Listed below are curves comparing the survival times of patients who responded sensitive to treatments and those who responded resistant.
These results published in the Journal of Clinical Oncology reveal a statistically significant correlation between drug sensitivity and time to progression. This seminal paper reintroduced platinum-based chemotherapy for the treatment of advanced breast cancer. Related combinations continue to provide significant improvement in advanced breast cancer survival.
This analysis published in Gynecologic Oncology represents a prospective correlation between drug sensitivity to the combination of cisplatin and gemcitabine in patients with a mixture of platinum-sensitive and platinum-resistant disease. Results reveal a statistically significant correlation between drug sensitivity and time to progression. In addition, this publication revealed a statistically significant correlation between drug sensitivity and clinical response, as well as drug sensitivity and overall survival. This drug combination, developed by Rational Therapeutics, received FDA approval in July 2006 predicated upon this landmark study and the subsequent GOG clinical trial written by Dr. Nagourney (Gyn Oncol, 2006)
Small Cell Lung Cancer
This analysis in small cell lung cancer, published by investigators at the National Cancer Institute, utilizing laboratory techniques developed and applied at Rational Therapeutics, correlates survival with the use of the “in vitro best regimen” (IVBR). With a 39 percent durable complete remission rate for patients receiving assay “sensitive” therapy, this remains one of the best outcomes in this lethal disease ever reported.
This analysis reveals a statistically significant survival advantage for patients receiving assay sensitive therapy in advanced metastatic malignant melanoma. Despite melanoma’s drug refractory nature, novel drug combinations provided durable responses in a high percentage of patients.
Chronic Lymphocytic Leukemia
CLL, the most common adult leukemia, is responsive to chemotherapy, but rarely curable. This analysis identifies a subset of patients with resistant disease who suffer early relapse and death. By identifying these patients at initial diagnosis, more effective therapies could be administered to provide more durable clinical response.