Impact on Survival of Early Versus Late Initiation of Adjuvant Chemotherapy After Pancreatic Adenocarcinoma Surgery: A Target Trial Emulation

Background We examined the impact of early (0–4 weeks after discharge) versus late (> 4–8 weeks after discharge) initiation of adjuvant chemotherapy on pancreatic adenocarcinoma survival. Methods We used Danish population-based healthcare registries to emulate a hypothetical target trial using the clone-censor-weight approach. All eligible patients were cloned with one clone assigned to ‘early initiation’ and one clone assigned to ‘late initiation’. Clones were censored when the assigned treatment was no longer compatible with the actual treatment. Informative censoring was addressed using inverse probability of censoring weighting. Results We included 1491 patients in a hypothetical target trial, of whom 32.3% initiated chemotherapy within 0–4 weeks and 38.3% between > 4 and 8 weeks after discharge for pancreatic adenocarcinoma surgery; 206 (13.8%) initiated chemotherapy after > 8 weeks, and 232 (15.6%) did not initiate chemotherapy. Median overall survival was 30.4 and 29.9 months in late and early initiators, respectively. The absolute differences in OS, comparing late with early initiators, were 3.2% (95% confidence interval [CI] − 1.5%, 7.9%), − 0.7% (95% CI − 7.2%, 5.8%), and 3.2% (95% CI − 2.8%, 9.3%) at 1, 3, and 5 years, respectively. Late initiators had a higher increase in albumin levels as well as higher pretreatment albumin values. Conclusions Postponement of adjuvant chemotherapy up to 8 weeks after discharge from pancreatic adenocarcinoma surgery is safe and may allow more patients to receive adjuvant therapy due to better recovery. Supplementary Information The online version contains supplementary material available at 10.1245/s10434-023-14497-x.

4][5][6][7][8][9] However, around half of the patients do not initiate adjuvant chemotherapy, which may be due to poor performance, early tumor recurrence, and postoperative complications. 10,113][14][15][16][17][18][19][20][21][22][23][24][25][26][27][28][29] However, both comparability between the studies and generalizability to other target populations are limited.There were major differences in the definitions of early and late initiation, median survival times ranged from 20 to 40 months, several studies did not specify the upper limit for allowed waiting times, and most studies used the same data source (the US-based National Cancer Database) and thus had overlapping study populations.More importantly, most studies Impact on Survival of Early … were substantially affected by immortal time bias (by using information captured after the start of follow-up to define exposure groups at baseline) or selection bias (introduced by exclusion of non-initiators), limiting interpretability.Both of these study design-related biases are known to introduce spurious associations when estimating treatment effects. 30,31arget trial emulation is a novel study design that specifically addresses the potential for immortal time bias and selection bias. 32Using this design, we aimed to provide evidence on the impact of timing of initiation of adjuvant chemotherapy on survival after pancreatic adenocarcinoma surgery, by examination of the effect of adjuvant chemotherapy initiated within 4 weeks compared with initiation between 4 and 8 weeks after discharge for pancreatic adenocarcinoma surgery.

Setting and Data Sources
4][35][36][37] We used information from The Danish National Patient Registry, 33 Danish Cancer Registry, 34 Civil Registration System, 35 Danish Anesthesia Database, 36 Danish Pathology Registry, 37 and the Register of Laboratory Results for Research. 38etailed descriptions of the data sources are provided in eTable 1 in the electronic supplementary material.

Study Design and Population
We specified a hypothetical target trial that would ideally be conducted to answer our research question, and then emulated this trial using observational data. 32e Target Trial Details of the target trial and our emulation are specified in ESM eTable 2. In brief, this would be a randomized trial of previously untreated patients undergoing radical resection for pancreatic adenocarcinoma without distant metastases, eligible for postoperative chemotherapy and randomized to either early (0-4 weeks after discharge) or late (> 4-8 weeks after discharge) initiation of adjuvant chemotherapy.The primary endpoint was the difference in median overall survival (mOS), while secondary endpoints were absolute difference in 1-, 3-, and 5-year survival.

Emulation Using Observational Data
To emulate the target trial using observational data, we initially included all patients aged at least 18 years who were undergoing surgery for pancreatic adenocarcinoma and who were registered in the Danish National Patient Registry during the period 2008-2022 (n = 2580).The index date was set to the date of discharge after surgery.We excluded patients who died during the index admission (n = 62), had less than 5 years of continuous residency in Denmark before surgery (n = 9), had an unknown area of residence (n = 11), had received neoadjuvant treatment (n = 197), or had missing information on pathological T or N status (n = 215).Furthermore, to avoid non-positivity, we restricted the study population to patients meeting the inclusion criteria of the target trial (i.e.patients assumed to be eligible for adjuvant chemotherapy at the time of discharge).Thus, we excluded patients with a metastatic tumor on postoperative pathology or a record of tumor recurrence before the index date (n = 82).Tumor recurrence was defined as either (1) a biopsy with verified malignancy compatible with pancreatic adenocarcinoma in the lung, liver, or peritoneum; (2) an International Classification of Diseases (ICD) code of metastatic malignancy; or (3) receipt of nab-paclitaxel, as this treatment regimen is only used in a palliative setting in Denmark (ESM eTable 3).We excluded patients with a diagnosis of another solid tumor (except biliary tract or duodenal cancers, as these were likely wrongly coded pancreatic cancers, and non-melanoma skin cancer) during the year before the index date (n = 79).We also required that patients were considered, in performance, to initiate adjuvant chemotherapy.We approximated this information by excluding patients with a length of stay after surgery of > 4 weeks (n = 181), Clavien-Dindo score of IV or American Society of Anesthesiologists (ASA) score of IV (n = 26), body mass index (BMI) < 17, or a Nordic Multimorbidity Index (NMI) 39 score of > 20 (combined n = 51).We furthermore excluded patients with latest available blood levels of bilirubin > 50 umol/L, hemoglobin < 5 mmol/L, platelets < 100 × 10 9 /L, creatinine > 100 umol/L, CA19-9 > 200 U/L, and albumin < 20 g/L (combined n = 176).For details, see ESM eFig. 1.

Treatment Strategies
In the target trial, treatment would be assigned randomly when eligibility was determined.In our trial emulation, we used an 8-week grace period from the index to capture the two treatment strategies of initiation of adjuvant chemotherapy within 0-4 weeks (early initiation) or > 4-8 weeks (late initiation) following discharge after surgery.A maximum of 8 weeks was chosen to decrease the risk of including patients receiving palliative treatment for recurrences prior to the index date.We restricted data to chemotherapy codes recorded at oncological departments.

Covariates
We included information on comorbidities, BMI, ASA score, and blood tests, in addition to information related to the index admission and postoperative complications.Missing values on BMI, ASA score, and blood samples were addressed using multiple imputation (except for CA19-9 due to a too-high proportion of missing values).For all patients, we retrieved a full medical history of diagnoses recorded up to 5 years before the index date (ESM eTable 4).To augment the assessment of comorbidities, we identified prescriptions used to treat the relevant comorbidities, restricting to a 1-year lookback period (ESM eTable 4).We constructed a composite score of the overall comorbidity burden for each patient using the NMI, a validated comorbidity index designed to predict 5-year mortality in a Danish population (ESM eTable 5). 39We obtained information on the length of stay for the admission related to the surgery (index admission) and Clavien-Dindo score. 40When information on the Clavien-Dindo score was unavailable, we used information on procedures and treatments recorded during the index admission (ESM eTable 6).We constructed a composite measure of postoperative complications defined as low (Clavien-Dindo score ≤ II) and high (Clavien-Dindo score III).Data sources of all covariates are shown in ESM eTable 1.For BMI, ASA score, and blood samples, we used the most recent measurement recorded in the period between the date of surgery and the index.

Statistical Analyses Main Analysis
We analyzed our study using the clone-censor-weight approach. 41,42First, each individual was duplicated in the dataset at the index date (date of discharge).One copy was then assigned to the early initiation strategy and the other copy to the late initiation strategy.Second, the copies were artificially censored over time when the observed treatment deviated from the assigned treatment.Copies assigned to the early initiation strategy were censored after 4 weeks if adjuvant chemotherapy was not initiated, and the copies assigned to the late initiation strategy were censored if adjuvant chemotherapy was initiated before 4 weeks or not initiated after 8 weeks.Follow-up ended at death, emigration (n < 5), after 5 years, or on 23 July 2023, whichever occurred first.
Since treatment was not randomized, potential confounding variables (age, sex, year of diagnosis, marital status, area of residence, comorbidity, BMI, ASA score, tumor stage, postoperative complications, blood samples) may have influenced the actual treatment decision, and thereby deviation from the assigned treatment strategy.Covariates were identified using a practice-and literatureinformed directed acyclic graph (ESM eFig.2).Therefore, in our third step, we used inverse probability of censoring weighting to account for the potential selection bias caused by informative censoring. 32Treatment-specific weights were derived using pooled logistic regression models as outlined in ESM eFig.3. Weights were truncated at the 1st and 99th percentile to reduce the impact of extreme weights. 43Throughout the grace period, comorbidity, BMI, ASA score, and blood samples were updated daily to guard against time-varying confounding (ESM eTable 7).To assess covariate balance, we calculated the standardized mean differences of potential confounders between the two strategies before and after weighting at the end of the grace period.A covariate with an absolute standardized mean difference of < 0.10 was considered sufficiently balanced. 43We report the mOS and overall survival at 1, 3, and 5 years after diagnosis, calculated using the Kaplan-Meier estimator.The treatment effects were contrasted using absolute differences.All estimates are presented with standard error-derived 95% confidence intervals (CIs), calculated using bootstrapping with 200 repetitions.We report estimates for all patients and stratified by N stage, which may introduce effect modification. 44tatistical analyses were conducted using Stata 18 (Stata-Corp LLC, College Station, TX, USA).

Supplemental and Sensitivity Analyses
To further explore and quantify the impact of timing of adjuvant chemotherapy on survival in pancreatic adenocarcinoma patients, we conducted a supplemental analysis on the non-cloned cohort using a Cox proportional hazards regression model.To investigate the impact of exposure dichotomization, 45 we started follow-up on the date of initiation of adjuvant chemotherapy, and modeled the time from discharge to start of adjuvant chemotherapy as a restricted cubic spline with three knots.Outcome was overall survival.All covariates were modeled similar to the target trial emulation, and this analysis was also stratified by N stage.As a marker of postsurgical recovery, 46 we also examined changes in albumin levels from the date of discharge to the date of treatment initiation.Paired data were analyzed using a Wilcoxon signed-rank test, and unpaired data were analyzed using a Wilcoxon rank-sum test.To examine the robustness of our findings, we conducted two sensitivity analyses designed to address potential positivity violations.First, we did not apply any restrictions on eligibility criteria, and second, we excluded patients with an ASA score of III to test a less and more restrictive approach, respectively.

Ethical Considerations
This study was approved by the Danish Data Protection Agency and the Danish Health Data Authority.Ethical approval is not required for registry-based studies in Denmark.Impact on Survival of Early …

Descriptive Characteristics
We included 1491 patients who were discharged alive within 4 weeks after surgery for pancreatic adenocarcinoma (Table 1).The median age was 69 years (interquartile range [IQR] 62-74 years), and 51.7% were men.Of the 1491 patients, 482 (32.3%) initiated adjuvant chemotherapy within 0-4 weeks and 571 (38.3%) initiated treatment between > 4 and 8 weeks after discharge for pancreatic adenocarcinoma surgery; 206 (13.8%) initiated chemotherapy after > 8 weeks, and 232 (15.6%) did not initiate adjuvant chemotherapy.Characteristics on pathology and surgical details are presented in Table 2.There were no differences according to type of chemotherapy (gemcitabine monotherapy, gemcitabine combinations, or mFOL-FIRINOX) received between early and late initiators.All characteristics according to receipt or non-receipt of adjuvant chemotherapy are presented in ESM eTables 8 and 9.

Supplemental and Sensitivity Analyses
When we started follow-up on the date of initiation of chemotherapy, we observed a tendency towards improved prognosis with longer time to initiation of adjuvant chemotherapy in patients with N+ disease but not N0 disease (Fig. 3).Neither of the sensitivity analyses had any major impact on our estimates (ESM eTable 10).

DISCUSSION
We used target trial emulation, a rigorous framework designed to mitigate selection bias and immortal time bias, to estimate the effect of early (0-4 weeks) versus late (> 4-8 weeks) initiation of adjuvant chemotherapy on survival in patients undergoing curative-intent surgery for pancreatic adenocarcinoma.Overall, late and early initiators had similar survival.
The literature on timing of adjuvant chemotherapy after pancreatic adenocarcinoma surgery is contradictory.4]29 Few studies found that early initiation (definition ranging from 5 to 10 weeks) was associated with an improved survival, 17,21,[26][27][28] whereas one study found that initiation after approximately 5 weeks conferred a survival benefit. 25In most studies, the magnitude of the differences was small and of limited clinical relevance; however, the studies were prone to immortal time bias and selection bias.Immortal time bias can be introduced when information on future treatments are used to create exposure groups at baseline. 30,31For example, when examining the impact of initiation of adjuvant chemotherapy before or after 8 weeks, patients in the > 8 weeks group will have 8 weeks of guaranteed survival time when this approach is used.If the patient had died or initiated treatment before 8 weeks, they would not be in the > 8-weeks group.Thus, immortal time bias can lead to inflated and spurious effect estimates.Selection bias can be introduced by exclusion of patients dying before treatment initiation, particularly in highly fatal malignancies such as pancreatic adenocarcinoma.It is not known which treatment these patients would have been allocated to, and it is likely to be different from that of patients who actually started adjuvant chemotherapy.Thus, inference from those in the study to the entire population is not straightforward.This may be prevalent in several papers, as suggested by the survival curves separating shortly after start of followup. 19,47Early separation of the survival curves are suggestive of selection bias, as any treatment effect would require some time to materialize.Prior research used the date of surgery as the index date, whereas we used the date of discharge.This was chosen as we used a target trial emulation.In order to mitigate immortal time bias with this approach, eligibility and time zero (index date) should be aligned.Thus, at the date of surgery, in contrast to the date of discharge, it is not possible to determine eligibility for adjuvant chemotherapy, because postoperative complications may occur, rendering the patient ineligible for adjuvant chemotherapy.Our findings are therefore not entirely comparable with the prior literature.However, median length of stay was limited to 10 days, and we excluded patients with admission after surgery of more than 4 weeks to avoid non-positivity by inclusion of patients, who would never be eligible for chemotherapy due to poor postoperative health status.
To mitigate the impact of immortal time bias and selection bias, we used target trial emulation, which is a novel rigorous framework specifically designed to address the potential for these study design-related biases. 32However, for the estimates to be interpreted in a causal context, some assumptions must be met.Importantly, all patients included should have a non-zero probability of receiving treatment (positivity).To meet this assumption, we applied some restrictions to the eligibility criteria.These restrictions were tested in sensitivity analyses.Furthermore, we did not have information on whether chemotherapy was adjuvant or palliative.To increase the probability of only considering adjuvant treatment regimens, we applied an algorithm to detect recurrences before treatment start based on pathology reports from biopsies, ICD codes, and type of chemotherapy administered.However, this algorithm has not been previously validated, and some patients receiving palliative treatment due to very early recurrence or metastatic disease not identified by the algorithm may have been included.We did not have information on whether R2 resections (macroscopically residual tumor) were performed; however, these are rare, with fewer than 10 cases a year in Denmark, and unlikely to have impacted our estimates. 48Residual or unmeasured confounding should be eliminated (exchangeability).Unmeasured confounding from missing information on performance status 49 may have contributed to our findings.To mitigate the impact of the missing information on performance status,  we included information on other variables that could be associated with both receipt of adjuvant chemotherapy and survival, e.g.comorbidity, ASA score, and albumin. 50The postoperative serum albumin recovery rate has been suggested to be a prognostic factor in patients with resected pancreatic adenocarcinoma. 46We saw that late initiators had a higher increase in albumin levels than early initiators, as well as higher pretreatment values.This may suggest that late initiators were in better shape when adjuvant chemotherapy was initiated because they had longer time to recover after surgery, although albumin is not a validated marker of postsurgical recovery.An improved performance status would increase the likelihood of patients receiving more efficient combination chemotherapy, although we found no major difference between the two groups according to type of adjuvant chemotherapy.
In our study, a total of 232 (15.6%) patients did not initiate adjuvant chemotherapy.The reason for this is unknown but these patients could potentially have benefited from neoadjuvant therapy.Contrary to adjuvant therapy, neoadjuvant therapy ensures early systemic delivery of chemotherapy and is not contingent on sufficient postoperative recovery.However, neoadjuvant chemotherapy introduces a delay in surgery which, if treatment is inefficient, may render the tumor unresectable.Overall, the use of neoadjuvant versus adjuvant chemotherapy in patients with resectable pancreatic adenocarcinoma is still controversial. 51

CONCLUSION
Our study supports that initiation of adjuvant chemotherapy in pancreatic adenocarcinoma patients can be safely postponed to up to 8 weeks after discharge from surgery, allowing for better recovery after surgery.

FIG. 1
FIG.1Overall survival since date of discharge for pancreatic adenocarcinoma surgery, comparing the early (blue) and late (orange) initiation strategies.Weighted estimates.Lines are shown with 95% confidence intervals

FIG. 2 50 0FIG. 3
FIG. 2 Median albumin levels among early and late initiators at the index date and the date of treatment initiation.0-4 weeks: comparison of the index date and treatment initiation: p < 0.05; > 4-8 weeks: comparison of the index date and treatment initiation: p < 0.05.Outliers not shown due to the protection of individual-level data

TABLE 1
Descriptive characteristics of the study population

TABLE 2
Tumor and surgery characteristics of the study population IQR interquartile range, AJCC American Joint Committee on Cancer

TABLE 3
Survival estimates at 1, 3, 5 years after discharge according to treatment in the target trial emulation