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Thresholds and timing of pre-operative thrombocytosis and ovarian cancer survival: analysis of laboratory measures from electronic medical records

BMC Cancer201616:612

https://doi.org/10.1186/s12885-016-2660-z

Received: 8 March 2016

Accepted: 1 August 2016

Published: 8 August 2016

Abstract

Background

Thrombocytosis has been associated with poor ovarian cancer prognosis. However, comparisons of thresholds to define thrombocytosis and evaluation of relevant timing of platelet measurement has not been previously conducted.

Methods

We selected Tumor Registry confirmed ovarian, primary peritoneal, and fallopian tube cancer cases diagnosed between 1995–2013 from the Vanderbilt University Medical Center. Laboratory measured platelet values from electronic medical records (EMR) were used to determine thrombocytosis at three thresholds: a platelet count greater than 350, 400, or 450 × 109/liter. Timing was evaluated with 5 intervals: on the date of diagnosis, and up to 1, 2, 4, and 8 weeks prior to the date of diagnosis. Cox regression was used to calculate hazard ratios (HR) and confidence intervals (CI) for association with overall survival; adjustment included age, stage, grade, and histologic subtype of disease.

Results

Pre-diagnosis platelet measures were available for 136, 241, 280, 297, and 304 cases in the five intervals. The prevalence of thrombocytosis decreased with increasing thresholds and was generally consistent across the five time intervals, ranging from 44.8–53.2 %, 31.6–39.4 %, and 19.9–26.1 % across the three thresholds. Associations with higher grade and stage of disease gained significance as the threshold increased. With the exception of the lowest threshold on the date of diagnosis (HR350: 1.55, 95 % CI: 0.97–2.47), all other survival associations were significant, with the highest reaching twice the risk of death for thrombocytosis on the date of diagnosis (HR400: 2.01, 95 % CI: 1.25–3.23).

Conclusions

Our EMR approach yielded associations comparable to published findings from medical record abstraction approaches. In addition, our results indicate that lower thrombocytosis thresholds and platelet measures up to 8 weeks before diagnosis may inform ovarian cancer characteristics and prognosis.

Keywords

Platelets Thrombocytosis Ovarian cancer Survival Electronic medical records

Background

Ovarian cancer is a rapidly progressive and lethal disease. In the United States (US), 22,280 new cases and 14,240 deaths due to ovarian cancer are estimated to occur [1]. Ovarian cancer is the 5th leading cause of cancer deaths among women and is responsible for more deaths per year than any other gynecologic malignancy [1]. Because of the anatomic location within the peritoneal cavity, ovarian cancer may be very advanced or even distantly metastatic before a patient experiences symptoms. Further, these symptoms are often initially vague and non-specific, and may mimic a variety of benign conditions [2]. Ovarian cancer also lacks a detectable pre-invasive stage that can be reliably evaluated by screening on a population level [2]. As a result, over 60 % of ovarian cancer presents with advanced stage disease [13]. Recent US data indicate a dismal five year relative survival rate of 46 %; this is reduced to 28 % among cases with distant metastases [1].

The association between thrombocytosis and the presence of an underlying solid tumor has long been recognized, prompting investigation of the role of platelets in disease progression [4]. Platelets promote cancer cell survival through a variety of mechanisms, including protection from immune surveillance, promotion of angiogenesis, and arrest of the cancer cell cycle [5]. Platelets have also been shown to increase the proliferation rate of ovarian cancer cells indepedent of direct contact with those cells and unaffected by blockade of adhesion receptors [6]. Molecular studies have proffered a possible mechanism for thrombocytosis in advancing tumor growth. Tumor derived interleukin-6 increases hepatic thrombopoietin, which stimulates bone marrow megakaryocytes and platelet production of TGF-β1, which in turn activates the TGF-β1/smad proliferation pathway in tumor cells [7]. Additionally, in vitro knockdown of TGF-βR1 in ovarian cancer cells by an anti-TGF-βR1 antibody halts proliferation of cancer cells when exposed to platelets [6]. Using an orthotopic mouse model of ovarian cancer, platelet transfusion resulted in increased tumor growth, and platelets were demonstrated to protect cancer cells from apoptosis [8]. The persistent paracrine cycle in which platelets promote tumor cell proliferation and sustain cancer cell viability may underlie differences in cancer prognosis according to platelet count.

The majority of ovarian malignancies are epithelial, which has worse survival than other ovarian tumors [3]. Known prognostic factors for epithelial ovarian cancer include age, stage, grade histologic subtype, and optimal cytoreduction [7, 9, 10]. In addition, pre-diagnosis thrombocytosis has been associated with poor prognosis [79, 1119]. To date, more than ten studies have evaluated the prognostic significance of preoperative thrombocytosis in ovarian cancer [79, 1120]; all but one found that thrombocytosis was an independent negative factor in ovarian cancer survival [20]. However, the diagnostic threshold used to define thrombocytosis has varied from 300 to 450 × 109/liter (L). Further, studies have used various time intervals for platelet measurements relative to diagnosis. Because of a lack of uniformity in thresholds and timing of platelet counts used to evaluate the association between thrombocytosis and overall survival in the existing literature, this study was undertaken to systematically compare three thresholds for thrombocytosis and the relevant timing of pre-diagnosis platelet counts in relation to ovarian cancer survival using Tumor Registry confirmed cases from the Vanderbilt University Medical Center (VUMC).

Methods

Study population

Appropriate Institutional Review Board (IRB) approval was garnered for this retrospective cohort study of de-identified EMR data (Vanderbilt University IRB #121299). Primary ovarian, peritoneal, and fallopian tube cancer cases were selected by International Classification of Disease-Oncology (ICD-O) codes C569 and C570 from the VUMC Tumor Registry (Fig. 1). Cases diagnosed before 1980, after 2013, or with unkown dates of diagnosis were excluded (N = 40). Germ cell tumors (ICD-O 9060, 9064, 9071, 9080, 9082, 9084, 9085), sex-cord stromal tumors (ICD-O 8620, 8634, 8640, 8670), and other tumors (ICD-O 8240, 8243, 8800, 8802, 8890, 8910, 9500, 9680) were excluded (N = 70). Epithelial ovarian cancer (EOC) cases were classified by histologic subtype: serous/papillary (ICD-O codes 8050, 8260, 8441, 8442, 8450, 8451, 8460, 8461, 8462); mucinous (ICD-O codes 8470, 8471, 8472, 8473, 8480, 8490); endometrioid (ICD-O codes 8380), clear cell (ICD-O codes 8310, 8313); and other (ICD-O codes 8013, 8041, 8046, 8070, 8120, 8320, 8570, 8950, 8951, 8980, 9000). Ovarian cancer cases with unknown histologic subtypes (ICD-O codes 8000, 8010, 8020, 8021, 8140, 8143, 8255, 8323, 8410, 8440, 8560) were retained, as the majority was likely to be epithelial. In addition to primary tumor site and histologic subtype, Tumor Registry data included date of diagnosis, stage, and grade of disease; women determined to have an age at diagnosis of less than 18 were excluded (N = 27). Women who had a prior epithelial or invasive carcinoma other than ovarian (N = 15), history of a myeloproliferative or myelodysplastic disorder (N = 2), or an autoimmune or inflammatory disorder (N = 10) were also excluded from analysis; no patients were found to have a history of total splenectomy (ICD code 41.5) prior to ovarian cancer diagnosis.
Fig. 1

Flow Chart of Tumor Registry and Platelet Lab Data Preparation of de-identified Electronic Medical Records from the Vanderbilt University Medical Center

Laboratory values for pre-diagnosis platelet counts were selected from the Synthetic Derivative (SD), a de-identified mirror of electronic medical records (EMR) from VUMC. Platelet count measurements (Current Procedural Terminology (CPT) code 85049) were from Sysmex assays conducted on whole blood samples with a reference range of 135–370 × 109/L by the Vanderbilt Pathology Lab Service. Thrombocytosis was defined using three thresholds: platelet counts greater than 350, 400, or 450 × 109/L. The relevant time frame of platelet measurement was evaluated with 5 time intervals: on the date of diagnosis, and up to 1 week, 2 weeks, 4 weeks, 8 weeks before and including the date of diagnosis. Only pre-diagnosis platelet counts were analyzed, as paraneoplastic mechanisms are thought to drive thrombocytsosis [7]. Further, post-operative platelet measures are intrinsically altered by inflammation secondary to surgical stress, and can be iatrogenically changed by transfusion or blood loss during debulking surgery for ovarian cancer [21, 22]. Death from any cause was determined from EMR and by linkage to the National Death Index (NDI). Cases were considered to have died if they were listed as deceased in the SD or if there was a date of death from the NDI. Otherwise, overall survival was censored at the date of last EMR entry.

Statistical analysis

Differences in clinical and histologic characteristics between cases with and without thrombocytosis were examined with Student’s t tests, χ2 tests, and Fisher’s exact test as appropriate. Cox proportional hazards regression was used to derive hazard ratios (HRs) and 95 % confidence intervals (CIs) for associations between thrombocytosis and overall ovarian cancer survival. Calendar time was used as the time scale for Cox regression models, with entry at date of ovarian cancer diagnosis and exit at date of death or last EMR entry. Due to low numbers, survival times were truncated at 10 years to prevent unstable estimates. Regression models included adjustment for known prognostic factors, including age at diagnosis, stage, grade, and histologic subtype of disease. Survival functions were visualized with Kaplan-Meier plots; the log-rank test was used to assess if differences were significant. Manual review of EMR was conducted to validate the date of diagnosis and timing of platelet measurement for a subset of cases. Sensitivity analyses were conducted by excluding cases with low malignant potential (LMP) tumors, synchronous cancers, non-White cases, and those with unknown stage of disease or histologic subtype. Data preparation was conducted with Excel and Python. In Python, the csv, datetime, time, matplotlib, and numpy modules were used along with dictionary and list stat structures to sort and filter data by platelet count and date relative to diagnosis date. All analyses were performed using SAS version 9.4 (SAS Institute, Cary, NC). A two-sided probability of 0.05 was used to determine statistical significance.

Results

Table 1 presents the demographic and histopathologic characteristics of 1,170 Tumor Registry confirmed cases diagnosed between 1980 and 2013, and 304 cases with pre-diagnostic platelet measures available from the VUMC SD. No cases diagnosed before 1995 were found to have laboratory measured platelet values available in their EMR. Although age at diagnosis, primary site, and histologic subtype were generally comparable, fewer cases with platelet count measures available had either unknown or unstaged disease (8.22 vs. 27.78 %) or unknown grade (27.63 vs. 38.97 %) than all cases. Among cases with pre-diagnosis platelet measures available, the majority were white (N = 266, 87.5 %), and had advanced stage (III or IV, N = 191, 62.83 %), high grade (poorly differentiated or undifferentiated, N = 155, 51.0 %), and serous histologic subtypes (N = 147, 48.4 %) of disease.
Table 1

Clinical Characteristics of Tumor Registry Confirmed Ovarian Cancer Cases from the Vanderbilt University Medical Center

 

All Epitheilal or Unknown Cases (N = 1170)

Cases With Pre-Diagnosis Platelets Measured (N = 304)

Characteristic

N or mean

% or std deva

N or mean

% or std deva

Age at Diagnosis, years

58.5

13.7

60.2

14.5

Date of Diagnosis, calendar year

 1980–1984

117

10.0

  

 1985–1989

143

12.2

  

 1990–1994

183

15.6

  

 1995–1999

202

17.3

62

20.4

 2000–2004

199

17.0

83

27.3

 2005–2009

208

17.8

100

32.9

 2010–2013

118

10.1

59

19.4

Race

 White

1036

88.6

266

87.5

 Black

68

5.8

25

8.2

 Asian

11

0.9

2

0.7

 Native

2

0.2

0

0.0

 Other/Unknown

53

4.5

11

3.6

Primary Site

 Ovary (C569)

1129

96.5

294

96.7

 Fallopian Tube (C570)

41

3.5

10

3.3

Histologic Subtype

 Serous

666

56.9

147

48.4

 Endometrioid

105

9.0

33

10.9

 Mucinous

75

6.4

24

7.9

 Clear Cell

45

3.9

15

4.9

 Other

47

4.0

18

5.9

 Unknown

232

19.8

67

22.0

Stage of Disease

 I

172

14.7

69

22.7

 II

52

4.4

19

6.3

 III

360

30.8

124

40.8

 IV

261

22.3

67

22.0

 Unknown/Unstaged

325

27.8

25

8.2

Disease Grade

 1, Well differentiated

58

5.0

21

6.9

 2, Moderately differentiated

161

13.8

44

14.5

 3, Poorly differentiated

412

35.2

120

39.5

 4, Undifferentiated

83

7.1

35

11.5

 Unknown

456

39.0

84

27.6

Overall Survival, years

4.1

3.4

3.4

3.1

aPercentages may not sum to 100 due to rounding error

Associations between thrombocytosis and clinical covariates are summarized in Table 2. When using the lowest thrombocytosis threshold, associations with higher stage (P-value =0.051) and grade (P-value =0.115) were suggestive, but not significant. Using either of the higher thresholds, cases were more likely to have stage IV or unstaged disease (P-value400 = 0.038, and P-value450 = 0.009) and undifferentiated grade 4 tumors (P-value400 = 0.008, and P-value450 = 0.010) than cases without thrombocytosis. A significant association was seen with primary site at the middle threshold (P-value400 = 0.015), but this did not evident at either of the other thresholds. Regardless of threshold used, there was no association between thrombocytosis and age, race, or histologic subtype of disease.
Table 2

Associations Between Thrombocytosis within 8 Weeks of Diagnosis and Clinical Covariates among Ovarian Cancer Cases from the Vanderbilt University Medical Center

 

Thrombocytosis (>350 × 109/L)

Thrombocytosis (>400 × 109/L)

Thrombocytosis (>450 × 109/L)

No (N = 145)

Yes (N = 159)

 

No (N = 190)

Yes (N = 114)

 

No (N = 228)

Yes (N = 76)

 

Characteristic

N or mean

(% or std dev)a

P-value**

N or mean

(% or std dev)a

P-value**

N or mean

(% or std dev)a

P-value**

Age at Diagnosis, years

60.7

(14.1)

59.9

(14.8)

0.631

60.9

(14.3)

59.1

(14.8)

0.275

60.4

(14.4)

59.8

(14.8)

0.746

Race

 White

128

(88.3)

138

(86.8)

0.696

169

(89.0)

97

(85.1)

0.325

202

(88.6)

64

(84.2)

0.317

 Other/Unknown

17

(11.7)

21

(13.2)

21

(11.1)

17

(14.9)

26

(11.4)

12

(15.8)

Primary Site

 Ovary (C569)

137

(94.5)

157

(98.7)

0.052 †

114

(100.0)

114

(100.0)

0.015 †

218

(95.6)

76

(100.0)

0.072 †

 Fallopian Tube (C570)

17

(5.5)

2

(1.3)

0

(0.0)

0

(0.0)

10

(4.4)

0

(0.0)

Histologic Subtype

 Serous

68

(46.9)

79

(49.7)

0.691

88

(46.3)

59

(51.8)

0.629

111

(48.7)

36

(47.4)

0.414

 Endometrioid

14

(9.7)

19

(12.0)

20

(10.5)

13

(11.4)

24

(10.5)

9

(11.8)

 Mucinous

15

(10.3)

9

(5.7)

19

(10.0)

5

(4.4)

22

(9.7)

2

(2.6)

 Clear Cell

6

(4.1)

9

(5.7)

9

(4.7)

6

(5.3)

10

(4.4)

5

(6.6)

 Other

9

(6.2)

9

(5.7)

11

(5.8)

7

(6.1)

12

(5.3)

6

(7.9)

 Unknown

33

(22.8)

34

(21.4)

43

(22.6)

24

(21.1)

49

(21.5)

18

(23.7)

 Serous

68

(46.9)

79

(49.7)

0.888

88

(46.3)

59

(51.8)

0.646

111

(48.7)

36

(47.4)

0.923

 Non-Serous

44

(30.3)

46

(28.9)

59

(31.1)

31

(27.2)

68

(29.8)

22

(29.0)

 Unknown

33

(22.8)

34

(21.4)

43

(22.6)

24

(21.1)

49

(21.5)

18

(23.7)

Stage of Disease

 I

43

(29.7)

26

(16.4)

0.051

52

(27.4)

17

(14.9)

0.038

59

(25.9)

10

(13.2)

0.009

 II

10

(6.9)

9

(5.7)

14

(7.4)

5

(4.4)

17

(7.5)

2

(2.6)

 III

56

(38.6)

68

(42.8)

76

(40.0)

48

(42.1)

94

(41.2)

30

(39.5)

 IV

25

(17.2)

42

(26.4)

35

(18.4)

32

(28.1)

43

(18.9)

24

(31.6)

 Unknown/Unstaged

11

(7.6)

14

(8.8)

13

(6.8)

12

(10.5)

15

(6.6)

10

(13.2)

Disease Grade

 1, Well differentiated

10

(6.9)

11

(6.9)

0.115

15

(7.9)

6

(5.3)

0.008

18

(7.9)

3

(4.0)

0.010

 2, Moderately differentiated

21

(14.5)

23

(14.5)

29

(15.3)

15

(13.2)

36

(15.8)

8

(10.5)

 3, Poorly differentiated

57

(39.3)

63

(39.6)

78

(41.1)

42

(36.8)

90

(39.5)

30

(39.5)

 4, Undifferentiated

10

(6.9)

25

(15.7)

12

(6.3)

23

(20.2)

18

(7.9)

17

(22.4)

 Unknown

47

(32.4)

37

(23.3)

56

(29.5)

28

(24.6)

66

(29.0)

18

(23.7)

aPercentages may not sum to 100 % due to rounding error

**P-values from χ2 test or Fisher’s exact test where indicated (†); bold values denote significant associations

In Table 3, associations between thrombocytosis and overall ovarian cancer survival are shown, including 5 time intervals and three thresholds. Within each threshold, the prevalence of thrombocytosis was lowest on the date of diagnosis, but this was not found to significantly differ from the other timeframes. In both unadjusted and multivariable adjusted analysis, thrombocytosis was significantly associated with worse survival across all five time intervals and three thresholds, except for the lowest threshold on the date of diagnosis (P-value350crude = 0.093 and P-value350adjusted = 0.070). Other associations at this threshold indicated a 79-83 % significantly increased risk of death with thrombocytosis. For both of the higher thresholds, associations were larger on the date of diagnosis (HR400: 2.01, 95 % CI 1.25–3.23, and HR450: 2.00, 95 % CI: 1.16–3.46), and smaller as time to diagnosis increased up to 8 weeks (HR400: 1.55, 95 % CI: 1.14–2.10, and HR450: 1.55, 95 % CI: 1.12–2.15). Kaplan-Meier analysis was found to be in general agreement, such that ovarian cancer cases with pre-diagnostic thrombocytosis were found to have significantly shorter survival across the 400 threshold regardless of timing, and significantly shorter survival for the 350 and 450 thresholds for all time periods except for those taken on the date of diagnosis (data not shown).
Table 3

Thrombocytosis and Overall Survival Among Ovarian Cancer Cases from the Vanderbilt University Medical Center

 

Thrombocytosis

No Thrombocytosis (Reference)

Unadjusted Association

Multivariable Associationa

Thrombocytosis

%

N Cases

N Events

N Cases

N Events

HR

95 % CI

P-value*

HR

95 % CI

P-value*

Defined by ≥350 × 109/L

 Date of diagnosis

44.8

61

42

75

46

1.45

0.94–2.23

0.093

1.55

0.97–2.47

0.070

 1 week prior to date of diagnosis

53.1

128

96

113

63

2.09

1.51–2.89

<0.001

1.83

1.30–2.58

0.001

 2 week prior to date of diagnosis

52.5

147

106

133

72

1.96

1.47–2.66

<0.001

1.79

1.31–2.44

<0.001

 4 week prior to date of diagnosis

53.2

158

110

139

73

1.94

1.44–2.62

<0.001

1.80

1.33–2.45

<0.001

 8 week prior to date of diagnosis

52.3

159

111

145

77

1.92

1.43–2.58

<0.001

1.80

1.33–2.43

<0.001

Defined by ≥400 × 109/L

 Date of diagnosis

31.6

43

33

93

60

1.98

1.27–3.09

0.003

2.01

1.25–3.23

0.004

 1 week prior to date of diagnosis

39.4

95

73

146

94

1.92

1.39–2.64

<0.001

1.62

1.16–2.26

0.005

 2 week prior to date of diagnosis

38.2

107

79

173

108

1.87

1.39–2.53

<0.001

1.60

1.17–2.18

0.003

 4 week prior to date of diagnosis

38.1

113

80

184

112

1.78

1.32–2.40

<0.001

1.54

1.14–2.09

0.006

 8 week prior to date of diagnosis

37.5

114

81

190

116

1.78

1.33–2.40

<0.001

1.55

1.14–2.10

0.005

Defined by ≥450 × 109/L

 Date of diagnosis

19.9

27

22

109

71

1.98

1.21–3.27

0.007

2.00

1.16–3.46

0.013

 1 week prior to date of diagnosis

26.1

63

51

178

116

2.01

1.43–2.82

<0.001

1.71

1.20–2.45

0.003

 2 week prior to date of diagnosis

25.7

72

55

208

132

1.91

1.38–2.65

<0.001

1.62

1.16–2.27

0.005

 4 week prior to date of diagnosis

24.9

74

56

223

136

1.88

1.37–2.59

<0.001

1.56

1.12–2.17

0.008

 8 week prior to date of diagnosis

25.0

76

57

228

140

1.79

1.30–2.45

<0.001

1.55

1.12–2.15

0.009

*Bold type denotes significant associations

aAdjusted for age at diagnosis, stage, grade, and histologic subtype

To validate dates of platelet measurement and diagnosis, EMR were manually reviewed for twenty cases. The Tumor Registry date of diagnosis matched the date of operative and/or pathology report for 75 % of reviewed cases. However, for 25 %, the Tumor Registry date of diagnosis was up to 2 weeks before the operative and/or pathology report, and usually coincided with the first presentation of symptoms that led to the diagnosis, e.g., computed tomography (CT) or ultrasound imaging. Based on this, we selected 2 weeks prior to and including the date of diagnosis as the interval most likely to best capture pre-diagnosis thrombocytosis in our data, and used this to conduct sensitivity analyses (Table 4). In agreement with our primary analysis, excluding cases with low malignant potential (N = 12), synchronous cancers (N = 26), not reported as White (N = 38), or unknown stage of disease (N = 36), did not materially alter our results. When unknown histologic subtypes (N = 86) were excluded, significance was attenuated for two of the three thresholds (P-value350 = 0.034; P-value400 = 0.089; P-value450 = 0.186). When all above exclusions were simultaneously applied, all associations were attenuated (P-value350 = 0.065; P-value400 = 0.072; P-value450 = 0.096), likely due to the small sample size remaining in the analysis (N = 152). Similar to Cox regression, Kaplan-Meier plots showed significant differences for cases with and without thrombocytosis within two weeks of diagnosis for all three thresholds evaluated (Fig. 2).
Table 4

Sensitivity Analysis of Thrombocytosis within 2 Weeks of Diagnosis and Overall Ovarian Cancer Survival

 

Thrombocytosis

No Thrombocytosis

Unadjusted Association

Multivariable Associationa

Thrombocytosis

N Cases

N Events

N Cases

N Events

HR

95 % CI

P-value*

HR

95 % CI

P-value*

Defined by ≥350 × 109/L

 2 weeks to date of diagnosis

147

106

133

72

1.96

1.45–2.66

<0.001

1.78

1.31–2.44

<0.001

  Excluding low malignant potential tumors

147

106

121

71

1.71

1.26–2.32

<0.001

1.67

1.22–2.28

0.001

  Excluding synchronous cancers

134

101

124

71

1.94

1.42–2.64

<0.001

1.72

1.26–2.36

<0.001

  Excluding non–Whites

128

91

114

61

1.92

1.38–2.68

<0.001

1.88

1.34–2.62

<0.001

  Excluding unknown stage of disease

134

95

124

67

1.89

1.37–2.60

<0.001

1.66

1.20–2.30

0.002

  Excluding unknown histologic subtypes

115

79

104

52

1.81

1.27–2.58

0.001

1.48

1.03–2.13

0.034

  Excluding all of the above cases

84

60

68

40

1.47

0.98–2.20

0.063

1.47

0.98–2.21

0.065

Defined by ≥400 × 109/L

 2 weeks to date of diagnosis

107

78

173

100

1.87

1.39–2.53

<0.001

1.60

1.17–2.18

0.003

  Excluding low malignant potential tumors

107

78

161

99

1.67

1.23–2.26

<0.001

1.50

1.10–2.06

0.010

  Excluding synchronous cancers

96

74

162

98

1.94

1.42–2.64

<0.001

1.61

1.17–2.20

0.003

  Excluding non–Whites

91

64

151

88

1.75

1.26–2.43

<0.001

1.58

1.13–2.21

0.008

  Excluding unknown stage of disease

96

69

162

93

1.84

1.34–2.52

<0.001

1.49

1.08–2.07

0.016

  Excluding unknown histologic subtypes

84

59

135

72

1.81

1.28–2.57

<0.001

1.37

0.95–1.97

0.089

  Excluding all of the above cases

59

44

93

56

1.69

1.13–2.53

0.011

1.46

0.97–2.20

0.072

Defined by ≥450 × 109/L

 2 weeks to date of diagnosis

72

55

208

123

1.91

1.38–2.65

<0.001

1.62

1.16–2.27

0.005

  Excluding low malignant potential tumors

72

55

196

122

1.73

1.25–2.39

<0.001

1.53

1.09–2.14

0.014

  Excluding synchronous cancers

64

51

194

121

1.92

1.38–2.68

<0.001

1.66

1.17–2.34

0.004

  Excluding non–Whites

60

44

182

108

1.82

1.27–2.61

0.001

1.65

1.14–2.40

0.008

  Excluding unknown stage of disease

63

47

195

115

1.88

1.33–2.65

<0.001

1.51

1.05–2.15

0.024

  Excluding unknown histologic subtypes

54

41

165

90

1.81

1.24–2.63

0.002

1.31

0.88–1.94

0.186

  Excluding all of the above cases

37

29

115

71

1.73

1.11–2.70

0.016

1.49

0.93–2.37

0.096

*Bold type denotes significant associations

aAdjusted for age at diagnosis, stage, grade, and histologic subtype as appropriate after exclusions

Fig. 2

Ovarian Cancer Overall Survival Kaplan-Meier functions for Thrombocytosis within two weeks of diagnosis.; Legend: a Thrombocytosis (350) two weeks prior to and including the date of diagnosis; b Thrombocytosis (400) two weeks prior to and including the date of diagnosis; and c Thrombocytosis (450) two weeks prior to and including the date of diagnosis

Discussion

In this large retrospective analysis of confirmed Tumor Registry cases from a single tertiary-care medical center with platelet measurments available in electronic medical records (EMR), we found that thrombocytosis, defined as a platelet count greater than 350, 400, or 450 × 109/L, and measured up to 8 weeks before diagnosis, was associated with significantly shorter overall ovarian cancer survival. This work adds to existing literature by providing a comprehensive comparison of thrombocytosis prevalence and associations with survival across three thresholds with uniform platelet measures in one study population, and indicates that elevated platelet counts up to eight weeks before diagnosis may be informative for ovarian cancer prognosis. In addition, this research demonstrates the power of combining Tumor Registry and EMR data to evaluate potential prognostic factors as an alternate approach to analysis based on data from retrospective medical chart review.

To date, more than ten studies have analyzed pre-operative thrombocytosis in relation to ovarian cancer survival [79, 1117, 19, 20]. The threshold to define thrombocytosis has varied from 300–450, with most studies using 400 [1115, 1720]. The relevant timing of thrombocytosis has also varied from within 1 week [12, 13, 18], to within 2 weeks from the date of diagnosis [14, 15, 19], although several publications lack specific details on timing other than qualifying measures as preoperative [8, 9, 11, 16, 20]. The prevalence of thrombocytosis has varied across studies, with ranges of 22.4 % [14] to 43.5 % [19]. Among those with significant associations with overall ovarian cancer survival, hazards have also ranged considerably. The largest association reported was a nearly five-fold increased risk of death among 136 cases, where adjustment included age, stage, histologic subtype, grade, cytoreduction, chemotherapy, CA-125, and fibrinogen [18]. In that study, the thrombocytosis threshold differs between the text (400) and table of results (300), but the reported prevalence was low (7.4 %) [18]. The largest study to date included 816 cases and had a prevalence of 22.8 % with a threshold of 400 [11]. After adjusting for age, menopausal status, histologic subtype, grade, stage, residual disease, ascites, CA-125, hemoglobin, and leukocyte count, cases with thrombocytosis had a more than two-fold higher risk of death [11]. The highest prevalence reported (42.9 %) used a threshold of 350 among 91 cases; after adjustment for age, menopausal status, stage, CA-125, and surgery, thrombocytosis was associated with a more than two-fold increased risk of death [16]. Meta-analysis of 5 studies with different statistical adjustments, but all using 400 as their threshold, yielded a thrombocytosis prevalence of 31.1 %, and a 52 % significantly increased risk of 5 year mortality [23]. Thus, our findings for the prevalence of pre-diagnosis thrombocytosis and associations with overall survival are in general agreement with existing literature, indicating that evaluation of VUMC Tumor Registry confirmed cases is a viable approach for ovarian cancer research.

Pre-operative thrombocytosis has been linked to decreased overall survival and to a host of clinical parameters and outcomes, which may in turn help elucidate the factors at play in increased mortality for those patients with thrombocytosis. Platelets are an acute phase reactant, meaning that platelet count transiently increases in response to inflammation [24]. Etiologies for reactive thrombocytosis include malignancy, tissue damage, infection, and chronic inflammation [22]. Factors influencing platelet count, in the absence of the the aforementioned reactive factors, include age, sex, race/ethnicity, nutritional status, drug exposure [24, 25], and inherent genetic variability [26]. Thrombocytosis in patients with ovarian cancer is associated with greater volumes of ascites [6, 13, 18], lower hemoglobin, receipt of peri-operative packed red blood cells transfusion [6], major post-operative complications [27] and post-operative death [25]. Thrombocytosis with concurrent leukocytosis, another marker of inflammation or infection, was associated with a higher risk of post-operative death (OR 5.4) than either thrombocytosis (OR 2.16) or leukocytosis alone (OR 1.78) [27]. Furthermore, pre-operative thrombocytosis was an independent negative prognostic factor for disease recurrence and progression-free survival [5, 6, 9, 12, 1517, 19]. Taken together, these factors may explain, at least in part, the association between thrombocytosis and shorter overall survival.

In addition to overall mortality, pre-operative thrombocytosis was found to be an independent predictor for the development of venous thromboembolism among clear cell ovarian carcinoma cases [28]. Risk factors for venous thromboembolism in ovarian cancer include increasing age, a higher number of chronic comorbid conditions, higher stage disease, invasive histology, and the absence of any major surgery [29]. In a multivariable model, women with symptomatic venous thromboembolism at the time of diagnosis prior to primary treatment had significantly shorter overall survival when compared with women without venous thromboembolism at diagnosis [30]. In accordance with the guidelines provided by the American Society of Clinical Oncology, oncology patients should receive venous thromboembolism prophylaxis 7–10 days prior to a major operation and extending up to 4 weeks post-operatively in patients with abdominal or pelvic surgery with high risk features [31]. As our data indicate that thrombocytosis up to 8 weeks pre-operative may confer worse survival, and thrombocytosis has been linked to development of venous thromboembolism, more investigation is needed to determine the possible efficacy of longer periods of pre-operative thromboembolism prophylaxis in helping to reduce ovarian cancer morbidity and mortality. Robust findings from our sensitivity analysis results indicate that pre-operative prophylaxis may have clinical utility for all types of ovarian cancer cases.

This study expands upon existing knowledge by directly comparing three thresholds for thrombocytosis. As expected, the prevalence of thrombocytosis decreased with increasing threshold. For both the 400 and 450 thresholds, we found significant associations with higher stage and grade of disease, and significant associations with overall survival even after adjusting for clinical and tumor characteristics. Our study also expands upon current knowledge by analyzing multiple time widows for the occurrence of thrombocytosis. For each threshold, the prevalence of thrombocytosis was lowest on the date of diagnosis, and was fairly consistent across the remaining time frames. With regard to survival associations, when using the smallest threshold of 350, the association on the date of diagnosis was not significant, but increasing time frames all had significant associations with worse survival. This pattern differed for both of the larger thresholds, where stronger associations occurred on the date of diagnosis, and smaller, but still significant associations, were found when measures up to 8 weeks pre-diagnosis were included. Larger associations closer to the date of diagnosis may be due to disease progression and subsequent worsening paraneoplastic thrombocytosis. Alternately, inclusion of values up to 8 weeks pre-diagnosis may increase measurement error, such that cases with thrombocytosis initially evaluated for a separate indication may have resolution of thrombocytosis by the time of cancer diagnosis. Such misclassification of a dichotomous exposure would be independent of the outcome and would therefore serve to attenuate associations toward the null. Notably, our validity sub-study indicated that all platelet measures were from before diagnosis. In addition, we found that among cases with thrombocytosis occurring within 8 weeks of diagnosis, more than 95 % also had thrombocytosis within 4 weeks, 2 weeks, or 1 week of diagnosis, regardless of the threshold. Only when evaluating the smallest timeframe, the date of diagnosis, was this reduced to 70 % of cases. Thus, misclassification of thrombocytosis is not likely to greatly influence the results of the current study.

Limitations of this investigation include the number of cases with preoperative platelet count data available, when compared with all confirmed Tumor Registry cases. Differences in disease presentation, preoperative course, and time to diagnosis likely contribute to variability in whether platelets were measured before or after diagnosis for each patient. Data on use of anti-platelet or anti-coagulant medications, which may alter the potential for adverse events in the setting of thrombocytosis, was not included in this study. Further, many cases were missing information on histologic subtype, stage, or grade of disease. Sensitivity analyses conducted by excluding these cases still yielded mostly significant survival associations, indicating that missing data is not greatly impacting our findings. Another limitation is the lack of data on optimal tumor cytoreduction, which has been shown to be an important negative predictor of ovarian cancer survival [10]. However, thrombocytosis has not been found to be associated with optimal debulking in prior studies, so this should not confound the current results. While sucessess of surgical debulking was unavailable from Tumor Registry data, all included cases were reviewed by trained Tumor Registry personnel, and information on stage, grade, and subtype of disease were reasonably standardized. Additional limitations of this analysis include the inherent retrospective nature of our analysis, the possibility of including deaths unrelated to ovarian cancer by use of all-cause mortality, and care limited to a single tertiary care center. Thus, our findings may not be generalizable to all ovarian cancer cases at all institutions. However, outcomes were ascertained by linkage to the NDI as well as by EMR notes on vital status, and our results are generally in agreement with those from other single and multi-center studies. Additional strengths of the current study include a robust analytic approach that included three thrombocytosis thresholds, exploration of relevant time frames for platelet measurement, and multivariable adjustment for all clinical covariates available. In addition, our study employed compuater programming methods to obtain EMR data, which differs from other studies in which manual chart review was conducted. Rather than including cases without evidence of thrombocytosis noted in medical records, our reference group included only cases where platelet values were actually measured, and were not found to be elevated.

Conclusions

Thrombocytosis was identified in 20-50 % of ovarian cancer cases, depending upon the pre-diagnostic time interval and diagnostic threshold. Regardless of timing or threshold, thrombocytosis was generally associated with more aggressive tumor characteristics and was an independent negative prognostic factor for overall survival. Our findings indicate that lower thrombocytosis thresholds and measures collected up to 8 weeks before diagnosis may inform ovarian cancer prognosis.

Abbreviations

CI, confidence interval; CPT, Current Procedural Terminology (code); CT, computed tomography; EMR, electronic medical records; HR, hazard ratio; ICD-O, International Classification of Disease-Oncology; IRB, institutional review board; L, liter; NDI, National Death Index; SAS, Statistical Analysis Software; SD, Synthetic Derivative; TGF-β1, transforming growth factor-beta 1; TGF-βR1, transforming growth factor-beta receptor 1; US, United States; VUMC, Vanderbilt University Medical Center

Declarations

Acknowledgements

We thank the members and supporters of the Vanderbilt Ovarian Cancer Alliance (VOCAL).

Funding

Dr. Beeghly-Fadiel and this research was supported, in part, by a Department of Defense Ovarian Cancer Research Program Pilot Award (W81XWH-14-1-0104). Datasets were obtained from the Vanderbilt University Medical Center Synthetic Derivative and BioVU which is supported by institutional funding, the 1S10RR025141-01 instrumentation award, and by the Vanderbilt CTSA grant UL1TR000445 from NCATS/NIH.

Availability of data and materials

Individual level clinical data from the VUMC Synthetic Derivative may not be made publically available; however, tabulated results and summary statistics may be shared via scientific presentations and publications of research findings.

Authors’ contributions

Concept and design: GDC, DK, ABF; acquisition and preparation of data: GDC, JMS, JTF, SK, ABF; analysis and interpretation of data: GDC, JMS, MAC, DK, ABF; writing and manuscript review: GDC, JMS, JTF, SK, MAC, DK, ABF; project supervision: ABF. All authors have read and approved the final manuscript.

Competing interests

All authors attest that they have no competing interests. For complete disclosure, Dr. Crispens has participated in clinical trials led by Astra-Zeneca and Jansen Pharmaceuticals.

Consent for publication

Not applicable.

Ethics approval and consent to participate

This retrospective cohort study of data from the VUMC Synthetic Derivative was not determined to qualify as human subject research; approved for this study was garnered from the Institutional Review Board (IRB) of Vanderbilt University, Nashville, Tennessee (IRB #121299). As only de-identified EMR data was included, individual patient consent was not required for this study.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Division of Epidemiology, Department of Medicine, Vanderbilt University Medical Center
(2)
Division of Gynecologic Oncology, Department of Obstetics and Gynecology, Vanderbilt University Medical Center
(3)
Vanderbilt-Ingram Cancer Center

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Copyright

© The Author(s). 2016