🔑 for those discussing or presenting results at @ASH_hematology! This also applies to us TWEETING about results #ASH25
- Present a balanced appraisal - remember, we are caregivers and scientists, not cheerleaders
- do not minimize toxicities or QOL!
https://t.co/fLJYnPZrKR
I don't practice myeloma but this is a very meaningful de-escalation trial with immediate global implications. This should set an example for the why and the how of de-escalation trials in oncology.
I was very impressed not just with the results but also with the methodology. This was not designed to show non-inferiority of fixed-duration over indefinite therapy but was appropriately designed to show superiority of indefinite over fixed-duration. As it should be. https://t.co/NEzaswuODs
Congratulations to the investigators, as well as to patients and health care systems.
⚽🩸 CHECKING OFFSIDE…
A leukemia cell has crossed the diagnostic line.
This week on WolverHeme Happy Hour, Dr. Dale Bixby joins us in the VAR booth for:
“VAR Review with Dr. Bixby: Reversing the Call on MPAL”
https://t.co/ZHabm1g616
➡️ Last year we published use of #pocketdex in patients on teclistamab.
🧠 🤓 Now hot off the press as a full manuscript, see how dex for low-grade CRS is safe and effective with talquetamab
https://t.co/H8ODIQ08Xl
The hottest take in myeloma right now:
☠️ “Cilta-cell is dead.”
With bispecifics delivering impressive results has CAR-T lost its crown?
We brought in @ManniMD1 for a discussion that every myeloma clinician should hear.
🎧 Listen here: https://t.co/emTP22tNgw
@JMaakaron Yup! We used to not know what to do for these pts, so we tried HD MTX prophy, hoping it would ⬇️ CNS relapse. But maybe we were wrong.
Gotta make clinical judgements with data we have, esp when there isn’t going to be an RCT! Another good editorial 👉 https://t.co/T5z2Fy9K92
A really well done analysis (n=1923!). In ultra high risk pts, no benefit to HD MTX in preventing cns relapse. Authors did a good job w/propensity score analysis for possible confounders
This practice comes with serious risks & patient burden, and it doesn’t seem to help.
It’s about time we remove CNS ppx in DLBCL from the NCCN guidelines.
High-Dose Methotrexate as CNS Prophylaxis in Ultra High-Risk Large B-Cell Lymphoma: An International Multicenter Analysis | Journal of Clinical Oncology https://t.co/cWhKcpvIzh
Does HD-MTX ppx reduce CNS relapse even in ultra-high-risk LBCL? #lymsm
- >1900 pts, all CNS-IPI 5-6; testicular, renal/adrenal, breast; ≥3 EN sites
- 3-yr CNS relapse: 9.3% (no HD-MTX) v 8.1% (HD-MTX), adjusted HR 1.13 [0.82, 1.57]
- no diff in isolated CNS relapse: 5.9% v 5.7%
- no diff in relapse rates for any high-risk subtypes
- DHL/THL not included
End of HD-MTX ppx, although DHL/THL is still a question. cc @tobyeyre82@mattwilson2287
https://t.co/80zAeJmlXo
@Eddie_Cliff@NatRevClinOncol@rajshekharucms@ManniMD1@DianaNrco Nice commentary. I mostly agree as I outlined in this friendly exchange with @Rfonsi1: https://t.co/vvUvMqtMxF
Cilta-cel still has a role after bsAb or before in pts who prefer it and fully understand risk. There are still many data gaps.
Hot off the press. Published just now in @NatRevClinOncol led by @OncologyBGLab current fellow @JavierDavidBen2 with past fellow @lateuwen !
https://t.co/NpHcI8vg6P
We dissect the RECITE trial and conclude that the excitement re romiplostim for chemo induced thrombocytopenia misses the point- we are supposed to treat patients, not platelets.
@JMaakaron@WolverHeme@Papa_Heme@FeeneyTate@ajperissinotti I’m guessing Joe didn’t listen to the episode or read the paper. Must have missed that quote 😂
It’s a tongue in cheek title about biases and beliefs that we ALL have in medicine, and we go through our own :)
Read the paper, it’s pretty cool
https://t.co/jbfQxVuUhk
Check out our latest episode "Cult-Like Thinking in BMT" with @Papa_Heme@FeeneyTate@ajperissinotti@Berninini! Comment below 👇what "cult-like" practices you've seen in medicine! https://t.co/x1JXzfSnfA
I know running clinical trials is tough but that doesn’t mean us clinicians have to accept the results as the new standard if we find the results not applicable to our current practice.
Young clinicians don’t need to make critical appraisal their primary academic focus, but it is a skill every clinician MUST learn as early as possible. No trial is perfect but understanding the implications of imperfections is 🔑.
And remember - critique trials, not people!
I know some have become experts at clinical appraisal and clinical trial critique. It’s important to have this dialogue and it helps physicians and patients understand the drawbacks of a given trial. But my advise to young investigators is to best not to make it your primary academic output.
Secondly, when critiquing it’s also worthwhile remembering that the investigators of trials may also fully aware of the issues but there are many barriers and often we have to choose between not doing a trial at all versus compromising. Perfect trials are not common; we can usually find some fault with almost all trials. So we must strive to avoid rudeness and condescension.
Third, try if possible to lead a clinical trial or at least get engaged with someone who leads trials and get a feel for the various stakeholders who have veto power during trial design, and more importantly the various competing priorities for what the trial seeks to accomplish, it will be easier to understand why a specific control arm was chosen, or a why a specific endpoint was chosen, even though you may think they are the wrong ones.