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Published in: International Journal of Clinical Oncology 6/2014

01-12-2014 | Original Article

Development of an integrated support system for hereditary cancer and its impact on gynecologic services

Authors: Mina Morii-Kashima, Hiroshi Tsubamoto, Chika Sato, Mariko Ushioda, Naohiro Tomita, Yasuo Miyoshi, Tomoko Hashimoto-Tamaoki, Kazuo Tamura, Hideaki Sawai, Hiroaki Shibahara

Published in: International Journal of Clinical Oncology | Issue 6/2014

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Abstract

Objective

Patients with hereditary cancer need an integrated support system. A recently launched project was evaluated in terms of its efficacy in screening patients with hereditary cancer at the gynecologic service.

Methods

The project team comprised gynecologists, surgeons, medical geneticists, and certified genetic counselors (CGCs) in our hospital. At the gynecologic service, a newly developed self-administered family history questionnaire (SAFHQ) was given to patients with ovarian, endometrial, or breast cancer as well as a history of multiple cancers. After an interview, a CGC constructed a pedigree and evaluated the risk for hereditary cancer. Patients at risk were recommended by a gynecologist to receive further genetic counseling at the Department of Genetics according to the modified Bethesda criteria, Amsterdam II criteria, and National Comprehensive Cancer Network (NCCN) guidelines 2012 for breast–ovarian cancer syndrome (HBOC). The numbers of newly screened patients were compared before and after the project launch.

Results

The SAFHQ was administered to 131 patients and 106 (81 %) pedigrees were constructed between August 2012 and July 2013. The number of newly screened patients according to the Bethesda criteria was 4 and 8 at 10 years before and 1 year after the project launch, respectively. Two and 31 patients met the NCCN criteria for HBOC excluding ovarian cancer alone, respectively, at these 2 time points. Of 54 patients who were recommended to undergo further counseling, 10 (19 %) visited the Department of Genetics.

Conclusion

After the launch of an integrated support system, the number of patients with hereditary cancers who were screened increased. The gynecologic service played a pivotal role in patient and family care.
Literature
1.
go back to reference Pal T, Permuth-Wey J, Betts JA et al (2005) BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases. Cancer 104:2807–2816PubMedCrossRef Pal T, Permuth-Wey J, Betts JA et al (2005) BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases. Cancer 104:2807–2816PubMedCrossRef
2.
go back to reference Lu KH (2008) Hereditary gynecologic cancers: differential diagnosis, surveillance, management and surgical prophylaxis. Fam Cancer 7:53–58PubMedCrossRef Lu KH (2008) Hereditary gynecologic cancers: differential diagnosis, surveillance, management and surgical prophylaxis. Fam Cancer 7:53–58PubMedCrossRef
3.
go back to reference Hampel H, Frankel W, Panescu J et al (2006) Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 66:7810–7817PubMedCrossRef Hampel H, Frankel W, Panescu J et al (2006) Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 66:7810–7817PubMedCrossRef
4.
go back to reference Dinh TA, Rosner BI, Atwood JC et al (2011) Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population. Cancer Prev Res (Phila) 4:9–22PubMedCentralCrossRef Dinh TA, Rosner BI, Atwood JC et al (2011) Health benefits and cost-effectiveness of primary genetic screening for Lynch syndrome in the general population. Cancer Prev Res (Phila) 4:9–22PubMedCentralCrossRef
5.
go back to reference Komata D, Yahata T, Kodama S et al (2009) The prevalence of hereditary breast/ovarian cancer risk in patients with a history of breast or ovarian cancer in Japanese subjects. Obstet Gynecol Res 35:912–917CrossRef Komata D, Yahata T, Kodama S et al (2009) The prevalence of hereditary breast/ovarian cancer risk in patients with a history of breast or ovarian cancer in Japanese subjects. Obstet Gynecol Res 35:912–917CrossRef
6.
go back to reference Aoki D, Udagawa Y, Ohwada M et al (2009) A report of Fujinka-Shuyo-Iinnkai. Acta Obstet Gynaecol Jpn 61:1540–1541 Aoki D, Udagawa Y, Ohwada M et al (2009) A report of Fujinka-Shuyo-Iinnkai. Acta Obstet Gynaecol Jpn 61:1540–1541
7.
go back to reference Kaneko K, Ohsumi S, Aogi K et al (2013) Genetic counseling and practice of hereditary cancers at Shikoku Cancer Center. Gan To Kagaku Ryoho 40:139–142PubMed Kaneko K, Ohsumi S, Aogi K et al (2013) Genetic counseling and practice of hereditary cancers at Shikoku Cancer Center. Gan To Kagaku Ryoho 40:139–142PubMed
8.
go back to reference Lu KH (2008) Hereditary gynecologic cancer: Risk, prevention, and management. Informa Healthcare Lu KH (2008) Hereditary gynecologic cancer: Risk, prevention, and management. Informa Healthcare
9.
go back to reference Umar A, Boland CR, Terdiman JP et al (2004) Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 96:261–268PubMedCentralPubMedCrossRef Umar A, Boland CR, Terdiman JP et al (2004) Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability. J Natl Cancer Inst 96:261–268PubMedCentralPubMedCrossRef
10.
go back to reference Vasen HF (2000) Clinical diagnosis and management of hereditary colorectal cancer syndromes. J Clin Oncol 18(21 Suppl):81–92 Vasen HF (2000) Clinical diagnosis and management of hereditary colorectal cancer syndromes. J Clin Oncol 18(21 Suppl):81–92
11.
go back to reference Masuda K, Banno K, Hirasawa A et al (2012) Relationship of lower uterine segment cancer with Lynch syndrome: a novel case with an hMLH1 germline mutation. Oncol Rep 28:1537–1543PubMedCentralPubMed Masuda K, Banno K, Hirasawa A et al (2012) Relationship of lower uterine segment cancer with Lynch syndrome: a novel case with an hMLH1 germline mutation. Oncol Rep 28:1537–1543PubMedCentralPubMed
13.
go back to reference Yang K, Allen B, Conrad P et al (2006) Awareness of gynecologic surveillance in women from hereditary non-polyposis colorectal cancer families. Fam Cancer 5:405–409PubMedCrossRef Yang K, Allen B, Conrad P et al (2006) Awareness of gynecologic surveillance in women from hereditary non-polyposis colorectal cancer families. Fam Cancer 5:405–409PubMedCrossRef
14.
go back to reference Domanska K, Carlsson C, Bendahl PO et al (2009) Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels. BMC Med Genet 10:30PubMedCentralPubMedCrossRef Domanska K, Carlsson C, Bendahl PO et al (2009) Knowledge about hereditary nonpolyposis colorectal cancer; mutation carriers and physicians at equal levels. BMC Med Genet 10:30PubMedCentralPubMedCrossRef
15.
go back to reference Ketabi Z, Mosgaard BJ, Gerdes AM et al (2012) Awareness of endometrial cancer risk and compliance with screening in hereditary nonpolyposis colorectal cancer. Obstet Gynecol 120:1005–1012PubMed Ketabi Z, Mosgaard BJ, Gerdes AM et al (2012) Awareness of endometrial cancer risk and compliance with screening in hereditary nonpolyposis colorectal cancer. Obstet Gynecol 120:1005–1012PubMed
16.
go back to reference Salemink S, Dekker N, Kets CM et al (2013) Focusing on patient needs and preferences may improve genetic counseling for colorectal cancer. J Genet Couns 22:118–124PubMedCentralPubMedCrossRef Salemink S, Dekker N, Kets CM et al (2013) Focusing on patient needs and preferences may improve genetic counseling for colorectal cancer. J Genet Couns 22:118–124PubMedCentralPubMedCrossRef
17.
go back to reference Soliman PT, Oh JC, Schmeler KM et al (2005) Risk factors for young premenopausal women with endometrial cancer. Obstet Gynecol 105:575–580PubMedCrossRef Soliman PT, Oh JC, Schmeler KM et al (2005) Risk factors for young premenopausal women with endometrial cancer. Obstet Gynecol 105:575–580PubMedCrossRef
18.
go back to reference Morgan D, Sylvester H, Lucas FL et al (2010) Hereditary breast and ovarian cancer: referral source for genetic assessment and communication regarding assessment with nongenetic clinicians in the community setting. Genet Med 12:25–31PubMedCrossRef Morgan D, Sylvester H, Lucas FL et al (2010) Hereditary breast and ovarian cancer: referral source for genetic assessment and communication regarding assessment with nongenetic clinicians in the community setting. Genet Med 12:25–31PubMedCrossRef
19.
go back to reference Loren AW, Mangu PB, Beck LN et al (2013) Fertility preservation for patients with cancer: American Society of Clinical Oncology Clinical Practice Guideline Update. J Clin Oncol 31:2500–2510PubMedCrossRef Loren AW, Mangu PB, Beck LN et al (2013) Fertility preservation for patients with cancer: American Society of Clinical Oncology Clinical Practice Guideline Update. J Clin Oncol 31:2500–2510PubMedCrossRef
20.
go back to reference Shulman LP (2010) Hereditary breast and ovarian cancer (HBOC): clinical features and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol Clin N Am 37:109–133CrossRef Shulman LP (2010) Hereditary breast and ovarian cancer (HBOC): clinical features and counseling for BRCA1 and BRCA2, Lynch syndrome, Cowden syndrome, and Li-Fraumeni syndrome. Obstet Gynecol Clin N Am 37:109–133CrossRef
21.
go back to reference Wood M, Kadlubek P, Lu KH et al (2012) Quality of cancer family history and referral for genetic counseling and testing among oncology practices: a pilot test of quality measures as part of the ASCO Quality Oncology Practice Initiative (QOPI). J Clin Oncol 30 (suppl; abstr CRA1505) Wood M, Kadlubek P, Lu KH et al (2012) Quality of cancer family history and referral for genetic counseling and testing among oncology practices: a pilot test of quality measures as part of the ASCO Quality Oncology Practice Initiative (QOPI). J Clin Oncol 30 (suppl; abstr CRA1505)
22.
go back to reference Murff HJ, Spigel DR, Syngal S (2004) Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history. JAMA 292:1480–1489PubMedCrossRef Murff HJ, Spigel DR, Syngal S (2004) Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history. JAMA 292:1480–1489PubMedCrossRef
23.
go back to reference Mai PL, Garceau AO, Graubard BI et al (2011) Confirmation of family cancer history reported in a population-based survey. J Natl Cancer Inst 103:788–797PubMedCentralPubMedCrossRef Mai PL, Garceau AO, Graubard BI et al (2011) Confirmation of family cancer history reported in a population-based survey. J Natl Cancer Inst 103:788–797PubMedCentralPubMedCrossRef
24.
go back to reference Vogel TJ, Stoops K, Bennett RL et al (2012) A self-administered family history questionnaire improves identification of women who warrant referral to genetic counseling for hereditary cancer risk. Gynecol Oncol 125:693–698PubMedCrossRef Vogel TJ, Stoops K, Bennett RL et al (2012) A self-administered family history questionnaire improves identification of women who warrant referral to genetic counseling for hereditary cancer risk. Gynecol Oncol 125:693–698PubMedCrossRef
25.
go back to reference Ooseto K, Arakawa A, Ando M et al (2012) Usefulness of the family career hearing in the interview vote with Lynch syndrome. Tokai Sanka Fujinka Gakkai Zasshi 49:303–307 Ooseto K, Arakawa A, Ando M et al (2012) Usefulness of the family career hearing in the interview vote with Lynch syndrome. Tokai Sanka Fujinka Gakkai Zasshi 49:303–307
26.
go back to reference Patenaude AF (2005) Genetic testing for cancer: psychological approaches for helping patients and families. American Psychological Association, Washington, DCCrossRef Patenaude AF (2005) Genetic testing for cancer: psychological approaches for helping patients and families. American Psychological Association, Washington, DCCrossRef
27.
go back to reference Rosenthal AN, Fraser L, Manchanda R et al (2013) Results of annual screening in phase I of the United Kingdom familial ovarian cancer screening study highlight the need for strict adherence to screening schedule. J Clin Oncol 31:49–57PubMedCentralPubMedCrossRef Rosenthal AN, Fraser L, Manchanda R et al (2013) Results of annual screening in phase I of the United Kingdom familial ovarian cancer screening study highlight the need for strict adherence to screening schedule. J Clin Oncol 31:49–57PubMedCentralPubMedCrossRef
28.
go back to reference Lancaster JM, Powell CB, Kauff ND et al (2007) Society of Gynecologic Oncologists Education Committee statement on risk assessment for inherited gynecologic cancer predispositions. Gynecol Oncol 107:159–162PubMedCrossRef Lancaster JM, Powell CB, Kauff ND et al (2007) Society of Gynecologic Oncologists Education Committee statement on risk assessment for inherited gynecologic cancer predispositions. Gynecol Oncol 107:159–162PubMedCrossRef
29.
go back to reference Resnick KE, Hampel H, Fishel R et al (2009) Current and emerging trends in Lynch syndrome identification in women with endometrial cancer. Gynecol Oncol 114:128–134PubMedCentralPubMedCrossRef Resnick KE, Hampel H, Fishel R et al (2009) Current and emerging trends in Lynch syndrome identification in women with endometrial cancer. Gynecol Oncol 114:128–134PubMedCentralPubMedCrossRef
30.
go back to reference Lu KH, Schorge JO, Rodabaugh KJ et al (2007) Prospective determination of prevalence of lynch syndrome in young women with endometrial cancer. J Clin Oncol 25:5158–5164PubMedCrossRef Lu KH, Schorge JO, Rodabaugh KJ et al (2007) Prospective determination of prevalence of lynch syndrome in young women with endometrial cancer. J Clin Oncol 25:5158–5164PubMedCrossRef
31.
32.
go back to reference Shih KK, Garg K, Levine DA et al (2011) Clinicopathologic significance of DNA mismatch repair protein defects and endometrial cancer in women 40 years of age and younger. Gynecol Oncol 123:88–94PubMedCrossRef Shih KK, Garg K, Levine DA et al (2011) Clinicopathologic significance of DNA mismatch repair protein defects and endometrial cancer in women 40 years of age and younger. Gynecol Oncol 123:88–94PubMedCrossRef
33.
go back to reference Ring KL, Connor EV, Atkins KA et al (2013) Women 50 years or younger with endometrial cancer: the argument for universal mismatch repair screening and potential for targeted therapeutics. Int J Gynecol Cancer 23:853–860PubMedCrossRef Ring KL, Connor EV, Atkins KA et al (2013) Women 50 years or younger with endometrial cancer: the argument for universal mismatch repair screening and potential for targeted therapeutics. Int J Gynecol Cancer 23:853–860PubMedCrossRef
34.
go back to reference Cohn DE, Frankel W, Resnick KE et al (2006) Improved survival with an intact DNA mismatch repair system in endometrial cancer. Obstet Gynecol 108:1208–1215PubMedCrossRef Cohn DE, Frankel W, Resnick KE et al (2006) Improved survival with an intact DNA mismatch repair system in endometrial cancer. Obstet Gynecol 108:1208–1215PubMedCrossRef
35.
go back to reference Kauff ND (2007) How should women with early-onset endometrial cancer be evaluated for lynch syndrome? J Clin Oncol 25:5143–5146PubMedCrossRef Kauff ND (2007) How should women with early-onset endometrial cancer be evaluated for lynch syndrome? J Clin Oncol 25:5143–5146PubMedCrossRef
36.
go back to reference Günther K, Horbach T, Hohenberger W et al (2000) Colonic late-onset familial adenomatous polyposis combined with severe duodenal polyposis and familial endometrial cancer. Am J Med 108:681–683PubMedCrossRef Günther K, Horbach T, Hohenberger W et al (2000) Colonic late-onset familial adenomatous polyposis combined with severe duodenal polyposis and familial endometrial cancer. Am J Med 108:681–683PubMedCrossRef
37.
go back to reference Oshima S, Miyake Y, Ikeda M et al (2007) A case of an uterine and pancreatic cancer with familial adenomatous polyposis detected by FDG-PET (in Japanese). Surgery 69:237–240 Oshima S, Miyake Y, Ikeda M et al (2007) A case of an uterine and pancreatic cancer with familial adenomatous polyposis detected by FDG-PET (in Japanese). Surgery 69:237–240
38.
go back to reference Iwama T, Tamura K, Morita T et al (2004) A clinical overview of familial adenomatous polyposis derived from the database of the Polyposis Registry of Japan. Int J Clin Oncol 9:308–316PubMedCrossRef Iwama T, Tamura K, Morita T et al (2004) A clinical overview of familial adenomatous polyposis derived from the database of the Polyposis Registry of Japan. Int J Clin Oncol 9:308–316PubMedCrossRef
39.
go back to reference Schorge JO, Modesitt SC, Coleman RL et al (2010) SGO White Paper on ovarian cancer: etiology, screening and surveillance. Gynecol Oncol 119:7–17PubMedCrossRef Schorge JO, Modesitt SC, Coleman RL et al (2010) SGO White Paper on ovarian cancer: etiology, screening and surveillance. Gynecol Oncol 119:7–17PubMedCrossRef
40.
go back to reference Auranen A, Joutsiniemi T (2011) A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families. Acta Obstet Gynecol Scand 90:437–444PubMedCrossRef Auranen A, Joutsiniemi T (2011) A systematic review of gynecological cancer surveillance in women belonging to hereditary nonpolyposis colorectal cancer (Lynch syndrome) families. Acta Obstet Gynecol Scand 90:437–444PubMedCrossRef
41.
go back to reference Inoue K, Tsubamoto H, Hao H et al (2013) Ovarian carcinoma in situ of presumable fallopian tube origin in a patient with Lynch syndrome: a case report. Gynecol Oncol Case Rep 5:61–63 Inoue K, Tsubamoto H, Hao H et al (2013) Ovarian carcinoma in situ of presumable fallopian tube origin in a patient with Lynch syndrome: a case report. Gynecol Oncol Case Rep 5:61–63
42.
go back to reference Kuppermann M, Wang G, Wong S et al (2013) Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome. Cancer 119:215–225PubMedCrossRef Kuppermann M, Wang G, Wong S et al (2013) Preferences for outcomes associated with decisions to undergo or forgo genetic testing for Lynch syndrome. Cancer 119:215–225PubMedCrossRef
43.
go back to reference Domchek SM, Friebel TM, Neuhausen SL et al (2006) Mortality after bilateral salpingo-oophorectomy in BRCA1 and BRCA2 mutation carriers: a prospective cohort study. Lancet Oncol 7:223–229PubMedCrossRef Domchek SM, Friebel TM, Neuhausen SL et al (2006) Mortality after bilateral salpingo-oophorectomy in BRCA1 and BRCA2 mutation carriers: a prospective cohort study. Lancet Oncol 7:223–229PubMedCrossRef
44.
go back to reference Grann VR, Jacobson JS, Thomason D et al (2002) Effect of prevention strategies on survival and quality-adjusted survival of women with BRCA1/2 mutations: an updated decision analysis. J Clin Oncol 20:2520–2529PubMedCrossRef Grann VR, Jacobson JS, Thomason D et al (2002) Effect of prevention strategies on survival and quality-adjusted survival of women with BRCA1/2 mutations: an updated decision analysis. J Clin Oncol 20:2520–2529PubMedCrossRef
45.
go back to reference Schmeler KM, Lynch HT, Chen LM et al (2006) Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome. N Engl J Med 354:261–269PubMedCrossRef Schmeler KM, Lynch HT, Chen LM et al (2006) Prophylactic surgery to reduce the risk of gynecologic cancers in the Lynch syndrome. N Engl J Med 354:261–269PubMedCrossRef
46.
go back to reference Dhar SU, Cooper HP, Wang T et al (2011) Significant differences among physician specialties in management recommendations of BRCA1 mutation carriers. Breast Cancer Res Treat 129:221–227PubMedCentralPubMedCrossRef Dhar SU, Cooper HP, Wang T et al (2011) Significant differences among physician specialties in management recommendations of BRCA1 mutation carriers. Breast Cancer Res Treat 129:221–227PubMedCentralPubMedCrossRef
47.
go back to reference Demsky R, McCuaig J, Maganti M et al (2013) Keeping it simple: genetics referrals for all invasive serous ovarian cancers. Gynecol Oncol 130:329–333PubMedCrossRef Demsky R, McCuaig J, Maganti M et al (2013) Keeping it simple: genetics referrals for all invasive serous ovarian cancers. Gynecol Oncol 130:329–333PubMedCrossRef
48.
49.
go back to reference Backes FJ, Mitchell E, Hampel H et al (2011) Endometrial cancer patients and compliance with genetic counseling: room for improvement. Gynecol Oncol 123:532–536PubMedCrossRef Backes FJ, Mitchell E, Hampel H et al (2011) Endometrial cancer patients and compliance with genetic counseling: room for improvement. Gynecol Oncol 123:532–536PubMedCrossRef
50.
go back to reference Deming WE (1986) Out of the crisis, 1st edn. MIT Press, Cambridge Deming WE (1986) Out of the crisis, 1st edn. MIT Press, Cambridge
51.
go back to reference Nakayama DK, Bushey TN, Hubbard I et al (2010) Using a Plan-Do-Study-Act cycle to introduce a new or service line. AORN J 92:335–343PubMedCrossRef Nakayama DK, Bushey TN, Hubbard I et al (2010) Using a Plan-Do-Study-Act cycle to introduce a new or service line. AORN J 92:335–343PubMedCrossRef
52.
go back to reference Vogel P, Vassilev G, Kruse B et al (2011) Morbidity and mortality conference as part of PDCA cycle to decrease anastomotic failure in colorectal surgery. Langenbecks Arch Surg 396:1009–1015PubMedCrossRef Vogel P, Vassilev G, Kruse B et al (2011) Morbidity and mortality conference as part of PDCA cycle to decrease anastomotic failure in colorectal surgery. Langenbecks Arch Surg 396:1009–1015PubMedCrossRef
53.
go back to reference Oh HC, Toh HG, Giap Cheong ES (2011) Realization of process improvement at a diagnostic radiology department with aid of simulation modeling. J Healthc Qual 33:40–47PubMedCrossRef Oh HC, Toh HG, Giap Cheong ES (2011) Realization of process improvement at a diagnostic radiology department with aid of simulation modeling. J Healthc Qual 33:40–47PubMedCrossRef
54.
go back to reference Michael M, Schaffer SD, Egan PL et al (2013) Improving wait times and patient satisfaction in primary care. J Healthc Qual 35:50–60PubMedCrossRef Michael M, Schaffer SD, Egan PL et al (2013) Improving wait times and patient satisfaction in primary care. J Healthc Qual 35:50–60PubMedCrossRef
55.
go back to reference Honda O, Tsubamoto H, Ito Y et al (2013) Regional coordination for end-of-life care in our department. Jpn J Gynecol Oncol 1:1–8 Honda O, Tsubamoto H, Ito Y et al (2013) Regional coordination for end-of-life care in our department. Jpn J Gynecol Oncol 1:1–8
Metadata
Title
Development of an integrated support system for hereditary cancer and its impact on gynecologic services
Authors
Mina Morii-Kashima
Hiroshi Tsubamoto
Chika Sato
Mariko Ushioda
Naohiro Tomita
Yasuo Miyoshi
Tomoko Hashimoto-Tamaoki
Kazuo Tamura
Hideaki Sawai
Hiroaki Shibahara
Publication date
01-12-2014
Publisher
Springer Japan
Published in
International Journal of Clinical Oncology / Issue 6/2014
Print ISSN: 1341-9625
Electronic ISSN: 1437-7772
DOI
https://doi.org/10.1007/s10147-013-0649-z

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