topotecan injection Clinical Studies

()

14 CLINICAL STUDIES

14.1 Small Cell Lung Cancer

The efficacy of topotecan was studied in 426 patients with recurrent or progressive SCLC in a randomized, comparative trial and in 3 single-arm trials.

Randomized Comparative Trial

In a randomized, comparative trial, 211 patients were randomized 1:1 to received topotecan (1.5 mg/m2 once daily intravenously for 5 days starting on Day 1 of a 21-day cycle) or CAV (cyclophosphamide 1,000 mg/m2, doxorubicin 45 mg/m2, vincristine 2 mg administered sequentially on Day 1 of a 21-day cycle). All patients were considered sensitive to first-line chemotherapy (responders who then subsequently progressed greater than or equal to 60 days after completion of first-line therapy). A total of 77% of patients treated with topotecan and 79% of patients treated with CAV received platinum/etoposide with or without other agents as first-line chemotherapy. The efficacy outcome measures were overall response rate, response duration, time to progression and overall survival (OS).

The results of the trial did not show statistically significant improvements in response rates, response duration, time to progression, and OS as shown in Table 2.

Table 2. Efficacy Results in Patients with Small Cell Lung Cancer Sensitive to First-Line Chemotherapy in Study 090
ParameterTopotecan
(n = 107)
CAV*
(n = 104)
Abbreviations: CI = confidence interval.
*
CAV = cyclophosphamide, doxorubicin and vincristine.
The calculation for duration of response was based on the interval between first response and time to progression.
Overall response rate (95% CI)24% (16% to 32%)18% (11% to 26%)
  Complete response rate0%1%
  Partial response rate24%17%
Response duration (months)
  Median (95% CI)3.3 (3.0 to 4.1)3.5 (3.0 to 5.3)
Time to progression (months)
  Median (95% CI)3.1 (2.6 to 4.1)2.8 (2.5 to 3.2)
  Hazard ratio (95% CI)0.92 (0.69 to 1.22)
Overall survival (months)
  Median (95% CI)5.8 (4.7 to 6.8)5.7 (5.0 to 7.0)
  Hazard ratio (95% CI)1.04 (0.78 to 1.39)

The median time to response was similar in both arms: topotecan 6 weeks (2.4 weeks to 3.6 months) versus CAV 6 weeks (5.1 weeks to 4.2 months).

Changes on a disease-related symptom scale are presented in Table 3. It should be noted that not all patients had all symptoms, nor did all patients respond to all questions. Each symptom was rated on a 4-category scale with an improvement defined as a change in 1 category from baseline sustained over 2 cycles. Limitations in interpretation of the rating scale and responses preclude formal statistical analysis.

Table 3. Symptom Improvement* in Patients with Small Cell Lung Cancer in Study 090
SymptomTopotecan
(n = 107)
CAV
(n = 104)
n%n%
*
Defined as improvement sustained over at least 2 cycles compared with baseline.
CAV = cyclophosphamide, doxorubicin and vincristine.
Number of patients with baseline and at least 1 post-baseline assessment.
Shortness of breath6828617
Interference with daily activity67276311
Fatigue7023659
Hoarseness40333813
Cough69256115
Insomnia57335319
Anorexia56325716
Chest pain44254117
Hemoptysis15271233

Single-Arm Trials

Topotecan was also studied in 3 open-label, non-comparative trials (Studies 014, 092 and 053) in a total of 319 patients with recurrent or progressive SCLC after treatment with first-line chemotherapy. In all 3 trials, patients were stratified as either sensitive (responders who then subsequently progressed greater than or equal to 90 days after completion of first-line therapy) or refractory (no response to first-line chemotherapy or who responded to first-line therapy and then progressed within 90 days of completing first-line therapy). Response rates ranged from 11% to 31% for sensitive patients and 2% to 7% for refractory patients. Median time to progression and median survival were similar in all 3 trials and the comparative trial.

Find topotecan injection medical information:

Find topotecan injection medical information:

Our scientific content is evidence-based, scientifically balanced and non-promotional. It undergoes rigorous internal medical review and is updated regularly to reflect new information.

topotecan injection Quick Finder

Prescribing Information
Download Prescribing Information

Health Professional Information

Clinical Studies

14 CLINICAL STUDIES

14.1 Small Cell Lung Cancer

The efficacy of topotecan was studied in 426 patients with recurrent or progressive SCLC in a randomized, comparative trial and in 3 single-arm trials.

Randomized Comparative Trial

In a randomized, comparative trial, 211 patients were randomized 1:1 to received topotecan (1.5 mg/m2 once daily intravenously for 5 days starting on Day 1 of a 21-day cycle) or CAV (cyclophosphamide 1,000 mg/m2, doxorubicin 45 mg/m2, vincristine 2 mg administered sequentially on Day 1 of a 21-day cycle). All patients were considered sensitive to first-line chemotherapy (responders who then subsequently progressed greater than or equal to 60 days after completion of first-line therapy). A total of 77% of patients treated with topotecan and 79% of patients treated with CAV received platinum/etoposide with or without other agents as first-line chemotherapy. The efficacy outcome measures were overall response rate, response duration, time to progression and overall survival (OS).

The results of the trial did not show statistically significant improvements in response rates, response duration, time to progression, and OS as shown in Table 2.

Table 2. Efficacy Results in Patients with Small Cell Lung Cancer Sensitive to First-Line Chemotherapy in Study 090
ParameterTopotecan
(n = 107)
CAV*
(n = 104)
Abbreviations: CI = confidence interval.
*
CAV = cyclophosphamide, doxorubicin and vincristine.
The calculation for duration of response was based on the interval between first response and time to progression.
Overall response rate (95% CI)24% (16% to 32%)18% (11% to 26%)
  Complete response rate0%1%
  Partial response rate24%17%
Response duration (months)
  Median (95% CI)3.3 (3.0 to 4.1)3.5 (3.0 to 5.3)
Time to progression (months)
  Median (95% CI)3.1 (2.6 to 4.1)2.8 (2.5 to 3.2)
  Hazard ratio (95% CI)0.92 (0.69 to 1.22)
Overall survival (months)
  Median (95% CI)5.8 (4.7 to 6.8)5.7 (5.0 to 7.0)
  Hazard ratio (95% CI)1.04 (0.78 to 1.39)

The median time to response was similar in both arms: topotecan 6 weeks (2.4 weeks to 3.6 months) versus CAV 6 weeks (5.1 weeks to 4.2 months).

Changes on a disease-related symptom scale are presented in Table 3. It should be noted that not all patients had all symptoms, nor did all patients respond to all questions. Each symptom was rated on a 4-category scale with an improvement defined as a change in 1 category from baseline sustained over 2 cycles. Limitations in interpretation of the rating scale and responses preclude formal statistical analysis.

Table 3. Symptom Improvement* in Patients with Small Cell Lung Cancer in Study 090
SymptomTopotecan
(n = 107)
CAV
(n = 104)
n%n%
*
Defined as improvement sustained over at least 2 cycles compared with baseline.
CAV = cyclophosphamide, doxorubicin and vincristine.
Number of patients with baseline and at least 1 post-baseline assessment.
Shortness of breath6828617
Interference with daily activity67276311
Fatigue7023659
Hoarseness40333813
Cough69256115
Insomnia57335319
Anorexia56325716
Chest pain44254117
Hemoptysis15271233

Single-Arm Trials

Topotecan was also studied in 3 open-label, non-comparative trials (Studies 014, 092 and 053) in a total of 319 patients with recurrent or progressive SCLC after treatment with first-line chemotherapy. In all 3 trials, patients were stratified as either sensitive (responders who then subsequently progressed greater than or equal to 90 days after completion of first-line therapy) or refractory (no response to first-line chemotherapy or who responded to first-line therapy and then progressed within 90 days of completing first-line therapy). Response rates ranged from 11% to 31% for sensitive patients and 2% to 7% for refractory patients. Median time to progression and median survival were similar in all 3 trials and the comparative trial.

Medication Guide

Health Professional Information

{{section_name_patient}}

{{section_body_html_patient}}

Resources

Didn’t find what you were looking for? Contact us.

MI Digital Assistant

Chat online with Pfizer Medical Information regarding your inquiry on a Pfizer medicine.

Call 800-438-1985*

*Speak with a Pfizer Medical Information Professional regarding your medical inquiry. Available 9AM-5PM ET Monday to Friday; excluding holidays.

Medical Inquiry

Submit a medical question for Pfizer prescription products.

Report Adverse Event

Pfizer Safety

To report an adverse event related to the Pfizer-BioNTech COVID-19 Vaccine, and you are not part of a clinical trial* for this product, click the link below to submit your information:

Pfizer Safety Reporting Site

*If you are involved in a clinical trial for this product, adverse events should be reported to your coordinating study site.

If you cannot use the above website, or would like to report an adverse event related to a different Pfizer product, please call Pfizer Safety at (800) 438-1985.

FDA Medwatch

You may also contact the U.S. Food and Drug Administration (FDA) directly to report adverse events or product quality concerns either online at www.fda.gov/medwatch or call (800) 822-7967.