6
High Dose Methotrexate as a Preoperative Adjuvant in the Treatment of Epidermoid Carcinoma of the Head and Neck A Feasibility Study and Clinical Trial John L. Tarpley, MD, Bethesda, Maryland Paul B. Chretien, MD, Bethesda, Maryland John C. Alexander, Jr, MD, Bethesda, Maryland Robert C. Hoye, MD, Bethesda, Maryland Jerome B. Block, MD, Bethesda, Maryland Alfred S. Ketcham, MD, Bethesda, Maryland The treatment of carcinoma of the head and neck presents the difficult problem of both local and systemic control. To improve survival rates over those achieved with surgery or radiotherapy alone, radiotherapy has been used as a preoperative adju- vant. The primary goal of these regimens was to reduce local recurrences; however, conclusive evi- dence that this has been achieved is lacking thus far. Preoperative irradiation, however, is frequent- ly associated with significant morbidity, such as impaired healing of the surgical wound, formation of fistulas, and, at least in one study, evidence of an increased incidence of systemic metastases [l- 31. To avoid the morbidity associated with radia- tion therapy used prior to surgery, trials of postop- erative radiation therapy are in progress. Thus far, sufficient data have not accrued to determine the efficacy of these regimens. Chemotherapy has been used in the treatment of carcinoma of the head and neck primarily for inoperable and recurrent tumors. When adminis- tered systemically, a significant number of cases of tumor regression in inoperable patients has been achieved with methotrexate [4-71. Local arterial infusion of chemotherapeutic agents, especially methotrexate, has effected marked tumor regres- sion and, as seen in limited follow-up studies, has reduced local recurrence rates after subsequent surgical resection. As with adjunctive radiation therapy, the ultimate effect of this combination on survival has not been assessed [8-121. From the Surgery Branch. National Cancer Institute, National Institutes of Health, Bethesda, Maryland. Reprint requests should be addressed to Paul B. Chretien. MD. Surgery Branch, National Cancer Institute. National Institutes of Health, Sethesda. Maryland 20014. Presented at the Combined Meeting of the James Ewing Sodety and the Society of Head and Neck Surgeons, New Orleans, Louisiana, March 25-29.1975. The beneficial effects of adjuvant chemotherapy in the management of malignant lesions classically treated by surgery alone are found in the experi- ences with osteogenic sarcoma, rhabdomyosarco- ma, soft tissue sarcoma, and breast cancer [13-191. Of these, the most dramatic effects have been achieved in the management of osteogenic sarco- ma. Methotrexate administered in extremely high doses immediately after amputation has reduced the incidence of recurrence from a historical rate of approximately 80 per cent in two years to pro- jected rates of 20 to 30 per cent [I&16]. The demonstrated efficacy of preoperative che- motherapy in the treatment of other forms of ma- lignancy and the regressions in inoperable tumors of the head and neck achieved with methotrexate led to this study to determine the effects of high dose methotrexate with leucovorin rescue when used preoperatively in patients with operable epi- dermoid carcinoma of the head and neck. Material and Methods Thirty consecutive patients with operable, previously untreated epidermoid carcinoma of the head and neck who had no medical contraindications to the adminis- tration of systemic methotrexate were studied. There were thirteen oral, four pharyngeal, and thirteen laryn- geal tumors. A control population of patients with simi- lar tumors who met all the medical and other criteria for eligibility for preoperative methotrexate were selected from the patients treated by surgery alone at the Na- tional Cancer Institute prior to the institution of this protocol. The tumor site, TNM classification, stage, and status of the methotrexate-treated patients is presented in Table I and the controls in Table II. A comparison of the two groups by these parameters is presented in Table III. V&an. 130, octobar 1975 481

High dose methotrexate as a preoperative adjuvant in the treatment of epidermoid carcinoma of the head and neck: A feasibility study and clinical trial

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High Dose Methotrexate as a Preoperative Adjuvant in the

Treatment of Epidermoid Carcinoma of the Head and Neck

A Feasibility Study and Clinical Trial

John L. Tarpley, MD, Bethesda, Maryland

Paul B. Chretien, MD, Bethesda, Maryland

John C. Alexander, Jr, MD, Bethesda, Maryland

Robert C. Hoye, MD, Bethesda, Maryland

Jerome B. Block, MD, Bethesda, Maryland

Alfred S. Ketcham, MD, Bethesda, Maryland

The treatment of carcinoma of the head and neck presents the difficult problem of both local and systemic control. To improve survival rates over those achieved with surgery or radiotherapy alone, radiotherapy has been used as a preoperative adju- vant. The primary goal of these regimens was to reduce local recurrences; however, conclusive evi- dence that this has been achieved is lacking thus far. Preoperative irradiation, however, is frequent- ly associated with significant morbidity, such as impaired healing of the surgical wound, formation of fistulas, and, at least in one study, evidence of an increased incidence of systemic metastases [l- 31. To avoid the morbidity associated with radia- tion therapy used prior to surgery, trials of postop- erative radiation therapy are in progress. Thus far, sufficient data have not accrued to determine the efficacy of these regimens.

Chemotherapy has been used in the treatment of carcinoma of the head and neck primarily for inoperable and recurrent tumors. When adminis- tered systemically, a significant number of cases of tumor regression in inoperable patients has been achieved with methotrexate [4-71. Local arterial infusion of chemotherapeutic agents, especially methotrexate, has effected marked tumor regres- sion and, as seen in limited follow-up studies, has reduced local recurrence rates after subsequent surgical resection. As with adjunctive radiation therapy, the ultimate effect of this combination on survival has not been assessed [8-121.

From the Surgery Branch. National Cancer Institute, National Institutes of Health, Bethesda, Maryland.

Reprint requests should be addressed to Paul B. Chretien. MD. Surgery Branch, National Cancer Institute. National Institutes of Health, Sethesda. Maryland 20014.

Presented at the Combined Meeting of the James Ewing Sodety and the Society of Head and Neck Surgeons, New Orleans, Louisiana, March 25-29.1975.

The beneficial effects of adjuvant chemotherapy in the management of malignant lesions classically treated by surgery alone are found in the experi- ences with osteogenic sarcoma, rhabdomyosarco- ma, soft tissue sarcoma, and breast cancer [13-191. Of these, the most dramatic effects have been achieved in the management of osteogenic sarco- ma. Methotrexate administered in extremely high doses immediately after amputation has reduced the incidence of recurrence from a historical rate of approximately 80 per cent in two years to pro- jected rates of 20 to 30 per cent [I&16].

The demonstrated efficacy of preoperative che- motherapy in the treatment of other forms of ma- lignancy and the regressions in inoperable tumors of the head and neck achieved with methotrexate led to this study to determine the effects of high dose methotrexate with leucovorin rescue when used preoperatively in patients with operable epi- dermoid carcinoma of the head and neck.

Material and Methods

Thirty consecutive patients with operable, previously untreated epidermoid carcinoma of the head and neck who had no medical contraindications to the adminis- tration of systemic methotrexate were studied. There were thirteen oral, four pharyngeal, and thirteen laryn- geal tumors. A control population of patients with simi- lar tumors who met all the medical and other criteria for eligibility for preoperative methotrexate were selected from the patients treated by surgery alone at the Na- tional Cancer Institute prior to the institution of this protocol. The tumor site, TNM classification, stage, and status of the methotrexate-treated patients is presented in Table I and the controls in Table II. A comparison of the two groups by these parameters is presented in Table III.

V&an. 130, octobar 1975 481

Tarpley et al

The preoperative methotrexate regimen was. as fol- lows: on day 1 methotrexate, 240 mg/m2, was given in- travenously in 1,000 ml of 5 per cent dextrose in water over a twenty-four hour interval. This was followed by leucovorin, 75 mg intravenously, in 500 ml of 5 per cent dextrose in water over twelve hours. Six hours later, leu- covorin, 12 mg, was given every six hours for a total of four doses. This regimen was repeated on day 5 and the operation was performed between days 12 and 15. Pa- tients who had intraoperative transection of tumor, tumor in surgical margins, or lymph node metastases demonstrated histologically received postoperative methotrexate. This regimen consisted of methotrexate, 30 mg/m2, intravenously weekly for four doses followed by escalation to 60 mg/m2 weekly for twelve doses, then the same dose monthly for two years.

The recurrence and survival rates were evaluated using the life table analysis method. Time of recurrence and time of death were evaluated using Student’s t test.

Results

Of the thirty patients treated with preoperative methotrexate, tumor regression occurred in twenty-three. Tumor regression is defined as any measurable decrease in size of the primary tumor

or lymph node metastases. In thirteen patients, re- gression of the primary tumor occurred, in four re- gression of lymph node metastases occurred, and in six regression of both primary tumor and the nodal metastases occurred. In seven patients, or 23 per cent, regression of tumor was not documented. (Table IV.)

Methotrexate toxicity was evaluated by labora- tory and clinical indexes. The laboratory indexes of toxicity are shown in Table V. The mean of the lowest platelet counts occurring in a two week in- terval after operation was 164,000 per mm3 with a range of 63,000 to 274,000. The mean of the lowest white blood cell counts during the same interval was 5,660 per mm3 with a range of 2,100 to 11,100. The mean of the highest white blood cell counts was 12,200 per mm3 with a range of 6,600 to 17,200. No renal or hepatic toxicity was docu- mented.

The clinical indexes used to determine possible methotrexate toxicity and a comparison of the same parameters in the controls are shown in Table VI. The average number of intraoperative blood transfusion in the methotrexate-treated

TABLE I Preoperative Tumor Extent and Current Status of the Patients Treated with Preoperative Methotrexate

Patient Site Txf’U’Jx Stage Status

1. LH 2. AB 3. JD 4. BM 5. AR 6. IE 7. JD 8. RM 9. cw

10. JS 11. AS 12. DB 13. GS 14. FD 15. WI-I 16. BG 17. EA 18. HD 19. EC 20. HG 21. LT 22. RC 23. HJ 24. ED 25. MM 26. ES 27. AK 28. JC 29. HB 30. WG

Larynx Tonsil Floor of the mouth Tongue Buccal mucosa Buccal mucosa Floor of the mouth Floor of the mouth Gingiva Tongue Palate Pyriform sinus Pyriform sinus Pyriform sinus Pyriform sinus Pyriform sinus Larynx Pyriform sinus Larynx Larynx Larynx Pyriform sinus Floor of the mouth Floor of the mouth Floor of the mouth Vallecula Base of the tongue Floor of the mouth Hypopharynx Vallecula

TaNaM, T,N,Mo T,N,Mo T,N,Mo T,N,Mo T,N,Mo T,N,Mo T,NoMo T,NJ% TJ%Mo T,N,% TJ’J,M, TM% T,N,Mo TJ’J,M, T,N,Mo T&,Mo T,N,W TN’% T,N,% T,W% TAM, T,W% T,W% TAM, T,N,Mo TJ’J,Mo T,N&‘o T,W% T,N,M,

III II III III II III III II II III IV IV II II II III IV III II III II IV II I IV III Ill II II III

No evidence of disease > 36 mo No evidence of disease, 20 mo Recurrence, 9 mo; dead of disease, 19 mo Recurrence, 18 mo; dead of disease, 26 mo Recurrence, 5 mo; dead of disease, 10 mo No evidence of disease, 26 mo Recurrence, 26 mo; alive with disease, 30 mo Recurrence, 12 mo; dead of disease, 21 mo No evidence of disease, 26 mo No evidence of disease, 35 mo No evidence of disease > 36 mo Recurrence, 13 mo; dead of disease, 20 mo Recurrence, 5 mo; dead of disease, 7 mo No evidence of disease, 27 mo Recurrence, 4 mo; dead of disease, 21 mo Recurrence, 9 mo; dead of disease, 21 mo No evidence of disease, 14 mo Recurrence, 11 mo; no evidence of disease, 20 mo No evidence of disease, 23 mo No evidence of disease, 28 mo No evidence of disease, 23 mo No evidence of disease, 19 mo No evidence of disease, 16 mo No evidence of disease, 17 mo Recurrence, 6 mo; no evidence of disease, 17 mo Recurrence, 9 mo;* no evidence of disease, 16 mo Recurrence, 9 mo;* no evidence of disease, 11 mo No evidence of disease, 9 mo No evidence of disease, 10 mo Recurrence, 5 mo; dead of disease, 15 mo

* Recurrence in opposite neck.

482 The Ame&an Journal d Surguy

Methotrexate in Epidermoid Carcinoma

group was 4.5 units with a range of 0 to 15 and in the controls, 4 units with a range of 0 to 15. Wound hematomas did not occur in the methotrexate- treated group but four occurred in the controls. In- fectious complications were divided into two cate- gories, local wound infections and pneumonitis. There were five wound infections in the metho- trexate-treated group and nine in the controls. Complications of wound healing led to two orocu- taneous fistulas in the methotrexate-treated group and five fist&as in the controls. Postoperative

pneumonia developed in four methotrexate-treat- ed patients and in nine controls. Postoperative temperatures greater than 38°C were noted in thirteen treated patients and in fifteen controls.

Life table analysis of the disease-free interval in the two groups is presented in Figure 1. There is no statistical difference in the incidence of recur- rence in the two groups. However, in the fifteen methotrexate-treated patients in whom recur- rences developed, the average postoperative inter- val before recurrence was 10.13 months and in the

TABLE II Preoperative Tumor Extent and Current Status of the Control Patients

Stage Status

1. RR 2. RS

3. HB 4. MD

5. MH

6. MS 7. PT

8. FK

9. AH

10. GM

11. IS 12. WK

13. HP

14. JK

15. TD

16. JW

17. ES

18. JP 19. RJ

20. HM

21. cc

22. WT

23. OC

24. GB

25. WS

26. MH 27. TH 28. LF

29. EM

30. RP

Larynx T,W% Tonsil T,N,Mo

Floor of the mouth Floor of the mouth

T,N,Mo TJ’J,Mo

Alveolar ridge Alveolar ridge

Tongue

TIN,% T,N,‘% T,N,‘“‘o

Floor of the mouth T,W%

Floor of the mouth

Tongue

Palate

Larynx

T,f’W’o T,N,Mo T,N,Mo -f’,N,Mo

Pyriform sinus T,N,Mo

Pyriform sinus -f-,N,Mo

Vallecula T,N,Mo

Larynx T,N,W

Pyriform sinus

Larynx

Larynx

Larynx

Larynx

Pyriform sinus TJ’J,Mo

Floor of the mouth T,NoMo

Floor of the mouth Floor of the mouth

Larnyx Vallecula Floor of the mouth

Floor of the mouth Floor of the mouth

II

III

III

III

III

III

III

II

I

I

III

III

III

III

III

Ill

III II II II II

III

I

I III III II III

II IV

No evidence of disease > 36 mo Recurrence, 6 mo; dead of disease, 15

mo No evidence of disease > 36 mo

Recurrence, 5 mo; dead of disease,

7 mo No evidence of disease > 36 mo

No evidence of disease > 36 mo

No evidence of disease, 26 mo; dead,

26 mo* No evidence of disease, 8 mo; dead,

8 mot

No evidence of disease > 36 mo

No evidence of disease > 36 mo

No evidence of disease > 36 mo

Recurrence, 6 mo; dead of disease, 21 mo

Recurrence, 7 mo; dead of disease,

13 mo Recurrence, 12 mo; no evidence of

disease > 36 mo Recurrence, 7 mo; dead of disease,

12 mo

Recurrence, 4 mo; dead of disease,

11 mo

No evidence of disease > 36 mo

No evidence of disease > 36 mo

No evidence of disease > 36 mo

No evidence of disease > 36 mo

Recurrence, 5 mo; dead of disease,

17 mo Recurrence, 11 mo; dead of disease,

25 mo

Recurrence, 7 mo; dead of disease,

9 mo No evidence of disease > 36 mo

Recurrence, 1 mo; dead, 1 mot No evidence of disease > 36 mo No evidence of disease > 36 mo

Recurrence, 11 mo; dead of disease, 28 mo

No evidence of disease > 36 mo Recurrence, 9 mo; dead of disease,

9 mo

* Dead of second primary lesion (malignant melanoma). t Dead of unrelated cause (myocardial infarction in both). $ Recurrence in opposite neck.

vohmo 130. Octobar 1975 463

Tarpley et al

TABLE III Comparison of Tumor Extent in the TABLE IV Preoperative Clinical Responses of Tumor Controt and Methotrexate-Treated Patients to Methotrexate in Thirty Patients

Patients Site Tumor Nodes Stage Response Number of Patients

Controls Oropharynx 13 T, 10 N, 12 I 4 Pharynx 3 T, 5 N, 17 II 8 Larynx 12 T, 13 N, 1 III 17

T, 2 N, 0 IV 1 Methotrexate- Oropharynx 13 T, 2 N, 14 I 1

treated Pharynx 4 T, 11 N, 11 II 12 Larynx 13 T, 15 N, 4 III 12

T, 2 N, 1 IV 5

TABLE V Laboratory index of Toxicity of Preoperative Methotrexate

Average Range

Lowest platelet count (per mm3)

Lowest white blood cell count (per mmJ)

Highest white blood cell count (per mm3)

Hepatic renal toxicity

164

5,660

12,220

None

(63-174)

(2,100-11,100)

(6,600-17,200)

TABLE VI Clinical index of Toxicity of Preoperative Methotrexate

Methotrexate- Treated

Index Controls Patients

Transfusions K = 4.0 R = 4.5 (O-15) (O-15)

Wound hematoma 2 0 Fistula 5 2 Wound infection 4 3 Total wound 9 5

complications Pneumonitis 9 4 Temperature > 38°C 15 13

METHOTREXATE

01 I I I I , I 1 1 I

0 4 a 12 18 20 24 28 32 36 TIME POST-OP IN MONTHS

Figure 1. Lite tabts ana&sts of postoperative d&ease- free lntervats tn the cm&at and methotrexate-treated pa- thts.

Positive response 23 (77%) Tumor only 13 Nodal only 4 Tumor and nodal 6

No response 7 (23%)

fourteen controls it was 6.78 months. The differ- ence is significant (p < 0.05). (Figure 2.)

Life table analysis of survival in the two groups is presented in Figure 3. The mean survival of the methotrexate-treated patients who thus far have died with disease was 16.4 months compared with 12.5 months in the controls. A trend toward longer survival in patients in whom recurrence develops after methotrexate treatment is suggested; how- ever, only eighteen of the treated patients have been followed up two years or longer compared with a follow-up interval of three years or longer for all controls. Thus, valid statistical comparison of the two groups by this parameter must await completion of the follow-up period in the treated group. (Figure 4.)

Comments

The goal of the use of methotrexate as an adju- vant in the surgical treatment of epidermoid carci- noma of the head and neck was to improve both recurrence and survival rates. The data show that there was no difference in recurrence rates com- pared with those in retrospective controls, but the postoperative disease-free interval was longer in the treated patients in whom recurrences devel- oped. Survival in the two groups did not differ sig- nificantly; however, there was a trend toward a longer survival in the treated patients who eventu- ally died of recurrent tumor.

These two observations consider different as- pects of the clinical course of patients after treat- ment. Thus, although methotrexate did not im- prove the cure rate, it appeared to change the dy- namics of tumor recurrence. At this dose level, methotrexate did not eradicate residual tumor, but it appeared to retard the growth rate of tumor that persisted after operation. Immunologic reac- tivity was not monitored in the postoperative in- terval in patients who received methotrexate after operation. However, correlations between immu- nologic reactivity and clinical course and the pre- viously demonstrated immunosuppressive effects

484 lho Amerkan Journal ol Surgery

Methotrexate in Epidermoid Carcinoma

MTX VS CDNT

t-2.066

df = 27

P<O.oS

.

. .

- x = 10.134

l 9.0 SEM-1.37 .

N- 15

. . . w x-6.70

l l . . . . SEM - 0.02

. . . N- 14

.

METMOTREXAT~ CONTROL

GROUP GROUP

Ft#ure 2. Compartson of the post@erattve iniervats be- fom tumor recwkcB h ftftaen conttvl and fourteen methotrexMe-treated pattents tn whoni recurkences havb developed.

of methotrexate provoke the speculation that the doses of methotrexate used postoperatively had a deleterious effect by suppressing immune compe- tence while failing to eradicate residual tumor.

The major conclusion of this study is that pa- tients with head and neck carcinoma, despite their relatively poor nutrition and susceptibility to post- operative pneumonia, undergo tumor resection without increased postoperative morbidity after high dose preoperative methotrexate therapy. The adjuvant did not increase the incidence of local in- fection, wound complications, or systemic infec- tion. This contrasts sharply with the morbidity of preoperative radiation therapy reported in several trials. These results warrant a determination of the adjunctive effect of other agents when used preoperatively; alone or in combination, which have a therapeutic effect on epidermoid carcino- ma.

Summary

Thirty patients with operable epidermoid carci- noma of the head and neck were treated with in- travenous high dose methotrexate and leucovorin rescue prior to resection. Their clinical courses were compared with those of thirty randomly se- lected patients matched for tumor site and clinical stage who were treated by surgery alone.

No medical or surgical complications associated with methotrexate were encountered. An objective

0 4 a 12 16 .ZO 24 26 32 36 TIME POST-OP IN MONTiiS

FIgwe 3. Life tabts anatysts of po&toperattve survtval In control and methotrexate-treated pattsnis.

24

r

20-

Y 5 16-

E”

r

E IZ-

ii

;;

i 0- F

. .

.

.

- X= 16.4

SEM = 2.1 .

N=7

.

.

.

.

.

.

: I= 12.5

. SEM = 1.73

N- 10

. .

.

4

t

.

METHOTREXATE CONTROL

TOTAL FOLLOWED TOTAL FOLLOWED

N- 16 N-36

Fwrre 4. Comparfson of the posto#eratlve interval befiwe death of the ten controt and seven methotrexate-treateU path?nts who have d&d.

decregse. in tumor size (primary lesion or nodal metastases) was noted prior to resection in twenty- three patients (77 per cent). The number of recur- rences in the two groups was similar. However, there was a significantly greater disease-free inter- val in the methotrexate-treated patients (p < 0.05). No significant differences in survival have been noted to date between the two groups. In view of the absence of complications, the regres- sions in tumor size, and the increase in postopera- tive disease-free interval in this trial, evaluation as preoperative adjuvants of higher doses of metho- trexate and of other chemotherapeutic agents in combination with methotrexate appears warrant- ed.

vohmm 130. ociobu 1975 485

Tarpley et al

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488 The Amrksn Journal of Suqery