BACKGROUND: Hand-foot syndrome or Hand-Foot skin reaction is a common adverse effect of certain chemotherapy agents, such as capecitabine or pegylated doxorubicin, where it is estimated to occur in 50% of cases. OBJECTIVES: The aim of this study is to develop and validate a hand-foot syndrome-specific quality of life scale in order to be able to measure the impact of the condition on patients and secondly to be able to assess the value of certain specific treatments in this indication METHODS: The questionnaire was developed after conducting a series of structured interviews with patients with forms of hand-foot syndrome of varying severity, which yielded a detailed and rigorous collection of verbatim transcripts. The Pilot-Testing are realised. RESULTS: Thirty-one items were identified, and 14 items were selected as being relevant and non-overlapping after initial evaluation. The first question in the HFS14 addresses which member is affected (hand, foot or both). The second question addresses the pain with three possible responses (very, moderately or not painful).  The 14 items can be organised in 2 modules: the first module more specifically assesses the handicap generated by involvement of the "feet" and the second assesses the handicap generated by involvement of the "hands". CONCLUSION: The hand-foot syndrome-specific HFS14 scale is easy to use and meets the requirements of a quality of life scale. This scale now needs to be tested in longitudinal studies (for example in clinical trials) to confirm its ability to measure a change in status.