-
Notifications
You must be signed in to change notification settings - Fork 0
/
Cholangiocarcinoma_Sequential-Chemotherapy_Predictive-Tests.Rmd
1078 lines (781 loc) · 35.4 KB
/
Cholangiocarcinoma_Sequential-Chemotherapy_Predictive-Tests.Rmd
1
2
3
4
5
6
7
8
9
10
11
12
13
14
15
16
17
18
19
20
21
22
23
24
25
26
27
28
29
30
31
32
33
34
35
36
37
38
39
40
41
42
43
44
45
46
47
48
49
50
51
52
53
54
55
56
57
58
59
60
61
62
63
64
65
66
67
68
69
70
71
72
73
74
75
76
77
78
79
80
81
82
83
84
85
86
87
88
89
90
91
92
93
94
95
96
97
98
99
100
101
102
103
104
105
106
107
108
109
110
111
112
113
114
115
116
117
118
119
120
121
122
123
124
125
126
127
128
129
130
131
132
133
134
135
136
137
138
139
140
141
142
143
144
145
146
147
148
149
150
151
152
153
154
155
156
157
158
159
160
161
162
163
164
165
166
167
168
169
170
171
172
173
174
175
176
177
178
179
180
181
182
183
184
185
186
187
188
189
190
191
192
193
194
195
196
197
198
199
200
201
202
203
204
205
206
207
208
209
210
211
212
213
214
215
216
217
218
219
220
221
222
223
224
225
226
227
228
229
230
231
232
233
234
235
236
237
238
239
240
241
242
243
244
245
246
247
248
249
250
251
252
253
254
255
256
257
258
259
260
261
262
263
264
265
266
267
268
269
270
271
272
273
274
275
276
277
278
279
280
281
282
283
284
285
286
287
288
289
290
291
292
293
294
295
296
297
298
299
300
301
302
303
304
305
306
307
308
309
310
311
312
313
314
315
316
317
318
319
320
321
322
323
324
325
326
327
328
329
330
331
332
333
334
335
336
337
338
339
340
341
342
343
344
345
346
347
348
349
350
351
352
353
354
355
356
357
358
359
360
361
362
363
364
365
366
367
368
369
370
371
372
373
374
375
376
377
378
379
380
381
382
383
384
385
386
387
388
389
390
391
392
393
394
395
396
397
398
399
400
401
402
403
404
405
406
407
408
409
410
411
412
413
414
415
416
417
418
419
420
421
422
423
424
425
426
427
428
429
430
431
432
433
434
435
436
437
438
439
440
441
442
443
444
445
446
447
448
449
450
451
452
453
454
455
456
457
458
459
460
461
462
463
464
465
466
467
468
469
470
471
472
473
474
475
476
477
478
479
480
481
482
483
484
485
486
487
488
489
490
491
492
493
494
495
496
497
498
499
500
501
502
503
504
505
506
507
508
509
510
511
512
513
514
515
516
517
518
519
520
521
522
523
524
525
526
527
528
529
530
531
532
533
534
535
536
537
538
539
540
541
542
543
544
545
546
547
548
549
550
551
552
553
554
555
556
557
558
559
560
561
562
563
564
565
566
567
568
569
570
571
572
573
574
575
576
577
578
579
580
581
582
583
584
585
586
587
588
589
590
591
592
593
594
595
596
597
598
599
600
601
602
603
604
605
606
607
608
609
610
611
612
613
614
615
616
617
618
619
620
621
622
623
624
625
626
627
628
629
630
631
632
633
634
635
636
637
638
639
640
641
642
643
644
645
646
647
648
649
650
651
652
653
654
655
656
657
658
659
660
661
662
663
664
665
666
667
668
669
670
671
672
673
674
675
676
677
678
679
680
681
682
683
684
685
686
687
688
689
690
691
692
693
694
695
696
697
698
699
700
701
702
703
704
705
706
707
708
709
710
711
712
713
714
715
716
717
718
719
720
721
722
723
724
725
726
727
728
729
730
731
732
733
734
735
736
737
738
739
740
741
742
743
744
745
746
747
748
749
750
751
752
753
754
755
756
757
758
759
760
761
762
763
764
765
766
767
768
769
770
771
772
773
774
775
776
777
778
779
780
781
782
783
784
785
786
787
788
789
790
791
792
793
794
795
796
797
798
799
800
801
802
803
804
805
806
807
808
809
810
811
812
813
814
815
816
817
818
819
820
821
822
823
824
825
826
827
828
829
830
831
832
833
834
835
836
837
838
839
840
841
842
843
844
845
846
847
848
849
850
851
852
853
854
855
856
857
858
859
860
861
862
863
864
865
866
867
868
869
870
871
872
873
874
875
876
877
878
879
880
881
882
883
884
885
886
887
888
889
890
891
892
893
894
895
896
897
898
899
900
901
902
903
904
905
906
907
908
909
910
911
912
913
914
915
916
917
918
919
920
921
922
923
924
925
926
927
928
929
930
931
932
933
934
935
936
937
938
939
940
941
942
943
944
945
946
947
948
949
950
951
952
953
954
955
956
957
958
959
960
961
962
963
964
965
966
967
968
969
970
971
972
973
974
975
976
977
978
979
980
981
982
983
984
985
986
987
988
989
990
991
992
993
994
995
996
997
998
999
1000
---
title: "Cholangiocarcinoma, Sequential Chemotherapy, and Predictive Tests"
author: "AJ Book"
output:
word_document: default
pdf_document: default
html_document: default
editor_options:
markdown:
wrap: 72
---
```{r setup, include=FALSE}
knitr::opts_chunk$set(echo = TRUE)
# Clear the entire environment
rm(list = ls())
setwd("C:/Users/ajboo/BookAbraham/RProjects/MZBSurvivalAnalysis")
# Define the output directory path
output_dir <- "output"
# Create the output directory if it doesn't exist
if (!dir.exists(output_dir)) {
dir.create(output_dir)
}
# Set the output directory for plots
knitr::opts_chunk$set(fig.path = paste0(output_dir, "/plot", "-"))
```
## Load Libraries
This section is reserved for libraries we will use throughout this RMD
file and any imported modules
```{python imports}
# Importing necessary libraries
import pandas as pd
import numpy as np
import matplotlib.pyplot as plt
import seaborn as sns
from lifelines import KaplanMeierFitter, CoxPHFitter
```
```{r libraries, echo=TRUE}
library(tidyverse)
library(survival)
library(survminer)
library(ggsci)
library(knitr)
library(ggsurvfit)
library(gt)
library(reticulate)
library(maxstat)
```
Import the data file
```{python load and convert data}
# Define the function to load and preprocess data
def load_and_convert_data(file_path, cancer_type):
# Load data from CSV file
df = pd.read_csv(file_path)
# Subset data for the specified cancer type
cancer_df = df[df['Cancer_Type'] == cancer_type].copy() # Create a copy
# Convert selected columns to categorical variables
factors = ['Gender', 'Cancer_Type', 'Prior_Tx', 'Resistant', 'Cancer_Status', 'Risk_Group_ALAN']
cancer_df[factors] = cancer_df[factors].astype('category')
# Print message indicating successful loading
print("Data for", cancer_type, "loaded successfully.")
return cancer_df
# Load and preprocess data for Cholangiocarcinoma
cholangio_df = load_and_convert_data("data/Organized_Bruckner_Data.csv", "Cholangiocarcinoma")
```
```{python recode ALAN}
# Recode Risk_Group_ALAN column
# Define the bins and labels
bins = [-1, 0, 2, 4]
labels = ['Low_Risk', 'Intermediate_Risk', 'High_Risk']
# Recode Risk_Group_ALAN column based on Prognostic_Score_ALAN
cholangio_df['Risk_Group_ALAN'] = pd.cut(cholangio_df['Prognostic_Score_ALAN'], bins=bins, labels=labels, include_lowest=False)
```
Examine the variables within your data
```{python examine subset}
# Glimpse at the subsetted data frames
print("\n Cholangiocarcinoma Data Frame:")
print(cholangio_df.head())
```
Determine the types of class each column contains as its datatype
```{python examine type}
# Check data types of columns in DataFrame
print(cholangio_df.dtypes)
```
## Numeric Summary
Step 1: calculate the numeric statistics of the cholangio_df
data frame #Note:You can specify percentiles, quantiles and normality or you can give specific percentiles depending on what you are interested in looking at this specific usage is looking at the 33rd and 67th percentiles of the data
Step 2: Create histograms, boxplots and distribution curves to visualize the descriptive statistics of the numeric variables.
```{python numeric summary}
def calculate_numeric_statistics(data):
# Select only numeric columns
numeric_data = data.select_dtypes(include=np.number)
# Calculate descriptive statistics
descriptive_stats = numeric_data.describe().transpose()
# Calculate interquartile range (IQR) and include quantiles (25th, 50th, and 75th percentiles)
quantiles = numeric_data.quantile([0.25, 0.5, 0.75], axis=0).transpose()
quantiles["IQR"] = quantiles[0.75] - quantiles[0.25]
quantiles.columns = ["Q1", "Median", "Q3", "IQR"]
# Calculate additional percentiles (33rd and 67th)
custom_percentiles = np.percentile(numeric_data, [33, 67], axis=0)
custom_percentiles_df = pd.DataFrame(custom_percentiles.T, columns=["33rd Percentile", "67th Percentile"], index=numeric_data.columns)
# Combine all statistics
stats_combined = pd.concat([descriptive_stats, quantiles, custom_percentiles_df], axis=1)
return stats_combined
# Create summary statistics table for NPT Cholangiocarcinoma
cholangio_stats = calculate_numeric_statistics(cholangio_df)
# Display the tables
print("Summary statistics for Cholangiocarcinoma:")
print(cholangio_stats)
```
```{r advanced numeric summary}
#Load Util functions
source("Utils.R")
# Generate the first table for Resistant Cholangiocarcinoma
cholangio_table <- calc_num_stats(py$cholangio_df, selected_labels = c("Quantiles", "Percentiles"), percentiles = c(33, 67), title = "Numeric Statistics for Cholangiocarcinoma")
# Save the table as an image
gtsave(cholangio_table, filename = file.path(output_dir, "cholangio_table.png"))
```
```{python numeric distribution, echo=FALSE}
import matplotlib.pyplot as plt
import seaborn as sns
# Define the function to plot histograms and boxplots for one variable
def plot_numeric_statistics(df, variable, subset):
# Create subplots
fig, (ax_box, ax_hist) = plt.subplots(2, sharex=True, gridspec_kw={"height_ratios": (.15, .85)})
# Plot boxplot
sns.boxplot(x=df[variable], ax=ax_box, color='orange', width=0.3, linewidth=1.5, showmeans=True, meanline=True,
meanprops=dict(color='black', linestyle='--', linewidth=2),
medianprops=dict(color='black', linewidth=2))
ax_box.set_ylabel(variable)
# Calculate mean and std_dev
mean = df[variable].mean()
std_dev = df[variable].std()
# Plot histogram with density function
sns.histplot(df[variable], kde=True, bins=12, stat='density', color='skyblue', ax=ax_hist)
ax_hist.set_xlabel(variable)
ax_hist.set_ylabel('Density')
# Add lines for mean and mean +/- std_dev to the histogram
ax_hist.axvline(mean, color='red', linestyle='--', linewidth=2, label=f'Mean: {mean:.2f}')
ax_hist.axvline(mean + std_dev, color='purple', linestyle='--', linewidth=2, label=f'Mean + Std Dev: {mean + std_dev:.2f}')
ax_hist.axvline(mean - std_dev, color='purple', linestyle='--', linewidth=2, label=f'Mean - Std Dev: {mean - std_dev:.2f}')
# Add label for the IQR on the boxplot
q1 = df[variable].quantile(0.25)
q3 = df[variable].quantile(0.75)
iqr = q3 - q1
ax_box.text(0.5, 0.5, 'IQR', color='black', ha='center', fontsize=10, transform=ax_box.transAxes)
# Remove y-axis ticks for boxplot
ax_box.set_yticks([])
# Despine the plots
sns.despine(ax=ax_hist)
sns.despine(ax=ax_box, left=True)
# Set common xlabel
plt.xlabel(variable)
# Add title to the entire plot
plt.suptitle(f'{subset} - by {variable}')
# Show the plot
plt.tight_layout()
# Save the plot as an image
plt.savefig(f'output/{subset}_{variable}_plot.png')
# Close the plot to release memory
plt.close()
# List of columns to exclude from numeric variables
exclude_columns = ['Prognostic_Score_ALAN', 'Event_Status']
# Iterate over each numeric variable in your dataset and call the plot_numeric_statistics function
for column in cholangio_df.select_dtypes(include=['int64', 'float64']).columns:
if column not in exclude_columns:
plot_numeric_statistics(cholangio_df, column, 'Cholangiocarcinoma')
```
```{r determine cutpoints}
# Define cutoff points for Albumin, LMR, PLT, LY, ANC, NLR, Alk_Phos, and Prognostic_Score_ALAN
cutoff_points <- list(
Albumin = 3.5,
LMR = 2.1,
PLT = 300,
LY = 1.5,
MON = 0.8,
ANC = c(4, 8),
NLR = c(3, 5),
Alk_Phos = c(135, 200),
Prognostic_Score_ALAN = c(0, 2, 4),
Age = c(60, 65, 70)
)
# Function to categorize values based on cutoff points
categorize_values <- function(df) {
for (variable in names(cutoff_points)) {
if (variable %in% colnames(df)) {
if (variable == "Prognostic_Score_ALAN") {
df[[paste0(variable, "_category")]] <- cut(df[[variable]],
breaks = c(-Inf, 0, 2, Inf),
labels = c("0", "1-2", "3-4"))
} else if (is.numeric(cutoff_points[[variable]])) {
for (cutoff in cutoff_points[[variable]]) {
category_column <- ifelse(df[[variable]] < cutoff,
paste0("< ", cutoff),
paste0(">= ", cutoff))
df <- cbind(df, category_column)
colnames(df)[ncol(df)] <- paste0(variable, "_", cutoff)
}
} else {
cutoff <- cutoff_points[[variable]]
category_column <- cut(df[[variable]],
breaks = c(-Inf, cutoff, Inf),
labels = c(paste0("< ", cutoff),
paste0(">= ", cutoff)))
df <- cbind(df, category_column)
colnames(df)[ncol(df)] <- paste0(variable, "_category")
}
} else {
cat(paste("Column '", variable, "' not found in the DataFrame.\n"))
}
}
return(df)
}
# Apply categorization to each DataFrame
categorized_cholangio_df <- categorize_values(py$cholangio_df)
# Check the result
print("Categorized cholangio DataFrame:")
print(head(categorized_cholangio_df))
```
```{r convert to factors}
# Function to convert specified columns to factors
convert_to_factors <- function(df, columns_to_convert) {
df[, columns_to_convert] <- lapply(df[, columns_to_convert], factor)
return(df)
}
# Columns to convert to factors
columns_to_convert <- c('Age_60', 'Age_65', 'Age_70', 'Albumin_3.5', 'LMR_2.1', 'PLT_300', 'LY_1.5', 'MON_0.8',
'ANC_4', 'ANC_8', 'NLR_3', 'NLR_5', 'Alk_Phos_135', 'Alk_Phos_200')
# Convert columns to factors for categorized_cholangio_df
categorized_cholangio_df <- convert_to_factors(categorized_cholangio_df, columns_to_convert)
# Check the structure of the dataframes
str(categorized_cholangio_df)
```
## Categoric Summary
Calculate the Categorical statistics for our new cholangio data frame
```{python calculate categoric}
def calculate_categorical_statistics(data, title="Categorical Statistics"):
# Check if data is a DataFrame
if not isinstance(data, pd.DataFrame):
raise ValueError("Input 'data' must be a pandas DataFrame.")
# Drop the 'ID' column if it exists
data = data.drop(columns=['ID'], errors='ignore')
# Initialize an empty list to store results
result_list = []
# Iterate over each non-numeric variable
for var in data.select_dtypes(exclude=['number']).columns:
# Get value counts for the current variable
categories = data[var].value_counts()
# Append the results to the list
result_list.append(pd.DataFrame({
'Variable': [var] * len(categories),
'Levels': categories.index,
'UniqueValues': len(categories),
'Frequencies': categories.values.tolist(),
'Proportions': (categories / categories.sum()).map(lambda x: f"{x:.2%}").tolist()
}))
# Concatenate the individual DataFrames into one
result = pd.concat(result_list, ignore_index=True)
# Return result DataFrame
return result
```
```{python categorized stats}
import warnings
# Suppress FutureWarnings
warnings.filterwarnings("ignore", category=FutureWarning)
# Calling the Python function on the R data frames
categorized_cholangio_stats = calculate_categorical_statistics(r.categorized_cholangio_df)
print(categorized_cholangio_stats)
```
```{r advanced categoric summary}
library(gt)
# Define a function to save gt tables as images
save_gt_as_image <- function(table, filename) {
gtsave(table, filename = filename, path = "output")
}
# Call the calc_cat_stats function and save the resulting gt tables
cat_stats_cholangio <- calc_cat_stats(categorized_cholangio_df, title = "Categoric Statistics for Cholangiocarcinoma")
save_gt_as_image(cat_stats_cholangio, "categoric_stats_cholangio.png")
```
```{python categoric distribution}
import seaborn as sns
import matplotlib.pyplot as plt
import numpy as np
def plot_combined_categorical_statistics(data, title="Categorical Statistics"):
# Create a copy of the data to avoid modifying the original DataFrame
data_copy = data.copy()
# Remove rows where the split is 100% to 0%
data_copy = data_copy[(data_copy['Proportions'] != '100.00%') & (data_copy['Proportions'] != '0.00%')]
# Exclude the 'Risk' column
data_copy = data_copy[data_copy['Variable'] != 'Risk_Group_ALAN']
# Convert Proportions column to numeric
data_copy['Proportions'] = data_copy['Proportions'].str.rstrip('%').astype(float)
# Combine similar variables
data_copy['Variable'] = data_copy['Variable'].str.split('_').str[0] # Extract the part before '_'
# Group by Variable and Levels, calculate mean and standard error of proportions
grouped_data = data_copy.groupby(['Variable', 'Levels'])['Proportions'].agg(['mean', 'sem']).reset_index()
# Initialize the plot
sns.set(style="whitegrid")
plt.figure(figsize=(16, 8)) # Increase figure width
# Create the bar plot
sns.barplot(data=grouped_data, x='Levels', y='mean', hue='Variable')
# Add error bars
plt.errorbar(x=np.arange(len(grouped_data['Levels'].unique())), y=grouped_data['mean'],
yerr=grouped_data['sem'], fmt='none', ecolor='black', capsize=3) # Adjust capsize
# Add labels above each bar
for index, row in grouped_data.iterrows():
plt.text(index, row['mean'], f"{row['mean']:.1f}", ha='center', va='bottom', fontsize=6)
# Set title and labels with adjusted font size
plt.title(title, fontsize=16)
plt.xlabel('Levels', fontsize=14)
plt.ylabel('Proportion', fontsize=14)
plt.xticks(rotation=45, fontsize=8, ha='right') # Rotate x-axis labels and adjust font size
plt.yticks(fontsize=8) # Adjust font size for y-axis labels
# Adjust legend size and position
plt.legend(title='Variable', fontsize=6, title_fontsize=8, loc='upper right')
# Adjust spacing
plt.tight_layout() # Adjust spacing
# Show plot
plt.show()
# Example usage:
# Plot combined categorical statistics
plot_combined_categorical_statistics(categorized_cholangio_stats, title="Categorical Statistics for Cholangiocarcinoma")
plt.close() # Close the plot to avoid displaying it again later
```
## Survival Analysis
```{r Suvival Object}
# Create survival object for categorized_cholangio_df
surv_obj <- Surv(time = categorized_cholangio_df$time_diff_months, event = categorized_cholangio_df$Event_Status)
```
# Overall Kaplan Meier
```{r Kaplan Meier}
# Load required libraries
library(survival)
library(survminer)
library(ggsci)
library(ggsurvfit)
library(ggplotify)
# Check if 'ggsurvplot' is loaded in the namespace
if (!"ggsurvplot" %in% loadedNamespaces()) {
library(survminer)
}
kmfit <- survfit(Surv(time = categorized_cholangio_df$time_diff_months, event = categorized_cholangio_df$Event_Status) ~1, data = categorized_cholangio_df)
kmplot <- ggsurvplot(kmfit,
data = categorized_cholangio_df,
title = "Survival Curve for Cholangiocarcinoma",
censor = TRUE,
xlab = "Time (Months)",
ylab = "Survival Probability",
conf.int = TRUE,
conf.int.style = "step",
conf.int.alpha = 0.2,
ggtheme = theme_minimal(),
surv.median.line = "hv",
xlim = c(0, 24),
break.time.by = 3,
breaks = seq(0, 24, by = 3),
surv.scale = "percent",
legend.labs = paste("Cholangiocarcinoma (N =", nrow(categorized_cholangio_df),")"),
palette = "lancet")
kmplot <- kmplot + ggsurvfit::theme_ggsurvfit_KMunicate()
kmplot
# Convert to gg objects
kmplot_gg <- kmplot$plot
# Save the ggplot objects
ggsave(filename = "output/kmplot.png", plot = kmplot_gg, width = 10, height = 6)
```
```{r}
levels <- levels(categorized_cholangio_df$Cancer_Status)
label1 <- paste(levels[1], " (N =", sum(categorized_cholangio_df$Cancer_Status == levels[1]), ")", sep = "")
label2 <- paste(levels[2], " (N =", sum(categorized_cholangio_df$Cancer_Status == levels[2]), ")", sep = "")
```
```{r resistant KM overall}
resistant_kmfit <- survfit(Surv(time = categorized_cholangio_df$time_diff_months, event = categorized_cholangio_df$Event_Status) ~ categorized_cholangio_df$Cancer_Status, data = categorized_cholangio_df)
resistant_kmplot <- ggsurvplot(resistant_kmfit,
data = categorized_cholangio_df,
title = "Survival Curve for Resistant- vs. NPT- Cholangiocarcinoma",
censor = TRUE,
xlab = "Time (Months)",
ylab = "Survival Probability",
conf.int = TRUE,
conf.int.style = "step",
conf.int.alpha = 0.2,
ggtheme = theme_minimal(),
surv.median.line = "hv",
xlim = c(0, 24),
break.time.by = 3,
breaks = seq(0, 24, by = 3),
legend.labs = c(label1, label2),
palette = "lancet")
resistant_kmplot <- resistant_kmplot + ggsurvfit::theme_ggsurvfit_KMunicate()
resistant_kmplot
resistant_gg <- resistant_kmplot$plot
# Save the ggplot objects
ggsave(filename = "output/resistant_v_npt_kmplot.png", plot = resistant_gg, width = 10, height = 6)
```
```{r rename df}
cca_df <- categorized_cholangio_df
colnames(cca_df)
```
## Km Fit Curve
```{r KM Fit}
# Define column names, variables, and cutoffs
column_names <- c("Cancer_Status","Albumin_3.5", "LMR_2.1", "MON_0.8", "LY_1.5", "ANC_4", "ANC_8", "NLR_3", "NLR_5", "PLT_300", "Alk_Phos_135", "Alk_Phos_200", "Age_60", "Age_65", "Age_70", "Prognostic_Score_ALAN_category")
# Initialize a list to store survival fits for NPT Cholangiocarcinoma
cca_kmfits <- list()
# Loop through variables for NPT Cholangiocarcinoma
for (col in column_names) {
# Construct formula with variable name extracted from column name
formula <- as.formula(paste("surv_obj ~", col))
# Fit Kaplan-Meier survival curve
cca_kmfit <- survfit(formula, data = cca_df)
# Store the fit in the list with a descriptive name
cca_kmfits[[paste("cca_kmfit_", col, sep = "")]] <- cca_kmfit
}
# Access results using names like km_fit_Albumin_3.5 etc.
print("Cholangiocarcinoma Survival Fits:")
print(cca_kmfits)
# Add a line of dashes for separation
cat("\n", paste(rep("-", 40), collapse = ""), "\n")
```
##LogRank
```{r Log-Rank Test}
# Define column names
column_names <- c("Albumin_3.5", "LMR_2.1", "MON_0.8", "LY_1.5", "ANC_4", "ANC_8", "NLR_3", "NLR_5", "PLT_300", "Alk_Phos_135", "Alk_Phos_200", "Age_60", "Age_65", "Age_70", "Prognostic_Score_ALAN_category", "Cancer_Status")
# Initialize an empty data frame to store log-rank test results for Cholangiocarcinoma
log_rank_results_df <- data.frame(
variable = character(),
cutoff = numeric(),
logrank_statistic = numeric(),
logrank_p_value = numeric(),
stringsAsFactors = FALSE
)
# Loop through variables for Cholangiocarcinoma
for (col in column_names) {
if (grepl("^Prognostic_Score_ALAN_Category", col)) {
# Treat categorical variable as a factor
formula <- as.formula(paste("surv_obj ~ factor(", col, ")"))
# Perform log-rank test
cca_logrank <- survdiff(formula, data = cca_df)
# Store log-rank test results in data frame
log_rank_results_df <- rbind(log_rank_results_df, data.frame(
variable = col,
cutoff = "N/A",
logrank_statistic = cca_logrank$chisq,
logrank_p_value = 1 - pchisq(cca_logrank$chisq, df = 1),
stringsAsFactors = FALSE
))
# Print log-rank test information for Cholangiocarcinoma
cat(rep("-", 20), "\n")
cat("Log-rank tests for Cholangiocarcinoma -", col, "\n")
cat(rep("-", 20), "\n")
print(cca_logrank)
} else {
# Extract cutoff from column name using regular expression
cutoff <- as.numeric(sub("^.*_(\\d+(\\.\\d+)?)$", "\\1", col))
formula <- as.formula(paste("surv_obj ~", col))
# Perform log-rank test
cca_logrank <- survdiff(formula, data = cca_df)
# Store log-rank test results in data frame
log_rank_results_df <- rbind(log_rank_results_df, data.frame(
variable = col,
cutoff = cutoff,
logrank_statistic = cca_logrank$chisq,
logrank_p_value = 1 - pchisq(cca_logrank$chisq, df = 1),
stringsAsFactors = FALSE
))
# Print log-rank test information for Cholangiocarcinoma
cat(rep("-", 20), "\n")
cat("Log-rank tests for Cholangiocarcinoma -", col, "\n")
cat(rep("-", 20), "\n")
print(cca_logrank)
}
}
# Display log-rank test results in a table
kable(log_rank_results_df, caption = "Log-rank Test Results for Cholangiocarcinoma")
```
### Pairwise LogRank
These results are pairwise log-rank tests comparing different levels of the variable "Prognostic_Score_ALAN_category" within the data. Let's interpret each pairwise comparison:
```{r Pairwise Logrank}
# Get unique levels of Prognostic_Score_ALAN_category
levels_cca <- unique(cca_df$Prognostic_Score_ALAN_category)
# Initialize a list to store pairwise log-rank test results
pairwise_results_cca <- list()
# Perform pairwise log-rank tests
for (i in 1:(length(levels_cca)-1)) {
for (j in (i+1):length(levels_cca)) {
level1 <- levels_cca[i]
level2 <- levels_cca[j]
cat("Pairwise log-rank test between", level1, "and", level2, "\n")
formula <- as.formula(paste("Surv(time_diff_months, Event_Status) ~ Prognostic_Score_ALAN_category"))
pairwise_test <- survdiff(formula, subset(cca_df, Prognostic_Score_ALAN_category %in% c(level1, level2)))
print(pairwise_test)
cat("\n")
# Store the pairwise test result
pairwise_results_cca[[paste("pairwise_test_", level1, "_vs_", level2, sep = "")]] <- pairwise_test
}
}
# Print the results
print("Pairwise log-rank test results for Cholangiocarcinoma:")
print(pairwise_results_cca)
```
##Cox Proportional Hazards
```{r Cox Proportional Hazards}
# Initialize lists to store Cox models, p-values, and hazard ratios for Cholangiocarcinoma
cox_p_values_list_cca <- list()
cox_hazard_ratios_list_cca <- list()
# Loop through variables for Cholangiocarcinoma
for (col in column_names) {
# Extract cutoff and variable name using regular expressions
cutoff <- as.numeric(sub("^.*_(\\d+(\\.\\d+)?)$", "\\1", col))
variable <- sub("^(.*)_\\d+(\\.\\d+)?$", "\\1", col)
# Create formula for Cox model
formula_cca <- as.formula(paste("Surv(time_diff_months, Event_Status) ~", col))
# Fit Cox model
cox_model_cca <- coxph(formula_cca, data = cca_df)
# Print Cox model for Cholangiocarcinoma
cat(rep("-", 30), "\n")
cat("Cox Proportional Hazards for Cholangiocarcinoma -", col, "\n")
cat(rep("-", 30), "\n")
print(cox_model_cca)
# Create properly formatted column name for p-value extraction
coef_name_cca <- paste(col, ">= ", cutoff, sep = "")
# Check if the variable is Prognostic_Score_ALAN_category
if (variable == "Prognostic_Score_ALAN_category") {
# Treat categorical variable as a factor
formula_cca <- as.formula(paste("Surv(time_diff_months, Event_Status) ~ factor(", col, ")"))
# Perform Cox model for Prognostic_Score_ALAN_category
cox_model_cca <- coxph(formula_cca, data = cca_df)
# Extract p-value
cox_p_value_cca <- as.numeric(format(summary(cox_model_cca)$coefficients[, "Pr(>|z|)"], scientific = TRUE, digits = 3))
# Print p-value for Cholangiocarcinoma
cat("P-value:", cox_p_value_cca, "\n")
} else if (variable == "Cancer_Status"){
# Treat categorical variable as a factor
formula_cca <- as.formula(paste("Surv(time_diff_months, Event_Status) ~ factor(", col, ")"))
# Perform Cox model for Cancer_Status
cox_model_cca <- coxph(formula_cca, data = cca_df)
# Extract p-value
cox_p_value_cca <- as.numeric(format(summary(cox_model_cca)$coefficients[, "Pr(>|z|)"], scientific = TRUE, digits = 3))
# Print p-value for Cholangiocarcinoma
cat("P-value:", cox_p_value_cca, "\n")
} else {
# Extract p-value
cox_p_value_cca <- as.numeric(format(summary(cox_model_cca)$coefficients[coef_name_cca, "Pr(>|z|)"], scientific = TRUE, digits = 3))
# Print p-value for Cholangiocarcinoma
cat("P-value:", cox_p_value_cca, "\n")
}
# Extract Hazard Ratio
cox_hazard_ratio_cca <- exp(coef(cox_model_cca))
# Print Hazard Ratio for Cholangiocarcinoma
cat("Hazard Ratio:", cox_hazard_ratio_cca, "\n")
# Append the results to respective lists for cca Cholangiocarcinoma
cox_p_values_list_cca[[length(cox_p_values_list_cca) + 1]] <- c(col, cutoff, cox_p_value_cca)
cox_hazard_ratios_list_cca[[length(cox_hazard_ratios_list_cca) + 1]] <- c(col, cutoff, cox_hazard_ratio_cca)
}
# Convert lists to data frames for cca Cholangiocarcinoma
cox_p_values_df_cca <- as.data.frame(do.call(rbind, cox_p_values_list_cca), stringsAsFactors = FALSE)
colnames(cox_p_values_df_cca) <- c("column_names", "cutoff", "cox_p_value")
cox_p_values_df_cca$cutoff <- as.numeric(cox_p_values_df_cca$cutoff)
cox_p_values_df_cca$cox_p_value <- as.numeric(cox_p_values_df_cca$cox_p_value)
cox_hazard_ratios_df_cca <- as.data.frame(do.call(rbind, cox_hazard_ratios_list_cca), stringsAsFactors = FALSE)
colnames(cox_hazard_ratios_df_cca) <- c("column_names", "cutoff", "cox_hazard_ratio")
cox_hazard_ratios_df_cca$cutoff <- as.numeric(cox_hazard_ratios_df_cca$cutoff)
cox_hazard_ratios_df_cca$cox_hazard_ratio <- as.numeric(cox_hazard_ratios_df_cca$cox_hazard_ratio)
# Merge the two data frames for cca Cholangiocarcinoma
coxph_df_cca <- merge(cox_p_values_df_cca, cox_hazard_ratios_df_cca, by = c("column_names", "cutoff"), sort = FALSE)
# Select only the relevant columns
coxph_df_cca <- coxph_df_cca[, c("column_names", "cutoff", "cox_p_value", "cox_hazard_ratio")]
# Print the combined data frame for cca Cholangiocarcinoma using kable
kable(coxph_df_cca, caption = "Cox Proportional Hazards Results for Cholangiocarcinoma")
# Print the structure of the combined data frame for cca Cholangiocarcinoma
str(coxph_df_cca)
```
##Schoenfeld Residuals Test
```{r Schoenfeld Test}
# Initialize lists to store Schoenfeld test results and plots for Resistant Cholangiocarcinoma
schoenfeld_results_list <- list()
schoenfeld_plots_list <- list()
# Loop through variables for Resistant Cholangiocarcinoma
for (col in column_names) {
# Create formula for Cox model
formula_cca <- as.formula(paste("Surv(time_diff_months, Event_Status) ~", col))
# Fit Cox model for Resistant Cholangiocarcinoma
cox_model_cca <- coxph(formula_cca, data = cca_df)
# Perform Schoenfeld test for Resistant Cholangiocarcinoma
schoenfeld_test_cca <- cox.zph(cox_model_cca)
# Print Schoenfeld test results for Resistant Cholangiocarcinoma
cat(rep("-", 45), "\n")
cat("Schoenfeld Test for Cholangiocarcinoma -", col, "\n")
cat(rep("-", 45), "\n")
print(schoenfeld_test_cca)
# Store Schoenfeld test result for Cholangiocarcinoma in the list
schoenfeld_results_list[[paste("schoenfeld_test", tolower(col), sep = "_")]] <- schoenfeld_test_cca
# Plot Schoenfeld residuals using ggcoxzph for Cholangiocarcinoma
schoenfeld_plot_cca <- ggcoxzph(schoenfeld_test_cca, caption = paste("Schoenfeld Plot of Cholangiocarcinoma for residuals of", col))
# Store Schoenfeld plot for Cholangiocarcinoma in the list
schoenfeld_plots_list[[paste("schoenfeld_plot", tolower(col), sep = "_")]] <- schoenfeld_plot_cca
# Print the plot for Resistant Cholangiocarcinoma
print(schoenfeld_plot_cca)
}
# Access results using names like schoenfeld_test_ly etc. for Cholangiocarcinoma
print(schoenfeld_results_list)
print(schoenfeld_plots_list)
```
#KM Plots
```{r legend labels}
# Define the column names
column_names <- c("Albumin_3.5", "LMR_2.1", "MON_0.8", "LY_1.5", "ANC_4", "ANC_8", "NLR_3", "NLR_5", "PLT_300", "Alk_Phos_135", "Alk_Phos_200", "Age_60", "Age_65", "Age_70", "Cancer_Status","Prognostic_Score_ALAN_category")
# Create a separate list of titles for legend labels
legend_titles <- c("Albumin ", "LMR ", "MON ", "LY ", "ANC ", "ANC ", "NLR ", "NLR ", "PLT ", "Alk_Phos ", "Alk_Phos ", "Age ", "Age ", "Age ","", "ALAN_Score:")
# Function to create legend labels for each variable
create_legend_labels <- function(df, column_names, legend_titles) {
legend_labels <- list()
for (i in seq_along(column_names)) {
variable <- column_names[i]
title <- legend_titles[i]
levels <- levels(df[[variable]])
if (length(levels) == 2) {
label1 <- paste(title, levels[1], " (N =", sum(df[[variable]] == levels[1]), ")", sep = "")
label2 <- paste(title, levels[2], " (N =", sum(df[[variable]] == levels[2]), ")", sep = "")
legend_labels[[variable]] <- c(label1, label2)
} else if (length(levels) == 3) {
label1 <- paste(title, levels[1], " (N =", sum(df[[variable]] == levels[1]), ")", sep = "")
label2 <- paste(title, levels[2], " (N =", sum(df[[variable]] == levels[2]), ")", sep = "")
label3 <- paste(title, levels[3], " (N =", sum(df[[variable]] == levels[3]), ")", sep = "")
legend_labels[[variable]] <- c(label1, label2, label3)
} else {
labels <- paste(title, levels, " (N =", table(df[[variable]]), ")", sep = "")
legend_labels[[variable]] <- labels
}
}
return(legend_labels)
}
# Call the function to create legend labels for each variable
legend_labels_cca <- create_legend_labels(cca_df, column_names, legend_titles)
print(legend_labels_cca)
```
```{r create our models}
# Define a function to fit Cox models for each variable in a data frame
fit_cox_models <- function(data, column_names) {
cox_models <- list()
for (col in column_names) {
formula <- as.formula(paste("Surv(time_diff_months, Event_Status) ~", col))
cox_model <- coxph(formula, data = data)
cox_models[[col]] <- cox_model
}
return(cox_models)
}
# Define a function to fit Kaplan-Meier models for each variable in a data frame
fit_km_models <- function(data, column_names) {
km_models <- list()
for (col in column_names) {
formula <- as.formula(paste("Surv(time_diff_months, Event_Status) ~", col))
km_model <- survfit(formula, data = data)
km_models[[col]] <- km_model
}
return(km_models)
}
# Fit Cox models for cca data frame
cox_models_cca <- fit_cox_models(cca_df, column_names)
# Fit Kaplan-Meier models for cca data frame
km_models_cca <- fit_km_models(cca_df, column_names)
```
```{r check logrank and HR}
# Print the Log-Rank P-value and Hazard Ratio for each variable
cat(rep("-", 40), "\n")
print("Log-Rank pvalue and HR for Cholangiocarcinoma")
cat(rep("-", 40), "\n")
for (col in names(km_models_cca)) {
logrank_p_cca <- log_rank_results_df$logrank_p_value[log_rank_results_df$variable == col]
cox_HR_cca <- coxph_df_cca$cox_hazard_ratio[coxph_df_cca$column_names == col]
cat("Variable:", col, "\n")
cat("Log-Rank P-value:", logrank_p_cca, "\n")
cat("Hazard Ratio:", cox_HR_cca, "\n")
}
```
```{r}
# Define the variables of interest for the dataset
variables_of_interest <- c("Albumin_3.5", "LMR_2.1", "MON_0.8", "LY_1.5", "ANC_4", "ANC_8",
"NLR_3", "NLR_5", "PLT_300", "Alk_Phos_135", "Alk_Phos_200",
"Age_60", "Age_65", "Age_70", "Cancer_Status")
```
```{r KM Plot }
# Open a PDF device
pdf("output/cca_km_plots.pdf")
# Loop through each variable and save its plot on a separate page
for (variable in variables_of_interest) {
legend_label <- legend_labels_cca[[variable]]
logrank_p <- log_rank_results_df$logrank_p_value[log_rank_results_df$variable == variable]
cox_HR <- coxph_df_cca$cox_hazard_ratio[coxph_df_cca$column_names == variable]
# Extract the variable values from the dataframe
variable_values <- cca_df[[variable]]
# Make sure the event status is logical
cca_df$Event_Status <- as.logical(cca_df$Event_Status)
# Create the survival object
surv_obj <- Surv(time = cca_df$time_diff_months, event = cca_df$Event_Status)
# Fit Kaplan-Meier model
km_fit <- survfit(surv_obj ~ variable_values, data = cca_df)
# Convert p-value and hazard ratio to scientific notation with 3 significant figures
logrank_p <- format(logrank_p, scientific = TRUE, digits = 3)
cox_HR <- format(cox_HR, scientific = TRUE, digits = 3)
# Create Kaplan-Meier plot
km_plot <- ggsurvplot(
km_fit,
data = cca_df,
title = paste("Kaplan-Meier Curve of Cholangiocarcinoma by", variable),
censor = TRUE,
xlab = "Time (Months)",
ylab = "Survival Probability",
conf.int = TRUE,
conf.int.style = "step",
conf.int.alpha = 0.2,
surv.median.line = "hv",
xlim = c(0, 24),
break.time.by = 3,
breaks = seq(0, 24, by = 3),
surv.scale = "percent",
legend.labs = c(legend_label[1], legend_label[2]), # Assuming two groups for now
palette = "lancet"
)
# Add annotation to the plot
km_plot <- km_plot$plot + annotate(
"text", x = 0, y = 0.05,
label = paste("Log-Rank p-value:", logrank_p, "\nHazard Ratio:", cox_HR),
hjust = 0, vjust = 0