine O, et al. Lancet. 2016; 388:565–75; 3. Delarue R, et al. Blood. 2013; 121:48–53; 4. Le Gouill S, et al. N Engl J Med. 2017; 377:1250–60; 5. Burrows S, et al. Presentation at BSH 2016. Abstract E970; 6. Chen RW, et al. Br J Haematol. 2017;176:759–69.
HD-cytarabine regimens
alt: alternating.
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HD-cytarabine trial outcomes
Trial PFS OS
NORDIC MCL21 8.5 years (median) 12.7 years (median)
MCL younger2 65% (5 years) 76% (5 years)
Lysa3 64% (5 years) 75% (5 years)
LyMa4 68% (4 years) 78% (4 years)
R-HD Ara-C5 61% (4 years) 78% (4 years)
1. Geisler CH, et al. Br J Haematol. 2012; 158:355–62; 2. Hermine O, et al. Lancet. 2016; 388:565–75; 3. Delarue R, et al. Blood. 2013; 121:48–53; 4. Le Gouill S, et al. N Engl J Med. 2017; 377:1250–60; 5. Burrows S, et al. Presentation at BSH 2016. Abstract E970.
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Case 1
• Started R-HD Ara-C
• C1D6 – chest pain
• Large inferoposterior MI → stent– Echo: normal LV function
– Aspirin and clopidogrel for three months
– Culture-negative neutropenic sepsis
• What now?
LV: left ventricular; MI: myocardial infarction.
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Case 1
• Received R-HD Ara-C x 4 → CR
• What now?
• ASCT (BEAM), August 2010
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Transplant – ASCT
• Only one prospective study comparing the outcome of ASCT with non-SCT strategies for first-line consolidation1
– CHOP-based induction then HDT + ASCT or IFN
– PFS: 39 months vs 17 months; no OS advantage
• Several phase 2 studies – difficult to separate the effects of intensive induction and consolidation HDT
– 4 to 5-year PFS: 56–73%; OS: 64–81% → SOC
Dreyling M, et al. Blood. 2005; 105:2677–84. HDT: high-dose therapy; IFN: interferon.
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Prognostic factors for favourable outcome of first-line consolidation HDT
• Low or intermediate MIPI
• Achievement of MRD-negative state
• Disease status at transplantation
Dr Pam McKay personal communication
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Allogeneic SCT1
• Limited data
• Heterogenous populations– First-line, relapse, +/- previous ASCT
• Substantial toxicity– Non-relapse mortality rates 9–25% at 1 year2–6
• cGVHD in 40–50%7
• Relapse rate: 15–38%3,6,8
• Suggestion of a plateau after four years
cGVHD: chronic graft vs host disease.
1. McKay, et al. Br J Haematol. 2018; 182:46–62; 2. Maris MB, et al. Blood. 2004;104:3535–42; 3. Tam CS, et al. Blood. 2009; 113:4144–52; 4. Cook G, et al. Biol Blood Marrow Transplant. 2010; 16:1419–27; 5. Le Gouill S, et al. Ann Oncol. 2012; 23:2695–703; 6. Fenske TS, et al. J Clin Oncol. 2014; 32:273–81; 7. Jagasia M, et al. Blood. 2012;119(1):296–307. 8. Robinson. Bone Marrow Transplant. 2017; 52:S17–155.
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Rituximab maintenance after SCT
• Previously untreated MCL <66 years, 53% MIPI low-risk
• R-DHAP x 4 (+ R-CHOP14 in NR), R-BEAM auto-SCT
• 299 enrolled, 240 randomised post-SCT to observation vs MR, once every two months for three years
• Four-year PFS: 83% MR vs 64% observation
• Four-year OS: 89% MR vs 80% observation
Conclusion: MR prolongs survival in younger MCL patients post-ASCT
Le Gouill S, et al. N Engl J Med. 2017; 377:1250–60. MR: maintenance rituximab; NR: non-responders
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Case 1
• Prostate cancer, March 2014
• Relapsed MCL (biopsy confirmed, Ki67 15–20%), November 2014
• CT scan: localised to L neck
• Management?
• Watch and wait
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Case 1
• November 2017 (three years later)
• CT scan showed progressive, widespread LNs
• Well; remained on watch and wait
• No cardiac issues; on aspirin
• February 2018: cervical LNs ~4 cm; LDH normal; platelets 87
• Management?
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Case 1
• January 2018: commenced ibrutinib
• Continued on aspirin
• February 2018: attended GP with sore throat and lymphadenopathy– Lymph 23.8
• Action?
• November 2018: no palpable LNs; normal LDH
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Management of the relapsed patient
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DrugNo. pts
Median prior lines
ORR (CR) %Median DOR
(months)Median PFS
(months)Median OS (months)
Trial
Temsirolimus 54** 3 22 (2) 7.1 4.8 12.8OPTIMAL1
Chemotherapy 53 4 2 (0) NA 1.9 9.7
Lenalidomide 170 2 40 (5) 16 8.7 27.8SPRINT2
Chemotherapy 84 2 11 (0) 10.4 5.2 21.2
Ibrutinib 139 2 72 (19) NR 14.6 NRRAY3
Temsirolimus 141 2 40 (1) 7 6.2 21.3
BR* 24* 1 71 (38) 17.6 35.3STiL4
FR* 23* 1 26 (13) 4.7 20.9
*results shown for subset with MCL; **results shown for 175/75 mg dose group. SPRINT trial single agent chemotherapy = rituximab, gemcitabine, fludarabine, chlorambucil, or cytarabine; OPTIMAL trial single agent chemotherapy = gemcitabine, fludarabine, chlorambucil, cladribine, etoposide, cyclophosphamide, thalidomide, vinblastine. Medianfollow-up: OPTIMAL trial = not reported, SPRINT trial = 15.9 months, RAY trial = 20 months, STiL trial = 96 months.
Randomised trials in relapsed/refractory MCL
DOR: duration of response; FR: fludarabine and rituximab;
mo: months; NA: not available. 1. Hess G, et al. J Clin Oncol. 2009; 27:3822–9; 2. Trneny M, et al. Lancet Oncol. 2016; 17:319–31; 3. Dreyling M, et al. Lancet. 2016; 287:770–8; 4. Rummel M, et al. Lancet Oncol. 2016; 17:57–66.
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1. Rule S, et al. Presentation at ASH 2015. Abstract 469.
High response rates for ibrutinib, irrespective of line of therapy
CR
PR
Number of prior lines of therapy
RAY trial: ORR by number of prior linesO
RR
1 2 ≥3
Ibr Tem Ibr Tem Ibr Tem
ibrutinib
Graph adapted from: Rule S, et al. 2015.1
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1. Rule S, et al. Presentation at ASH 2015. Abstract 469. 36
Ibr ≥2 prior
0 3 6 129 15
Months
18 21 24
0
30
10
20
40
50
60
70
80
90
100
% a
live
wit
ho
ut
pro
gre
ssio
n
Patients at risk
Ibr 1 prior 57 47 43 39 37 21 19 3 2
Tem 1 prior 50 33 24 13 11 6 4 0 0
82 67 58 44 40 24 15 5 3
91 60 45 32 22 13 7 3 1
Temsirolimus prior line 1
Ibrutinib prior line 1
Tem ≥2 prior
Ibrutinib prior line ≥ 2
Temsirolimus prior line ≥ 2
RAY trial: PFS by line of therapy
However, best outcomes for ibrutinib in second-line
Graph adapted from: Rule S, et al. 2015.1
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PFS and OS by prior line of therapy; 3.5-year follow-up of ibrutinib-treated relapsed/refractory mantle cell lymphoma patients: pooled analysis
Median PFS was just over two years in patients with one prior line of therapy
Patients censored from OS analysis upon study discontinuation. 1. Rule S, et al. Presentation at the 2018 Korean Society of Hematology Conference and 59th Annual Meeting. Abstract 57.
OS
Median NR (36.0–NE)
Median 22.5 mo(16.2–26.7)
PFS
Median 25.4 mo(17.5–57.5)
Median 10.3 mo(8.1–12.5)
Median PFS overall (95% CI): 12.5 (9.8–16.6) months Median OS overall (95% CI): 26.7 (22.5–38.4) months
Patients at risk
1 prior
> 1 prior
99
271
81
193
66
147
61
117
55
97
51
79
47
67
38
60
36
54
31
47
27
43
16
30
12
22
5
12
3
5
2
2
2
1
2
1
0
0
Patients at risk
1 prior
> 1 prior
99
271
88
227
81
186
70
158
66
139
66
122
59
103
50
83
46
68
41
59
36
50
20
37
15
29
8
16
4
8
3
3
3
2
2
2
0
1
0
0
NE: not estimable.
Graphs adapted from: Rule S, et al. 2018.1
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• Ibrutinib had improved tolerability vs temsirolimus
– Fewer Grade ≥3 TEAEs: 68% vs 87%– Fewer discontinuations of study medication due to AEs:
6% vs 26%
• Most common side effects with ibrutinib were diarrhoea, fatigue, cough, thrombocytopenia and anaemia
• Grade ≥3 atrial fibrillation: 4% ibrutinib vs 1% tem
• Major bleeding: 10% ibrutinib vs 6% tem
• In the phase 1 trial (PCYC 1123), the prevalence of infection, diarrhoea, and bleeding was highest for the first six months of therapy and less thereafter2
1. Dreyling M, et al. Lancet. 2016; 287:770–8; 2. Wang ML, et al. N Engl J Med. 2013; 369:507–16.
Ibrutinib safety
AEs: adverse events; TEAEs: treatment-emergent adverse events.
Common TEAEs (20% or more of patients) in the safety population
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Learning points from case 1
• Management of the younger, fitter patient– Cytarabine-containing regimen
o Unclear which is best
– Role of ASCT
– Maintenance rituximab
• Management of relapse– Role of observation
– Ibrutinib vs second-line chemotherapy
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Adapted from: Haematological Malignancy Research Network. Incidence. [Accessed: July 2019]. Available at: www.hmrn.org/statistics/incidence
Median age in the UK is 73 years
>50% ‘too old’
Incidence of haematological neoplasms
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Case 2
• 74-year-old man, presented December 2017
• R cervical LN mass, ~6 x 4 cm; abdominal LNs, splenomegaly, BM infiltration
• Stage IVA
• MIPIc = 6.4 (intermediate-risk, median OS: 58 months)
• No comorbidities (aneurysm noted on CT scan)
• How would you manage him?
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Options
No standard of care– R-CHOP
– R-bendamustine
– VR-CAP
– R-chlorambucil
• Maintenance R
VR-CAP: bortezomib, rituximab, cyclophosphamide, doxorubicin, prednisone.
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Adapted from: Kluin-Nelemans HC, et al. N Engl J Med. 2012; 367:520–31.
R-CHOP vs FCR followed by IFN vs maintenance REuropean MCL elderly trial
Maintenance continued until progression
N=560 patients
FCR: fludarabine, cyclophosphamide, rituximab; Peg: pegylated.
R
A
N
D
O
M
I
S
E
D
R
A
N
D
O
M
I
S
E
D
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Improved results with maintenance R vs IFNα(R-CHOP patients)
• Median PFS NR for R-CHOP + R at a median follow-up of 36 monthsMedian survival not reached at median follow-up of 36 months
Improved results with R-CHOP vs FCR• Comparable response• Less haem toxicity• Fewer progressions (5% vs 14%)• Longer four-year survival (62% vs 47%)
Results favour R-CHOP followed by maintenance REuropean MCL Elderly Trial: Final results
1. Kluin-Nelemans HC, et al. N Engl J Med. 2012; 367:520–31.
OS, patients assigned to R-CHOP
Time since start of induction (months)
OS
(p
rob
ab
ility
)
Median follow-up: 36 months
P=0.0023
FCR, median: 36 months
R-CHOP, median: 77 months
Graphs adapted from: Kluin-Nelemans HC, et al. 2012.1
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• B-R vs R-CHOP (no maintenance)
• n=514 analysed (94 MCL)
• Non-inferiority margin 10%
• Comparable response rates
• PFS at 45 months= 35 months (B-R) vs 22 months (R-CHOP)
Data shown are for MCL subgroup.1. Rummel MJ, et al. Lancet. 2013; 381:1203–10.
Is R-bendamustine better than R-CHOP?
STiL NHL 1-2003 trial
B-R: bendamustine, rituximab; IQR: interquartile range.
Time (months)
Pro
bab
ility
PFS in histological subtypes of MCL
0 12 24 36 48 60 72 84 96
Graph adapted from: Rummel MJ, et al. 2013.1
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• BR vs R-CHOP and BR vs R-CVP; non-inferiority design
• n=447 randomised (74 MCL)
• R-CVP least effective overall
• BR non-inferior: ORR 97% (BR) and 91% (R-CVP/R-CHOP); p=0.0102
• PFS/OS not reported
Data shown are for MCL subgroup.1. Flinn IW, et al. Blood. 2014; 123:2944–52.
Is R-bendamustine better than R-CHOP?BRIGHT trial
R-CVP: rituximab, cyclophosphamide, vincristine, prednisone; SD: stable disease.
Table adapted from: Flinn IW, et al. 2014.1
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BR R-CHOP
How well tolerated is R-bendamustine?
BRIGHT trial2
STiL NHL 1-2003 trial1
• Less Grade 3–4 neutropenia for BR vs R-CHOP (39% vs 87%)
• More Grade 3–5 infection for BR vs R-CHOP (12% vs 5%)
• More opportunistic infection (all grades) for BR vs R-CHOP (10% vs 7%)
§p<0.0001, Pearson’s χ-square test.1. Rummel MJ, et al. Lancet. 2013; 381:1203–10; 2. Flinn IW, et al. Blood. 2014; 123:2944–52.
Tables adapted from: Rummel MJ, et al. 2013;1
Flinn IW, et al. 2014.2
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Is there a role for maintenance rituximab after R-bendamustine?
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STiL NHL7-2008 trial1
NCT00877214 N=122 of 168 (73%)
European MCL Elderly2
NCT00209209 N=184 of 280 (66%)
RB RB + R R-CHOP + INF R-CHOP + R
DoRMedian since randomisation 57 months 68 months* 23 months NR
Rate at six years 49% 40% 12% 50%
OSMedian since randomisation NR NR 64 months NR
Rate at six years 70% 66% 50% 71%
*p=0.341. Rummel MJ, et al. Presentation at ASCO 2016. Abstract 7503; 2. Kluin-Nelemans HC, et al. N Engl J Med. 2012; 367:520–31.
STiL NHL7-2008 trial (MAINTAIN) Subgroup analysis1
Eligibility criteria • Patients with MCL• Not eligible for ASCT
PR
Rituximab every two months for two years (N=60)
RB
Up to six cycles
N=122
Cross-study comparison
Observation (N=62)
At this time (4.5 year follow-up) there is no PFS benefit for
maintenance R after first-line RB
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1. Robak T, et al. N Engl J Med. 2015; 372:944–53.
Is VR-CAP better than R-CHOP?• VR-CAP (LYM-3002 trial)
• Untreated MCL unsuitable for transplant
• No maintenance rituximab
bortezomib
Diagram adapted from: Robak T, et al. 2015.1
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1. Robak T, et al. N Engl J Med. 2015; 372:944–53; 2. NICE. Technology appraisal 370. [Published: October 2015], [Accessed July 2019]. Available at: www.nice.org.uk/guidance/ta370.
VR-CAP leads to longer PFS than R-CHOP1
• N=487 patients
• ORR 92% vs 89%
• VR-CAP superior for CR rate (53% vs 42%) and PFS (25 vs 14 months)
• But more toxic…
• SAEs 38% vs 30% – Peripheral neuropathy 30% vs 27%– Thrombocytopenia 57% vs 6%– Neutropenia 85% vs 67%– Infections 21% vs 14%
NICE approval: December 2015 as option for first-line treatment for adult patients unfit for transplant2
ITT: intent-to-treat; SAEs: serious adverse events.
PFS according to independent review (ITT population)
Graph adapted from: Robak T, et al. 2015.1
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• CGA ‘fit’ patents aged 61–80 years with untreated MCL
Induction phase x 6 cycles q3 weeks
rituximab(375 mg/m2)
bendamustine(70 mg/m2)
cytarabine
(500 mg/m2)*
Day 1 2 3 4*Former 800 mg dose too toxic.Visco C, et al. Lancet Haematol. 2017; 4:e15–23
Does cytarabine improve survival when added to R-B?
FIL phase 2 trial of RBAC-500
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Does cytarabine improve survival in elderly MCL?• n=57 evaluable, median age 71 years
(range: 61–79)• 91% advanced stage disease • 45% high MIPI• 9% blastoid
Efficacy:• ORR 96% (CMR 93%)• MRD-negative: 76% blood, 55% marrow • Two-year PFS 81 +/- 5%
Toxicity:• ~50% Grade 3–4 neutropenia
and thrombocytopenia• 6% febrile neutropenia• 26% stopped due to toxicity
FIL phase 2 trial of RBAC-500
Improved two-year PFS, randomised data needed to establish a PFS or survival advantage for addition of cytarabine
Median 5.3 cycles delivered/patient. Median follow-up of 34 months.1. Visco C, et al. Lancet Haematol. 2017; 4:e15–23. CMR: complete molecular response.
Graph adapted from: Visco C, et al. 2017.1
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Case 2 management
• Patient received R-bendamustine on clinical trial
• Achieved CR after six cycles
• On maintenance R for two years
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Learning points from case 2
• Multiple options for first-line treatment of patients“unsuitable” for HDT and transplant
• Influenced by:– Age
– Fitness
– Comorbidities
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Case 3
• WF, 65-year-old female
• Previously fit and well, ECOG 0
• Presented in April 2017 with fatigue, weight loss and enlarging neck nodes
• CT scan: bilateral neck, axillae, mediastinal, abdominal, retroperitoneal, groin nodes. Spleen 16.9 cm
• Core biopsy neck node:– MCL: CD20, CD5, cyclin D1 and SOX11 positive. Ki67 40–50%;
Classical MCL
ECOG: Eastern Cooperative Oncology Group.
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Case 3
• Stage IVB
• Hb 116, WCC 4.0, lymph 1.7
• LDH 423
• MIPI score 6.9 (high-risk)
• Rituximab and high-dose cytarabine 2 g/m2 (age >60 years)
• Completed six cycles and achieved VGPR
• BEAM-conditioned ASCT, November 2017
• Commenced maintenance R
• Day 100 assessment: VGPR. Largest node (periportal) 19x10 mm, spleen 10.9 cm, bone marrow clear
VGPR: very good partial response.
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Case 3
• Remained well until August 2018
• Presented with fevers, sweats and fatigue (PS 3)
• Subsequently developed nausea, reduced appetite and headache
• Documented fevers to 39⁰C; blood cultures negative
• 22/8/18: Hb 140, platelets 145, WCC 5.0, neutrophils 3.8, lymph 0.5
• Cr 61, albumin 42, bilirubin 17, ALT 73, AST 32, ALP 70; LDH 277 – rose to 469 over two weeks, CRP <5
• CT NCAP: no LNs. Spleen 10.5 cm. No focus of infection
ALP: alkaline phosphatase; ALT: alanine aminotransferase; AST: aspartate aminotransferase; Cr: creatinine;
CRP: C-reactive protein; NCAP: neck-chest-abdomen-pelvis.
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Case 3
• CT head: right frontal lobe lesion with surrounding oedema
• MRI brain: right frontal lobe mass involving the corpus callosum. Local mass effect. Possible additional mass in right temporal lobe
• Differential diagnosis: primary brain tumour or relapsed lymphoma
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Case 3
• Biopsy frontal lobe tumour
• Cerebral involvement by MCL
• Positive: CD5, CD20, BCL2, cyclin D1, SOX11
• Ki67 proliferation 70%
• Thought to represent blastoid variation of MCL on this occasion
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CNS involvement in MCL
• Rare at diagnosis
• 4.1–7.8%
• Median onset 15–20 months
• Ki-67 and blastoid histology
• >90% leptomeningeal
• Poor survival: 3–8 months
Cheah et a. J Clin Oncol. 2016; 34:1256–1269; Chihara et al. Annals Oncol. 2015; 26:966–973; Conconi et al. Leuk & Lymphoma. 2013; 54:1908–1914; Chea et al. Annals Oncol. 2013; 24:2119–2123.
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Case 3
• Treatment options?– Ibrutinib single agent
• Patient 64 years old, but fit
• Started dexamethasone 8 mg bd post-biopsy
• Weaned quickly due to side effects (agitation)
• Ibrutinib started three weeks post-biopsy (8/10/18)
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Case 3
Response:
• Fevers and sweats resolved within one week
• Nausea and headache also resolved quickly, 1–2 weeks
• LDH normalised
• Fatigue improving weekly
• No side effects from ibrutinib
• MRI of brain repeated post-five-week treatment with ibrutinib
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MRI brain: five weeks post-treatment with ibrutinib
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Comparison: pre- and post-ibrutinib (five weeks of treatment)
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Case 3
As of 22/11/18:
• Seven weeks on ibrutinib
• Off dexamethasone
• Well
– No headache or nausea
– No B symptoms
• Energy improving – out to shops, travelling by train, etc.
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BSH treatment algorithm for MCL
Diagram adapted from: McKay P, et al. Br J Haematol. 2018; 182:46–62.
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Beatson Cancer Centre
Thank you for listening
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TP53 mutations identify younger mantle cell lymphoma patients who do not benefit from intensive chemoimmunotherapy
• 183 patients on MCL2 and MCL3 studies
• Genomic studies on DNA from diagnostic BM
Inferior outcomes noted with mutations of:
– TP53 (11%)
– NOTCH1 (4%)
– delTP53 (16%)
– CDKN2A (20%)
• MIPI and MIPI-c
• Blastoid morphology
• Ki67 >30%
• TP53 mutation associated with Ki67 >30%, blastoid morphology, high-risk MIPI, inferior response to induction and HDT
• Multivariate analysis – only TP53 mutation retained prognostic impact on OS
• TP53 mutated patients:
– Median OS 1.8 years
– 50% relapsed at one year
• TP53 unmutated cases:
– Median OS not reached, p<.0001
Eskelund CW, et al. Blood. 2017; 130:1903–10.
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Prognostic impact of TP53 mutations on OS in MCL
Graph adapted from: Cohen JC. Blood. 2017; 130:1876–77.
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TP53-mutated patients
• Difficult not to offer HDT in younger patients
• Consider experimental front-line therapy with novel agents, e.g. R-I-Len
R-I-Len: rituximab, ifosfamide, lenalidomide.