2017
DOI: 10.1016/s1470-2045(17)30672-1
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GeDDiS: insight into frontline therapy in soft tissue sarcoma

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Cited by 4 publications
(3 citation statements)
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“…The authors concluded that the combination should not be recommended as routine in the first‐line setting for patients with advanced soft‐tissue sarcoma. This conclusion has however been challenged, as some oncologists believe that the combination of gemcitabine‐docetaxel could be used in the first line setting on a histology‐ driven basis …”
Section: Leiomyosarcomamentioning
confidence: 99%
“…The authors concluded that the combination should not be recommended as routine in the first‐line setting for patients with advanced soft‐tissue sarcoma. This conclusion has however been challenged, as some oncologists believe that the combination of gemcitabine‐docetaxel could be used in the first line setting on a histology‐ driven basis …”
Section: Leiomyosarcomamentioning
confidence: 99%
“…On the other hand, standard first-line chemotherapy for disseminated or unresectable disease generally involves palliative systemic chemotherapy regimens with poor prognosis with a median overall survival (OS) of ∼12 months [ 10 ]. The most active first-line chemotherapy for advanced or recurrent disease has not changed for the last ∼30 years and remains doxorubicin with or without ifosfamide [ 11 ] and other nonapproved active but more toxic treatments such as gemcitabine alone or in combination with docetaxel [ 12 , 13 , 14 ]. A variety of newer cytotoxic agents, including trabectedin, pazopanib, and olaratumab, have already been approved by the US Food and Drug Administration (FDA), whilst others such as targeted therapies, aromatase inhibitors, and immunotherapies have demonstrated very modest activity in uLMS and are still under active investigation.…”
Section: Introductionmentioning
confidence: 99%
“…While no survival or progression-free survival differences were found between the groups, patients who received gemcitabine + docetaxel experienced more dose modifications and treatment discontinuation due to toxicity, as well as lower quality of life scores. While the GeDDiS trial did not report a statistically significant difference in progression-free survival between the treatment arms, some physicians may have interpreted this as meaning gemcitabine + docetaxel was still a viable treatment option [22].…”
Section: Sarcomamentioning
confidence: 98%