1/ Our latest - @JAMAOncology Viewpoint! Ablative radiotherapy has a dual effect on metastatic cancer that changes how we should interpret progression after treatment.
@DrewMoghanaki@rweichselbaum@piet_ost We are pleased to share PersonaCRC - the first clinically validated biomarker for oligometastatic CRC - is available to order: https://t.co/IBAFlTat6C
Based on prior work from our group:
https://t.co/p6L6OKLHcA
https://t.co/3g74FHMxuY
https://t.co/Lb8bfMQsur
@DrewMoghanaki@rweichselbaum@piet_ost We are pleased to share PersonaCRC - the first clinically validated biomarker for oligometastatic CRC - is available to order: https://t.co/IBAFlTat6C
Based on prior work from our group:
https://t.co/p6L6OKLHcA
https://t.co/3g74FHMxuY
https://t.co/Lb8bfMQsur
Hot Topics in Lung Cancer Basic and Translational Research is coming up! Submit your abstract by april 15 and come and visit in (hopefully) sunny Dublin!
Speakers include Drew Pardoll, @FSkoulidis@DrJNaidoo@CottrellLab@SeanPitroda among a glittering line up! #lcsm
IFN signaling at the nexus of the radiotherapy response in malignant peripheral nerve sheath tumors: https://t.co/an90PV9wdD
Sean P. Pitroda @SeanPitroda, Ralph Weichselbaum @rweichselbaum & team @UChicago provide a Commentary on Iowis Zhu et al.: https://t.co/e5hJOOyM4W
💬 Viewpoint: The badscopal effect following ablative radiotherapy signals not failure but biological reorganization, prompting serial metastasis-directed therapy in selected patients. https://t.co/aNk5EQpv4i
@ebludmir@ChadTangMD@drdavidpalma@CJTsaiMDPhD Agree - Important to develop additional data in this clinical context to move treatment paradigms forward and test these preclinical predictions.
1/ Our latest - @JAMAOncology Viewpoint! Ablative radiotherapy has a dual effect on metastatic cancer that changes how we should interpret progression after treatment.
I think Sean's thinking here has been clear from the get go. There's no claim of accelerated progression of non-irradiated mets in the SBRT arm compared to the non-SBRT arm.
The claim is simply that one biological driver of out-of-field progression, when it occurs post-SBRT, acknowledging it occurs LESS FREQUENTLY in the SBRT arms of the trials mentioned, may be amphiregulin driven immune suppression. His work has identified a druggable target that may make the SBRT arms of oligomet trials even more successful than they've already been. Kudos to him! #radonc
@CJTsaiMDPhD@drdavidpalma@NiuSanford@piet_ost@rweichselbaum We don't know the source of post-RT mets. Easy to assume pre-existing lesions destined to grow, but may be more complex. RT controls treated lesions and reduces seeding, yet progression occurs. Why not study mechanisms rather than assume we understand them?