Diagnostic and Therapeutic Approach in a Metastatic Vaginal Adenocarcinoma: A Case Report.
Adenocarcinoma
/ drug therapy
Adenocarcinoma of Lung
/ drug therapy
Antibodies, Monoclonal, Humanized
/ administration & dosage
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Bevacizumab
/ administration & dosage
Cisplatin
/ administration & dosage
DNA-Binding Proteins
/ genetics
Female
Humans
Immunotherapy
Middle Aged
Mutation
Paclitaxel
/ administration & dosage
Receptor, ErbB-2
/ metabolism
Transcription Factors
/ genetics
Vaginal Neoplasms
/ drug therapy
abscopal effect
immune checkpoint blockade
mutational burden
trastuzumab
vaginal adenocarcinoma
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2021
2021
Historique:
received:
28
03
2021
accepted:
05
07
2021
entrez:
9
8
2021
pubmed:
10
8
2021
medline:
29
10
2021
Statut:
epublish
Résumé
Vaginal adenocarcinomas (VAC) are most often reported after intrauterine exposition to diethylstilbestrol (DES). Rarely, VACs are reported as a malignant transformation of vaginal adenosis or endometriosis, in the context of chromosomal abnormalities or malformations of the uterus or the vagina. VACs without DES exposition have a poor prognosis and a significantly worse outcome compared to vaginal squamous cell carcinomas or DES-associated VACs. Here, we report the case of a primarily metastatic VAC, treated successfully with different lines of chemo-, antiangiogenic, antibody, and immunotherapy. The 49-year-old patient presented in 5/2018 with a primarily pulmonary metastatic VAC. Significant tumor reduction was seen after six cycles of carboplatin AUC5/paclitaxel 175 mg/m²/bevacizumab 15 mg/kg q3w. Bevacizumab maintenance therapy and later cisplatin mono 50 mg/m² q2w led to local and distant tumor progression. To identify a potential targeted therapy, new tumor biopsies were obtained. Immunohistochemistry revealed ERBB2 expression, and paclitaxel 80 mg/m² weekly plus trastuzumab 4 mg/m² respectively 2 mg/m² q3w was administered. Due to local and pulmonal tumor progression after 6 months and persistent ERBB2 positivity, the therapy was adjusted to trastuzumab emtansine (T-DM1) 3.6 mg/kg q3w; however, the patient remained locally progressive after three cycles of T-DM1 and additionally showed a new bone metastasis. The new tumor biopsies revealed a combined positive score (CPS) of 2 regarding PD-L1, and pembrolizumab 200 mg q3w was initiated. The bone metastasis was radiated and treated with denosumab 120 mg q4w. Extreme tumor regression followed by stable disease was maintained for 9 months. Due to a slow locoregional progress only with new inguinal lymph node and pararectal lymph node metastases, a new tumor biopsy was taken. Molecular profiling showed an ARID1A mutation, a mutational burden of 5.1 mutations per megabase, and no genfusions. Based on these findings, therapy with PD-L1 antibodies, PD-1 antibodies, gemcitabine, or dasatinib was suggested. Therefore, administration of pembrolizumab was continued and local radiation therapy was performed. This led to a decrease in local tumor manifestations and a stable systemic disease. Our case demonstrates the diagnostic and therapeutic approach in a patient with primary metastatic vaginal adenocarcinoma. By tumorgenetic profiling, different lines of systemic therapy, namely, antiangiogenic therapy, monoclonal antibody therapy, immunotherapy, and local radiation therapy, were identified and successfully administered.
Sections du résumé
Background
Vaginal adenocarcinomas (VAC) are most often reported after intrauterine exposition to diethylstilbestrol (DES). Rarely, VACs are reported as a malignant transformation of vaginal adenosis or endometriosis, in the context of chromosomal abnormalities or malformations of the uterus or the vagina. VACs without DES exposition have a poor prognosis and a significantly worse outcome compared to vaginal squamous cell carcinomas or DES-associated VACs.
Objective
Here, we report the case of a primarily metastatic VAC, treated successfully with different lines of chemo-, antiangiogenic, antibody, and immunotherapy.
Case
The 49-year-old patient presented in 5/2018 with a primarily pulmonary metastatic VAC. Significant tumor reduction was seen after six cycles of carboplatin AUC5/paclitaxel 175 mg/m²/bevacizumab 15 mg/kg q3w. Bevacizumab maintenance therapy and later cisplatin mono 50 mg/m² q2w led to local and distant tumor progression. To identify a potential targeted therapy, new tumor biopsies were obtained. Immunohistochemistry revealed ERBB2 expression, and paclitaxel 80 mg/m² weekly plus trastuzumab 4 mg/m² respectively 2 mg/m² q3w was administered. Due to local and pulmonal tumor progression after 6 months and persistent ERBB2 positivity, the therapy was adjusted to trastuzumab emtansine (T-DM1) 3.6 mg/kg q3w; however, the patient remained locally progressive after three cycles of T-DM1 and additionally showed a new bone metastasis. The new tumor biopsies revealed a combined positive score (CPS) of 2 regarding PD-L1, and pembrolizumab 200 mg q3w was initiated. The bone metastasis was radiated and treated with denosumab 120 mg q4w. Extreme tumor regression followed by stable disease was maintained for 9 months. Due to a slow locoregional progress only with new inguinal lymph node and pararectal lymph node metastases, a new tumor biopsy was taken. Molecular profiling showed an ARID1A mutation, a mutational burden of 5.1 mutations per megabase, and no genfusions. Based on these findings, therapy with PD-L1 antibodies, PD-1 antibodies, gemcitabine, or dasatinib was suggested. Therefore, administration of pembrolizumab was continued and local radiation therapy was performed. This led to a decrease in local tumor manifestations and a stable systemic disease.
Conclusion
Our case demonstrates the diagnostic and therapeutic approach in a patient with primary metastatic vaginal adenocarcinoma. By tumorgenetic profiling, different lines of systemic therapy, namely, antiangiogenic therapy, monoclonal antibody therapy, immunotherapy, and local radiation therapy, were identified and successfully administered.
Identifiants
pubmed: 34367146
doi: 10.3389/fimmu.2021.686879
pmc: PMC8342998
doi:
Substances chimiques
ARID1A protein, human
0
Antibodies, Monoclonal, Humanized
0
DNA-Binding Proteins
0
Transcription Factors
0
Bevacizumab
2S9ZZM9Q9V
pembrolizumab
DPT0O3T46P
Receptor, ErbB-2
EC 2.7.10.1
Paclitaxel
P88XT4IS4D
Cisplatin
Q20Q21Q62J
Types de publication
Case Reports
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
686879Informations de copyright
Copyright © 2021 Egger, Ralser, Lindner, Recker, Marinova, Savchenko, Lau and Mustea.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Références
Oncotarget. 2017 May 2;8(18):30606-30616
pubmed: 28389628
CA Cancer J Clin. 2021 May;71(3):209-249
pubmed: 33538338
Clin Cancer Res. 2015 Dec 15;21(24):5480-7
pubmed: 26672085
Int J Gynecol Pathol. 1986;5(4):362-70
pubmed: 3643169
N Engl J Med. 1971 Apr 15;284(15):878-81
pubmed: 5549830
J Hematol Oncol. 2018 Aug 16;11(1):104
pubmed: 30115069
Int J Mol Sci. 2021 Feb 19;22(4):
pubmed: 33669559
Antioxidants (Basel). 2020 Nov 26;9(12):
pubmed: 33256059
Oncotarget. 2015 Nov 3;6(34):36219-30
pubmed: 26435481
J Clin Oncol. 2019 Nov 1;37(31):2825-2834
pubmed: 31487218
Gynecol Oncol. 2014 Apr;133(1):117-23
pubmed: 24486604
Gynecol Oncol. 2007 May;105(2):470-4
pubmed: 17292459
J Hematol Oncol. 2018 Jun 25;11(1):86
pubmed: 29941010
Lancet Oncol. 2020 Oct;21(10):1353-1365
pubmed: 32919526
Lancet. 2017 Oct 7;390(10103):1654-1663
pubmed: 28756902
Semin Oncol. 2020 Oct;47(5):259-269
pubmed: 32896428
Am J Obstet Gynecol. 2017 Oct;217(4):432.e1-432.e17
pubmed: 28599900
J Clin Oncol. 2019 Jun 10;37(17):1470-1478
pubmed: 30943124
Gynecol Oncol. 1994 Nov;55(2):259-64
pubmed: 7959294
BMC Cancer. 2019 Aug 13;19(1):798
pubmed: 31409310
Int J Gynaecol Obstet. 2015 Oct;131 Suppl 2:S84-7
pubmed: 26433679
Arch Gynecol Obstet. 2020 Dec;302(6):1429-1439
pubmed: 32780160
Nature. 2014 Feb 20;506(7488):371-5
pubmed: 24390348