‘FLARE’ of tumor marker in advanced gastric cancer treated with first-line systemic therapy

Abstract

Background:

Transient tumor marker elevations caused by chemotherapy were defined as ‘Flare’ and have been demonstrated in some solid tumors. In clinical practice, we observed that some patients were accompanied by elevated tumor markers during treatment, but subsequent imaging proved that the treatment they received was effective.

Objectives:

We aimed to study the Flare and the prognosis in advanced gastric cancer.

Design:

This is an observational retrospective study. A total of 167 patients were enrolled in this study. Carcinoembryonic antigen (CEA), carbohydrate antigen (CA) 19-9 and CA125 values were obtained before the first, second, third, fourth, fifth and sixth cycles of treatment, respectively.

Methods:

Imaging for the first efficacy assessment was reviewed according to the Response Evaluation Criteria in Solid Tumors 1.1 (RECIST 1.1) criteria. Kaplan–Meier analyses and log-rank tests were performed for overall survival (OS) analyses. Univariate and multivariate Cox analyses were used to determine the prognostic factor for OS and progression-free survival (PFS).

Results:

37.1% of patients were accompanied with at least one tumor marker Flare during the course of treatment. The median time to tumor marker peak was 24–30 days and the Flare duration lasted 49–53 days. Patients with tumor markers Flare had a worse OS. Flare may be associated with the use of 5-fluorouracil. Baseline CEA and CA125 levels were the independent prognostic factors for OS and baseline CA125 level was the independent prognostic factor for PFS.

Conclusion:

Initial elevation of tumor markers during treatment is not an indication of tumor progression. Patients with tumor markers ‘Flare’ may had a worse OS.

Keywords

FLARE CA19-9 CA125 CEA gastric cancer prognosis tumor marker

Introduction

The Response Evaluation Criteria in Solid Tumors 1.1 (RECIST 1.1) criteria more applicable to cytotoxic agents¹ was an attempt to assess the chemotherapeutic efficacy. According to RECIST 1.1 criteria, radiology remains the optimal recommendation for evaluating the efficacy of gastric cancer chemotherapy. However, especially in patients with only bone or peritoneal metastases, radiology is insensitive to evaluate the efficacy of the primary lesion of gastric cancer. Although the changes in iodine concentration on spectral computed tomography (CT)² or tumor volume on CT³ may be able to predict the pathological response of gastric primary lesion, it has not been extensively validated. Previous studies have demonstrated that carcinoembryonic antigen (CEA), CA125 and CA19-9 can improve the accuracy of the diagnosis of gastric cancer and have prognostic significance.^4–6 Furthermore, tumor markers have been shown to be valuable in predicting the efficacy of chemotherapy considering the convenience.^7,8 Tumor markers often show three types of changes during the treatment process: decreasing, increasing and normal. The viewpoint that an increasing tumor marker as a predictor of disease progression and a decreasing tumor marker as a predictor of disease control is generally accepted. In clinical practice, however, we observed that the majority of patients with elevated tumor markers during the initial treatment did not indicate clinical disease progression. This phenomenon in other solid tumors has been demonstrated and has been named the ‘Flare or Surge’.^9–19 Sikander Ailawadhi et al. defined CEA Flare as ‘an increase of >20% from baseline followed by a >20% drop in one or more subsequent CEA levels compared to baseline’⁹. However, the elevated values of other tumor markers Flare compared to baseline were not clearly defined. Elevated tumor markers due to Flare were not the symbol of treatment failure in either prostate cancer or metastatic colorectal cancer.^10,11,14,17 Therefore, the existence of Flare may lead us to make erroneous judgments about the efficacy of the treatment.

In gastric cancer, tumor marker Flare has also been reported in the literature.²⁰ However, studies on the ‘Flare’ of carbohydrate antigen 125 (CA125) in gastric cancer are rare and the prognosis for patients with ‘Flare’ is unknown. This article takes a deeper look at the value of tumor markers Flare in predicting chemotherapeutic efficacy, and the relationship between ‘Flare’ and prognosis in gastric cancer.

Patients and methods

This retrospective study included 167 eligible patients at Cancer Center, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology between June 2017 and May 2021 (Supplemental Figure 1). CEA, CA19-9 and CA125 values in peripheral blood were collected before the first, second, third, fourth, fifth and sixth cycles of treatment, respectively. The recommended cutoff levels of serum CEA, CA19-9 and CA125 were 5, 37 and 35 U/mL, respectively. Treatment response was assessed radiologically (CT/magnetic resonance imaging) according to RECIST 1.1 criteria.

Flare phenomenon was defined as a tumor marker (CEA, CA19-9 or CA125) initially increased from baseline and then declined during first-line treatment of gastric cancer. Positive tumor marker referred to tumor marker with a value of greater than or equal to recommended cutoff value. Negative tumor marker referred to tumor marker with a value of less than recommended cutoff value. Overall survival (OS) was calculated as the time from diagnosis to the date of any cause of death and progression-free survival (PFS) was calculated as the time from diagnosis to the date of identification of disease progressive.

Survival curves of different groups were estimated and compared by Kaplan–Meier method and log-rank test using Medcalc software at a significance level of p < 0.05. Categorical variables were compared using χ² and Fisher’s exact tests in IBM SPSS 26.0 version. Univariate and multivariate Cox model analyses were used to identify independent prognostic factors affecting OS and PFS among numerous clinical factors. To analyze independent prognostic factors, univariate Cox regression analysis was first performed with each variable and variables with p value <0.2 were selected. Multivariate Cox regression analysis using enter selection was performed, and the independent prognostic variables of OS and PFS were then determined. The reporting of this study conforms to the STROBE statement.

Results

Patient clinical features

The median follow-up was 14.9 [95% confidence interval (CI): 13.2–16.6] months. The average age of 167 patients was 56.6 years. In all, 73 patients were males and 94 were females. Lung, bone, liver, lymph nodes and peritoneal metastases accounted for 9.0% (15/167), 6.6% (11/167), 25.7% (43/167), 56.3% (94/167) and 28.1% (47/167), respectively. Treatment regimens containing oxaliplatin, Teggio, 5-fluorouracil and capecitabine in ratios of 84.4% (141/167), 45.5% (76/167), 27.5% (46/167) and 21.6% (36/167), respectively (Table 1).

Table 1.

Patients characteristics and univariable analyses of clinical variables in relation to FLARE.

	Non-Flare	Flare	χ² value	p Value
Age (years)
⩾60	51	25	1.070	0.301
<60	54	37
Sex
Female	63	31	1.584	0.208
Male	42	31
Lung metastasis
Yes	12	3	1.343	0.246
No	93	59
Bone metastasis
Yes	5	6	0.836	0.361
No	100	56
Liver metastasis
Yes	23	20	2.186	0.139
No	82	42
Lymph node metastasis
Yes	60	34	0.084	0.772
No	45	28
Peritoneal metastasis
Yes	33	14	1.509	0.219
No	72	48
Oxaliplatin
Yes	88	53	0.083	0.773
No	17	9
Teggio
Yes	50	26	0.508	0.476
No	55	36
5-Fluorouracil
Yes	21	25	8.067	0.005
No	84	37
Capecitabine
Yes	24	12	0.283	0.595
No	81	50

Changes in tumor markers during first-line treatment

Clinically, we always pay more attention to positive tumor markers. Therefore, we defined the changes of tumor markers in patients with negative CEA, CA19-9 and CA125 as normal tumor markers. Patients with at least one tumor marker positive was divided into five categories (regardless of negative tumor markers): (1) decrease; (2) increase; (3) increase after decrease; (4) FLARE: ‘Flare’ exists in at least one tumor marker, whether or not accompanied with (1)–(3); and (5) Other: it cannot be classified as any of the above. Our study suggests that during the first-line treatment, 21% (35/167) of patients are negative for three tumor markers, 30.5% (51/167) of patients have a continuous decrease in tumor markers, 4.8% (8/167) of patients have a progressive upward trend in tumor markers and 37.1% (62/167) of patients are accompanied with the ‘Flare’ of at least one tumor marker. There were 70 patients with elevated tumor markers after treatment, and 88.6% (62/70) of them were caused by ‘Flare’ and the other eight patients were due to disease progression (Supplemental Figure 2).

Relationship between changes in tumor markers and response to systemic therapy

Among the 51 patients with continuous decrease of tumor markers, the overall response to treatment was 94.1% (48/51) [standard deviation (SD): 52.9%, 27/51; partial remission (PR): 41.2%, 21/51]. Of the 62 patients with ‘Flare’, 93.5% (58/62) could benefit from the treatment (SD: 67.7%, 42/62; PR: 25.8%, 16/62). All eight patients (100%) with continuous increase of tumor markers had radiographic evidence of ineffective treatment (Supplemental Figure 2).

CEA Flare

In the biweekly regimen, the peak of CEA Flare occurred before the second and third cycles in 57.14% and 42.86% of the patients, respectively. In the triweekly therapy, the peak of CEA Flare occurred before the second and third cycles in 85% and 15% of the patients, respectively. The Flare peak of CEA emerged at a median of 30 (95% CI: 27–34) days from the beginning of treatment. The Flare duration was 53 (95% CI: 48–58) days (Tables 2 and 3).

Table 2.

The relationship between the timing of CEA, CA199 and CA125 Flare peaks and therapeutic schedule.

	Therapeutic schedule	Pre-C2 (%)	Pre-C3	Pre-C4
CEA (n = 27)	2w (n = 7)	4 (57.14)	3 (42.86)	0
	3w (n = 20)	17 (85)	3 (15%)	0
CA125 (n = 32)	2w (16)	12 (75)	4 (25%)	0
	3w (n = 16)	14 (87.5)	2 (12.5%)	0
CA19-9 (n = 21)	2w (n = 9)	7 (70)	2 (20%)	1 (10%)
	3w (n = 11)	8 (72.73)	3 (27.27%)	0

2w, biweekly treatment; 3w, triweekly treatment; CA, carbohydrate antigen; CEA, carcinoembryonic antigen; Pre-C2, before the second cycle of treatment; Pre-C3, before the third cycle of treatment; Pre-C4, before the fourth cycle of treatment.

Table 3.

The median time of peak and duration of CEA, CA19-9 and CA125 Flare.

	The median time of Flare peak (95% CI, days)	Duration of Flare (95% CI, days)
CEA	30 (27–34)	53 (48–58)
CA125	28 (23–33)	52 (42–58)
CA19-9	24 (21–32)	49 (37–54)

CA, carbohydrate antigen; CEA, carcinoembryonic antigen; CI, confidence interval.

CA125 Flare

The majority of the peaks in CA125 Flare appeared before the second cycle for both biweekly (75%) and triweekly treatment (87.5%). The emergence of the CA125 Flare median time was 24 (95% CI: 21–32) days and the CA125 Flare lasted a median 52 (95% CI: 42–58) days (Tables 2 and 3).

CA19-9 Flare

Similar to CEA and CA125, CA19-9 Flare was most frequently observed before the second cycle of treatment, with only one patient having a Flare peak before the fourth cycle. The median time to peak and duration of CA19-9 Flare was 24 (95% CI: 21–32) days and 49 (95% CI: 37–54) days, respectively (Tables 2 and 3).

Influencing factors of ‘Flare’

Using χ² test, the associations in age, gender, lung, bone, liver, lymph node or peritoneal metastasis in the ‘Flare’ group versus the ‘Non-Flare’ group were not be observed. There were no significant differences in the use of Teggio, oxaliplatin or capecitabine between ‘Flare’ group and the ‘Non-Flare’ group. However, the use of 5-fluorouracil was associated with ‘Flare’ (p = 0.004) (Table 1).

‘Flare’ and prognosis

For the total cohort, the median OS and PFS were 16.4 (95% CI: 14.4–18.4) months and 8.1 (95% CI: 6.7–9.4) months, respectively. Furthermore, the absence or presence of any of the tumor markers Flare in CEA, CA19-9 and CA125 was associated with OS [17.9 versus 12.1 months, p = 0.0238, hazard ratio (HR): 0.58, 95% CI: 0.36–0.94]. Although there was a benefit in PFS for patients without FLARE, there was no statistically significant differences (8.9 versus 7.1 months, p = 0.2038).

In addition, we analyzed the three tumor markers separately and excluded the interference of the other two tumor markers Flare. For CEA and CA125, the occurrence of ‘Flare’ was associated with reduced OS (CEA: 17.9 versus 8.4 months, p = 0.0411, HR: 0.44, 95% CI: 0.20–0.99; CA125: 17.9 versus 11.6 months, p = 0.0297, HR, 0.49, 95% CI: 0.26–0.95). No differences in PFS between patients with ‘Flare’ and without ‘Flare’ were observed. There were no significant differences between OS/PFS and ‘Flare’ for CA19-9 (Figure 1).

Figure 1.

Kaplan–Meier analysis of OS and PFS of the patients in the ‘Non-Flare’ group versus the ‘Flare’ group.

Prognostic factors associated with OS and PFS

Survival analyses of the total cohort were performed for the following 10 criteria: (1) Flare, (2) Age, (3) Sex, (4) Lung metastasis, (5) Bone metastasis, (6) Liver metastasis, (7) Lymph node metastasis, (8) Baseline CEA, (9) Baseline CA19-9, (10) Baseline CA125. Univariate Cox regression showed that three variables (Flare, baseline CEA level ⩾5 ng/mL and baseline CA125 level ⩾35 U/mL) were significant prognostic factors for OS; one variable (baseline CA125 level ⩾35 U/mL) was significant prognostic factor for PFS. Multivariate Cox regression using enter regression techniques was performed with the variables (p < 0.2) that showed that baseline CEA level ⩾5 ng/mL (HR: 0.912, 95% CI: 0.561–1.483) and baseline CA125 level ⩾35 U/mL (HR: 1.714, 95% CI: 1.055–2.783) were selected as the independent factor for OS and baseline CA125 level ⩾35 U/mL (HR: 1.726, 95% CI: 1.170–2.548) was chosen as the independent factor for PFS (Table 4).

Table 4.

Univariate and multivariate cox model analyses of clinicopathological characteristics for OS and PFS (all patients).

Prognostic factor	OS				PFS
	Univariate		Multivariate		Univariate		Multivariate
	p Value	HR (95% CI)	p Value	HR (95% CI)	p Value	HR (95% CI)	p Value	HR (95% CI)
Flare
Yes	0.026	1.719 (1.068–2.768)	0.481	1.208 (0.714–2.042)	0.207	1.286 (0.870–1.901)
No		1				1
Age (years)
⩾60	0.947	1.017 (0.625–1.654)			0.685	1.083 (0.737–1.589)
<60		1				1
Sex
Female	0.743	0.923 (0.574–1.485)			0.883	0.972 (0.665–1.421)
Male		1				1
Lung metastasis
Yes	0.442	0.699 (0.280–1.741)			0.745	0.901 (0.481–1.688)
No		1				1
Bone metastasis
Yes	0.162	1.750 (0.799–3.830)	0.130	1.870 (0.831–4.207)	0.426	1.340 (0.651–2.759)
No		1				1
Liver metastasis
Yes	0.481	1.214(0.708–2.084)			0.416	1.193 (0.780–1.826)
No		1				1
Lymph node metastasis
Yes	0.862	1.055 (0.656–1.696)			0.441	0.862 (0.592–1.257)
No		1				1
Baseline CEA
⩾5	0.008	1.930 (1.187–3.140)	0.016	1.903 (1.129–3.208)	0.086	1.400 (0.953–2.057)	0.065	1.448 (0.977–2.148)
<5		1				1
Baseline CA19-9
⩾37	0.710	0.912 (0.561–1.483)			0.738	1.068 (0.728–1.566)
<37		1				1
Baseline CA125
⩾35	0.029	1.714 (1.055–2.783)	0.043	1.676 (1.016–2.766)	0.005	1.730 (1.178–2.543)	0.006	1.726 (1.170–2.548)
<35		1				1

CA, carbohydrate antigen; CEA, carcinoembryonic antigen; CI, confidence interval; HR, hazard ratio; OS, overall survival; PFS, progression-free survival.

Survival analyses of the Flare cohort were performed for the following nine criteria: (1) Age, (2) Sex, (3) Lung metastasis, (4) Bone metastasis, (5) Liver metastasis, (6) Lymph node metastasis, (7) Baseline CEA, (8) Baseline CA19-9 and (9) Baseline CA125. Univariate Cox regression and multivariate Cox regression showed that none of the nine included variables was a significant prognostic factor for OS. Baseline CA125 level ⩾35 U/mL (HR: 2.243, 95% CI: 1.106–4.547) was significant prognostic factors for PFS. However, multivariate Cox regression could not be performed due to the lack of sufficient significant variables (Supplemental Table 1).

Discussion

It is commonly believed that there is a consistency between the elevation of tumor markers and disease progression during chemotherapy. However, this viewpoint is untenable in some solid tumors due to the ‘Flare’. 11.1–15% of patients with advanced colorectal cancer will develop CEA surge during chemotherapy,^9,12,14,17 three of these studies analyzed the relationship between Flare and chemotherapy efficacy and showed that 100% CEA Flare patients had radiological confirmation of disease control. In prostate cancer, chemotherapy caused prostate-specific antigen (PSA) Flare in 11–18% of patients,^7,8,12,21 and in Avishay Sella’s study, 87.5% of the patients who presented with PSA Flare were able to benefit from chemotherapy. This suggested that the presence of Flare did not mean therapeutic failure, on the contrary, most patients can benefit from chemotherapy. Ineffective treatment is not only a waste of resources, but also bring irreversible physical damage to patients, so it is extremely important to properly assess the effectiveness of treatment. In this study, 37.1% of patients could be seen to have at least one tumor marker surge and of these patients, approximately 90% were confirmed to have a clinical response. The median time to tumor marker peak was 24–30 days (CEA: 30 days, CA19-9: 24 days, CA125: 28 days) and the surge duration lasted 49–53 days (CEA: 53 days, CA19-9: 49 days, CA125: 52 days). In addition, 57.1–87.5% of tumor markers surge occurred before the second cycle treatment. Therefore, we should be cautious about the initial elevation of tumor markers during first-line chemotherapy for gastric cancer, especially for patients receiving biweekly regimens.

It is reported that depression and anxiety were detected in 24.5 and 27.7% of gastric patients, respectively.²² Unfortunately, the quality of life of anxious patients is inferior to that of anxious-free patients.²³ Likewise, negative emotions such as depression can lead to poor prognosis and decreased compliance in cancer patients.²⁴ Most patients have a weak understanding of the ‘Flare’ and often deem that elevated tumor markers are equivalent to ineffective treatment, which will exacerbate the level of patient distress and increase the prevalence of anxiety. Therefore, helping patients to correctly recognize the initial elevation of tumor markers during chemotherapy can inhibit the growth of adverse emotions in patients.

In prostate cancer, there was no statistical difference in OS between the Flare and non-Flare groups.^10,11,15 CEA Flare was a favorable prognostic factor, and the CEA Flare group had better OS (median 17.7 months versus 10.9 months), PFS (median 8.3 months versus 3.1 months) and ORR (73% versus 11%) compared to the CEA elevated group in advanced colorectal cancer.¹² However, alpha fetoprotein (AFP) Flare is an adverse prognostic factor for patients with non-seminomatous testicular cancer¹³. In this study, patients with tumor markers surge had a worse OS (median OS: 17.9 months versus 12.1 months, p = 0.0238). Although patients with tumor markers surge had a worse PFS, there was no statistical difference. For the total cohort, baseline CEA and CA125 levels were the independent prognostic factors for OS and baseline CA125 level was the independent prognostic factor for PFS. We tried to explore the reasons for the appearance of tumor markers surge, but ultimately found that it was independent of age, sex and metastases in lung, bone, liver, lymph nodes or peritoneum. We conjecture that ‘Flare’ may be related to tumor burden, but we were unable to verify this conjecture due to the limitations of measuring the overall tumor burden of the patients. In patients with advanced colorectal cancer who develop CEA Flare, 70% receive oxaliplatin-based regimens and 99% receive fluoropyrimidine-based regimens.¹² In addition to this, irinotecan can also cause CEA Flare.¹⁴ In our cohort, tumor marker Flare was triggered by the use of 5-fluorouracil in gastric cancer patients, whereas oxaliplatin, Teggio and captabine did not. 5-Fluorouracil induced the expression of CEA mRNA which may be the reason of CEA Flare.^25,26

With the announcement of CheckMate-649 clinical trial result, immune checkpoint inhibitors have made a new breakthrough in gastric cancer, bringing new hope to more gastric cancer patients.²⁷ In the National Comprehensive Cancer Network guidelines, nivolumab plus chemotherapy is recommended as the optimal first-line therapy for patients with gastric cancer with programmed death ligand-1 combined positivity score ⩾5. Due to the scarcity of samples of patients receiving immunotherapy in first-line treatment, however, we did not verify the ‘Flare’ separately in this cohort. Nevertheless, the significance of Flare phenomenon in immunotherapy deserves further study.

Conclusion

In conclusion, our study shown that initial elevation of tumor markers during first-line treatment in gastric cancer is not an indication of tumor progression. Elevation of the initial tumor marker cannot be used as evidence for a change in treatment regimen. At the same time, patients with the tumor marker Flare had a worse OS.

Supplemental Material

sj-docx-3-tag-10.1177_17562848221124029 – Supplemental material for ‘FLARE’ of tumor marker in advanced gastric cancer treated with first-line systemic therapy

Supplemental material, sj-docx-3-tag-10.1177_17562848221124029 for ‘FLARE’ of tumor marker in advanced gastric cancer treated with first-line systemic therapy by Fangyuan Zhang, Menglan Zhai, Jinru Yang, Lei Zhao, Zhenyu Lin, Jing Wang, Tao Zhang and Dandan Yu in Therapeutic Advances in Gastroenterology

Supplemental Material

sj-pptx-1-tag-10.1177_17562848221124029 – Supplemental material for ‘FLARE’ of tumor marker in advanced gastric cancer treated with first-line systemic therapy

Supplemental material, sj-pptx-1-tag-10.1177_17562848221124029 for ‘FLARE’ of tumor marker in advanced gastric cancer treated with first-line systemic therapy by Fangyuan Zhang, Menglan Zhai, Jinru Yang, Lei Zhao, Zhenyu Lin, Jing Wang, Tao Zhang and Dandan Yu in Therapeutic Advances in Gastroenterology

Supplemental Material

sj-pptx-2-tag-10.1177_17562848221124029 – Supplemental material for ‘FLARE’ of tumor marker in advanced gastric cancer treated with first-line systemic therapy

Supplemental material, sj-pptx-2-tag-10.1177_17562848221124029 for ‘FLARE’ of tumor marker in advanced gastric cancer treated with first-line systemic therapy by Fangyuan Zhang, Menglan Zhai, Jinru Yang, Lei Zhao, Zhenyu Lin, Jing Wang, Tao Zhang and Dandan Yu in Therapeutic Advances in Gastroenterology

Footnotes

Acknowledgements

None.

Declarations

ORCID iD

Fangyuan Zhang

Supplemental material

Supplemental material for this article is available online.

References

Eisenhauer

Therasse

Bogaerts

, et al. New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer 2009; 45: 228–247.

Tang

, et al. Evaluating the response of gastric carcinomas to neoadjuvant chemotherapy using iodine concentration on spectral CT: a comparison with pathological regression. Clin Radiol 2015; 70: 1198–1204.

Sang

Kim

Lee

, et al. Usefulness of CT volumetry for primary gastric lesions in predicting pathologic response to neoadjuvant chemotherapy in advanced gastric cancer. Abdom Imaging 2009; 34: 430–440.

Wang

Jiang

Ren

, et al. The significance of preoperative serum carcinoembryonic antigen levels in the prediction of lymph node metastasis and prognosis in locally advanced gastric cancer: a retrospective analysis. BMC Gastroenterol 2020; 20: 100.

Wang

Tian

, et al. Gastrin-17 combined with CEA, CA12-5 and CA19-9 improves the sensitivity for the diagnosis of gastric cancer. Int J Gen Med 2021; 14: 8087–8095.

Yasuhito

Mitsuro

Seiji

, et al. Prognostic significance of perioperative tumor marker levels in stage II/III gastric cancer. World J Gastrointest Oncol 2019; 11: 17–27.

Jong

Deneer

VHM

Kelder

, et al. Association between serum biomarkers CEA and LDH and response in advanced non-small cell lung cancer patients treated with platinum-based chemotherapy. Thorac Cancer 2020; 11: 1790–1800.

Tuxen

Sölétormos

Dombernowsky

Serum tumour marker CA 125 in monitoring of ovarian cancer during first-line chemotherapy. Br J Cancer 2001; 84: 1301–1307.

Ailawadhi

Sunga

Rajput

, et al. Chemotherapy-induced carcinoembryonic antigen surge in patients with metastatic colorectal cancer. Oncology 2006; 70: 49–53.

10.

Olbert

Hegele

Kraeuter

, et al. Clinical significance of a prostate-specific antigen flare phenomenon in patients with hormone-refractory prostate cancer receiving docetaxel. Anticancer Drugs 2006; 17: 993–996.

11.

Sella

Sternberg

Skoneczna

, et al. Prostate-specific antigen flare phenomenon with docetaxel-based chemotherapy in patients with androgen-independent prostate cancer. BJU Int 2010; 102: 1607–1609.

12.

Strimpakos

Cunningham

Mikropoulos

, et al. The impact of carcinoembryonic antigen flare in patients with advanced colorectal cancer receiving first-line chemotherapy. Ann Oncol 2010; 21: 1013–1019.

13.

Wit

Collette

Sylvester

, et al. Serum alpha-fetoprotein surge after the initiation of chemotherapy for non-seminomatous testicular cancer has an adverse prognostic significance. Br J Cancer 1998; 78: 1350–1355.

14.

Ding

Xiang

, et al. Carcinoembryonic antigen surge in metastatic colorectal cancer patients responding to irinotecan combination chemotherapy. Biomarkers 2010; 15: 243–248.

15.

Nelius

Klatte

Riese

, et al. Impact of PSA flare-up in patients with hormone-refractory prostate cancer undergoing chemotherapy. Int Urol Nephrol 2008; 40: 97–104.

16.

Vogelzang

Lange

Goldman

, et al. Acute changes of α-fetoprotein and human chorionic gonadotropin during induction chemotherapy of germ cell tumors. Cancer Res 1982; 42: 4855–4861.

17.

Sørbye

Dahl

Transient CEA increase at start of oxaliplatin combination therapy for metastatic colorectal cancer. Acta Oncol 2004; 43: 495–498.

18.

Hermunen

Lantto

Poussa

, et al. Can carcinoembryonic antigen replace computed tomography in response evaluation of metastatic colorectal cancer? Acta Oncol 2018; 57: 750–758.

19.

Loprinzi

Tormey

Rasmussen

, et al. Prospective evaluation of carcinoembryonic antigen levels and alternating chemotherapeutic regimens in metastatic breast cancer. J Clin Oncol 1986; 4: 46–56.

20.

Kim

Lee

Kim

, et al. Chemotherapy-induced transient CEA and CA19-9 surges in patients with metastatic or recurrent gastric cancer. Acta Oncol 2008; 48: 385–390.

21.

Castello

Macapinlac

Lopci

, et al. Prostate-specific antigen flare induced by 223RaCl2 in patients with metastatic castration-resistant prostate cancer. Eur J Nucl Med Mol Imaging 2018; 45: 2256–2263.

22.

Brintzenhofe-Szoc

Levin

, et al. Mixed anxiety/depression symptoms in a large cancer cohort: prevalence by cancer type. Psychosomatics 2009; 50: 383–391.

23.

Yan-Mei

Cai-Feng

Yu-Bin

Analysis of factors affecting the life quality of the patients with late stomach cancer. J Clin Nurs 2014; 23: 1257–1262.

24.

Arrieta

Angulo

Núñez-Valencia

, et al. Association of depression and anxiety on quality of life, treatment adherence, and prognosis in patients with advanced non-small cell lung cancer. Ann Surg Oncol 2013; 20: 1941–1948.

25.

Ohtsukasa

Okabe

Yamashita

, et al. Increased expression of CEA and MHC class I in colorectal cancer cell lines exposed to chemotherapy drugs. J Cancer Res Clin Oncol 2003; 129: 719–726.

26.

Modrak

Gold

Goldenberg

, et al. Colonic tumor CEA, CSAp and MUC-1 expression following radioimmunotherapy or chemotherapy. Tumor Biol 2003; 24: 32–39.

27.

Janjigian

Shitara

Moehler

, et al. First-line nivolumab plus chemotherapy versus chemotherapy alone for advanced gastric, gastro-oesophageal junction, and oesophageal adenocarcinoma (CheckMate 649): a randomised, open-label, phase 3 trial. Lancet 2021; 398: 27–40.

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