Background We conducted 20 years of follow-up of women enrolledin a randomized trial to compare the efficacy of radical (Halsted)mastectomy with that of breast-conserving surgery.
Methods From 1973 to 1980, 701 women with breast cancers measuringno more than 2 cm in diameter were randomly assigned to undergoradical mastectomy (349 patients) or breast-conserving surgery(quadrantectomy) followed by radiotherapy to the ipsilateralmammary tissue (352 patients). After 1976, patients in bothgroups who had positive axillary nodes also received adjuvantchemotherapy with cyclophosphamide, methotrexate, and fluorouracil.
Conclusions The long-term survival rate among women who undergobreast-conserving surgery is the same as that among women whoundergo radical mastectomy. Breast-conserving surgery is thereforethe treatment of choice for women with relatively small breastcancers.
The radical mastectomy introduced by Halsted1 was the treatmentof choice for breast cancer of any size or type, regardlessof the patient's age, for 80 years. Apart from a few modifications,such as enlarging the extent of the dissection to include theinternal mammary nodes or reducing it to spare the pectoralismuscles, the Halsted mastectomy was performed as originallydescribed throughout this period. The possibility of attemptinga surgical procedure that would conserve the breast was notwidely considered during those years.2,3
In 1969, a randomized study to compare radical mastectomy withbreast-conserving surgery, which was termed "quadrantectomy,"was approved by the World Health Organization Committee of Investigatorsfor Evaluation of Methods of Diagnosis and Treatment of BreastCancer.4 The recruitment of patients began at the Milan CancerInstitute in 1973, after the new procedure was standardized,and preliminary data showing that survival rates were equalafter radical and breast-conserving surgery were published in19775 and 1981.6
The main criticism of the data was that they were too preliminary;patients with small breast cancers must be followed for a verylong time, even decades, to ensure that the evaluation of theefficacy of any new treatment is accurate. We carefully monitoredthe 701 women in the trial for up to 29 years, and we now reportthe results.
Methods
Study Design
Enrollment in the trial began in 1973 and ended in May 1980after the recruitment of 701 patients who had breast cancerswith a maximal diameter of 2 cm or less on physical examination(stage T1) and no palpable axillary nodes (N0). Patients whowere older than 70 years of age or who had a history of cancerwere excluded. The patients underwent excisional biopsy undergeneral anesthesia, and those who had an infiltrating carcinomathat was no more than 2 cm in diameter on gross examinationand microscopical examination of a frozen section were stratifiedaccording to menopausal status and randomly assigned to undergoeither radical (Halsted) mastectomy alone or a breast-conservingquadrantectomy in combination with complete axillary dissectionand postoperative radiotherapy to the ipsilateral mammary tissue.The details of the surgical techniques and the radiation procedureshave been described previously.5,6 A complete axillary dissectionwas performed, and radiotherapy was delivered to the breastat a dose of 50 Gy plus a boost of 10 Gy. From 1973 to 1975,33 patients with axillary metastases were further randomly assignedto receive additional radiotherapy to the supraclavicular andinternal mammary nodes (40 to 45 Gy over a period of four tofive weeks) and 23 to receive no further radiotherapy (P=0.22for the difference in the numbers of patients in the two subgroups).
Beginning in 1976, all patients with positive axillary nodeswere given 12 monthly cycles of chemotherapy according to thefollowing schedule: 100 mg of cyclophosphamide per square meterof body-surface area per day orally for 14 days and 40 mg ofmethotrexate per square meter plus 600 mg of fluorouracil persquare meter intravenously on days 1 and 8. Chemotherapy wasbegun 15 to 30 days after radical mastectomy and simultaneouslywith radiotherapy in the group assigned to breast-conservingtherapy. No patient received tamoxifen during the trial or follow-up.For the first 10 years, patients were seen at the clinic every3 months and underwent a complete examination, including chestand skeletal radiography, liver ultrasonography, and mammography,every year. Thereafter, the patients were seen once a year andunderwent annually routine mammography. Other examinations wereperformed whenever they were clinically indicated. Three patientswere lost to follow-up. The median follow-up was 20 years. Themain data for all patients were recorded, updated, and storedin an automated data system after the accuracy of the data wasverified.
Statistical Analysis
The estimated crude cumulative incidence of recurrent tumorin the same breast in the quadrantectomy group and local recurrencein the radical-mastectomy group, as well as of contralateral-breastcarcinomas, regional or distant metastases, and other primarytumors, whichever occurred first, was calculated according toa competing-risk framework, as described by Marubini and Valsecchi,7and compared with use of the Gray test.8 The time to the occurrenceof these events was computed from the date of surgery. Becauseof the limited number of end-point events, multivariate analyseswere deemed an inappropriate method of comparing the effectsof treatment on recurrent tumor in the same breast and localrecurrences among stratified patients. For exploratory purposes,we computed the event rate (the cumulative number of eventsduring follow-up) according to the main characteristics of thepatients and the disease.
The overall survival curves for each treatment group were obtainedwith use of the KaplanMeier method and compared withuse of the log-rank test.9 Because of the long follow-up period,many deaths were not caused by breast cancer. Therefore, wealso estimated the cause-specific mortality rate on the basisof available information on the cause of death, using a competing-riskframework and the Gray test. We validated this approach by estimatingthe crude cumulative cause-specific mortality rate on the basisof life-tables,10 rather than information on the cause of death,since such information is often unreliable and unsuitable forstatistical analyses. All tests were two-sided, and a P valueof less than 0.05 was considered to indicate statistical significance.
Results
Of the 701 patients who entered the trial, 349 underwent a radical(Halsted) mastectomy and 352 underwent breast-conserving surgery.The primary carcinoma was palpable in 698 patients, whereasit was discovered only on mammography in 3 patients. The mean(±SD) age of the patients was 51±10.1 years inthe radical-mastectomy group and 50±10.4 years in thequadrantectomy group. At base line, similar proportions of patientsin the two groups were premenopausal, had tumors that were lessthan 1 cm in diameter, had a tumor in the upper or central quadrantor the lower quadrant, had a history of biopsy, and had axillary-nodemetastases (Table 1).
Table 1. Base-Line Characteristics of the Women Who Underwent Radical Mastectomy and Those Who Underwent Breast-Conserving Therapy.
Recurrent Tumors
The probability of recurrent tumor was significantly higherin the group that received breast-conserving therapy than inthe radical-mastectomy group (30 of 352 vs. 8 of 349 patients,P<0.001) (Figure 1). The mean (±SE) crude cumulativeincidence of recurrent tumor in the same breast was 8.8±3.2percent after 20 years among patients treated with breast-conservingsurgery and 2.3±0.8 percent in the radical-mastectomygroup. Of the 30 patients with a recurrent tumor in the samebreast, 29 underwent total mastectomy and 1 patient underwenta second local resection. Of these 30 cases of recurrent tumor,10 appeared in the scar and were thus defined as true recurrences,whereas 20 occurred in other quadrants of the breast and weretherefore classified as second ipsilateral carcinomas.
Figure 1. Crude Cumulative Incidence of Local Recurrences after Radical Mastectomy and Recurrences in the Same Breast after Breast-Conserving Therapy.
Table 2 shows the event rates according to age, tumor size,and the extent of axillary-node involvement at base line. Inthe radical-mastectomy group, the overall rate of local recurrenceswas low (average, 0.17 per 100 woman-years of observation) andwas not significantly affected by the patient's age and thesize of the tumor at base line. The rate of recurrences wasrelatively high among women with more than three axillary nodescontaining metastases, but the importance of this finding isuncertain because of the small number of such patients. In thegroup that received breast-conserving therapy, the average eventrate was almost four times as high (0.63 per 100 woman-yearsof observation) as the rate in the radical-mastectomy group.The rate in this group varied with age and was highest amongthe women who were 45 years of age or younger at base line (1.05per 100 woman-years of observation).
Table 2. Rates of Local Recurrences among Women Who Underwent Radical Mastectomy and of Recurrent Tumor in the Same Breast among Women Who Underwent Breast-Conserving Surgery, According to Base-Line Characteristics.
When true recurrences and second ipsilateral carcinomas wereconsidered separately, the rates were 0.21 and 0.42 per 100woman-years of observation, respectively. The timing of thetwo kinds of events also differed: true recurrences appeareda median of 92 months after quadrantectomy, and second ipsilateralcarcinomas appeared a median of 117 months afterward. In comparison,the median time to local recurrence was 54 months in the radical-mastectomygroup.
Other Events
Table 3 shows the cumulative incidence of neoplastic eventsother than local recurrences and recurrences in the same breast.There were no statistically significant differences betweenthe two groups in the 20-year crude cumulative incidence ofcontralateral-breast carcinomas, distant metastases, or otherprimary cancers. The overall rate of contralateral-breast cancerwas 0.66 per 100 woman-years of observation, a figure that wasnearly identical to the rate of recurrent tumors in the samebreast in the group that received breast-conserving therapy(0.63 per 100 woman-years of observation).
Table 3. Numbers and Crude Cumulative Incidence of Events over the 20-Year Period in the Two Groups of Patients.
Mortality
Of the 701 women who entered the trial, 308 died 152in the radical-mastectomy group and 156 in the group that receivedbreast-conserving therapy. Among these women, 177 (57 percent)died of breast cancer (86 in the radical-mastectomy group and91 in the group that received breast-conserving therapy), 42(14 percent) died of other primary cancers, and 73 (24 percent)died of nonneoplastic diseases. The cause of death could notbe ascertained in 16 patients (5 percent). The overall survivalcurves overlapped in the two groups (Figure 2). Twenty yearsafter surgery, the rate of death from all causes was 41.2 percentin the radical-mastectomy group and 41.7 percent in the groupthat received breast-conserving therapy (P=1.0). The observedrate of death from breast cancer was 24.3 percent and 26.1 percent,respectively (P=0.8), similar to the rates expected on the basisof calculations in age-matched Italian women (23.6 percent and24.8 percent, respectively). The survival curves were also similarwhen the two groups were stratified according to the size ofthe primary carcinoma at base line (Figure 3).
Figure 2. KaplanMeier Estimates of Survival after Radical Mastectomy or Breast-Conserving Therapy.
The two lower curves correspond to observed survival, taking into account deaths from any cause. The upper curves (which are almost identical in the two groups) show the expected survival rate on the basis of mortality rates in age-matched cohorts of Italian women.
Figure 3. KaplanMeier Estimates of Survival after Radical Mastectomy or Breast-Conserving Therapy, According to the Size of the Primary Carcinoma.
The two upper curves (which are almost identical in the two groups) show the expected survival rate on the basis of mortality rates in age-matched cohorts of Italian women. The four lower curves show the survival rates in the two groups stratified according to the maximal diameter of the breast cancer at base line.
Among the 33 patients with positive axillary nodes who wereassigned to receive additional radiotherapy to the supraclavicularlymph nodes in the early years of the study, the mortality ratewas 64 percent (21 of 33), as compared with a rate of 48 percent(11 of 23) among the 23 similar patients who were assigned toreceive no additional radiotherapy (P=0.08).
Discussion
Our results show that the long-term survival of women with earlybreast cancer who were treated with breast-conserving surgeryand postoperative radiotherapy to the ipsilateral breast wasvirtually identical to the rate among women who underwent radicalmastectomy. After a median follow-up of 20 years, the overalland breast-cancerspecific survival rates were also similarin the two groups. Our observation is in line with the 20-yearresults of trial B-06 of the National Surgical Adjuvant Breastand Bowel Project, presented by Fisher et al. elsewhere in thisissue of the Journal.11 These results should dispel any lingeringdoubts about the safety and efficacy of breast-conserving surgeryas a treatment for breast cancer.
The goal of the surgical technique we used was complete removalof the primary carcinoma, together with the removal of a generousamount of the surrounding normal breast tissue (extending 1.5to 2.0 cm from the edge of the tumor). The objective was todissect the entire area from which the tumor originated. Portionsof the overlying skin and deep muscular fascia were also removed.The operation was termed "quadrantectomy" to indicate the extentof the resection.
The patients assigned to radical mastectomy underwent the classicHalsted procedure, because at the time the study began, themodified radical mastectomy had not been accepted by most surgeons.If we had compared breast-conserving surgery with modified radicalmastectomy, the difference in the rate of local recurrencesbetween the two groups might have been smaller than the differencewith the Halsted procedure.
Although scattered radiation beams certainly reached the oppositebreast, the incidence of contralateral-breast carcinomas waslower in the group that underwent breast-conserving surgeryplus radiotherapy than in the radical-mastectomy group. Thisfinding suggests that the doses of radiotherapy delivered inthe study were not carcinogenic.12 Among 56 patients with positiveaxillary nodes who were assigned to receive either prophylacticsupraclavicular radiotherapy or no such treatment, the respectivemortality rates were 64 percent and 48 percent.
Patients with intraductal noninvasive carcinomas were not eligiblefor our trial. Other studies have shown that a breast-conservingapproach should also be the treatment of choice for women within situ breast carcinomas that are relatively small.13,14 Ourdata apply only to patients with a primary tumor of limitedsize (maximal diameter, 2 cm). Other studies have successfullyused breast-conserving procedures in women with larger primarytumors.15,16,17 In clinical practice it is important to considerthe size of the primary tumor in relation to the size of thebreast, because quadrantectomy is technically difficult in patientswith small breasts and large cancers. In these women, mastectomywith immediate reconstruction may be the best choice.
The 20-year rate of death from breast cancer in node-negativepatients who received no systemic adjuvant therapy was 20.8percent. This result is notable, because 20 to 30 years agothe results of pathological examination of the lymph nodes werenot as accurate as they are now. In our recent trial involvingpatients with the same stage of disease as patients in our earlierstudy (T1 and N0), 36 percent had positive axillary nodes onpathological examination, as compared with 26 percent in theearlier trial (unpublished data). For this reason, we believethat about 10 percent of the patients who were originally consideredto be node-negative were actually node-positive.
We believe that the use of a breast-conserving procedure thatis associated with a high quality of life is one reason forthe increasing awareness of and participation in early-detectionprograms on the part of women. The early results of our studywere confirmed by other European and American trials in 198316and 1985.17 We believe that as a result of these trials, about300,000 women with early breast cancer worldwide each year undergobreast-conserving surgery rather than radical mastectomy.
Supported by the Italian Association for Cancer Research.
We are indebted to Mrs. F. Falcetta and Mrs. L. Morandi fordata management.
Source Information
From the Department of Senology, European Institute of Oncology (U.V., A.L., M.A.); the Departments of Senology (N.C., M.G., R.S.) and Biometrics (L.M.), Istituto Nazionale per lo Studio e la Cura dei Tumori; and the Institute of Medical Statistics and Biometry, Università degli Studi (E.M.) all in Milan, Italy.
Address reprint requests to Dr. Veronesi at the European Institute of Oncology, 435 Via G. Ripamonti, I-20141 Milan, Italy, or at umberto.veronesi{at}ieo.it.
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