Prognostic factors of adjuvant chemotherapy discontinuation among stage III colon cancer patients: A survey of medical oncologists and a systematic review and meta‐analysis

Abstract Background Factors that are prognostic of early discontinuation of adjuvant chemotherapy among stage III colon cancer patients have yet to be described. To address this gap, a survey of medical oncologists and a systematic review and meta‐analysis were conducted. Methods A survey was distributed in March 2019 to medical oncologists who treat colon cancer within Alberta, Canada. Clinicians were asked to rank the prognostic importance of a set of variables using a Likert scale and agreement was quantified using a weighted Cohen's kappa. In addition, we systematically searched four databases up to July 2019. Meta‐analyses were conducted using a random‐effects model. Results Of the 25 clinicians who were sent the survey, 14 responded. Overall, there was no agreement regarding which variables were prognostic of early discontinuation (weighted Cohen's kappa = 0.12; 95% CI = 0.05‐0.18). From an initial 3927 articles, 18 investigations were identified for inclusion in our review. Based upon evidence from both the survey and the systematic review, the following four variables were identified as being prognostic of early discontinuation: (a) comorbidity (OR2+ vs 0 = 1.53; 95% CI = 1.30‐1.79); (b) performance status (ORECOG 2+ vs 0‐1 = 1.33; 95%CI = 1.07‐1.65); (c) T stage (ORT4 vs T1‐2 = 1.57; 95% CI = 0.99‐2.50); and (d) chemotherapy regimen (estimates not pooled due to heterogeneity). In addition to these factors, there was some suggestion that age, marital status/social support, muscle mass, N stage, and tumor grade had prognostic value. Conclusions Current evidence is heterogeneous and limited. Additional research is needed to confirm our findings and to explore additional prognostic factors.


| INTRODUCTION
Among individuals diagnosed with stage III colon cancer, treatment with adjuvant chemotherapy has been shown to increase six-year survival from approximately 50% to 73%. 1,2 Despite such benefits, there are side-effects to adjuvant chemotherapy which have been well-documented in this patient population. During the course of their treatment, patients often experience a variety of mild to severe toxicities which include neuropathy, diarrhea, nausea, vomiting, fatigue, and hand-foot syndrome. [3][4][5] In the recent IDEA Trial (2018), for example, which assessed the effect of a shortened duration of adjuvant chemotherapy on disease-free survival among individuals with stage III colon cancer, one in two patients in the 6-month duration arm experienced at least one grade 3 or 4 adverse event. 4 As a result of such toxicities, some patients willingly or are mandated by their oncologist to discontinue their prescribed chemotherapy regimen prematurely which may compromise the efficacy of adjuvant treatment. In addition to treatment side-effects, non-medical factors may contribute an individual's willingness to complete chemotherapy such as barriers related to treatment costs and ease of access. Other less common medical reasons for discontinuation of adjuvant chemotherapy include disease progression and death.
Variables that are prognostic of early discontinuation of adjuvant chemotherapy among stage III colon cancer patients have not been systematically described and quantified. Previous reviews have focused on qualitatively synthesizing results from investigations targeting breast cancer patients, 6,7 elderly cancer patients, 8,9 and patients prescribed oral antineoplastic medications. 6,10 While these studies have reported high percentages of patients discontinuing chemotherapy and have identified potential prognostic factors of early discontinuation, 6-10 such findings may not be generalizable to patients with stage III colon cancer. The identification of prognostic factors for early discontinuation among stage III colon cancer patients may help to improve clinical practice and research. Such an understanding may, for example, help to inform the appropriateness of treatment and the intensity of follow-up care. The identification of prognostic factors could also help in the development of clinical prediction models by narrowing the list of candidate variables. In addition, this knowledge may help to identify potential confounders which would assist with the adjustment for confounding in etiologic studies examining the association between chemotherapy duration and patient outcomes. In a previous review of the association between chemotherapy duration and survival, we recently identified the need for such etiologic research in order to validate subgroup findings from the IDEA Trial (2018) and highlighted the lack of adjustment for potential confounders as a limitation of many of the observational studies conducted to date. 11 To address this gap, we surveyed the opinions of medical oncologists and conducted a systematic review and meta-analysis in order to identify variables that were prognostic of adjuvant chemotherapy discontinuation. The purpose of this study was to provide evidence that would support: (a) the development of clinical tools used to predict the risk of discontinuation at the patient-level by helping to narrow a list of candidate variables and; (b) the estimation of the effect of chemotherapy duration on patient outcomes within observational settings by helping to identify a list of potential baseline confounders that should be considered in the analyses. By examining both sources of evidence, we hoped to increase our certainty regarding variable importance and better identify areas for future research. The specific objectives of this investigation were to: (a) survey a group of medical oncologists and describe their perceptions regarding the prognostic importance of variables with respect to chemotherapy discontinuation; (b) determine if there was any agreement between clinicians regarding objective one; (c) systematically review the evidence to date and quantify the association between various patient, tumor, treatment, and provider characteristics and chemotherapy discontinuation; and (d) estimate the proportion of patients with stage III colon cancer who discontinue adjuvant chemotherapy.

BOYNE Et al.
This survey was originally intended to guide the selection of variables for a separate study in which we developed a clinical tool for predicting chemotherapy discontinuation. The list of variables included in the survey was limited to variables that were routinely and reliably captured within the administrative datasets that would support this project. For this reason, we did not include variables such as performance status within our survey. In addition, we did not include type of chemotherapy within our survey because we had decided to include this variable within the clinical prediction model a priori.

| Statistical analysis of survey responses
Overall agreement between clinicians was assessed using the model-based method of estimating the weighted Cohen's kappa developed by Nelson and Edwards (2015). 12 This method can be used to assess the degree of agreement between three or more raters when the outcome is ordinal. The variables were also examined using two summary scores: (a) the percentage of clinicians who classified the variable as being at least "Somewhat Important"; and (b) the median response. In all analyses, responses coded as "Unsure" were treated as missing values.

| Systematic search and study eligibility
The systematic review and meta-analysis were conducted following the guidance of the Cochrane Handbook 13 and Riley et al (2019) 14 and reported in accordance with the PRISMA statement. 15 The protocol used for this study was adopted from an existing protocol used for a separate investigation which examined the association between a shortened duration of adjuvant chemotherapy and survival among individuals with stage II or III colon cancer (PROSPERO identifier of original protocol: CRD42018108711). 11 The search strategy used for the current review was originally created for and is available in the supplemental file of the systematic review on chemotherapy duration and survival that we previously published. 11 The original search was conducted on August 10th, 2018, and covered English abstracts in the MEDLINE, EMBASE, CENTRAL, and CINAHL databases. The database search was re-run on July 8th, 2019 to identify studies published since the date of the original search.
Given our focus on prognostic factors, we adopted the PICOTS modification of the PICO mnemonic when developing our research question and eligibility criteria. 14 The Population of interest was individuals with stage III colon cancer who underwent surgical resection of their tumor and were prescribed adjuvant chemotherapy in the form of 5-flourouracil or capecitabine alone or in combination with oxaliplatin. We placed no restriction on the Index prognostic factors or the Comparator prognostic factors (ie other prognostic factors included in a multivariable model) which could consist of any patient, clinician, tumor, treatment, or health-system variables. The Outcome of interest was the risk or odds of discontinuation of adjuvant chemotherapy defined in part or entirely by the number of cycles or months of treatment completed by the patient. With respect to Timing our interest was in variables measured prior to the initiation of adjuvant chemotherapy that could be used to predict discontinuation during the course of their prescribed treatment regimen. We made no restrictions on the clinical Setting in which individuals were administered adjuvant chemotherapy (eg tertiary, community, academic, private, etc).
All articles were reviewed by DJB and EH for eligibility. The title and abstract of each study were first assessed for relevance and then the full-texts of the remaining studies were examined. Any disagreements were resolved through discussion. We excluded articles if they: (a) were review articles, case studies, or case series; (b) were not conducted on human participants; (c) did not assess the association between any patient, tumor, provider, or contextual variables and the odds or risk of adjuvant chemotherapy discontinuation; (d) did not include patients with stage III colon cancer; (e) did not explore treatment discontinuation defined according to the duration of 5-flourouracil or capecitabine alone or in combination with oxaliplatin; and (f) had a sample size that was less than 200 individuals. A minimum sample size of 200 was chosen because approximately 200 individuals are needed to estimate the proportion of patients who discontinue chemotherapy within two exposure categories with 95% confidence limits that are within ± 10 percentage points of the point estimate which we felt was the minimal degree of precision needed for an estimate to be clinically informative. 16 We chose to examine the complete cessation of adjuvant chemotherapy as an outcome rather than periodic dose-reductions or dose-omissions in order to focus on the form of non-adherence with the greatest potential to impact treatment efficacy.

| Meta-analysis
All meta-analyses were conducted using a random-effects model estimated using restricted maximum likelihood (REML). For objective three, the log odds ratio was estimated for each study and the natural exponential function was used to convert the pooled results back to the original scale. When a study reported stratified results, the estimates were pooled such that each study contributed a single estimate in the meta-analysis. When multiple measures of effect were reported, we used the estimate adjusted for the greatest number of variables. When synthesizing the association between age and the odds of discontinuation, a log-linear association was first estimated for each study using the Greenland-Longnecker method prior to the quantitative synthesis in a "two-stage" approach. 17 If it was not reported, the median value of the different age categories was taken as the midpoint (eg midpoint of 65-75 year category = 70 years). If the maximum and minimum values of an age category were not reported, we the distance between intermediary categories to estimate the median value of the upper or lower-most categories (eg 65-70, 70-75, 75-80, 80 + year categories; we would estimate a median of 82.5 years for the 80 + year category). In cases where a meta-analysis was not possible (ie there was only one estimate) or inappropriate because of heterogeneity, then results were qualitatively described. For objective four, the log odds of discontinuation was first estimated within each study and the inverse logit transformation was used to return the pooled estimate as a proportion. For all meta-analyses, heterogeneity was assessed using the tau-squared, I-squared, and 95% prediction intervals. 18,19 Publication bias was examined using a funnel plot. In accordance with recommendations in the Cochrane Handbook, we did not examine publication bias within meta-analyses involving less than 10 studies. 13

| Risk of BIAS
Risk of bias was assessed independently and in duplicate by DJB and DEO using the Quality in Prognostic Factor Studies (QUIPS) tool as per the recommendations of Riley et al (2019). 14,20 Discrepancies were resolved through discussion. With respect to the "prognostic factor measurement" domain, we assigned a "moderate" risk of bias to studies that dichotomized one or more continuous exposure variables because this practice is known to be statistically problematic. 21 Regarding the "adjustment for other prognostic factors" domain, we assigned a "high" risk of bias to studies presenting crude estimates, a "moderate" risk of bias to studies in which there were four or fewer variables in total within the multivariable model, and a "low" risk of bias to studies that included five or more factors within a multivariable model or to studies where participants were randomly assigned to different exposure categories. When assessing the risk of bias within this domain, we did not identify a minimal adjustment set of covariates because no factors to date have been established as being prognostic of chemotherapy discontinuation within this patient population. Specific to the "statistical analysis and reporting" domain, we assigned a "moderate" risk of bias to studies in which there was evidence that the reporting of results was related to the precision or the statistical significance of the estimates. No additional criteria beyond those described in the QUIPS tool were used to assess the risk of bias within the remaining domains.

| Software
Statistical analyses were conducted using R Studio version 1.1.463. 22 The R code used to carry out the estimation of the weighted kappa statistic was taken from the supplemental file of Mitani et al (2017). 23 Meta-analyses were conducted using the metafor package 24 and the Greenland-Longnecker method was implemented using the dosresmeta package in R Studio. 25

| Survey of medical oncologists
Of the 25 medical oncologists contacted, 14 (56%) responded to our survey. Overall, there was no agreement between clinicians beyond what would be expected due to chance alone (weighted Cohen's kappa = 0.12; 95% CI: 0.05-0.18). Age was the only variable where 100% of clinicians thought that it was at least "somewhat important" and where the median response was "very important" (Table 1). Besides age, 70% or more of the clinicians thought that the following variables were at least "somewhat important" prognostic factors for chemotherapy discontinuation: (a) a history of cardiovascular disease, cancer, or diabetes; (b) time from surgery to chemotherapy initiation; (c) baseline laboratory values; and (d) T and N stage. The majority of clinicians were of the opinion that the following variables were "not important" prognostic factors of chemotherapy discontinuation: (a) body mass index; (b) gender; and (c) tumor side. The following is a list of additional variables not included in our survey that were considered by one or more clinician to be an important prognostic factors: (a) use of or interest in alternative medicines; (b) social support; (c) health literacy; (d) performance status; (e) the type of chemotherapy regimen; (f) body composition and muscle mass; (g) distance from home to treatment facility; (h) mental health; (i) post-operative complications; and (j) religious or spiritual beliefs.

| Systematic review
From an initial 3927 articles, 18 investigations were identified for inclusion in our review (14 observational studies and four randomized trials) ( Figure 1 and Table 2). [3][4][5][26][27][28][29][30][31][32][33][34][35][36][37][38][39][40] Among the observational studies, the pooled estimate of the proportion of patients who discontinued chemotherapy was 25.1% (95% CI: 18.3%-33.3%) (Figure 2). There was substantial heterogeneity in these estimates, likely arising from the disparity in the definitions of chemotherapy discontinuation (I 2 : 98.8%; tau 2 : 0.567; 95% prediction interval: 6.8%-60.7%). Among the four randomized trials included in this review, the pooled proportion of patients who discontinued was 18.3% (95% CI: 16.0%-20.7%; I 2 : 89.6%; tau 2 : 0.148; 95% prediction interval: 13.8%-23.7%) (Figure 2). Of the 18 studies included, eight had a specific objective to examine the association between multiple potential prognostic factors and chemotherapy discontinuation ( Table  2). In general, there were little to no missing covariate data within the studies included in this review (Table S1). Nine of the 18 studies analyzed the data using multivariable logistic regression whereas crude, strata-specific proportions were reported for the other nine studies (Table S1). With respect to multivariable adjustment, only one study used backwards elimination with a liberal p-value to select which subset of covariates to include in the multivariable model (Table S1). The other investigations that reported a multivariable-adjusted analysis included all covariates that were examined with the exception of Cespedes Feliciano et al (2017) which adjusted for three variables based upon their expert opinion (Table S1). 28 All of the observational cohort studies collected data retrospectively using medical records and/or routinely collected administrative data (eg hospital or pharmacy dispensary records). The exception to this rule was the study by Cespedes Feliciano (2017) which also used prospectively collected muscle mass data assessed via a computed tomography scan. 28 The following sections detail results from the meta-analyses (Table 3). A forest plot for each individual meta-analysis is available in the supplemental (Figures S1-S17). Following this section is a narrative summary of results for variables not included in the quantitative synthesis.

| Patient characteristics
Results from the meta-analysis suggested that the odds of discontinuation was higher among patients who had two or more comorbidities vs none (OR: 1.53; 95% CI: 1.30-1.79) and among patients who had an ECOG score of two or greater vs zero or one (OR: 1.33; 95% CI: 1.07-1.65) ( Table  3). Although the meta-analysis suggested that being older and being female were associated with an increased odds of discontinuation, the evidence base was heterogeneous and the 95% prediction intervals included values below the null. There was no evidence of an association between socioeconomic status and chemotherapy discontinuation. Indicator for whether or not one of the study objectives was to examine the association between multiple potential prognostic variables and chemotherapy discontinuation b

Study
The age variable was not included in the synthesis as we were unable to extract an estimate suitable for meta-analysis

| Tumor variables
There was evidence that the odds of discontinuation was higher among patients with a high vs low grade tumor (OR: 1.29; 95% CI: 1.14-1.47) and among patients with a T4 vs T1-2 stage tumor (OR: 1.57; 95% CI: 0.99-2.50). There was no evidence that discontinuation was associated with tumor stage III vs II or N2 vs N1 or the presence of lymphovascular or perineural invasion (Table 3).

| Provider-related factors
There was some suggestion in the meta-analysis that patients who received treatment in a community centre instead of an academic centre and that patients who had a prolonged postoperative hospital stay had an increased odds of discontinuation, however, there was a great deal of imprecision in these estimates and the 95% prediction intervals included values below 1.00 (Table 3).

| Patient characteristics
There were reports from individual studies of a higher odds of discontinuation among individuals who were white vs black (OR: 1.48; 95% CI: 1.12-1.95), 29 33 Kumar et al (2015) found that the presence of an obstruction or a perforation was associated with an increased odds of discontinuation (OR: 1.82; 95% CI: 1.08-3.05). 32 In contrast, Morris et al (2007) found that the presence of a perforation only was not associated with discontinuation (OR: 0.68; 95% CI: 0.32-1.43). 33

| Chemotherapy regimen
A quantitative synthesis of the evidence surrounding chemotherapy regimen and the odds of discontinuation was not conducted because of clinical heterogeneity in the study populations and statistical heterogeneity in the effect estimates. Instead, the results from these studies will be qualitatively described. In the MOSAIC Trial (2004), patients randomized to 5-flourouracil F I G U R E 2 The proportion of stage III colon cancer patients who discontinued chemotherapy among studies included in systematic review (n = 18). This figure presents results from a meta-analysis of the proportion of patients who discontinued chemotherapy stratified by study design plus oxaliplatin (FOLFOX) had a significantly higher odds of discontinuation than those randomized to 5-flourouracil alone (OR: 2.16; 95% CI: 1.74-2.69). 3 Similarly, van Erning (2016) found that patients aged 70 + years who were prescribed capecitabine plus oxaliplatin (CAPOX) in a real-world setting had a higher odds of discontinuation relative to those prescribed capecitabine monotherapy (OR: 2.51; 95% CI: 1.63-3.86). 39 In contrast, Abrams et al (2011) found that, in a real-world cancer patient population, combination therapy was associated with a reduced odds of discontinuation relative to monotherapy (OR: 0.78; 95% CI: 0.62-0.98). 26 With respect to monotherapies, patients in the X-ACT Trial (2012) who were randomized to capecitabine monotherapy had a higher odds of discontinuation than those randomized to 5-flououracil monotherapy (OR: 1.37; 95% CI: 1.07-1.76). 5 While CAPOX and FOLFOX have never been compared in a head-to-head trial, non-randomized analyses from the IDEA Trial (2018) 4 and from Sha (2018) 36 suggest that the odds of discontinuation is higher among patients who receive CAPOX relative to those who receive FOLFOX (IDEA Trial (2018)

| Provider and other treatmentrelated factors
There were reports of a higher odds of discontinuation among patients seen by medical oncologists (OR 6 or fewer patients annually vs

| Risk of bias assessment
Since all of the studies included in this review were based on administrative, registry, and medical abstract data and because of the short duration of follow-up needed to assess chemotherapy discontinuation, the risk of bias in the "study population", "study attrition", and "outcome measurement" domains of the QUIP tool were judged to be low within all studies ( Table 4). Three of the 18 studies were assigned a moderate risk of bias in the "prognostic factor measurement" domain because they dichotomized one or more continuous variables. Regarding the "adjustment for other prognostic factors" domain, nine studies were deemed to have a high risk of bias. Lastly, three studies were judged to have a moderate risk of bias in the "statistical analysis and reporting" domain as the reporting of outcomes appeared to be guided by a P-value.

| Publication bias
There was no evidence of publication bias among the agespecific results based on an examination of a funnel plot ( Figure S18). An assessment of publication bias was not conducted for any other variables because the number of studies was less than 10. 13

| DISCUSSION
The evidence to date suggests that as many as 2 in 3 patients will discontinue adjuvant chemotherapy in real-world settings depending upon the outcome definition and study population. The primary objective of this study was to identify factors that are prognostic of adjuvant chemotherapy discontinuation among stage III colon cancer patients. With respect to the survey of Some studies did not include all measured covariates within the multivariable model. As such, the number of prognostic factors examined within the study (as reported in Table 2) may not correspond with the number of variables within the multivariable model (as reported in Table 4). b Multivariable adjusted estimates were available for some variables whereas only crude estimates were available for others (see Table S1) medical oncologists, firm conclusions cannot be made given the lack of agreement across clinicians which suggests that medical oncologists may be unable to accurately determine which patients have a high risk of treatment discontinuation. Nonetheless, there was some suggestion that clinicians thought that age, comorbidity, time to chemotherapy initiation, baseline laboratory values, and tumor stage were important prognostic factors for chemotherapy discontinuation in this population. Results from the systematic review and meta-analysis suggested that comorbidity, chemotherapy regimen, performance status, t stage, and tumor grade were significantly associated with chemotherapy discontinuation. Summarizing across these bodies of evidence, the following variables were identified as having strong evidence of being prognostic of early discontinuation because they were supported by both the opinions of medical oncologists and by findings from multiple investigations: (a) comorbidity; (b) t stage; (c) performance status; and (d) chemotherapy regimen (Table 5). With respect to chemotherapy regimen, the literature suggests that CAPOX has the highest odds of discontinuation followed by FOLFOX, capecitabine monotherapy, and 5-flououracil monotherapy. The finding from Abrams et al (2011) that patients prescribed a combination therapy had a lower odds of discontinuation relative to those prescribed a monotherapy is noteworthy. 26 This finding suggests that receipt of a monotherapy may be a proxy of poor candidacy for oxaliplatin and that patients who are poor candidates for oxaliplatin have a higher odds of discontinuing chemotherapy.

| Limitations
There are limitations of this investigation that should be acknowledged. With respect to our survey of medical oncologists, the absolute number of participants was small. In addition, our survey targeted clinicians who treated colon cancer within Alberta, Canada. For these reasons, our findings may not be generalizable, particularly to medical oncologists who work within other geographic regions and who treat other types of cancer. In addition, our method of expert elicitation was simplistic in that the interpretation of variable importance likely differed between clinicians which could account for the low degree of agreement. For many of the variables examined in our systematic review and metaanalysis, the number of investigations was small, the estimates were imprecise, and/or the degree of heterogeneity was substantial. Therefore, the strength of the conclusions that can be drawn from these findings is limited. Similarly, the number of participants included in the analyses was small for a number of the comparisons within this review, particularly those describe within the narrative summary. The lack of statistical significance that was observed for some of these comparisons may therefore be attributable to a lack of statistical power arising from limited sample sizes. Also, our study population of interest was stage III colon cancer patients. As such, these findings are not generalizable to individuals with metastatic disease or with malignancies in other sites. Lastly, the studies included in this review were limited with respect to the scope of the covariates that were examined as they relied primarily on routinely collected clinical data. As such, there are likely important prognostic factors that have yet to be quantitatively examined.

| Areas for future research
There is a need for additional research to identify factors that are prognostic of early discontinuation of adjuvant chemotherapy among stage III colon cancer patients. New investigations should target variables that we identified as being prognostic or potentially prognostic to confirm the findings from our systematic review and meta-analysis. In addition to these variables, researchers should focus on the variables that medical oncologists considered to be potentially important that were not examined within any of the studies included in our systematic review. These variables included patient-level factors such as mental health, interest in alternative medicines, degree of social support, and health care delivery factors such as distance from home to treatment facility. Additional qualitative research and large-scale population-based surveys of patients and clinicians may help to expand this list by identifying additional prognostic factors that have yet to be examined within the quantitative literature. In addition, many of the studies in this review relied upon retrospective administrative data and, as a result, were unable to assess easily measured lifestyle factors such as a history of tobacco or alcohol use which could be explored in future analyses. Several randomized trials were excluded because they did not provide a comparison between a prognostic factor and chemotherapy discontinuation or because they compared the risk of discontinuation relative to a treatment not used within clinical practice (eg FOLFOX versus FOLFOX + bevacizumab or FOLFOX + cetuximab). 41,42 In addition, the MOSIAC Trial, X-ACT Trial, and IDEA Trial were included in this review solely because we were able to indirectly estimate an association between treatment regimen and discontinuation using reported data. [3][4][5] We therefore highlight the existence of a large amount of clinical trial data that could be used to further help identify determinants of chemotherapy discontinuation. Researchers could leverage these data by conducting multivariable-adjusted analyses that are restricted to patients who received a regimen currently approved for use within this patient population. While many of the studies included in this review used a multivariable model, no investigation to date assessed the performance of a multivariable model as a clinical prediction tool. Moreover, it would be difficult to assess the external validity of existing multivariable models because the regression coefficient corresponding to the intercept was not reported. Future research should report the intercept from multivariable models and could focus on the development of clinician decision support tools for predicting early chemotherapy discontinuation. It is noteworthy that only one study included within this review examined cancer stage according to the overall TNM stage variable and that all other studies modeled T and N stage as separate covariates in which additivity was assumed. Future researchers should consider using the overall TNM stage variable since the number of parameters needed to fully specify all possible T1-4 and N1-2 strata would be seven whereas only two parameters are needed to fully specify strata defined by TNM stage IIIA-C. Additionally, there is a great deal of heterogeneity in the literature regarding the operationalization of chemotherapy discontinuation and there is a need to reach consensus regarding the definition that should be used in future investigations. Lastly, it should be noted that none of the investigations stratified the analyses by reason for discontinuation. Such stratification may provide additional insight regarding the prognostic value of the variables examined.

| CONCLUSIONS
While the literature is heterogeneous and limited, there is evidence that comorbidity, chemotherapy regimen, performance status, and T stage are prognostic factors for early discontinuation of chemotherapy. Further research is needed to confirm these findings, to assess additional variables that have yet to be examined, to develop clinical prediction tools, and to reach consensus regarding the definition of chemotherapy discontinuation that should be used within this body of literature.