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Clinical Trials/JPRN-C000000084
JPRN-C000000084
Completed
Phase 2

Second line chemotherapy consisting of weekly irinotecan and cisplatin for relapsed/first line resistant non-small cell lung carcinoma - phase II study - Second line chemotherapy consisting of weekly irinotecan and cisplatin for relapsed/first line resistant non-small cell lung carcinoma - phase II study

Chiba Lung Cancer Study Group0 sites48 target enrollmentSeptember 1, 2005

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
on-small-cell lung carcinoma
Sponsor
Chiba Lung Cancer Study Group
Enrollment
48
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

Even with the standard first-line chemotherapy, advanced non-small cell lung cancer (NSCLC) recurs in most cases. The purpose of this study is to develop a new chemotherapeutic regimen for patients with NSCLC that has relapsed or was refractory to previous chemotherapy. Patients with proven NSCLC refractory or recurrent after previous single-regimen chemotherapy, PS of 0 to 2, age of 15 years or older, adequate organ functions and measurable lesions were treated with irinotecan at 60 mg/m2 and cisplatin at 25 mg/m2 with 1,000 ml hydration on day 1. This administration, considered as one cycle, was repeated every week without rest unless encountering defined skip and dose-reduction criteria. The treatment was administered for 6 cycles over a 49-day period, both median values, to 48 patients, with a response rate of 26%, progression free and median survival times of 3 and 11 months, respectively, and a 1-year survival rate of 46%. The most frequent grade 3 or 4 toxicities were neutropenia, anaemia and nausea, which were manageable. Subset analyses suggested that the response rate was independent of response to the first-line chemotherapy. In conclusion, second-line chemotherapy of weekly irinotecan and cisplatin with minimum hydration seemed effective, with tolerable toxicity, and is potentially useful irrespective of the outcome of previous chemotherapy.

Registry
who.int
Start Date
September 1, 2005
End Date
December 1, 2006
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Chiba Lung Cancer Study Group

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Prior chemotherapy including irinotecan 2\) Prior chemotherapy by 2 or more chemotherapeutic regimens 3\) Prior resection 4\) Requirement of thoracic irradiation 5\) Any contraindication for irinotecan, such as interstitial pneumonitis 6\) Pleural effusion/ascites requiring treatment 7\) Pericardial effusion 8\) Serious concomitant medical conditions, including uncontrolled diabetes mellitus, angina pectoris, myocardial infarction within 3 months, and others 9\) Brain metastasis requiring treatment 10\) Concomitant malignancy 11\) History of serious drug allergy 12\) Pregnancy, potential pregnancy, or breast feeding 13\) Others

Outcomes

Primary Outcomes

Not specified

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