๐ง๐๐ฟ๐ป๐ถ๐ป๐ด ๐ฃ๐ฎ๐ด๐ฒ๐ ๐ง๐๐ฒ๐๐ฑ๐ฎ๐ | #ASH2026 edition
๐ญ๐ฌ ๐บ๐๐ฒ๐น๐ผ๐บ๐ฎ ๐ฎ๐ฏ๐๐๐ฟ๐ฎ๐ฐ๐๐ ๐โ๐บ ๐๐ฎ๐๐ฐ๐ต๐ถ๐ป๐ด ๐ณ๐ฟ๐ผ๐บ ๐๐ป๐ฑ๐ถ๐ฎ
With teclistamab (Tec), elranatamab (Elra), talquetamab (Tal) and SC Dara in our toolkit, my questions are about sequencing, duration, safety and access.
๐ญ. ๐ ๐ผ๐ป๐๐บ๐ฒ๐ป๐ง๐๐-๐ฒ | #426
At 13.4 monthsโ median follow-up, Tec+Tal vs EPd/PVd: PFS HR 0.11; Tal+Pom also improved PFS/OS. ~80% were anti-CD38-refractory. Watch the planned 26-cycle bispecific cap and immunoglobulin replacement burden.
๐ฎ. ๐ ๐ฎ๐ด๐ป๐ฒ๐๐ถ๐๐ ๐ -๐ฑ | #424
Elra vs DPd: PFS HR 0.56. Only 5.9% had prior anti-CD38 exposure: important when interpreting this for Dara-refractory relapse.
๐ฏ. ๐ช๐ต๐ถ๐ฐ๐ต ๐ฏ๐ถ๐๐ฝ๐ฒ๐ฐ๐ถ๐ณ๐ถ๐ฐ ๐ป๐ฒ๐ ๐? | #2205
In a retrospective 187-patient series, 136 target-switchers had median PFS ~4 months with the second bispecific. Activity remains possible; the best order is unresolved.
๐ฐ. ๐๐ฎ๐ป ๐๐ฒ ๐๐๐ผ๐ฝ ๐ฏ๐ถ๐๐ฝ๐ฒ๐ฐ๐ถ๐ณ๐ถ๐ฐ๐? | #845
43 selected responders stopped; 12-month treatment-free PFS was 85.4%. Relevant to financial and infectious toxicity; selection bias limits conclusions.
๐ฑ. ๐๐ป๐ณ๐ฒ๐ฐ๐๐ถ๐ผ๐ป ๐ฝ๐ฟ๐ฒ๐๐ฒ๐ป๐๐ถ๐ผ๐ป | #2275
Modelled 1-year grade โฅ3 infection risk: 21.0% with continuous vs 38.3% with observed immunoglobulin replacement. Supportive care belongs in the budget; replacement was not randomized.
๐ฒ. ๐ช๐ต๐ผ ๐๐ต๐ผ๐๐น๐ฑ ๐ฟ๐ฒ๐ฐ๐ฒ๐ถ๐๐ฒ ๐ง๐ฎ๐น? | #934
Among 43 IHC-evaluable Tal patients, none of 19 with low/negative GPRC5D responded. Could pretreatment IHC improve selection? Retrospective data need validation.
๐ณ. ๐ฃ๐๐ฅ๐ฆ๐๐จ๐ฆ | #111
After ASCT, 236 patients stopped Dara per protocol; lenalidomide continued. Eligibility required โฅ24 months maintenance, โฅCR and โฅ12 months sustained MRD negativity by serial NGS.
๐ด. ๐๐ค๐จ๐๐๐ | #112
In high-risk smoldering MM, 7-year OS: 87.8% vs 78.7% with 3 years of SC Dara vs monitoring. Risk definitions and reliable follow-up are central before treating asymptomatic patients.
๐ต. ๐๐ฒ๐น๐ฎ๐ป๐๐ฎ๐บ๐ฎ๐ฏ ๐ฒ๐๐ฒ ๐บ๐ผ๐ป๐ถ๐๐ผ๐ฟ๐ถ๐ป๐ด | #419
A 30-patient BelaRd study in newly diagnosed MM tests symptom-guided dosing. Both groups still had eye examinations. A practical implementation question for belantamab.
๐ญ๐ฌ. ๐๐ซ๐๐๐๐๐๐๐ฅ-๐ฅ๐ฅ๐ ๐ : ๐ถ๐ฏ๐ฒ๐ฟ๐ฑ๐ผ๐บ๐ถ๐ฑ๐ฒ | #114
IberDd vs DVd: 10โปโต flow MRD-negative CR, 41.1% vs 20.7%. PFS results await presentation. A CELMoD future-access watch: 84.3% grade 3/4 neutropenia; anti-CD38-refractory patients excluded.
For MRD, 10โปโต is not 10โปโถ; matching sensitivity also does not automatically make flow and NGS interchangeable for a trialโs treatment decisions.
These are abstracts to examine closely, with fuller data still to come.
#TurningPagesTuesday #MMsm
๐๐ผ๐ ๐น๐ผ๐ป๐ด ๐ฐ๐ฎ๐ป ๐ฟ๐ฒ๐บ๐ถ๐๐๐ถ๐ผ๐ป ๐น๐ฎ๐๐ ๐ฎ๐ณ๐๐ฒ๐ฟ ๐ฏ๐ถ๐๐ฝ๐ฒ๐ฐ๐ถ๐ณ๐ถ๐ฐ ๐๐ต๐ฒ๐ฟ๐ฎ๐ฝ๐ ๐๐๐ผ๐ฝ๐?
Iโm inviting colleagues across India to collaborate on ๐๐๐ก๐๐ง๐-๐ ๐ ๐๐ป๐ฑ๐ถ๐ฎ, studying treatment-free outcomes after stopping #BiTesโ in #MutipleMyeloma.
We plan to include:
โข ๐ฅ๐ฒ๐๐ฟ๐ผ๐๐ฝ๐ฒ๐ฐ๐๐ถ๐๐ฒ ๐ฐ๐ฎ๐๐ฒ๐: Treatment already stopped in CR because of infections, toxicity, financial constraints or a response-led decision.
โข ๐ฃ๐ฟ๐ผ๐๐ฝ๐ฒ๐ฐ๐๐ถ๐๐ฒ ๐ฐ๐ฎ๐๐ฒ๐: Patients in whom discontinuation is planned, with systematic follow-up.
๐ฃ๐ฟ๐ผ๐ฝ๐ผ๐๐ฒ๐ฑ ๐ฐ๐ฟ๐ถ๐๐ฒ๐ฟ๐ถ๐ฎ:
โข โฅ6 months of BiTe monotherapy
โข Confirmed CR or better within four weeks before stopping
We will assess treatment-free survival, relapse, infections, IVIG needs and retreatment outcomes-including early failures.
๐๐๐ฒ๐ป ๐ผ๐ป๐ฒ ๐ฒ๐น๐ถ๐ด๐ถ๐ฏ๐น๐ฒ ๐ฐ๐ฎ๐๐ฒ ๐ถ๐ ๐๐ฒ๐น๐ฐ๐ผ๐บ๐ฒ. Please DM for details/any patients.
Synopsis attached. Prospective enrolment will follow protocol finalisation and required.
#mmsm
@Papa_Heme For us bmt is the easiest way to stay rich when one suffers from myeloma ! It gives us PFS which helps to see the sun rise of 2030 by which time we will have generic bites and car t cell at a fraction of the cost
Everspan is innovation - whole genome sequencing plus the preventive genomics with proteomics and whole body mri. @deepigoyal along with wearable device with a longitudinal follow up