Individualized AML Treatment
This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.
About the trial
Every patient responds differently to their cancer treatment, and some treatments work better for some patients more than others. For patients with relapsed, refractory ( R/R) AML, there may be fewer approved treatment options remaining. In this research study, the investigators are testing whether high throughput drug screening (HTS) in combination with robust molecular testing by HopeSeq (includes DNA sequencing for \>500 genes and 160 gene rearrangements and RNAseq for \>5,000 genes) can help doctors determine which treatment might work best for each individual patient. HTS tests how the patient's own AML cells respond to different treatment options including individual drugs and triple drug regimens and recommends for the best treatment options for an individual patient. Participants will provide extra bone marrow and/or blood at the time of routine procedure, and these extra sample(s) will be tested using the Cancer Drug Sensitivity Test ( CDST) HTS, CLIA approved in Washington state since 2014. A committee (the Functional Molecular Tumor Board) will review the HopeSeq and HTS results, past treatments, and clinical description, and give a recommendation for the best AML treatment options for each individual patient. The patient's doctor will get a copy of the recommendation and discuss treatment options with the patient. The patient and their doctor will decide on the best treatment plan for the patient, one which will be approved by insurance. Patients will not be treated with any drugs as part of this study. Then at 6 and 12 months, there will be retrospective review of medical records to determine how will the testing predicted the response, drug sensitivity or resistance, and overall and disease-free survival will be monitored.
Original English text from ClinicalTrials.gov
Who can (and can't) join
✓ Qualifies
- •Wiek 18 lat lub więcej
- •Potwierdzona diagnoza białaczki szpikowej
- •Choroba nawrotowa lub oporna na poprzednie leczenie
- •Ogólny stan zdrowia pozwalający na uczestnictwo (ECOG ≤ 3)
- •Wystarczająca ilość komórek z szpiku kostnego lub krwi do badań
- •Oczekiwana długość życia ponad 100 dni
- •Pełne wyleczenie się z poprzednich skutków ubocznych leczenia
- •Świadoma zgoda na uczestnictwo w badaniu
✗ Disqualifies
- •Aktywna choroba w ośrodkowym układzie nerwowym (mózg i rdzeń kręgowy)
- •Znaczna choroba serca (zawał serca w ostatnich 6 miesięcy, niekontrolowana arytmia)
- •Ciąża lub karmienie piersią
- •Niekontrolowana aktywna infekcja
- •Szczepienie żywą szczepionką podczas udziału w badaniu
- •Pewne rzadkie typy białaczki szpikowej (z zaburzeniem chromosomu 15;17)
- •Reakcja przeszczepienia przeciwko organizmowi (GVHD)
- •Inne nowotwory wymagające leczenia
Simplified criteria — AI translation
Trial details
- Minimum age
- 18 Years
- Last updated (source)
- August 21, 2026
- Sex
- No restrictions
Therapies / drugs in trial
Locations (1)
City of Hope Medical Center
Duarte, United States
Trial contact
Pamela Becker, MD
Contact information from ClinicalTrials.gov. Contact in English.
Share this trial
Data from ClinicalTrials.gov. AI-assisted translation, last sync: 8/22/2026.
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