Neoadjuvant chemotherapy in high-risk soft tissue sarcomas: A Sarculator-based risk stratification analysis of the ISG-STS 1001 randomized trial.


Journal

Cancer
ISSN: 1097-0142
Titre abrégé: Cancer
Pays: United States
ID NLM: 0374236

Informations de publication

Date de publication:
01 Jan 2022
Historique:
revised: 25 05 2021
received: 21 04 2021
accepted: 07 06 2021
pubmed: 14 10 2021
medline: 11 3 2022
entrez: 13 10 2021
Statut: ppublish

Résumé

The value of neoadjuvant chemotherapy in soft tissue sarcoma (STS) is not completely understood. This study investigated the benefit of neoadjuvant chemotherapy according to prognostic stratification based on the Sarculator nomogram for STS. This study analyzed data from ISG-STS 1001, a randomized study that tested 3 cycles of neoadjuvant anthracycline plus ifosfamide (AI) or histology-tailored (HT) chemotherapy in adult patients with STS. The 10-year predicted overall survival (pr-OS) was estimated with the Sarculator and was stratified into higher (10-year pr-OS < 60%) and lower risk subgroups (10-year pr-OS ≥ 60%). The median pr-OS was 0.63 (interquartile range [IQR], 0.51-0.72) for the entire study population, 0.62 (IQR, 0.51-0.70) for the AI arm, and 0.64 (IQR, 0.51-0.73) for the HT arm. Three- and 5-year overall survival (OS) were 0.86 (95% confidence interval [CI], 0.82-0.93) and 0.81 (95% CI, 0.71-0.86) in lower risk patients and 0.69 (95% CI, 0.70-0.85) and 0.59 (95% CI, 0.51-0.72) in the higher risk patients (log-rank test, P = .004). In higher risk patients, the 3- and 5-year Sarculator-predicted and study-observed OS rates were 0.68 and 0.58, respectively, and 0.85 and 0.66, respectively, in the AI arm (P = .04); the corresponding figures in the HT arm were 0.69 and 0.60, respectively, and 0.69 and 0.55, respectively (P > .99). In lower risk patients, the 3- and 5-year Sarculator-predicted and study-observed OS rates were 0.85 and 0.80, respectively, and 0.89 and 0.82, respectively, in the AI arm (P = .507); the corresponding figures in the HT arm were 0.87 and 0.81, respectively, and 0.86 and 0.74, respectively (P = .105). High-risk patients treated with AI performed better than predicted, and this adds to the evidence for the efficacy of neoadjuvant AI in STS. People affected by soft tissue sarcomas of the extremities and trunk wall are at some risk of developing metastasis after surgery. Preoperative or postoperative chemotherapy has been tested in clinical trials to reduce the chances of distant metastasis. However, study findings have not been conclusive. This study stratified the risk of metastasis for people affected by sarcomas who were included in a clinical trial testing neoadjuvant chemotherapy. Exploiting the prognostic nomogram Sarculator, it found a benefit for chemotherapy when the predicted risk, based on patient and tumor characteristics, was high.

Sections du résumé

BACKGROUND BACKGROUND
The value of neoadjuvant chemotherapy in soft tissue sarcoma (STS) is not completely understood. This study investigated the benefit of neoadjuvant chemotherapy according to prognostic stratification based on the Sarculator nomogram for STS.
METHODS METHODS
This study analyzed data from ISG-STS 1001, a randomized study that tested 3 cycles of neoadjuvant anthracycline plus ifosfamide (AI) or histology-tailored (HT) chemotherapy in adult patients with STS. The 10-year predicted overall survival (pr-OS) was estimated with the Sarculator and was stratified into higher (10-year pr-OS < 60%) and lower risk subgroups (10-year pr-OS ≥ 60%).
RESULTS RESULTS
The median pr-OS was 0.63 (interquartile range [IQR], 0.51-0.72) for the entire study population, 0.62 (IQR, 0.51-0.70) for the AI arm, and 0.64 (IQR, 0.51-0.73) for the HT arm. Three- and 5-year overall survival (OS) were 0.86 (95% confidence interval [CI], 0.82-0.93) and 0.81 (95% CI, 0.71-0.86) in lower risk patients and 0.69 (95% CI, 0.70-0.85) and 0.59 (95% CI, 0.51-0.72) in the higher risk patients (log-rank test, P = .004). In higher risk patients, the 3- and 5-year Sarculator-predicted and study-observed OS rates were 0.68 and 0.58, respectively, and 0.85 and 0.66, respectively, in the AI arm (P = .04); the corresponding figures in the HT arm were 0.69 and 0.60, respectively, and 0.69 and 0.55, respectively (P > .99). In lower risk patients, the 3- and 5-year Sarculator-predicted and study-observed OS rates were 0.85 and 0.80, respectively, and 0.89 and 0.82, respectively, in the AI arm (P = .507); the corresponding figures in the HT arm were 0.87 and 0.81, respectively, and 0.86 and 0.74, respectively (P = .105).
CONCLUSIONS CONCLUSIONS
High-risk patients treated with AI performed better than predicted, and this adds to the evidence for the efficacy of neoadjuvant AI in STS.
LAY SUMMARY BACKGROUND
People affected by soft tissue sarcomas of the extremities and trunk wall are at some risk of developing metastasis after surgery. Preoperative or postoperative chemotherapy has been tested in clinical trials to reduce the chances of distant metastasis. However, study findings have not been conclusive. This study stratified the risk of metastasis for people affected by sarcomas who were included in a clinical trial testing neoadjuvant chemotherapy. Exploiting the prognostic nomogram Sarculator, it found a benefit for chemotherapy when the predicted risk, based on patient and tumor characteristics, was high.

Identifiants

pubmed: 34643947
doi: 10.1002/cncr.33895
doi:

Substances chimiques

Ifosfamide UM20QQM95Y

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

85-93

Subventions

Organisme : DEPGYN
ID : RHU4
Organisme : EUROSARC FP7
ID : 278472
Organisme : LYRICAN
ID : INCA-DGOS-INSERM 12563

Commentaires et corrections

Type : CommentIn
Type : ErratumIn

Informations de copyright

© 2021 American Cancer Society.

Références

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Auteurs

Sandro Pasquali (S)

Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Emanuela Palmerini (E)

Osteoncology, Bone and Soft Tissue Sarcomas, and Innovative Therapies Unit, IRCCS Istituto Ortopedico Rizzoli, Bologna, Italy.

Vittorio Quagliuolo (V)

Department of Surgery, IRCCS Humanitas Research Hospital, Rozzano, Italy.

Javier Martin-Broto (J)

Medical Oncology Department, University Hospital Virgen del Rocio, Seville, Spain.
Institute of Biomedicine of Seville, University of Seville, Seville, Spain.

Antonio Lopez-Pousa (A)

Department of Cancer Medicine, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Giovanni Grignani (G)

Department of Cancer Medicine, Fondazione del Piemonte per l'Oncologia IRCCS Candiolo, Turin, Italy.

Antonella Brunello (A)

Department of Oncology, Medical Oncology 1 Unit, Istituto Oncologico Veneto, IRCCS, Padua, Italy.

Jean-Yves Blay (JY)

Department of Cancer Medicine, Léon Bérard Cancer Center, Lyon, France.
Université Claude Bernard Lyon I, Lyon, France.

Oscar Tendero (O)

Department of Surgery, Hospital Universitari Son Espases, Palma de Mallorca, Spain.

Robert Diaz-Beveridge (R)

Department of Cancer Medicine, Hospital Universitari i Politècnic La Fe, Valencia, Spain.

Virginia Ferraresi (V)

Department of Cancer Medicine, Istituto Regina Elena, Rome, Italy.

Iwona Lugowska (I)

Department of Soft Tissue/Bone Sarcoma and Melanoma, Centrum Onkologii Instytut im Marii Skłodowskiej Curie, Warsaw, Poland.

Gabriele Infante (G)

Clinical Epidemiology and Trial Organization, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Luca Braglia (L)

Research and Statistics Infrastructure, Azienda Unità Sanitaria Locale-IRCCS, Reggio Emilia, Italy.

Domenico Franco Merlo (DF)

Research and Statistics Infrastructure, Azienda Unità Sanitaria Locale-IRCCS, Reggio Emilia, Italy.

Valeria Fontana (V)

Clinical Trial Center and Department of Epidemiology, IRCCS Azienda Ospedaliera Universitaria San Martino, IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy.

Emanuela Marchesi (E)

Clinical Trial Center, Italian Sarcoma Group, Bologna, Italy.

Davide Maria Donati (DM)

Department of Orthopedic Oncology, Istituto Ortopedico Rizzoli, Bologna, Italy.

Elena Palassini (E)

Department of Cancer Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Giuseppe Bianchi (G)

Department of Orthopedic Oncology, Istituto Ortopedico Rizzoli, Bologna, Italy.

Andrea Marrari (A)

Department of Cancer Medicine, Istituto Clinico Humanitas, Rozzano, Italy.

Carlo Morosi (C)

Department of Radiology, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Silvia Stacchiotti (S)

Department of Cancer Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Silvia Bagué (S)

Department of Pathology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.

Jean Michel Coindre (JM)

Department of Pathology, Institut Bergonié, Bordeaux, France.

Angelo Paolo Dei Tos (AP)

Department of Pathology, Treviso General Hospital, Padua, Italy.
University of Padua, Padua, Italy.

Piero Picci (P)

Laboratory of Oncologic Research, Istituto Ortopedico Rizzoli, Bologna, Italy.

Paolo Bruzzi (P)

Clinical Trial Center and Department of Epidemiology, IRCCS Azienda Ospedaliera Universitaria San Martino, IST Istituto Nazionale per la Ricerca sul Cancro, Genoa, Italy.

Rosalba Miceli (R)

Clinical Epidemiology and Trial Organization, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

Paolo Giovanni Casali (PG)

Department of Orthopedic Oncology, Istituto Ortopedico Rizzoli, Bologna, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, Milan, Italy.

Alessandro Gronchi (A)

Department of Surgery, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

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