- Meric-Bernstam, Funda;
- Lloyd, Michael;
- Koc, Soner;
- Evrard, Yvonne;
- McShane, Lisa;
- Lewis, Michael;
- Evans, Kurt;
- Li, Dali;
- Rubinstein, Lawrence;
- Welm, Alana;
- Dean, Dennis;
- Srivastava, Anuj;
- Grover, Jeffrey;
- Ha, Min;
- Chen, Huiqin;
- Huang, Xuelin;
- Varadarajan, Kaushik;
- Wang, Jing;
- Roth, Jack;
- Welm, Bryan;
- Govinden, Ramaswamy;
- Ding, Li;
- Kaochar, Salma;
- Mitsiades, Nicholas;
- Carvajal-Carmona, Luis;
- Herylyn, Meenhard;
- Davies, Michael;
- Shapiro, Geoffrey;
- Fields, Ryan;
- Trevino, Jose;
- Harrell, Joshua;
- Doroshow, James;
- Chuang, Jeffrey;
- Moscow, Jeffrey
Although patient-derived xenografts (PDX) are commonly used for preclinical modeling in cancer research, a standard approach to in vivo tumor growth analysis and assessment of antitumor activity is lacking, complicating the comparison of different studies and determination of whether a PDX experiment has produced evidence needed to consider a new therapy promising. We present consensus recommendations for assessment of PDX growth and antitumor activity, providing public access to a suite of tools for in vivo growth analyses. We expect that harmonizing PDX study design and analysis and assessing a suite of analytical tools will enhance information exchange and facilitate identification of promising novel therapies and biomarkers for guiding cancer therapy.