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|Articles|June 21, 2010

Oncology NEWS International

  • Oncology NEWS International Vol 19 No 6
  • Volume 19
  • Issue 6

Personalized medicine advances in non-small–cell lung cancer treatment

Author(s)Ed Susman

Success of adaptive randomization in BATTLE could provide new strategy in cancer trials. NSCLC also gain another tool for maintenance therapy.

ABSTRACT: Success of adaptive randomization in BATTLE could provide new strategy in cancer trials. NSCLC also gain another tool for maintenance therapy.

The treatment armamentarium for nonsmall- cell lung cancer has received fresh ammunition in the past few months with FDA approval of erlotinib (Tarceva) for maintenance therapy (see News Briefs) and positive preliminary results from a trial that looked at the value of biomarkers in NSCLC.

While the BATTLE trial confirmed the vital role biomarkers play in designing NSCLC treatment, the study also offered proof that adaptive randomization-pairing patients with the therapies that offered them the best chances-was workable. BATTLE leaders suggested that the experience demonstrated a new way to approach and conduct all cancer clinical trials.

microRNA serves as potential target for lung cancer therapy



Knocking down microRNA-31 production suppressed lung cancer growth in an animal study conducted at the National Cancer Institute, leading the investigators to suggest that microRNA-31 may be a key oncomir in lung cancer.

Xi Liu, PhD

, a postdoctoral fellow at the NCI, said that, based on his research, microRNA-31 was overexpressed in malignant lung tissue when compared with normal tissue. In his animal model study, knocking down microRNA-31 production suppressed lung cancer growth. Also, expression of miR-31 was inversely related to LATS2 and PPP2R2A in both mouse and human lung cancers. "We hypothesize that microRNA-31 is a target to repress for lung cancer therapy and prevention," he said. (AACR 2010 abstract 5698).

"This trial has shown us that we can learn as we go," said Edward S. Kim, MD, an associate professor of thoracic/head and neck medical oncology at Houston's M.D. Anderson Cancer Center and the principle investigator of the BATTLE trial. "We decided that instead of running the same studies over and over again, adding new drugs to old drugs and hoping for a benefit, we had to stop looking at the drugs and start looking at the patients."

In the BATTLE (Biomarker-integrated Approaches of Targeted Therapy for Lung Cancer Elimination: Personalizing Therapy for Lung Cancer) trials, biomarkers were pitted against different drugs. This technique of adaptive randomization allowed patients to be paired with the therapies most likely to benefit them.

"The purpose of BATTLE was to biopsy patients in real-time so we could determine their individual biomarkers," Dr. Kim said. The researchers enrolled patients with progressing lung cancer, performed biopsies, "and tried to figure out which therapies were best for them," he added.

Patients enrolled in the phase II study tested 11 biomarkers from four non-small–cell lung cancer (NSCLC) pathways:

EGFR, KRAS, and BRAF mutation
EGFR and Cyclin D1 (as assessed by FISH) copy number and VEGF
VEGFR
3 RXR receptors and Cyclin D1 (assessed by immunohistochemistry)


TABLE
BATTLE trial treatment arms
150 mg/day of erlotinib (Tarceva)
400 mg/day of sorafenib (Nexavar)
300 mg/day of vandetanib (Zactima)
150 mg/day of erlotinib + 400 mg/m
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