Combination Olaparib and Temozolomide in Relapsed Small-Cell Lung Cancer.
Anna F FaragoBeow Y YeapMarcello StanzioneYin Pun HungRebecca S HeistJ Paul MarcouxJun ZhongDeepa RangachariDavid A BarbieSarah PhatDavid T MyersRobert MorrisMarina KemTaronish D DubashElizabeth A KennedySubba R DigumarthyLecia V SequistAaron N HataShyamala MaheswaranDaniel A HaberMichael S LawrenceAlice T ShawMari A Mino-KenudsonNicholas J DysonBenjamin J DrapkinPublished in: Cancer discovery (2019)
Small-cell lung cancer (SCLC) is an aggressive malignancy in which inhibitors of PARP have modest single-agent activity. We performed a phase I/II trial of combination olaparib tablets and temozolomide (OT) in patients with previously treated SCLC. We established a recommended phase II dose of olaparib 200 mg orally twice daily with temozolomide 75 mg/m2 daily, both on days 1 to 7 of a 21-day cycle, and expanded to a total of 50 patients. The confirmed overall response rate was 41.7% (20/48 evaluable); median progression-free survival was 4.2 months [95% confidence interval (CI), 2.8-5.7]; and median overall survival was 8.5 months (95% CI, 5.1-11.3). Patient-derived xenografts (PDX) from trial patients recapitulated clinical OT responses, enabling a 32-PDX coclinical trial. This revealed a correlation between low basal expression of inflammatory-response genes and cross-resistance to both OT and standard first-line chemotherapy (etoposide/platinum). These results demonstrate a promising new therapeutic strategy in SCLC and uncover a molecular signature of those tumors most likely to respond. SIGNIFICANCE: We demonstrate substantial clinical activity of combination olaparib/temozolomide in relapsed SCLC, revealing a promising new therapeutic strategy for this highly recalcitrant malignancy. Through an integrated coclinical trial in PDXs, we then identify a molecular signature predictive of response to OT, and describe the common molecular features of cross-resistant SCLC.See related commentary by Pacheco and Byers, p. 1340.This article is highlighted in the In This Issue feature, p. 1325.
Keyphrases
- phase ii
- newly diagnosed
- small cell lung cancer
- clinical trial
- phase iii
- end stage renal disease
- study protocol
- free survival
- ejection fraction
- inflammatory response
- open label
- acute lymphoblastic leukemia
- chronic kidney disease
- acute myeloid leukemia
- prognostic factors
- squamous cell carcinoma
- randomized controlled trial
- diffuse large b cell lymphoma
- peritoneal dialysis
- dna damage
- machine learning
- poor prognosis
- oxidative stress
- patient reported outcomes
- brain metastases
- double blind
- dna repair
- single cell
- transcription factor
- binding protein
- single molecule
- locally advanced
- chemotherapy induced