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Related Concept Videos

Treatment Resistant Cancers02:56

Treatment Resistant Cancers

Cancer is the second leading cause of death in the United States. A cancer cell is genetically unstable and hence can mutate faster. They can also modify their microenvironment and escape immune surveillance. The difficulties in treating cancer are further compounded by the emergence of rapid resistance to anticancer drugs. The most common ways to attain resistance in cancer cells include alteration in drug transport and metabolism, modification of drug target, elevated DNA damage response, or...
Drug Administration and Therapy Phases: Overview01:26

Drug Administration and Therapy Phases: Overview

Drugs, the chemical agents used in diagnosing, treating, or preventing diseases, undergo a four-phase process of development: pharmaceutic, pharmacokinetics, pharmacodynamics, and therapeutic.
The pharmaceutical phase focuses on leveraging the physicochemical properties of the drug to design and manufacture an effective product. Variants include orally administered tablets or capsules, topical creams or ointments, and parenteral-delivery solutions or emulsions.
The pharmacokinetic phase...
Targeted Cancer Therapies02:57

Targeted Cancer Therapies

The targeted cancer therapies, also known as “molecular targeted therapies,” take advantage of the molecular and genetic differences between the cancer cells and the normal cells. It needs a thorough understanding of the cancer cells to develop drugs that can target specific molecular aspects that drive the growth, progression, and spread of cancer cells without affecting the growth and survival of other normal cells in the body.
There are several types of targeted therapies against specific...
Clinical Trials: Overview01:11

Clinical Trials: Overview

Clinical development focuses on how the drug will interact with the human body and encompasses four key phases of clinical trials, each serving a specific purpose in assessing the safety and effectiveness of new drugs. These phases overlap and build upon one another. Phase I involves a small group of healthy volunteers (typically 20-80 individuals) or, in cases where significant toxicity is expected, patients with the targeted disease, such as cancer or AIDS. The volunteers are tested for...
Cancer Therapies02:49

Cancer Therapies

Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Tumor Immunotherapy01:27

Tumor Immunotherapy

Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.

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Related Experiment Video

Updated: May 9, 2026

Y-90 Radioembolization and PD-1 Inhibitor as Neoadjuvant Treatment in Hepatocellular Carcinoma
09:11

Y-90 Radioembolization and PD-1 Inhibitor as Neoadjuvant Treatment in Hepatocellular Carcinoma

Published on: May 24, 2024

Neoadjuvant therapy: what are the lessons so far?

Gunter von Minckwitz1

  • 1German Breast Group, Martin-Behaim-Str. 12, Neu-Isenburg 63263, Germany. gunter.vonminckwitz@germanbreastgroup.de

Hematology/Oncology Clinics of North America
|August 7, 2013
PubMed
Summary
This summary is machine-generated.

Neoadjuvant chemotherapy offers benefits for high-risk breast cancer patients, but pathologic complete response (pCR) surrogacy for survival is debated. Further research is needed to identify treatment benefits and guide therapy selection.

Keywords:
Breast cancerLocoregional relapseNeoadjuvant chemotherapyPathologic complete responsePostneoadjuvant treatmentSubtypesSurrogate marker

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Last Updated: May 9, 2026

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Potentiation of Anticancer Antibody Efficacy by Antineoplastic Drugs: Detection of Antibody-drug Synergism Using the Combination Index Equation
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Potentiation of Anticancer Antibody Efficacy by Antineoplastic Drugs: Detection of Antibody-drug Synergism Using the Combination Index Equation

Published on: January 19, 2019

Area of Science:

  • Oncology
  • Breast Cancer Research
  • Clinical Trials

Background:

  • Neoadjuvant chemotherapy is increasingly used for high-risk breast cancer.
  • Accurate assessment of treatment response is crucial for patient outcomes.
  • Current methods for predicting treatment benefit require refinement.

Purpose of the Study:

  • To review recent advancements in neoadjuvant chemotherapy for high-risk breast cancer.
  • To evaluate the utility of pathologic complete response (pCR) as a surrogate for long-term survival.
  • To discuss strategies for managing patients who do not achieve pCR and future clinical trial directions.

Main Methods:

  • Review of current literature and clinical trial data on neoadjuvant chemotherapy in breast cancer.
  • Analysis of the prognostic value of pathologic complete response (pCR).
  • Discussion of translational biomarker utility and future clinical trial designs.

Main Results:

  • Diagnosis of pathologic complete response (pCR) can avert poor prognosis in high-risk breast cancer.
  • The surrogacy of pCR for long-term survival remains uncertain.
  • Translational biomarker studies have not effectively identified patients likely to benefit from treatment.
  • Prognostic assessment for non-pCR patients is key for risk stratification and trial enrollment.

Conclusions:

  • Optimizing neoadjuvant chemotherapy requires better prediction of treatment response.
  • Further investigation is needed to validate pCR surrogacy and identify predictive biomarkers.
  • Future clinical trials should focus on non-pCR patients and de-escalation of locoregional treatment where appropriate.