Title

Inhalation SLIT Cisplatin (Liposomal) for the Treatment of Osteosarcoma Metastatic to the Lung
Phase Ib/IIa Study of SLIT Cisplatin by Inhalation in the Treatment of Patients Wtih Relapsed/Progressive Osteosarcoma Metastatic to the Lung
  • Phase

    Phase 1/Phase 2
  • Study Type

    Interventional
  • Intervention/Treatment

    cisplatin ...
  • Study Participants

    19
Phase Ib/IIa open label safety and efficacy study designed to determine the maximum tolerated dose of inhaled cisplatin liposomal (SLIT cisplatin) administered every 14 days to patients with relapsed/progressive osteosarcoma metastatic to the lung.
Study Started
Jan 12
2005
Primary Completion
Mar 31
2008
Study Completion
Mar 17
2008
Results Posted
Aug 01
2017
Last Update
Aug 01
2017

Drug Cisplatin liposomal

  • Other names: SLIT Cisplatin

Cisplatin liposomal 24 mg/m2 Experimental

Inhaled liposomal cisplatin was administered over 1 day in a 14-day treatment cycle by inhalation for a maximum of 6 cycles.

Cisplatin liposomal 36 mg/m2 Experimental

The study allowed for a dose escalation of liposomal cisplatin to 36 mg/m2 if no adverse events of Grade 3 or higher occurred after at least 3 cycles of drug administration at 24 mg/m2

Criteria

Inclusion Criteria:

Histologically proven, Progressive or recurrent high grade osteosarcoma metastatic to the lung
Patients with histologically proven, fully malignant high-grade osteosarcoma of bone
Measureable pulmonary metastases
Less than grade 3 neuropathies, insignificant decreases in cardiac or auditory function
ECOG performance status of 0, 1 or 2
FEV1 of 50% or greater of predicted value
FEV1/FVC ratio of 65% or greater
Serum creatinine of ≤ 1.5 mg/dl
Total bilirubin ≤ 1.5mg/dl and SGOT or SGPT < 2.5 times upper normal limit
ANC of ≥ 1,000/mm3 and platelet count of ≥ 100,000/mm3

Exclusion Criteria:

Grade 3 or higher painful neuropathy persisting after a prior platinum containing regimen
Patients who are pregnant or are of childbearing potential and not using methods to avoid pregnancy
Concurrent systemic chemotherapy
Greater than Grade 2 pulmonary toxicity
Pulmonary atelectasis
Reactive airway disease which has resulted in hospitalization within the last year or which requires daily treatment with bronchodilator therapy
Concurrent serious infections
Unstable or serious concurrent medical condition
Recent major surgery or thoracic radiation therapy or chemotherapy
Significant pulmonary fibrosis secondary to prior radiation
Major ventilatory distribution abnormalities
Osteosarcoma secondary to radiation or premalignant conditions
History of prior malignancy
Low grade osteosarcoma, parosteal or periosteal sarcoma

Summary

Cisplatin Liposomal 24 mg/m2

Cisplatin Liposomal 36 mg/m2

All Events

Event Type Organ System Event Term Cisplatin Liposomal 24 mg/m2 Cisplatin Liposomal 36 mg/m2

The Study Medication Was to be Considered Effective if the Population Response Rate Was Found to be Greater Than 20% and Individuals Who Demonstrated a CR or PR or Whose Tumours Demonstrated a Grade 3 or 4 Histologic Response at the Time of Surgery.

Cisplatin Liposomal 24 mg/m2

CR/PR

2.0
participants

Histological response

1.0
participants

Cisplatin Liposomal 36 mg/m2

CR/PR

2.0
participants

Histological response

1.0
participants

Total

19
Participants

Age, Continuous

18.2
years (Mean)
Standard Deviation: 3.4

Race (NIH/OMB)

Region of Enrollment

Sex: Female, Male

Overall Study

Cisplatin Liposomal 24 mg/m2

Cisplatin Liposomal 36 mg/m2

Drop/Withdrawal Reasons

Cisplatin Liposomal 24 mg/m2

Cisplatin Liposomal 36 mg/m2