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Kaliff, Malin
Publications (9 of 9) Show all publications
Bergengren, L., Kaliff, M., Lillsunde-Larsson, G., Karlsson, M. & Helenius, G. (2018). Comparison between professional sampling and self-sampling for HPV-based cervical cancer screening among postmenopausal women. International Journal of Gynecology & Obstetrics, 142(3), 359-364
Open this publication in new window or tab >>Comparison between professional sampling and self-sampling for HPV-based cervical cancer screening among postmenopausal women
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2018 (English)In: International Journal of Gynecology & Obstetrics, ISSN 0020-7292, E-ISSN 1879-3479, Vol. 142, no 3, p. 359-364Article in journal (Refereed) Published
Abstract [en]

OBJECTIVE: To investigate whether self-sampling is as reliable as professional sampling for HPV testing and genotype detection among postmenopausal women.

METHODS: In the present prospective cross-sectional study, women in Örebro County, Sweden, who had high-risk HPV (hrHPV) and normal cytology results in exit screening tests conducted in between January 1, 2012, and December 31, 2014, were invited to follow-up screenings between February 24, 2015 and May 15, 2015, that included professional sampling and self-sampling. HPV genotypes were identified by a DNA-based assay that could detect 35 HPV genotypes. Findings between the different sampling methods were compared.

RESULTS: Of 143 women who participated, 119 returned a self-sample. Completely concordant results were observed in 67 of these samples when both hrHPV and low-risk HPV genotypes were analyzed. Overall, 99 (83.2%) women had the same clinically relevant finding from both sampling methods. Twenty women had discordant hrHPV results (hrHPV detected in 10 self-samples vs 10 professionally collected samples; Cohen κ 0.66, 95% confidence interval 0.53-0.80). There was no significant difference between the two sampling methods for clinically significant infections (P>0.99) or extended genotyping (P=0.827).

CONCLUSION: Postmenopausal women could be offered self-sampling devices to increase screening-program coverage while maintaining test quality.

Place, publisher, year, edition, pages
Wiley-Blackwell Publishing Inc., 2018
Keywords
Cervical cancer, HPV, Postmenopausal women, Professional sampling, Screening, Self-sample
National Category
Cancer and Oncology Obstetrics, Gynecology and Reproductive Medicine
Identifiers
urn:nbn:se:oru:diva-67134 (URN)10.1002/ijgo.12538 (DOI)000440652000017 ()29856071 (PubMedID)2-s2.0-85051073715 (Scopus ID)
Note

Funding Agencies:

Region Örebro County Research Committee  

Örebro University Hospital Research Foundation  

BBMRI.se

Available from: 2018-06-04 Created: 2018-06-04 Last updated: 2018-08-30Bibliographically approved
Helenius, G., Ottestig, E., Kaliff, M., Lillsunde-Larsson, G., Karlsson, M. & Bergengren, L. (2018). Distribution of HPV-genotypes in a Swedish screening population. In: : . Paper presented at Eurogin 2018 International multidisciplinary HPV Congress, Lisabon Portugal, December 2-5, 2018.
Open this publication in new window or tab >>Distribution of HPV-genotypes in a Swedish screening population
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2018 (English)Conference paper, Poster (with or without abstract) (Refereed)
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-69348 (URN)
Conference
Eurogin 2018 International multidisciplinary HPV Congress, Lisabon Portugal, December 2-5, 2018
Available from: 2018-10-08 Created: 2018-10-08 Last updated: 2018-10-08Bibliographically approved
Kaliff, M., Sorbe, B., Mordhorst, L. B., Helenius, G., Karlsson, M. G. & Lillsunde-Larsson, G. (2018). Findings of multiple HPV genotypes in cervical carcinoma are associated with poor cancer-specific survival in a Swedish cohort of cervical cancer primarily treated with radiotherapy. OncoTarget, 9(27), 18786-18796
Open this publication in new window or tab >>Findings of multiple HPV genotypes in cervical carcinoma are associated with poor cancer-specific survival in a Swedish cohort of cervical cancer primarily treated with radiotherapy
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2018 (English)In: OncoTarget, ISSN 1949-2553, E-ISSN 1949-2553, Vol. 9, no 27, p. 18786-18796Article in journal (Refereed) Published
Abstract [en]

Cervical cancer (CC) is one of the most common cancers in women and virtually all cases of CC are a result of a persistent infection of human papillomavirus (HPV). For disease detected in early stages there is curing treatment but when diagnosed late with recurring disease and metastasis there are limited possibilities. Here we evaluate HPV impact on treatment resistance and metastatic disease progression. Prevalence and distribution of HPV genotypes and HPV16 variants in a Swedish CC patient cohort (n=209) was evaluated, as well as HPV influence on patient prognosis. Tumor samples suitable for analysis (n=204) were genotyped using two different real-time PCR methods. HPV16 variant analysis was made using pyrosequencing. Results showed that HPV prevalence in the total series was 93%. Of the HPV-positive samples, 13% contained multiple infections, typically with two high-risk HPV together. Primary cure rate for the complete series was 95%. Recurrence rate of the complete series was 28% and distant recurrences were most frequent (20%). Patients with tumors containing multiple HPV-strains and particularly HPV genotypes belonging to the alpha 7 and 9 species together had a significantly higher rate of distant tumor recurrences and worse cancer-specific survival rate.

Place, publisher, year, edition, pages
Impact Journals LLC, 2018
Keywords
HPV, cervical cancer, recurrences, survival
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-71672 (URN)10.18632/oncotarget.24666 (DOI)29721161 (PubMedID)2-s2.0-85045206587 (Scopus ID)
Available from: 2019-01-22 Created: 2019-01-22 Last updated: 2019-01-24Bibliographically approved
Lillsunde-Larsson, G., Kaliff, M., Ottestig, E. & Helenius, G. (2018). HPV genotyping of HPV primary screening positive samples in Örebro, Sweden. In: : . Paper presented at 33rd World congress of Biomedical Laboratory Science (IFBLS), Florens, Italy, 22-26 Sep., 2018.
Open this publication in new window or tab >>HPV genotyping of HPV primary screening positive samples in Örebro, Sweden
2018 (English)Conference paper, Poster (with or without abstract) (Other academic)
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-73851 (URN)
Conference
33rd World congress of Biomedical Laboratory Science (IFBLS), Florens, Italy, 22-26 Sep., 2018
Available from: 2019-04-17 Created: 2019-04-17 Last updated: 2019-04-17Bibliographically approved
Lillsunde-Larsson, G., Kaliff, M., Sorbe, B., Helenius, G. & Karlsson, M. (2018). HPV16 VIRAL CHARACTERISTICS IN PRIMARY AND RECURRENT VULVAR CARCINOMA. In: : . Paper presented at 32nd International Papillomavirus Conference IPVC 2018, Sydney, Australia, 2-6 October, 2018.
Open this publication in new window or tab >>HPV16 VIRAL CHARACTERISTICS IN PRIMARY AND RECURRENT VULVAR CARCINOMA
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2018 (English)Conference paper, Poster (with or without abstract) (Other academic)
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-73753 (URN)
Conference
32nd International Papillomavirus Conference IPVC 2018, Sydney, Australia, 2-6 October, 2018
Available from: 2019-04-15 Created: 2019-04-15 Last updated: 2019-04-16Bibliographically approved
Lillsunde Larsson, G., Kaliff, M., Sorbe, B., Helenius, G. & Karlsson, M. G. (2018). HPV16 viral characteristics in primary, recurrent and metastatic vulvar carcinoma. Papillomavirus research, 6, 63-69
Open this publication in new window or tab >>HPV16 viral characteristics in primary, recurrent and metastatic vulvar carcinoma
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2018 (English)In: Papillomavirus research, ISSN 2405-8521, Vol. 6, p. 63-69Article in journal (Refereed) Published
Abstract [en]

Vulvar carcinoma is the fourth most common gynecological malignancy. Two separate carcinogenic pathways are suggested, where one is associated with the human papillomavirus (HPV) and HPV16 the most common genotype.

The aim of this study was to evaluate HPV-markers in a set of primary tumors, metastases and recurrent lesions of vulvar squamous cell carcinomas (VSCC). Ten HPV16-positive VSCC with metastatic regional lymph nodes, distant lymphoid/hematogenous metastases or local recurrent lesions were investigated for HPV genotype, HPV16 variant, HPV16 viral load, HPV16 integration and HPV16 E2BS3 and 4 methylation.

In all 10 analyzed case series, the same HPV genotype (HPV16), HPV16 variant and level of viral load were detected in all lesions within a patient case. Primary tumors with a high E2/E6 ratio were found to have fewer vulvar recurrences and/or metastases after diagnosis and treatment. Also, a significantly lower viral load was evident in regional lymph nodes compared to primary tumors.

The data presented strengthens the evidence for a clonal HPV-induced pathway for vulvar carcinoma.

Place, publisher, year, edition, pages
Elsevier, 2018
Keywords
Vulvar carcinoma, human papillomavirus, integration, metastases, recurrences, viral load
National Category
Cancer and Oncology Dermatology and Venereal Diseases
Identifiers
urn:nbn:se:oru:diva-69992 (URN)10.1016/j.pvr.2018.10.008 (DOI)000452069800012 ()30391517 (PubMedID)2-s2.0-85056569332 (Scopus ID)
Note

Funding Agency:

Örebro County Council Research Committee

Available from: 2018-11-07 Created: 2018-11-07 Last updated: 2018-12-17Bibliographically approved
Lillsunde-Larsson, G., Kaliff, M., Hansen, M. & Helenius, G. (2017). Comparison of mRNA and DNA HPV levels in HRHPV-positive primary screening samples using digital droplet PCR. In: : . Paper presented at EUROGIN 2017, Amsterdam, Netherlands, October 8-11, 2017.
Open this publication in new window or tab >>Comparison of mRNA and DNA HPV levels in HRHPV-positive primary screening samples using digital droplet PCR
2017 (English)Conference paper, Poster (with or without abstract) (Refereed)
National Category
Microbiology Infectious Medicine
Identifiers
urn:nbn:se:oru:diva-67184 (URN)
Conference
EUROGIN 2017, Amsterdam, Netherlands, October 8-11, 2017
Available from: 2018-06-05 Created: 2018-06-05 Last updated: 2018-08-30Bibliographically approved
Viegas, E. O., Augusto, O., Ismael, N., Kaliff, M., Lillsunde-Larsson, G., Ramqvist, T., . . . Andersson, S. (2017). Human papillomavirus prevalence and genotype distribution among young women and men in Maputo city, Mozambique. BMJ Open, 7(7), Article ID e015653.
Open this publication in new window or tab >>Human papillomavirus prevalence and genotype distribution among young women and men in Maputo city, Mozambique
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2017 (English)In: BMJ Open, ISSN 2044-6055, E-ISSN 2044-6055, Vol. 7, no 7, article id e015653Article in journal (Refereed) Published
Abstract [en]

OBJECTIVES: Human papillomavirus (HPV) is a well-known cause of cervical cancer, the second most frequent cancer in female African populations. This study aimed at determining the prevalence of HPV infections and the genotype distribution in young adults aged 18-24, in Maputo city, Mozambique, and to assess the suitability of commercially available HPV vaccines.

METHODS: This cross-sectional study was conducted between 2009 and 2011 at a youth clinic in Maputo Central Hospital. Cervical and urethral samples were obtained from 236 women and 176 men, respectively. Demographic and behavioural data were collected using structured questionnaires. HPV genotyping was performed for 35 different high, probably or possibly high-risk and low-risk HPV types using the CLART Human Papillomavirus 2.

RESULTS: HPV prevalence was 168/412 (40.8%; 95% CI 36.0 to 45.5) and was significantly higher in women than in men (63.6%vs10.2%). HPV52 was the most frequent type found in women, followed by HPV35, -16,-53, -58,-6 and -51. In men, HPV51 ranked the highest, followed by HPV6, -11,-52, -59 and -70. HIV infection and sexual debut before 18 years of age were associated with multiple HPV infections (OR 3.03; 95% CI 1.49 to 6.25 and OR 6.03; 95% CI 1.73 to 21.02, respectively). Women had a significantly higher HPV infection prevalence than men (p<0.001). The 9-valent HPV vaccine would cover 36.8% of the high-risk genotypes circulating in women in this study, compared with 26.3% and 15.8% coverage by the bivalent and quadrivalent vaccines, respectively.

CONCLUSION: This study confirmed the high burden of HPV infections in young women in Maputo city, Mozambique. The HPV prevalence was associated with high-risk sexual behaviour. Sex education and sexually transmitted infection prevention interventions should be intensified in Mozambique. Only a proportion of the high-risk HPV genotypes (37%) were covered by currently available vaccines.

Place, publisher, year, edition, pages
BMJ Publishing Group Ltd, 2017
Keywords
Epidemiology, INFECTIOUS DISEASES, Molecular diagnostics, Public health, SEXUAL MEDICINE
National Category
Obstetrics, Gynecology and Reproductive Medicine Public Health, Global Health, Social Medicine and Epidemiology
Identifiers
urn:nbn:se:oru:diva-61759 (URN)10.1136/bmjopen-2016-015653 (DOI)000410203700116 ()28716790 (PubMedID)2-s2.0-85025065144 (Scopus ID)
Note

Funding Agencies:

Regional HIV/AIDS Team for Africa, Embassy of Sweden, Lusaka - Sweden (Sida)  2150012801 

Regional HIV/AIDS Team for Africa, Embassy of Sweden, Lusaka - Norway (Sida)  2150012801 

Available from: 2017-10-25 Created: 2017-10-25 Last updated: 2018-08-31Bibliographically approved
Kumakech, E., Berggren, V., Wabinga, H., Lillsunde-Larsson, G., Helenius, G., Kaliff, M., . . . Andersson, S. (2016). Significantly Reduced Genoprevalence of Vaccine-Type HPV-16/18 Infections among Vaccinated Compared to Non-Vaccinated Young Women 5.5 Years after a Bivalent HPV-16/18 Vaccine (Cervarix®) Pilot Project in Uganda. PLoS ONE, 11(8), Article ID e0160099.
Open this publication in new window or tab >>Significantly Reduced Genoprevalence of Vaccine-Type HPV-16/18 Infections among Vaccinated Compared to Non-Vaccinated Young Women 5.5 Years after a Bivalent HPV-16/18 Vaccine (Cervarix®) Pilot Project in Uganda
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2016 (English)In: PLoS ONE, ISSN 1932-6203, E-ISSN 1932-6203, Vol. 11, no 8, article id e0160099Article in journal (Refereed) Published
Abstract [en]

The objective of this study was to determine the prevalence and some predictors for vaccine and non-vaccine types of HPV infections among bivalent HPV vaccinated and non-vaccinated young women in Uganda. This was a comparative cross sectional study 5.5 years after a bivalent HPV 16/18 vaccination (Cervarix®, GlaxoSmithKline, Belgium) pilot project in western Uganda. Cervical swabs were collected between July 2014-August 2014 and analyzed with a HPV genotyping test, CLART® HPV2 assay (Genomica, Madrid Spain) which is based on PCR followed by microarray for determination of genotype. Blood samples were also tested for HIV and syphilis infections as well as CD4 and CD8 lymphocyte levels. The age range of the participants was 15-24 years and mean age was 18.6(SD 1.4). Vaccine-type HPV-16/18 strains were significantly less prevalent among vaccinated women compared to non-vaccinated women (0.5% vs 5.6%, p 0.006, OR 95% CI 0.08(0.01-0.64). At type-specific level, significant difference was observed for HPV16 only. Other STIs (HIV/syphilis) were important risk factors for HPV infections including both vaccine types and non-vaccine types. In addition, for non-vaccine HPV types, living in an urban area, having a low BMI, low CD4 count and having had a high number of life time sexual partners were also significant risk factors. Our data concurs with the existing literature from other parts of the world regarding the effectiveness of bivalent HPV-16/18 vaccine in reducing the prevalence of HPV infections particularly vaccine HPV- 16/18 strains among vaccinated women. This study reinforces the recommendation to vaccinate young girls before sexual debut and integrate other STI particularly HIV and syphilis interventions into HPV vaccination packages.

Place, publisher, year, edition, pages
San Francisco, USA: Public Library of Science, 2016
National Category
Cancer and Oncology
Identifiers
urn:nbn:se:oru:diva-51618 (URN)10.1371/journal.pone.0160099 (DOI)000381110700023 ()27482705 (PubMedID)2-s2.0-84982091440 (Scopus ID)
Funder
Sida - Swedish International Development Cooperation Agency, SWE-2010-146/348-2013-6172
Available from: 2016-08-09 Created: 2016-08-09 Last updated: 2019-03-06Bibliographically approved
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