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DOI 10.1002/cncr.33895

Медицинская библиотека · Cancer · 2021

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

Pasquali Sandro, Palmerini Emanuela, Quagliuolo Vittorio, Martin-Broto Javier, Lopez-Pousa Antonio, Grignani Giovanni, Brunello Antonella, Blay Jean-Yves, Tendero Oscar, Diaz-Beveridge Robert, Ferraresi Virginia, Lugowska Iwona, Infante Gabriele, Braglia Luca, Merlo Domenico Franco, Fontana Valeria, Marchesi Emanuela, Donati Davide Maria, Palassini Elena, Bianchi Giuseppe, Marrari Andrea, Morosi Carlo, Stacchiotti Silvia, Bagué Silvia, Coindre Jean Michel, Dei Tos Angelo Paolo, Picci Piero, Bruzzi Paolo, Miceli Rosalba, Casali Paolo Giovanni, Gronchi Alessandro

СтатьяРандомизированное исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

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

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

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

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: 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.

Для цитирования: Pasquali Sandro, Palmerini Emanuela, Quagliuolo Vittorio, Martin-Broto Javier, Lopez-Pousa Antonio, Grignani Giovanni, Brunello Antonella, Blay Jean-Yves, Tendero Oscar, Diaz-Beveridge Robert, Ferraresi Virginia, Lugowska Iwona, Infante Gabriele, Braglia Luca, Merlo Domenico Franco, Fontana Valeria, Marchesi Emanuela, Donati Davide Maria, Palassini Elena, Bianchi Giuseppe, Marrari Andrea, Morosi Carlo, Stacchiotti Silvia, Bagué Silvia, Coindre Jean Michel, Dei Tos Angelo Paolo, Picci Piero, Bruzzi Paolo, Miceli Rosalba, Casali Paolo Giovanni, Gronchi Alessandro. Neoadjuvant chemotherapy in high-risk soft tissue sarcomas: A Sarculator-based risk stratification analysis of the ISG-STS 1001 randomized trial.. Cancer. 2021. DOI: 10.1002/cncr.33895.

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