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Explore cases using Daratumumab in myeloma patients, detailing demographics, outcomes, toxicity, and impact on the healthcare system. Follow three patient journeys with insights on experiences and challenges.
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Clinical cases and experiences of using Daratumumab therapy in the DGH setting Dr Rachel Hall Consultant Haematologist Royal Bournemouth and Christchurch NHS Foundation Trust
Clinical use of anti-CD38 MAb in Myeloma • Setting: open labelled Daratumumab single agent in • Relapsed after 3 prior therapies (IMID and PI x 2 cycles) • Double refractory (PD within 60 days of last IMID/PI) • Weekly Dara infusions cycles 1 and 2 (8 doses) • Fortnightly Dara infusions cycles 3-6 (8 doses) • Monthly Dara infusions cycle 9 and thereafter
Clinical use of anti-CD38 MAb in Myeloma • 3 clinical cases • Demographics • Outcomes • Toxicities • Impact on DGH work load • Experiences of staff with the drug
Case 1: GW 52yr man • Diagnosis IgG kappa aged 47 yrs Jan 2010 Hants • Renal impairment: Creatinine 215 • Anaemia: Hb 95 • ISS 3 • Kappa 36,850 • No bone lesions on skeletal survey • FISH not performed • MGUS 2002 • NIDDM
Case 1: GW 52yr man • CTD commenced x 6 cycles no issues • VGPR achieved • Renal function normal • Peripheral sensory neuropathy • HDM ASCT Oct 2010 • VGPR post • April 2012 PD • Lenalidomide/Dexa x 7 cycles • PD on treatment (refractory)
Case 1: GW 52yr man • Feb 2013 Velcade/Dexa x 4 cycles; CR • July 2014 Velcade/Dexax 4 cycles; VGPR • ‘no funding for continued cycles’ • Jan 2016 PD: referred for consideration of clinical trial • Kappa 860, IgG15g (pp10g) • Creatinine normal • Hb normal • ECOG 0 • Eligible for Daratumumab study: commenced March 2016
Case 1: GW 52yr man • Ist infusion nasal congestion: • Pre med M-Pred D1, oral Prednisolone D2-3 • D1 Antihistamine, Paracetamol • No further infusional reactions • From #1 D15 down to 3 hour infusion • IDDM medication changes required (Pred related) • In a PR (monoclonal pp 4g) • Kappa 135 with ratio 19 • Attending once monthly for 3 hours • No side effects • Working and looking after 11 year old son
Case 2: AS 69yr man • Diagnosis IgG kappa aged 55yr 2002 London • Anaemia, hypercalcaemia, bone disease • CTD x 6, Mel 200 ASCT Nov 2002 • Thalidomide maintenance study Feb 2003 • Feb 2007 PD: Dexa added in to Thal maintenance • Oct 2008 PD: VCD #5 (PR) • 2nd Mel 200 ASCT July 2009
Case 2: AS 69yr man • March 2011 PD: Lenalidomide/Dexa (PR) to Sept 2013 • Dec 2013 PD: MUK 6 (Pano/Vel/Thal/Dexa) 16 cycles (PR) • Maintenance panobinostat to March 2015 • Moved to Poole 2014 • May 2015 PD: BCMA antibody conjugate phase 1 trial • May 15 – April 16 (MR) • PD with bony lesions R humerus and L5 spine • Bone pain +++ Referred to Poole for local RT to bone lesions
Case 2: AS 69yr man • Latest bony relapse Aug 2016; • # R humerus post RT requires humeral nail • Fall results in # L clavicle • Bone marrow with 10% PC • FISH: 1q21 gain • Hb and creatinine normal • IgG 13g (pp12g) • Kappa 206, ratio 36 • ECOG 2 • Eligible for Daratumumab study: commenced Sept 2016
Case 2: AS 69yr man • Ist infusion nasal congestion and wheeze: • Pre med M-Pred D1, oral Prednisolone D2-3 • D1 Antihistamine, Paracetamol • No further infusional reactions • From #1 D15 down to 3 hour infusion • In a PR (monoclonal pp 3g) • Kappa 29 with ratio 5.3 • Attending once weekly for 3 hours • No side effects • Bone pain improved, off morphine
Case 3: SR 67yr woman • Diagnosis IgA lambda aged 57yr 2008 Bournemouth • Likely MGUS IgA 6.7g W+W • 2014: lambda 4149, IgA 0.5g • Hb 104, creatinine normal, B2m 7.4 • Marrow 22% PC • FISH: sample unsuitable for processing • Skeletal survey normal • Feb 2014: CTD x 6 (PR lambda 369) • Sept 2014: Mel 200 ASCT (VGPR) • August 2015: PD lambda 957, quickly rising to 5000 Nov 15
Case 3: SR 67yr woman • Nov 15: MUK 5 study: Carfilzomib/Cyclo/Dexa • Initial PR • Refractory disease cycle 5 lambda 1609 May 16 • Holiday to Ireland • July 16 lambda 9750, sternal and L acetabular lesions • Commenced Lenalidomide/Dexa (+Ixazomib) • PR to lambda 1780 Aug 16 • Sept 2016 PD lambda 5000, ^ sternal lesion ECOG 2 • Eligible for Daratumumab study: commenced Oct 2016
Case 3: SR 67yr woman • 3 infusions • Minor infusional reaction with #1 D1 • #1 D22 bloods: • Hb 77 g/L, WCC 2.0 (neuts 0.8), platelets 4 x 109/l • Creatinine 174, eGFR 20 • Expanding sternal lesion • PD, taken off trial, palliative care
Toxicities/tolerability • Minimal toxicities • Grade 1-2 infusional reaction in all patients D1 #1 • ‘instant flu’ • Nasal drip • Bronchospasm • Nausea • Stop infusion, antihistamine, paracetamol • All D1 infusions completed fully • No further reactions with later doses • 3 hour infusions from D15 #1
Toxicities/tolerability • Mild ALT / AST rise in few patients • Resolved spontaneously, no delays • All anaemic patients (except rapid PD patient) Hb resolved to normal on treatment. • No neutropenia or thrombocytopenia
Impact on service provision • Heavy impact on day unit initially • Mon - Sat 8am – 6pm • 1st infusion up to 10 hours • Close nursing monitoring /observations • Intervention for reactions • Once #1 D15 3 hour infusion rate: less onerous • Monthly infusions very well tolerated by all
Summary • Current experience in heavily pre treated patient group +/- refractory disease • Very well tolerated in all with minimal toxicities • Excellent responses in most patients • NOT double refractory / aggressive disease group • Quick responses (PR post cycle 1) • ? Duration of responses