TRImodal DEfinitive invasive vagiNal carcinoma Treatment (TRIDENT protocol): how a standardized approach may change prognostic outcomes

Author:

Lancellotta ValentinaORCID,Macchia Gabriella,Garganese Giorgia,Fionda Bruno,Pezzulla DonatoORCID,De Angeli Martina,Autorino Rosa,Zinicola Tiziano,Gui BenedettaORCID,Russo Luca,Fragomeni Simona Maria,Ferrandina Gabriella,Rovirosa Angeles,Sala Evis,Scambia GiovanniORCID,Gambacorta Maria Antonietta,Tagliaferri Luca

Abstract

ObjectiveVaginal carcinoma is a rare malignancy accounting for 1–2% of all gynecological cancers. Surgery has a limited role, while definitive radiotherapy–chemotherapy followed by interventional radiotherapy is considered a valid alternative. The aim of the TRIDENT (TRImodal DEfinitive invasive vagiNal carcinoma Treatment) pilot study was to report the results of a modern standardized trimodal protocol treatment consisting of image guided definitive radiotherapy–chemotherapy followed by image guided interventional radiotherapy in terms of safety and efficacy.MethodsBetween January 2019 and December 2021, we analyzed 21 consecutive patients with primary vaginal cancer who had received radiotherapy–chemotherapy followed by interventional radiotherapy. The primary study endpoint was local control, and secondary endpoints were metastasis free survival, overall survival, and rate and severity of acute and late toxicities.Results14 patients had FIGO (International Federation of Gynecology and Obstetrics) stage II, five patients had stage III, and two had stage IVB disease. Median total external beam radiotherapy dose for the tumor was 45 Gy. Median total dose on positive nodes was 60 Gy. Median total dose for interventional radiotherapy was 28 Gy over four high dose rate fractions to achieve between 85 and 95 Gy equivalent dose, in 2 Gy fractions (EQD2)α/β10, to the high risk clinical target volume, and 60 Gy EQD2α/β10 to the intermediate risk clinical target volume. All patients received weekly platinum based chemotherapy. Median follow-up was 20 months (range 10–56 months). Two year actuarial local control, metastasis free survival, and overall survival rate were 79.4%, 90.5%, and 79.4%, respectively. In terms of acute toxicity, there were no grade 4 events and only one acute grade (G) 3 toxicity (skin). Only vaginal stenosis (G3) was documented 12 months after therapy due to late toxicity.ConclusionsIn this study, definitive radiotherapy–chemotherapy followed by interventional radiotherapy was a safe and effective treatment modality for primary vaginal cancer.

Publisher

BMJ

Subject

Obstetrics and Gynecology,Oncology

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