Cancer Imaging strongly encourages that all datasets on which the conclusions of the paper rely should be available to readers. We encourage authors to ensure that their datasets are either deposited in publicly available repositories (where available and appropriate) or presented in the main manuscript or additional supporting files whenever possible. Please see Springer Nature’s information on recommended repositories.
Cancer Imaging supports the complete and transparent reporting of research. The Editor requires the submission of a populated checklist and figure from the relevant reporting guidelines, including CONSORT for completed randomized controlled trials and PRISMA for systematic reviews. The checklist should be provided as an additional file and if available, the flow diagram should be included in the main body of the text, both the checklist and flow diagram should be referenced in the text. Submissions received without these elements will be requested by the Editor. A Word file of the checklists (and flow diagrams) can be downloaded via the EQUATOR Network.
It is understood that for some studies certain aspects of the report may not comply fully with the pre-specified checklist. The checklist will not be used as a tool for judging the suitability of manuscripts for publication in Cancer Imaging, but is intended as an aid to authors to clearly, completely, and transparently let reviewers and readers know what authors did and found. Using these guidelines to write the report, completing the checklist, and constructing a flow diagram are likely to optimize the quality of reporting and make the peer review process more efficient.
Preparing your manuscript
The information below details the section headings that you should include in your manuscript and what information should be within each section.
Please note that your manuscript must include a 'Declarations' section including all of the subheadings (please see below for more information).
The title page should:
- present a title that includes, if appropriate, the study design e.g.:
- "A versus B in the treatment of C: a randomized controlled trial", "X is a risk factor for Y: a case control study", "What is the impact of factor X on subject Y: A systematic review"
- or for non-clinical or non-research studies a description of what the article reports
- list the full names, institutional addresses and email addresses for all authors
- if a collaboration group should be listed as an author, please list the Group name as an author. If you would like the names of the individual members of the Group to be searchable through their individual PubMed records, please include this information in the “Acknowledgements” section in accordance with the instructions below
- indicate the corresponding author
The Abstract should not exceed 350 words. Please minimize the use of abbreviations and do not cite references in the abstract. Reports of randomized controlled trials should follow the CONSORT extension for abstracts. The abstract must include the following separate sections:
- Background: the context and purpose of the study
- Methods: how the study was performed and statistical tests used
- Results: the main findings
- Conclusions: brief summary and potential implications
- Trial registration: If your article reports the results of a health care intervention on human participants, it must be registered in an appropriate registry and the registration number and date of registration should be in stated in this section. If it was not registered prospectively (before enrollment of the first participant), you should include the words 'retrospectively registered'. See our editorial policies for more information on trial registration
Three to ten keywords representing the main content of the article.
The Background section should explain the background to the study, its aims, a summary of the existing literature and why this study was necessary or its contribution to the field.
The methods section should include:
- the aim, design and setting of the study
- the characteristics of participants or description of materials
- a clear description of all processes, interventions and comparisons. Generic drug names should generally be used. When proprietary brands are used in research, include the brand names in parentheses
- the type of statistical analysis used, including a power calculation if appropriate
This should include the findings of the study including, if appropriate, results of statistical analysis which must be included either in the text or as tables and figures.
This section should discuss the implications of the findings in context of existing research and highlight limitations of the study.
This should state clearly the main conclusions and provide an explanation of the importance and relevance of the study reported.
List of abbreviations
If abbreviations are used in the text they should be defined in the text at first use, and a list of abbreviations should be provided.