Anemia Is a Significant Prognostic Factor in Local Relapse-Free Survival of Premenopausal Primary Breast Cancer Patients Receiving Adjuvant Cyclophosphamide/Methotrexate/5-Fluorouracil Chemotherapy

Patients and Experimental Design

Between 1990 and 1999, a total of 1,099 premenopausal patients with primary breast cancer were included in a prospective, randomized, multicenter, phase III trial of the ABCSG Trial 5. Of these patients, 523 were randomized to the polychemotherapy arm consisting of six cycles of i.v. CMF (cyclophosphamide 600 mg/m², methotrexate 40 mg/m², and 5-fluorouracil 600 mg/m²) on days 1 and 8 every 4 weeks. All trial patients undergoing breast-conserving surgery received mandatory radiotherapy, which was optional in women who underwent modified radical mastectomy. The sandwich technique was used with irradiation conducted after the first three cycles of CMF. Radiation therapy consisted of external irradiation of the breast with ∼50 cGy and a boost irradiation of an additional 8 to 12 cGy of the tumor bed.

Study design, patient eligibility, and patient evaluation. All details on the design of ABCSG Trial 5, patient eligibility for the trial, and patient evaluation have previously been published (21). ABCSG Trial 5 was a prospective, randomized, multicenter study conducted in Austria that compared the effectiveness of endocrine treatment with that of standard chemotherapy regimens (in 1990: CMF) in endocrine-responsive, premenopausal women.

Eligibility for this analysis included all exclusion and inclusion criteria of ABCSG Trial 5. For the current retrospective study of the data, patients who did not receive at least three cycles of CMF, or in whom no Hb levels were documented before the start of chemotherapy, were excluded from the analysis.

Patient follow-up in ABCSG Trial 5 has previously been described (21). Patients' first relapse, local recurrence, and cancer in the opposite breast served as primary end points for RFS, and death served as the primary end point for OS. Whenever possible, local or regional relapses and contralateral incidences required histologic confirmation. Relapses in supraclavicular lymph nodes were classified as distant metastases. Survival parameters were calculated as the time between date of primary surgery and date of histologic diagnosis of local relapse, relapse, or death.

Anemia was defined as the incidence of at least one serum Hb level <12 g/dL during the period of adjuvant chemotherapy through the first follow-up date 3 months after the end of adjuvant treatment. Serum Hb levels were determined before each cycle of adjuvant polychemotherapy and at the time of the first follow-up visit.

Statistical analysis. Frequency distributions (patient characteristics) were analyzed using the χ² test. Serum Hb was analyzed as a binary variable; values of <12 g/dL were defined as anemia. Univariate analysis of patient LRFS, RFS, and OS was done using Kaplan-Meier analysis, and survival curves were compared using the log-rank test. A Cox proportional hazards regression model was used to identify independent prognostic factors including age, stage of disease, axillary lymph node status, estrogen and progesterone receptor status, type of surgery, postoperative irradiation, histologic grading, and anemia.

Results

A Hb level <12 g/dL occurred in a total of 18% of patients in the chemotherapy arm and was a very rare event (<1%) in the hormonal treatment arm. Because treatment groups were assigned by prospective, adaptive randomization and patient characteristics (including the type of surgery and the use of radiotherapy) were well balanced between the two groups, the inclusion of polychemotherapy within the treatment regimen was most likely responsible for the difference in anemia rates. Because univariate analysis gave no indication of differential outcome of anemic patients in the endocrine treatment arm, only the CMF arm was further analyzed for the effect of anemia on survival.

Patients who did not receive at least three cycles of the CMF regimen, or in whom no serum Hb level was documented at the beginning of polychemotherapy, were excluded from this analysis (n = 81). Of the remaining 442 patients, no serum Hb level was available between cycles 3 and 6 in 9 patients; another 9 patients were lost to follow-up after the last cycle of CMF chemotherapy. Therefore, 424 patients were included in this analysis of prospectively collected data.

Patient characteristics are shown in Table 1 . Of 424 patients, 77 (18.2%) had at least one serum Hb level <12 g/dL during adjuvant treatment with the CMF regimen or follow-up. The only parameters that correlated with anemia were type of surgery and postoperative irradiation. Patients who had undergone modified radical mastectomy had a significantly higher rate of anemia (26.0%) than patients who had undergone breast-conserving surgery (13.7%; P = 0.002). Because radiotherapy was given largely according to type of surgery, this may have affected the result that patients who did not receive radiotherapy (mostly modified radical mastectomy patients) had a significantly higher risk of anemia (27.6%) than patients who did receive radiotherapy (14.1%; P = 0.001).

After a median follow-up time of 61 months, a total of 39 (9.2%) local relapses had occurred among the population of 424 premenopausal breast cancer patients (Table 2 ). Local relapse was diagnosed in 6.9% of nonanemic patients versus 19.5% of anemic patients (P = 0.0006, log-rank test). The overall relapse rate and the number of deaths were equal among anemic and nonanemic patients.

As seen in Fig. 1 , LRFS was significantly longer in nonanemic than in anemic patients (P = 0.0006, log-rank test). At 5 years, 8.2% of nonanemic versus 19.6% of anemic patients had developed local relapse. RFS and OS curves did not differ significantly between the anemic and nonanemic groups.

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Fig. 1.

LRFS for patients with Hb ≥12 g/dL versus Hb <12 g/dL.

According to a multivariate Cox proportional hazards model of all relevant prognostic factors in early-stage breast cancer patients, only age (as a continuous variable), axillary lymph node status, and anemia were shown to be significant prognostic factors for LRFS (P < 0.005 for all; Table 3 ). Anemic patients had a 2.96-fold increased relative risk of developing local relapse compared with nonanemic patients. Radiotherapy, type of surgery, and tumor stage had no significant effect on LRFS. Anemia was not shown to be an independent prognostic factor for RFS or OS (Tables 4 and 5 ).

Discussion

The results from our prospective, randomized, phase III trial showed that anemia during adjuvant polychemotherapy and radiotherapy in premenopausal primary breast cancer patients has a significant negative effect on LRFS. Local recurrence occurred in 6.9% of nonanemic patients and in 19.5% of patients with Hb levels <12 g/dL. According to the results of our retrospective multivariate analysis, this could not be explained by a correlation between anemia and tumor size, postoperative irradiation, or type of surgery.

In young women with regular menstrual cycles, anemia or at least lower levels of Hb resulting from iron deficiency are common. In the current study, this might be the most common predisposition for developing anemia under adjuvant therapy because anemia caused by stage I to II breast cancer alone is unlikely. Other factors leading to low Hb levels are well distributed between treatment groups due to the prospective randomization procedure. Indeed, there were no differences between the rate of mastectomies and the use of radiotherapy between treatment groups in ABCSG Trial 5 (21). It is thus safe to conclude that the apparent difference in anemia rates was due to the inclusion of polychemotherapy in the treatment regimen.

Anemia, even in primary operable breast cancer, has prognostic effect in breast cancer patients (2, 5). With regard to the observed effect on LRFS, anemia should be discussed in the context of its interaction with chemotherapy and, maybe most importantly, the influence of anemia on radiotherapy outcome.

With regard to the interaction of chemotherapy and anemia, at least two published reports indicate that patients with Hb levels <12 g/dL have a poor response to preoperative cytotoxic therapy. Bottini et al. (11) reported Hb levels to predict tumor response to primary chemotherapy. In a total of 157 patients treated with either a preoperative CMF + tamoxifen regimen or single agent epirubicin, response at the time of surgery was reduced in patients starting at a cutoff of 12.5 g/dL. The authors suggest an inhibition of antiproliferative activity in anemic patients as a possible mechanism. Beresford et al. made similar observations. Although the influence of anemia (threshold 12 g/dL) did not reach a level of statistical significance in view of response rates, a trend of reduced response in anemic patients was reported. Of note, patients with complete response in this study had a high Hb range between 12.8 and 15.7 g/dL (12).

With regard to the reported data, the influence of Hb levels on the effectiveness of radiotherapy is of particular relevance. In head and neck cancer, the negative effect of low Hb levels on outcome was reported over 20 years ago (22). In breast cancer, a link between low Hb and response to radiotherapy has also been reported: Kamby et al. studied a cohort of 99 patients with isolated local recurrence after mastectomy. Patients were treated with radical excision and radiotherapy and followed up for survival, interval to second local failure, and distant metastasis. Hemoglobin levels at the time of first recurrence were identified as a prognostic factor of survival (23). Further data linking Hb levels to local control via the interaction with radiotherapy were reported by Henke et al. (10). In this report, low Hb not only influenced disease-free survival but further analysis of the data also suggests that the effect only occurs when radiotherapy was included in the therapeutic regimen.

Finally, a wide range of experimental data serves as a biological basis for the clinical observations summarized above. Tumor hypoxia (most likely aggravated in anemic breast cancer patients; ref. 13) leads to signaling pathways that regulate proliferation, angiogenesis, and apoptosis. These signals are mediated by hypoxia-inducible factors (16). As a consequence, tumor types with a dedifferentiated phenotype may emerge. In breast cancer, this has been established for ductal carcinoma in situ lesions (15). Furthermore, hypoxia-inducible factors have been shown to activate pathways associated with stem cell self renewal (Oct4), a finding of utmost importance in view of cancer stem cells (24).

The same line of data linking anemia with tumor hypoxia also explains the interaction of anemia with both chemotherapy and radiotherapy. Low blood flow in tumors can serve as an effective barrier against systemic agents. Effective radiotherapy kills tumor cells by generating reactive oxygen species (25). Thus, in hypoxic tumors, resistance to ionizing radiation can occur.

Experimental advances in the description of molecular pathways associated with tumor hypoxia have identified several new targets for therapy (26). Currently, several small molecule inhibitors of hypoxia-inducible factor-1α activity, although none with specificity for hypoxia-inducible factor 1, are under experimental investigation or moving toward clinical trials (27).

Both clinical observation and experimental data have inspired a series of prospectively randomized trials in which erythropoietin-stimulating agents have been combined with chemotherapy and/or radiotherapy. The disappointing results from these trials have recently been reviewed and commented on (18). As a consequence, the Food and Drug Administration has issued an alert describing an increased risk for thromboembolic disease, promotion of tumor growth, and decreased survival due to erythropoiesis-stimulating agent treatment.¹¹

The current report identifies treatment-associated anemia in early breast cancer as an important factor in local tumor control. In view of the recent pitfalls in the treatment of cancer-associated anemia, the use of erythropoiesis-stimulating agents can hardly be recommended as a viable treatment option. Molecular targets associated with tumor hypoxia and distinct from erythropoiesis merit further experimental and clinical investigation.

Appendix

Members of the Austrian Breast and Colorectal Cancer Study Group who participated in Trial 5 were as follows:

M. Gnant, D. Kandioler, M. Schmidinger, B. Gebhard, S. Taucher, P. Dubsky (Departments of Surgery, Medical University of Vienna, Vienna)

G. Steger, G. Altorjai, R. Bartsch. U. Pluschnig, C. Wenzel, C. Zielinski (Department of Internal Medicine I, Division of Oncology, Medical University of Vienna, Vienna)

P. Mayer, C. Menzel, B. Mlineritsch, C. Rass, R. Reitsamer, G. Russ (Third Medical Department and Department of Special Gynecology, Salzburg Hospital, Salzburg)

T. Bauernhofer, H.-J. Mischinger, M. Schmid, M. Smola, P. Steindorfer, H. Stöger (Departments of Internal Medicine and Surgery, Graz University, and Second Department of Surgery, Graz Hospital, Graz)

E. Asseryanis, A. Galid, R. Möslinger-Gehmayr, M. Seifert (Department of Special Gynecology, Vienna University, Vienna);.

D. Depisch, K. Haider, W. Kwasny, A. Lenauer, T. Payrits (Department of Surgery, Wiener Neustadt Hospital, Wiener Neustadt)

M. Fridrik, R. Greul, G. Hochreiner, G. Wahl (Department of Internal Medicine 3, AKH-Linz, Linz)

G. Jatzko, V. Wette (Department of Surgery, Sankt Veit Hospital, Sankt Veit)

H. Spoula, M. Stierer (Department of Surgery, Hanusch Hospital, Vienna)

U. Schmidbauer, M. Wunderlich (Department of Surgery, Barmherzige Schwestern Hospital, Vienna)

F. Hofbauer, M. Lang (Department of Surgery, Oberpullendorf Hospital, Oberpullendorf)

P. Kier, K. Renner (Second Medical Department and Department of Surgery, Sozialmedizinisches Zentrum Ost Hospital, Vienna)

R. Kocher, F. Stangl (Department of Surgery, Leoben Hospital, Leoben)

G. Luschin-Ebengreuth, R. Winter (Department of Gynecology, Graz University, Graz)

W. Schennach, H. Zoller (Department of Surgery, Zams Hospital, Zams)

F. Kugler, C. Tausch (Department of Surgery, Barmherzige Schwestern Hospital, Linz)

E. Hanzal, C. Sam (Department of Gynecology, Vienna University, Vienna)

A. Haid, R. Köberle-Wührer (Department of Surgery, Feldkirch Hospital, Feldkirch)

W. Döller, E. Melbinger (Department of Surgery, Wolfsberg Hospital, Wolfsberg)

J. Berger, R. Lenzhofer (Medical Department, Schwarzach Hospital, Schwarzach)

H. Ludwig, P. Sagaster (First Medical Department, Wilhelminenspital, Vienna)

G. Reiner, D. Semmler (Department of Surgery, Mistelbach Hospital, Mistelbach)

J. Omann (Department of Surgery, Klagenfurt Hospital, Klagenfurt)

W. Neunteufel (Department of Gynecology, Dornbirn Hospital, Dornbirn).