Individualized Prediction of Menses Recovery After Chemotherapy for Early-stage Breast Cancer: A Nomogram Developed From UNICANCER PACS04 and PACS05 Trials.


Journal

Clinical breast cancer
ISSN: 1938-0666
Titre abrégé: Clin Breast Cancer
Pays: United States
ID NLM: 100898731

Informations de publication

Date de publication:
02 2019
Historique:
received: 25 04 2018
revised: 06 06 2018
accepted: 16 08 2018
pubmed: 23 9 2018
medline: 27 3 2020
entrez: 23 9 2018
Statut: ppublish

Résumé

The likelihood of menses recovery varies greatly in premenopausal patients receiving adjuvant chemotherapy for breast cancer. Quantifying this probability for each patient could better inform the chemotherapy discussion and individualize fertility counseling. We performed a pooled analysis of the PACS04 and PACS05 adjuvant randomized trials to develop a nomogram to estimate the probability of menses recovery at 3, 6, and 18 months after the end of adjuvant chemotherapy. Women who were premenopausal and aged ≤ 50 years at randomization in the PACS04 and PACS05 trials were included in the present analysis. The primary endpoint was the probability of menses recovery within 18 months of chemotherapy completion. Multivariable Cox proportional hazards regression was used to estimate the association of each variable with the likelihood of menses resumption. A nomogram was developed to predict menses recovery at different intervals. The factors associated with menses recovery were assessed for 1210 patients. At a median follow-up of 90 months (range, 3-189 months), 342 of 1210 patients (28.2%) had recovered menses. The probability of menses recovery at 18 months was 25.5% (range, 23.0%-27.9%). After backward elimination, age, final body mass index, type of chemotherapy, and hormone therapy were selected to build the nomogram to predict the probability of menstrual resumption at 3, 6, and 18 months after chemotherapy. An accurate and individualized prediction of menses recovery is feasible for premenopausal patients eligible for adjuvant chemotherapy for early-stage breast cancer. Our nomogram will be externally validated in a large prospective cohort.

Sections du résumé

BACKGROUND
The likelihood of menses recovery varies greatly in premenopausal patients receiving adjuvant chemotherapy for breast cancer. Quantifying this probability for each patient could better inform the chemotherapy discussion and individualize fertility counseling. We performed a pooled analysis of the PACS04 and PACS05 adjuvant randomized trials to develop a nomogram to estimate the probability of menses recovery at 3, 6, and 18 months after the end of adjuvant chemotherapy.
PATIENTS AND METHODS
Women who were premenopausal and aged ≤ 50 years at randomization in the PACS04 and PACS05 trials were included in the present analysis. The primary endpoint was the probability of menses recovery within 18 months of chemotherapy completion. Multivariable Cox proportional hazards regression was used to estimate the association of each variable with the likelihood of menses resumption. A nomogram was developed to predict menses recovery at different intervals.
RESULTS
The factors associated with menses recovery were assessed for 1210 patients. At a median follow-up of 90 months (range, 3-189 months), 342 of 1210 patients (28.2%) had recovered menses. The probability of menses recovery at 18 months was 25.5% (range, 23.0%-27.9%). After backward elimination, age, final body mass index, type of chemotherapy, and hormone therapy were selected to build the nomogram to predict the probability of menstrual resumption at 3, 6, and 18 months after chemotherapy.
CONCLUSION
An accurate and individualized prediction of menses recovery is feasible for premenopausal patients eligible for adjuvant chemotherapy for early-stage breast cancer. Our nomogram will be externally validated in a large prospective cohort.

Identifiants

pubmed: 30241966
pii: S1526-8209(18)30264-7
doi: 10.1016/j.clbc.2018.08.005
pii:
doi:

Types de publication

Clinical Trial, Phase III Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

63-70

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Barbara Pistilli (B)

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France. Electronic address: barbara.pistilli@gustaveroussy.fr.

Chafika Mazouni (C)

Department of Surgical Oncology, Institut Gustave Roussy, Villejuif, France.

Anna Zingarello (A)

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France; U.O. Oncologia Medica 2, IRCCS AOU San Martino-IST, Genova, Italy.

Matthieu Faron (M)

Department of Surgical Oncology, Institut Gustave Roussy, Villejuif, France; Department of Biostatistics and Epidemiology, Institut Gustave Roussy, Villejuif, France.

Mahasti Saghatchian (M)

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.

Michael Grynberg (M)

Department of Reproductive Medicine and Fertility Preservation, Hopital Antoine Béclère, Clamart, and Université Paris Sud XI, Paris, France.

Marc Spielmann (M)

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.

Paul Kerbrat (P)

Department of Oncology, Centre Eugene Marquis, Rennes, France.

Henri Roché (H)

Department of Medical Oncology, Institut Claudius Regaud, IUCT Oncopole, Toulouse, France.

Veronique Lorgis (V)

Department of Medical Oncology, Centre Georges François Leclerc, Dijon, France.

Thomas Bachelot (T)

Department of Medical Oncology, Centre Léon Bérard, Lyon, France.

Mario Campone (M)

Department of Medical Oncology, Institut de Cancérologie de l'Ouest, Angers, France.

Christelle Levy (C)

Department of Medical Oncology, Centre Franois Baclesse, Caen, France.

Anthony Gonçalves (A)

Department of Medical Oncology, Institut Paoli-Calmettes, Marseille, France.

Anne Lesur (A)

Department of Medical Oncology, Institut de Cancérologie de Lorriane, Nancy, France.

Corinne Veyret (C)

Department of Medical Oncology, Centre Henri Becquerel, Rouen, France.

Laurence Vanlemmens (L)

Department of Medical Oncology, Centre Oscar Lambret, Lille, France.

Jerome Lemonnier (J)

National Federation of French Cancer Centres, Paris, France.

Suzette Delaloge (S)

Department of Medical Oncology, Institut Gustave Roussy, Villejuif, France.

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