177 655
656
Enhancement of cytotoxic activity of mediastinal lymphnodes by trans-tracheal injection to the subcarinal lymphnode of recombinant Interleukin-2 (rIL-2). Kazuhiro Tani, Soji Namikewa, Minoru Kusagawa Department of Thoracic Surgery, Mie University School of Medicine, Mie, Japan To enhance the cytotoxic activity of mediastinal lymphwe have nodes of the patients with lung cancer, using injected rIL-2 into the subcarinal lymphnode bronchoscopic needle 2 or 4 days before radical operations. 18 patients received trans-tracheal injection (2@*105 units) and/or intravenous administration (10*105 units/day) of rIL-2 for 4 days. Wediastinal lymphnodes resected at the operations were mesured for natural killer(NK) and Lymphokine-activated killer(LAK) activity of lymphcytes employing 51Cr release assay. Control patients (n=6) without the rIL-2 treatment represented low activity (NK=1.9%,LAK=0.5%). Patients receiving single trans-tracheal injection of at the rlL-2 revealed enhanced cytotoxic activity second day after injection (NK=E.lL,LAK=3.3~~), followed by decreased LAK activity at the fourth day (NK=7.6%, LAK=Z.O%). Patients receiving only intravenous revealed low administration of rIL-2 for 4 days cytotoxic activity (NK-7.85,LAK:Z.OX). Patients treated with a combination of trans-tracheal and intravenous administration of rIL-2 revealed the most potent cytoWe conclude from toxic activity (NK=18.3%,LAK=7.6%). these results that the combination of trans-tracheal and intravenous administration of rIL-2 is an effective therapy to kill micrometastatic cancer cells of which of opposite side were mediastinal lymphnodes undetected preoperatively.
657
Tr..tm.nt
on 561
by Traditional 2h.w
Lun.
co...
Chin... Ghan
Of Lung
C.nc.r
l*dlcln.
Ruirheng
Dept. of Tumor Rereerch Guanozhou College of TradItional Chin... Ifad. CHllfR Lung cancer 1. rePIdly incresrlng in the *orId. GuangZhou ie one of the high incidence areas. rhere he. Increased from 25. 42.11100.000 In 1981.Ve have sccunulatrd 561 6JlOO.OOO ln 1876 c.... of lung c.nc.r treated based on the differentiation of
to
.s!mnom. and
elgn..
P.thoIow
1*ich
have
beon
prowed
by
evtolo~y
or
snd X P.Y. Rmng 581 a.... 402 o.... IP. ml... 159 old,.nd the oldeet we 87. 0.1.. fa*sl... The The P.rc.ntae. of the high lncldenc. ~lro”~ bctteeen 50 to 58 yeer. old .I* 48.1%. POeltiVe coincidence ret. by X P.Y teet we. 13.7X. The ewtum emear and the euwortinp ceil. W. 38.1% and 59.6% r..P.CtIV.IY. The tu.wr<3cm---19.OX>7cm---28.9~. commonlv eeen 3
!m”“g..t*(I. 17Y..P.
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T-her. 44.4Xof
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In hietopstholosy
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cell
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and
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Pulmonum ea. 3.11. of the four method. of TOM -.x.“in.t,on. .ho*rd Th. .o.lv.i. that wwl. tow”. we. 76.31. thick and OP...Y fur we. 67. 41 subllnoual green colour tendon. we. 81.01. There me marked dlfferenc. in PC 0.01 conpared with normel pereon.. There we. c.nc.r
cell
wee
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15.21:
and
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,
ei9niflc.nce MterI.Ie of d.t.rmln.tion wwtom.
torln
and
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33.1X.
for
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of th. tr..tm.Bnt based eion.. There were four
obeeruation.
pr.cL.. on
d.t.
type.: .t.~n.tion
34.01.both
stagnation
deficiency
of phlegm
due
to deficiency
of
wr.
comtonlv
In the
P.."
In the
lung energy mt.phs.e
of vital lung type and
for
differentistlon
energy
.nd
of
of
Phleg,,
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type
18.51
and
phlegm
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two
late
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Th.
The the
type h..t type.
tr..t,..,,t
01)
treated bv chemtherepv end rediotherepv those rho M.P. in.fflctlvelY sea 130 C.888. In which lvlrked effectlv. we. 4.31, .ff.ctlv. 14s 58. 31. The tot.1 eff.EtlV. ret. u.. 81. II The eurvivel Deriod of the Petlent. were that ROP. then on. yeer ,... 5% 3X. more then two veer. we. I. 27.. mop. than three yeer. I... 4X. and the were~e rurvival period MB 11 month.. The wretlue ret.. of .q”.ID”B cell cerci~me end eden,,,.. we?. high 39154. 40155. Wo effect for undliferentlated center cell. It we. better then combined chemotherepy. P
652
A phase
photodynnmic
II pmtientr with
inoperable
therapy ?? m8ll
non
may
cell
in
lung
Cancer. G&&&j& P. Baas. N. van Zandwijk. Department of Medical Oncology. The Netherlands Cancer Institute - Antoni van Lccuwenhoekhuis. Amsterdam - the Netherlands.
Twenty-six patients with inoperable non small cell lung cancer (NSCLC) were treated with photodynamk therapy [PDTj. InteMitial tumour Uhuntnation was performed 48 hours after Photofrin II injection, using a cylindrtcal diffuser laser fibre to transmtt red light of 830 nm. wavelength from an Argon-dye laser.A>50?6 impmWMntoftheainvaylrrmenwasregani~as a partial response. For a complete response, negative histology and/or cytology was required. Median follow-up was 8 months.
mhdea
tomow
~0i0mc
n complete rerponee Significant rerponre NO remponse Laser
Of
D.t.rnin.tion
bllure
aala
15 0 11 2 2
11
tote1 26
00
2”
<2cm3
10 1
10 12
All treatments were well tolerated and grade II skin photosensitivIty was seen in 4 patients. PDT could achieve complete responses in patients with small tumour volume. In large tumour volume. local palliation was obtained in the majority of patients. Four pattents died because of puhnonary haemorrhage during follow-up (1.5-8 months), and this was probably related to extralumenal disease. Further study is warranted to define the exact value of PDT in the palltation of locally advanced disease.
A RANDOMIZED STUDY OF A NEW BRM -- SAPYLIN COMPARING WITH CHEMOTHERAPY TREATED ON CANCEROUS PLEUPAL EFFUSION - L. Mei-lin, Z. Jia-mei et al 104 cases of canerous pleural effusion proved by cytology or histology were randomized into 2 groups, 52 cases each, group A, Sapylin was injected into the pleural cavity after fluid tapping,which is a new biological response modifier, a kind of streptococus product, also a simulator of OK 432 and made by Shanghai Institute of Pharmaceutical Industry. Group B chemotherapy regime of MFT(Mitomycin + 5Fu + Thiotepa) or CD(CTX + DDP) was used by the same route. The response rate of group a was 88.5%(46/52), CR was of 36.5% (19/52). Mean time to response was 9.7 days, 72.3% of cases showed its response at the dose of