Impact of HPV-16 Lineages Infection in Response to Radio-Chemotherapy in Cervical Cancer

被引:1
作者
de Figueiredo, Fabio Vidal [1 ]
Santos, Gerusinete Rodrigues Bastos dos [1 ]
Vidal, Flavia Castello Branco [1 ]
da Silva, Marcos Antonio Custodio Neto [2 ]
da Silva, Rodrigo Lopes [1 ]
Batista, Zulmira da Silva [1 ]
de Andrade, Marcelo Souza [1 ]
Barbosa, Maria do Carmo Lacerda [3 ]
Manicoba, Anna Cyntia Brandao Nascimento [4 ]
da Silva, Mayara Cristina Pinto [1 ]
Nascimento, Maria do Desterro Soares Brandao [1 ]
机构
[1] Univ Fed Maranhao, Postgrad Program Adult Hlth, BR-65020070 Sao Luis, Brazil
[2] Univ Fed Maranhao, Sci Ctr Imperatriz, Med Course, BR-65905240 Imperatriz, Brazil
[3] Univ Fed Maranhao, Med I Dept, BR-65020070 Sao Luis, Brazil
[4] Univ Fed Maranhao, Univ Hosp, BR-65020070 Sao Luis, Brazil
关键词
cervical cancer; HPV-16; variants; radiotherapy; follow-up; HUMAN-PAPILLOMAVIRUS TYPE-16; SQUAMOUS-CELL CARCINOMA; RADIATION; RADIOTHERAPY; CISPLATIN; VARIANTS; GENOTYPE; ADENOCARCINOMA; CHEMOTHERAPY; PERSISTENCE;
D O I
10.3390/biomedicines11072069
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: HPV is strongly related to cervical cancer. HPV lineages can contribute to a response to cervical cancer therapy. The aim of this research was to estimate the frequency of human papillomavirus (HPV)-16 lineages in specimens of cervical cancer, relate the pathological factors in these variants, and assess their response to treatment with radical chemoradiotherapy. Methods: Samples of cervical cancer were collected from women who were referred to a reference cancer hospital to test the presence of human papillomavirus-type DNA. The standard protocol of this service consisted of cisplatin-based chemotherapy of 40 mg/m(2), plus conventional pelvic irradiation in doses of 45-50.4 Gy and high dose-rate brachytherapy of 28-30 Gy to Point A. The response to chemotherapy was evaluated after three months in patients with the HPV-16 lineage. Results: HPV DNA was detected in 104 (88.1%) of the 118 patients. HPV-16 was present in 63 patients (53%). Lineages of HPV-16 were identified in 57 patients and comprised 33 instances of (57.8%) lineage A, 2 instances of lineage B (3.5%), 2 instances of lineage C (3.5%), and 20 instances of (35.0%) lineage D. The median age of the patients was 48.4 years (range 25-85 years). Squamous cell carcinoma was detected 48 times (84.2%). Adenocarcinoma was more likely to occur in lineage D, as three of the four cases occurred in this lineage. A total of 11 patients with the HPV-16 variant were treated with chemoradiotherapy. After three months, it was observed that nine of the eleven patients (81.8%) achieved a complete response, five with the lineage A type, two with the lineage C type, and two with the lineage D type. The two cases of partial response and disease progression, one of each, occurred in lineage A. Conclusions: In addition to the small number of patients and HPV variants, we noticed a better response in patients with the HPV-16 lineage A. Increasing the sample size could be helpful to better assess the impact of HPV variants on cervical cancer treatment.
引用
收藏
页数:14
相关论文
共 46 条
[1]   Comparison of human papillomavirus genotypes, sexual, and reproductive risk factors of cervical adenocarcinoma and squamous cell carcinoma: Northeastern United States [J].
Altekruse, SF ;
Lacey, JV ;
Brinton, LA ;
Gravitt, PE ;
Silverberg, SG ;
Barnes, WA ;
Greenberg, MD ;
Hadjimichael, OC ;
McGowan, L ;
Mortel, R ;
Schwartz, PE ;
Hildesheim, A .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 2003, 188 (03) :657-663
[2]  
[Anonymous], 2002, INT J GYNECOL OBSTET, V78, P79
[3]   STRUCTURES OF BOVINE AND HUMAN PAPILLOMAVIRUSES - ANALYSIS BY CRYOELECTRON MICROSCOPY AND 3-DIMENSIONAL IMAGE-RECONSTRUCTION [J].
BAKER, TS ;
NEWCOMB, WW ;
OLSON, NH ;
COWSERT, LM ;
OLSON, C ;
BROWN, JC .
BIOPHYSICAL JOURNAL, 1991, 60 (06) :1445-1456
[4]   Genome variation of human papillomavirus types: Phylogenetic and medical implications [J].
Bernard, HU ;
Calleja-Macias, IE ;
Dunn, ST .
INTERNATIONAL JOURNAL OF CANCER, 2006, 118 (05) :1071-1076
[5]   PREVALENCE OF HUMAN PAPILLOMAVIRUS IN CERVICAL-CANCER - A WORLDWIDE PERSPECTIVE [J].
BOSCH, FX ;
MANOS, MM ;
MUNOZ, N ;
SHERMAN, M ;
JANSEN, AM ;
PETO, J ;
SCHIFFMAN, MH ;
MORENO, V ;
KURMAN, R ;
SHAH, KV ;
ALIHONOU, E ;
BAYO, S ;
MOKHTAR, HC ;
CHICAREON, S ;
DAUDT, A ;
DELOSRIOS, E ;
GHADIRIAN, P ;
KITINYA, JN ;
KOULIBALY, M ;
NGELANGEL, C ;
TINTORE, LMP ;
RIOSDALENZ, JL ;
SARJADI ;
SCHNEIDER, A ;
TAFUR, L ;
TEYSSIE, AR ;
ROLON, PA ;
TORROELLA, M ;
TAPIA, AV ;
WABINGA, HR ;
ZATONSKI, W ;
SYLLA, B ;
VIZCAINO, P ;
MAGNIN, D ;
KALDOR, J ;
GREER, C ;
WHEELER, C .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1995, 87 (11) :796-802
[6]  
Bray F, 2018, CA-CANCER J CLIN, V68, P394, DOI [10.3322/caac.21609, 10.3322/caac.21492]
[7]   Human papillomavirus genome variants [J].
Burk, Robert D. ;
Harari, Ariana ;
Chen, Zigui .
VIROLOGY, 2013, 445 (1-2) :232-243
[8]   Human papillomavirus 16 sub-lineage dispersal and cervical cancer risk worldwide: Whole viral genome sequences from 7116 HPV16-positive women [J].
Clifford, Gary M. ;
Tenet, Vanessa ;
Georges, Damien ;
Alemany, Laia ;
Angel Pavon, Miquel ;
Chen, Zigui ;
Yeager, Meredith ;
Cullen, Michael ;
Boland, Joseph F. ;
Bass, Sara ;
Steinberg, Mia ;
Raine-Bennett, Tina ;
Lorey, Thomas ;
Wentzensen, Nicolas ;
Walker, Joan ;
Zuna, Rosemary ;
Schiffman, Mark ;
Mirabello, Lisa .
PAPILLOMAVIRUS RESEARCH, 2019, 7 :67-74
[9]   HPV16 genetic variation and the development of cervical cancer worldwide [J].
Cornet, I. ;
Gheit, T. ;
Iannacone, M. R. ;
Vignat, J. ;
Sylla, B. S. ;
Del Mistro, A. ;
Franceschi, S. ;
Tommasino, M. ;
Clifford, G. M. .
BRITISH JOURNAL OF CANCER, 2013, 108 (01) :240-244
[10]   OBESITY Insensitive issue [J].
Crow, James Mitchell .
NATURE, 2012, 486 (7403) :S12-S13