De-escalation, escalation and response-adapted therapy
Giving less treatment to patients who are doing well and more to those who are not, using a marker such as scan response, ctDNA or MRD to decide. The aim is to cure the same number of people with less harm.
Examples: omitting chemotherapy in low-risk HR-positive breast cancer by genomic assays (TAILORx, MINDACT) or in HER2-positive disease by PET response (PHERGain); shortening adjuvant FOLFOX to 3 months (IDEA); ctDNA-guided omission or escalation of adjuvant chemotherapy in colon cancer (DYNAMIC, CIRCULATE); PET-guided omission of radiotherapy or bleomycin in lymphoma; 12 versus 6 months of trastuzumab (PERSEPHONE); radiotherapy dose reduction in HPV-positive oropharynx cancer (which has repeatedly failed); and MRD-guided stopping in CLL and myeloma. De-escalation trials need non-inferiority designs and large numbers, and are rarely funded by industry. Escalation trials add drugs to non-responders (KEYNOTE-522 residual disease, CheckMate 577).
Pages like this
not linked directly; found by shared links- TermControl arm and comparator (investigator's choice)
Shares Backbone, add-on and monotherapy, Non-inferiority trial.
- TermSecondary malignancy (therapy-related cancer)
Shares ABVD, BEACOPP and BrECADD (Hodgkin lymphoma regimens), Late effects and survivorship toxicity.
- IdeaFormally qualify tumour-DNA blood tests as a surrogate endpoint for adjuvant trials
Shares DYNAMIC, CIRCULATE-Japan (GALAXY / VEGA / ALTAIR), Circulating tumour DNA (ctDNA).
- TermColectomy
- TermComplete response (CR) and partial response (PR)
Shares Deauville score and PET-adapted therapy, Undetectable MRD (uMRD / MRD-negative).
- IdeaStrip the platelet coat off travelling tumour cells in ctDNA-positive patients
- IdeaA national platform trial that every ctDNA-positive patient can join
- IdeactDNA-guided adjuvant therapy as the default in stage II-III colon cancer