Objective: To synthesize the latest evidence regarding the association of a priori and a posteriori dietary patterns with robust outcome measures, such as total mortality and cancer-specific mortality.

Eligibility criteria: Studies will be eligible to be included if: (i) they have a cohort design, prospective

or retrospective, (ii) examine the association of a priori i or a posteriori i dietary pattern or patterns after cancer diagnosis with at least one of the primary endpoints of interest, all-cause mortality and

cancer-specific mortality, (iii) the study population consists of cancer survivors, defined as women and men aged 18 years and older with a diagnosis of primary cancer (from the time of diagnosis through the remainder of their lives), (iv) the minimum sample size is 100 participants, (v) the length of follow-up is at least six months, and (vi) provide a measure of association, such as Hazard Ratio (HR), and the corresponding 95% confidence intervals (CIs), or sufficient information for their calculation, for the comparison between the highest versus the lowest category of adherence to on a priori ri o a posteriori ri dietary pattern. The search will exclude editorials, letters to the Editor, comments, conference abstracts, systematic reviews and meta-analyses and it will be

limited to English articles.

Literature search: The literature search will be performed in three electronic databases MEDLINE,

Scopus and Web of Science from January 2000 up to 09 October 2022. Reference

lists of previous meta-analyses and systematic reviews, as well as, from the

identified articles in the present review, will be also hand-searched in order

to retrieve any additional relevant articles.

Data extraction: The following data will be extracted: first author, publication year, study

, cancer site, cancer stage (where available), sample size, age and sex

distribution, follow-up duration, outcome assessed (all-cause mortality and

cancer-specific mortality), types of dietary patterns and dietary assessment

method used, increments or categories used for the analysis of dietary patterns

(i.e. values from quartiles/quintiles used to define the highest category and

the lowest category taken as reference), adjustment covariates and the reported

measures of associations (i.e HR with associated 95% CIs).

Risk of bias: The risk of bias in the included cohort studies will be

evaluated with the ROBINS-I tool, which takes into account seven domains of bias: confounding, selection of participants into the study, classification of exposures, deviations from

intended exposures during follow-up, missing data, outcome measurement, and

selection of reported result.

Data analysis: The pooled estimate for the association of the

highest vs. the lowest categories of adherence to post-diagnosis a priori iand a posteriori i dietary patterns, grouped by cancer site and overall, with each of the outcomes of interest, i.e. all-cause and cancer-specific mortality, will be estimated by random effects meta-analysis models to take into account the between-study heterogeneity. The between-studies variance will be

estimated using the approach by Der Simonian and Laird. Heterogeneity will be

assessed by th² I2 statistic, with values > 50% considered as substantial heterogeneity, and graphically by Galbraith plots. Publication bias will be assessed by funnel plots and Egger’s test will investigate the asymmetry in the case of more than 10 studies in the meta-analyses. We will

further apply subgroup analysis among studies by their assessment of the overall risk of bias. A cumulative meta-analysis by year of publication will be also performed for all-cause mortality and cancer-specific mortality. A sensitivity analysis with influence plots investigating the impact of a priori dietary patterns on overall mortality and cancer mortality by omitting one study at a

time and assessing its effect on the overall estimate will be also applied.