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Dacarbazine for Metastatic Soft Tissue and Bone Sarcoma

Ní féidir ach le húsáideoirí cláraithe ailt a aistriú
Logáil Isteach / Cláraigh
Sábháiltear an nasc chuig an gearrthaisce
StádasCríochnaithe
Urraitheoirí
Washington University School of Medicine

Keywords

Coimriú

The purpose of this study is to determine the overall best tumor response rate to dacarbazine given until disease progression as assessed by RECIST criteria, CT and clinical exams in patients with metastatic sarcomas.

Cur síos

The two reasons why dacarbazine was eliminated from treatment options for patients with metastatic sarcoma included inability to effectively address the drug's major toxicities (emesis and neutropenia) and the prevailing opinion that the drug was less effective than other chemotherapeutic agents.

Specific Aim #1: The primary endpoint of this study is to determine the overall best tumor anatomic response rate (CR- complete response, PR - partial response, SD - stable disease, or PD - progressive disease) to dacarbazine given until disease progression as assessed by RECIST criteria using CT and clinical examination in patients with metastatic sarcoma.

The prevailing opinion that dacarbazine was less effective than other chemotherapeutic agents in this setting was not based on data from controlled randomized clinical trials. Indeed, we are not aware of a single randomized trial that was conducted and reported which compared the anti-tumor activity of single agent dacarbazine to that of other active single agents in this patient population. However, phase two trials clearly established that dacarbazine had anti-tumor activity in the treatment of metastatic sarcoma, and our personal experience at this institution has confirmed that this is true. In addition, randomized trials demonstrated that the addition of dacarbazine to doxorubicin increased tumor response rates over doxorubicin alone.12 The literature supports the conclusion that dacarbazine has anti-tumor activity in the treatment of metastatic sarcoma.

Historically, in most studies, tumor response to dacarbazine was assessed by WHO criteria. However, current assessment of tumor response usually is based on RECIST criteria, which differ from the WHO criteria, as shown:

Studies have not been performed to determine the tumor anatomic response rate of single agent dacarbazine using RECIST criteria. This study will determine the tumor anatomic response rate as assessed by RECIST criteria to dacarbazine in patients with metastatic sarcoma. Modern methods of CT scans will be used to assess tumor response which contrasts with the earlier methods to assess tumor response to dacarbazine used in most of the published reports. These methods included physical examination and conventional X-ray or first generation, lower resolution CT scans. The current methods of radiologic assessment of tumor response are superior to those used over 15 years ago. The latest generation of CT scans more accurately measure and image a tumor mass, which may better assess tumor response to therapy.

Specific Aim #2: To determine the overall risk of nausea/emesis (any grade) and neutropenia (grade 3 or 4) with dacarbazine when given with current antiemetic agents (5-hydroxytryptamine-3 serotonin antagonist, dexamethasone, and aprepitant) and with pegfilgrastim.

Historically, dacarbazine-induced toxicities such as emesis and myelosuppression were common and led to significant dose reductions and delays which could have negatively impacted the drug's anti-tumor activity. When dacarbazine was initially identified as a potentially effective agent for the treatment of sarcoma, the anti-emetic drugs available had limited efficacy. Also, there were no measures available to prevent chemotherapy-induced neutropenia. Today, there are very effective drugs that can prevent and reduce the frequency of both chemotherapy-induced emesis and neutropenia.

Dacarbazine carries the risk of emesis (all grades) of >90% of cases when administered without antiemetics13. A three-drug anti-emetic combination of a 5-hydroxytryptamine-3 serotonin antagonist, dexamethasone, and aprepitant is the current recommendation from ASCO when administering highly emetogenic chemotherapy drugs13. Hesketh, et al reported that the risk of emesis (all grades) following highly emetogenic chemotherapy (cisplatin) and pre-medication with this three drug anti-emetic regimen was 27% compared to a two drug regimen of ondansetron and dexamethasone in which the risk was 48% (p< 0.001)14.

Prior studies showed that the risk of grade 3 or 4 neutropenia following dacarbazine given without granulocyte- colony stimulating factors was 36%15. Granulocyte- colony stimulating factors (pegfilgrastim or neupogen) are effective agents in preventing chemotherapy-induced neutropenia. Crawford, et al showed in a randomized trial that risk of chemotherapy- induced grade four neutropenia was one day with G-CSF compared to six days with placebo15. Subsequent randomized trials showed equivalent efficacy of pegfilgrastim compared with neupogen16. Vogel, et al reported in a phase three double blinded randomized trial of patients with breast cancer receiving docetaxel 100 mg/m2 that pegfilgrastim compared to placebo reduced the incidence of febrile neutropenia ( 1% vs 17%, p< 0.001) and febrile neutropenia-related hospitalization (1% vs 14%, p< 0.001)17.

In this trial, we hypothesize that the implementation of these newer anti-nausea agents (5-hydroxytryptamine-3 serotonin antagonist, dexamethasone, and aprepitant) and granulocyte-colony stimulating factor (pegfilgrastim) as a primary prophylactic strategy will reduce the frequency of dacarbazine-induced nausea/emesis (any grade) and neutropenia (grade 3 or 4).

Specific Aim #3: To compare the SUV at up to three target tumor sites and to determine the overall tumor metabolic response (complete metabolic response, partial metabolic response, stable metabolic disease or progressive metabolic disease (CMR, PMR, SMD, or PMD) as assessed by FDG-PET/CT performed at baseline and then after every three cycles of treatment with dacarbazine.

Studies have not been performed to determine the changes in FDG uptake by PET imaging following dacarbazine in patients with metastatic sarcoma. There is limited published data about changes in FDG uptake by PET imaging following other chemotherapy agents in patients with metastatic sarcoma. However, there is an emerging body of data showing the prognostic impact of early tumor response to targeted agents (imatinib or sunitinib) as assessed by FDG-PET in patients with metastatic GIST18. In this trial, we will determine the tumor metabolic response to dacarbazine as assessed by FDG-PET/CT and correlate this to the tumor anatomic response as assessed by CT scans.

Dátaí

Fíoraithe Deireanach: 11/30/2016
Cuireadh isteach den chéad uair: 12/03/2008
Clárú Measta Curtha isteach: 12/03/2008
Arna chur suas ar dtús: 12/04/2008
Nuashonrú Deireanach Curtha isteach: 12/19/2016
Nuashonrú Deireanach Postáilte: 02/12/2017
Dáta na gcéad torthaí a cuireadh isteach: 06/15/2016
Dáta na dtorthaí QC a cuireadh isteach den chéad uair: 12/19/2016
Dáta na gcéad torthaí a cuireadh sa phost: 02/12/2017
Dáta Tosaigh an Staidéir Iarbhír: 02/28/2009
Dáta Críochnaithe Bunscoile Measta: 12/31/2014
Dáta Críochnaithe an Staid Mheasta: 12/31/2014

Coinníoll nó galar

Sarcoma

Idirghabháil / cóireáil

Drug: Dacarbazine

Céim

Céim 2

Grúpaí Láimhe

LámhIdirghabháil / cóireáil
Experimental: Dacarbazine
Dacarbazine 850 mg/m^2 IV Day 1 of each 21 day cycle.
Drug: Dacarbazine

Critéir Incháilitheachta

Aois Incháilithe le haghaidh Staidéir 18 Years Chun 18 Years
Gnéas Incháilithe le haghaidh StaidéirAll
Glacann Oibrithe Deonacha SláintiúlaSea
Critéir

Inclusion Criteria:

- Histologically proven diagnosis of soft tissue or bone sarcoma

- Metastatic or locally recurrent and unresectable sarcoma which progressed after one or more prior chemotherapy regimens (excluding adjuvant chemotherapy).

- At least one measurable tumor lesion (by CT scan) At least one FDG avid (SUV ≥ 3) tumor lesion (by PET/CT) which must have been performed at this institution. At least one of these target lesions must be ≥ 1.5 cm in smallest dimension as measured on the baseline CT

- Age greater than 18 yrs old

- ECOG Performance Status of 0-2

- Baseline ANC ≥ 1000/uL, Hgb ≥ 8 Gr/dL, platelets ≥ 100,000/ dL.

- Baseline serum creatinine

- Baseline serum total bilirubin

- No active infection

- Signed Informed Consent by patient or legally authorized representative

Exclusion Criteria:

- Current pregnancy or breast feeding.

- A serious uncontrolled medical disorder that in the opinion of the Investigator would impair the ability of the subject to receive protocol therapy.

- Chemotherapy, radiation therapy, or investigational agents given with the last 21 days.

- Investigational agents given with the last 30 days

- Uncontrolled diabetes mellitus. (Subjects with a fasting blood glucose > 200 at time of PET scanning may need to reschedule to another day after consulting with appropriate physicians.)

Toradh

Bearta Toraidh Príomhúla

1. Best Anatomical Tumor Response [After completion of 3 cycles]

Complete response (CR): disappearance of all target lesions, disappearance of all non-target lesions, normalization of tumor level marker Partial response (PR): at least 30% decrease in the sum of the longest diameter (LD) of target lesions taking as reference the baseline sum LD, persistence of one or more non-target lesion and/or maintenance of tumor marker level above the upper limits of normal Stable disease (SD): neither sufficient shrinkage in target lesions to qualify for PR nor sufficient increase to qualify for progressive disease taking as references the smallest sum LD since the treatment started, persistence of one or more non-target lesion and/or maintenance of tumor marker level above the normal limits of normal Progressive disease (PD): at least 20% increase in the sum of the LD of target lesions and/or appearance of one or more new lesions and/or unequivocal progression of existing non-target lesions

Bearta Torthaí Tánaisteacha

1. Rate of Neutropenia (Grade 3/4) [Completion of 6 cycles of treatment (18 weeks)]

Grade 3 neutropenia = absolute neutrophil count of <1000 - 500/mm^3 Grade 4 neutropenia = absolute neutrophil count of <500/mm^3

2. Rate of Nausea/Emesis (Any Grade) [Completion of 6 cycles of treatment (18 weeks)]

Approximately 18 weeks

3. Comparison of the SUV at up to 3 Tumor Sites [Baseline and after every three cycles of treatment (up to 1 year)]

4. Overall Tumor Metabolic Response [After completion of 3 cycles]

Complete metabolic response (CMR)-complete resolution of all metabolically active target and non-target lesions, and no interval development of new lesions. Partial metabolic response (PMR) Target lesions: 20% or greater decrease in maximum SUV from baseline. No unequivocal metabolic progression of non-target disease, and no unequivocal new lesions. Non-target lesions: decrease in total number of non-target lesions, without complete resolution of metabolically active disease, or unequivocal decrease in degree of FDG activity within >50% of the lesions. No unequivocal new lesions. Stable metabolic disease (SMD): does not qualify for CMR, PMR, or PMD. Progressive metabolic disease (PMD): Unequivocal development of one more new metabolically active lesions Target lesion: 20% or greater increase in maximum SUV from baseline. Non-target lesions: unequivocal increase in FDG activity

5. Correlate the Tumor Metabolic Response Rate With the Tumor Anatomic Response Rate [After completion of 3 cycles]

6. Overall Disease Control Rate [12 months]

7. Time to Progression (TTP) [Until completion of follow-up (estimated to be 1 year)]

-Progression - At least a 20% increase in the sum of the longest diameter (LD) of target lesions taking as references the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions.

8. Overall Survival [Until completion of follow-up or patient death (estimated to be 1 year)]

9. Correlate the Time to Progression With Best Anatomic Response [Completion of follow-up (estimated to be 1 year)]

-Progression - At least a 20% increase in the sum of the longest diameter (LD) of target lesions taking as references the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions.

10. Correlate Time to Progression With Best Metabolic Response [Completion of follow-up (estimated to be 1 year)]

-Progression - At least a 20% increase in the sum of the longest diameter (LD) of target lesions taking as references the smallest sum LD recorded since the treatment started or the appearance of one or more new lesions.

11. Correlate Overall Survival With Best Anatomic Response [Completion of follow-up (estimated to be 1 year)]

12. Correlate Overall Survival With Best Metabolic Response [Completion of follow-up (estimated to be 1 year)]

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