Precision oncology often relies on treating patients with a single, molecularly matched therapy that targets one mutation in their tumor. In a report, published online in Nature Medicine on April 22, 2019, University of California San Diego School of Medicine researchers found that treating patients with personalized, combination therapies improved outcomes in patients with therapy resistant cancers.
“Response rates to therapies that target one alteration can be low and not durable. Our approach went beyond targeting a single alteration,” said first author and co-principal investigator Jason K. Sicklick, MD, associate professor of surgery at UC San Diego School of Medicine and surgical oncologist at Moores Cancer Center at UC San Diego Health. “In collaboration with a multi-specialty team of oncology experts, we formulated a personalized combination therapy for each patient. With this approach, we saw an increased response rate, as well as improved overall survival and progression-free survival in patients who were highly matched to treatment versus those who were unmatched or less well-matched.”
In general, patients considered highly matched were those who had more than 50 percent of their tumor mutations matched to drugs.
Of the patients treated who were highly matched with combination treatments that targeted multiple alterations, 50 percent saw their disease respond compared to 22 percent that were unmatched or less well matched.
The prospective navigation trial — Investigation of Profile-Related Evidence Determining Individualized Cancer Therapy or I-PREDICT — enrolled patients with previously treated metastatic cancers at either Moores Cancer Center or Avera Cancer Institute in Sioux Falls, South Dakota.
Molecular data, including genomic profiling using next generation sequencing technology developed by study collaborator Foundation Medicine, was gathered for each patient and presented to a molecular tumor board consisting of oncologists, pharmacologists, cancer biologists, geneticists, surgeons, radiologists, pathologists, and bioinformatics experts who focused on creating customized, multidrug combinations to target a majority of the genomic alterations in each patient’s tumors.
The study consented 149 participants with metastatic, treatment-refractory disease, and, of these, 73 (49 percent) were matched to a therapy. Sixty-six were unable to be treated on the study, most commonly because their disease progressed too rapidly and they were placed in hospice or died, reflecting the advanced nature of their diseases.
“The percentage of patients matched was much higher than in most precision medicine studies because we implemented a team who instituted immediate review of genomic results, as well as navigators who helped patients and physicians access clinical trials, and off-label FDA-approved drugs,” said Shumei Kato, MD, assistant professor of medicine at UC San Diego School of Medicine and one of the lead investigators.
The therapies ultimately administered to each of the 83 treated patients were based on the treating oncologists’ choice and an individual patient’s preference. Only 10 patients had completely unmatched treatment. Seventy-three of the patients and their treating physicians chose a personalized, combination therapy that was matched to genomic alterations. The drugs included gene product-targeted drugs, hormone therapies, immunotherapies and chemotherapies.
“Having 50 percent of patients with heavily pretreated disease responding when highly matched speaks to the importance of personalized, precision medicine combination approaches,” said senior author and co-principal investigator Razelle Kurzrock, MD, director of the Center for Personalized Cancer Therapy at Moores Cancer Center. “Our next step is to determine if we can increase the benefit rate further if this strategy is instituted earlier in the course of the disease.”
Patient outcomes were monitored until the disease progressed, treatment was no longer tolerated or the patient died.
“Personalized, multi-drug therapies have not been used as standard treatment because there are concerns about the safety of administering drug combinations that have not been previously studied together,” said Sicklick. “Yet personalized combinations are necessary since no two tumors are exactly the same and so no two regimens will be the same. Our findings demonstrate that this approach is feasible and safe when patients are monitored closely and started on reduced doses.”
Researchers say larger follow up studies are needed to confirm the findings.
Co-authors include: Ryosuke Okamura, Maria Schwaederle, Michael E. Hahn, David E. Piccioni, Paul T. Fanta and Scott M. Lippman, all at UC San Diego; Pradip De, Amy Krie and Brian Leyland-Jones, Avera Cancer Institute; Vincent A. Miller and Jennifer Webster, Foundation Medicine; Jeffrey S. Ross, Foundation Medicine and SUNY Upstate Medical University; Adam Benson, Scipher Medicine; Philip J. Stephens, Grail, Inc.; and J. Jack Lee, University of Texas MD Anderson Cancer Center.
Funding for this research came, in part, from the National Institutes of Health (grants P30CA023100, K08CA168999 and R21CA192072); Foundation Medicine, Inc.; Joan and Irwin Jacobs Philanthropic Fund; the Jon Schneider Memorial Cancer Research Fund; Padres Pedal the Cause; The David Foundation; and Kristen Ann Carr Fund.
Disclosures: Sicklick receives research funds from Foundation Medicine, Inc., Novartis Pharmaceuticals, Blueprint Medicines, and Amgen, as well as consultant fees from Loxo Oncology, Biotheranostics, and Grand Rounds. Kurzrock has research funding from Incyte, Genentech, Merck Serono, Pfizer, Sequenom, Grifols, OmniSeq, Foundation Medicine, Inc., Guardant Health, and Konica Minolta, as well as consultant fees from Loxo Oncology, Actuate Therapeutics, Roche, XBiotech, and NeoMed. She serves as an advisor to Soluventis; receives speaker fees from Roche; and has an equity interest in IDbyDNA, CureMatch, Inc. and Soluventis. Hahn receives research funds from General Electric and is an equity holder in Illumina, Inc. Williams receives research support from Takeda, TESARO, and Pfizer, as well as consultant fees from Takeda. Miller, Ross, and Webster are employees and equity holders in Foundation Medicine, Inc. Miller is also on the Board of Directors for Revolution Medicines and has patent royalties for EGFR T790M testing issued to the Memorial Sloan Kettering Cancer Center. Benson is formerly an employee and is an equity holder in Foundation Medicine, Inc. He is now an employee of Scipher Medicine. Stephens is formerly an employee and is formerly an equity holder in Foundation Medicine, Inc. He is now an employee of GRAIL, Inc. Lee served on the Statistical Advisory Board of AbbVie.
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