3D conformal postoperative radiotherapy with concomitant boost in uterine cancer: results of a phase I-II study (ADA-RT-1)

Gabriella Macchia; Maria Gabriella Ferrandina; Francesco Deodato; R Bibbò; Mariangela Massaccesi; Edy Ippolito; Numa Cellini; Giovanni Scambia; Vincenzo Valentini; Alessio Giuseppe Morganti

doi:10.1016/j.ygyno.2010.11.021

3D conformal postoperative radiotherapy with concomitant boost in uterine cancer: results of a phase I-II study (ADA-RT-1)

Gabriella Macchia^*
, Maria Gabriella Ferrandina
, Francesco Deodato
, R Bibbò
, Mariangela Massaccesi
, Edy Ippolito
, Numa Cellini
, Giovanni Scambia
, Vincenzo Valentini
, Alessio Giuseppe Morganti

^*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivista › Articolo

Abstract

A phase I-II prospective clinical trial of adjuvant accelerated radiation therapy (ADA-RT-1 trial) was set up in order to investigate the feasibility and efficacy of a pelvic conformal radiotherapy technique with concomitant boost (CB technique) to the vaginal vault in high-risk uterine cancers.

Lingua originale	Inglese
pagine (da-a)	485-488
Numero di pagine	4
Rivista	Gynecologic Oncology
Volume	120
Numero di pubblicazione	3
DOI	https://doi.org/10.1016/j.ygyno.2010.11.021
Stato di pubblicazione	Pubblicato - 2011

OSS delle Nazioni Unite

Questo processo contribuisce al raggiungimento dei seguenti obiettivi di sviluppo sostenibile

SDG 3 Salute e benessere

All Science Journal Classification (ASJC) codes

Oncologia
Ostetricia e Ginecologia

Keywords

80 and over
Adult
Aged
Combined Modality Therapy
Conformal
Female
Humans
Middle Aged
Neoplasm Staging
Prospective Studies
Radiotherapy
Uterine Neoplasms

Accesso al documento

10.1016/j.ygyno.2010.11.021

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title = "3D conformal postoperative radiotherapy with concomitant boost in uterine cancer: results of a phase I-II study (ADA-RT-1)",

abstract = "A phase I-II prospective clinical trial of adjuvant accelerated radiation therapy (ADA-RT-1 trial) was set up in order to investigate the feasibility and efficacy of a pelvic conformal radiotherapy technique with concomitant boost (CB technique) to the vaginal vault in high-risk uterine cancers.",

keywords = "80 and over, Adult, Aged, Combined Modality Therapy, Conformal, Female, Humans, Middle Aged, Neoplasm Staging, Prospective Studies, Radiotherapy, Uterine Neoplasms, 80 and over, Adult, Aged, Combined Modality Therapy, Conformal, Female, Humans, Middle Aged, Neoplasm Staging, Prospective Studies, Radiotherapy, Uterine Neoplasms",

author = "Gabriella Macchia and Ferrandina, \{Maria Gabriella\} and Francesco Deodato and R Bibb{\`o} and Mariangela Massaccesi and Edy Ippolito and Numa Cellini and Giovanni Scambia and Vincenzo Valentini and Morganti, \{Alessio Giuseppe\}",

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doi = "10.1016/j.ygyno.2010.11.021",

language = "English",

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pages = "485--488",

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AU - Macchia, Gabriella

AU - Ferrandina, Maria Gabriella

AU - Deodato, Francesco

AU - Bibbò, R

AU - Massaccesi, Mariangela

AU - Ippolito, Edy

AU - Cellini, Numa

AU - Scambia, Giovanni

AU - Valentini, Vincenzo

AU - Morganti, Alessio Giuseppe

PY - 2011

Y1 - 2011

N2 - A phase I-II prospective clinical trial of adjuvant accelerated radiation therapy (ADA-RT-1 trial) was set up in order to investigate the feasibility and efficacy of a pelvic conformal radiotherapy technique with concomitant boost (CB technique) to the vaginal vault in high-risk uterine cancers.

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KW - Adult

KW - Aged

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KW - Humans

KW - Middle Aged

KW - Neoplasm Staging

KW - Prospective Studies

KW - Radiotherapy

KW - Uterine Neoplasms

KW - 80 and over

KW - Adult

KW - Aged

KW - Combined Modality Therapy

KW - Conformal

KW - Female

KW - Humans

KW - Middle Aged

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KW - Prospective Studies

KW - Radiotherapy

KW - Uterine Neoplasms

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JO - Gynecologic Oncology

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IS - 3

ER -

3D conformal postoperative radiotherapy with concomitant boost in uterine cancer: results of a phase I-II study (ADA-RT-1)

Abstract

OSS delle Nazioni Unite

All Science Journal Classification (ASJC) codes

Keywords

Accesso al documento

Altri file e collegamenti

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