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Heterogeneity of drug resistance in human breast and ovarian cancers
1Oncotech, Inc., Irvine, CA 92714, USA.
Purpose:
This study quantitates the extent of heterogeneity of drug resistance in breast and ovarian cancers. Identification of drug-specific resistance in tumors from multiple sites provides information necessary to understand the unique biology of a patient's disease.
Materials And Methods:
Drug resistance to cisplatin, paclitaxel, and doxorubicin was measured in multiple synchronous or metachronous tumors using the extreme drug resistance (EDR) assay. The degree of resistance for each tumor was classified into one of three categories: low drug resistance (LDR), EDR, or intermediate drug resistance (IDR).
Results:
When tested against cisplatin, 66% of primary ovarian cancers and their paired synchronous distant metastases (N = 88) shared the same resistance category, while 4% of the results were discordant (one site had EDR and the other site had LDR). Of the paired results for paclitaxel (N = 68), 54% were in the same resistance category, while 13% of the comparisons were discordant. Heterogeneity of drug response to cisplatin was also measured in primary ovarian cancers and paired recurrent tumors from 108 women. Median time to recurrence was 9.6 months. Only 55% of the paired results fell into the same resistance category, while 19% of the results were discordant. Drug resistance to doxorubicin was measured in primary breast cancers and paired synchronous metastases from 23 women: 74% of the paired results fell into the same resistance category, while 13% of the results were discordant. Metastatic sites had a slightly higher incidence of EDR than primary sites (26% and 17%, respectively). Heterogeneity of drug response to doxorubicin was then determined in primary breast cancers and paired recurrent tumors from 26 women with a median time to recurrence of 14.3 months. Only 52% of the paired results fell into the same resistance category, while 24% of the results were discordant.
Discussion:
Heterogeneity of drug resistance for ovarian and breast cancer is a serious clinical problem encountered in administering chemotherapy for overt metastatic or recurrent cancers. The first step in managing this problem is to recognize that heterogeneity of drug resistance exists. Drug resistance tests may then help the physician avoid administering certain chemotherapeutic agents when a patient's metastatic or recurrent tumor is found to be resistant to those agents.
Insights
Drug resistance varies significantly between tumor sites in breast and ovarian cancers, complicating chemotherapy. Understanding this drug resistance heterogeneity is crucial for effective cancer treatment.
Area of Science:
- Oncology
- Cancer Biology
- Pharmacology
Background:
- Drug resistance is a major challenge in treating advanced breast and ovarian cancers.
- Tumor heterogeneity can lead to differential responses to chemotherapy agents.
- Understanding resistance patterns is vital for personalized treatment strategies.
Purpose of the Study:
- To quantify the extent of drug resistance heterogeneity in breast and ovarian cancers.
- To identify drug-specific resistance patterns in tumors from multiple sites.
- To provide insights into the unique biology of individual patient diseases.
Main Methods:
- The extreme drug resistance (EDR) assay was used to measure resistance to cisplatin, paclitaxel, and doxorubicin.
- Resistance was assessed in multiple synchronous or metachronous tumors.
- Tumor resistance was classified into low drug resistance (LDR), EDR, or intermediate drug resistance (IDR) categories.
Main Results:
- Significant heterogeneity in drug resistance was observed for cisplatin, paclitaxel, and doxorubicin across different tumor sites and recurrence.
- Discordant resistance categories (e.g., EDR vs. LDR) were found in 4-24% of paired tumor samples.
- Metastatic sites showed a slightly higher incidence of extreme drug resistance (EDR) compared to primary sites.
Conclusions:
- Drug resistance heterogeneity is a significant clinical issue in managing metastatic and recurrent breast and ovarian cancers.
- Recognizing this heterogeneity is the first step toward optimizing chemotherapy administration.
- Drug resistance testing can guide physicians in selecting effective chemotherapeutic agents and avoiding resistant ones.
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