Bhagirath Dholaria, MD

207 posts

Bhagirath Dholaria, MD

Bhagirath Dholaria, MD

@DholariaMD

Katılım Eylül 2018
100 Takip Edilen340 Takipçiler
Decera Clinical Education
Decera Clinical Education@DeceraClinEdu·
🔥 Featured Faculty Spotlight: @MichaelDJain As we prepare for #ASH2025, we’re honored to highlight Dr. Michael D. Jain, a leading expert in cellular immunotherapy whose work continues to shape the future of lymphoma treatment. Dr. Jain brings deep expertise in CAR T-cell therapy, translating emerging evidence into practical, patient-centered guidance for clinicians navigating this rapidly evolving landscape. Join us in Orlando for our Hematology Symposia!! It's not too late to register for in-person or online attendance: bit.ly/4nyUrXZ #HematologySymposia #DeceraClinicalEducation
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Bhagirath Dholaria, MD
Bhagirath Dholaria, MD@DholariaMD·
@JanakiramMurali @mmejia91 @SusanBal9 not surprised. We have not found any benefit of dex or toci prophy in ICANS prevention either with CD19 CAR T. Need mechanistic studies first to define pathophysio of delayed NT before we start planning interventions.
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Murali Janakiram
Murali Janakiram@JanakiramMurali·
Interesting abstract on suppressive dexamethasone, ALC and delayed neurotox -single-center retrospective, N=56, -From the results no effect of suppressive dex for ALC >3 on delayed neurotox. Need to consider different strategies. a/w publication ALC highly predictive meetings-api.hematology.org/api/abstract/v…
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Frederick L. Locke
Frederick L. Locke@DrFredLocke·
From our first transplant in 1989 to our 10,000th today 🎉 We celebrated with our faculty, nurses, pharmacists & APPs (photo: faculty), with deepest gratitude to the patients & families who entrust us with their care. @MoffittNews
Frederick L. Locke tweet media
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Rahul Banerjee, MD, FACP
Rahul Banerjee, MD, FACP@RahulBanerjeeMD·
@End_myeloma @bdermanmd @Rfonsi1 Very well stated as always!! Although you all can guess what I would say... If you had to draw a line throuh Dara/V/R/d to delineate the drugs that actually matter, I know where I'd draw mine 🤣
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Luciano J Costa
Luciano J Costa@End_myeloma·
The S-MRD-5 vs. S-MRD-6 created some good questions and surprised some. It comes down to the difference between "what produces the best classifying model" and "what is the best result to have". They are often different things. To use an analogy, and still stay in MM: B2M 1/x
Rahul Banerjee, MD, FACP@RahulBanerjeeMD

As usual, masterfully written (no pun intended) by @End_myeloma @smith__giri et al. #MMsm sMRD- at 10^-5 performed better than sMRD- at 10^-6. Turned many heads at #ASH24. May be small n, or: 👇🏼 Maybe sMRD ≤10^-5 catches the most pts and gives us the prognostic info we need!

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Vincent Rajkumar
Vincent Rajkumar@VincentRK·
So the belantamab ODAC is on. Personally I hope the belantamab is approved for relapsed myeloma. It has many advantages and there is a unique need for the drug in relapsed refractory myeloma. If available we will have an important option to tackle very difficult situations for which other options are not possible or far more riskier. See thread. Yes there is a problem with belantamab dosing. But there is no question the drug works and with appropriate modification of dose frequency we won’t have the type of eye toxicity that’s been seen in the phase III trials. Note that we did not have the best dose for many myeloma drugs when they were first approved. Many are just not used in the dose that they were approved at: bortezomib, pomalidomide, carfilzomib, even bispecifics. But there is no question lives were saved due to early approval of these drugs even though the dosing was not ideal in regulatory trials of these drugs. It’s a balance between the risk of approving an effective life saving drug tested with a less than ideal dose in the regulatory phase III versus the risk of delaying approval and access by a very long time to find the best dose. In the case of belantamab, that would be years. In clinical practice we are able to modify dosing to the extent that’s not possible in a clinical trial. We also have learnt a lot since the regulatory trials already that help with optimizing dosing. So I hope for the best because in my opinion myeloma patients with relapsed refractory disease need belantamab available as an option.
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Luciano J Costa
Luciano J Costa@End_myeloma·
Patients with standard risk MM treated with QUADs + ASCT, achieving S-MRD negativity and stopping therapy have <10% risk of progression or MRD resurgence in 4 years!
Luciano J Costa@End_myeloma

Optimal MRD-based end point to support response-adapted treatment cessation in NDMM. ⁦@smith__giri⁩ ⁦@nsc_natalie⁩ ⁦@SusanBal9⁩ ⁦@DholariaMD⁩ ⁦@bhemato⁩ ⁦@Chhabra_mayo⁩ ⁦@KellyGodbyashpublications.org/blood/article/…

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Rahul Banerjee, MD, FACP
Rahul Banerjee, MD, FACP@RahulBanerjeeMD·
@HiraSMian I think primarily just P-BCMA-ALLO1 and the Caribou Camouflage one! I think the others are no longer in commercial development - more or less accurate, @DholariaMD ? Certainly there’s a role for these if infectious risks lower, especially if they work post-failure of auto CAR!
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Rahul Banerjee, MD, FACP
Rahul Banerjee, MD, FACP@RahulBanerjeeMD·
#DAVAWhistler great presentation by Ken Shain about allo-CARs in #MMsm myeloma. The list of abandoned candidates is almost as long as the number of patients treated on the remaining ones, but these do look quite promising! Easy to give, not as much lymphodepletion as before…
Rahul Banerjee, MD, FACP tweet media
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Bhagirath Dholaria, MD
Bhagirath Dholaria, MD@DholariaMD·
@bdermanmd @End_myeloma I have noticed this pattern too in last 3-4 yrs. Many requiring steroids. Also, 3 cases of severe auto-GVHD (bx proven) involving skin+ gut. Not sure if there is a pattern here.
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Ben Derman
Ben Derman@bdermanmd·
13% incidence of engraftment syndrome. Seems odd that the median cd34+ cell dose was only 1.75x10^6/kg (we aim for 3-5 & always >2). Dara was used only for patients who needed add’l disease reduction before transplant. Despite these peculiarities, we have noted more ES in recent years which coincides with quad induction. Would be really interesting to know if patients collected in the quad era who defer transplant have higher incidence of ES when they proceed to transplant later.
Muzaffar Qazilbash@Transplant_Doc

Daratumumab-based induction may increase the risk of engraftment syndrome (12.7%) after an autoSCT for MM. #mmsm #bmtsm @BMTjournal nature.com/articles/s4140…

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Bhagirath Dholaria, MD
Bhagirath Dholaria, MD@DholariaMD·
@MediHumdani donor original T LGL. I have a few who recovered ANC with FK taper, rest needed low dose steroid/MTX.
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Mehdi Hamadani, MD
Mehdi Hamadani, MD@MediHumdani·
❓Quiz ⏲️⏲️: 68yr old MDS patient day +167 post ptCY-based matched Allo HCT. No #GvHD - On 0.5mg of tacrolimus - CBC showed WBC of 2.0; platelets 204. ANC 600/uL - On exam no adenopathy - T-cell chimerism fully donor - PB flow shown below Diagnosis & Rx?? #bmtsm Allo 🦪
Mehdi Hamadani, MD tweet media
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IACH
IACH@TheIACH·
📢 Don't miss the next @TheIACH post #ASH24 webinar: the Most Important Cellular Therapy Studies 🎙️ Speaker: Dr. Bhagirathbhai Dholaria 🗓️ Friday, January 17, 2025 🕔 5 PM CET 🎟️ Register for FREE: 👉 bit.ly/3DSZHni @DholariaMD @Mohty_EBMT
IACH tweet media
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Bhagirath Dholaria, MD
Bhagirath Dholaria, MD@DholariaMD·
@MediHumdani Bi-specifics are currently at a stage where CAR T therapy was in early 2000. They will outpace CAR given ease of logistics, and combinations.
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Narendra Modi
Narendra Modi@narendramodi·
Historic and exemplary! Congratulations to Gukesh D on his remarkable accomplishment. This is the result of his unparalleled talent, hard work and unwavering determination. His triumph has not only etched his name in the annals of chess history but has also inspired millions of young minds to dream big and pursue excellence. My best wishes for his future endeavours. @DGukesh
Narendra Modi tweet media
International Chess Federation@FIDE_chess

🇮🇳 Gukesh D is the YOUNGEST WORLD CHAMPION in history! 🔥 👏

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