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Original Research| Volume 109, P51-60, March 2019

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The impact of chemotherapy on survival of patients with extremity and trunk wall soft tissue sarcoma: revisiting the results of the EORTC-STBSG 62931 randomised trial

Published:January 25, 2019DOI:https://doi.org/10.1016/j.ejca.2018.12.009

      Highlights

      • The EORTC 62931 failed to detect an OS benefit for adjuvant chemotherapy in soft tissue sarcoma (STS).
      • The prognostic tool Sarculator was used to stratify prognosis of enrolled patients.
      • Sixty percent of patients were at low risk and did not benefit from adjuvant chemotherapy.
      • Adjuvant chemotherapy halved the risk of death in high-risk participants.
      • This analysis explains conflicting results on adjuvant chemotherapy for STS.

      Abstract

      Background

      This study was aimed at determining whether patients with high-risk soft tissue sarcoma (STS), as identified using the nomogram Sarculator, benefitted from adjuvant chemotherapy in the EORTC-STBSG 62931 randomised controlled trial (RCT), which failed to detect an impact for adjuvant doxorubicin plus ifosfamide (Adj) over observation (Obs).

      Methods

      Patients with extremity and trunk wall STS in the EORTC-STBSG 62931 RCT were analysed (N = 290/351). Ten-year predicted probability of overall survival (pr-OS) was calculated using the prognostic nomogram Sarculator. Patients were grouped into three categories of predicted pr-OS: high (pr-OS>66%), intermediate (51<pr-OS≤66) and low (pr-OS≤51%). OS and disease-free survival (DFS) were calculated.

      Results

      Nomogram pr-OS was dispersed (median 72%, interquartile range 57–83%) and had prognostic value for OS and DFS (log-rank test: P < 0.001). One hundred seventy, 68 and 52 patients had high (58.6%, 90 Obs/80 Adj), intermediate (23.5%, 34 Obs/34 Adj) and low pr-OS (17.9%, 24 Obs/28 Adj), respectively. Adjuvant chemotherapy halved the risk of recurrence (hazard ratio [HR] = 0.46, 95% confidence interval [CI] 0.24–0.89) and death (HR = 0.46, 95% CI 0.23–0.94) in the low pr-OS category, while no effect was detected in intermediate and high pr-OS categories. To strengthen these findings, study participants with pr-OS<60% were combined (N = 80, 27.6%, 39 Obs/41 Adj), and a significant DFS (HR = 0.49, 95% CI 0.28–0.85) and OS (HR = 0.50, 95% CI 0.30–0.90) benefit was detected.

      Conclusion

      Patients of the EORTC-STBSG 62931 RCT with extremity and trunk wall STS and a low predicted pr-OS (high-risk patients) had better outcomes when treated with adjuvant chemotherapy. This may help reconcile the disparate results of clinical studies on adjuvant/neoadjuvant chemotherapy in STS.

      Keywords

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      References

        • Gronchi A.
        • Maki R.G.
        • Jones R.L.
        Treatment of soft tissue sarcoma: a focus on earlier stages.
        Future Oncol. 2017; 13: 13-21
        • Loong H.H.
        • Wong K.H.
        • Tse T.
        Controversies and consensus of neoadjuvant chemotherapy in soft-tissue sarcomas.
        ESMO Open. 2018; 3: e000293
      1. Adjuvant chemotherapy for localised resectable soft-tissue sarcoma of adults: meta-analysis of individual data. Sarcoma Meta-analysis Collaboration.
        Lancet. 1997; 350: 1647-1654
      2. Adjuvant chemotherapy for localised resectable soft tissue sarcoma in adults. Sarcoma Meta-analysis Collaboration (SMAC).
        Cochrane Database Syst Rev. 2000; : CD001419
        • Pervaiz N.
        • Colterjohn N.
        • Farrokhyar F.
        • Tozer R.
        • Figueredo A.
        • Ghert M.
        A systematic meta-analysis of randomized controlled trials of adjuvant chemotherapy for localized resectable soft-tissue sarcoma.
        Cancer. 2008; 113: 573-581
        • Benjamin R.S.
        Adjuvant and neoadjuvant chemotherapy for soft tissue sarcomas: a personal point of view.
        Tumori. 2017; 103: 213-216
        • van der Graaf W.T.A.
        • Jones R.L.
        Neoadjuvant chemotherapy in localised soft-tissue sarcomas: where do we go from here?.
        Lancet Oncol. 2017; 18: 706-707
        • Nathenson M.J.
        • Sausville E.
        Looking for answers: the current status of neoadjuvant treatment in localized soft tissue sarcomas.
        Cancer Chemother Pharmacol. 2016; 78: 895-919
        • Canter R.J.
        Chemotherapy: does neoadjuvant or adjuvant therapy improve outcomes?.
        Surg Oncol Clin N Am. 2016; 25: 861-872
        • Rothermundt C.
        • Fischer G.F.
        • Bauer S.
        • Blay J.Y.
        • Grunwald V.
        • Italiano A.
        • et al.
        Pre- and postoperative chemotherapy in localized extremity soft tissue sarcoma: a European organization for Research and treatment of cancer expert survey.
        Oncol. 2018; 23: 461-467
        • Sherman K.L.
        • Wayne J.D.
        • Chung J.
        • Agulnik M.
        • Attar S.
        • Hayes J.P.
        • et al.
        Assessment of multimodality therapy use for extremity sarcoma in the United States.
        J Surg Oncol. 2014; 109: 395-404
        • George S.
        • Wagner A.J.
        Low levels of evidence for neoadjuvant chemotherapy to treat soft-tissue sarcoma.
        JAMA Oncol. 2018; 4: 1169-1170
        • Gronchi A.
        • Jones R.L.
        The value of neoadjuvant chemotherapy in localized high-risk soft-tissue sarcoma of the extremities and trunk.
        JAMA Oncol. 2018; 4: 1167-1168
        • Woll P.J.
        • Reichardt P.
        • Le Cesne A.
        • Bonvalot S.
        • Azzarelli A.
        • Hoekstra H.J.
        • et al.
        Adjuvant chemotherapy with doxorubicin, ifosfamide, and lenograstim for resected soft-tissue sarcoma (EORTC 62931): a multicentre randomised controlled trial.
        Lancet Oncol. 2012; 13: 1045-1054
        • Le Cesne A.
        • Ouali M.
        • Leahy M.G.
        • Santoro A.
        • Hoekstra H.J.
        • Hohenberger P.
        • et al.
        Doxorubicin-based adjuvant chemotherapy in soft tissue sarcoma: pooled analysis of two STBSG-EORTC phase III clinical trials.
        Ann Oncol. 2014; 25: 2425-2432
        • von Mehren M.
        • Randall R.L.
        • Benjamin R.S.
        • Boles S.
        • Bui M.M.
        • Ganjoo K.N.
        • et al.
        Soft tissue sarcoma, version 2.2018, NCCN clinical practice guidelines in oncology.
        J Natl Compr Canc Netw. 2018; 16: 536-563
        • Casali P.G.
        • Abecassis N.
        • Bauer S.
        • Biagini R.
        • Bielack S.
        • Bonvalot S.
        • et al.
        Soft tissue and visceral sarcomas: ESMO-EURACAN Clinical Practice Guidelines for diagnosis, treatment and follow-up.
        Ann Oncol. 2018; 29: iv268-iv269
        • Gronchi A.
        • Ferrari S.
        • Quagliuolo V.
        • Martin Broto J.
        • Lopez-Pousa A.
        • Grignani G.
        • et al.
        Neoadjuvant chemotherapy in high-risk soft tissue sarcomas: a randomised clinical trial from the Italian sarcoma group, the Spanish sarcoma group (GEIS), the Italian French group (FSG) and the the polish sarcoma group (PSG).
        Lancet Oncol. 2017; 18: 812-822
        • Callegaro D.
        • Miceli R.
        • Bonvalot S.
        • Ferguson P.
        • Strauss D.C.
        • Levy A.
        • et al.
        Development and external validation of two nomograms to predict overall survival and occurrence of distant metastases in adults after surgical resection of localised soft-tissue sarcomas of the extremities: a retrospective analysis.
        Lancet Oncol. 2016; 17: 671-680
        • Callegaro D.
        • Miceli R.
        • Mariani L.
        • Raut C.P.
        • Gronchi A.
        Soft tissue sarcoma nomograms and their incorporation into practice.
        Cancer. 2017; 123: 2802-2820
        • Smith H.G.
        • Memos N.
        • Thomas J.M.
        • Smith M.J.
        • Strauss D.C.
        • Hayes A.J.
        Patterns of disease relapse in primary extremity soft-tissue sarcoma.
        Br J Surg. 2016; 103: 1487-1496
        • Amin M.B.
        • Edge S.
        • Greene F.
        • Byrd D.R.
        • Brookland R.K.
        • Washington M.K.
        • et al.
        AJCC cancer staging manual.
        Springer, 2017
        • Gronchi A.
        • Frustaci S.
        • Mercuri M.
        • Martin J.
        • Lopez-Pousa A.
        • Verderio P.
        • et al.
        Short, full-dose adjuvant chemotherapy in high-risk adult soft tissue sarcomas: a randomized clinical trial from the Italian Sarcoma Group and the Spanish Sarcoma Group.
        J Clin Oncol. 2012; 30: 850-856
        • Gronchi A.
        • Stacchiotti S.
        • Verderio P.
        • Ferrari S.
        • Martin Broto J.
        • Lopez-Pousa A.
        • et al.
        Short, full-dose adjuvant chemotherapy (CT) in high-risk adult soft tissue sarcomas (STS): long-term follow-up of a randomized clinical trial from the Italian Sarcoma Group and the Spanish Sarcoma Group.
        Ann Oncol. 2016; 27: 2283-2288
        • Pasquali S.
        • Colombo C.
        • Pizzamiglio S.
        • Verderio P.
        • Callegaro D.
        • Stacchiotti S.
        • et al.
        High-risk soft tissue sarcomas treated with perioperative chemotherapy: improving prognostic classification in a randomised clinical trial.
        Eur J Cancer. 2018; 93: 28-36
        • Kaplan E.L.
        • Meier P.
        Nonparametric estimation from incomplete observations.
        J Am Stat Assoc. 1958; 53: 457-481
        • Cox R.D.
        Regression models and life tables.
        J Roy Stat Soc B. 1972; 34: 187-220
        • Altman D.G.
        • Andersen P.K.
        Calculating the number needed to treat for trials where the outcome is time to an event.
        BMJ. 1999; 319: 1492-1495
        • Sundby Hall K.
        • Bruland O.S.
        • Bjerkehagen B.
        • Zaikova O.
        • Engellau J.
        • Hagberg O.
        • et al.
        Adjuvant chemotherapy and postoperative radiotherapy in high-risk soft tissue sarcoma patients defined by biological risk factors-A Scandinavian Sarcoma Group study (SSG XX).
        Eur J Cancer. 2018; 99: 78-85
        • Issels R.D.
        • Lindner L.H.
        • Verweij J.
        • Wessalowski R.
        • Reichardt P.
        • Wust P.
        • et al.
        Effect of neoadjuvant chemotherapy plus regional hyperthermia on long-term outcomes among patients with localized high-risk soft tissue sarcoma: the EORTC 62961-ESHO 95 randomized clinical trial.
        JAMA Oncol. 2018; 4: 483-492
        • Issels R.D.
        • Lindner L.H.
        • Verweij J.
        • Wust P.
        • Reichardt P.
        • Schem B.C.
        • et al.
        Neo-adjuvant chemotherapy alone or with regional hyperthermia for localised high-risk soft-tissue sarcoma: a randomised phase 3 multicentre study.
        Lancet Oncol. 2010; 11: 561-570
        • Angele M.K.
        • Albertsmeier M.
        • Prix N.J.
        • Hohenberger P.
        • Abdel-Rahman S.
        • Dieterle N.
        • et al.
        Effectiveness of regional hyperthermia with chemotherapy for high-risk retroperitoneal and abdominal soft-tissue sarcoma after complete surgical resection: a subgroup analysis of a randomized phase-III multicenter study.
        Ann Surg. 2014; 260 (discussion 754-6): 749-754
        • Le Guellec S.
        • Lesluyes T.
        • Sarot E.
        • Valle C.
        • Filleron T.
        • Rochaix P.
        • et al.
        Validation of the Complexity INdex in SARComas prognostic signature on formalin-fixed, paraffin-embedded, soft tissue sarcomas.
        Ann Oncol. 2018; 29: 1828-1835
        • Chibon F.
        • Lagarde P.
        • Salas S.
        • Perot G.
        • Brouste V.
        • Tirode F.
        • et al.
        Validated prediction of clinical outcome in sarcomas and multiple types of cancer on the basis of a gene expression signature related to genome complexity.
        Nat Med. 2010; 16: 781-787
        • Bertucci F.
        • De Nonneville A.
        • Finetti P.
        • Perrot D.
        • Nilbert M.
        • Italiano A.
        • et al.
        The Genomic Grade Index predicts postoperative clinical outcome in patients with soft-tissue sarcoma.
        Ann Oncol. 2018; 29: 459-465