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The 16-year experience in treating low-risk gestational trophoblastic neoplasia patients with failed primary
Xiaodong Wu1, Jiale Qin2,3, Tao Shen1
1Department of Gynecologic Oncology, Women's Hospital, School of Medicine Zhejiang University, Hangzhou, China.
Objective:
To assess the outcomes and toxic effects of 5-day actinomycin D (Act-D) salvage therapy and to explore the predictors of Act-D resistance in patients with low-risk gestational trophoblastic neoplasia (GTN)who failed 5-day methotrexate (MTX) chemotherapy.
Methods:
This retrospective study analyzed patients with low-risk GTN administered Act-D salvage therapy after failing MTX chemotherapy at Women's Hospital, School of Medicine Zhejiang University between January 2000 and December 2015. The clinical parameters of these patients were collected and analyzed.
Results:
The final analysis included 89 cases. Of these, 73 cases (82.02%) responded to salvage Act-D. The remaining 16 resistant cases were switched to etoposide, MTX, Act-D/cyclophosphamide, and vincristine chemotherapy and achieved complete remission. Serum human chorionic gonadotrophin levels before Act-D salvage therapy (hCGAct-D)in the Act-D-resistant cases were significantly higher than those in the Act-D responders (median 605 vs. 103 IU/L, p=0.009). However, the range of hCGAct-D values in Act-D responders was wider than that in Act-D-resistant cases (5.76-16,664 IU/L vs. 11.43-6,732 IU/L). Thus, assigning a general cut-off value was difficult considering the individual setting. Except for 2 cases requiring other salvage regimens due to Act-D toxicity, 97.80% of cases (89/91) tolerated the toxicity. During at least 1-year follow-up, the survival rate was 100.00% and no case developed recurrence.
Conclusion:
Based on the good therapeutic effect and tolerable toxicity, we recommend Act-D salvage therapy for all patients with low-risk GTN who fail primary MTX chemotherapy. The higher serum hCG levels before Act-D salvage therapy may be associated with resistance to this treatment.
Insights
Actinomycin D (Act-D) is effective salvage therapy for low-risk gestational trophoblastic neoplasia (GTN) after methotrexate (MTX) failure. Higher hCG levels before Act-D may predict resistance, but toxicity is generally well-tolerated.
Area of Science:
- Gynecology
- Oncology
- Pharmacology
Background:
- Low-risk gestational trophoblastic neoplasia (GTN) can be challenging to treat.
- Methotrexate (MTX) chemotherapy is a primary treatment for low-risk GTN.
- Some patients with low-risk GTN fail to respond to initial MTX chemotherapy.
Purpose of the Study:
- To evaluate the efficacy and toxicity of 5-day actinomycin D (Act-D) as salvage therapy for low-risk GTN.
- To identify predictors of resistance to Act-D in patients with low-risk GTN who previously failed MTX therapy.
Main Methods:
- Retrospective analysis of 89 patients with low-risk GTN treated with Act-D salvage therapy after MTX failure.
- Data collected included clinical parameters and treatment outcomes.
- Serum human chorionic gonadotrophin (hCG) levels before Act-D salvage therapy were analyzed.
Main Results:
- Act-D salvage therapy achieved an 82.02% response rate in 89 patients.
- Act-D resistant cases (16/89) achieved remission with alternative chemotherapy regimens.
- Higher pre-Act-D hCG levels were associated with Act-D resistance (p=0.009).
- Act-D toxicity was generally well-tolerated, with a 100% survival rate and no recurrence at 1-year follow-up.
Conclusions:
- Actinomycin D (Act-D) salvage therapy is recommended for low-risk GTN patients who fail methotrexate (MTX) chemotherapy due to its good efficacy and tolerable toxicity.
- Elevated serum hCG levels prior to Act-D treatment may indicate a higher risk of resistance to this salvage regimen.
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