Introduction to Survival Analysis Flashcards

1
Q

Does survival analysis necessarily mean death?

A

The methods for analysing time-to-event data are usually called survival analysis, even though the event of interest does not have to be death.

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2
Q

Why do we use rates rather than proportions with survival analysis?

A

To allow for differing length of follow-up between groups of patients.

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3
Q

What does it mean to have censored data?

A

In survival analysis, observations are censored if their follow-up finishes before they have had an event.

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4
Q

In general we assume that censored data happens randomly. How might censored data undermine the validity of the analysis if it is not random?

A

In practice, people who are censored may be more likely (or less likely) to experience the outcome. This would limit the validity of the analysis, especially if many people are censored.

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5
Q

What is a suitable method of survival analysis when we do not have access to exact dates of events/censoring?

A

Life table method (requires probabilities to be adjusted for censoring)

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6
Q

How is survival data usually presented in clinical trials?

A

Kaplan-Meier Method

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7
Q

What two types of Kaplan-Meier curve can you construct?

A
Survival rate 
Failure rate (1 - S-rate)
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8
Q

Why is the failure rate often more useful visually?

A

The upward graph is more informative if the cumulative probability of the event is low until the end of the trial (as in the RITA-2 dataset). In such cases, the downward graph uses only a small part of the data range, e.g. the RITA-2 survival curve goes from 1 to 0.81, but the axis range is from 1 to 0. By contrast, the upward graph can cover all its data range (0 to 0.19 for RITA-2) with no empty space.

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9
Q

How can we assess if there is a significant difference in survival outcomes using Kaplan-Meier Curves?

A

Logrank tests (for of Chi-squared tests)

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10
Q

What statistical components go into survival analysis?

A

Plots of survival probability
Hypothesis test (Logrank test)
Estimand for magnitude of difference

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11
Q

How do we estimate the magnitude of the difference in survival analysis in clinical trials?

A

Poisson or Cox regressions (most commonly Cox)

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12
Q

What does a COx regression model?

A

Hazard ratios (the proportional effect of treatment on event rates in those still at risk at each timepoint)

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13
Q

Why is Cox regression most popular for calculation of proportional hazards?

A

It does not assume any particular for for the hazard rate in the control arm. The baseline hazard rate can vary over time.

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14
Q

What assumption does the Cox regression method make?

A

It assume that the ratio of hazard rates between arms is constant. Called ‘proportional hazards’.

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15
Q

What is the best way to test Cox regression validity for proportional hazard ratio?

A

Look at the KM curve (there are also formal tests)

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16
Q

What do you look for to assess the validity of the hazard proportion in KM curves?

A

If the HR is constant and not equal to 1, the lines will grow apart (=valid)

If lines touch or intersect this is a sign it may not be alid

17
Q

What do you do if the HR is not proportional/constant?

A

Quote different hazard ratios at defined points in the trial to give a fair overview