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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1157811 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type& ?& H  H0 F, E
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 $ f0 `* p7 P: u) }, O
+ Author Affiliations. Q4 b' l8 [$ V2 t$ m0 C

7 N0 F7 b  H6 }4 M1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ' Q: U: K6 Y* E6 O1 L* H; e$ a
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 e; y, `1 g4 P5 Q: n5 f: U& D3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan   ~& B5 c8 k; ]+ ]" Y. t: A) Q: r0 B
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 7 W4 [/ _" _1 {4 \9 Z7 m2 j
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
3 ~$ L( N' _5 h  s, \6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
( F! E( V$ W! h' E8 h1 X0 s. j5 b7Kinki University School of Medicine, Osaka 589-8511, Japan 0 R5 b, b* W1 z. d) j* K
8Izumi Municipal Hospital, Osaka 594-0071, Japan
) S, m, W0 E& U, f9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
  e, x0 ?3 G3 o/ P, @1 H  [4 A4 hCorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp   ^! q5 R7 k/ P9 ?1 c9 H
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type. 5 c  A( `, g6 y. Z0 D
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type
2 J& m! |* B4 [8 ?
5 R" \- [' Y6 [. k# d' n# DAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato ) x; `6 {/ c* Y) y9 ~5 E6 H9 ]
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Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    `) w8 D. Z+ W7 X7 g$ @0 n4 x( z

. q; z7 N1 f! q( OPublished online on: Thursday, December 1, 2011
4 A, `3 \! x: ~+ J, ]5 [, b7 W7 ]; @' E# f! ?& c$ }, T# j" T
Doi: 10.3892/ol.2011.507
# ]: b; T' b' y6 W! j) U
7 l! {/ p/ U. t% i/ v  \1 IPages: 405-410
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9 e, e4 g) R( K7 i9 O9 O. a1 a$ V9 S' X* sAbstract:
% p5 Y( ?: I% ^! T% c5 [' BS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.) T; b' o2 R, g5 e( V
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population
# w% Y  ~& D6 E% F- a6 Y- C) _, @F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 # c& ]* w4 E' F; k
+ Author Affiliations# C* p" B4 o3 O! p! X) u4 F
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu 3 F! @7 ^3 m; ?( \8 Z
2Department of Thoracic Surgery, Kyoto University, Kyoto ) W! @0 c& K& {* j+ g
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
0 K7 s+ C+ t% o5 Q# n" M- d% |  @&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp , I+ d6 }9 ?% q& P# s- N0 l
Received September 3, 2010. 5 v# l. E6 t! k! J) c  a
Revision received November 11, 2010.
: _+ c7 x) Z( J" _5 w; AAccepted November 17, 2010. : w( D1 K8 E& o7 s* a4 U
Abstract4 h: C0 l" C; a* Z3 u, W
Background: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed.
) j( g. i# e, I& pPatients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes. 7 n, c9 m/ _8 r
Results: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. % @% i& T+ ~$ E2 x8 d/ D. y
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. / |6 S5 C. u* \  h7 e! j! t, l
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。$ p, r9 }3 b5 b7 |/ U* g
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?
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老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy9 g2 K8 H- `% Z" p" N7 o; m
http://clinicaltrials.gov/ct2/show/NCT01523587" e) y" v( N$ h: v
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC/ v7 {+ W. v8 Y  D: y* q3 H
http://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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  |2 K/ ~( Z/ q8 Y& m从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。& s. a7 L0 r4 h4 D  z
至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦

5 Q. E0 w) u' m  {. W3 M6 _没有副作用是第一追求,效果显著是第二追求。
" M" N" I  h5 e: y) Y" |不错。

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