Exercise 9. Localised melanoma: modelling cause-specific mortality using Cox regression
In exercise 7 we modelled the cause-specific mortality of patients diagnosed with localised melanoma using Poisson regression. We will now model cause-specific mortality using Cox regression and compare the results to those we obtained using the Poisson regression model.
To fit a Cox proportional hazards model (for cause-specific survival) with calendar period as the only explanatory variable, the following commands can be used. Note that we are censoring all survival times at 120 months (10 years) in order to facilitate comparisons with the Poisson regression model in exercise 7.
You may have to install the required packages the first time you use
them. You can install a package by
install.packages("package_of_interest")
for each package
you require.
library(biostat3)
library(dplyr) # for data manipulation
library(splines) # ns (recommended package)
## Read melanoma data, select subcohorts and create a death indicator
melanoma.l <- biostat3::melanoma |>
subset(stage=="Localised") |>
transform(death_cancer = as.numeric(status=="Dead: cancer"))
melanoma.l2 <-
transform(melanoma.l,
## Create a death indicator (only count deaths within 120 months)
death_cancer = ifelse(surv_mm<=120, death_cancer, 0),
## Create a new time variable
surv_mm = pmin(surv_mm, 120))
(a)
## Call:
## coxph(formula = Surv(surv_mm, death_cancer) ~ year8594, data = melanoma.l2)
##
## n= 5318, number of events= 960
##
## coef exp(coef) se(coef) z Pr(>|z|)
## year8594Diagnosed 85-94 -0.25297 0.77649 0.06579 -3.845 0.000121 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## exp(coef) exp(-coef) lower .95 upper .95
## year8594Diagnosed 85-94 0.7765 1.288 0.6825 0.8834
##
## Concordance= 0.533 (se = 0.008 )
## Likelihood ratio test= 14.83 on 1 df, p=1e-04
## Wald test = 14.78 on 1 df, p=1e-04
## Score (logrank) test = 14.86 on 1 df, p=1e-04
Patients diagnosed during 1985–94 experience only 77.7% of the cancer mortality experienced by those diagnosed 1975–84. That is, mortality due to skin melanoma has decreased by 22.3% in the latter period compared to the earlier period. This estimate is not adjusted for potential confounders. There is strong evidence of a statistically significant difference in survival between the two periods (based on the test statistic or the fact that the CI for the hazard ratio does not contain 1).
The regression equation is
\[\begin{align*} h(t|\text{year8594}) &= h_0(t) \exp(\beta_1 I(\text{year8594}="\text{Diagnosed 85-94}")) \end{align*}\] where \(h(t|\text{year8594})\) is the hazard at time \(t\) given covariate \(\text{year8594}\), with baseline hazard \(h_0(t)\) and regression coefficient \(\beta_1\) for the log hazard ratio for the calendar period 1985–1994 compared with the reference calendar period 1974–1984.
(b)
## Call:
## survdiff(formula = Surv(surv_mm, death_cancer) ~ year8594, data = melanoma.l)
##
## N Observed Expected (O-E)^2/E (O-E)^2/V
## year8594=Diagnosed 75-84 2145 572 512 7.03 15.5
## year8594=Diagnosed 85-94 3173 441 501 7.18 15.5
##
## Chisq= 15.5 on 1 degrees of freedom, p= 8e-05
## Call:
## coxph(formula = Surv(surv_mm, death_cancer) ~ year8594, data = melanoma.l)
##
## n= 5318, number of events= 1013
##
## coef exp(coef) se(coef) z Pr(>|z|)
## year8594Diagnosed 85-94 -0.25790 0.77267 0.06565 -3.928 8.56e-05 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## exp(coef) exp(-coef) lower .95 upper .95
## year8594Diagnosed 85-94 0.7727 1.294 0.6794 0.8788
##
## Concordance= 0.533 (se = 0.008 )
## Likelihood ratio test= 15.49 on 1 df, p=8e-05
## Wald test = 15.43 on 1 df, p=9e-05
## Score (logrank) test = 15.51 on 1 df, p=8e-05
The three test statistics are
log-rank
: 14.85
Wald
: $-3.84^2=14.75$ (from the $z$ test above)
Likelihood ratio
: 14.78 (from the output above)
The three test statistics are very similar. We would expect each of these test statistics to be similar since they each test the same null hypothesis that survival is independent of calendar period. The null hypothesis in each case is that survival is not associated with calendar period.
(c)
summary(coxfit9c <- coxph(Surv(surv_mm, death_cancer) ~ year8594 + sex + agegrp,
data = melanoma.l2))
## Call:
## coxph(formula = Surv(surv_mm, death_cancer) ~ year8594 + sex +
## agegrp, data = melanoma.l2)
##
## n= 5318, number of events= 960
##
## coef exp(coef) se(coef) z Pr(>|z|)
## year8594Diagnosed 85-94 -0.33339 0.71649 0.06618 -5.037 4.72e-07 ***
## sexFemale -0.53061 0.58825 0.06545 -8.107 5.19e-16 ***
## agegrp45-59 0.28283 1.32688 0.09417 3.003 0.00267 **
## agegrp60-74 0.62006 1.85904 0.09088 6.823 8.90e-12 ***
## agegrp75+ 1.21801 3.38045 0.10443 11.663 < 2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## exp(coef) exp(-coef) lower .95 upper .95
## year8594Diagnosed 85-94 0.7165 1.3957 0.6293 0.8157
## sexFemale 0.5882 1.7000 0.5174 0.6688
## agegrp45-59 1.3269 0.7536 1.1032 1.5959
## agegrp60-74 1.8590 0.5379 1.5557 2.2215
## agegrp75+ 3.3804 0.2958 2.7547 4.1483
##
## Concordance= 0.646 (se = 0.009 )
## Likelihood ratio test= 212.7 on 5 df, p=<2e-16
## Wald test = 217.9 on 5 df, p=<2e-16
## Score (logrank) test = 226.8 on 5 df, p=<2e-16
## Loading required package: carData
##
## Attaching package: 'car'
## The following object is masked from 'package:dplyr':
##
## recode
## Linear hypothesis test
##
## Hypothesis:
## agegrp45-59 = 0
## agegrp60-74 = 0
## agegrp75+ = 0
##
## Model 1: restricted model
## Model 2: Surv(surv_mm, death_cancer) ~ year8594 + sex + agegrp
##
## Res.Df Df Chisq Pr(>Chisq)
## 1 5316
## 2 5313 3 154.38 < 2.2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
The regression equation is
\[\begin{align*} h(t|\text{year8594},\text{sex},\text{agegrp}) &= h_0(t) \exp(\beta_1 I(\text{year8594}="\text{Diagnosed 85-94}")+\beta_2 I(\text{sex}="\text{Female}")+\beta_3 I(\text{agegrp}="\text{45-59}")+\beta_4 I(\text{agegrp}="\text{60-74}")+\beta_5 I(\text{agegrp}="\text{75+}")) \end{align*}\] where \(h(t|\text{year8594},\text{sex},\text{agegrp})\) is the hazard at time \(t\) given covariates \(\text{year8594}\), \(\text{sex}\) and \(\text{agegrp}\), with baseline hazard \(h_0(t)\) and regression coefficients representing log hazard ratios for \(\beta_1\) for the calendar period 1985–1994, \(\beta_2\) for females, \(\beta_3\) for those aged 45–59 years at diagnosis, \(\beta_4\) for those aged 60–74 years and \(\beta_5\) for those aged 75 years and over.
For patients of the same sex diagnosed in the same calendar period, those aged 60–74 at diagnosis have an estimated 86% higher risk of death due to skin melanoma than those aged 0–44 at diagnosis. The difference is statistically significant.
If this were an exam question the previous paragraph would be awarded full marks. It is worth noting, however, that the analysis is adjusted for the fact that mortality may depend on time since diagnosis (since this is the underlying time scale) and the mortality ratio between the two age groups is assumed to be the same at each point during the follow-up (i.e., proportional hazard).
The parameter estimate for period changes from 0.78 to 0.72 when age and sex are added to the model. Whether this is ‘strong confounding’, or even ‘confounding’, is a matter of judgement. I would consider this confounding but not strong confounding but there is no correct answer to this question.
Age (modelled as a categorical variable with 4 levels) is highly significant in the model.
(d)
## Test if the effect of age is significant
## Use an LR test with the anova function
## The model without agegrp
summary(coxfit9d <- coxph(Surv(surv_mm, death_cancer) ~ year8594 + sex,
data = melanoma.l2))
## Call:
## coxph(formula = Surv(surv_mm, death_cancer) ~ year8594 + sex,
## data = melanoma.l2)
##
## n= 5318, number of events= 960
##
## coef exp(coef) se(coef) z Pr(>|z|)
## year8594Diagnosed 85-94 -0.27976 0.75596 0.06588 -4.246 2.17e-05 ***
## sexFemale -0.47825 0.61987 0.06494 -7.364 1.78e-13 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## exp(coef) exp(-coef) lower .95 upper .95
## year8594Diagnosed 85-94 0.7560 1.323 0.6644 0.8602
## sexFemale 0.6199 1.613 0.5458 0.7040
##
## Concordance= 0.578 (se = 0.009 )
## Likelihood ratio test= 69.32 on 2 df, p=9e-16
## Wald test = 69.03 on 2 df, p=1e-15
## Score (logrank) test = 70.02 on 2 df, p=6e-16
## Analysis of Deviance Table
## Cox model: response is Surv(surv_mm, death_cancer)
## Model 1: ~ year8594 + sex + agegrp
## Model 2: ~ year8594 + sex
## loglik Chisq Df Pr(>|Chi|)
## 1 -7792.7
## 2 -7864.4 143.37 3 < 2.2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
## Analysis of Deviance Table
## Cox model: response is Surv(surv_mm, death_cancer)
## Terms added sequentially (first to last)
##
## loglik Chisq Df Pr(>|Chi|)
## NULL -7899.0
## year8594 -7891.6 14.829 1 0.0001177 ***
## sex -7864.4 54.495 1 1.559e-13 ***
## agegrp -7792.7 143.365 3 < 2.2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
Age (modelled as a categorical variable with 4 levels) is highly significant in the model. The Wald test is an approximation to the LR test and we would expect the two to be similar (which they are).
(e)
summary(coxfit9e <- coxph(Surv(surv_mm, death_cancer) ~ year8594 + sex + agegrp,
data = melanoma.l2))
## Call:
## coxph(formula = Surv(surv_mm, death_cancer) ~ year8594 + sex +
## agegrp, data = melanoma.l2)
##
## n= 5318, number of events= 960
##
## coef exp(coef) se(coef) z Pr(>|z|)
## year8594Diagnosed 85-94 -0.33339 0.71649 0.06618 -5.037 4.72e-07 ***
## sexFemale -0.53061 0.58825 0.06545 -8.107 5.19e-16 ***
## agegrp45-59 0.28283 1.32688 0.09417 3.003 0.00267 **
## agegrp60-74 0.62006 1.85904 0.09088 6.823 8.90e-12 ***
## agegrp75+ 1.21801 3.38045 0.10443 11.663 < 2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## exp(coef) exp(-coef) lower .95 upper .95
## year8594Diagnosed 85-94 0.7165 1.3957 0.6293 0.8157
## sexFemale 0.5882 1.7000 0.5174 0.6688
## agegrp45-59 1.3269 0.7536 1.1032 1.5959
## agegrp60-74 1.8590 0.5379 1.5557 2.2215
## agegrp75+ 3.3804 0.2958 2.7547 4.1483
##
## Concordance= 0.646 (se = 0.009 )
## Likelihood ratio test= 212.7 on 5 df, p=<2e-16
## Wald test = 217.9 on 5 df, p=<2e-16
## Score (logrank) test = 226.8 on 5 df, p=<2e-16
## Split follow up by year
melanoma.spl <- survSplit(melanoma.l2, cut=12*(0:10), end="surv_mm", start="start",
event="death_cancer")
## Calculate persontime and
## recode start time as a factor
melanoma.spl <- transform(melanoma.spl,
pt = surv_mm - start,
fu = as.factor(start))
## Run Poisson regression
summary(poisson9e <- glm(death_cancer ~ fu + year8594 + sex + agegrp + offset(log(pt)),
family = poisson,
data = melanoma.spl))
##
## Call:
## glm(formula = death_cancer ~ fu + year8594 + sex + agegrp + offset(log(pt)),
## family = poisson, data = melanoma.spl)
##
## Coefficients:
## Estimate Std. Error z value Pr(>|z|)
## (Intercept) -6.85172 0.14322 -47.841 < 2e-16 ***
## fu12 1.26827 0.13592 9.331 < 2e-16 ***
## fu24 1.30657 0.13806 9.464 < 2e-16 ***
## fu36 1.07575 0.14627 7.354 1.92e-13 ***
## fu48 0.89517 0.15559 5.753 8.75e-09 ***
## fu60 0.81370 0.16368 4.971 6.65e-07 ***
## fu72 0.58637 0.17957 3.265 0.00109 **
## fu84 0.25361 0.20758 1.222 0.22181
## fu96 0.36427 0.21006 1.734 0.08290 .
## fu108 -0.22796 0.27844 -0.819 0.41296
## year8594Diagnosed 85-94 -0.32516 0.06618 -4.913 8.97e-07 ***
## sexFemale -0.53180 0.06545 -8.125 4.48e-16 ***
## agegrp45-59 0.28352 0.09417 3.011 0.00261 **
## agegrp60-74 0.62185 0.09088 6.843 7.76e-12 ***
## agegrp75+ 1.22386 0.10444 11.718 < 2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## (Dispersion parameter for poisson family taken to be 1)
##
## Null deviance: 8651.5 on 34308 degrees of freedom
## Residual deviance: 8233.4 on 34294 degrees of freedom
## AIC: 10183
##
## Number of Fisher Scoring iterations: 7
## exp(beta) 2.5 % 97.5 %
## (Intercept) 0.00105764 0.0007987845 0.001400381
## fu12 3.55468470 2.7233409232 4.639809589
## fu24 3.69349752 2.8178702496 4.841217922
## fu36 2.93219656 2.2013365582 3.905707478
## fu48 2.44775331 1.8043764564 3.320535593
## fu60 2.25623262 1.6370304171 3.109646344
## fu72 1.79745329 1.2641700059 2.555699257
## fu84 1.28866663 0.8579195554 1.935684625
## fu96 1.43945962 0.9536609622 2.172726024
## fu108 0.79615726 0.4613049163 1.374072448
## year8594Diagnosed 85-94 0.72241051 0.6345232662 0.822470947
## sexFemale 0.58754651 0.5168075778 0.667967959
## agegrp45-59 1.32779475 1.1040048878 1.596948453
## agegrp60-74 1.86237635 1.5585268021 2.225464233
## agegrp75+ 3.40028687 2.7708463710 4.172714492
Both models adjust for the same factors. When fitting the Poisson regression model we split time since diagnosis into annual intervals and explicitly estimated the effect of this factor in the model. The Cox model does not estimate the effect of ‘time’ but the other estimates are adjusted for ‘time’.
Since the two models are conceptually similar we would expect the parameter estimates to be similar, which they are.
Yes, both models assume ‘proportional hazards’. The proportional hazards assumption implies that the rate ratios for sex, period, and age are constant across all levels of follow-up time. In other words, the assumption is that there is no effect modification by follow-up time. This assumption is implicit in Poisson regression (as it is in logistic regression) where it is assumed that estimated rate ratios are constant across all combination of the other covariates. We can, of course, relax this assumption by fitting interaction terms.
(f)
sfit9f <- survfit(Surv(surv_mm, event=death_cancer) ~ 1,
data = melanoma.l2 )
## Have a look at the fitted object
str(sfit9f, 1)
## List of 16
## $ n : int 5318
## $ time : num [1:121] 0.5 1.5 2.5 3.5 4.5 5.5 6.5 7.5 8.5 9.5 ...
## $ n.risk : num [1:121] 5318 5315 5304 5298 5292 ...
## $ n.event : num [1:121] 0 5 1 4 4 7 5 8 7 11 ...
## $ n.censor : num [1:121] 3 6 5 2 11 9 6 7 9 6 ...
## $ surv : num [1:121] 1 0.999 0.999 0.998 0.997 ...
## $ std.err : num [1:121] 0 0.000421 0.000461 0.000596 0.000706 ...
## $ cumhaz : num [1:121] 0 0.000941 0.001129 0.001884 0.00264 ...
## $ std.chaz : num [1:121] 0 0.000421 0.000461 0.000596 0.000706 ...
## $ type : chr "right"
## $ logse : logi TRUE
## $ conf.int : num 0.95
## $ conf.type: chr "log"
## $ lower : num [1:121] 1 0.998 0.998 0.997 0.996 ...
## $ upper : num [1:121] 1 1 1 0.999 0.999 ...
## $ call : language survfit(formula = Surv(surv_mm, event = death_cancer) ~ 1, data = melanoma.l2)
## - attr(*, "class")= chr "survfit"
## [1] 0.5 1.5 2.5 3.5 4.5 5.5
## Split follow up by event times
melanoma.spl2 <- survSplit(melanoma.l2, cut=sfit9f$time, end="surv_mm", start="start",
event="death_cancer")
## Calculate persontime and
## recode start time as a factor
melanoma.spl2 <- transform(melanoma.spl2,
pt = surv_mm - start,
fu = as.factor(start))
## Collapse
library(dplyr)
melanoma.spl3 <- melanoma.spl2 |>
group_by(fu,year8594,sex,agegrp) |>
summarise(pt=sum(pt), death_cancer=sum(death_cancer)) |>
data.frame()
## `summarise()` has grouped output by 'fu', 'year8594', 'sex'. You can override
## using the `.groups` argument.
## Run Poisson regression
poisson9f <- glm(death_cancer ~ fu + year8594 + sex + agegrp + offset(log(pt)),
family = poisson,
data = melanoma.spl3 )
## IRR
coef9f <- eform(poisson9f)
## We are not interested in nuisance parameters fu1, fu2, etc
npar <- nrow(coef9f)
pars <- (npar-4):npar
coef9f[pars,]
## exp(beta) 2.5 % 97.5 %
## year8594Diagnosed 85-94 0.7168836 0.6296723 0.8161739
## sexFemale 0.5888144 0.5179256 0.6694059
## agegrp45-59 1.3263971 1.1028413 1.5952697
## agegrp60-74 1.8573227 1.5542946 2.2194298
## agegrp75+ 3.3726522 2.7483711 4.1387363
## Call:
## coxph(formula = Surv(surv_mm, death_cancer) ~ year8594 + sex +
## agegrp, data = melanoma.l2)
##
## n= 5318, number of events= 960
##
## coef exp(coef) se(coef) z Pr(>|z|)
## year8594Diagnosed 85-94 -0.33339 0.71649 0.06618 -5.037 4.72e-07 ***
## sexFemale -0.53061 0.58825 0.06545 -8.107 5.19e-16 ***
## agegrp45-59 0.28283 1.32688 0.09417 3.003 0.00267 **
## agegrp60-74 0.62006 1.85904 0.09088 6.823 8.90e-12 ***
## agegrp75+ 1.21801 3.38045 0.10443 11.663 < 2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## exp(coef) exp(-coef) lower .95 upper .95
## year8594Diagnosed 85-94 0.7165 1.3957 0.6293 0.8157
## sexFemale 0.5882 1.7000 0.5174 0.6688
## agegrp45-59 1.3269 0.7536 1.1032 1.5959
## agegrp60-74 1.8590 0.5379 1.5557 2.2215
## agegrp75+ 3.3804 0.2958 2.7547 4.1483
##
## Concordance= 0.646 (se = 0.009 )
## Likelihood ratio test= 212.7 on 5 df, p=<2e-16
## Wald test = 217.9 on 5 df, p=<2e-16
## Score (logrank) test = 226.8 on 5 df, p=<2e-16
(g)
This R code demonstates how to predict rates and survival for those diagnosed 1985–94 who are male aged 45–59 years:
## split and collapse
library(dplyr)
cuts.splines <- seq(0,max(sfit9f$time),by=3)
mid.splines <- cuts.splines + 1.5
melanoma.spl4 <-
survSplit(Surv(surv_mm,death_cancer)~., data=melanoma.l2, cut=cuts.splines,
start="tstart", end="tstop") |>
mutate(cut=cut(tstop,cuts.splines),
mid=mid.splines[unclass(cut)]) |>
group_by(mid,year8594,sex,agegrp) |>
summarise(pt=sum(tstop-tstart), death_cancer=sum(death_cancer), .groups="keep")
poisson9g <- glm( death_cancer ~ ns(mid,df=3) + year8594 + sex + agegrp,
offset=log(pt), # for effects::Effect() - rather than in the formula
family = poisson,
data = melanoma.spl4 )
summary(poisson9g)
##
## Call:
## glm(formula = death_cancer ~ ns(mid, df = 3) + year8594 + sex +
## agegrp, family = poisson, data = melanoma.spl4, offset = log(pt))
##
## Coefficients:
## Estimate Std. Error z value Pr(>|z|)
## (Intercept) -6.57844 0.12618 -52.134 < 2e-16 ***
## ns(mid, df = 3)1 -0.81303 0.16775 -4.847 1.26e-06 ***
## ns(mid, df = 3)2 1.24995 0.27265 4.584 4.55e-06 ***
## ns(mid, df = 3)3 -0.99353 0.19434 -5.112 3.18e-07 ***
## year8594Diagnosed 85-94 -0.32337 0.06622 -4.884 1.04e-06 ***
## sexFemale -0.53157 0.06545 -8.121 4.61e-16 ***
## agegrp45-59 0.28455 0.09417 3.022 0.00251 **
## agegrp60-74 0.62317 0.09088 6.857 7.01e-12 ***
## agegrp75+ 1.22532 0.10445 11.731 < 2e-16 ***
## ---
## Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
##
## (Dispersion parameter for poisson family taken to be 1)
##
## Null deviance: 1101.87 on 639 degrees of freedom
## Residual deviance: 733.79 on 631 degrees of freedom
## AIC: 1781
##
## Number of Fisher Scoring iterations: 5
## exp(beta) 2.5 % 97.5 %
## (Intercept) 0.001390012 0.001085452 0.001780027
## ns(mid, df = 3)1 0.443510637 0.319238413 0.616159200
## ns(mid, df = 3)2 3.490164898 2.045326838 5.955650114
## ns(mid, df = 3)3 0.370266633 0.252983714 0.541921761
## year8594Diagnosed 85-94 0.723704143 0.635618981 0.823996297
## sexFemale 0.587678725 0.516922269 0.668120343
## agegrp45-59 1.329162191 1.105140512 1.598595030
## agegrp60-74 1.864821637 1.560572459 2.228387231
## agegrp75+ 3.405250925 2.774846360 4.178874200
times <- seq(0,max(cuts.splines),length=1000)
delta <- times[2]-times[1]
newdata <- data.frame(mid=times, year8594="Diagnosed 85-94",
sex="Male", agegrp="45-59",
pt=1)
## plot predicted rates and 95% CI
library(tinyplot)
cbind(newdata,
predict(poisson9g, newdata=newdata, se.fit=TRUE) |> as.data.frame()) |>
transform(rate = exp(fit),
lower = exp(fit-1.96*se.fit),
upper = exp(fit+1.96*se.fit)) |>
with(plt(rate~mid, type="ribbon",
ymin=lower, ymax=upper,
xlab="Time since diagnosis (months)",
ylab="Rate", main="Males aged 45-59 years diagnosed 1985-94"))
##
## Attaching package: 'rstpm2'
## The following objects are masked from 'package:biostat3':
##
## colon, eform, popmort
## The following object is masked from 'package:survival':
##
## colon
logcumhaz <-
rstpm2::predictnl(poisson9g,
fun=function(fit,newdata)
log(cumsum(delta*predict(fit, newdata, type="response"))),
newdata=newdata) |>
transform(surv = exp(-exp(Estimate)),
lower.ci=exp(-exp(cbind(Estimate-1.96*SE))),
upper.ci=exp(-exp(cbind(Estimate+1.96*SE)))) |>
cbind(newdata)
with(logcumhaz, plt(surv~mid, ymin=lower.ci, ymax=upper.ci, type="ribbon",
xlab="Time since diagnosis (months)",
ylab="Survival", main="Males aged 45-59 years diagnosed 1985-94"))