1.The effect of inductive chemotherapy with FAC regimen on breast cancer.
Journal of the Korean Cancer Association 1991;23(4):783-789
No abstract available.
Breast Neoplasms*
;
Breast*
;
Drug Therapy*
2.Effectiveness of postoperative adjuvant treatment between radiation alone and chemotherapy plus radiation in locally advanced breast cancer.
Kyung Ran PARK ; John Kyu LOH JUHN ; Chang Ok SUH ; Gwi Eon KIM ; Eun Hee KOH ; Byung Soo KIM ; Kyung Sik LEE
Journal of the Korean Cancer Association 1991;23(1):107-119
No abstract available.
Breast Neoplasms*
;
Breast*
;
Drug Therapy*
3.Quadrantectomy and axillary node dissection in breast cancer after preoperative inductive chemotherapy.
Journal of the Korean Cancer Association 1992;24(6):840-847
No abstract available.
Breast Neoplasms*
;
Breast*
;
Drug Therapy*
4.Chemotherapy of breast cancer.
Korean Journal of Medicine 2000;58(5):497-509
No abstract available.
Breast Neoplasms*
;
Breast*
;
Drug Therapy*
5.Systemic adjuvant therapy in breast cancer.
Jin Hee AHN ; Sung Bae KIM ; Woo Kun KIM
Korean Journal of Medicine 2005;69(3):243-254
No abstract available.
Breast Neoplasms*
;
Breast*
;
Drug Therapy
;
Neoadjuvant Therapy
6.Mono- and Combination Chemotherapy for Metastatic Breast Cancer: An Increamental Step Forward.
Journal of Korean Breast Cancer Society 2003;6(3):137-140
No abstract available.
Breast Neoplasms*
;
Breast*
;
Drug Therapy, Combination*
7.Pathologic Evaluation of Breast Cancer after Neoadjuvant Therapy.
Cheol Keun PARK ; Woo Hee JUNG ; Ja Seung KOO
Journal of Pathology and Translational Medicine 2016;50(3):173-180
Breast cancer, one of the most common cancers in women, has various treatment modalities. Neoadjuvant therapy (NAT) has been used in many clinical trials because it is easy to evaluate the treatment response to therapeutic agents in a short time period; consequently, NAT is currently a standard treatment modality for large-sized and locally advanced breast cancers, and its use in early-stage breast cancer is becoming more common. Thus, chances to encounter breast tissue from patients treated with NAT is increasing. However, systems for handling and evaluating such specimens have not been established. Several evaluation systems emphasize a multidisciplinary approach to increase the accuracy of breast cancer assessment. Thus, detailed and systematic evaluation of clinical, radiologic, and pathologic findings is important. In this review, we compare the major problems of each evaluation system and discuss important points for handling and evaluating NAT-treated breast specimens.
Breast Neoplasms*
;
Breast*
;
Female
;
Humans
;
Neoadjuvant Therapy*
8.The effect of adjuvant CMF(cyclophosphamide, methotrexate, 5-FU) chemotherapy of breast cancer.
Joon PARK ; Jung Han YOON ; Young Jong JEGAL
Journal of the Korean Cancer Association 1993;25(6):928-934
No abstract available.
Breast Neoplasms*
;
Breast*
;
Drug Therapy*
;
Methotrexate*
9.Hormone Replacement Therapy and the Risk of Breast Cancer.
Journal of the Korean Medical Association 2000;43(5):438-447
No abstract available.
Breast Neoplasms*
;
Breast*
;
Hormone Replacement Therapy*
10.Clinical and pathologic tumor response following response-guided neoadjuvant chemotherapy for locally-advanced breast cancer in a Tertiary Hospital Breast Center in the Philippines
Shiela S. Macalindong ; Ralph Lazarus R. Rapacon
Philippine Journal of Surgical Specialties 2024;79(1):42-53
Rationale/Objective:
Neoadjuvant chemotherapy (NAC) is
recommended for locally-advanced breast cancer (LABC) to improve
resectability and provide in-vivo tumor response assessment. This
study aimed to describe the clinical and pathologic tumor response
of LABC patients after response-guided NAC.
Methods:
This is a retrospective cohort analysis of 128 LABC patients
who underwent NAC using sequential doxorubicin/cyclophosphamide
(AC) – docetaxel (T) regimen at the Philippine General Hospital
Breast Care Center. Clinical and pathologic response rates were
analyzed according to clinicopathologic variables including tumor
intrinsic subtype.
Results:
Objective clinical response (complete and partial) was
observed in 88% (111/128) of patients with 11% (14/128) achieving
pathologic complete response (pCR). The hormone receptor-negative/
Her2-enriched (HR-/Her2+) subtype had the highest pCR rate (23.5%)
followed by triple negative subtype (HR-/Her2-) at 19%. The hormone
receptor-positive/Her2-positive (HR+/Her2+) subtype had the lowest
pCR (4.7%). Two patients with initial poor response to AC but had
good response upon shifting to T achieved pCR. Twelve patients
(9.4%) had poor response to AC and T chemotherapy. Patients who
were pre-menopausal (p=0.04), had ductal histology (p=0.03), with
a HR-/Her2- (p=0.002) or HR+/Her2+ subtype (p=0.03) had good
response to AC. Intrinsic subtype was not significantly associated
with treatment response in those who received docetaxel. There was
strong association between the pathologic and clinical responses
(Spearman’s Rho score 0.69, p-value <0.0001).
Conclusion
Clinical and pathologic response to NAC was highly
dependent on tumor subtype. Clinical response was predictive of
pathologic response. Response-guided NAC allowed direct and early
evaluation of tumor treatment response that allowed for treatment
modifications.
Breast Neoplasms
;
Neoadjuvant Therapy
;
Drug Therapy