| Literature DB >> 30315379 |
Audrey E Kam1, Gopichand Pendurti2,3, Umang H Shah1, Mohammad H Ghalib1, Imran Chaudhary1, Jennifer Chuy1,3, Lakshmi Rajdev1,3, Andreas Kaubisch1,3, Santiago Aparo1,3, Ioannis Mantzaris1,3, Sanjay Goel4,5.
Abstract
Background Patients with metastatic colorectal cancer (mCRC) who progress on standard therapies may be eligible for phase I trials. To better delineate the risk-benefit ratio, we assessed toxicities, clinical outcomes and prognostic factors. Methods Records of mCRC patients on phase I trials at our institution over 18 years were reviewed. Univariable (UVA) and multivariable analyses (MVA) were undertaken and a prognostic model developed. Results There were 187 enrollments on 37 phase I trials. Median age was: 59 (29-83) years and number of prior therapies: 3 (0-8). The clinical benefit rate (CBR): response (5.6%) + stable disease, was 43.1%. Median progression free survival (PFS) and overall survival (OS) was 7.7 weeks and 43.7 weeks, respectively. The MVA identified age > 60 years (HR 1.63, p < 0.004), albumin<3.5 g/dL (HR 3.69, p < 0.001), direct bilirubin>ULN (HR1.69, p < 0.01), and WBC ≥ 5.2 k/uL (HR 1.97, p < 0.001) as negative prognostic factors. A risk score based on the MVA revealed that patients with a score of 0-1 had an improved OS (58.7 weeks) compared to a score of 2 (49.9 weeks, p < 0.01) and 3 (14.1 weeks, p < 0.001). Conclusions Phase 1 trials may offer similar or better clinical outcome for mCRC patients than standard third line therapies; the prognostic model could assist in selecting appropriate patients.Entities:
Keywords: Colorectal cancer; Phase I trials; Survival
Mesh:
Year: 2018 PMID: 30315379 PMCID: PMC6461536 DOI: 10.1007/s10637-018-0675-9
Source DB: PubMed Journal: Invest New Drugs ISSN: 0167-6997 Impact factor: 3.850